Dilevalol Hydrochloride

CHEMBL1204165 Phase 4 Đã phê duyệt Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
364.9 g/mol
LogP
Phase
4

A hydrochloride salt form of dilevalol with the same antihypertensive and vasodilating properties as the parent compound. It is used to manage high blood pressure.

Khối lượng phân tử

364,9000 g/mol

TPSA

95,60 Ų

Lĩnh vực điều trị

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Cấu trúc 2D

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SMILES

C[C@H](CCc1ccccc1)NC[C@H](O)c1ccc(O)c(C(N)=O)c1.Cl

InChI

InChI=1S/C19H24N2O3.ClH/c1-13(7-8-14-5-3-2-4-6-14)21-12-18(23)15-9-10-17(22)16(11-15)19(20)24;/h2-6,9-11,13,18,21-23H,7-8,12H2,1H3,(H2,20,24);1H/t13-,18+;/m1./s1

Molecular Formula

C19H25ClN2O3

HBD / HBA

5 / 4

Liên kết có thể quay

8

Nguyên tử nặng

25

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.

Câu hỏi thường gặp

A hydrochloride salt form of dilevalol with the same antihypertensive and vasodilating properties as the parent compound. It is used to manage high blood pressure.

Yes, Dilevalol Hydrochloride 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). CHEMBL1204165. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 636407. Chemical information database.

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

Tuyên bố miễn trách y tế

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.