Drug Information

Drug General Information
Drug ID
D0F2HJ
Former ID
DNC014167
Drug Name
2-Cinnamamido-N1-hydroxy-N4-pentylsuccinamide
Drug Type
Small molecular drug
Indication Discovery agent Investigative [530409]
Structure
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2D MOL

3D MOL
Formula
C18H25N3O4
Canonical SMILES
CCCCCNC(=O)CC(C(=O)NO)NC(=O)C=CC1=CC=CC=C1
InChI
1S/C18H25N3O4/c1-2-3-7-12-19-17(23)13-15(18(24)21-25)20-16(22)11-10-14-8-5-4-6-9-14/h4-6,8-11,15,25H,2-3,7,12-13H2,1H3,(H,19,23)(H,20,22)(H,21,24)/b11-10+/t15-/m1/s1
InChIKey
GEWJSTSZXRZGCY-AUECHBEKSA-N
PubChem Compound ID
45257111
Target and Pathway
Target(s) Aminopeptidase N Target Info Inhibitor [530409]
BioCyc Pathway Glutathione-mediated detoxification
KEGG Pathway Glutathione metabolism
Metabolic pathways
Renin-angiotensin system
Hematopoietic cell lineage
Pathway Interaction Database C-MYB transcription factor network
PathWhiz Pathway Glutathione Metabolism
Reactome Metabolism of Angiotensinogen to Angiotensins
WikiPathways Metabolism of Angiotensinogen to Angiotensins
Cardiac Progenitor Differentiation
miR-targeted genes in squamous cell - TarBase
miR-targeted genes in muscle cell - TarBase
miR-targeted genes in lymphocytes - TarBase
miR-targeted genes in leukocytes - TarBase
Glutathione metabolism
References
Ref 530409Bioorg Med Chem. 2009 Oct 15;17(20):7398-404. Epub 2009 Sep 24.Design, synthesis, and preliminary studies of the activity of novel derivatives of N-cinnamoyl-L-aspartic acid as inhibitors of aminopeptidase N/CD13.
Ref 530409Bioorg Med Chem. 2009 Oct 15;17(20):7398-404. Epub 2009 Sep 24.Design, synthesis, and preliminary studies of the activity of novel derivatives of N-cinnamoyl-L-aspartic acid as inhibitors of aminopeptidase N/CD13.

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