Found 92 hits of ic50 for UniProtKB: P14151 Target/Host
(Institution) | Ligand | Target/Host
Links | Ligand
Links | Trg + Lig
Links | Ki
nM | ΔG°
kcal/mole | IC50
nM | Kd
nM | EC50/IC50
nM | koff
s-1 | kon
M-1s-1 | pH | Temp
°C |
|---|
L-selectin
(Homo sapiens (Human)) | BDBM50060512
((R)-4-Methylcarbamoyl-4-[(R)-2-(2-tetradecyl-hexad...)Show SMILES CCCCCCCCCCCCCCC(CCCCCCCCCCCCCC)C(=O)N[C@H](COC1OC(C)C(O)C(O)C1O)C(=O)N[C@H](CCC(O)=O)C(=O)NC Show InChI InChI=1S/C45H85N3O10/c1-5-7-9-11-13-15-17-19-21-23-25-27-29-35(30-28-26-24-22-20-18-16-14-12-10-8-6-2)42(54)48-37(33-57-45-41(53)40(52)39(51)34(3)58-45)44(56)47-36(43(55)46-4)31-32-38(49)50/h34-37,39-41,45,51-53H,5-33H2,1-4H3,(H,46,55)(H,47,56)(H,48,54)(H,49,50)/t34?,36-,37-,39?,40?,41?,45?/m1/s1 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet 
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 700 | n/a | n/a | n/a | n/a | n/a | n/a |
Kanebo
Curated by ChEMBL
| Assay Description
Inhibition of Selectin L binding |
J Med Chem 41: 4279-87 (1998)
Article DOI: 10.1021/jm980267x
BindingDB Entry DOI: 10.7270/Q2474BHN |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50205383
((5-{4-[(2',3',4'-trihydroxy-biphenyl-3-carbonyl)-a...)Show SMILES OC(=O)Cc1ccc(s1)-c1ccc(NC(=O)c2cccc(c2)-c2ccc(O)c(O)c2O)cc1 Show InChI InChI=1S/C25H19NO6S/c27-20-10-9-19(23(30)24(20)31)15-2-1-3-16(12-15)25(32)26-17-6-4-14(5-7-17)21-11-8-18(33-21)13-22(28)29/h1-12,27,30-31H,13H2,(H,26,32)(H,28,29) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 790 | n/a | n/a | n/a | n/a | n/a | n/a |
Revotar Biopharmaceuticals AG
Curated by ChEMBL
| Assay Description
Inhibition of human L-selectin after 2 hrs |
J Med Chem 50: 1101-15 (2007)
Article DOI: 10.1021/jm060536g
BindingDB Entry DOI: 10.7270/Q2TB17Q6 |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50060511
((R)-4-Methylcarbamoyl-4-[(S)-2-(2-tetradecyl-hexad...)Show SMILES CCCCCCCCCCCCCCC(CCCCCCCCCCCCCC)C(=O)N[C@@H](COC1OC(C)C(O)C(O)C1O)C(=O)N[C@H](CCC(O)=O)C(=O)NC Show InChI InChI=1S/C45H85N3O10/c1-5-7-9-11-13-15-17-19-21-23-25-27-29-35(30-28-26-24-22-20-18-16-14-12-10-8-6-2)42(54)48-37(33-57-45-41(53)40(52)39(51)34(3)58-45)44(56)47-36(43(55)46-4)31-32-38(49)50/h34-37,39-41,45,51-53H,5-33H2,1-4H3,(H,46,55)(H,47,56)(H,48,54)(H,49,50)/t34?,36-,37+,39?,40?,41?,45?/m1/s1 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 800 | n/a | n/a | n/a | n/a | n/a | n/a |
Kanebo
Curated by ChEMBL
| Assay Description
Inhibition of Selectin L binding |
J Med Chem 41: 4279-87 (1998)
Article DOI: 10.1021/jm980267x
BindingDB Entry DOI: 10.7270/Q2474BHN |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50072620
(1-[4-Methoxy-3-(3,4,5-trihydroxy-6-hydroxymethyl-t...)Show SMILES COc1ccc(cc1C1OC(CO)C(O)C(O)C1O)C1(CCCCC1)C(O)=O Show InChI InChI=1S/C20H28O8/c1-27-13-6-5-11(20(19(25)26)7-3-2-4-8-20)9-12(13)18-17(24)16(23)15(22)14(10-21)28-18/h5-6,9,14-18,21-24H,2-4,7-8,10H2,1H3,(H,25,26) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| PubMed
| n/a | n/a | 1.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sankyo Co. Ltd.
Curated by ChEMBL
| Assay Description
Inhibitory activity of the compound against L-selectin IgG chimeras binding to sLex coating 96 wells using competitive cell-free ELISA assay was dete... |
Bioorg Med Chem Lett 8: 3307-10 (1999)
BindingDB Entry DOI: 10.7270/Q2W0953H |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50205368
((5-{3-[(2',3',4'-trihydroxy-biphenyl-3-carbonyl)-a...)Show SMILES OC(=O)Cc1ccc(s1)-c1cccc(NC(=O)c2cccc(c2)-c2ccc(O)c(O)c2O)c1 Show InChI InChI=1S/C25H19NO6S/c27-20-9-8-19(23(30)24(20)31)14-3-1-5-16(11-14)25(32)26-17-6-2-4-15(12-17)21-10-7-18(33-21)13-22(28)29/h1-12,27,30-31H,13H2,(H,26,32)(H,28,29) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 1.10E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Revotar Biopharmaceuticals AG
Curated by ChEMBL
| Assay Description
Inhibition of human L-selectin after 2 hrs |
J Med Chem 50: 1101-15 (2007)
Article DOI: 10.1021/jm060536g
BindingDB Entry DOI: 10.7270/Q2TB17Q6 |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50205396
(3-[2-(3,4,5-trihydroxy-phenyl)-acetylamino]-benzoi...)Show InChI InChI=1S/C15H13NO6/c17-11-4-8(5-12(18)14(11)20)6-13(19)16-10-3-1-2-9(7-10)15(21)22/h1-5,7,17-18,20H,6H2,(H,16,19)(H,21,22) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 1.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Revotar Biopharmaceuticals AG
Curated by ChEMBL
| Assay Description
Inhibition of human L-selectin after 2 hrs |
J Med Chem 50: 1101-15 (2007)
Article DOI: 10.1021/jm060536g
BindingDB Entry DOI: 10.7270/Q2TB17Q6 |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50205377
(CHEMBL220254 | {2'-[(3,4,5-trihydroxybenzoyl)oxy]-...)Show SMILES OC(=O)Cc1cccc(c1)-c1ccccc1OC(=O)c1cc(O)c(O)c(O)c1 Show InChI InChI=1S/C21H16O7/c22-16-10-14(11-17(23)20(16)26)21(27)28-18-7-2-1-6-15(18)13-5-3-4-12(8-13)9-19(24)25/h1-8,10-11,22-23,26H,9H2,(H,24,25) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 1.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Revotar Biopharmaceuticals AG
Curated by ChEMBL
| Assay Description
Inhibition of human L-selectin after 2 hrs |
J Med Chem 50: 1101-15 (2007)
Article DOI: 10.1021/jm060536g
BindingDB Entry DOI: 10.7270/Q2TB17Q6 |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50205403
(5-{2-[(2'3',4'-hydroxy-biphenyl-3-carbonyl)-amino]...)Show SMILES OC(=O)c1ccc(s1)-c1ccccc1NC(=O)c1cccc(c1)-c1ccc(O)c(O)c1O Show InChI InChI=1S/C24H17NO6S/c26-18-9-8-15(21(27)22(18)28)13-4-3-5-14(12-13)23(29)25-17-7-2-1-6-16(17)19-10-11-20(32-19)24(30)31/h1-12,26-28H,(H,25,29)(H,30,31) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 1.60E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Revotar Biopharmaceuticals AG
Curated by ChEMBL
| Assay Description
Inhibition of human L-selectin after 2 hrs |
J Med Chem 50: 1101-15 (2007)
Article DOI: 10.1021/jm060536g
BindingDB Entry DOI: 10.7270/Q2TB17Q6 |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50060514
((S)-4-Methylcarbamoyl-4-[(R)-2-(2-tetradecyl-hexad...)Show SMILES CCCCCCCCCCCCCCC(CCCCCCCCCCCCCC)C(=O)N[C@H](COC1OC(C)C(O)C(O)C1O)C(=O)N[C@@H](CCC(O)=O)C(=O)NC Show InChI InChI=1S/C45H85N3O10/c1-5-7-9-11-13-15-17-19-21-23-25-27-29-35(30-28-26-24-22-20-18-16-14-12-10-8-6-2)42(54)48-37(33-57-45-41(53)40(52)39(51)34(3)58-45)44(56)47-36(43(55)46-4)31-32-38(49)50/h34-37,39-41,45,51-53H,5-33H2,1-4H3,(H,46,55)(H,47,56)(H,48,54)(H,49,50)/t34?,36-,37+,39?,40?,41?,45?/m0/s1 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 1.60E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Kanebo
Curated by ChEMBL
| Assay Description
Inhibition of Selectin L binding |
J Med Chem 41: 4279-87 (1998)
Article DOI: 10.1021/jm980267x
BindingDB Entry DOI: 10.7270/Q2474BHN |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50205394
((5-{2-[(2',3',4'-trihydroxy-biphenyl-4-carbonyl)-a...)Show SMILES OC(=O)Cc1ccc(s1)-c1ccccc1NC(=O)c1ccc(cc1)-c1ccc(O)c(O)c1O Show InChI InChI=1S/C25H19NO6S/c27-20-11-10-17(23(30)24(20)31)14-5-7-15(8-6-14)25(32)26-19-4-2-1-3-18(19)21-12-9-16(33-21)13-22(28)29/h1-12,27,30-31H,13H2,(H,26,32)(H,28,29) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 1.60E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Revotar Biopharmaceuticals AG
Curated by ChEMBL
| Assay Description
Inhibition of human L-selectin after 2 hrs |
J Med Chem 50: 1101-15 (2007)
Article DOI: 10.1021/jm060536g
BindingDB Entry DOI: 10.7270/Q2TB17Q6 |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50060515
((S)-4-Methylcarbamoyl-4-[(S)-2-(2-tetradecyl-hexad...)Show SMILES CCCCCCCCCCCCCCC(CCCCCCCCCCCCCC)C(=O)N[C@@H](COC1OC(C)C(O)C(O)C1O)C(=O)N[C@@H](CCC(O)=O)C(=O)NC Show InChI InChI=1S/C45H85N3O10/c1-5-7-9-11-13-15-17-19-21-23-25-27-29-35(30-28-26-24-22-20-18-16-14-12-10-8-6-2)42(54)48-37(33-57-45-41(53)40(52)39(51)34(3)58-45)44(56)47-36(43(55)46-4)31-32-38(49)50/h34-37,39-41,45,51-53H,5-33H2,1-4H3,(H,46,55)(H,47,56)(H,48,54)(H,49,50)/t34?,36-,37-,39?,40?,41?,45?/m0/s1 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 1.80E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Kanebo
Curated by ChEMBL
| Assay Description
Inhibition of Selectin L binding |
J Med Chem 41: 4279-87 (1998)
Article DOI: 10.1021/jm980267x
BindingDB Entry DOI: 10.7270/Q2474BHN |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50205375
(CHEMBL220419 | {3-[3-(3,4,5-trihydroxy-phenyl)-pro...)Show InChI InChI=1S/C17H17NO6/c19-13-7-11(8-14(20)17(13)24)4-5-15(21)18-12-3-1-2-10(6-12)9-16(22)23/h1-3,6-8,19-20,24H,4-5,9H2,(H,18,21)(H,22,23) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
| Article
PubMed
| n/a | n/a | 2.30E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Revotar Biopharmaceuticals AG
Curated by ChEMBL
| Assay Description
Inhibition of human L-selectin after 2 hrs |
J Med Chem 50: 1101-15 (2007)
Article DOI: 10.1021/jm060536g
BindingDB Entry DOI: 10.7270/Q2TB17Q6 |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50091501
(3-[(2S,5R)-3,6-Dioxo-7-(2-tetradecyl-hexadecyl)-5-...)Show SMILES CCCCCCCCCCCCCCC(CCCCCCCCCCCCCC)CN1CCCS[C@@H](CCC(O)=O)C(=O)N[C@H](CO[C@H]2O[C@H](CO)[C@@H](O)[C@@H](O)[C@@H]2O)C1=O Show InChI InChI=1S/C47H88N2O10S/c1-3-5-7-9-11-13-15-17-19-21-23-25-28-37(29-26-24-22-20-18-16-14-12-10-8-6-4-2)34-49-32-27-33-60-40(30-31-41(51)52)45(56)48-38(46(49)57)36-58-47-44(55)43(54)42(53)39(35-50)59-47/h37-40,42-44,47,50,53-55H,3-36H2,1-2H3,(H,48,56)(H,51,52)/t38-,39?,40+,42?,43?,44?,47?/m1/s1 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
| PubMed
| n/a | n/a | 2.34E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Nippon Organon K.K.
Curated by ChEMBL
| Assay Description
In vitro inhibitory activity of compound was determined against Selectin L binding by ELISA assay |
Bioorg Med Chem Lett 10: 1827-30 (2000)
BindingDB Entry DOI: 10.7270/Q2ZP46M8 |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50067552
(2-[(R)-2-(2-Tetradecyl-hexadecanoylamino)-3-(3,4,5...)Show SMILES CCCCCCCCCCCCCCC(CCCCCCCCCCCCCC)C(=O)N[C@H](COC1OC(C)C(O)C(O)C1O)C(=O)NC(CCC(O)=O)C(=O)OC Show InChI InChI=1S/C45H84N2O11/c1-5-7-9-11-13-15-17-19-21-23-25-27-29-35(30-28-26-24-22-20-18-16-14-12-10-8-6-2)42(53)47-37(33-57-45-41(52)40(51)39(50)34(3)58-45)43(54)46-36(44(55)56-4)31-32-38(48)49/h34-37,39-41,45,50-52H,5-33H2,1-4H3,(H,46,54)(H,47,53)(H,48,49)/t34?,36?,37-,39?,40?,41?,45?/m1/s1 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 2.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Kanebo
Curated by ChEMBL
| Assay Description
Inhibition of Selectin L binding |
J Med Chem 41: 4279-87 (1998)
Article DOI: 10.1021/jm980267x
BindingDB Entry DOI: 10.7270/Q2474BHN |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50072621
(CHEMBL112485 | [4-Methoxy-3-(3,4,5-trihydroxy-6-me...)Show InChI InChI=1S/C15H20O7/c1-7-12(18)13(19)14(20)15(22-7)9-5-8(6-11(16)17)3-4-10(9)21-2/h3-5,7,12-15,18-20H,6H2,1-2H3,(H,16,17) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| PubMed
| n/a | n/a | 3.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sankyo Co. Ltd.
Curated by ChEMBL
| Assay Description
Inhibitory activity of the compound against L-selectin IgG chimeras binding to sLex coating 96 wells using competitive cell-free ELISA assay was dete... |
Bioorg Med Chem Lett 8: 3307-10 (1999)
BindingDB Entry DOI: 10.7270/Q2W0953H |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50205384
((5-{2-[2-(3,4,5-trihydroxy-phenyl)-acetylamino]-ph...)Show SMILES OC(=O)Cc1ccc(s1)-c1ccccc1NC(=O)Cc1cc(O)c(O)c(O)c1 Show InChI InChI=1S/C20H17NO6S/c22-15-7-11(8-16(23)20(15)27)9-18(24)21-14-4-2-1-3-13(14)17-6-5-12(28-17)10-19(25)26/h1-8,22-23,27H,9-10H2,(H,21,24)(H,25,26) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 3.10E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Revotar Biopharmaceuticals AG
Curated by ChEMBL
| Assay Description
Inhibition of human L-selectin after 2 hrs |
J Med Chem 50: 1101-15 (2007)
Article DOI: 10.1021/jm060536g
BindingDB Entry DOI: 10.7270/Q2TB17Q6 |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50205370
(4-{[2-(3,4,5-trihydroxy-phenyl)-acetylamino]-methy...)Show SMILES OC(=O)[C@H]1CC[C@@H](CC1)NC(=O)Cc1cc(O)c(O)c(O)c1 |wU:3.2,wD:6.9,(3.02,-25.63,;3.03,-24.09,;4.37,-23.33,;1.7,-23.32,;.36,-24.08,;-.97,-23.31,;-.97,-21.77,;.37,-21,;1.7,-21.78,;-2.3,-21.01,;-3.63,-21.78,;-3.63,-23.32,;-4.97,-21.01,;-6.3,-21.78,;-6.29,-23.3,;-7.62,-24.08,;-7.61,-25.62,;-8.96,-23.31,;-10.29,-24.08,;-8.96,-21.77,;-10.29,-21,;-7.63,-21,)| Show InChI InChI=1S/C15H19NO6/c17-11-5-8(6-12(18)14(11)20)7-13(19)16-10-3-1-9(2-4-10)15(21)22/h5-6,9-10,17-18,20H,1-4,7H2,(H,16,19)(H,21,22)/t9-,10- | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 3.30E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Revotar Biopharmaceuticals AG
Curated by ChEMBL
| Assay Description
Inhibition of human L-selectin after 2 hrs |
J Med Chem 50: 1101-15 (2007)
Article DOI: 10.1021/jm060536g
BindingDB Entry DOI: 10.7270/Q2TB17Q6 |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50067553
(CHEMBL133134 | N-Methyl-3-[(R)-2-(2-tetradecyl-hex...)Show SMILES CCCCCCCCCCCCCCC(CCCCCCCCCCCCCC)C(=O)N[C@H](COC1OC(C)C(O)C(O)C1O)C(=O)NC(CC(O)=O)C(=O)NC Show InChI InChI=1S/C44H83N3O10/c1-5-7-9-11-13-15-17-19-21-23-25-27-29-34(30-28-26-24-22-20-18-16-14-12-10-8-6-2)41(53)47-36(43(55)46-35(31-37(48)49)42(54)45-4)32-56-44-40(52)39(51)38(50)33(3)57-44/h33-36,38-40,44,50-52H,5-32H2,1-4H3,(H,45,54)(H,46,55)(H,47,53)(H,48,49)/t33?,35?,36-,38?,39?,40?,44?/m1/s1 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 3.80E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Kanebo
Curated by ChEMBL
| Assay Description
Inhibition of Selectin L binding |
J Med Chem 41: 4279-87 (1998)
Article DOI: 10.1021/jm980267x
BindingDB Entry DOI: 10.7270/Q2474BHN |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50091500
((R)-4-Methylcarbamoyl-4-[(S)-2-(2-tetradecyl-hexad...)Show SMILES CCCCCCCCCCCCCCC(CCCCCCCCCCCCCC)C(=O)N[C@@H](CO[C@@H]1O[C@@H](CO)[C@H](O)[C@H](O)[C@H]1O)C(=O)N[C@H](CCC(O)=O)C(=O)NC Show InChI InChI=1S/C45H85N3O11/c1-4-6-8-10-12-14-16-18-20-22-24-26-28-34(29-27-25-23-21-19-17-15-13-11-9-7-5-2)42(55)48-36(44(57)47-35(43(56)46-3)30-31-38(50)51)33-58-45-41(54)40(53)39(52)37(32-49)59-45/h34-37,39-41,45,49,52-54H,4-33H2,1-3H3,(H,46,56)(H,47,57)(H,48,55)(H,50,51)/t35-,36+,37?,39?,40?,41?,45?/m1/s1 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| PubMed
| n/a | n/a | 4.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Nippon Organon K.K.
Curated by ChEMBL
| Assay Description
In vitro inhibitory activity of compound was determined against Selectin L binding by ELISA assay |
Bioorg Med Chem Lett 10: 1827-30 (2000)
BindingDB Entry DOI: 10.7270/Q2ZP46M8 |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50422276
(CHEMBL2303755)Show SMILES CCCCCCCCCCCCCCC(CCCCCCCCCCCCCC)C(=O)N[C@H](CO[C@H]1O[C@H](CO)[C@@H](O)[C@@H](O)[C@@H]1O)C(=O)N[C@@H](CCC(O)=O)C(=O)NC |r| Show InChI InChI=1S/C45H85N3O11/c1-4-6-8-10-12-14-16-18-20-22-24-26-28-34(29-27-25-23-21-19-17-15-13-11-9-7-5-2)42(55)48-36(44(57)47-35(43(56)46-3)30-31-38(50)51)33-58-45-41(54)40(53)39(52)37(32-49)59-45/h34-37,39-41,45,49,52-54H,4-33H2,1-3H3,(H,46,56)(H,47,57)(H,48,55)(H,50,51)/t35-,36+,37+,39+,40+,41-,45-/m0/s1 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 4.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Kanebo
Curated by ChEMBL
| Assay Description
Inhibition of Selectin L binding |
J Med Chem 41: 4279-87 (1998)
Article DOI: 10.1021/jm980267x
BindingDB Entry DOI: 10.7270/Q2474BHN |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50422275
(CHEMBL2303665)Show SMILES CCCCCCCCCCCCCCC(CCCCCCCCCCCCCC)C(=O)N[C@@H](CO[C@H]1O[C@H](CO)[C@@H](O)[C@@H](O)[C@@H]1O)C(=O)N[C@H](CCC(O)=O)C(=O)NC |r| Show InChI InChI=1S/C45H85N3O11/c1-4-6-8-10-12-14-16-18-20-22-24-26-28-34(29-27-25-23-21-19-17-15-13-11-9-7-5-2)42(55)48-36(44(57)47-35(43(56)46-3)30-31-38(50)51)33-58-45-41(54)40(53)39(52)37(32-49)59-45/h34-37,39-41,45,49,52-54H,4-33H2,1-3H3,(H,46,56)(H,47,57)(H,48,55)(H,50,51)/t35-,36+,37-,39-,40-,41+,45+/m1/s1 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 4.20E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Kanebo
Curated by ChEMBL
| Assay Description
Inhibition of Selectin L binding |
J Med Chem 41: 4279-87 (1998)
Article DOI: 10.1021/jm980267x
BindingDB Entry DOI: 10.7270/Q2474BHN |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50205371
(4-methyl-3-[3-(3,4,5-trihydroxy-phenyl)-propionyla...)Show InChI InChI=1S/C17H17NO6/c1-9-2-4-11(17(23)24)8-12(9)18-15(21)5-3-10-6-13(19)16(22)14(20)7-10/h2,4,6-8,19-20,22H,3,5H2,1H3,(H,18,21)(H,23,24) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 4.20E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Revotar Biopharmaceuticals AG
Curated by ChEMBL
| Assay Description
Inhibition of human L-selectin after 2 hrs |
J Med Chem 50: 1101-15 (2007)
Article DOI: 10.1021/jm060536g
BindingDB Entry DOI: 10.7270/Q2TB17Q6 |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50205374
((5-{2-[3-(2,3,4-trihydroxy-phenyl)-acryloylamino]-...)Show SMILES OC(=O)Cc1ccc(s1)-c1ccccc1NC(=O)\C=C\c1ccc(O)c(O)c1O Show InChI InChI=1S/C21H17NO6S/c23-16-8-5-12(20(27)21(16)28)6-10-18(24)22-15-4-2-1-3-14(15)17-9-7-13(29-17)11-19(25)26/h1-10,23,27-28H,11H2,(H,22,24)(H,25,26)/b10-6+ | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 4.30E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Revotar Biopharmaceuticals AG
Curated by ChEMBL
| Assay Description
Inhibition of human L-selectin after 2 hrs |
J Med Chem 50: 1101-15 (2007)
Article DOI: 10.1021/jm060536g
BindingDB Entry DOI: 10.7270/Q2TB17Q6 |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50422275
(CHEMBL2303665)Show SMILES CCCCCCCCCCCCCCC(CCCCCCCCCCCCCC)C(=O)N[C@@H](CO[C@H]1O[C@H](CO)[C@@H](O)[C@@H](O)[C@@H]1O)C(=O)N[C@H](CCC(O)=O)C(=O)NC |r| Show InChI InChI=1S/C45H85N3O11/c1-4-6-8-10-12-14-16-18-20-22-24-26-28-34(29-27-25-23-21-19-17-15-13-11-9-7-5-2)42(55)48-36(44(57)47-35(43(56)46-3)30-31-38(50)51)33-58-45-41(54)40(53)39(52)37(32-49)59-45/h34-37,39-41,45,49,52-54H,4-33H2,1-3H3,(H,46,56)(H,47,57)(H,48,55)(H,50,51)/t35-,36+,37-,39-,40-,41+,45+/m1/s1 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 4.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Kanebo
Curated by ChEMBL
| Assay Description
Inhibition of Selectin L binding |
J Med Chem 41: 4279-87 (1998)
Article DOI: 10.1021/jm980267x
BindingDB Entry DOI: 10.7270/Q2474BHN |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50205401
(4-{[3-(3,4,5-trihydroxy-phenyl)-propionylamino]-me...)Show SMILES OC(=O)[C@H]1CC[C@@H](CC1)NC(=O)CCc1cc(O)c(O)c(O)c1 |wU:3.2,wD:6.9,(23.8,-27.36,;23.8,-25.82,;25.14,-25.06,;22.47,-25.04,;21.13,-25.81,;19.81,-25.04,;19.81,-23.5,;21.14,-22.72,;22.47,-23.5,;18.47,-22.73,;17.14,-23.5,;17.14,-25.04,;15.81,-22.73,;14.47,-23.5,;13.14,-22.73,;11.84,-23.55,;10.49,-22.82,;9.18,-23.62,;10.45,-21.27,;9.1,-20.53,;11.77,-20.47,;11.73,-18.93,;13.12,-21.2,)| Show InChI InChI=1S/C16H21NO6/c18-12-7-9(8-13(19)15(12)21)1-6-14(20)17-11-4-2-10(3-5-11)16(22)23/h7-8,10-11,18-19,21H,1-6H2,(H,17,20)(H,22,23)/t10-,11- | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
| Article
PubMed
| n/a | n/a | 5.70E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Revotar Biopharmaceuticals AG
Curated by ChEMBL
| Assay Description
Inhibition of human L-selectin after 2 hrs |
J Med Chem 50: 1101-15 (2007)
Article DOI: 10.1021/jm060536g
BindingDB Entry DOI: 10.7270/Q2TB17Q6 |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50205376
((2'-{[(3,4,5-trihydroxyphenyl)acetyl]amino}-1,1'-b...)Show SMILES OC(=O)Cc1cccc(c1)-c1ccccc1NC(=O)Cc1cc(O)c(O)c(O)c1 Show InChI InChI=1S/C22H19NO6/c24-18-9-14(10-19(25)22(18)29)11-20(26)23-17-7-2-1-6-16(17)15-5-3-4-13(8-15)12-21(27)28/h1-10,24-25,29H,11-12H2,(H,23,26)(H,27,28) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
| Article
PubMed
| n/a | n/a | 8.70E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Revotar Biopharmaceuticals AG
Curated by ChEMBL
| Assay Description
Inhibition of human L-selectin after 2 hrs |
J Med Chem 50: 1101-15 (2007)
Article DOI: 10.1021/jm060536g
BindingDB Entry DOI: 10.7270/Q2TB17Q6 |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50205392
((5-{2-[2-(2',3',4'-trihydroxy-biphenyl-3-yl)-acety...)Show SMILES OC(=O)Cc1ccc(s1)-c1ccccc1NC(=O)Cc1cccc(c1)-c1ccc(O)c(O)c1O Show InChI InChI=1S/C26H21NO6S/c28-21-10-9-18(25(32)26(21)33)16-5-3-4-15(12-16)13-23(29)27-20-7-2-1-6-19(20)22-11-8-17(34-22)14-24(30)31/h1-12,28,32-33H,13-14H2,(H,27,29)(H,30,31) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 9.70E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Revotar Biopharmaceuticals AG
Curated by ChEMBL
| Assay Description
Inhibition of human L-selectin after 2 hrs |
J Med Chem 50: 1101-15 (2007)
Article DOI: 10.1021/jm060536g
BindingDB Entry DOI: 10.7270/Q2TB17Q6 |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50205389
((5-{2-[(2',3',4'-trihydroxy-biphenyl-3-carbonyl)-a...)Show SMILES OC(=O)Cc1ccc(s1)-c1ccccc1NC(=O)c1cccc(c1)-c1ccc(O)c(O)c1O Show InChI InChI=1S/C25H19NO6S/c27-20-10-9-17(23(30)24(20)31)14-4-3-5-15(12-14)25(32)26-19-7-2-1-6-18(19)21-11-8-16(33-21)13-22(28)29/h1-12,27,30-31H,13H2,(H,26,32)(H,28,29) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 9.80E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Revotar Biopharmaceuticals AG
Curated by ChEMBL
| Assay Description
Inhibition of human L-selectin after 2 hrs |
J Med Chem 50: 1101-15 (2007)
Article DOI: 10.1021/jm060536g
BindingDB Entry DOI: 10.7270/Q2TB17Q6 |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50072618
(1-[4-Methoxy-3-(3,4,5-trihydroxy-tetrahydro-pyran-...)Show SMILES COc1ccc(cc1C1OCC(O)C(O)C1O)C1(CCCCC1)C(O)=O Show InChI InChI=1S/C19H26O7/c1-25-14-6-5-11(19(18(23)24)7-3-2-4-8-19)9-12(14)17-16(22)15(21)13(20)10-26-17/h5-6,9,13,15-17,20-22H,2-4,7-8,10H2,1H3,(H,23,24) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| PubMed
| n/a | n/a | 1.10E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Sankyo Co. Ltd.
Curated by ChEMBL
| Assay Description
Inhibitory activity of the compound against L-selectin IgG chimeras binding to sLex coating 96 wells using competitive cell-free ELISA assay was dete... |
Bioorg Med Chem Lett 8: 3307-10 (1999)
BindingDB Entry DOI: 10.7270/Q2W0953H |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50067554
(4-Methylcarbamoyl-4-[(R)-3-(3,4,5-trihydroxy-6-met...)Show SMILES CCCCCCCCCCCC(CCCCCCCCCCC)C(=O)N[C@H](COC1OC(C)C(O)C(O)C1O)C(=O)NC(CCC(O)=O)C(=O)NC Show InChI InChI=1S/C39H73N3O10/c1-5-7-9-11-13-15-17-19-21-23-29(24-22-20-18-16-14-12-10-8-6-2)36(48)42-31(27-51-39-35(47)34(46)33(45)28(3)52-39)38(50)41-30(37(49)40-4)25-26-32(43)44/h28-31,33-35,39,45-47H,5-27H2,1-4H3,(H,40,49)(H,41,50)(H,42,48)(H,43,44)/t28?,30?,31-,33?,34?,35?,39?/m1/s1 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 1.20E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Kanebo
Curated by ChEMBL
| Assay Description
Inhibition of Selectin L binding |
J Med Chem 41: 4279-87 (1998)
Article DOI: 10.1021/jm980267x
BindingDB Entry DOI: 10.7270/Q2474BHN |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50205395
((5-{2-[3-(3,4,5-trihydroxy-phenyl)-propionylamino]...)Show SMILES OC(=O)Cc1ccc(s1)-c1ccccc1NC(=O)CCc1cc(O)c(O)c(O)c1 Show InChI InChI=1S/C21H19NO6S/c23-16-9-12(10-17(24)21(16)28)5-8-19(25)22-15-4-2-1-3-14(15)18-7-6-13(29-18)11-20(26)27/h1-4,6-7,9-10,23-24,28H,5,8,11H2,(H,22,25)(H,26,27) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 1.36E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Revotar Biopharmaceuticals AG
Curated by ChEMBL
| Assay Description
Inhibition of human L-selectin after 2 hrs |
J Med Chem 50: 1101-15 (2007)
Article DOI: 10.1021/jm060536g
BindingDB Entry DOI: 10.7270/Q2TB17Q6 |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50205404
((5-{2-[2-(2,3,4-trihydroxy-phenyl)-acetylamino]-ph...)Show SMILES OC(=O)Cc1ccc(s1)-c1ccccc1NC(=O)Cc1ccc(O)c(O)c1O Show InChI InChI=1S/C20H17NO6S/c22-15-7-5-11(19(26)20(15)27)9-17(23)21-14-4-2-1-3-13(14)16-8-6-12(28-16)10-18(24)25/h1-8,22,26-27H,9-10H2,(H,21,23)(H,24,25) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 1.46E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Revotar Biopharmaceuticals AG
Curated by ChEMBL
| Assay Description
Inhibition of human L-selectin after 2 hrs |
J Med Chem 50: 1101-15 (2007)
Article DOI: 10.1021/jm060536g
BindingDB Entry DOI: 10.7270/Q2TB17Q6 |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50205386
(2,3,4-trihydroxybenzoic acid | CHEMBL220779)Show InChI InChI=1S/C7H6O5/c8-4-2-1-3(7(11)12)5(9)6(4)10/h1-2,8-10H,(H,11,12) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
MCE
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 1.52E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Revotar Biopharmaceuticals AG
Curated by ChEMBL
| Assay Description
Inhibition of human L-selectin after 2 hrs |
J Med Chem 50: 1101-15 (2007)
Article DOI: 10.1021/jm060536g
BindingDB Entry DOI: 10.7270/Q2TB17Q6 |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50205391
((5-{2-[3-(3,4,5-trihydroxy-phenyl)-acryloylamino]-...)Show SMILES OC(=O)Cc1ccc(s1)-c1ccccc1NC(=O)\C=C\c1cc(O)c(O)c(O)c1 Show InChI InChI=1S/C21H17NO6S/c23-16-9-12(10-17(24)21(16)28)5-8-19(25)22-15-4-2-1-3-14(15)18-7-6-13(29-18)11-20(26)27/h1-10,23-24,28H,11H2,(H,22,25)(H,26,27)/b8-5+ | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 2.13E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Revotar Biopharmaceuticals AG
Curated by ChEMBL
| Assay Description
Inhibition of human L-selectin after 2 hrs |
J Med Chem 50: 1101-15 (2007)
Article DOI: 10.1021/jm060536g
BindingDB Entry DOI: 10.7270/Q2TB17Q6 |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50205373
(4-{[2-(3,4,5-trihydroxy-phenyl)-acetylamino]-methy...)Show InChI InChI=1S/C16H15NO6/c18-12-5-10(6-13(19)15(12)21)7-14(20)17-8-9-1-3-11(4-2-9)16(22)23/h1-6,18-19,21H,7-8H2,(H,17,20)(H,22,23) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
| Article
PubMed
| n/a | n/a | 2.62E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Revotar Biopharmaceuticals AG
Curated by ChEMBL
| Assay Description
Inhibition of human L-selectin after 2 hrs |
J Med Chem 50: 1101-15 (2007)
Article DOI: 10.1021/jm060536g
BindingDB Entry DOI: 10.7270/Q2TB17Q6 |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50085536
(3,4,5-Trihydroxybenzoate, X | 3,4,5-trihydroxybenz...)Show InChI InChI=1S/C7H6O5/c8-4-1-3(7(11)12)2-5(9)6(4)10/h1-2,8-10H,(H,11,12) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
MCE
KEGG
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 2.76E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Revotar Biopharmaceuticals AG
Curated by ChEMBL
| Assay Description
Inhibition of human L-selectin after 2 hrs |
J Med Chem 50: 1101-15 (2007)
Article DOI: 10.1021/jm060536g
BindingDB Entry DOI: 10.7270/Q2TB17Q6 |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50408284
(CHEMBL2029056)Show SMILES CCCCCCCCCCCCCCC(CCCCCCCCCCCCCC)CO[C@@H]1O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](OS([O-])(=O)=O)[C@H]2O)[C@H](O[C@@H]2O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]2O)[C@H]1O |r| Show InChI InChI=1S/C48H92O18S/c1-4-6-8-10-12-14-16-18-20-22-24-26-28-34(29-27-25-23-21-19-17-15-13-11-9-7-5-2)32-60-46-42(56)45(65-47-40(54)39(53)37(51)33(3)61-47)43(36(31-50)63-46)64-48-41(55)44(66-67(57,58)59)38(52)35(30-49)62-48/h33-56H,4-32H2,1-3H3,(H,57,58,59)/p-1/t33-,35+,36+,37+,38-,39+,40-,41+,42+,43+,44-,45+,46+,47-,48-/m0/s1 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
KEGG
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 3.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Kanebo
Curated by ChEMBL
| Assay Description
Inhibition of Selectin L binding |
J Med Chem 41: 4279-87 (1998)
Article DOI: 10.1021/jm980267x
BindingDB Entry DOI: 10.7270/Q2474BHN |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50050500
(CHEMBL3085443 | Sodium; 3,5-dihydroxy-2-[5-hydroxy...)Show SMILES [Na+].CCCCCCCCCCCCCCC(CCCCCCCCCCCCCC)CO[C@@H]1O[C@@H](CO)[C@@H](O[C@@H]2O[C@@H](CO)[C@H](O)[C@@H]([C@@H]2O)S([O-])(=O)=O)[C@H](O[C@H]2O[C@@H](C)[C@@H](O)[C@H](O)[C@@H]2O)[C@@H]1O |r| Show InChI InChI=1S/C48H92O17S.Na/c1-4-6-8-10-12-14-16-18-20-22-24-26-28-34(29-27-25-23-21-19-17-15-13-11-9-7-5-2)32-60-46-41(55)44(65-47-40(54)39(53)37(51)33(3)61-47)43(36(31-50)63-46)64-48-42(56)45(66(57,58)59)38(52)35(30-49)62-48;/h33-56H,4-32H2,1-3H3,(H,57,58,59);/q;+1/p-1/t33-,35-,36-,37+,38-,39-,40-,41-,42-,43+,44+,45-,46+,47+,48-;/m0./s1 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 3.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
New Drug Research Laboratory
Curated by ChEMBL
| Assay Description
Inhibitory concentration against blocking of Selectin L during migration of inflammatory cells to inflammatory site |
J Med Chem 39: 2055-9 (1996)
Article DOI: 10.1021/jm950877m
BindingDB Entry DOI: 10.7270/Q2KH0P0B |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50408284
(CHEMBL2029056)Show SMILES CCCCCCCCCCCCCCC(CCCCCCCCCCCCCC)CO[C@@H]1O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](OS([O-])(=O)=O)[C@H]2O)[C@H](O[C@@H]2O[C@@H](C)[C@@H](O)[C@@H](O)[C@@H]2O)[C@H]1O |r| Show InChI InChI=1S/C48H92O18S/c1-4-6-8-10-12-14-16-18-20-22-24-26-28-34(29-27-25-23-21-19-17-15-13-11-9-7-5-2)32-60-46-42(56)45(65-47-40(54)39(53)37(51)33(3)61-47)43(36(31-50)63-46)64-48-41(55)44(66-67(57,58)59)38(52)35(30-49)62-48/h33-56H,4-32H2,1-3H3,(H,57,58,59)/p-1/t33-,35+,36+,37+,38-,39+,40-,41+,42+,43+,44-,45+,46+,47-,48-/m0/s1 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
KEGG
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 3.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Kanebo Ltd.
Curated by ChEMBL
| Assay Description
Inhibitory activity against Selectin L expressed in endothelial cells |
J Med Chem 40: 362-9 (1997)
Article DOI: 10.1021/jm9606103
BindingDB Entry DOI: 10.7270/Q2QV3KM0 |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50205393
(4-{[3-(3,4,5-trihydroxy-phenyl)-propionylamino]-me...)Show InChI InChI=1S/C17H17NO6/c19-13-7-11(8-14(20)16(13)22)3-6-15(21)18-9-10-1-4-12(5-2-10)17(23)24/h1-2,4-5,7-8,19-20,22H,3,6,9H2,(H,18,21)(H,23,24) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
| Article
PubMed
| n/a | n/a | 3.08E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Revotar Biopharmaceuticals AG
Curated by ChEMBL
| Assay Description
Inhibition of human L-selectin after 2 hrs |
J Med Chem 50: 1101-15 (2007)
Article DOI: 10.1021/jm060536g
BindingDB Entry DOI: 10.7270/Q2TB17Q6 |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50050461
(5-(2-{2-[5-Acetylamino-2-hydroxymethyl-4-(2,3,4-tr...)Show SMILES C[C@@H]1O[C@@H](O[C@@H]2[C@H](CO[C@H](CO)[C@H]2O[C@@H]2O[C@H](O)[C@H](O[C@@]3(C[C@H](O)[C@@H](NC(C)=O)[C@@H](O3)[C@H](O)[C@H](O)CO)C(O)=O)[C@H](O)[C@H]2O)NC(C)=O)[C@@H](O)[C@H](O)[C@@H]1O Show InChI InChI=1S/C30H50N2O22/c1-8-16(39)18(41)20(43)27(49-8)50-22-11(31-9(2)35)7-48-14(6-34)23(22)51-28-21(44)19(42)25(26(45)52-28)54-30(29(46)47)4-12(37)15(32-10(3)36)24(53-30)17(40)13(38)5-33/h8,11-28,33-34,37-45H,4-7H2,1-3H3,(H,31,35)(H,32,36)(H,46,47)/t8-,11-,12-,13+,14+,15+,16+,17+,18+,19+,20-,21+,22+,23+,24+,25+,26-,27-,28+,30-/m0/s1 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
KEGG
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 3.50E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Institute of Cancer Research Laboratories
Curated by ChEMBL
| Assay Description
Inhibitory activity against human chimeric L-selectin-Ig |
J Med Chem 39: 1339-43 (1996)
Article DOI: 10.1021/jm9506478
BindingDB Entry DOI: 10.7270/Q2513ZWW |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50403679
(CHEMBL2111731)Show SMILES COc1ccc(cc1[C@H]1O[C@@H](C)[C@H](O)[C@H](O)[C@@H]1O)C1(CCCCC1)C(O)=O |r| Show InChI InChI=1S/C20H28O7/c1-11-15(21)16(22)17(23)18(27-11)13-10-12(6-7-14(13)26-2)20(19(24)25)8-4-3-5-9-20/h6-7,10-11,15-18,21-23H,3-5,8-9H2,1-2H3,(H,24,25)/t11-,15-,16-,17-,18+/m0/s1 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| PubMed
| n/a | n/a | 3.50E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Sankyo Co. Ltd.
Curated by ChEMBL
| Assay Description
Inhibitory activity of the compound against L-selectin IgG chimeras binding to sLex coating 96 wells using competitive cell-free ELISA assay was dete... |
Bioorg Med Chem Lett 8: 3307-10 (1999)
BindingDB Entry DOI: 10.7270/Q2W0953H |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50205381
((5-{2-[(3',4',5'-trihydroxy-biphenyl-3-carbonyl)-a...)Show SMILES OC(=O)Cc1ccc(s1)-c1ccccc1NC(=O)c1cccc(c1)-c1cc(O)c(O)c(O)c1 Show InChI InChI=1S/C25H19NO6S/c27-20-11-16(12-21(28)24(20)31)14-4-3-5-15(10-14)25(32)26-19-7-2-1-6-18(19)22-9-8-17(33-22)13-23(29)30/h1-12,27-28,31H,13H2,(H,26,32)(H,29,30) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 3.76E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Revotar Biopharmaceuticals AG
Curated by ChEMBL
| Assay Description
Inhibition of human L-selectin after 2 hrs |
J Med Chem 50: 1101-15 (2007)
Article DOI: 10.1021/jm060536g
BindingDB Entry DOI: 10.7270/Q2TB17Q6 |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50205372
(5-methylbenzene-1,2,3-triol | CHEMBL374735)Show InChI InChI=1S/C7H8O3/c1-4-2-5(8)7(10)6(9)3-4/h2-3,8-10H,1H3 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
MCE
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 3.85E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Revotar Biopharmaceuticals AG
Curated by ChEMBL
| Assay Description
Inhibition of human L-selectin after 2 hrs |
J Med Chem 50: 1101-15 (2007)
Article DOI: 10.1021/jm060536g
BindingDB Entry DOI: 10.7270/Q2TB17Q6 |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50422136
(CHEMBL2303852)Show SMILES CCCCCCCCCCCCCCC(CCCCCCCCCCCCCC)CO[C@@H]1O[C@@H](CO)[C@@H](O[C@@H]2O[C@@H](CO)[C@H](O)[C@H](OC(=O)C3CC(O)C(NC(C)=O)C(O3)C(O)C(O)CO)[C@@H]2O)[C@H](O[C@@H]2O[C@@H](C)[C@@H](O)[C@H](O)[C@@H]2O)[C@@H]1NC(C)=O |r| Show InChI InChI=1S/C61H112N2O22/c1-6-8-10-12-14-16-18-20-22-24-26-28-30-40(31-29-27-25-23-21-19-17-15-13-11-9-7-2)36-78-59-47(63-39(5)68)56(85-60-52(75)51(74)48(71)37(3)79-60)54(45(35-66)82-59)84-61-53(76)57(50(73)44(34-65)81-61)83-58(77)43-32-41(69)46(62-38(4)67)55(80-43)49(72)42(70)33-64/h37,40-57,59-61,64-66,69-76H,6-36H2,1-5H3,(H,62,67)(H,63,68)/t37-,41?,42?,43?,44-,45-,46?,47-,48+,49?,50-,51-,52-,53-,54+,55?,56+,57-,59+,60-,61-/m0/s1 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 4.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
New Drug Research Laboratory
Curated by ChEMBL
| Assay Description
Inhibitory concentration against blocking of Selectin L during migration of inflammatory cells to inflammatory site |
J Med Chem 39: 2055-9 (1996)
Article DOI: 10.1021/jm950877m
BindingDB Entry DOI: 10.7270/Q2KH0P0B |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50205382
((5-{2-[4-(2,3,4-trihydroxy-phenyl)-butyrylamino]-p...)Show SMILES OC(=O)Cc1ccc(s1)-c1ccccc1NC(=O)CCCc1ccc(O)c(O)c1O Show InChI InChI=1S/C22H21NO6S/c24-17-10-8-13(21(28)22(17)29)4-3-7-19(25)23-16-6-2-1-5-15(16)18-11-9-14(30-18)12-20(26)27/h1-2,5-6,8-11,24,28-29H,3-4,7,12H2,(H,23,25)(H,26,27) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 4.17E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Revotar Biopharmaceuticals AG
Curated by ChEMBL
| Assay Description
Inhibition of human L-selectin after 2 hrs |
J Med Chem 50: 1101-15 (2007)
Article DOI: 10.1021/jm060536g
BindingDB Entry DOI: 10.7270/Q2TB17Q6 |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50205380
(3-[3-(3,4,5-trihydroxy-phenyl)-propionylamino]-ben...)Show InChI InChI=1S/C16H15NO6/c18-12-6-9(7-13(19)15(12)21)4-5-14(20)17-11-3-1-2-10(8-11)16(22)23/h1-3,6-8,18-19,21H,4-5H2,(H,17,20)(H,22,23) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 4.66E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Revotar Biopharmaceuticals AG
Curated by ChEMBL
| Assay Description
Inhibition of human L-selectin after 2 hrs |
J Med Chem 50: 1101-15 (2007)
Article DOI: 10.1021/jm060536g
BindingDB Entry DOI: 10.7270/Q2TB17Q6 |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50205402
(4-methyl-3-[2-(3,4,5-trihydroxy-phenyl)-acetylamin...)Show InChI InChI=1S/C16H15NO6/c1-8-2-3-10(16(22)23)7-11(8)17-14(20)6-9-4-12(18)15(21)13(19)5-9/h2-5,7,18-19,21H,6H2,1H3,(H,17,20)(H,22,23) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 6.45E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Revotar Biopharmaceuticals AG
Curated by ChEMBL
| Assay Description
Inhibition of human L-selectin after 2 hrs |
J Med Chem 50: 1101-15 (2007)
Article DOI: 10.1021/jm060536g
BindingDB Entry DOI: 10.7270/Q2TB17Q6 |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50205398
(CHEMBL426378 | {2'-[3-(3,4,5-trihydroxy-phenyl)-pr...)Show SMILES OC(=O)Cc1cccc(c1)-c1ccccc1NC(=O)CCc1cc(O)c(O)c(O)c1 Show InChI InChI=1S/C23H21NO6/c25-19-11-15(12-20(26)23(19)30)8-9-21(27)24-18-7-2-1-6-17(18)16-5-3-4-14(10-16)13-22(28)29/h1-7,10-12,25-26,30H,8-9,13H2,(H,24,27)(H,28,29) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
| Article
PubMed
| n/a | n/a | 6.49E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Revotar Biopharmaceuticals AG
Curated by ChEMBL
| Assay Description
Inhibition of human L-selectin after 2 hrs |
J Med Chem 50: 1101-15 (2007)
Article DOI: 10.1021/jm060536g
BindingDB Entry DOI: 10.7270/Q2TB17Q6 |
More data for this
Ligand-Target Pair | |
L-selectin
(Homo sapiens (Human)) | BDBM50205378
((5-{2-[3-(2,3,4-trihydroxy-phenyl)-propionylamino]...)Show SMILES OC(=O)Cc1ccc(s1)-c1ccccc1NC(=O)CCc1ccc(O)c(O)c1O Show InChI InChI=1S/C21H19NO6S/c23-16-8-5-12(20(27)21(16)28)6-10-18(24)22-15-4-2-1-3-14(15)17-9-7-13(29-17)11-19(25)26/h1-5,7-9,23,27-28H,6,10-11H2,(H,22,24)(H,25,26) | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 8.58E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Revotar Biopharmaceuticals AG
Curated by ChEMBL
| Assay Description
Inhibition of human L-selectin after 2 hrs |
J Med Chem 50: 1101-15 (2007)
Article DOI: 10.1021/jm060536g
BindingDB Entry DOI: 10.7270/Q2TB17Q6 |
More data for this
Ligand-Target Pair | |
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