Gamma-Hydroxyvaleric acid

<span title="International nonproprietary name (INN): <nowiki>*gamma*-Hydroxyvaleric acid</nowiki>">*gamma*-Hydroxyvaleric acid
Clinical data
Other names	γ-Hydroxyvaleric acid; ; ; ; GVB
Legal status
Legal status	Page Àtụ:Plainlist/styles.css has no content. <abbr class="country-name" title="<nowiki>United States</nowiki>">US: DEA na-ewere GHV dị ka ihe yiri ya.; N'ozuzu: enweghị nchịkwa;
Ihe ndị na-eme ka a mata ya
	Aha IUPAC 4-Hydroxyvaleric acid;
Nọmba CAS	13532-37-1;
PubChem <abbr title="<nowiki>Compound ID</nowiki>">CID	114539;
ChemSpider	102591;
UNII	58B139Q3RL;
CompTox Dashboard (<abbr title="<nowiki>U.S. Environmental Protection Agency</nowiki>">EPA)	DTXSID60928958 ;
<span title="echa.europa.eu">ECHA InfoCard</span>	100.033.516
Ihe omuma kemịkal na nke anụ ahụ
Nhazi	C5H10O3
Ọkpụkpụ nke ọkpụkpụ	118.132 g·mol-1

γ-Hydroxyvaleric acid (GHV), nke a makwaara dị ka 4-methyl-GHB, bụ ọgwụ mmepụta metụtara γ-hydroxybutyric acid (GHB). A na-ahụ ya mgbe ụfọdụ n'ahịa na-acha ntụ ntụ ụlọ na ụdị nke ụwa họrọ site n'ime ka ndị ọzọ na ụdị nke dị ka ihe ọzọ iwu kwadoro na GHB, mana na-enwe ike dị ala na nsị dị elu, ihe onwunwe ndị na-egbochi ojiji ntụrụndụ ya.^[2]^[3]

γ-Valerolactone (GVL) na-arụ ọrụ dị ka prodrug na GHV, n'ụzọ yiri otú γ-butyrolactone (GBL) si bụrụ prodrug na ГHB.^[4]

Hụkwa[dezie | dezie ebe o si]

1,4-Butanediol (1-4-BD)
Aceburic acid
Valerenic acid
Valeric acid

Ntụaka[dezie | dezie ebe o si]

↑ "GHB and Analogues: Fast Facts". National Drug Intelligence Center. January 1, 2006. Archived from the original on July 5, 2023. Retrieved July 5, 2023.
↑ Carter LP (April 2005). "Comparison of the behavioral effects of gamma-hydroxybutyric acid (GHB) and its 4-methyl-substituted analog, gamma-hydroxyvaleric acid (GHV)". Drug and Alcohol Dependence 78 (1): 91–9. DOI:10.1016/j.drugalcdep.2004.10.002. PMID 15769562.
↑ Fred Smith (31 December 2004). Handbook of Forensic Drug Analysis. Academic Press, 462–. ISBN 978-0-08-047289-8.
↑ (2013) "Uptake of gamma-valerolactone--detection of gamma-hydroxyvaleric acid in human urine samples". J Anal Toxicol 37 (4): 250–4. DOI:10.1093/jat/bkt013. PMID 23486087.

[1] "GHB and Analogues: Fast Facts". National Drug Intelligence Center. January 1, 2006. Archived from the original on July 5, 2023. Retrieved July 5, 2023.

[pmid15769562-2] Carter LP (April 2005). "Comparison of the behavioral effects of gamma-hydroxybutyric acid (GHB) and its 4-methyl-substituted analog, gamma-hydroxyvaleric acid (GHV)". Drug and Alcohol Dependence 78 (1): 91–9. DOI:10.1016/j.drugalcdep.2004.10.002. PMID 15769562.

[Smith2004-3] Fred Smith (31 December 2004). Handbook of Forensic Drug Analysis. Academic Press, 462–. ISBN 978-0-08-047289-8.

[pmid23486087-4] (2013) "Uptake of gamma-valerolactone--detection of gamma-hydroxyvaleric acid in human urine samples". J Anal Toxicol 37 (4): 250–4. DOI:10.1093/jat/bkt013. PMID 23486087.

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