Enoxacin
Penetrex (enoxacin) is a small molecule pharmaceutical. Enoxacin was first approved as Penetrex on 1991-12-31. It is used to treat escherichia coli infections, gonorrhea, haemophilus infections, klebsiella infections, and proteus infections amongst others in the USA. It is known to target V-type proton ATPase subunit B, brain isoform.
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Therapeutic Areas
Therapeutic Area | MeSH |
---|---|
infections | D007239 |
urogenital diseases | D000091642 |
Trade Name
FDA
EMA
No data
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
Enoxacin
Tradename | Company | Number | Date | Products |
---|---|---|---|---|
PENETREX | Sanofi | N-019616 DISCN | 1991-12-31 | 2 products |
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Labels
FDA
EMA
Brand Name | Status | Last Update |
---|---|---|
penetrex(r) arthritis pain relief | unapproved drug other | 2022-06-20 |
Indications
FDA
EMA
Indication | Ontology | MeSH | ICD-10 |
---|---|---|---|
escherichia coli infections | EFO_1001318 | D004927 | B96.20 |
gonorrhea | DOID_7551 | D006069 | A54 |
haemophilus infections | EFO_1001127 | D006192 | — |
klebsiella infections | EFO_1001353 | D007710 | — |
proteus infections | EFO_1001130 | D011512 | — |
pseudomonas infections | EFO_0001076 | D011552 | — |
staphylococcal infections | — | D013203 | A49.01 |
urinary tract infections | EFO_0003103 | D014552 | N39.0 |
Agency Specific
FDA
EMA
No data
Patent Expiration
No data
HCPCS
No data
Clinical
Clinical Trials
39 clinical trials
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Indications Phases 4
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Indications Phases 2
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Myelomonocytic leukemia chronic | D015477 | C93.1 | 2 | 3 | — | — | — | 5 | |
Hematologic neoplasms | D019337 | 2 | 1 | — | — | — | 2 | ||
Multiple myeloma | D009101 | C90.0 | 2 | 1 | — | — | — | 2 | |
Neoplasms | D009369 | C80 | 2 | 2 | — | — | — | 2 | |
Biphenotypic leukemia acute | D015456 | C95.0 | — | 1 | — | — | — | 1 | |
Glioma | D005910 | EFO_0000520 | 1 | 1 | — | — | — | 1 | |
Cholangiocarcinoma | D018281 | C22.1 | 1 | 1 | — | — | — | 1 | |
Chondrosarcoma | D002813 | 1 | 1 | — | — | — | 1 | ||
Leukemia | D007938 | C95 | 1 | 1 | — | — | — | 1 |
Indications Phases 1
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Healthy volunteers/patients | — | 4 | — | — | — | — | 4 | ||
Hepatic insufficiency | D048550 | 2 | — | — | — | — | 2 | ||
Prostatic neoplasms | D011471 | C61 | 1 | — | — | — | — | 1 | |
Castration-resistant prostatic neoplasms | D064129 | 1 | — | — | — | — | 1 | ||
Breast neoplasms | D001943 | EFO_0003869 | C50 | 1 | — | — | — | — | 1 |
Pancreatic neoplasms | D010190 | EFO_0003860 | C25 | 1 | — | — | — | — | 1 |
Non-hodgkin lymphoma | D008228 | C85.9 | 1 | — | — | — | — | 1 | |
Primary myelofibrosis | D055728 | D47.4 | 1 | — | — | — | — | 1 | |
Precursor cell lymphoblastic leukemia-lymphoma | D054198 | C91.0 | 1 | — | — | — | — | 1 | |
B-cell chronic lymphocytic leukemia | D015451 | C91.1 | 1 | — | — | — | — | 1 |
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Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common name | ENOXACIN |
INN | enoxacin |
Description | Enoxacin is a 1,8-naphthyridine derivative that is 1,4-dihydro-1,8-naphthyridine with an ethyl group at the 1 position, a carboxy group at the 3-position, an oxo sustituent at the 4-position, a fluoro substituent at the 5-position and a piperazin-1-yl group at the 7 position. An antibacterial, it is used in the treatment of urinary-tract infections and gonorrhoea. It has a role as an antibacterial drug and a DNA synthesis inhibitor. It is a monocarboxylic acid, an amino acid, a 1,8-naphthyridine derivative, a N-arylpiperazine, a quinolone antibiotic and a fluoroquinolone antibiotic. |
Classification | Small molecule |
Drug class | antibacterials (quinolone derivatives) |
Image (chem structure or protein) | |
Structure (InChI/SMILES or Protein Sequence) | CCn1cc(C(=O)O)c(=O)c2cc(F)c(N3CCNCC3)nc21 |
Identifiers
PDB | — |
CAS-ID | 74011-58-8 |
RxCUI | 3925 |
ChEMBL ID | CHEMBL826 |
ChEBI ID | 157175 |
PubChem CID | 3229 |
DrugBank | DB00467 |
UNII ID | 325OGW249P (ChemIDplus, GSRS) |
Target
Agency Approved
No data
Alternate
ATP6V1B2
ATP6V1B2
Organism
Homo sapiens
Gene name
ATP6V1B2
Gene synonyms
ATP6B2, VPP3
NCBI Gene ID
Protein name
V-type proton ATPase subunit B, brain isoform
Protein synonyms
ATPase, H+ transporting, lysosomal 56/58kDa, V1 subunit B2, Endomembrane proton pump 58 kDa subunit, H+ transporting two-sector ATPase, HO57, testicular secretory protein Li 65, V-ATPase B2 subunit, V-ATPase subunit B 2, vacuolar H+-ATPase 56,000 subunit, Vacuolar proton pump subunit B 2
Uniprot ID
Mouse ortholog
Atp6v1b2 (11966)
V-type proton ATPase subunit B, brain isoform (Q3UAW7)
Variants
Clinical Variant
No data
Financial
No data
Trends
PubMed Central
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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2,268 adverse events reported
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