Found 47 hits with Last Name = 'gibbs' and Initial = 'bs' Target/Host
(Institution) | Ligand | Target/Host
Links | Ligand
Links | Trg + Lig
Links | Ki
nM | ΔG°
kJ/mole | IC50
nM | Kd
nM | EC50/IC50
nM | koff
s-1 | kon
M-1s-1 | pH | Temp
°C |
|---|
Protein farnesyltransferase subunit beta/geranylgeranyltransferase type-1 subunit alpha
(Rattus norvegicus-Rattus norvegicus (rat)) | BDBM50060140
(CHEMBL115943 | [(S)-1-{(4-Benzyloxy-benzyl)-[(2-cy...)Show SMILES O=C(CN(Cc1ccc(OCc2ccccc2)cc1)C(=O)[C@H](Cc1cnc[nH]1)NC(=O)OCc1ccccc1)NCC(C#N)c1ccccc1 Show InChI InChI=1S/C39H38N6O5/c40-21-33(32-14-8-3-9-15-32)22-42-37(46)25-45(24-29-16-18-35(19-17-29)49-26-30-10-4-1-5-11-30)38(47)36(20-34-23-41-28-43-34)44-39(48)50-27-31-12-6-2-7-13-31/h1-19,23,28,33,36H,20,22,24-27H2,(H,41,43)(H,42,46)(H,44,48)/t33?,36-/m0/s1 | PDB
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UniProtKB/SwissProt
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| n/a | n/a | 2 | n/a | n/a | n/a | n/a | n/a | n/a |
Warner-Lambert Company
Curated by ChEMBL
| Assay Description
In vitro inhibition of rat farnesyltransferase. |
J Med Chem 40: 3319-22 (1997)
Article DOI: 10.1021/jm970470c
BindingDB Entry DOI: 10.7270/Q2V69HQG |
More data for this
Ligand-Target Pair | |
Protein farnesyltransferase subunit beta/geranylgeranyltransferase type-1 subunit alpha
(Rattus norvegicus-Rattus norvegicus (rat)) | BDBM50060144
(CHEMBL325073 | [(S)-1-{(4-Benzyloxy-benzyl)-[((R)-...)Show SMILES C[C@H](Cc1ccccc1)NC(=O)CN(Cc1ccc(OCc2ccccc2)cc1)C(=O)[C@H](Cc1cnc[nH]1)NC(=O)OCc1ccccc1 Show InChI InChI=1S/C39H41N5O5/c1-29(21-30-11-5-2-6-12-30)42-37(45)25-44(24-31-17-19-35(20-18-31)48-26-32-13-7-3-8-14-32)38(46)36(22-34-23-40-28-41-34)43-39(47)49-27-33-15-9-4-10-16-33/h2-20,23,28-29,36H,21-22,24-27H2,1H3,(H,40,41)(H,42,45)(H,43,47)/t29-,36+/m1/s1 | PDB
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| n/a | n/a | 3 | n/a | n/a | n/a | n/a | n/a | n/a |
Warner-Lambert Company
Curated by ChEMBL
| Assay Description
In vitro inhibition of rat farnesyltransferase. |
J Med Chem 40: 3319-22 (1997)
Article DOI: 10.1021/jm970470c
BindingDB Entry DOI: 10.7270/Q2V69HQG |
More data for this
Ligand-Target Pair | |
Protein farnesyltransferase subunit beta/geranylgeranyltransferase type-1 subunit alpha
(Rattus norvegicus-Rattus norvegicus (rat)) | BDBM50060141
(CHEMBL431440 | [(S)-1-{(4-Benzyloxy-benzyl)-[(2-me...)Show SMILES CC(C)(CNC(=O)CN(Cc1ccc(OCc2ccccc2)cc1)C(=O)[C@H](Cc1cnc[nH]1)NC(=O)OCc1ccccc1)c1ccccc1 Show InChI InChI=1S/C40H43N5O5/c1-40(2,33-16-10-5-11-17-33)28-42-37(46)25-45(24-30-18-20-35(21-19-30)49-26-31-12-6-3-7-13-31)38(47)36(22-34-23-41-29-43-34)44-39(48)50-27-32-14-8-4-9-15-32/h3-21,23,29,36H,22,24-28H2,1-2H3,(H,41,43)(H,42,46)(H,44,48)/t36-/m0/s1 | PDB
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Warner-Lambert Company
Curated by ChEMBL
| Assay Description
In vitro inhibition of rat farnesyltransferase. |
J Med Chem 40: 3319-22 (1997)
Article DOI: 10.1021/jm970470c
BindingDB Entry DOI: 10.7270/Q2V69HQG |
More data for this
Ligand-Target Pair | |
Protein farnesyltransferase subunit beta/geranylgeranyltransferase type-1 subunit alpha
(Rattus norvegicus-Rattus norvegicus (rat)) | BDBM50060145
(CHEMBL115669 | [(S)-1-{(4-Benzyloxy-benzyl)-[((S)-...)Show SMILES C[C@H](CNC(=O)CN(Cc1ccc(OCc2ccccc2)cc1)C(=O)[C@H](Cc1cnc[nH]1)NC(=O)OCc1ccccc1)c1ccccc1 Show InChI InChI=1S/C39H41N5O5/c1-29(33-15-9-4-10-16-33)22-41-37(45)25-44(24-30-17-19-35(20-18-30)48-26-31-11-5-2-6-12-31)38(46)36(21-34-23-40-28-42-34)43-39(47)49-27-32-13-7-3-8-14-32/h2-20,23,28-29,36H,21-22,24-27H2,1H3,(H,40,42)(H,41,45)(H,43,47)/t29-,36+/m1/s1 | PDB
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| n/a | n/a | 5 | n/a | n/a | n/a | n/a | n/a | n/a |
Warner-Lambert Company
Curated by ChEMBL
| Assay Description
In vitro inhibition of rat farnesyltransferase. |
J Med Chem 40: 3319-22 (1997)
Article DOI: 10.1021/jm970470c
BindingDB Entry DOI: 10.7270/Q2V69HQG |
More data for this
Ligand-Target Pair | |
Protein farnesyltransferase subunit beta/geranylgeranyltransferase type-1 subunit alpha
(Rattus norvegicus-Rattus norvegicus (rat)) | BDBM50060149
(CHEMBL112512 | [(S)-1-{(4-Benzyloxy-benzyl)-[(2-ph...)Show SMILES CCC(CNC(=O)CN(Cc1ccc(OCc2ccccc2)cc1)C(=O)[C@H](Cc1cnc[nH]1)NC(=O)OCc1ccccc1)c1ccccc1 Show InChI InChI=1S/C40H43N5O5/c1-2-33(34-16-10-5-11-17-34)23-42-38(46)26-45(25-30-18-20-36(21-19-30)49-27-31-12-6-3-7-13-31)39(47)37(22-35-24-41-29-43-35)44-40(48)50-28-32-14-8-4-9-15-32/h3-21,24,29,33,37H,2,22-23,25-28H2,1H3,(H,41,43)(H,42,46)(H,44,48)/t33?,37-/m0/s1 | PDB
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| n/a | n/a | 5 | n/a | n/a | n/a | n/a | n/a | n/a |
Warner-Lambert Company
Curated by ChEMBL
| Assay Description
In vitro inhibition of rat farnesyltransferase. |
J Med Chem 40: 3319-22 (1997)
Article DOI: 10.1021/jm970470c
BindingDB Entry DOI: 10.7270/Q2V69HQG |
More data for this
Ligand-Target Pair | |
Protein farnesyltransferase subunit beta/geranylgeranyltransferase type-1 subunit alpha
(Rattus norvegicus-Rattus norvegicus (rat)) | BDBM50060139
(CHEMBL326352 | [(S)-1-((4-Benzyloxy-benzyl)-{[(1-p...)Show SMILES O=C(CN(Cc1ccc(OCc2ccccc2)cc1)C(=O)[C@H](Cc1cnc[nH]1)NC(=O)OCc1ccccc1)NCC1(CCC1)c1ccccc1 Show InChI InChI=1S/C41H43N5O5/c47-38(43-29-41(21-10-22-41)34-15-8-3-9-16-34)26-46(25-31-17-19-36(20-18-31)50-27-32-11-4-1-5-12-32)39(48)37(23-35-24-42-30-44-35)45-40(49)51-28-33-13-6-2-7-14-33/h1-9,11-20,24,30,37H,10,21-23,25-29H2,(H,42,44)(H,43,47)(H,45,49)/t37-/m0/s1 | PDB
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Warner-Lambert Company
Curated by ChEMBL
| Assay Description
In vitro inhibition of rat farnesyltransferase. |
J Med Chem 40: 3319-22 (1997)
Article DOI: 10.1021/jm970470c
BindingDB Entry DOI: 10.7270/Q2V69HQG |
More data for this
Ligand-Target Pair | |
Protein farnesyltransferase subunit beta/geranylgeranyltransferase type-1 subunit alpha
(Rattus norvegicus-Rattus norvegicus (rat)) | BDBM50060146
(CHEMBL407445 | [(S)-1-((4-Benzyloxy-benzyl)-{[(1-p...)Show SMILES O=C(CN(Cc1ccc(OCc2ccccc2)cc1)C(=O)[C@H](Cc1cnc[nH]1)NC(=O)OCc1ccccc1)NCC1(CC1)c1ccccc1 Show InChI InChI=1S/C40H41N5O5/c46-37(42-28-40(20-21-40)33-14-8-3-9-15-33)25-45(24-30-16-18-35(19-17-30)49-26-31-10-4-1-5-11-31)38(47)36(22-34-23-41-29-43-34)44-39(48)50-27-32-12-6-2-7-13-32/h1-19,23,29,36H,20-22,24-28H2,(H,41,43)(H,42,46)(H,44,48)/t36-/m0/s1 | PDB
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| n/a | n/a | 7 | n/a | n/a | n/a | n/a | n/a | n/a |
Warner-Lambert Company
Curated by ChEMBL
| Assay Description
In vitro inhibition of rat farnesyltransferase. |
J Med Chem 40: 3319-22 (1997)
Article DOI: 10.1021/jm970470c
BindingDB Entry DOI: 10.7270/Q2V69HQG |
More data for this
Ligand-Target Pair | |
Protein farnesyltransferase subunit beta/geranylgeranyltransferase type-1 subunit alpha
(Rattus norvegicus-Rattus norvegicus (rat)) | BDBM50060138
(CHEMBL324827 | [(S)-1-{(4-Benzyloxy-benzyl)-[(2-ph...)Show SMILES CC(CNC(=O)CN(Cc1ccc(OCc2ccccc2)cc1)C(=O)[C@H](Cc1cnc[nH]1)NC(=O)OCc1ccccc1)c1ccccc1 Show InChI InChI=1S/C39H41N5O5/c1-29(33-15-9-4-10-16-33)22-41-37(45)25-44(24-30-17-19-35(20-18-30)48-26-31-11-5-2-6-12-31)38(46)36(21-34-23-40-28-42-34)43-39(47)49-27-32-13-7-3-8-14-32/h2-20,23,28-29,36H,21-22,24-27H2,1H3,(H,40,42)(H,41,45)(H,43,47)/t29?,36-/m0/s1 | PDB
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| n/a | n/a | 8 | n/a | n/a | n/a | n/a | n/a | n/a |
Warner-Lambert Company
Curated by ChEMBL
| Assay Description
In vitro inhibition of rat farnesyltransferase. |
J Med Chem 40: 3319-22 (1997)
Article DOI: 10.1021/jm970470c
BindingDB Entry DOI: 10.7270/Q2V69HQG |
More data for this
Ligand-Target Pair | |
Protein farnesyltransferase subunit beta/geranylgeranyltransferase type-1 subunit alpha
(Rattus norvegicus-Rattus norvegicus (rat)) | BDBM50060150
(CHEMBL114281 | [(S)-1-{(4-Benzyloxy-benzyl)-[((R)-...)Show SMILES C[C@@H](CNC(=O)CN(Cc1ccc(OCc2ccccc2)cc1)C(=O)[C@H](Cc1cnc[nH]1)NC(=O)OCc1ccccc1)c1ccccc1 Show InChI InChI=1S/C39H41N5O5/c1-29(33-15-9-4-10-16-33)22-41-37(45)25-44(24-30-17-19-35(20-18-30)48-26-31-11-5-2-6-12-31)38(46)36(21-34-23-40-28-42-34)43-39(47)49-27-32-13-7-3-8-14-32/h2-20,23,28-29,36H,21-22,24-27H2,1H3,(H,40,42)(H,41,45)(H,43,47)/t29-,36-/m0/s1 | PDB
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Warner-Lambert Company
Curated by ChEMBL
| Assay Description
In vitro inhibition of rat farnesyltransferase. |
J Med Chem 40: 3319-22 (1997)
Article DOI: 10.1021/jm970470c
BindingDB Entry DOI: 10.7270/Q2V69HQG |
More data for this
Ligand-Target Pair | |
Protein farnesyltransferase subunit beta/geranylgeranyltransferase type-1 subunit alpha
(Rattus norvegicus-Rattus norvegicus (rat)) | BDBM50060142
(CHEMBL326127 | [(S)-1-((4-Benzyloxy-benzyl)-{[(1-p...)Show SMILES O=C(CN(Cc1ccc(OCc2ccccc2)cc1)C(=O)[C@H](Cc1cnc[nH]1)NC(=O)OCc1ccccc1)NCC1(CCCC1)c1ccccc1 Show InChI InChI=1S/C42H45N5O5/c48-39(44-30-42(22-10-11-23-42)35-16-8-3-9-17-35)27-47(26-32-18-20-37(21-19-32)51-28-33-12-4-1-5-13-33)40(49)38(24-36-25-43-31-45-36)46-41(50)52-29-34-14-6-2-7-15-34/h1-9,12-21,25,31,38H,10-11,22-24,26-30H2,(H,43,45)(H,44,48)(H,46,50)/t38-/m0/s1 | PDB
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| n/a | n/a | 17 | n/a | n/a | n/a | n/a | n/a | n/a |
Warner-Lambert Company
Curated by ChEMBL
| Assay Description
In vitro inhibition of rat farnesyltransferase. |
J Med Chem 40: 3319-22 (1997)
Article DOI: 10.1021/jm970470c
BindingDB Entry DOI: 10.7270/Q2V69HQG |
More data for this
Ligand-Target Pair | |
Protein farnesyltransferase subunit beta/geranylgeranyltransferase type-1 subunit alpha
(Rattus norvegicus-Rattus norvegicus (rat)) | BDBM50060148
(CHEMBL325331 | [(S)-1-{(4-Benzyloxy-benzyl)-[(2-ph...)Show SMILES CCCC(CNC(=O)CN(Cc1ccc(OCc2ccccc2)cc1)C(=O)[C@H](Cc1cnc[nH]1)NC(=O)OCc1ccccc1)c1ccccc1 Show InChI InChI=1S/C41H45N5O5/c1-2-12-35(34-17-10-5-11-18-34)24-43-39(47)27-46(26-31-19-21-37(22-20-31)50-28-32-13-6-3-7-14-32)40(48)38(23-36-25-42-30-44-36)45-41(49)51-29-33-15-8-4-9-16-33/h3-11,13-22,25,30,35,38H,2,12,23-24,26-29H2,1H3,(H,42,44)(H,43,47)(H,45,49)/t35?,38-/m0/s1 | PDB
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Warner-Lambert Company
Curated by ChEMBL
| Assay Description
In vitro inhibition of rat farnesyltransferase. |
J Med Chem 40: 3319-22 (1997)
Article DOI: 10.1021/jm970470c
BindingDB Entry DOI: 10.7270/Q2V69HQG |
More data for this
Ligand-Target Pair | |
Protein farnesyltransferase subunit beta/geranylgeranyltransferase type-1 subunit alpha
(Homo sapiens (Human)) | BDBM50081229
(10-(tert-butyl)-2,6-dimethyl-(6E,10Z)-2,6,10-dodec...)Show SMILES [#6]\[#6](-[#6])=[#6]\[#6]-[#6]\[#6](-[#6])=[#6]\[#6]-[#6]\[#6](=[#6]\[#6]-[#8]P([#8-])(=O)[#8]P([#8-])([#8-])=O)C([#6])([#6])[#6] Show InChI InChI=1S/C18H34O7P2/c1-15(2)9-7-10-16(3)11-8-12-17(18(4,5)6)13-14-24-27(22,23)25-26(19,20)21/h9,11,13H,7-8,10,12,14H2,1-6H3,(H,22,23)(H2,19,20,21)/p-3/b16-11+,17-13- | PDB
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| n/a | n/a | 31 | n/a | n/a | n/a | n/a | n/a | n/a |
Parke-Davis Pharmaceutical Research
Curated by ChEMBL
| Assay Description
Inhibition of recombinant farnesyltransferase (mFTase) in scintillation proximity assay |
J Med Chem 42: 3800-8 (1999)
BindingDB Entry DOI: 10.7270/Q2Z89D3S |
More data for this
Ligand-Target Pair | |
Protein farnesyltransferase subunit beta/geranylgeranyltransferase type-1 subunit alpha
(Rattus norvegicus-Rattus norvegicus (rat)) | BDBM50060152
(CHEMBL112879 | [(S)-1-{(4-Benzyloxy-benzyl)-[(2-et...)Show SMILES CCC(CC)(CNC(=O)CN(Cc1ccc(OCc2ccccc2)cc1)C(=O)[C@H](Cc1cnc[nH]1)NC(=O)OCc1ccccc1)c1ccccc1 Show InChI InChI=1S/C42H47N5O5/c1-3-42(4-2,35-18-12-7-13-19-35)30-44-39(48)27-47(26-32-20-22-37(23-21-32)51-28-33-14-8-5-9-15-33)40(49)38(24-36-25-43-31-45-36)46-41(50)52-29-34-16-10-6-11-17-34/h5-23,25,31,38H,3-4,24,26-30H2,1-2H3,(H,43,45)(H,44,48)(H,46,50)/t38-/m0/s1 | PDB
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Warner-Lambert Company
Curated by ChEMBL
| Assay Description
In vitro inhibition of rat farnesyltransferase. |
J Med Chem 40: 3319-22 (1997)
Article DOI: 10.1021/jm970470c
BindingDB Entry DOI: 10.7270/Q2V69HQG |
More data for this
Ligand-Target Pair | |
Protein farnesyltransferase subunit beta/geranylgeranyltransferase type-1 subunit alpha
(Rattus norvegicus-Rattus norvegicus (rat)) | BDBM50060143
(CHEMBL324345 | [(S)-1-{(4-Benzyloxy-benzyl)-[((S)-...)Show SMILES C[C@@H](Cc1ccccc1)NC(=O)CN(Cc1ccc(OCc2ccccc2)cc1)C(=O)[C@H](Cc1cnc[nH]1)NC(=O)OCc1ccccc1 Show InChI InChI=1S/C39H41N5O5/c1-29(21-30-11-5-2-6-12-30)42-37(45)25-44(24-31-17-19-35(20-18-31)48-26-32-13-7-3-8-14-32)38(46)36(22-34-23-40-28-41-34)43-39(47)49-27-33-15-9-4-10-16-33/h2-20,23,28-29,36H,21-22,24-27H2,1H3,(H,40,41)(H,42,45)(H,43,47)/t29-,36-/m0/s1 | PDB
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Warner-Lambert Company
Curated by ChEMBL
| Assay Description
In vitro inhibition of rat farnesyltransferase. |
J Med Chem 40: 3319-22 (1997)
Article DOI: 10.1021/jm970470c
BindingDB Entry DOI: 10.7270/Q2V69HQG |
More data for this
Ligand-Target Pair | |
Protein farnesyltransferase subunit beta/geranylgeranyltransferase type-1 subunit alpha
(Rattus norvegicus-Rattus norvegicus (rat)) | BDBM50059857
(CHEMBL102955 | [(S)-1-[(4-Benzyloxy-benzyl)-(phene...)Show SMILES O=C(CN(Cc1ccc(OCc2ccccc2)cc1)C(=O)[C@H](Cc1cnc[nH]1)NC(=O)OCc1ccccc1)NCCc1ccccc1 Show InChI InChI=1S/C38H39N5O5/c44-36(40-21-20-29-10-4-1-5-11-29)25-43(24-30-16-18-34(19-17-30)47-26-31-12-6-2-7-13-31)37(45)35(22-33-23-39-28-41-33)42-38(46)48-27-32-14-8-3-9-15-32/h1-19,23,28,35H,20-22,24-27H2,(H,39,41)(H,40,44)(H,42,46)/t35-/m0/s1 | PDB
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| n/a | n/a | 62 | n/a | n/a | n/a | n/a | n/a | n/a |
Warner-Lambert Company
Curated by ChEMBL
| Assay Description
In vitro inhibition of rat farnesyltransferase. |
J Med Chem 40: 3319-22 (1997)
Article DOI: 10.1021/jm970470c
BindingDB Entry DOI: 10.7270/Q2V69HQG |
More data for this
Ligand-Target Pair | |
Protein farnesyltransferase subunit beta/geranylgeranyltransferase type-1 subunit alpha
(Rattus norvegicus-Rattus norvegicus (rat)) | BDBM50059876
(CHEMBL217423 | [(S)-1-[(S)-1-{(S)-2-Benzyloxy-1-[(...)Show SMILES C[C@@H](NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](COCc1ccccc1)NC(=O)[C@H](Cc1ccc(OCc2ccccc2)cc1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)OCc1ccccc1)C(N)=O Show InChI InChI=1S/C54H57N9O9/c1-35(49(55)64)59-50(65)46(26-40-28-57-44-20-12-11-19-43(40)44)61-53(68)48(33-70-30-37-13-5-2-6-14-37)62-51(66)45(25-36-21-23-42(24-22-36)71-31-38-15-7-3-8-16-38)60-52(67)47(27-41-29-56-34-58-41)63-54(69)72-32-39-17-9-4-10-18-39/h2-24,28-29,34-35,45-48,57H,25-27,30-33H2,1H3,(H2,55,64)(H,56,58)(H,59,65)(H,60,67)(H,61,68)(H,62,66)(H,63,69)/t35-,45+,46+,47+,48+/m1/s1 | PDB
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| n/a | n/a | 76 | n/a | n/a | n/a | n/a | n/a | n/a |
Warner-Lambert Company
Curated by ChEMBL
| Assay Description
In vitro inhibition of rat farnesyltransferase. |
J Med Chem 40: 3319-22 (1997)
Article DOI: 10.1021/jm970470c
BindingDB Entry DOI: 10.7270/Q2V69HQG |
More data for this
Ligand-Target Pair | |
GTPase HRas
(Homo sapiens (Human)) | BDBM50060139
(CHEMBL326352 | [(S)-1-((4-Benzyloxy-benzyl)-{[(1-p...)Show SMILES O=C(CN(Cc1ccc(OCc2ccccc2)cc1)C(=O)[C@H](Cc1cnc[nH]1)NC(=O)OCc1ccccc1)NCC1(CCC1)c1ccccc1 Show InChI InChI=1S/C41H43N5O5/c47-38(43-29-41(21-10-22-41)34-15-8-3-9-16-34)26-46(25-31-17-19-36(20-18-31)50-27-32-11-4-1-5-12-32)39(48)37(23-35-24-42-30-44-35)45-40(49)51-28-33-13-6-2-7-14-33/h1-9,11-20,24,30,37H,10,21-23,25-29H2,(H,42,44)(H,43,47)(H,45,49)/t37-/m0/s1 | PDB
MMDB
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| n/a | n/a | 88 | n/a | n/a | n/a | n/a | n/a | n/a |
Warner-Lambert Company
Curated by ChEMBL
| Assay Description
Concentration required to inhibit 50% of the cultured colonies of H-Ras-Fcells . |
J Med Chem 40: 3319-22 (1997)
Article DOI: 10.1021/jm970470c
BindingDB Entry DOI: 10.7270/Q2V69HQG |
More data for this
Ligand-Target Pair | |
Protein farnesyltransferase subunit beta/geranylgeranyltransferase type-1 subunit alpha
(Homo sapiens (Human)) | BDBM50081234
(3-[(Z)-ethylidene]-7,11-dimethyl-(6E)-1,6,10-dodec...)Show SMILES [#6]\[#6](-[#6])=[#6]/[#6]-[#6]\[#6](-[#6])=[#6]\[#6]-[#6]\[#6](-[#6]=[#6])=[#6]\[#6]-[#8]P([#8-])(=O)[#8]P([#8-])([#8-])=O Show InChI InChI=1S/C16H28O7P2/c1-5-16(11-7-10-15(4)9-6-8-14(2)3)12-13-22-25(20,21)23-24(17,18)19/h5,8,10,12H,1,6-7,9,11,13H2,2-4H3,(H,20,21)(H2,17,18,19)/p-3/b15-10+,16-12+ | PDB
MMDB
Reactome pathway
KEGG
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antibodypedia
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| PubMed
| n/a | n/a | 173 | n/a | n/a | n/a | n/a | n/a | n/a |
Parke-Davis Pharmaceutical Research
Curated by ChEMBL
| Assay Description
Inhibition of recombinant farnesyltransferase (mFTase) in scintillation proximity assay |
J Med Chem 42: 3800-8 (1999)
BindingDB Entry DOI: 10.7270/Q2Z89D3S |
More data for this
Ligand-Target Pair | |
GTPase HRas
(Homo sapiens (Human)) | BDBM50060141
(CHEMBL431440 | [(S)-1-{(4-Benzyloxy-benzyl)-[(2-me...)Show SMILES CC(C)(CNC(=O)CN(Cc1ccc(OCc2ccccc2)cc1)C(=O)[C@H](Cc1cnc[nH]1)NC(=O)OCc1ccccc1)c1ccccc1 Show InChI InChI=1S/C40H43N5O5/c1-40(2,33-16-10-5-11-17-33)28-42-37(46)25-45(24-30-18-20-35(21-19-30)49-26-31-12-6-3-7-13-31)38(47)36(22-34-23-41-29-43-34)44-39(48)50-27-32-14-8-4-9-15-32/h3-21,23,29,36H,22,24-28H2,1-2H3,(H,41,43)(H,42,46)(H,44,48)/t36-/m0/s1 | PDB
MMDB
KEGG
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| n/a | n/a | 180 | n/a | n/a | n/a | n/a | n/a | n/a |
Warner-Lambert Company
Curated by ChEMBL
| Assay Description
Concentration required to inhibit 50% of the cultured colonies of H-Ras-Fcells . |
J Med Chem 40: 3319-22 (1997)
Article DOI: 10.1021/jm970470c
BindingDB Entry DOI: 10.7270/Q2V69HQG |
More data for this
Ligand-Target Pair | |
GTPase HRas
(Homo sapiens (Human)) | BDBM50060146
(CHEMBL407445 | [(S)-1-((4-Benzyloxy-benzyl)-{[(1-p...)Show SMILES O=C(CN(Cc1ccc(OCc2ccccc2)cc1)C(=O)[C@H](Cc1cnc[nH]1)NC(=O)OCc1ccccc1)NCC1(CC1)c1ccccc1 Show InChI InChI=1S/C40H41N5O5/c46-37(42-28-40(20-21-40)33-14-8-3-9-15-33)25-45(24-30-16-18-35(19-17-30)49-26-31-10-4-1-5-11-31)38(47)36(22-34-23-41-29-43-34)44-39(48)50-27-32-12-6-2-7-13-32/h1-19,23,29,36H,20-22,24-28H2,(H,41,43)(H,42,46)(H,44,48)/t36-/m0/s1 | PDB
MMDB
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PubMed
| n/a | n/a | 180 | n/a | n/a | n/a | n/a | n/a | n/a |
Warner-Lambert Company
Curated by ChEMBL
| Assay Description
Concentration required to inhibit 50% of the cultured colonies of H-Ras-Fcells . |
J Med Chem 40: 3319-22 (1997)
Article DOI: 10.1021/jm970470c
BindingDB Entry DOI: 10.7270/Q2V69HQG |
More data for this
Ligand-Target Pair | |
Protein farnesyltransferase subunit beta/geranylgeranyltransferase type-1 subunit alpha
(Homo sapiens (Human)) | BDBM50081235
(3-substituted farnesyl diphosphate analogue | 4-[(...)Show SMILES [#6]\[#6](-[#6])=[#6]\[#6]-[#6]\[#6](-[#6])=[#6]\[#6]-[#6]\[#6](-[#6]-[#6]=[#6])=[#6]\[#6]-[#8]P([#8-])(=O)[#8]P([#8-])([#8-])=O Show InChI InChI=1S/C17H30O7P2/c1-5-8-17(12-7-11-16(4)10-6-9-15(2)3)13-14-23-26(21,22)24-25(18,19)20/h5,9,11,13H,1,6-8,10,12,14H2,2-4H3,(H,21,22)(H2,18,19,20)/p-3/b16-11+,17-13+ | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
antibodypedia
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| KEGG
PC cid
PC sid
UniChem
Similars
| PubMed
| n/a | n/a | 189 | n/a | n/a | n/a | n/a | n/a | n/a |
Parke-Davis Pharmaceutical Research
Curated by ChEMBL
| Assay Description
Inhibition of recombinant farnesyltransferase (mFTase) in scintillation proximity assay |
J Med Chem 42: 3800-8 (1999)
BindingDB Entry DOI: 10.7270/Q2Z89D3S |
More data for this
Ligand-Target Pair | |
GTPase HRas
(Homo sapiens (Human)) | BDBM50060140
(CHEMBL115943 | [(S)-1-{(4-Benzyloxy-benzyl)-[(2-cy...)Show SMILES O=C(CN(Cc1ccc(OCc2ccccc2)cc1)C(=O)[C@H](Cc1cnc[nH]1)NC(=O)OCc1ccccc1)NCC(C#N)c1ccccc1 Show InChI InChI=1S/C39H38N6O5/c40-21-33(32-14-8-3-9-15-32)22-42-37(46)25-45(24-29-16-18-35(19-17-29)49-26-30-10-4-1-5-11-30)38(47)36(20-34-23-41-28-43-34)44-39(48)50-27-31-12-6-2-7-13-31/h1-19,23,28,33,36H,20,22,24-27H2,(H,41,43)(H,42,46)(H,44,48)/t33?,36-/m0/s1 | PDB
MMDB
KEGG
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PubMed
| n/a | n/a | 190 | n/a | n/a | n/a | n/a | n/a | n/a |
Warner-Lambert Company
Curated by ChEMBL
| Assay Description
Concentration required to inhibit 50% of the cultured colonies of H-Ras-Fcells . |
J Med Chem 40: 3319-22 (1997)
Article DOI: 10.1021/jm970470c
BindingDB Entry DOI: 10.7270/Q2V69HQG |
More data for this
Ligand-Target Pair | |
Protein farnesyltransferase subunit beta/geranylgeranyltransferase type-1 subunit alpha
(Homo sapiens (Human)) | BDBM50081227
(10-ethyl-2,6-dimethyl-(6E,10E)-2,6,10-dodecatriene...)Show SMILES [#6]-[#6]\[#6](-[#6]-[#6]\[#6]=[#6](/[#6])-[#6]-[#6]\[#6]=[#6](/[#6])-[#6])=[#6]/[#6]-[#8]P([#8-])(=O)[#8]P([#8-])([#8-])=O Show InChI InChI=1S/C16H30O7P2/c1-5-16(11-7-10-15(4)9-6-8-14(2)3)12-13-22-25(20,21)23-24(17,18)19/h8,10,12H,5-7,9,11,13H2,1-4H3,(H,20,21)(H2,17,18,19)/p-3/b15-10+,16-12+ | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
antibodypedia
GoogleScholar
AffyNet
| KEGG
PC cid
PC sid
UniChem
Similars
| PubMed
| n/a | n/a | 215 | n/a | n/a | n/a | n/a | n/a | n/a |
Parke-Davis Pharmaceutical Research
Curated by ChEMBL
| Assay Description
Inhibition of recombinant farnesyltransferase (mFTase) in scintillation proximity assay |
J Med Chem 42: 3800-8 (1999)
BindingDB Entry DOI: 10.7270/Q2Z89D3S |
More data for this
Ligand-Target Pair | |
Protein farnesyltransferase subunit beta/geranylgeranyltransferase type-1 subunit alpha
(Rattus norvegicus-Rattus norvegicus (rat)) | BDBM50060151
(CHEMBL408134 | [(S)-1-{(4-Benzyloxy-benzyl)-[(1,1-...)Show SMILES CC(C)(Cc1ccccc1)NC(=O)CN(Cc1ccc(OCc2ccccc2)cc1)C(=O)[C@H](Cc1cnc[nH]1)NC(=O)OCc1ccccc1 Show InChI InChI=1S/C40H43N5O5/c1-40(2,23-30-12-6-3-7-13-30)44-37(46)26-45(25-31-18-20-35(21-19-31)49-27-32-14-8-4-9-15-32)38(47)36(22-34-24-41-29-42-34)43-39(48)50-28-33-16-10-5-11-17-33/h3-21,24,29,36H,22-23,25-28H2,1-2H3,(H,41,42)(H,43,48)(H,44,46)/t36-/m0/s1 | PDB
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| n/a | n/a | 270 | n/a | n/a | n/a | n/a | n/a | n/a |
Warner-Lambert Company
Curated by ChEMBL
| Assay Description
In vitro inhibition of rat farnesyltransferase. |
J Med Chem 40: 3319-22 (1997)
Article DOI: 10.1021/jm970470c
BindingDB Entry DOI: 10.7270/Q2V69HQG |
More data for this
Ligand-Target Pair | |
Protein farnesyltransferase subunit beta/geranylgeranyltransferase type-1 subunit alpha
(Homo sapiens (Human)) | BDBM50081226
(1-[1-[(Z)-ethylidene]-5,9-dimethyl-(4E)-4,8-decadi...)Show SMILES [#6]\[#6](-[#6])=[#6]/[#6]-[#6]\[#6](-[#6])=[#6]\[#6]-[#6]\[#6](=[#6]\[#6]-[#8]P([#8-])(=O)[#8]P([#8-])([#8-])=O)-c1ccccc1 Show InChI InChI=1S/C20H30O7P2/c1-17(2)9-7-10-18(3)11-8-14-20(19-12-5-4-6-13-19)15-16-26-29(24,25)27-28(21,22)23/h4-6,9,11-13,15H,7-8,10,14,16H2,1-3H3,(H,24,25)(H2,21,22,23)/p-3/b18-11+,20-15- | PDB
MMDB
Reactome pathway
KEGG
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DrugBank
antibodypedia
antibodypedia
GoogleScholar
AffyNet
| KEGG
PC cid
PC sid
UniChem
Similars
| PubMed
| n/a | n/a | 299 | n/a | n/a | n/a | n/a | n/a | n/a |
Parke-Davis Pharmaceutical Research
Curated by ChEMBL
| Assay Description
Inhibition of recombinant farnesyltransferase (mFTase) in scintillation proximity assay |
J Med Chem 42: 3800-8 (1999)
BindingDB Entry DOI: 10.7270/Q2Z89D3S |
More data for this
Ligand-Target Pair | |
GTPase HRas
(Homo sapiens (Human)) | BDBM50060145
(CHEMBL115669 | [(S)-1-{(4-Benzyloxy-benzyl)-[((S)-...)Show SMILES C[C@H](CNC(=O)CN(Cc1ccc(OCc2ccccc2)cc1)C(=O)[C@H](Cc1cnc[nH]1)NC(=O)OCc1ccccc1)c1ccccc1 Show InChI InChI=1S/C39H41N5O5/c1-29(33-15-9-4-10-16-33)22-41-37(45)25-44(24-30-17-19-35(20-18-30)48-26-31-11-5-2-6-12-31)38(46)36(21-34-23-40-28-42-34)43-39(47)49-27-32-13-7-3-8-14-32/h2-20,23,28-29,36H,21-22,24-27H2,1H3,(H,40,42)(H,41,45)(H,43,47)/t29-,36+/m1/s1 | PDB
MMDB
KEGG
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DrugBank
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Similars
| Article
PubMed
| n/a | n/a | 300 | n/a | n/a | n/a | n/a | n/a | n/a |
Warner-Lambert Company
Curated by ChEMBL
| Assay Description
Concentration required to inhibit 50% of the cultured colonies of H-Ras-Fcells . |
J Med Chem 40: 3319-22 (1997)
Article DOI: 10.1021/jm970470c
BindingDB Entry DOI: 10.7270/Q2V69HQG |
More data for this
Ligand-Target Pair | |
GTPase HRas
(Homo sapiens (Human)) | BDBM50060138
(CHEMBL324827 | [(S)-1-{(4-Benzyloxy-benzyl)-[(2-ph...)Show SMILES CC(CNC(=O)CN(Cc1ccc(OCc2ccccc2)cc1)C(=O)[C@H](Cc1cnc[nH]1)NC(=O)OCc1ccccc1)c1ccccc1 Show InChI InChI=1S/C39H41N5O5/c1-29(33-15-9-4-10-16-33)22-41-37(45)25-44(24-30-17-19-35(20-18-30)48-26-31-11-5-2-6-12-31)38(46)36(21-34-23-40-28-42-34)43-39(47)49-27-32-13-7-3-8-14-32/h2-20,23,28-29,36H,21-22,24-27H2,1H3,(H,40,42)(H,41,45)(H,43,47)/t29?,36-/m0/s1 | PDB
MMDB
KEGG
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B.MOAD
DrugBank
GoogleScholar
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| CHEMBL
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PC sid
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| Article
PubMed
| n/a | n/a | 310 | n/a | n/a | n/a | n/a | n/a | n/a |
Warner-Lambert Company
Curated by ChEMBL
| Assay Description
Concentration required to inhibit 50% of the cultured colonies of H-Ras-Fcells . |
J Med Chem 40: 3319-22 (1997)
Article DOI: 10.1021/jm970470c
BindingDB Entry DOI: 10.7270/Q2V69HQG |
More data for this
Ligand-Target Pair | |
Protein farnesyltransferase subunit beta/geranylgeranyltransferase type-1 subunit alpha
(Rattus norvegicus-Rattus norvegicus (rat)) | BDBM50059879
(CHEMBL102492 | [(S)-1-{(4-Benzyloxy-benzyl)-[(2-be...)Show SMILES O=C(CN(Cc1ccc(OCc2ccccc2)cc1)C(=O)[C@H](Cc1cnc[nH]1)NC(=O)OCc1ccccc1)NCCOCc1ccccc1 Show InChI InChI=1S/C39H41N5O6/c45-37(41-20-21-48-26-31-10-4-1-5-11-31)25-44(24-30-16-18-35(19-17-30)49-27-32-12-6-2-7-13-32)38(46)36(22-34-23-40-29-42-34)43-39(47)50-28-33-14-8-3-9-15-33/h1-19,23,29,36H,20-22,24-28H2,(H,40,42)(H,41,45)(H,43,47)/t36-/m0/s1 | PDB
KEGG
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GoogleScholar
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| Article
PubMed
| n/a | n/a | 320 | n/a | n/a | n/a | n/a | n/a | n/a |
Warner-Lambert Company
Curated by ChEMBL
| Assay Description
In vitro inhibition of rat farnesyltransferase. |
J Med Chem 40: 3319-22 (1997)
Article DOI: 10.1021/jm970470c
BindingDB Entry DOI: 10.7270/Q2V69HQG |
More data for this
Ligand-Target Pair | |
GTPase HRas
(Homo sapiens (Human)) | BDBM50060142
(CHEMBL326127 | [(S)-1-((4-Benzyloxy-benzyl)-{[(1-p...)Show SMILES O=C(CN(Cc1ccc(OCc2ccccc2)cc1)C(=O)[C@H](Cc1cnc[nH]1)NC(=O)OCc1ccccc1)NCC1(CCCC1)c1ccccc1 Show InChI InChI=1S/C42H45N5O5/c48-39(44-30-42(22-10-11-23-42)35-16-8-3-9-17-35)27-47(26-32-18-20-37(21-19-32)51-28-33-12-4-1-5-13-33)40(49)38(24-36-25-43-31-45-36)46-41(50)52-29-34-14-6-2-7-15-34/h1-9,12-21,25,31,38H,10-11,22-24,26-30H2,(H,43,45)(H,44,48)(H,46,50)/t38-/m0/s1 | PDB
MMDB
KEGG
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B.MOAD
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| Article
PubMed
| n/a | n/a | 330 | n/a | n/a | n/a | n/a | n/a | n/a |
Warner-Lambert Company
Curated by ChEMBL
| Assay Description
Concentration required to inhibit 50% of the cultured colonies of H-Ras-Fcells . |
J Med Chem 40: 3319-22 (1997)
Article DOI: 10.1021/jm970470c
BindingDB Entry DOI: 10.7270/Q2V69HQG |
More data for this
Ligand-Target Pair | |
GTPase HRas
(Homo sapiens (Human)) | BDBM50060149
(CHEMBL112512 | [(S)-1-{(4-Benzyloxy-benzyl)-[(2-ph...)Show SMILES CCC(CNC(=O)CN(Cc1ccc(OCc2ccccc2)cc1)C(=O)[C@H](Cc1cnc[nH]1)NC(=O)OCc1ccccc1)c1ccccc1 Show InChI InChI=1S/C40H43N5O5/c1-2-33(34-16-10-5-11-17-34)23-42-38(46)26-45(25-30-18-20-36(21-19-30)49-27-31-12-6-3-7-13-31)39(47)37(22-35-24-41-29-43-35)44-40(48)50-28-32-14-8-4-9-15-32/h3-21,24,29,33,37H,2,22-23,25-28H2,1H3,(H,41,43)(H,42,46)(H,44,48)/t33?,37-/m0/s1 | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
GoogleScholar
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| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 400 | n/a | n/a | n/a | n/a | n/a | n/a |
Warner-Lambert Company
Curated by ChEMBL
| Assay Description
Concentration required to inhibit 50% of the cultured colonies of H-Ras-Fcells . |
J Med Chem 40: 3319-22 (1997)
Article DOI: 10.1021/jm970470c
BindingDB Entry DOI: 10.7270/Q2V69HQG |
More data for this
Ligand-Target Pair | |
Protein farnesyltransferase subunit beta/geranylgeranyltransferase type-1 subunit alpha
(Homo sapiens (Human)) | BDBM50081238
(4-[(Z)-ethylidene]-8,12,16-trimethyl-(7E,11E)-1,7,...)Show SMILES [#6]\[#6](-[#6])=[#6]/[#6]-[#6]\[#6](-[#6])=[#6]\[#6]-[#6]\[#6](-[#6])=[#6]\[#6]-[#6]\[#6](-[#6]-[#6]=[#6])=[#6]\[#6]-[#8]P([#8-])(=O)[#8]P([#8-])([#8-])=O Show InChI InChI=1S/C22H38O7P2/c1-6-10-22(17-18-28-31(26,27)29-30(23,24)25)16-9-15-21(5)14-8-13-20(4)12-7-11-19(2)3/h6,11,13,15,17H,1,7-10,12,14,16,18H2,2-5H3,(H,26,27)(H2,23,24,25)/p-3/b20-13+,21-15+,22-17+ | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
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antibodypedia
antibodypedia
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| n/a | n/a | 453 | n/a | n/a | n/a | n/a | n/a | n/a |
Parke-Davis Pharmaceutical Research
Curated by ChEMBL
| Assay Description
Inhibition of recombinant farnesyltransferase (mFTase) in scintillation proximity assay |
J Med Chem 42: 3800-8 (1999)
BindingDB Entry DOI: 10.7270/Q2Z89D3S |
More data for this
Ligand-Target Pair | |
GTPase HRas
(Homo sapiens (Human)) | BDBM50060150
(CHEMBL114281 | [(S)-1-{(4-Benzyloxy-benzyl)-[((R)-...)Show SMILES C[C@@H](CNC(=O)CN(Cc1ccc(OCc2ccccc2)cc1)C(=O)[C@H](Cc1cnc[nH]1)NC(=O)OCc1ccccc1)c1ccccc1 Show InChI InChI=1S/C39H41N5O5/c1-29(33-15-9-4-10-16-33)22-41-37(45)25-44(24-30-17-19-35(20-18-30)48-26-31-11-5-2-6-12-31)38(46)36(21-34-23-40-28-42-34)43-39(47)49-27-32-13-7-3-8-14-32/h2-20,23,28-29,36H,21-22,24-27H2,1H3,(H,40,42)(H,41,45)(H,43,47)/t29-,36-/m0/s1 | PDB
MMDB
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UniProtKB/SwissProt
B.MOAD
DrugBank
GoogleScholar
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| CHEMBL
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PubMed
| n/a | n/a | 570 | n/a | n/a | n/a | n/a | n/a | n/a |
Warner-Lambert Company
Curated by ChEMBL
| Assay Description
Concentration required to inhibit 50% of the cultured colonies of H-Ras-Fcells . |
J Med Chem 40: 3319-22 (1997)
Article DOI: 10.1021/jm970470c
BindingDB Entry DOI: 10.7270/Q2V69HQG |
More data for this
Ligand-Target Pair | |
GTPase HRas
(Homo sapiens (Human)) | BDBM50060144
(CHEMBL325073 | [(S)-1-{(4-Benzyloxy-benzyl)-[((R)-...)Show SMILES C[C@H](Cc1ccccc1)NC(=O)CN(Cc1ccc(OCc2ccccc2)cc1)C(=O)[C@H](Cc1cnc[nH]1)NC(=O)OCc1ccccc1 Show InChI InChI=1S/C39H41N5O5/c1-29(21-30-11-5-2-6-12-30)42-37(45)25-44(24-31-17-19-35(20-18-31)48-26-32-13-7-3-8-14-32)38(46)36(22-34-23-40-28-41-34)43-39(47)49-27-33-15-9-4-10-16-33/h2-20,23,28-29,36H,21-22,24-27H2,1H3,(H,40,41)(H,42,45)(H,43,47)/t29-,36+/m1/s1 | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
GoogleScholar
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| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 710 | n/a | n/a | n/a | n/a | n/a | n/a |
Warner-Lambert Company
Curated by ChEMBL
| Assay Description
Concentration required to inhibit 50% of the cultured colonies of H-Ras-Fcells . |
J Med Chem 40: 3319-22 (1997)
Article DOI: 10.1021/jm970470c
BindingDB Entry DOI: 10.7270/Q2V69HQG |
More data for this
Ligand-Target Pair | |
Protein farnesyltransferase subunit beta/geranylgeranyltransferase type-1 subunit alpha
(Homo sapiens (Human)) | BDBM50081233
(3-[(Z)-ethylidene]-7,11,15-trimethyl-(6E,10E)-1,6,...)Show SMILES [#6]\[#6](-[#6])=[#6]\[#6]-[#6]\[#6](-[#6])=[#6]\[#6]-[#6]\[#6](-[#6])=[#6]\[#6]-[#6]\[#6](-[#6]=[#6])=[#6]\[#6]-[#8]P([#8-])(=O)[#8]P([#8-])([#8-])=O Show InChI InChI=1S/C21H36O7P2/c1-6-21(16-17-27-30(25,26)28-29(22,23)24)15-9-14-20(5)13-8-12-19(4)11-7-10-18(2)3/h6,10,12,14,16H,1,7-9,11,13,15,17H2,2-5H3,(H,25,26)(H2,22,23,24)/p-3/b19-12+,20-14+,21-16+ | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
antibodypedia
GoogleScholar
AffyNet
| KEGG
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PC sid
UniChem
Similars
| PubMed
| n/a | n/a | 715 | n/a | n/a | n/a | n/a | n/a | n/a |
Parke-Davis Pharmaceutical Research
Curated by ChEMBL
| Assay Description
Inhibition of recombinant farnesyltransferase (mFTase) in scintillation proximity assay |
J Med Chem 42: 3800-8 (1999)
BindingDB Entry DOI: 10.7270/Q2Z89D3S |
More data for this
Ligand-Target Pair | |
GTPase HRas
(Homo sapiens (Human)) | BDBM50060152
(CHEMBL112879 | [(S)-1-{(4-Benzyloxy-benzyl)-[(2-et...)Show SMILES CCC(CC)(CNC(=O)CN(Cc1ccc(OCc2ccccc2)cc1)C(=O)[C@H](Cc1cnc[nH]1)NC(=O)OCc1ccccc1)c1ccccc1 Show InChI InChI=1S/C42H47N5O5/c1-3-42(4-2,35-18-12-7-13-19-35)30-44-39(48)27-47(26-32-20-22-37(23-21-32)51-28-33-14-8-5-9-15-33)40(49)38(24-36-25-43-31-45-36)46-41(50)52-29-34-16-10-6-11-17-34/h5-23,25,31,38H,3-4,24,26-30H2,1-2H3,(H,43,45)(H,44,48)(H,46,50)/t38-/m0/s1 | PDB
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B.MOAD
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| CHEMBL
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PubMed
| n/a | n/a | >1.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Warner-Lambert Company
Curated by ChEMBL
| Assay Description
Concentration required to inhibit 50% of the cultured colonies of H-Ras-Fcells . |
J Med Chem 40: 3319-22 (1997)
Article DOI: 10.1021/jm970470c
BindingDB Entry DOI: 10.7270/Q2V69HQG |
More data for this
Ligand-Target Pair | |
GTPase HRas
(Homo sapiens (Human)) | BDBM50060148
(CHEMBL325331 | [(S)-1-{(4-Benzyloxy-benzyl)-[(2-ph...)Show SMILES CCCC(CNC(=O)CN(Cc1ccc(OCc2ccccc2)cc1)C(=O)[C@H](Cc1cnc[nH]1)NC(=O)OCc1ccccc1)c1ccccc1 Show InChI InChI=1S/C41H45N5O5/c1-2-12-35(34-17-10-5-11-18-34)24-43-39(47)27-46(26-31-19-21-37(22-20-31)50-28-32-13-6-3-7-14-32)40(48)38(23-36-25-42-30-44-36)45-41(49)51-29-33-15-8-4-9-16-33/h3-11,13-22,25,30,35,38H,2,12,23-24,26-29H2,1H3,(H,42,44)(H,43,47)(H,45,49)/t35?,38-/m0/s1 | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
GoogleScholar
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| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | >1.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Warner-Lambert Company
Curated by ChEMBL
| Assay Description
Concentration required to inhibit 50% of the cultured colonies of H-Ras-Fcells . |
J Med Chem 40: 3319-22 (1997)
Article DOI: 10.1021/jm970470c
BindingDB Entry DOI: 10.7270/Q2V69HQG |
More data for this
Ligand-Target Pair | |
Geranylgeranyl transferase type-1 subunit beta/Protein farnesyltransferase/geranylgeranyltransferase type-1 subunit alpha
(Homo sapiens (Human)) | BDBM50081233
(3-[(Z)-ethylidene]-7,11,15-trimethyl-(6E,10E)-1,6,...)Show SMILES [#6]\[#6](-[#6])=[#6]\[#6]-[#6]\[#6](-[#6])=[#6]\[#6]-[#6]\[#6](-[#6])=[#6]\[#6]-[#6]\[#6](-[#6]=[#6])=[#6]\[#6]-[#8]P([#8-])(=O)[#8]P([#8-])([#8-])=O Show InChI InChI=1S/C21H36O7P2/c1-6-21(16-17-27-30(25,26)28-29(22,23)24)15-9-14-20(5)13-8-12-19(4)11-7-10-18(2)3/h6,10,12,14,16H,1,7-9,11,13,15,17H2,2-5H3,(H,25,26)(H2,22,23,24)/p-3/b19-12+,20-14+,21-16+ | PDB
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antibodypedia
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| n/a | n/a | 3.05E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Parke-Davis Pharmaceutical Research
Curated by ChEMBL
| Assay Description
Inhibition of recombinant Geranylgeranyl transferase type I in scintillation proximity assay |
J Med Chem 42: 3800-8 (1999)
BindingDB Entry DOI: 10.7270/Q2Z89D3S |
More data for this
Ligand-Target Pair | |
Geranylgeranyl transferase type-1 subunit beta/Protein farnesyltransferase/geranylgeranyltransferase type-1 subunit alpha
(Homo sapiens (Human)) | BDBM50081238
(4-[(Z)-ethylidene]-8,12,16-trimethyl-(7E,11E)-1,7,...)Show SMILES [#6]\[#6](-[#6])=[#6]/[#6]-[#6]\[#6](-[#6])=[#6]\[#6]-[#6]\[#6](-[#6])=[#6]\[#6]-[#6]\[#6](-[#6]-[#6]=[#6])=[#6]\[#6]-[#8]P([#8-])(=O)[#8]P([#8-])([#8-])=O Show InChI InChI=1S/C22H38O7P2/c1-6-10-22(17-18-28-31(26,27)29-30(23,24)25)16-9-15-21(5)14-8-13-20(4)12-7-11-19(2)3/h6,11,13,15,17H,1,7-10,12,14,16,18H2,2-5H3,(H,26,27)(H2,23,24,25)/p-3/b20-13+,21-15+,22-17+ | PDB
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B.MOAD
antibodypedia
antibodypedia
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UniChem
Similars
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| n/a | n/a | 3.38E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Parke-Davis Pharmaceutical Research
Curated by ChEMBL
| Assay Description
Inhibition of recombinant Geranylgeranyl transferase type I in scintillation proximity assay |
J Med Chem 42: 3800-8 (1999)
BindingDB Entry DOI: 10.7270/Q2Z89D3S |
More data for this
Ligand-Target Pair | |
Protein farnesyltransferase subunit beta/geranylgeranyltransferase type-1 subunit alpha
(Rattus norvegicus-Rattus norvegicus (rat)) | BDBM50060147
(CHEMBL114495 | [(S)-1-{(4-Benzyloxy-benzyl)-[(meth...)Show SMILES CN(CCc1ccccc1)C(=O)CN(Cc1ccc(OCc2ccccc2)cc1)C(=O)[C@H](Cc1cnc[nH]1)NC(=O)OCc1ccccc1 Show InChI InChI=1S/C39H41N5O5/c1-43(22-21-30-11-5-2-6-12-30)37(45)26-44(25-31-17-19-35(20-18-31)48-27-32-13-7-3-8-14-32)38(46)36(23-34-24-40-29-41-34)42-39(47)49-28-33-15-9-4-10-16-33/h2-20,24,29,36H,21-23,25-28H2,1H3,(H,40,41)(H,42,47)/t36-/m0/s1 | PDB
KEGG
UniProtKB/SwissProt
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| CHEMBL
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Similars
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PubMed
| n/a | n/a | 4.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Warner-Lambert Company
Curated by ChEMBL
| Assay Description
In vitro inhibition of rat farnesyltransferase. |
J Med Chem 40: 3319-22 (1997)
Article DOI: 10.1021/jm970470c
BindingDB Entry DOI: 10.7270/Q2V69HQG |
More data for this
Ligand-Target Pair | |
GTPase HRas
(Homo sapiens (Human)) | BDBM50059857
(CHEMBL102955 | [(S)-1-[(4-Benzyloxy-benzyl)-(phene...)Show SMILES O=C(CN(Cc1ccc(OCc2ccccc2)cc1)C(=O)[C@H](Cc1cnc[nH]1)NC(=O)OCc1ccccc1)NCCc1ccccc1 Show InChI InChI=1S/C38H39N5O5/c44-36(40-21-20-29-10-4-1-5-11-29)25-43(24-30-16-18-34(19-17-30)47-26-31-12-6-2-7-13-31)37(45)35(22-33-23-39-28-41-33)42-38(46)48-27-32-14-8-3-9-15-32/h1-19,23,28,35H,20-22,24-27H2,(H,39,41)(H,40,44)(H,42,46)/t35-/m0/s1 | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
GoogleScholar
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| CHEMBL
PC cid
PC sid
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Similars
| Article
PubMed
| n/a | n/a | 4.30E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Warner-Lambert Company
Curated by ChEMBL
| Assay Description
Concentration required to inhibit 50% of the cultured colonies of H-Ras-Fcells . |
J Med Chem 40: 3319-22 (1997)
Article DOI: 10.1021/jm970470c
BindingDB Entry DOI: 10.7270/Q2V69HQG |
More data for this
Ligand-Target Pair | |
GTPase HRas
(Homo sapiens (Human)) | BDBM50060143
(CHEMBL324345 | [(S)-1-{(4-Benzyloxy-benzyl)-[((S)-...)Show SMILES C[C@@H](Cc1ccccc1)NC(=O)CN(Cc1ccc(OCc2ccccc2)cc1)C(=O)[C@H](Cc1cnc[nH]1)NC(=O)OCc1ccccc1 Show InChI InChI=1S/C39H41N5O5/c1-29(21-30-11-5-2-6-12-30)42-37(45)25-44(24-31-17-19-35(20-18-31)48-26-32-13-7-3-8-14-32)38(46)36(22-34-23-40-28-41-34)43-39(47)49-27-33-15-9-4-10-16-33/h2-20,23,28-29,36H,21-22,24-27H2,1H3,(H,40,41)(H,42,45)(H,43,47)/t29-,36-/m0/s1 | PDB
MMDB
KEGG
UniProtKB/SwissProt
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DrugBank
GoogleScholar
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| CHEMBL
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PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 6.30E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Warner-Lambert Company
Curated by ChEMBL
| Assay Description
Concentration required to inhibit 50% of the cultured colonies of H-Ras-Fcells . |
J Med Chem 40: 3319-22 (1997)
Article DOI: 10.1021/jm970470c
BindingDB Entry DOI: 10.7270/Q2V69HQG |
More data for this
Ligand-Target Pair | |
GTPase HRas
(Homo sapiens (Human)) | BDBM50059879
(CHEMBL102492 | [(S)-1-{(4-Benzyloxy-benzyl)-[(2-be...)Show SMILES O=C(CN(Cc1ccc(OCc2ccccc2)cc1)C(=O)[C@H](Cc1cnc[nH]1)NC(=O)OCc1ccccc1)NCCOCc1ccccc1 Show InChI InChI=1S/C39H41N5O6/c45-37(41-20-21-48-26-31-10-4-1-5-11-31)25-44(24-30-16-18-35(19-17-30)49-27-32-12-6-2-7-13-32)38(46)36(22-34-23-40-29-42-34)43-39(47)50-28-33-14-8-3-9-15-33/h1-19,23,29,36H,20-22,24-28H2,(H,40,42)(H,41,45)(H,43,47)/t36-/m0/s1 | PDB
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| Article
PubMed
| n/a | n/a | 1.43E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Warner-Lambert Company
Curated by ChEMBL
| Assay Description
Concentration required to inhibit 50% of the cultured colonies of H-Ras-Fcells . |
J Med Chem 40: 3319-22 (1997)
Article DOI: 10.1021/jm970470c
BindingDB Entry DOI: 10.7270/Q2V69HQG |
More data for this
Ligand-Target Pair | |
Geranylgeranyl transferase type-1 subunit beta/Protein farnesyltransferase/geranylgeranyltransferase type-1 subunit alpha
(Homo sapiens (Human)) | BDBM50081229
(10-(tert-butyl)-2,6-dimethyl-(6E,10Z)-2,6,10-dodec...)Show SMILES [#6]\[#6](-[#6])=[#6]\[#6]-[#6]\[#6](-[#6])=[#6]\[#6]-[#6]\[#6](=[#6]\[#6]-[#8]P([#8-])(=O)[#8]P([#8-])([#8-])=O)C([#6])([#6])[#6] Show InChI InChI=1S/C18H34O7P2/c1-15(2)9-7-10-16(3)11-8-12-17(18(4,5)6)13-14-24-27(22,23)25-26(19,20)21/h9,11,13H,7-8,10,12,14H2,1-6H3,(H,22,23)(H2,19,20,21)/p-3/b16-11+,17-13- | PDB
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PC sid
UniChem
Similars
| PubMed
| n/a | n/a | 5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Parke-Davis Pharmaceutical Research
Curated by ChEMBL
| Assay Description
Inhibition of recombinant Geranylgeranyl transferase type I in scintillation proximity assay |
J Med Chem 42: 3800-8 (1999)
BindingDB Entry DOI: 10.7270/Q2Z89D3S |
More data for this
Ligand-Target Pair | |
Geranylgeranyl transferase type-1 subunit beta/Protein farnesyltransferase/geranylgeranyltransferase type-1 subunit alpha
(Homo sapiens (Human)) | BDBM50081234
(3-[(Z)-ethylidene]-7,11-dimethyl-(6E)-1,6,10-dodec...)Show SMILES [#6]\[#6](-[#6])=[#6]/[#6]-[#6]\[#6](-[#6])=[#6]\[#6]-[#6]\[#6](-[#6]=[#6])=[#6]\[#6]-[#8]P([#8-])(=O)[#8]P([#8-])([#8-])=O Show InChI InChI=1S/C16H28O7P2/c1-5-16(11-7-10-15(4)9-6-8-14(2)3)12-13-22-25(20,21)23-24(17,18)19/h5,8,10,12H,1,6-7,9,11,13H2,2-4H3,(H,20,21)(H2,17,18,19)/p-3/b15-10+,16-12+ | PDB
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antibodypedia
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PC sid
UniChem
Similars
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| n/a | n/a | 1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Parke-Davis Pharmaceutical Research
Curated by ChEMBL
| Assay Description
Inhibition of recombinant Geranylgeranyl transferase type I in scintillation proximity assay |
J Med Chem 42: 3800-8 (1999)
BindingDB Entry DOI: 10.7270/Q2Z89D3S |
More data for this
Ligand-Target Pair | |
Geranylgeranyl transferase type-1 subunit beta/Protein farnesyltransferase/geranylgeranyltransferase type-1 subunit alpha
(Homo sapiens (Human)) | BDBM50081226
(1-[1-[(Z)-ethylidene]-5,9-dimethyl-(4E)-4,8-decadi...)Show SMILES [#6]\[#6](-[#6])=[#6]/[#6]-[#6]\[#6](-[#6])=[#6]\[#6]-[#6]\[#6](=[#6]\[#6]-[#8]P([#8-])(=O)[#8]P([#8-])([#8-])=O)-c1ccccc1 Show InChI InChI=1S/C20H30O7P2/c1-17(2)9-7-10-18(3)11-8-14-20(19-12-5-4-6-13-19)15-16-26-29(24,25)27-28(21,22)23/h4-6,9,11-13,15H,7-8,10,14,16H2,1-3H3,(H,24,25)(H2,21,22,23)/p-3/b18-11+,20-15- | PDB
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PC sid
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Similars
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| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Parke-Davis Pharmaceutical Research
Curated by ChEMBL
| Assay Description
Inhibition of recombinant Geranylgeranyl transferase type I in scintillation proximity assay |
J Med Chem 42: 3800-8 (1999)
BindingDB Entry DOI: 10.7270/Q2Z89D3S |
More data for this
Ligand-Target Pair | |
Geranylgeranyl transferase type-1 subunit beta/Protein farnesyltransferase/geranylgeranyltransferase type-1 subunit alpha
(Homo sapiens (Human)) | BDBM50081227
(10-ethyl-2,6-dimethyl-(6E,10E)-2,6,10-dodecatriene...)Show SMILES [#6]-[#6]\[#6](-[#6]-[#6]\[#6]=[#6](/[#6])-[#6]-[#6]\[#6]=[#6](/[#6])-[#6])=[#6]/[#6]-[#8]P([#8-])(=O)[#8]P([#8-])([#8-])=O Show InChI InChI=1S/C16H30O7P2/c1-5-16(11-7-10-15(4)9-6-8-14(2)3)12-13-22-25(20,21)23-24(17,18)19/h8,10,12H,5-7,9,11,13H2,1-4H3,(H,20,21)(H2,17,18,19)/p-3/b15-10+,16-12+ | PDB
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
antibodypedia
GoogleScholar
AffyNet
| KEGG
PC cid
PC sid
UniChem
Similars
| PubMed
| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Parke-Davis Pharmaceutical Research
Curated by ChEMBL
| Assay Description
Inhibition of recombinant Geranylgeranyl transferase type I in scintillation proximity assay |
J Med Chem 42: 3800-8 (1999)
BindingDB Entry DOI: 10.7270/Q2Z89D3S |
More data for this
Ligand-Target Pair | |
Geranylgeranyl transferase type-1 subunit beta/Protein farnesyltransferase/geranylgeranyltransferase type-1 subunit alpha
(Homo sapiens (Human)) | BDBM50081235
(3-substituted farnesyl diphosphate analogue | 4-[(...)Show SMILES [#6]\[#6](-[#6])=[#6]\[#6]-[#6]\[#6](-[#6])=[#6]\[#6]-[#6]\[#6](-[#6]-[#6]=[#6])=[#6]\[#6]-[#8]P([#8-])(=O)[#8]P([#8-])([#8-])=O Show InChI InChI=1S/C17H30O7P2/c1-5-8-17(12-7-11-16(4)10-6-9-15(2)3)13-14-23-26(21,22)24-25(18,19)20/h5,9,11,13H,1,6-8,10,12,14H2,2-4H3,(H,21,22)(H2,18,19,20)/p-3/b16-11+,17-13+ | PDB
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
antibodypedia
GoogleScholar
AffyNet
| KEGG
PC cid
PC sid
UniChem
Similars
| PubMed
| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Parke-Davis Pharmaceutical Research
Curated by ChEMBL
| Assay Description
Inhibition of recombinant Geranylgeranyl transferase type I in scintillation proximity assay |
J Med Chem 42: 3800-8 (1999)
BindingDB Entry DOI: 10.7270/Q2Z89D3S |
More data for this
Ligand-Target Pair | |
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