Cangrelor

CHEMBL334966 Phase 4 Одобрено Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
776.4 g/mol
LogP
-1.0
Phase
4

A short-acting intravenous antiplatelet drug that rapidly inhibits the P2Y12 receptor to prevent platelet aggregation during and after heart procedures such as percutaneous coronary intervention. Its very short half-life allows quick reversal of antiplatelet effects, which is useful when bridging to oral therapy. It is used in patients who have not been pre-treated with oral P2Y12 inhibitors.

Молекулярная масса

776,4000 g/mol

LogP

-1,00

TPSA

307,00 Ų

Правило пяти Липинского

Не соответствует

Терапевтические области

Pharmacokinetics (PK)

Pharmacodynamics (PD)

2D Структура

SVG PNG

Cite this structure


                        

Embed this structure


                        

SMILES

CSCCNc1nc(SCCC(F)(F)F)nc2c1ncn2[C@@H]1O[C@H](COP(=O)(O)OP(=O)(O)C(Cl)(Cl)P(=O)(O)O)[C@@H](O)[C@H]1O

InChI

InChI=1S/C17H25Cl2F3N5O12P3S2/c1-43-5-3-23-12-9-13(26-15(25-12)44-4-2-16(20,21)22)27(7-24-9)14-11(29)10(28)8(38-14)6-37-42(35,36)39-41(33,34)17(18,19)40(30,31)32/h7-8,10-11,14,28-29H,2-6H2,1H3,(H,33,34)(H,35,36)(H,23,25,26)(H2,30,31,32)/t8-,10-,11-,14-/m1/s1

Molecular Formula

C17H25Cl2F3N5O12P3S2

HBD / HBA

7 / 21

Вращаемые Связи

15

Тяжёлые Атомы

44

No targets recorded

Target interaction data is not yet available for this drug.

No interactions recorded

Drug interaction data is not yet available for this compound.

No side effects recorded

Side effect data is not yet available for this drug.

Часто задаваемые вопросы

A short-acting intravenous antiplatelet drug that rapidly inhibits the P2Y12 receptor to prevent platelet aggregation during and after heart procedures such as percutaneous coronary intervention. Its very short half-life allows quick reversal of antiplatelet effects, which is useful when bridging to oral therapy. It is used in patients who have not been pre-treated with oral P2Y12 inhibitors.

Yes, Cangrelor is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.

{# References & Data Sources section for drug detail pages. Renders standard pharmacological database links plus the drug's data_sources field. #}

References & Data Sources

  • ChEMBL — European Bioinformatics Institute (EBI). CHEMBL334966. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 9854012. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.

Медицинский отказ от ответственности

This content is for educational and informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider before making medication decisions.

Data sources: ChEMBL, PubChem, DailyMed.