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Polpharma European CDMO Partner & API Manufacturer since 1951 Polpharma European CDMO Partner & API Manufacturer since 1951

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Technical details about Fisogatinib, learn more about the structure, uses, toxicity, action, side effects and more

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2D Structure
1. Also known as: Blu-554, 1707289-21-1, Blu554, N-((3s,4s)-3-((6-(2,6-dichloro-3,5-dimethoxyphenyl)quinazolin-2-yl)amino)tetrahydro-2h-pyran-4-yl)acrylamide, Blu111362, Fisogatinib [inn]
Molecular Formula
C24H24Cl2N4O4
Molecular Weight
503.4  g/mol
InChI Key
MGZKYOAQVGSSGC-DLBZAZTESA-N
FDA UNII
5Q7R99CKV2

Fisogatinib is an orally bioavailable inhibitor of human fibroblast growth factor receptor 4 (FGFR4), with potential antineoplastic activity. Upon oral administration, fisogatinib specifically binds to and blocks the binding of the ligand FGF19 to FGFR4. This prevents the activation of FGFR4, inhibits FGFR4-mediated signaling and leads to an inhibition of tumor cell proliferation in FGFR4-overexpressing cells. FGFR4 is a receptor tyrosine kinase and is involved in tumor cell proliferation, differentiation, angiogenesis, and survival. FGF19 is overexpressed by certain tumor cell types.
1 2D Structure

2D Structure

2 Identification
2.1 Computed Descriptors
2.1.1 IUPAC Name
N-[(3S,4S)-3-[[6-(2,6-dichloro-3,5-dimethoxyphenyl)quinazolin-2-yl]amino]oxan-4-yl]prop-2-enamide
2.1.2 InChI
InChI=1S/C24H24Cl2N4O4/c1-4-20(31)28-16-7-8-34-12-17(16)30-24-27-11-14-9-13(5-6-15(14)29-24)21-22(25)18(32-2)10-19(33-3)23(21)26/h4-6,9-11,16-17H,1,7-8,12H2,2-3H3,(H,28,31)(H,27,29,30)/t16-,17+/m0/s1
2.1.3 InChI Key
MGZKYOAQVGSSGC-DLBZAZTESA-N
2.1.4 Canonical SMILES
COC1=CC(=C(C(=C1Cl)C2=CC3=CN=C(N=C3C=C2)NC4COCCC4NC(=O)C=C)Cl)OC
2.1.5 Isomeric SMILES
COC1=CC(=C(C(=C1Cl)C2=CC3=CN=C(N=C3C=C2)N[C@@H]4COCC[C@@H]4NC(=O)C=C)Cl)OC
2.2 Other Identifiers
2.2.1 UNII
5Q7R99CKV2
2.3 Synonyms
2.3.1 MeSH Synonyms

1. 2-propenamide, N-((3s,4s)-3-((6-(2,6-dichloro-3,5-dimethoxyphenyl)-2-quinazolinyl)amino)tetrahydro-2h-pyran-4-yl)-

2. Blu-554

3. N-((3s,4s)-3-((6-(2,6-dichloro-3,5-dimethoxyphenyl)quinazolin-2-yl)amino)oxan-4-yl)prop-2-enamide

4. N-((3s,4s)-3-((6-(2,6-dichloro-3,5-dimethoxyphenyl)quinazolin-2-yl)amino)tetrahydro-2h-pyran-4-yl)acrylamide

2.3.2 Depositor-Supplied Synonyms

1. Blu-554

2. 1707289-21-1

3. Blu554

4. N-((3s,4s)-3-((6-(2,6-dichloro-3,5-dimethoxyphenyl)quinazolin-2-yl)amino)tetrahydro-2h-pyran-4-yl)acrylamide

5. Blu111362

6. Fisogatinib [inn]

7. Fisogatinib [usan]

8. X439161

9. Blu-111362

10. 5q7r99ckv2

11. Blu 554

12. X-439161

13. 2-propenamide, N-((3s,4s)-3-((6-(2,6-dichloro-3,5-dimethoxyphenyl)-2-quinazolinyl)amino)tetrahydro-2h-pyran-4-yl)-

14. N-((3s,4s)-3-((6-(2,6-dichloro-3,5-dimethoxyphenyl)quinazolin-2-yl)amino)oxan-4-yl)prop-2-enamide

15. N-[(3s,4s)-3-[[6-(2,6-dichloro-3,5-dimethoxyphenyl)quinazolin-2-yl]amino]oxan-4-yl]prop-2-enamide

16. Blu554(fisogatinib)

17. Fisogatinib (usan/inn)

18. Unii-5q7r99ckv2

19. Fisogatinib [who-dd]

20. Blu 554 [who-dd]

21. Chembl4514636

22. Schembl16668287

23. Gtpl10220

24. Ex-a841

25. Amy16699

26. Bdbm50575072

27. Cs3008

28. Mfcd30496704

29. Nsc795718

30. S8503

31. Who 10947

32. Akos030632994

33. Ccg-269714

34. Cs-5986

35. Nsc-795718

36. Ac-29871

37. As-55934

38. Bb160379

39. Hy-100492

40. D11737

41. Q29209801

42. N-[(3s,4s)-3-[[6-(2,6-dichloro-3,5-dimethoxyphenyl)-2-quinazolinyl]amino]tetrahydro-2h-pyran-4-yl]-2-propenamide

2.4 Create Date
2015-09-28
3 Chemical and Physical Properties
Molecular Weight 503.4 g/mol
Molecular Formula C24H24Cl2N4O4
XLogP34.7
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count7
Rotatable Bond Count7
Exact Mass502.1174606 g/mol
Monoisotopic Mass502.1174606 g/mol
Topological Polar Surface Area94.6 Ų
Heavy Atom Count34
Formal Charge0
Complexity688
Isotope Atom Count0
Defined Atom Stereocenter Count2
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently Bonded Unit Count1
4 Pharmacology and Biochemistry
4.1 MeSH Pharmacological Classification

Antineoplastic Agents

Substances that inhibit or prevent the proliferation of NEOPLASMS. (See all compounds classified as Antineoplastic Agents.)


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