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E-7090

CAS No.
1622204-21-0
Chemical Name:
E-7090
Synonyms
tasurgratinib;E-7090;E7090 (E 7090);1H-Indole-1-carboxamide, 5-[[2-[[4-[1-(2-hydroxyethyl)-4-piperidinyl]benzoyl]amino]-4-pyridinyl]oxy]-6-(2-methoxyethoxy)-N-methyl-
CBNumber:
CB53166236
Molecular Formula:
C32H37N5O6
Molecular Weight:
587.67
MDL Number:
MFCD32204515
MOL File:
1622204-21-0.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-04-24 14:58:46

E-7090 Properties

form Solid
color White to off-white
FDA UNII TN7CUD1NGA

E-7090 price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
ChemScene CS-0021430 E7090 98.11% 1622204-21-0 5mg $769 2026-06-04 Buy
ChemScene CS-0021430 E7090 98.11% 1622204-21-0 10mg $1246 2026-06-04 Buy
ChemScene CS-0021430 E7090 98.11% 1622204-21-0 25mg $2167 2026-06-04 Buy
ChemScene CS-0021430 E7090 98.11% 1622204-21-0 50mg $3250 2026-06-04 Buy
ChemScene CS-0021430 E7090 98.11% 1622204-21-0 100mg $4875 2026-06-04 Buy
Product number Packaging Price Buy
CS-0021430 5mg $769 Buy
CS-0021430 10mg $1246 Buy
CS-0021430 25mg $2167 Buy
CS-0021430 50mg $3250 Buy
CS-0021430 100mg $4875 Buy

E-7090 Chemical Properties, Uses, Production

Uses

E7090 is an orally available, potent, and selective FGFR inhibitor with IC50s of 0.71 nM, 0.50 nM, 1.2 nM, and 120 nM for FGFR1/FGFR2/FGFR3/FGFR4, respectively[1].

in vivo

Pharmacodynamics analysis reveals that E7090 inhibits phosphorylation of FGFRs in SNU-16 xenograft tumors in a dose-dependent manner[1].
E7090 (6.25-50 mg/kg, orally, once daily) treatment prolongs survival in a 4T1 mouse lung metastasis model[2].

Animal Model:Mouse xenograft model of SNU-16 human gastric cancer[2]
Dosage:6.25 to 50 mg/kg
Administration:Orally, once daily for 14 days
Result:Inhibited tumor growth in a dose-dependent manner.

IC 50

FGFR1: 0.71 nM (IC50); FGFR2: 0.50 nM (IC50); FGFR3: 1.2 nM (IC50); FGFR4: 120 nM (IC50)

References

[1] Saori Watanabe Miyano, et al. E7090: A potent and selective FGFR inhibitor with activity in multiple FGFR-driven cancer models with distinct mechanisms of activation. AACR 106th Annual Meeting 2015; April 18-22, 2015; Philadelphia, PA.
[2] Saori Watanabe Miyano, et al. E7090, a Novel Selective Inhibitor of Fibroblast Growth Factor Receptors, Displays Potent Antitumor Activity and Prolongs Survival in Preclinical Models. Mol Cancer Ther. 2016 Nov;15(11):2630-2639. DOI:10.1158/1535-7163.MCT-16-0261

E-7090 Preparation Products And Raw materials

Raw materials

Preparation Products

E-7090 Suppliers

Global Suppliers ( 18)
Supplier Tel Email Country ProdList Advantage
WUHAN SUN-SHINE BIO-TECHNOLOGY Co., Ltd. 17702719238 sales@sun-shinechem.com China 1197 64
Shanghai Lollane Biological Technology Co.,Ltd. 021-52996696,15000506266 15000506266 China 4860 55
Hangzhou ChangCun Biotechnology Co., Ltd. 0571-; 13567100326 158848739@qq.com China 108 50
Zhongshan Geometric Biological Technology Co., Ltd. 2953972351@qq.com China 253 58
Chuzhou KeMail Chemical Technology Co., Ltd 0550-5196001 15000891977 wj520wjxby@126.com China 1940 55
Tianjin Kaifu Pharmaceutical Technology Co., Ltd. 18081075745 chemflowtech@sina.com China 1883 58
TargetMol Chemicals Inc. +1-781-999-5354; +1-00000000000 marketing@targetmol.com United States 32431 58
Changzhou Chenhong Biotechnology Co., Ltd. +86-0519-85788828 +86-13775037613 sales@chemrenpharm.com China 4058 58
ShangHai ChuanQian Chemcial Technique Centre 15869524721 3525679403@qq.com China 4565 58
Chunchuang (Wuhan) Technology Co., Ltd 15727060112 yutianchun2007@126.com China 9867 58
E-7090 E7090 (E 7090) 1H-Indole-1-carboxamide, 5-[[2-[[4-[1-(2-hydroxyethyl)-4-piperidinyl]benzoyl]amino]-4-pyridinyl]oxy]-6-(2-methoxyethoxy)-N-methyl- tasurgratinib 1622204-21-0