A 967079

A 967079 구조식 이미지
카스 번호:
1170613-55-4
상품명:
A 967079
동의어(영문):
A 967079;(1E,3E)-1-(4-Fluorophenyl)-2-Methyl-1-penten-3-one oxiMe;(1E,3E)-1-(4-Fluorophenyl)-2-methyl-1-pentene-3-one oxime;1-Penten-3-one, 1-(4-fluorophenyl)-2-methyl-, oxime, (1E,3E)-;TRP Channel,inhibit,Transient receptor potential channels,A 967079,Inhibitor,A-967079,A967079
CBNumber:
CB22650391
분자식:
C12H14FNO
포뮬러 무게:
207.24
MOL 파일:
1170613-55-4.mol
MSDS 파일:
SDS

A 967079 속성

끓는 점
324.4±34.0 °C(Predicted)
밀도
1.03±0.1 g/cm3 (20 ºC 760 Torr)
저장 조건
2-8°C
용해도
DMSO: ≥12mg/mL
산도 계수 (pKa)
12.23±0.40(Predicted)
물리적 상태
가루
색상
흰색에서 황갈색까지
안정성
-20°C에서 DMSO에 최대 2개월 동안 보관 가능
InChI
InChI=1S/C12H14FNO/c1-3-12(14-15)9(2)8-10-4-6-11(13)7-5-10/h4-8,15H,3H2,1-2H3/b9-8+,14-12+
InChIKey
HKROEBDHHKMNBZ-CHBKHGQFSA-N
SMILES
C(/C1=CC=C(F)C=C1)=C(/C)\C(=N\O)\CC

안전

WGK 독일 3
HS 번호 2928009090

A 967079 C화학적 특성, 용도, 생산

용도

(1E,3E)- 1-(4-Fluorophenyl)-2-methyl-1-penten-3-one Oxime is a transient receptor potential ankyrin 1 (TRPA1) antagonist and has been investigated as potential analgesic drug for the treatment of chronic pain.

일반 설명

A-967079 prevents neuropathic and inflammatory pain. It reduces cold allodynia, which is produced by nerve injury.

Biochem/physiol Actions

A-967079 is a potent and selective antagonist of Transient Receptor Potential Anykrin 1 (TRPA1) with IC50′s of 67 nM and 289 nM at human and rat TRPA1 receptors, respectively, and minimal or no activity at other TRP channels or G-protein-coupled receptors, enzymes, transporters, and ion channels out of 89 tested. A-967079 blocks TRPA1 activation in human and rat cell lines and has been shown to reduce the responses of wide dynamic range (WDR) and nociceptive specific (NS) neurons to high-intensity mechanical stimulation.

Advantages

(1E,3E)-1-(4-Fluorophenyl)-2-methyl-1-pentene-3-one oxime (A-967079) has shown impressive efficacy as an antagonist to TRPA1 and has multiple advantages over other compounds, including high selectivity, potency, and oral bioavailability. A-967079 has IC50 values of 67 and 289 nM for human and rat TRPA1 receptors, respectively. It displays 1000-fold selectivity for TRPA1 over other TRP channels, and >150-fold selectivity for over 75 other ion channels, enzymes and G-protein-coupled receptors. Oral administration of A-967079 in rats produced robust bioavailability and analgesic efficacy for TIH-induced pain response (i.e., sneezing, tearing, coughing, etc.) and osteoarthritic pain. Intravenous injection of A-967079 has shown to decrease the reactive gas response of wide dynamic range neurons (i.e., a second-order neuron that responds to more than one type of stimulus) and pain specific-neurons. Aditionally, A-967079 produces no known locomotor or cardiovascular effects, a common side effect of other TRP antagonists[2].

A 967079 준비 용품 및 원자재

원자재

준비 용품


A 967079 공급 업체

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