PF-04691502

PF-04691502 구조식 이미지
카스 번호:
1013101-36-4
상품명:
PF-04691502
동의어(영문):
CS-305;CS-2640;PF4691502;PF-04691502;PF 04691502; PF04691502;PF-04691502 ISO 9001:2015 REACH;PF-04691502, 98%, a potent and selective inhibitor of PI3K and mTOR kinases;2-Amino-8-((1r,4r)-4-(2-hydroxyethoxy)cyclohexyl)-6-(6-methoxypyridin-3-yl)-4-methylpyrido[2,3;2-amino-8-[4-(2-hydroxyethoxy)cyclohexyl]-6-(6-methoxypyridin-3-yl)-4-methylpyrido[2,3-d]pyrimidin-7-one;2-Amino-8-[trans-4-(2-hydroxyethoxy)cyclohexyl]-6-(6-methoxy-3-pyridinyl)-4-methylpyrido[2,3-d]pyrimidin-7(8H)-one
CBNumber:
CB22589602
분자식:
C22H27N5O4
포뮬러 무게:
425.48
MOL 파일:
1013101-36-4.mol
MSDS 파일:
SDS

PF-04691502 속성

녹는점
219-221°C
끓는 점
682.5±65.0 °C(Predicted)
밀도
1.36
저장 조건
Refrigerator
용해도
클로로포름(약간 용해됨, 가열, 초음파 처리), 메탄올(약간 용해됨, 초음파 처리)
물리적 상태
고체
물리적 상태
단단한 모양
산도 계수 (pKa)
14.39±0.10(Predicted)
색상
연한 노란색에서 밝은 녹색까지

안전

PF-04691502 C화학적 특성, 용도, 생산

화학적 성질

Pale Yellow Solid

용도

PF-04691502 is an ATP-competitive PI3K/mTOR inhibitor with IC50 of 32 nM and also inhibits Akt T308/S473 with IC50 of 7.5 nM/3.8 nM.

효소 저해제

This ATP-competitive PI3K/mTOR dual inhibitor (FW = 325.49 g/mol; CAS 1013101-36-4; Solubility = 14 mg/mL DMSO, < 1 mg/ML H2O), also systematically named 2-amino-8-((1R,4R)-4-(2-hydroxyethoxy)cyclohexyl)-6-(6-methoxypyridin-3-yl)-4-methylpyrido[2,3-d]pyrimidin-7(8H)- one, potently inhibits recombinant Class-I PI3Kα (Ki = 1.8 nM), PI3Kβ (Ki = 2.1 nM), PI3Kδ (Ki = 1.6 nM), PI3Kγ (Ki = 1.9 nM), and mTOR (Ki = 16 nM) in biochemical assays, with little activity against either Vps34, AKT, PDK1, p70S6K, MEK, ERK, p38, or JNK. PF-04691502 also suppresses avian fibroblast transformation mediated by wild-type PI3K γ, δ, or mutant PI3Kα. In PIK3CA-mutant and PTEN-deleted cancer cell lines, PF- 04691502 reduces phosphorylation of AKT T308 (IC50 = 7.5–47 nM) and AKT S473 (IC50 = 3.8–20 nM) and inhibits cell proliferation (IC50 = 180– 310 nM). PF-04691502 also inhibite mTORC1 activity within cells, asmeasured by PI3K-independent, nutrient-stimulated assay (IC50 = 32 nM) and inhibited the activation of PI3K and mTOR downstream effectors, including AKT, FKHRL1, PRAS40, p70S6K, 4EBP1, and S6RP. Shortterm exposure to PF-04691502 predominantly inhibits PI3K, whereas mTOR inhibition persists for 24 to 48 hours. PF-04691502 also induces cell cycle G1 arrest, concomitant with upregulation of p27 Kip1 and reduction of retinbalstoma protein, or Rb. At doses below the maximal tolerable dose, PD-0325901 potently inhibits tumor growth, when Kras and/or PI3K are drivers of tumor growth and progression.

PF-04691502 준비 용품 및 원자재

원자재

준비 용품


PF-04691502 공급 업체

글로벌( 142)공급 업체
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Capot Chemical Co.,Ltd.
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sales@capotchem.com China 29797 60
career henan chemical co
+86-0371-86658258
sales@coreychem.com China 29914 58
Biochempartner
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candy@biochempartner.com CHINA 967 58
BOC Sciences
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inquiry@bocsci.com United States 19553 58
Chongqing Chemdad Co., Ltd
+86-023-61398051 +8613650506873
sales@chemdad.com China 39916 58
Alchem Pharmtech,Inc.
8485655694
sales@alchempharmtech.com United States 63711 58
HANGZHOU CLAP TECHNOLOGY CO.,LTD
86-571-88216897,88216896 13588875226
sales@hzclap.com CHINA 6313 58
ANHUI WITOP BIOTECH CO., LTD
+8615255079626
eric@witopchemical.com China 23556 58
Dideu Industries Group Limited
+86-29-89586680 +86-15129568250
1026@dideu.com China 27894 58
Shenzhen Shengda Pharma Limited
755-85269922 +8613424394241
sales@shengdapharm.com CHINA 310 58

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