A2734
α5IA
≥98% (HPLC)
동의어(들):
1,2,4-Triazolo[3,4-a]phthalazine, 3-(5-methyl-3-isoxazolyl)-6-[(1-methyl-1H-1,2,3-triazol-4-yl)methoxy]-, 3-(5-Methylisoxazol-3-yl)-6-(1-methyl-1,2,3-triazol-4-yl)methoxy-1,2,4-triazolo[3,4-a]phthalazine
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모든 사진(1)
About This Item
실험식(Hill 표기법):
C17H14N8O2
CAS Number:
Molecular Weight:
362.35
MDL number:
UNSPSC 코드:
12352200
PubChem Substance ID:
NACRES:
NA.77
분석
≥98% (HPLC)
양식
powder
색상
off-white to light yellow
solubility
DMSO: >2 mg/mL
주관자
Merck & Co., Inc., Kenilworth, NJ, U.S.
저장 온도
2-8°C
SMILES string
Cc1cc(no1)-c2nnc3c4ccccc4c(OCc5cn(C)nn5)nn23
InChI
1S/C17H14N8O2/c1-10-7-14(22-27-10)16-20-19-15-12-5-3-4-6-13(12)17(21-25(15)16)26-9-11-8-24(2)23-18-11/h3-8H,9H2,1-2H3
InChI key
NZMJFRXKGUCYNP-UHFFFAOYSA-N
생화학적/생리학적 작용
α5IA is a selective inverse agonist for Α5 subtype of GABAA receptor with a higher intrinsic activity at the A5 subtype than other drugs. α5IA enhances cognition in laboratory animals without being proconvulsant or anxiogenic. α5IA acts as an "alcohol antagonist," markedly reducing the amnesic effect of alcohol and partially attenuating sedation, similar to Ro15-4513, but without the anxiogenic effect. α5IA offers promise as a tool to study cognitive disorders, memory function, and treatment of alcohol-related disorders.
α5IA is a selective inverse agonist for a5 subtype of GABAA receptor.
특징 및 장점
This compound was developed by Merck & Co., Inc., Kenilworth, NJ, U.S.. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.
Storage Class Code
13 - Non Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Gloves, type N95 (US)
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