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Compile Data Set for Download or QSAR

Found 6 hits with Last Name = 'rocheblave' and Initial = 'l'   
Target/Host
(Institution)
LigandTarget/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
pHTemp
°C
Gag-Pol polyprotein [489-587]


(Human immunodeficiency virus type 1)
BDBM577
PNG
((3S)-oxolan-3-yl N-[(2S,3R)-4-[(4-aminobenzene)(2-...)
Show SMILES CC(C)CN(C[C@@H](O)[C@H](Cc1ccccc1)NC(=O)O[C@H]1CCOC1)S(=O)(=O)c1ccc(N)cc1 |r|
Show InChI InChI=1S/C25H35N3O6S/c1-18(2)15-28(35(31,32)22-10-8-20(26)9-11-22)16-24(29)23(14-19-6-4-3-5-7-19)27-25(30)34-21-12-13-33-17-21/h3-11,18,21,23-24,29H,12-17,26H2,1-2H3,(H,27,30)/t21-,23-,24+/m0/s1
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n/an/a 1n/an/an/an/an/an/a



Université de la Méditerranée

Curated by ChEMBL


Assay Description
Concentration required to inhibit HIV-1 protease cleavage by 50%.


J Med Chem 45: 3321-4 (2002)


BindingDB Entry DOI: 10.7270/Q2VQ3211
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Gag-Pol polyprotein [489-587]


(Human immunodeficiency virus type 1)
BDBM196
PNG
(A-74704 | CHEMBL307193 | benzyl N-[(1S)-1-{[(2S,4S...)
Show SMILES CC(C)[C@H](NC(=O)OCc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C(O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)OCc1ccccc1)C(C)C
Show InChI InChI=1S/C43H52N4O7/c1-29(2)37(46-42(51)53-27-33-21-13-7-14-22-33)40(49)44-35(25-31-17-9-5-10-18-31)39(48)36(26-32-19-11-6-12-20-32)45-41(50)38(30(3)4)47-43(52)54-28-34-23-15-8-16-24-34/h5-24,29-30,35-39,48H,25-28H2,1-4H3,(H,44,49)(H,45,50)(H,46,51)(H,47,52)/t35-,36-,37-,38-/m0/s1
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n/an/a 3n/an/an/an/an/an/a



Université de la Méditerranée

Curated by ChEMBL


Assay Description
Inhibitory activity of the compound was evaluated against HIV-protease was evaluated


Bioorg Med Chem Lett 8: 1861-6 (1999)


BindingDB Entry DOI: 10.7270/Q25T3JNQ
More data for this
Ligand-Target Pair
Gag-Pol polyprotein [489-587]


(Human immunodeficiency virus type 1)
BDBM50115670
PNG
(CHEMBL115329 | {3-[(4-Amino-benzenesulfonyl)-isobu...)
Show SMILES CC(C)CN(C[C@@H](O)[C@H](NC(=O)O[C@@H]1CCOC1)Sc1ccccc1)S(=O)(=O)c1ccc(N)cc1
Show InChI InChI=1S/C24H33N3O6S2/c1-17(2)14-27(35(30,31)21-10-8-18(25)9-11-21)15-22(28)23(34-20-6-4-3-5-7-20)26-24(29)33-19-12-13-32-16-19/h3-11,17,19,22-23,28H,12-16,25H2,1-2H3,(H,26,29)/t19-,22-,23-/m1/s1
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n/an/a 1.40E+3n/an/an/an/an/an/a



Université de la Méditerranée

Curated by ChEMBL


Assay Description
Concentration required to inhibit HIV-1 protease cleavage by 50%.


J Med Chem 45: 3321-4 (2002)


BindingDB Entry DOI: 10.7270/Q2VQ3211
More data for this
Ligand-Target Pair
Gag-Pol polyprotein [489-587]


(Human immunodeficiency virus type 1)
BDBM50115673
PNG
(CHEMBL324319 | {3-[(4-Amino-benzenesulfonyl)-isobu...)
Show SMILES CC(C)CN(C[C@H](O)[C@H](NC(=O)O[C@@H]1CCOC1)Sc1ccccc1)S(=O)(=O)c1ccc(N)cc1
Show InChI InChI=1S/C24H33N3O6S2/c1-17(2)14-27(35(30,31)21-10-8-18(25)9-11-21)15-22(28)23(34-20-6-4-3-5-7-20)26-24(29)33-19-12-13-32-16-19/h3-11,17,19,22-23,28H,12-16,25H2,1-2H3,(H,26,29)/t19-,22+,23-/m1/s1
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n/an/a 1.16E+4n/an/an/an/an/an/a



Université de la Méditerranée

Curated by ChEMBL


Assay Description
Concentration required to inhibit HIV-1 protease cleavage by 50%.


J Med Chem 45: 3321-4 (2002)


BindingDB Entry DOI: 10.7270/Q2VQ3211
More data for this
Ligand-Target Pair
Gag-Pol polyprotein [489-587]


(Human immunodeficiency virus type 1)
BDBM50115671
PNG
(CHEMBL112703 | {3-[(4-Amino-benzenesulfonyl)-isobu...)
Show SMILES CC(C)CN(C[C@H](O)[C@@H](NC(=O)O[C@@H]1CCOC1)Sc1ccccc1)S(=O)(=O)c1ccc(N)cc1
Show InChI InChI=1S/C24H33N3O6S2/c1-17(2)14-27(35(30,31)21-10-8-18(25)9-11-21)15-22(28)23(34-20-6-4-3-5-7-20)26-24(29)33-19-12-13-32-16-19/h3-11,17,19,22-23,28H,12-16,25H2,1-2H3,(H,26,29)/t19-,22+,23+/m1/s1
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n/an/a 1.25E+4n/an/an/an/an/an/a



Université de la Méditerranée

Curated by ChEMBL


Assay Description
Concentration required to inhibit HIV-1 protease cleavage by 50%.


J Med Chem 45: 3321-4 (2002)


BindingDB Entry DOI: 10.7270/Q2VQ3211
More data for this
Ligand-Target Pair
Gag-Pol polyprotein [489-587]


(Human immunodeficiency virus type 1)
BDBM50115672
PNG
(CHEMBL113559 | {3-[(4-Amino-benzenesulfonyl)-isobu...)
Show SMILES CC(C)CN(C[C@@H](O)[C@@H](NC(=O)O[C@@H]1CCOC1)Sc1ccccc1)S(=O)(=O)c1ccc(N)cc1
Show InChI InChI=1S/C24H33N3O6S2/c1-17(2)14-27(35(30,31)21-10-8-18(25)9-11-21)15-22(28)23(34-20-6-4-3-5-7-20)26-24(29)33-19-12-13-32-16-19/h3-11,17,19,22-23,28H,12-16,25H2,1-2H3,(H,26,29)/t19-,22-,23+/m1/s1
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n/an/a 1.67E+4n/an/an/an/an/an/a



Université de la Méditerranée

Curated by ChEMBL


Assay Description
Concentration required to inhibit HIV-1 protease cleavage by 50%.


J Med Chem 45: 3321-4 (2002)


BindingDB Entry DOI: 10.7270/Q2VQ3211
More data for this
Ligand-Target Pair