코비메티닙

코비메티닙
코비메티닙 구조식 이미지
카스 번호:
934660-93-2
한글명:
코비메티닙
동의어(한글):
코비메티닙
상품명:
XL518
동의어(영문):
CobiMetinib;GDC-0973;XL518;RG7420;CS-1977;Cobimetinib-D4;GDC-0973/RG7420;XL518 ,GDC-0973;XL518 USP/EP/BP;GDC-0973(XL-518)
CBNumber:
CB32551361
분자식:
C21H21F3IN3O2
포뮬러 무게:
531.31
MOL 파일:
934660-93-2.mol

코비메티닙 속성

녹는점
165 - 166°C
끓는 점
565.9±50.0 °C(Predicted)
밀도
1.706
저장 조건
Refrigerator
용해도
클로로포름(약간 용해됨), DMSO(약간 용해됨), 에틸아세테이트(약간 용해됨), 메탄올(약간 용해됨)
물리적 상태
고체
물리적 상태
단단한 모양
산도 계수 (pKa)
13.13±0.20(Predicted)
색상
회백색
안전
  • 위험 및 안전 성명
HS 번호 29333990
그림문자(GHS): GHS hazard pictograms
신호 어: Warning
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
예방조치문구:
NFPA 704
0
2 0

코비메티닙 C화학적 특성, 용도, 생산

개요

Cobimetinib, codeveloped by Genentech and Exelixis, was approved in August 2015 in Switzerland and November 2015 in the U.S. and Europe for the treatment of unresectable or metastatic BRAFV600 mutationpositive melanoma when used in combination with vemurafenib. Cobimetinib is a potent, highly selective reversible inhibitor of mitogen-activated protein kinases (MEK) 1 and 2,120 which serves to inhibit phosphorylation of ERK1/2,121 disrupting the MAPK pathway which is responsible for cell proliferation, cell survival, and migration.122 Combination of cobimetinib with vemurafenib, an important BRAF inhibitor,123 enables targeting of multiple points on the MAPK pathway, leading to overall enhanced tumor cell apoptosis and response as compared to stand-alone treatment with vemurafenib.124 Specifically, in a representative trial of previously untreated patients with BRAFV600 mutation-positive, unresectable, stage IIIc or IV melanoma, combination of these two therapies led to a significantly improved progression-free survival and overall response rate versus patients treated only with vemurafenib.

용도

A potent, selective, orally bioavailable inhibitor of MEK1, a component of the RAS/RAF/MEK/ERK pathway. It inhibits proliferation and stimulates apoptosis in a variety of human tumor cell lines. In preclinical xenograft models, oral administration of XL518 results in sustained inhibition of pERK in tumor tissue, but not brain tissue, leading to tumor growth inhibition and regression at well tolerated doses.

상표명

Cotellic

Pharmacokinetics

Cobimetinib has only moderate oral bioavailability (46%), likely due to metabolism rather than incomplete absorption. However, it displays prolonged elimination half-life (44 h), which supports a once-daily dosing regimen (60 mg). Following oral administration, the unchanged cobimetinib and metabolite 4 were the major circulating components in the plasma up to 48 hours post dose (AUC0–48), accounting for 21% and 18% of all the circulating drug-related components, respectively (Fig. 4).
Figure 4. Major metabolic pathway of cobimetinib in  humans.

target

Primary target: MEK1/2

코비메티닙 준비 용품 및 원자재

원자재

준비 용품


코비메티닙 공급 업체

글로벌( 177)공급 업체
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Hangzhou FandaChem Co.,Ltd.
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ATK CHEMICAL COMPANY LIMITED
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career henan chemical co
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Biochempartner
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Standardpharm Co. Ltd.
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BOC Sciences
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Chongqing Chemdad Co., Ltd
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Shanghai VastPro Technology Development Co., Ltd.
021-20608178 18930468532
sales@vastprotech.com CHINA 12 58
Shanghai Rochi Pharmaceutical Co.,Ltd.
21-38751876 +8615000076078
info@rochipharma.com China 431 58
Dideu Industries Group Limited
+86-29-89586680 +86-15129568250
1026@dideu.com China 24330 58

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