2-Chloro-5-[[5-[[5-(4,5-Dimethyl-2-nitrophenyl)-2-furanyl]methylene]-4,5-dihydro-4-oxo-2-thiazolyl]amino]benzoicacid

2-Chloro-5-[[5-[[5-(4,5-Dimethyl-2-nitrophenyl)-2-furanyl]methylene]-4,5-dihydro-4-oxo-2-thiazolyl]amino]benzoicacid 구조식 이미지
카스 번호:
331002-70-1
상품명:
2-Chloro-5-[[5-[[5-(4,5-Dimethyl-2-nitrophenyl)-2-furanyl]methylene]-4,5-dihydro-4-oxo-2-thiazolyl]amino]benzoicacid
동의어(영문):
RTHRCOIONCZINZ-JMIUGGIZSA-N;2-Chloro-5-[[5-[[5-(4,5-Dimethyl-2-nitrophenyl)-2-furanyl]methylene]-4,5-dihydro-4-oxo-2-thiazolyl]amino]benzoicacid;Benzoic acid, 2-chloro-5-[[5-[[5-(4,5-dimethyl-2-nitrophenyl)-2-furanyl]methylene]-4,5-dihydro-4-oxo-2-thiazolyl]amino]-
CBNumber:
CB02518882
분자식:
C23H16ClN3O6S
포뮬러 무게:
497.91
MOL 파일:
331002-70-1.mol

2-Chloro-5-[[5-[[5-(4,5-Dimethyl-2-nitrophenyl)-2-furanyl]methylene]-4,5-dihydro-4-oxo-2-thiazolyl]amino]benzoicacid 속성

끓는 점
696.8±65.0 °C(Predicted)
밀도
1.53±0.1 g/cm3(Predicted)
저장 조건
Store at -20°C
용해도
DMSO에 용해됨
물리적 상태
고체
물리적 상태
단단한 모양
산도 계수 (pKa)
2.74±0.25(Predicted)
색상
갈색
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
그림문자(GHS): GHS hazard pictograms
신호 어: Warning
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
H302 삼키면 유해함 급성 독성 물질 - 경구 구분 4 경고 GHS hazard pictograms P264, P270, P301+P312, P330, P501
예방조치문구:
P264 취급 후에는 손을 철저히 씻으시오.
P264 취급 후에는 손을 철저히 씻으시오.
P270 이 제품을 사용할 때에는 먹거나, 마시거나 흡연하지 마시오.
P301+P312 삼켜서 불편함을 느끼면 의료기관(의사)의 진찰을 받으시오.
P330 입을 씻어내시오.
P501 ...에 내용물 / 용기를 폐기 하시오.
NFPA 704
0
2 0

2-Chloro-5-[[5-[[5-(4,5-Dimethyl-2-nitrophenyl)-2-furanyl]methylene]-4,5-dihydro-4-oxo-2-thiazolyl]amino]benzoicacid C화학적 특성, 용도, 생산

효소 저해제

This AMPK activator (FW = 497.91 g/mol; CAS 331002-70-1), systematically named 2-chloro-5-[[5-[[5- (4,5-dimethyl-2-nitrophenyl) -2- furanyl]methylene]-4,5-dihydro-4-oxo-2-thiazolyl]amino]benzoic acid, targets AMP-activated protein kinase (EC50 = 0.3 μM) by antagonizing its built-in autoinhibition mechanism. PT1 dose-dependently activates AMPK α1394, α1335, α2398, and even the heterotrimer α1β1γ1 form. Based on the structure of PT1 docked to AMPK α1 subunit, it appears that PT1 interacts with Glu-96 and Lys-156 near the autoinhibitory domain, directly relieving autoinhibition. In studies using L6 myotubes, the phosphorylation of AMPK and its downstream substrate, acetyl-CoA carboxylase, were dose-dependently and time-dependently increased by PT1 without any change in cellular AMP:ATP concentration ratio.

2-Chloro-5-[[5-[[5-(4,5-Dimethyl-2-nitrophenyl)-2-furanyl]methylene]-4,5-dihydro-4-oxo-2-thiazolyl]amino]benzoicacid 준비 용품 및 원자재

원자재

준비 용품


2-Chloro-5-[[5-[[5-(4,5-Dimethyl-2-nitrophenyl)-2-furanyl]methylene]-4,5-dihydro-4-oxo-2-thiazolyl]amino]benzoicacid 공급 업체

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