General Information of the Drug (ID: M6ADRUG0134)
Name
Methyl piperidine-3-carboxylate
Synonyms
methyl piperidine-3-carboxylate, 50585-89-2, Piperidine-3-carboxylic acid methyl ester, methyl nipecotate, Methylpiperidine-3-carboxylate, MFCD00797850, 3-Piperidinecarboxylic acid, methyl ester, MFCD09752680, METHYL 3-PIPERIDINECARBOXYLATE, NSC522506, nipecotic acid methylester, 3-methoxycarbonylpiperidine, SCHEMBL763374, DTXSID20325989, BCDBHIAXYFPJCT-UHFFFAOYSA-N, Methyl (S)-3-piperidinecarboxylate, BBL101450, STL555246, AKOS005259002, AC-5453, CS-W005063, FM56436, NSC-522506, PB17641, PB34398, SB10235, 3-piperidinecarboxylic acid methyl ester, DS-10878, SY003160, SY030269, DB-007697, EN300-25335, A828186, Piperidine-3-carboxylic acid methyl ester;Methyl nipecotate
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Structure
3D MOL
Formula
C7H13NO2
InChI
InChI=1S/C7H13NO2/c1-10-7(9)6-3-2-4-8-5-6/h6,8H,2-5H2,1H3
InChIKey
BCDBHIAXYFPJCT-UHFFFAOYSA-N
PubChem CID
351626
References
Ref 1 Metabolism of capsaicin by cytochrome P450 produces novel dehydrogenated metabolites and decreases cytotoxicity to lung and liver cells. Chem Res Toxicol. 2003 Mar;16(3):336-49. doi: 10.1021/tx025599q.