Contact us: +91 9550333722 040 - 40102781
Structured search
India
Choose your country
Different countries will display different contents
Try our best to find the right business for you.
My chemicalbook

Welcome back!

HomeProduct name listFGFR inhibitor

FGFR inhibitor

FGFR inhibitor Structural

What is FGFR inhibitor?

The Uses of FGFR inhibitor

SSR128129E (SSR) is an potent FGFR inhibitor, which inhibits fibroblast growth factor receptor (FGFR). Oral delivery of SSR128129E inhibits arthritis and tumors that are relatively refractory to anti-vascular endothelial growth factor receptor-2 antibodies.

Definition

ChEBI: Sodium 2-amino-5-[(1-methoxy-2-methylindolizin-3-yl)carbonyl]benzoate is an organic sodium salt having 2-amino-5-[(1-methoxy-2-methylindolizin-3-yl)carbonyl]benzoate as the counterion. It has a role as an antineoplastic agent and a fibroblast growth factor receptor antagonist. It contains a 2-amino-5-[(1-methoxy-2-methylindolizin-3-yl)carbonyl]benzoate.

Biological Activity

ssr128129e is an allosteric inhibitor of fgfr1 with ic50 value of 1.9 μm [1].the fibroblast growth factor receptors (fgfrs) are receptor tyrosine kinases for fibroblast growth factors (fgfs) and play an important role in cancer and inflammation. fgf2 plays an important role in angiogenesis [1] [2].ssr128129e is an orally-active and allosteric fgfr1 inhibitor. in human umbilical venous endothelial cells (huvecs), ssr128129e inhibited fgf2-induced endothelial cells (ecs) proliferation and migration with ic50 values of 31 and 15.2 nm respectively and also inhibited lamellipodia formation. ssr128129e inhibited responses mediated by fgfr1-4. in fgfr2-expressing hek293 cells, ssr128129e inhibited phosphorylation of frs2 and erk1/2 induced by fgf2 [1].in arthritis mice, ssr128129e inhibited bone and joint damage and reduced angiogenesis in the inflamed joints. in orthotopic panc02 tumor model, ssr128129e (30 mg/kg) inhibited tumor growth by 44%. in murine 4t1 breast tumors, ssr128129e (30 mg/kg) reduced tumor weight and size by 40% and 53%, respectively [1]. in atherosclerosis-prone apolipoprotein e (apoe)-deficient mice, ssr128129e (50 mg/kg) reduced neointimal proliferation and reduced fgfr2 mrna levels and lesion size in the aortic sinus [2].

References

[1]. bono f, de smet f, herbert c, et al. inhibition of tumor angiogenesis and growth by a small-molecule multi-fgf receptor blocker with allosteric properties. cancer cell, 2013, 23(4): 477-488.
[2]. dol-gleizes f, delesque-touchard n, marès am, et al. a new synthetic fgf receptor antagonist inhibits arteriosclerosis in a mouse vein graft model and atherosclerosis in apolipoprotein e-deficient mice. plos one, 2013, 8(11): e80027.

Properties of FGFR inhibitor

Melting point: >230°C (dec.)
storage temp.  Hygroscopic, -20°C Freezer, Under inert atmosphere
solubility  DMSO (Slightly), Methanol (Slightly)
form  Solid
color  Yellow
Stability: Hygroscopic

Safety information for FGFR inhibitor

Computed Descriptors for FGFR inhibitor

Related products of tetrahydrofuran

You may like

Statement: All products displayed on this website are only used for non medical purposes such as industrial applications or scientific research, and cannot be used for clinical diagnosis or treatment of humans or animals. They are not medicinal or edible.