TTD Drug ID: DAP000999

Drug Information
Name	Cinoxacin
Synonyms	ST044511; Azolinic Acid; NCGC00023754-04; EINECS 249-133-8; DB00827; Compound 64716; HMS500P20; Cinoxacine; NCGC00023754-03; UNII-LMK22VUH23; AC1L1EEQ; NSC304467; Oprea1_131085; Cinobactin; NCGC00023754-06; Lopac-C-8645; Prestwick3_000780; 1-Ethyl-6,7-methylenedioxy-4(1H)-oxocinnoline-3-carboxylic acid; Uronorm; KBio3_001263; KBio2_000632; Cinoxacine [INN-French]; NCGC00023754-05; C8645_SIGMA; (1,3)Dioxolo(4,5-g)cinnoline-3-carboxylic acid, 1-ethyl-1,4-dihydro-4-oxo-; MolPort-001-794-447; (1,3)Dioxolo(4,5-g)cinnoline-3-carboxylic acid, 1,4-dihydro-1-ethyl-4-oxo-; 1-Ethyl-1,4-dihydro-4-oxo(1,3)dioxolo(4,5-g)cinnoline-3-carboxylic acid; KBio1_000318; KBioSS_000632; cinoxacin; Cinoxacin [USAN:BAN:INN:JAN]; BRD-K14704277-001-05-1; Lopac0_000309; Lilly 64716; D00872; Spectrum_000152; BSPBio_000860; Cinoxacinum; LS-62687; Cinobac; SPECTRUM1500190; EU-0100309; NCGC00015277-04; SPBio_000360; Spectrum2_000570; SPBio_002799; BPBio1_000946; NSC 304467; NCGC00015277-01; Prestwick0_000780; NINDS_000318; AC1Q317Y; BRN 1084304; KBio2_003200; 1-Ethyl-1,4-dihydro-4-oxo[1,3]dioxolo[4,5-g]cinnoline-3-carboxylic acid; Prestwick1_000780; C08052; Spectrum5_000749; CCRIS 8206; NCGC00023754-07; CHEBI:3716; 1-Ethyl-4-oxo-1,4-dihydro[1,3]dioxolo[4,5-g]cinnoline-3-carboxylic acid; NCGC00015277-14; 28657-80-9; KBio2_005768; Clinoxacin; TNP00246; NCGC00015277-02; Prestwick2_000780; C12H10N2O5; Spectrum3_000352; BSPBio_002043; NCGC00015277-03; MLS001148076; SMR000058232; CHEMBL1208; HMS2091E18; [1,3]Dioxolo[4,5-g]cinnoline-3-carboxylic acid, 1-ethyl-1,4-dihydro-4-oxo-; DivK1c_000318; 1-ethyl-4-oxo-[1,3]dioxolo[4,5-g]cinnoline-3-carboxylic acid; C 8645; CAS-28657-80-9; Spectrum4_000289; IDI1_000318; Cinoxacinum [INN-Latin]; Prestwick_239; Cinoxacino [INN-Spanish]; KBioGR_000818; NCGC00015277-07; MLS000069630; Cinoxacin (JAN/USP/INN); CID2762; Cinoxacino; HMS1920O11; Cinx; HMS1570K22; Cinobac (TN)
Indication	Urinary tract infections			Approved    [1]
Structure	Click to save drug structure in 3D MOL format Click to save drug structure in 2D MOL format
Therapeutic Class	Antiinfective Agents
CAS Number	CAS 28657-80-9
Formular	C12H10N2O5
PubChem Compound ID	CID 2762.
PubChem Substance ID	SID 10252.
SuperDrug ATC ID	J01MB06;
SuperDrug CAS ID	028657809;
Target	DNA gyrase			Inhibitor	[2]
Ref 1	FDA Approved Drug Products from FDA Official Website. 2009. Application Number: (NDA) 018067 To Reference
Ref 2	The interaction and transport of beta-lactam antibiotics with the cloned rat renal organic anion transporter 1. J Pharmacol Exp Ther. 1999 Aug;290(2):672-7. To Reference

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