General Information of DTT (ID: TTFK8YB)

DTT Name Bacterial DNA topoisomerase 4A (Bact parC) DTT Info
Gene Name Bact parC

Molecule-Related Drug & Molecule List

Molecule-Related Drug List
Molecule Type:
DTT
DTP
DME
Drug Status:
Approved Drug(s)
Clinical Trial Drug(s)
Investigative Drug(s)
1 Approved Drug(s) Transported by This DTP
Drug Name Drug ID Indication ICD 11 Highest Status REF
Prulifloxacin DMOK965 Urinary tract infection GC08 Approved [1]
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5 Clinical Trial Drug(s) Transported by This DTP
Drug Name Drug ID Indication ICD 11 Highest Status REF
Pazufloxacin DMHXTAQ Conjunctivitis 9A60 Phase 3 [2]
Sitafloxacin DMTV5XC Escherichia coli infection 1A03 Phase 2/3 [3]
JNJ-32729463 DMQD1GN Community-acquired pneumonia CA40.Z Phase 2 [4]
TNP-2092 DM8DZKI Skin and skin-structure infection 1F28-1G0Z Phase 2 [5]
VB 1953 DM0YWQ4 Acne vulgaris ED80 Phase 2 [6]
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1 Investigative Drug(s) Transported by This DTP
Drug Name Drug ID Indication ICD 11 Highest Status REF
A-62824 DMJ6IMZ Discovery agent N.A. Investigative [7]
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Molecule Interaction Atlas

References

1 Prulifloxacin: a new antibacterial fluoroquinolone. Expert Rev Anti Infect Ther. 2006 Feb;4(1):27-41.
2 Target preference of 15 quinolones against Staphylococcus aureus, based on antibacterial activities and target inhibition. Antimicrob Agents Chemother. 2001 Dec;45(12):3544-7.
3 Dual-targeting properties of the 3-aminopyrrolidyl quinolones, DC-159a and sitafloxacin, against DNA gyrase and topoisomerase IV: contribution to reducing in vitro emergence of quinolone-resistant Streptococcus pneumoniae. J Antimicrob Chemother. 2008 Jul;62(1):98-104.
4 Antistaphylococcal activities of the new fluoroquinolone JNJ-Q2. Antimicrob Agents Chemother. 2011 Dec;55(12):5512-21.
5 Clinical pipeline report, company report or official report of TenNor Therapeutics.
6 Clinical pipeline report, company report or official report of Vyome Therapeutics.
7 Isothiazoloquinolones containing functionalized aromatic hydrocarbons at the 7-position: synthesis and in vitro activity of a series of potent anti... Bioorg Med Chem Lett. 2006 Mar 1;16(5):1272-6.