Tenofovir Alafenamide Fumarate

CHEMBL2364637 Phase 4 معتمد Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
1069.0 g/mol
LogP
Phase
4

Tenofovir alafenamide fumarate is the fumarate salt form of tenofovir alafenamide (TAF), a prodrug NRTI that is converted intracellularly to tenofovir diphosphate to inhibit HIV-1 and HBV reverse transcriptase. See tenofovir-alafenamide for complete pharmacological details. This salt form is used in numerous fixed-dose combination antiretroviral products.

الوزن الجزيئي

1069,0000 g/mol

TPSA

362,00 Ų

المجالات العلاجية

آلية العمل

Administered as an inactive precursor that is metabolically converted to its active form in the body. This prodrug design improves bioavailability, absorption, or targeted delivery compared to the active compound.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

الآلية

Administered as an inactive precursor that is metabolically converted to its active form in the body. This prodrug design improves bioavailability, absorption, or targeted delivery compared to the active compound.

البنية ثنائية الأبعاد

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SMILES

CC(C)OC(=O)[C@H](C)N[P@](=O)(CO[C@H](C)Cn1cnc2c(N)ncnc21)Oc1ccccc1.CC(C)OC(=O)[C@H](C)N[P@](=O)(CO[C@H](C)Cn1cnc2c(N)ncnc21)Oc1ccccc1.O=C(O)/C=C/C(=O)O

InChI

InChI=1S/2C21H29N6O5P.C4H4O4/c2*1-14(2)31-21(28)16(4)26-33(29,32-17-8-6-5-7-9-17)13-30-15(3)10-27-12-25-18-19(22)23-11-24-20(18)27;5-3(6)1-2-4(7)8/h2*5-9,11-12,14-16H,10,13H2,1-4H3,(H,26,29)(H2,22,23,24);1-2H,(H,5,6)(H,7,8)/b;;2-1+/t2*15-,16+,33+;/m11./s1

Molecular Formula

C46H62N12O14P2

HBD / HBA

6 / 24

الروابط القابلة للدوران

26

الذرات الثقيلة

74

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.

الأسئلة الشائعة

Tenofovir alafenamide fumarate is the fumarate salt form of tenofovir alafenamide (TAF), a prodrug NRTI that is converted intracellularly to tenofovir diphosphate to inhibit HIV-1 and HBV reverse transcriptase. See tenofovir-alafenamide for complete pharmacological details. This salt form is used in numerous fixed-dose combination antiretroviral products.

Administered as an inactive precursor that is metabolically converted to its active form in the body. This prodrug design improves bioavailability, absorption, or targeted delivery compared to the active compound.

Yes, Tenofovir Alafenamide Fumarate 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). CHEMBL2364637. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 71492247. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.

إخلاء المسؤولية الطبية

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.