Tepotinib

Tepotinib 구조식 이미지
카스 번호:
1100598-32-0
상품명:
Tepotinib
동의어(영문):
Tepotinib;EMD-1214063;Veledimex;CS-977;MSC2156119;EMD1214063,Tepotinib;epotinib(EMD 1214063);Tepotinib (EMD 1214063);EMD 1214063; EMD1214063;EMD-1214063|||MSC2156119
CBNumber:
CB72550731
분자식:
C29H28N6O2
포뮬러 무게:
492.57
MOL 파일:
1100598-32-0.mol

Tepotinib 속성

끓는 점
626.5±65.0 °C(Predicted)
밀도
1.25
저장 조건
Store at -20°C
물리적 상태
Solid
산도 계수 (pKa)
8.93±0.10(Predicted)
수용성
≥ 4.93 mg/mL in DMSO, <2.52 mg/mL in EtOH, <2.56 mg/mL in Water
InChIKey
AHYMHWXQRWRBKT-UHFFFAOYSA-N
SMILES
C(#N)C1=CC=CC(C2=NN(CC3=CC=CC(C4=NC=C(OCC5CCN(C)CC5)C=N4)=C3)C(=O)C=C2)=C1
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:
P280 보호장갑/보호의/보안경/안면보호구를 착용하시오.
P305+P351+P338 눈에 묻으면 몇 분간 물로 조심해서 씻으시오. 가능하면 콘택트렌즈를 제거하시오. 계속 씻으시오.

Tepotinib C화학적 특성, 용도, 생산

개요

Tepotinib is a highly selective inhibitor against MET. In xenograft models, acquired resistance to EGFR TKIs via secondary EGFR T790 M mutations can be overcome with tepotinib treatment.

용도

EMD 1214063 is a novel ATP-comptetitive inhibitor of the MET hepatocyte growth factor receptor and a novel kinase inhibitor and a therapeutic agent for neuroblastoma. Potent c-MET inhibitor.

상표명

Tepmetko

Mechanism of action

Tepotinib is a Kinase Inhibitor. The mechanism of action of tepotinib is as a Mesenchymal Epithelial Transition Inhibitor, and P-Glycoprotein Inhibitor.

Clinical Use

Tepotinib is currently being evaluated in combination with EGFR TKI gefitinib and also a separate trial in NSCLC patients with MET exon 14 skipping mutation and MET amplification.

Drug interactions

Tepotinib is indicated for the treatment of adult patients with metastatic non-small cell lung cancer (NSCLC) who have mesenchymal-epithelial transition (_MET_) exon 14 skipping alterations.

신진 대사

Tepotinib is metabolized primarily by CYP3A4 and CYP2C8, with some apparent contribution by unspecified UGT enzymes. The metabolite M506 is the major circulating metabolite, comprising approximately 40.4% of observed drug material in plasma, while the M668 glucuronide metabolite has been observed in plasma at much lower quantities (~4% of an orally administered dose). A total of 10 phase I and phase II metabolites have been detected following tepotinib administration, most of which are excreted in the feces.

Tepotinib 준비 용품 및 원자재

원자재

준비 용품


Tepotinib 공급 업체

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ATK CHEMICAL COMPANY LIMITED
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Shenzhen Shengda Pharma Limited
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Zhejiang J&C Biological Technology Co.,Limited
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sales@sarms4muscle.com China 10522 58
InvivoChem
+1-708-310-1919 +1-13798911105
sales@invivochem.cn United States 6393 58
Shanghai Innopharm Industrial Co., Ltd.
+86-21-59960785 +86-17701845089
sales@hoyaopharm.com China 314 58

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