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Mubritinib

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Mubritinib
Clinical data
Routes of
administration
Oral
ATC code
  • none
Legal status
Legal status
  • In general: uncontrolled
Identifiers
  • 1-(4-{4-[(2-{(E)-2-[4-(trifluoromethyl)phenyl]ethenyl}-1,3-oxazol-4-yl)methoxy]phenyl}butyl)-1H-1,2,3-triazole
CAS Number
PubChemCID
IUPHAR/BPS
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC25H23F3N4O2
Molar mass468.480 g·mol−1
3D model (JSmol)
  • FC(F)(F)c1ccc(cc1)\C=C\c2nc(co2)COc3ccc(cc3)CCCCn4nncc4
  • InChI=1S/C25H23F3N4O2/c26-25(27,28)21-9-4-20(5-10-21)8-13-24-30-22(18-34-24)17-33-23-11-6-19(7-12-23)3-1-2-15-32-16-14-29-31-32/h4-14,16,18H,1-3,15,17H2/b13-8+
  • Key:ZTFBIUXIQYRUNT-MDWZMJQESA-N

Mubritinib (TAK-165) is aprotein kinase inhibitor which was under development byTakeda for the treatment ofcancer.[1][2][3] It completedphase Iclinical trials but appears to have been discontinued, as no new information on the drug has surfaced since December 2008.[4]

See also

[edit]

References

[edit]
  1. ^McCormick F, Fabbro D (2005).Protein Tyrosine Kinases: From Inhibitors to Useful Drugs (Cancer Drug Discovery and Development). Totowa, NJ: Humana Press.doi:10.1385/1-59259-962-1:001.ISBN 1-58829-384-X.
  2. ^Mitscher LA, Lednicer D (1977).The organic chemistry of drug synthesis. New York: Wiley.ISBN 0-470-10750-2.
  3. ^Lednicer D (2008).Strategies for Organic Drug Synthesis and Design. New York: Wiley-Interscience.ISBN 978-0-470-19039-5.
  4. ^Clinical trial numberNCT00034281 for "Safety and Tolerability Study of TAK-165 in Subjects With Tumors Expressing HER2" atClinicalTrials.gov


SPs/MIs
(M phase)
Blockmicrotubule assembly
Block microtubule disassembly
DNA replication
inhibitor
DNA precursors/
antimetabolites
(S phase)
Folic acid
Purine
Pyrimidine
Deoxyribonucleotide
Topoisomerase inhibitors
(S phase)
I
II
II+Intercalation
Crosslinking of DNA
(CCNS)
Alkylating
Platinum-based
Nonclassical
Intercalation
Photosensitizers/PDT
Other
Enzyme inhibitors
Receptor antagonists
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CImonoclonal antibodies ("-mab")
Receptor tyrosine kinase
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Tyrosine kinase inhibitors ("-nib")
Receptor tyrosine kinase
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Angiopoietin
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Unsorted
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IGF
IGF-1
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Others
LNGF (p75NTR)
PDGF
RET (GFL)
GFRα1
GFRα2
GFRα3
GFRα4
Unsorted
SCF (c-Kit)
TGFβ
Trk
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