FGFR(成纤维细胞生长因子)
FGFRs (fibroblast growth factor receptors) are transmembrane tyrosine kinase receptor. It is involved in carcinogenesis and plays an important role in cell differentiation, survival and proliferation etc.
Products for FGFR
- Cat.No. 产品名称 Information
- GC19187 H3B-6527 An FGFR4 inhibitor
- GC19156 TAS-120 An orally bioavailable, irreversible inhibitor of FGFRs
- GC19155 FGFR4-IN-1 An inhibitor of FGFR4
- GC19154 Roblitinib An FGFR4 inhibitor
- GC19142 Erdafitinib A pan-FGFR inhibitor
- GC19075 BLU-554 A potent inhibitor of FGFR4
- GC10759 CH5183284 (Debio-1347) An inhibitor of FGFR1, 2, and 3
- GC10833 BLU9931 A selective FGFR4 inhibitor
- GC15801 ACTB-1003 A multi-kinase inhibitor
- GC17323 FIIN-2 An FGFR inhibitor
- GC12049 PD 161570 An inhibitor of FGFR1
- GC10491 SSR128129E An FGFR inhibitor
- GC12730 Pazopanib Hydrochloride A multi-kinase inhibitor
- GC14005 AZD4547 A selective inhibitor of FGFR tyrosine kinases
- GC17283 AP26113 A potent ALK inhibitor
- GC14396 Ponatinib (AP24534) An inhibitor of native and mutant Bcr-Abl
- GC16732 TSU-68 (SU6668,Orantinib) An inhibitor of select receptor tyrosine kinases
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GC15454
Lenvatinib (E7080)
An inhibitor of VEGFR2 and VEGFR3
- GC13547 Dovitinib (TKI-258, CHIR-258) A multi-kinase inhibitor
- GC13410 Masitinib (AB1010) An inhibitor of c-Kit
- GC17943 PD 173074 Inhibitor of tyrosine kinase activity of fibroblast growth factor receptors
- GC11705 Nintedanib (BIBF 1120) A VEGFR, FGFR, and PDGFR inhibitor
- GC12776 SKLB610 An inhibitor of VEGFR2
- GC11622 TG 100801 TG 100801 是一种前药,可通过在开发过程中的去酯化作用产生 TG 100572,以治疗年龄相关性黄斑变性。 TG 100572 是一种多靶点激酶抑制剂,可抑制受体酪氨酸激酶和 Src 激酶;对于 VEGFR1、VEGFR2、FGFR1、FGFR2、PDGFRβ、Fgr、Fyn、Hck、Lck、Lyn、Src、Yes , 分别。
- GC14660 SU 5402 An inhibitor of VEGFR2, FGFR1, and PDGFRβ
- GC16028 NVP-BGJ398 phosphate NVP-BGJ398 phosphate (BGJ-398 phosphate; NVP-BGJ398 phosphate) 是一种有效的 FGFR 家族抑制剂,对 FGFR1、FGFR2、FGFR3 和 FGFR4 的 IC50 分别为 0.9 nM、1.4 nM、1 nM 和 60 nM。
- GC13424 LY2874455 A pan-FGFR inhibitor
- GC12149 E-3810 E-3810 (E-3810) 是一种新型的 VEGFR 和 FGFR 双重抑制剂,有效且选择性地抑制 VEGFR1、VEGFR2、VEGFR3、FGFR1 和 FGFR2,IC50 为 7 nM、25 nM、10 nM、17.5 nM 和 82.5 nM,分别。
- GC14592 KW 2449 A multi-kinase inhibitor
- GC15217 Danusertib (PHA-739358) A pan-Aurora kinase and Abl inhibitor
- GC16519 ENMD-2076 A multi-kinase inhibitor
- GC12145 ENMD-2076 L-(+)-Tartaric acid ENMD-2076 L-(+)-Tartaric acid 是一种多靶点激酶抑制剂,对 Aurora A、Flt3、KDR/VEGFR2、Flt4/VEGFR3、FGFR1 的 IC50 为 1.86、14、58.2、15.9、92.7、70.8、56.4 nM , FGFR2, Src, PDGFRα, 分别。
- GC13848 LY2784544 Potent inhibitor of JAK2
- GC16327 Pazopanib (GW-786034) A multi-kinase inhibitor
- GC10055 BGJ398 An FGFR inhibitor
- GN10540 Fumalic acid A phenol with diverse biological activities
- GN10527 Formononetin An isoflavone