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Technical details about Besifloxacin Hydrochloride, learn more about the structure, uses, toxicity, action, side effects and more

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2D Structure
1. Also known as: Besifloxacin hcl, 405165-61-9, Besivance, Besifloxacin (hydrochloride), Bol-303224-a, Besifloxacin hydrochloride [usan]
Molecular Formula
C19H22Cl2FN3O3
Molecular Weight
430.3  g/mol
InChI Key
PMQBICKXAAKXAY-HNCPQSOCSA-N
FDA UNII
7506A6J57T

1 2D Structure

2D Structure

2 Identification
2.1 Computed Descriptors
2.1.1 IUPAC Name
7-[(3R)-3-aminoazepan-1-yl]-8-chloro-1-cyclopropyl-6-fluoro-4-oxoquinoline-3-carboxylic acid;hydrochloride
2.1.2 InChI
InChI=1S/C19H21ClFN3O3.ClH/c20-15-16-12(18(25)13(19(26)27)9-24(16)11-4-5-11)7-14(21)17(15)23-6-2-1-3-10(22)8-23;/h7,9-11H,1-6,8,22H2,(H,26,27);1H/t10-;/m1./s1
2.1.3 InChI Key
PMQBICKXAAKXAY-HNCPQSOCSA-N
2.1.4 Canonical SMILES
C1CCN(CC(C1)N)C2=C(C=C3C(=C2Cl)N(C=C(C3=O)C(=O)O)C4CC4)F.Cl
2.1.5 Isomeric SMILES
C1CCN(C[C@@H](C1)N)C2=C(C=C3C(=C2Cl)N(C=C(C3=O)C(=O)O)C4CC4)F.Cl
2.2 Other Identifiers
2.2.1 UNII
7506A6J57T
2.3 Synonyms
2.3.1 MeSH Synonyms

1. 7-((3r)-aminohexahydro-1h-azepin-1-yl)-8-chloro-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic Acid

2. 7-(3-aminohexahydro-1h-azepin-1-yl)-8-chloro-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic Acid

3. Besifloxacin

4. Besivance

5. Bol-303224-a

2.3.2 Depositor-Supplied Synonyms

1. Besifloxacin Hcl

2. 405165-61-9

3. Besivance

4. Besifloxacin (hydrochloride)

5. Bol-303224-a

6. Besifloxacin Hydrochloride [usan]

7. Ss734

8. Besifloxacin Hcl (besivance)

9. Besifloxacin (as Hydrochloride)

10. Ss-734

11. 7506a6j57t

12. 405165-61-9 (hcl)

13. Unii-7506a6j57t

14. Besifloxacin Hydrochloride (usan)

15. (+)-7-((3r)-3-aminohexahydro-1h-azepin-1-yl)-8-chloro-1-cyclopropyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic Acid Hydrochloride

16. (+)-7-[(3r)-3-aminohexahydro-1h-azepin-1-yl]-8-chloro-1- Cyclopropyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic Acid Hydrochloride.

17. (r)-7-(3-aminoazepan-1-yl)-8-chloro-1-cyclopropyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic Acid Hydrochloride

18. 3-quinolinecarboxylic Acid, 7-((3r)-3-aminohexahydro-1h-azepin-1-yl)-8-chloro-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-, Monohydrochloride

19. 7-[(3r)-3-aminoazepan-1-yl]-8-chloro-1-cyclopropyl-6-fluoro-4-oxoquinoline-3-carboxylic Acid;hydrochloride

20. Bol 303224a

21. Besivance (tn)

22. Besivance Hydrochloride

23. 7-[(3r)-3-aminohexahydro-1h-azepin-1-yl]-8-chloro-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic Acid Hydrochloride

24. Schembl291598

25. Chembl1201761

26. Dtxsid20193529

27. Besifloxacin Hydrochloride- Bio-x

28. Amy18155

29. Ex-a1339

30. Mfcd14636632

31. S3055

32. Akos025401618

33. Besifloxacin Hydrochloride [mi]

34. Ccg-221259

35. Cs-0713

36. Ac-23367

37. Bb164241

38. Besifloxacin Hydrochloride [mart.]

39. Besifloxacin Hydrochloride [vandf]

40. Hy-17028

41. Besifloxacin Hydrochloride [who-dd]

42. Besifloxacin Hydrochloride [orange Book]

43. C75052

44. D08872

45. 165b619

46. A848253

47. J-519840

48. Q27266315

49. Besifloxacin Hydrochloride 100 Microg/ml In Acetonitrile:water

50. (r)-7-(3-aminohexahydro-1h-azepin-1-yl)-8-chloro-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic Acid Hydrochloride

2.4 Create Date
2006-10-25
3 Chemical and Physical Properties
Molecular Weight 430.3 g/mol
Molecular Formula C19H22Cl2FN3O3
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count7
Rotatable Bond Count3
Exact Mass429.1022251 g/mol
Monoisotopic Mass429.1022251 g/mol
Topological Polar Surface Area86.9 Ų
Heavy Atom Count28
Formal Charge0
Complexity656
Isotope Atom Count0
Defined Atom Stereocenter Count1
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently Bonded Unit Count2
4 Pharmacology and Biochemistry
4.1 MeSH Pharmacological Classification

Anti-Bacterial Agents

Substances that inhibit the growth or reproduction of BACTERIA. (See all compounds classified as Anti-Bacterial Agents.)


Topoisomerase II Inhibitors

Compounds that inhibit the activity of DNA TOPOISOMERASE II. Included in this category are a variety of ANTINEOPLASTIC AGENTS which target the eukaryotic form of topoisomerase II and ANTIBACTERIAL AGENTS which target the prokaryotic form of topoisomerase II. (See all compounds classified as Topoisomerase II Inhibitors.)


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