Heparin Sodium

CHEMBL1201657 Phase 4 Aprovado Oligosaccharide
Half-Life
Bioavailability
Protein Binding
Molecular Weight
1157.9 g/mol
LogP
Phase
4

The sodium salt form of heparin, a widely used injectable anticoagulant that prevents clot formation by enhancing the activity of antithrombin against multiple clotting factors. This is the standard pharmaceutical formulation of heparin available for intravenous and subcutaneous administration. Bleeding risk, platelet counts, and clotting times must be monitored during therapy.

Peso Molecular

1157,9000 g/mol

TPSA

652,00 Ų

Áreas Terapêuticas

Mecanismo de Ação

Binds to antithrombin III, dramatically accelerating its inhibition of thrombin (Factor IIa), Factor Xa, and other serine proteases of the coagulation cascade. This produces rapid anticoagulation proportional to the dose administered.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mecanismo

Binds to antithrombin III, dramatically accelerating its inhibition of thrombin (Factor IIa), Factor Xa, and other serine proteases of the coagulation cascade. This produces rapid anticoagulation proportional to the dose …

Estrutura 2D

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SMILES

CC(=O)NC1C(C(C(OC1O)COS(=O)(=O)O)OC2C(C(C(C(O2)C(=O)O)OC3C(C(C(C(O3)CO)OC4C(C(C(C(O4)C(=O)O)O)O)OS(=O)(=O)O)OS(=O)(=O)O)NS(=O)(=O)O)O)OS(=O)(=O)O)O.[Na+]

InChI

InChI=1S/C26H42N2O37S5.Na/c1-4(30)27-7-9(31)13(6(56-23(7)39)3-55-67(43,44)45)58-26-19(65-70(52,53)54)12(34)16(20(62-26)22(37)38)60-24-8(28-66(40,41)42)15(63-68(46,47)48)14(5(2-29)57-24)59-25-18(64-69(49,50)51)11(33)10(32)17(61-25)21(35)36;/h5-20,23-26,28-29,31-34,39H,2-3H2,1H3,(H,27,30)(H,35,36)(H,37,38)(H,40,41,42)(H,43,44,45)(H,46,47,48)(H,49,50,51)(H,52,53,54);/q;+1

Molecular Formula

C26H42N2NaO37S5+

HBD / HBA

15 / 38

Ligações Rotacionáveis

21

Átomos Pesados

71

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.

Perguntas frequentes

The sodium salt form of heparin, a widely used injectable anticoagulant that prevents clot formation by enhancing the activity of antithrombin against multiple clotting factors. This is the standard pharmaceutical formulation of heparin available for intravenous and subcutaneous administration. Bleeding risk, platelet counts, and clotting times must be monitored during therapy.

Binds to antithrombin III, dramatically accelerating its inhibition of thrombin (Factor IIa), Factor Xa, and other serine proteases of the coagulation cascade. This produces rapid anticoagulation proportional to the dose administered.

Yes, Heparin Sodium is an approved drug. It has reached clinical phase 4. It is classified as a Oligosaccharide.

{# 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). CHEMBL1201657. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 92044406. Chemical information database.

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

Aviso Médico

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.