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 | ClH |
| Molecular Weight | 36.461 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| 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
| Title | Date | PubMed |
|---|---|---|
| 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 |
|
| Design, synthesis and anticonvulsive activities of potential prodrugs linked by two-carbon chain. | 2003 Oct |
|
| Energetic characterization of short helical polyalanine peptides in water: analysis of 13C=O chemical shift data. | 2005 Dec 7 |
|
| Design, synthesis, and structure-activity relationships of piperidine and dehydropiperidine carboxylic acids as novel, potent dual PPARalpha/gamma agonists. | 2008 Jun 15 |
|
| 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
Edited
Fri Dec 15 15:53:28 GMT 2023
by
admin
on
Fri Dec 15 15:53:28 GMT 2023
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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 Fri Dec 15 15:53:28 GMT 2023 , Edited by admin on Fri Dec 15 15:53:28 GMT 2023
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PRIMARY | Merck Index |