Drug Information
Drug General Information | Top | |||
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Drug ID |
D0Y1NM
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Former ID |
DNC006031
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Drug Name |
(R)-2-(biphenyl-4-sulfonylamino)-propionic acid
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Synonyms |
SCHEMBL4651862; CHEMBL198184; BDBM24034; biphenylsulfonamide carboxylate, 11; (2R)-2-[(4-phenylbenzene)sulfonamido]propanoic acid
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Drug Type |
Small molecular drug
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Indication | Discovery agent [ICD-11: N.A.] | Investigative | [1] | |
Structure |
Download2D MOL |
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Formula |
C15H15NO4S
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Canonical SMILES |
CC(C(=O)O)NS(=O)(=O)C1=CC=C(C=C1)C2=CC=CC=C2
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InChI |
1S/C15H15NO4S/c1-11(15(17)18)16-21(19,20)14-9-7-13(8-10-14)12-5-3-2-4-6-12/h2-11,16H,1H3,(H,17,18)/t11-/m1/s1
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InChIKey |
KXVXZFCETOKHTC-LLVKDONJSA-N
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PubChem Compound ID |
Target and Pathway | Top | |||
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Target(s) | Aggrecanase-1 (ADAMTS4) | Target Info | Inhibitor | [1] |
Reactome | Degradation of the extracellular matrix | |||
O-glycosylation of TSR domain-containing proteins | ||||
WikiPathways | Endochondral Ossification |
References | Top | |||
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REF 1 | Synthesis and biological evaluation of biphenylsulfonamide carboxylate aggrecanase-1 inhibitors. Bioorg Med Chem Lett. 2006 Jan 15;16(2):311-6. |
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