Drug General Information
Drug ID
D02YPU
Former ID
DNCL002966
Drug Name
Pyridoxamine
Synonyms
Pyridorin (TN)
Drug Type
Small molecular drug
Indication Diabetic kidney disease; Diabetic nephropathy [ICD9: 250.4; ICD10:E11.22, E11.21] Phase 3 [524788]
Company
Nephrogenex
Structure
Download
2D MOL

3D MOL

Formula
C8H12N2O2
Canonical SMILES
CC1=NC=C(C(=C1O)CN)CO
InChI
1S/C8H12N2O2/c1-5-8(12)7(2-9)6(4-11)3-10-5/h3,11-12H,2,4,9H2,1H3
InChIKey
NHZMQXZHNVQTQA-UHFFFAOYSA-N
PubChem Compound ID
PubChem Substance ID
ChEBI ID
ChEBI:16410
Target and Pathway
Target(s) Advanced glycosylation end product-specific receptor Target Info Inhibitor [526411], [530891]
Pathway Interaction Database amb2 Integrin signaling
Reactome RIP-mediated NFkB activation via ZBP1
DEx/H-box helicases activate type I IFN and inflammatory cytokines production
TAK1 activates NFkB by phosphorylation and activation of IKKs complex
Advanced glycosylation endproduct receptor signaling
TRAF6 mediated NF-kB activation
WikiPathways NRF2 pathway
Nuclear Receptors Meta-Pathway
Cytosolic sensors of pathogen-associated DNA
TAK1 activates NFkB by phosphorylation and activation of IKKs complex
AGE/RAGE pathway
RIG-I/MDA5 mediated induction of IFN-alpha/beta pathways
Advanced glycosylation endproduct receptor signaling
References
Ref 524788ClinicalTrials.gov (NCT02156843) Pyridorin in Diabetic Nephropathy. U.S. National Institutes of Health.
Ref 526411The AGE inhibitor pyridoxamine inhibits development of retinopathy in experimental diabetes. Diabetes. 2002 Sep;51(9):2826-32.
Ref 530891Pyridoxamine, an inhibitor of advanced glycation end product (AGE) formation ameliorates insulin resistance in obese, type 2 diabetic mice. Protein Pept Lett. 2010 Sep;17(9):1177-81.

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