loader
Please Wait
Applying Filters...

AbbVie Header AbbVie Header

X

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

Client Email Product
Menu
2D Structure
1. Also known as: 1218779-75-9, Rivoceranib mesylate, Yn968d1, Yn-968d1, Yn 968d1, Tk02x14asj
Molecular Formula
C25H27N5O4S
Molecular Weight
493.6  g/mol
InChI Key
FYJROXRIVQPKRY-UHFFFAOYSA-N
FDA UNII
TK02X14ASJ

Rivoceranib Mesylate is the mesylate salt of rivoceranib, an orally bioavailable, small-molecule receptor tyrosine kinase inhibitor with potential antiangiogenic and antineoplastic activities. Rivoceranib selectively binds to and inhibits vascular endothelial growth factor receptor 2, which may inhibit VEGF-stimulated endothelial cell migration and proliferation and decrease tumor microvessel density. In addition, this agent mildly inhibits c-Kit and c-SRC tyrosine kinases.
1 2D Structure

2D Structure

2 Identification
2.1 Computed Descriptors
2.1.1 IUPAC Name
N-[4-(1-cyanocyclopentyl)phenyl]-2-(pyridin-4-ylmethylamino)pyridine-3-carboxamide;methanesulfonic acid
2.1.2 InChI
InChI=1S/C24H23N5O.CH4O3S/c25-17-24(11-1-2-12-24)19-5-7-20(8-6-19)29-23(30)21-4-3-13-27-22(21)28-16-18-9-14-26-15-10-18;1-5(2,3)4/h3-10,13-15H,1-2,11-12,16H2,(H,27,28)(H,29,30);1H3,(H,2,3,4)
2.1.3 InChI Key
FYJROXRIVQPKRY-UHFFFAOYSA-N
2.1.4 Canonical SMILES
CS(=O)(=O)O.C1CCC(C1)(C#N)C2=CC=C(C=C2)NC(=O)C3=C(N=CC=C3)NCC4=CC=NC=C4
2.2 Other Identifiers
2.2.1 UNII
TK02X14ASJ
2.3 Synonyms
2.3.1 MeSH Synonyms

1. Apatinib

2. Rivoceranib

3. Rivoceranib Mesylate

4. Yn-968d1

5. Yn968d1

2.3.2 Depositor-Supplied Synonyms

1. 1218779-75-9

2. Rivoceranib Mesylate

3. Yn968d1

4. Yn-968d1

5. Yn 968d1

6. Tk02x14asj

7. Rivoceranib Mesylate (usan)

8. 3-pyridinecarboxamide, N-(4-(1-cyanocyclopentyl)phenyl)-2-((4-pyridinylmethyl)amino)-, Methanesulfonate (1:1)

9. Rivoceranib Mesylate [usan]

10. N-(4-(1-cyanocyclopentyl)phenyl)-2-((pyridin-4-ylmethyl)amino)nicotinamide Mesylate

11. N-[4-(1-cyanocyclopentyl)phenyl]-2-(pyridin-4-ylmethylamino)pyridine-3-carboxamide;methanesulfonic Acid

12. Unii-tk02x14asj

13. Apatinib?mesylate

14. 3-pyridinecarboxamide, N-[4-(1-cyanocyclopentyl)phenyl]-2-[(4-pyridinylmethyl)amino]-, Methanesulfonate (1:1)

15. Alitan (tn)

16. Apatinib-yn968d1

17. Apatinib - Yn968d1

18. Mls006011286

19. Chembl3545414

20. Schembl21847695

21. Dtxsid80153427

22. Hms3655h12

23. Bcp15234

24. Apatinib (registered Name In China)

25. Bdbm50152828

26. S2221

27. Rivoceranib Mesylate [who-dd]

28. Akos026750547

29. Bcp9000308

30. Ccg-269641

31. Cs-0694

32. Sb16589

33. N-(4-(1-cyanocyclopentyl)phenyl)-2-((pyridin-4-ylmethyl)amino)nicotinamide Methanesulfonate

34. Ac-35390

35. Hy-13342

36. Smr004703036

37. Sw220296-1

38. D11289

39. N-(4-(1-cyanocyclopentyl)phenyl)-2-(pyridin-4-ylmethylamino)nicotinamide Mesylate

40. N-(4-(1-cyanocyclopentyl)phenyl)-2-((pyridin-4-ylmethyl)amino)pyridine-3-carboxamide Mesylate

41. N-(4-(1-cyanocyclopentyl)phenyl)-2-((pyridin-4-ylmethyl)amino)pyridine-3-carboxamide Monomethanesulfonate Salt

2.4 Create Date
2010-04-26
3 Chemical and Physical Properties
Molecular Weight 493.6 g/mol
Molecular Formula C25H27N5O4S
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count8
Rotatable Bond Count6
Exact Mass493.17837553 g/mol
Monoisotopic Mass493.17837553 g/mol
Topological Polar Surface Area153 Ų
Heavy Atom Count35
Formal Charge0
Complexity701
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently Bonded Unit Count2
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.)


Protein Kinase Inhibitors

Agents that inhibit PROTEIN KINASES. (See all compounds classified as Protein Kinase Inhibitors.)


Post Enquiry
POST ENQUIRY