Drug Information

Drug General Information
Drug ID
D0B9ZE
Former ID
DIB019496
Drug Name
compound 40
Synonyms
H(3)N(+)CH(CH(2)CH(2)SO(3)(-))CH(SH)CO-Ile-(3-COOH)Pro
Drug Type
Small molecular drug
Indication Discovery agent Investigative [525655]
Structure
Download
2D MOL
Formula
C17H29N3O9S2
InChI
InChI=1S/C17H29N3O9S2/c1-3-8(2)11(19-14(21)13(30)10(18)5-7-31(27,28)29)15(22)20-6-4-9(16(23)24)12(20)17(25)26/h8-13,30H,3-7,18H2,1-2H3,(H,19,21)(H,23,24)(H,25,26)(H,27,28,29)/t8-,9?,10-,11+,12+,13-/m1/s1
InChIKey
HUWSZNZAROKDRZ-RRLWZMAJSA-N
PubChem Compound ID
44365325
PubChem Substance ID
103393310, 252166830
Target and Pathway
Target(s) Glutamyl aminopeptidase Target Info Inhibitor [525655]
KEGG Pathway Renin-angiotensin system
NetPath Pathway IL2 Signaling Pathway
Reactome Metabolism of Angiotensinogen to Angiotensins
WikiPathways Metabolism of Angiotensinogen to Angiotensins
References
Ref 525655Investigation of subsite preferences in aminopeptidase A (EC 3.4.11.7) led to the design of the first highly potent and selective inhibitors of this enzyme. J Med Chem. 1999 Dec 16;42(25):5197-211.
Ref 525655Investigation of subsite preferences in aminopeptidase A (EC 3.4.11.7) led to the design of the first highly potent and selective inhibitors of this enzyme. J Med Chem. 1999 Dec 16;42(25):5197-211.

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