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Details

Stereochemistry ACHIRAL
Molecular Formula C6H11NO2
Molecular Weight 129.157
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Isonipecotic acid

SMILES

OC(=O)C1CCNCC1

InChI

InChIKey=SRJOCJYGOFTFLH-UHFFFAOYSA-N
InChI=1S/C6H11NO2/c8-6(9)5-1-3-7-4-2-5/h5,7H,1-4H2,(H,8,9)

HIDE SMILES / InChI

Molecular Formula C6H11NO2
Molecular Weight 129.157
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Alternative splicing of a Drosophila GABA receptor subunit gene identifies determinants of agonist potency.
2001
Zwitterionic 4-piperidinecarboxylic acid monohydrate.
2001 Aug
Xanthamide fluorescent dyes.
2002 Dec 15
Phosphinic, phosphonic and seleninic acid bioisosteres of isonipecotic acid as novel and selective GABA(C) receptor antagonists.
2003 Jun
Synthetic methodology utilized to prepare substituted imidazole p38 MAP kinase inhibitors.
2003 Nov
Design, synthesis and anticonvulsive activities of potential prodrugs linked by two-carbon chain.
2003 Oct
Highly water-soluble derivatives of the anesthetic agent propofol: in vitro and in vivo evaluation of cyclic amino acid esters.
2003 Sep
Characterization and crystal structure of cadmium(II) halide complexes with amino acids and their derivatives VI. The comparison of crystal structures of cadmium(II) halide complexes with three kinds of piperidine carboxylic acids.
2004 Dec
Facile synthesis of 4-substituted-4-aminopiperidine derivatives, the key building block of piperazine-based CCR5 antagonists.
2004 Jul 16
Activation of single heteromeric GABA(A) receptor ion channels by full and partial agonists.
2004 Jun 1
Design, synthesis and anticonvulsive activity of analogs of gamma-vinyl GABA.
2004 May
Energetic characterization of short helical polyalanine peptides in water: analysis of 13C=O chemical shift data.
2005 Dec 7
Temperature effects on the hydrogen-bond patterns in 4-piperidinecarboxylic acid.
2005 Feb
Discovery of leukotriene A4 hydrolase inhibitors using metabolomics biased fragment crystallography.
2009 Aug 13
Aqua-bis(4-nitro-benzoato)-κO,O';κO-(piperidinium-4-carboxyl-ato-κO,O')cadmium(II).
2009 May 20
Intercepting the synthesis of triazine dendrimers with nucleophilic pharmacophores: a general strategy toward drug delivery vehicles.
2009 Oct 7
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 02:24:32 GMT 2023
Edited
by admin
on Sat Dec 16 02:24:32 GMT 2023
Record UNII
M5TZP1RWIE
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
Isonipecotic acid
MI  
Systematic Name English
NSC-61049
Code English
Isonipecotinic acid
Common Name English
Piperidin-4-carboxylic acid
Systematic Name English
Hexahydroisonicotinic acid
Systematic Name English
ISONIPECOTIC ACID [MI]
Common Name English
4-Carboxypiperidine
Systematic Name English
4-Piperidinecarboxylic acid
Systematic Name English
Code System Code Type Description
NSC
61049
Created by admin on Sat Dec 16 02:24:32 GMT 2023 , Edited by admin on Sat Dec 16 02:24:32 GMT 2023
PRIMARY
PUBCHEM
3773
Created by admin on Sat Dec 16 02:24:32 GMT 2023 , Edited by admin on Sat Dec 16 02:24:32 GMT 2023
PRIMARY
EPA CompTox
DTXSID9060100
Created by admin on Sat Dec 16 02:24:32 GMT 2023 , Edited by admin on Sat Dec 16 02:24:32 GMT 2023
PRIMARY
ECHA (EC/EINECS)
207-872-3
Created by admin on Sat Dec 16 02:24:32 GMT 2023 , Edited by admin on Sat Dec 16 02:24:32 GMT 2023
PRIMARY
FDA UNII
M5TZP1RWIE
Created by admin on Sat Dec 16 02:24:32 GMT 2023 , Edited by admin on Sat Dec 16 02:24:32 GMT 2023
PRIMARY
WIKIPEDIA
ISONIPECOTIC ACID
Created by admin on Sat Dec 16 02:24:32 GMT 2023 , Edited by admin on Sat Dec 16 02:24:32 GMT 2023
PRIMARY
MERCK INDEX
m6505
Created by admin on Sat Dec 16 02:24:32 GMT 2023 , Edited by admin on Sat Dec 16 02:24:32 GMT 2023
PRIMARY Merck Index
CAS
498-94-2
Created by admin on Sat Dec 16 02:24:32 GMT 2023 , Edited by admin on Sat Dec 16 02:24:32 GMT 2023
PRIMARY