BindingDB logo
myBDB logout

BDBM50063137 (R)-3-Methyl-2-{4-[2-(4-methylsulfanyl-phenyl)-2H-tetrazol-5-yl]-benzenesulfonylamino}-butyric acid::CHEMBL160153

SMILES: CSc1ccc(cc1)-n1nnc(n1)-c1ccc(cc1)S(=O)(=O)N[C@H](C(C)C)C(O)=O

InChI Key: InChIKey=CTGTUEAFFDISNJ-QGZVFWFLSA-N

Data: 8 IC50

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 8 hits for monomerid = 50063137   
Target/Host
(Institution)
LigandTarget/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
pHTemp
°C
Matrix metalloproteinase-9


(Homo sapiens (Human))
BDBM50063137
PNG
((R)-3-Methyl-2-{4-[2-(4-methylsulfanyl-phenyl)-2H-...)
Show SMILES CSc1ccc(cc1)-n1nnc(n1)-c1ccc(cc1)S(=O)(=O)N[C@H](C(C)C)C(O)=O
Show InChI InChI=1S/C19H21N5O4S2/c1-12(2)17(19(25)26)22-30(27,28)16-10-4-13(5-11-16)18-20-23-24(21-18)14-6-8-15(29-3)9-7-14/h4-12,17,22H,1-3H3,(H,25,26)/t17-/m1/s1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 5.90n/an/an/an/an/an/a



Shionogi & Co., Ltd.

Curated by ChEMBL


Assay Description
Inhibitory activity against human gelatinase B (Matrix metalloproteinase-9)


J Med Chem 41: 640-9 (1998)


Article DOI: 10.1021/jm9707582
BindingDB Entry DOI: 10.7270/Q2HD7TS9
More data for this
Ligand-Target Pair
Interstitial collagenase


(Homo sapiens (Human))
BDBM50063137
PNG
((R)-3-Methyl-2-{4-[2-(4-methylsulfanyl-phenyl)-2H-...)
Show SMILES CSc1ccc(cc1)-n1nnc(n1)-c1ccc(cc1)S(=O)(=O)N[C@H](C(C)C)C(O)=O
Show InChI InChI=1S/C19H21N5O4S2/c1-12(2)17(19(25)26)22-30(27,28)16-10-4-13(5-11-16)18-20-23-24(21-18)14-6-8-15(29-3)9-7-14/h4-12,17,22H,1-3H3,(H,25,26)/t17-/m1/s1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a>1.00E+3n/an/an/an/an/an/a



Shionogi & Co., Ltd.

Curated by ChEMBL


Assay Description
Inhibitory activity against Matrix metalloproteinase-1


J Med Chem 41: 640-9 (1998)


Article DOI: 10.1021/jm9707582
BindingDB Entry DOI: 10.7270/Q2HD7TS9
More data for this
Ligand-Target Pair
Matrix metalloproteinase-7 (MMP7)


(Homo sapiens (Human))
BDBM50063137
PNG
((R)-3-Methyl-2-{4-[2-(4-methylsulfanyl-phenyl)-2H-...)
Show SMILES CSc1ccc(cc1)-n1nnc(n1)-c1ccc(cc1)S(=O)(=O)N[C@H](C(C)C)C(O)=O
Show InChI InChI=1S/C19H21N5O4S2/c1-12(2)17(19(25)26)22-30(27,28)16-10-4-13(5-11-16)18-20-23-24(21-18)14-6-8-15(29-3)9-7-14/h4-12,17,22H,1-3H3,(H,25,26)/t17-/m1/s1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a>1.00E+3n/an/an/an/an/an/a



Shionogi & Co., Ltd.

Curated by ChEMBL


Assay Description
Inhibitory activity against Matrix metalloproteinase-7


J Med Chem 41: 640-9 (1998)


Article DOI: 10.1021/jm9707582
BindingDB Entry DOI: 10.7270/Q2HD7TS9
More data for this
Ligand-Target Pair
72 kDa type IV collagenase


(Homo sapiens (Human))
BDBM50063137
PNG
((R)-3-Methyl-2-{4-[2-(4-methylsulfanyl-phenyl)-2H-...)
Show SMILES CSc1ccc(cc1)-n1nnc(n1)-c1ccc(cc1)S(=O)(=O)N[C@H](C(C)C)C(O)=O
Show InChI InChI=1S/C19H21N5O4S2/c1-12(2)17(19(25)26)22-30(27,28)16-10-4-13(5-11-16)18-20-23-24(21-18)14-6-8-15(29-3)9-7-14/h4-12,17,22H,1-3H3,(H,25,26)/t17-/m1/s1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 13n/an/an/an/an/an/a



Shionogi & Co., Ltd.

Curated by ChEMBL


Assay Description
Inhibitory activity against human gelatinase A (matrix metalloproteinase-2 MMP2)


J Med Chem 41: 640-9 (1998)


Article DOI: 10.1021/jm9707582
BindingDB Entry DOI: 10.7270/Q2HD7TS9
More data for this
Ligand-Target Pair
Neutral Endopeptidase (NEP)


(Rattus norvegicus (Rat))
BDBM50063137
PNG
((R)-3-Methyl-2-{4-[2-(4-methylsulfanyl-phenyl)-2H-...)
Show SMILES CSc1ccc(cc1)-n1nnc(n1)-c1ccc(cc1)S(=O)(=O)N[C@H](C(C)C)C(O)=O
Show InChI InChI=1S/C19H21N5O4S2/c1-12(2)17(19(25)26)22-30(27,28)16-10-4-13(5-11-16)18-20-23-24(21-18)14-6-8-15(29-3)9-7-14/h4-12,17,22H,1-3H3,(H,25,26)/t17-/m1/s1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a>1.00E+3n/an/an/an/an/an/a



Shionogi & Co., Ltd.

Curated by ChEMBL


Assay Description
Inhibitory activity against neutral endopeptidase (NEP)


J Med Chem 41: 640-9 (1998)


Article DOI: 10.1021/jm9707582
BindingDB Entry DOI: 10.7270/Q2HD7TS9
More data for this
Ligand-Target Pair
Stromelysin-1


(Homo sapiens (Human))
BDBM50063137
PNG
((R)-3-Methyl-2-{4-[2-(4-methylsulfanyl-phenyl)-2H-...)
Show SMILES CSc1ccc(cc1)-n1nnc(n1)-c1ccc(cc1)S(=O)(=O)N[C@H](C(C)C)C(O)=O
Show InChI InChI=1S/C19H21N5O4S2/c1-12(2)17(19(25)26)22-30(27,28)16-10-4-13(5-11-16)18-20-23-24(21-18)14-6-8-15(29-3)9-7-14/h4-12,17,22H,1-3H3,(H,25,26)/t17-/m1/s1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a>1.00E+3n/an/an/an/an/an/a



Shionogi & Co., Ltd.

Curated by ChEMBL


Assay Description
Inhibitory activity against Matrix metalloproteinase-3


J Med Chem 41: 640-9 (1998)


Article DOI: 10.1021/jm9707582
BindingDB Entry DOI: 10.7270/Q2HD7TS9
More data for this
Ligand-Target Pair
Angiotensin-converting enzyme


(Homo sapiens (Human))
BDBM50063137
PNG
((R)-3-Methyl-2-{4-[2-(4-methylsulfanyl-phenyl)-2H-...)
Show SMILES CSc1ccc(cc1)-n1nnc(n1)-c1ccc(cc1)S(=O)(=O)N[C@H](C(C)C)C(O)=O
Show InChI InChI=1S/C19H21N5O4S2/c1-12(2)17(19(25)26)22-30(27,28)16-10-4-13(5-11-16)18-20-23-24(21-18)14-6-8-15(29-3)9-7-14/h4-12,17,22H,1-3H3,(H,25,26)/t17-/m1/s1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a>1.00E+3n/an/an/an/an/an/a



Shionogi & Co., Ltd.

Curated by ChEMBL


Assay Description
Inhibitory activity against Angiotensin I converting enzyme


J Med Chem 41: 640-9 (1998)


Article DOI: 10.1021/jm9707582
BindingDB Entry DOI: 10.7270/Q2HD7TS9
More data for this
Ligand-Target Pair
Endothelin-converting enzyme 1 (ECE1)


(Homo sapiens (Human))
BDBM50063137
PNG
((R)-3-Methyl-2-{4-[2-(4-methylsulfanyl-phenyl)-2H-...)
Show SMILES CSc1ccc(cc1)-n1nnc(n1)-c1ccc(cc1)S(=O)(=O)N[C@H](C(C)C)C(O)=O
Show InChI InChI=1S/C19H21N5O4S2/c1-12(2)17(19(25)26)22-30(27,28)16-10-4-13(5-11-16)18-20-23-24(21-18)14-6-8-15(29-3)9-7-14/h4-12,17,22H,1-3H3,(H,25,26)/t17-/m1/s1
PDB

UniProtKB/SwissProt
UniProtKB/TrEMBL

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a>1.00E+3n/an/an/an/an/an/a



Shionogi & Co., Ltd.

Curated by ChEMBL


Assay Description
Inhibitory activity against endothelin converting enzyme (ECE)


J Med Chem 41: 640-9 (1998)


Article DOI: 10.1021/jm9707582
BindingDB Entry DOI: 10.7270/Q2HD7TS9
More data for this
Ligand-Target Pair