Glesatinib Explained

Iupac Name:N-[(3-Fluoro-4-<nowiki/>{[2-(5-<nowiki/>{[(2-methoxyethyl)amino]methyl}-2-pyridinyl)thieno[3,2-b]pyridin-7-yl]oxy}phenyl)carbamothioyl]-2-(4-fluorophenyl)acetamide
Routes Of Administration:By mouth
Legal Status:Investigational
Cas Number:936694-12-1
Atc Prefix:None
Pubchem:25181472
Chemspiderid:52084900
Unii:7Q29OXD98N
Kegg:D11136
C:31
H:27
F:2
N:5
O:3
S:2
Smiles:COCCNCc1ccc(nc1)c2cc3c(s2)c(ccn3)Oc4ccc(cc4F)NC(=S)NC(=O)Cc5ccc(cc5)F
Stdinchi:1S/C31H27F2N5O3S2/c1-40-13-12-34-17-20-4-8-24(36-18-20)28-16-25-30(43-28)27(10-11-35-25)41-26-9-7-22(15-23(26)33)37-31(42)38-29(39)14-19-2-5-21(32)6-3-19/h2-11,15-16,18,34H,12-14,17H2,1H3,(H2,37,38,39,42)
Stdinchikey:YRCHYHRCBXNYNU-UHFFFAOYSA-N

Glesatinib (MGCD265) is an experimental anti-cancer drug.[1] [2]

It is in phase 2 clinical trials for non-small cell lung cancer (NSCLC).

It is a spectrum selective tyrosine[1] kinase inhibitor "for the treatment of non-small cell lung cancer (NSCLC) patients with genetic alterations of MET".[3]

See also

External links

Notes and References

  1. Web site: Glesatinib . National Cancer Institute at the National Institutes of Health . NCI Dictionaries . U.S. Department of Health and Human Services . 2017-01-15 . 2017-01-16 . https://web.archive.org/web/20170116182844/https://www.cancer.gov/publications/dictionaries/cancer-drug?cdrid=597305 . live .
  2. Cui Q, Cai CY, Gao HL, Ren L, Ji N, Gupta P, Yang Y, Shukla S, Ambudkar SV, Yang DH, Chen ZS . Glesatinib, a c-MET/SMO Dual Inhibitor, Antagonizes P-glycoprotein Mediated Multidrug Resistance in Cancer Cells . Frontiers in Oncology . 9 . 313 . 2019 . 31106148 . 6494935 . 10.3389/fonc.2019.00313 . free .
  3. Web site: Mirati Therapeutics Provides Update On Glesatinib And Sitravatinib Clinical Trials And Pipeline Programs . January 2017 . PipelineReview.com .