Drug General Information
Drug ID
D04ADG
Former ID
DCL001004
Drug Name
SU5416
Synonyms
Semaxanib; Semaxinib; Semaxnib; Semoxind; S 8442; SU 5416; VEGF Receptor 2 Kinase Inhibitor III; InSolution™ SU-5416; TSU-16; Semaxanib (USAN/INN); Methylene]-2H-indol-2-one; (3Z)-3-[(3,5-dimethyl-1H-pyrrol-2-yl)methylidene]-1,3-dihydro-2H-indol-2-one; (3Z)-3-[(3,5-dimethyl-1H-pyrrol-2-yl)methylidene]-1H-indol-2-one; 1,3-Dihydro-3-[(3,5-dimethyl-1H-pyrrol-2-yl); 1,3-Dihydro-3-[(3,5-dimethyl-1H-pyrrol-2-yl)methylene]-2H-indol-2-one; 3-((Z)-(3,5-Dimethylpyrrol-2-yl)methylene)-2-indolinone; 3-(1-(3,5-Dimethyl-1H-pyrrol-2-yl)meth-(Z)-ylidene)-2-oxo-2,3-dihydroindole; 3-(2,4-dimethylpyrrol-5-yl)methylidene-indolin-2-one; 3-[(2,4-Dimethylpyrrol-5-yl)methylidene]-indolin-2-one; 3-[(2,4-dimethylpyrrol-5-yl)methylidenyl]indolin-2-one; 3-[(3,5-dimethyl-1H-pyrrol-2-yl)methylidene]-1,3-dihydro-2H-indol-2-one
Drug Type
Small molecular drug
Indication Multiple myeloma; HIV infections [ICD9: 001-139, 042, 203.0; ICD10:B20-B24, C90] Phase 2 [468143], [527804], [537114]
Company
Sugen
Structure
Download
2D MOL

3D MOL

Formula
C15H14N2O
InChI
InChI=1S/C15H14N2O/c1-9-7-10(2)16-14(9)8-12-11-5-3-4-6-13(11)17-15(12)18/h3-8,16H,1-2H3,(H,17,18)/b12-8-
InChIKey
WUWDLXZGHZSWQZ-WQLSENKSSA-N
CAS Number
CAS 204005-46-9
PubChem Compound ID
PubChem Substance ID
Target and Pathway
Target(s) Aryl hydrocarbon receptor Target Info Modulator [527804]
References
Ref 468143(http://www.guidetopharmacology.org/) Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Ligand id: 5056).
Ref 527804A Phase I study of the angiogenesis inhibitor SU5416 (semaxanib) in solid tumours, incorporating dynamic contrast MR pharmacodynamic end points. Br J Cancer. 2005 Oct 17;93(8):876-83.
Ref 537114Emerging therapies for multiple myeloma. Expert Opin Emerg Drugs. 2009 Mar;14(1):99-127.
Ref 527804A Phase I study of the angiogenesis inhibitor SU5416 (semaxanib) in solid tumours, incorporating dynamic contrast MR pharmacodynamic end points. Br J Cancer. 2005 Oct 17;93(8):876-83.

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