Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C6H11NO2.ClH |
| Molecular Weight | 165.618 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.OC(=O)C1CCNCC1
InChI
InChIKey=NVUYWKBRSRPYMH-UHFFFAOYSA-N
InChI=1S/C6H11NO2.ClH/c8-6(9)5-1-3-7-4-2-5;/h5,7H,1-4H2,(H,8,9);1H
| 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 |
| Molecular Formula | ClH |
| Molecular Weight | 36.461 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Intercepting the synthesis of triazine dendrimers with nucleophilic pharmacophores: a general strategy toward drug delivery vehicles. | 2009-10-07 |
|
| Discovery of leukotriene A4 hydrolase inhibitors using metabolomics biased fragment crystallography. | 2009-08-13 |
|
| Aqua-bis(4-nitro-benzoato)-κO,O';κO-(piperidinium-4-carboxyl-ato-κO,O')cadmium(II). | 2009-05-20 |
|
| The identification of orally bioavailable thrombopoietin agonists. | 2009-03-01 |
|
| Modifications of the isonipecotic acid fragment of SNS-032: analogs with improved permeability and lower efflux ratio. | 2008-12-01 |
|
| Design, synthesis, and structure-activity relationships of piperidine and dehydropiperidine carboxylic acids as novel, potent dual PPARalpha/gamma agonists. | 2008-06-15 |
|
| Energetic characterization of short helical polyalanine peptides in water: analysis of 13C=O chemical shift data. | 2005-12-07 |
|
| Temperature effects on the hydrogen-bond patterns in 4-piperidinecarboxylic acid. | 2005-02 |
|
| 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. | 2004-12 |
|
| Facile synthesis of 4-substituted-4-aminopiperidine derivatives, the key building block of piperazine-based CCR5 antagonists. | 2004-07-16 |
|
| Activation of single heteromeric GABA(A) receptor ion channels by full and partial agonists. | 2004-06-01 |
|
| Design, synthesis and anticonvulsive activity of analogs of gamma-vinyl GABA. | 2004-05 |
|
| Synthetic methodology utilized to prepare substituted imidazole p38 MAP kinase inhibitors. | 2003-11 |
|
| Design, synthesis and anticonvulsive activities of potential prodrugs linked by two-carbon chain. | 2003-10 |
|
| Highly water-soluble derivatives of the anesthetic agent propofol: in vitro and in vivo evaluation of cyclic amino acid esters. | 2003-09 |
|
| Phosphinic, phosphonic and seleninic acid bioisosteres of isonipecotic acid as novel and selective GABA(C) receptor antagonists. | 2003-06 |
|
| Xanthamide fluorescent dyes. | 2002-12-15 |
|
| Zwitterionic 4-piperidinecarboxylic acid monohydrate. | 2001-08 |
|
| Short, solubilized polyalanines are conformational chameleons: exceptionally helical if N- and C-capped with helix stabilizers, weakly to moderately helical if capped with rigid spacers. | 2001-01-16 |
|
| Alternative splicing of a Drosophila GABA receptor subunit gene identifies determinants of agonist potency. | 2001 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:12:15 GMT 2025
by
admin
on
Mon Mar 31 18:12:15 GMT 2025
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| Record UNII |
9Y7QNE4DH3
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| Record Status |
Validated (UNII)
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| Record Version |
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9Y7QNE4DH3
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DTXSID00208564
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5984-56-5
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22298
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m6505
Created by
admin on Mon Mar 31 18:12:15 GMT 2025 , Edited by admin on Mon Mar 31 18:12:15 GMT 2025
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PRIMARY | Merck Index |