Alatrofloxacin Mesylate

CHEMBL1200498 Phase 4 Disetujui Small molecule

Half-Life

—

Bioavailability

—

Protein Binding

—

Molecular Weight

654.6 g/mol

LogP

—

Phase

4

The mesylate salt form of alatrofloxacin, a prodrug that converts to trovafloxacin after administration to treat serious bacterial infections. Like the parent compound, it disrupts bacterial DNA synthesis by inhibiting topoisomerase enzymes, and this salt form is formulated for intravenous delivery.

Berat Molekul

654,6000 g/mol

TPSA

221,00 Å²

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Struktur 2D

SVG PNG

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SMILES

CS(=O)(=O)O.C[C@H](N)C(=O)N[C@@H](C)C(=O)N[C@H]1[C@@H]2CN(c3nc4c(cc3F)c(=O)c(C(=O)O)cn4-c3ccc(F)cc3F)C[C@@H]21

InChI

InChI=1S/C26H25F3N6O5.CH4O3S/c1-10(30)24(37)31-11(2)25(38)32-20-14-7-34(8-15(14)20)23-18(29)6-13-21(36)16(26(39)40)9-35(22(13)33-23)19-4-3-12(27)5-17(19)28;1-5(2,3)4/h3-6,9-11,14-15,20H,7-8,30H2,1-2H3,(H,31,37)(H,32,38)(H,39,40);1H3,(H,2,3,4)/t10-,11-,14-,15+,20+;/m0./s1

Molecular Formula

C27H29F3N6O8S

HBD / HBA

5 / 15

Ikatan yang Dapat Dirotasi

7

Atom Berat

45

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.

Pertanyaan yang Sering Diajukan

The mesylate salt form of alatrofloxacin, a prodrug that converts to trovafloxacin after administration to treat serious bacterial infections. Like the parent compound, it disrupts bacterial DNA synthesis by inhibiting topoisomerase enzymes, and this salt form is formulated for intravenous delivery.

Yes, Alatrofloxacin Mesylate 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). CHEMBL1200498. Open-access bioactivity database.
PubChem — National Center for Biotechnology Information (NCBI). CID 5282517. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-08-20.

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Struktur

Data Cepat

Rumus: C27H29F3N6O8S

Tautan Eksternal

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Penyangkalan Medis

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.