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Chemical compound
α-Hydroxyetizolam
Other names α-Hydroxyetizolam
Dependence liability Moderate
Routes of administration Oral, sublingual, rectal
Metabolism
Hepatic
Elimination half-life 8.2 hours
[1]
Excretion
Kidney
1-[7-(2-chlorophenyl)-13-methyl-3-thia-1,8,11,12-tetrazatricyclo[8.3.0.02,6]trideca-2(6),4,7,10,12-pentaen-4-yl]ethanol
CAS Number
PubChem
CID
ChemSpider
UNII
CompTox Dashboard (
EPA )
Formula C 17 H 15 Cl N 4 O S
Molar mass 358.84 g·mol−1 3D model (
JSmol )
CC1=NN=C2N1C3=C(C=C(S3)C(C)O)C(=NC2)C4=CC=CC=C4Cl
InChI=1S/C17H15ClN4OS/c1-9(23)14-7-12-16(11-5-3-4-6-13(11)18)19-8-15-21-20-10(2)22(15)17(12)24-14/h3-7,9,23H,8H2,1-2H3
Key:YRJXUAYHZCDGDO-UHFFFAOYSA-N
α-Hydroxyetizolam is the pharmacologically
active metabolite of
etizolam .
[2] α-Hydroxyetizolam has a half-life of approximately 8.2 hours.
[3]
Etizolam's other non-pharmacologically active metabolite in humans is 8-hydroxyetizolam.
[2]
See also
References
^ Fracasso C, Confalonieri S, Garattini S, Caccia S (1991-02-01). "Single and multiple dose pharmacokinetics of etizolam in healthy subjects". European Journal of Clinical Pharmacology . 40 (2): 181–185.
doi :
10.1007/BF00280074 .
PMID
2065698 .
S2CID
10176681 .
^
a
b
"alpha-Hydroxyetizolam" . PubChem . U.S. National Library of Medicine. Retrieved 2021-02-23 .
^ Nakamae T, Shinozuka T, Sasaki C, Ogamo A, Murakami-Hashimoto C, Irie W, et al. (November 2008). "Case report: Etizolam and its major metabolites in two unnatural death cases". Forensic Science International . 182 (1–3): e1-6.
doi :
10.1016/j.forsciint.2008.08.012 .
PMID
18976871 .
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