E 7820

HCID 196970CAS 289483-69-8

기본 정보

표준 SMILES
Cc1ccc(NS(=O)(=O)c2cccc(C#N)c2)c2[nH]cc(C#N)c12
InChIKey
LWGUASZLXHYWIV-UHFFFAOYSA-N
분자식
C17H12N4O2S
평균 분자량
336.4 g/mol
단동위원소 질량
336.06809662

개요

E7820 has been investigated for the treatment of Colon Cancer and Rectal Cancer.

이름 및 식별자

우선 이름
E 7820
IUPAC
3-cyano-N-(3-cyano-4-methyl-1H-indol-7-yl)benzenesulfonamide
영어명
E-7820
분자식
C17H12N4O2S
분자량
336.37

이름 및 동의어

289483-69-8E7820E-7820E 7820Benzenesulfonamide, 3-cyano-N-(3-cyano-4-methyl-1H-indol-7-yl)-TVH5K7949N3-cyano-N-(3-cyano-4-methyl-1H-indol-7-yl)benzene-1-sulfonamideER-68203-00DTXSID20183142RefChem:920775DTXCID301056333-cyano-N-(3-cyano-4-methyl-1H-indol-7-yl)benzenesulfonamide
이름 더 보기
CS-2701ER 68203-00E7820, 10 mM in DMSOER68203-003-Cyano-N-(3-cyano-4-methyl-7-indolyl)benzenesulfonamide
N-(3-cyano-4-methyl-1H-indol-7-yl)-3-cyanobenzene-sulfonamideUNII-TVH5K7949NN-(3-cyano-4-methyl-1H-indol-7-yl)-3-cyanobenzenesulfonamideNSC-7192393-Cyano-N-(3-cyano-4-methyl-1H-indole-7-yl)benzensulfonamideLWGUASZLXHYWIV-UHFFFAOYSA-NO6MMFCD09833234

데이터베이스 식별자

CAS
289483-69-8
PubChem CID
196970
DTXSID
DTXSID20183142
ChEMBL
CHEMBL4297376
UNII
TVH5K7949N
Nikkaji
J1.844.794K

물성

구조 계산 물성

XLogP
2.4
극성 표면적
118 Ų
수소 결합 공여자 수
2
수소 결합 수용자 수
5
회전 가능 결합 수
3
무거운 원자 수
24

실험 및 물리화학적 성질

DrugsPharmaceuticals -> Listed in ZINC15

물리화학적 성질

끓는 점
626.2 · 626.2±65.0 °C(Predicted)
밀도
1.48 · 1.48±0.1 g/cm3(Predicted)
저장 조건
-20 °C · Store at -20°C
용해도
67 · DMSO:67.0(Max Conc. mg/mL);199.19(Max Conc. mM)
물리적 상태
결정성 고체
산도 계수 (pKa)
8.17 · 8.17±0.30(Predicted)

안전 및 규제

안전 데이터

wgk
WGK 3
스토리지 클래스
11 - Combustible Solids

화학 및 산업

응용 분야 · 1건

개요E7820 is a sulfonamide derivative and an angiogenesis inhibitor that inhibits bFGF- and VEGF-stimulated human umbilical vein endothelial cell (HUVEC) proliferation (IC50s = 0.1 and 0.081 μg/ml, respectively). It inhibits bFGF- and VEGF-stimulated tube formation of HUVECs in a concentration-dependent manner (IC50s = 0.2 and 0.24 μg/ml, respectively). E7820 selectively decreases the surface expression and mRNA levels of integrin α2 over CD31 and VE-cadherin in HUVECs. In vivo, E7820 (200 and 400 mg/kg) reduces tumor growth and inhibits angiogenesis in a WiDr colorectal cancer mouse xenograft model. It also reduces tumor weight in a panel of seven human colon, breast, pancreas, and kidney cancer mouse xenograft models, completely inhibits tumor growth in KP-1 pancreatic and LoVo colon cancer mouse xenograft models, and inhibits tumor growth in KP-1 and COLO 320DM mouse orthotopic transplantation models.

공급사50 곳

陕西缔都医药有限责任公司029-81124775 17791530730 · [email protected]
Career Henan Chemica Co+86-0371-86658258 +86-13203830695 · [email protected]
武汉英诺医药科技有限公司+86-027-59232304 15387063101 · [email protected]
上海麦克林生化科技股份有限公司021-50706066 15221275939 · [email protected]
上海毕得医药科技股份有限公司400-1647117 13681763483 · [email protected]

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3건

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