AMG 900

AMG 900 구조식 이미지
카스 번호:
945595-80-2
상품명:
AMG 900
동의어(영문):
AMG 900;AMG-900;AMG900;AMG 900 USP/EP/BP;N-(4-((3-(2-Aminopyrimidin-4-yl)pyridin-2-yl)oxy)phenyl)-4-(4-methylthiophen-2-yl)phthalazin-1;N-[4-[[3-(2-Amino-4-pyrimidinyl)-2-pyridinyl]oxy]phenyl]-4-(4-methyl-2-thienyl)-1-phthalazinamine;1-Phthalazinamine, N-[4-[[3-(2-amino-4-pyrimidinyl)-2-pyridinyl]oxy]phenyl]-4-(4-methyl-2-thienyl)-;N-[4-[[3-(2-Amino-4-pyrimidinyl)-2-pyridinyl]oxy]phenyl]-4-(4-methyl-2-thienyl)-1-phthalazinamine AMG 900
CBNumber:
CB82554079
분자식:
C28H21N7OS
포뮬러 무게:
503.58
MOL 파일:
945595-80-2.mol

AMG 900 속성

끓는 점
778.7±70.0 °C(Predicted)
밀도
1.380
저장 조건
2-8°C(protect from light)
용해도
≥25.2 mg/mL in DMSO; insoluble in H2O; insoluble in EtOH
물리적 상태
고체
물리적 상태
단단한 모양
산도 계수 (pKa)
4.79±0.30(Predicted)
색상
Light yellow to yellow

안전

AMG 900 C화학적 특성, 용도, 생산

개요

Three Aurora kinases, A-C, are involved in phosphorylation events that are critical for the completion of mitosis. Their expression is elevated in a variety of human cancers. AMG 900 is an orally bioavailable, selective Aurora kinase inhibitor with IC50 values of 5, 4, and 1 nM for Aurora A, B, and C, respectively. It is greater than 10-fold selective for Aurora kinases over p38α, TYK2, JNK2, Met, and Tie2 (IC50s = 53, 220, 520, 550, and 650 nM, respectively). At 2-3 nM, AMG 900 has been shown to inhibit the proliferation of 26 different tumor cell lines in vitro, including cell lines resistant to either the antimitotic agent paclitaxel or to other Aurora kinase inhibitors. Furthermore, AMG 900 is reported to be broadly active in multiple xenograft models, including three multidrug-resistant xenograft models, representing five tumor types.

효소 저해제

This potent and highly selective mitotic protein kinase inhibitor (FW = 503.58 g/mol; CAS 945595-80-2; Solubility: 100 mg/mL DMSO), also named N-(4-(3-(2-aminopyrimidin-4-yl)pyridin-2-yloxy)phenyl)-4-(4- methylthiophen-2-yl)phthalazin-1-amine, targets Aurora A (IC50 = 5 nM), Aurora B (IC50 = 4 nM), and Aurora C (IC50 = 1 nM) protein kinases, with >10-fold selectivity versus p38α, Tyk2, JNK2, Met and Tie2. The modal tumor cell response to AMG 900 treatment is aborted cell division without prolonged mitotic arrest, ultimately resulting in cell death. AMG 900 exhibits acceptable PK properties in preclinical species and is predicted to have low clearance in humans. Male rats metabolize AMG 900 primarily through hydroxylation with subsequent sulfate conjugation on the pyrimidinyl-pyridine side-chain, whereas female rats favor oxidation on the thiophene ring's methyl group, which is then metabolized to a carboxylic acid, attended by conjugation to an acyl glucuronide. At low-nM concentrations, AMG 900, whether administered alone or in combination with microtubule-targeting drugs (paclitaxel or ixabepilone), may be an effective intervention strategy for the treatment of metastatic breast cancer and provide potential therapeutic options for patients with multidrug-resistant tumors. It is, in fact, also active against taxaneresistant tumor cell lines.

AMG 900 준비 용품 및 원자재

원자재

준비 용품


AMG 900 공급 업체

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ATK CHEMICAL COMPANY LIMITED
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support@targetmol.com United States 19973 58
Zibo Hangyu Biotechnology Development Co., Ltd
+86-0533-2185556 +8617865335152
Mandy@hangyubiotech.com China 11027 58

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