Norfloxacin - Moligand™, analytical standard , Bacterial DNA gyrase inhibitor, CAS No.70458-96-7, Bacterial DNA gyrase inhibitor

CAS: 70458-96-7 Cat. No.: N114261 Formula: C16H18FN3O3 Peso molecolare: 319.33 Numero EC: 274-614-4
Disponibile su ordine
QUALITÀ & PUREZZA Analytical standard ? Analytical standard — certified-purity material for quantitative calibration. Use to prepare calibration standards and validate analytical methods. Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools.
Synonyms
Chibroxine|Norfloxacin - Norxacin|NORFLOXACIN (USP IMPURITY)|Noroxin|Norfloxacine|1-ethyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid|1-Ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-3-quinolinecarboxylic acid|3-Quinolinecarboxylic acid, 1,4-dihydro-1-ethyl-6-fluoro-4-oxo-7-(1-piperazinyl)-|Noracin|1-Ethyl-6-fluoro-4-oxo-7-(1-piperazinyl)-1,4-dihydro-3-quinolinecarboxylic acid|Norfloxacine,(S)|Zoroxin|Norfloxacin (JP17/USP/INN)|Noflo|Noroxine|Utinor|NORFLOXACIN (USP-RS)|norfloxacina|Chibroxin|norphloxacine|Norflo|NORFLOXACIN [USP IMPURITY]|Norocin|Noraxin|Norfloxacinum (INN-Latin)|AM 715|NORFLOXACIN [VANDF]|Norfloxacino (INN-Spanish)|NORFLOXACIN [MI]|NORFLOXACIN [USAN]|Sebercim|Chibroxol|Gonorcin|norfloxacin|Norfloxacin protomer II|1,4-Dihydro-1-ethyl-6-fluoro-4-oxo-7-(1-piperazinyl)-3-quinolinecarboxylic acid|Baccidal|1-Ethyl-6-fluor-1,4-dihydro-4-oxo-7-(1-piperazinyl)-3-chinolincarbonsaeure|Nolicin|Norfloxacin (Norxacin)|Barazan|Fulgram|Noroxin (TN)|NORFLOXACIN (MART.)|NORFLOXACIN [USP-RS]|MK 0366|Norfloxacine [INN-French]|Uroxacin|NFLX|Norfloxacinum|AM-715|NORFLOXACIN (EP MONOGRAPH)|NORFLOXACIN [EP MONOGRAPH]|Norfloxacin [USAN:USP:INN:BAN:JAN]|1-ethyl-6-fluoro-4-oxo-7-piperazin-1-ylquinoline-3-carboxylic acid|Lexinor|MK-0366|Opera_ID_1423|Norfloxacino|1-Ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-3-quinoline carboxylic acid|3-Quinolinecarboxylic acid, 1-ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-|Norfloxacin (USAN:USP:INN:BAN:JAN)|Norfloxacin protomer I|Norfloxacine (INN-French)|Norfloxacinum [INN-Latin]|NORFLOXACIN [JAN]|Norxacin|NORFLOXACIN [WHO-DD]
Storage
Store at 2-8°C
Shipped In
Wet ice
★
Dimensione
Germania (EU)
USA*
Prezzo
Qtà
100mg
N114261-100mg
—
5 Disponibile
260,23€
Enter a quantity for the sizes you want to add.

Specifiche

Sinonimi
Chibroxine | Norfloxacin - Norxacin | NORFLOXACIN (USP IMPURITY) | Noroxin | Norfloxacine | 1-ethyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid | 1-Ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-3-quinolinecarboxylic acid | 3-Quinolinecarboxylic acid, 1,4-dihydro-1-ethyl-6-fluoro-4-oxo-7-(1-piperazinyl)- | Mostra altro
Specifiche e purezza
Moligand™, analytical standard
Condizioni di conservazione di stoccaggio
Store at 2-8°C
Spedito in
Wet ice
Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.
Grado
Moligand™, Standard analitico
Tipo di azione
INHIBITOR
Meccanismo d'azione
Bacterial DNA gyrase inhibitor
Proprietà del prodotto
ALogP
-1
Nomi e identificatori
Pubchem Sid
Sorrisi canonici
CCN1C=C(C(=O)C2=CC(=C(C=C21)N3CCNCC3)F)C(=O)O
IUPAC Name
1-ethyl-6-fluoro-4-oxo-7-piperazin-1-ylquinoline-3-carboxylic acid
InChIKey
OGJPXUAPXNRGGI-UHFFFAOYSA-N
INCHI
1S/C16H18FN3O3/c1-2-19-9-11(16(22)23)15(21)10-7-12(17)14(8-13(10)19)20-5-3-18-4-6-20/h7-9,18H,2-6H2,1H3,(H,22,23)
Isomeri SMILES
CCN1C=C(C(=O)C2=CC(=C(C=C21)N3CCNCC3)F)C(=O)O
Peso molecolare
319.33
Reaxy-Rn
567897
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=567897&ln=

Dati avanzati

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClasseQuinolines and derivatives
SubclassQuinoline carboxylic acids
Intermediate Tree Nodes Not available
Direct ParentQuinoline carboxylic acids
Alternative Parents Fluoroquinolones  N-arylpiperazines  Haloquinolines  Hydroquinolones  Aminoquinolines and derivatives  Hydroquinolines  Pyridinecarboxylic acids  Dialkylarylamines  Benzenoids  Aryl fluorides  Heteroaromatic compounds  Vinylogous amides  Amino acids  Azacyclic compounds  Monocarboxylic acids and derivatives  Dialkylamines  Carboxylic acids  Hydrocarbon derivatives  Organic oxides  Organofluorides  Organooxygen compounds  Organopnictogen compounds  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Quinoline-3-carboxylic acid - Fluoroquinolone - N-arylpiperazine - Aminoquinoline - Haloquinoline - Dihydroquinolone - Dihydroquinoline - Pyridine carboxylic acid - Pyridine carboxylic acid or derivatives - Tertiary aliphatic/aromatic amine - Dialkylarylamine - Aryl fluoride - Aryl halide - 1,4-diazinane - Piperazine - Pyridine - Benzenoid - Vinylogous amide - Heteroaromatic compound - Amino acid or derivatives - Amino acid - Tertiary amine - Azacycle - Secondary amine - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Carboxylic acid - Secondary aliphatic amine - Amine - Organic oxygen compound - Organic nitrogen compound - Organopnictogen compound - Organic oxide - Organohalogen compound - Organofluoride - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Aromatic heteropolycyclic compound
DescrizioneThis compound belongs to the class of organic compounds known as quinoline carboxylic acids. These are quinolines in which the quinoline ring system is substituted by a carboxyl group at one or more positions.
External Descriptors Fluoroquinolones
Struttura 3D
Modello di struttura chimica interattiva





Obiettivi associati (umani)
PDE5A Tclin Phosphodiesterase 5A (5113 Activities)
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EGFR Tclin Epidermal growth factor receptor erbB1 (33727 Activities)
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CA2 Tclin Carbonic anhydrase II (17698 Activities)
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ESR1 Tclin Estrogen receptor alpha (17718 Activities)
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HMGCR Tclin HMG-CoA reductase (2475 Activities)
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NR3C1 Tclin Glucocorticoid receptor (14987 Activities)
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INSR Tclin Insulin receptor (5558 Activities)
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PGR Tclin Progesterone receptor (8562 Activities)
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ADRB2 Tclin Beta-2 adrenergic receptor (11824 Activities)
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CHRM2 Tclin Muscarinic acetylcholine receptor M2 (10671 Activities)
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ADRB1 Tclin Beta-1 adrenergic receptor (6630 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR1A Tclin Serotonin 1a (5-HT1a) receptor (14969 Activities)
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ADRA2A Tclin Alpha-2a adrenergic receptor (9450 Activities)
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AR Tclin Androgen Receptor (11781 Activities)
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CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)
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ACE Tclin Angiotensin-converting enzyme (1423 Activities)
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DRD2 Tclin Dopamine D2 receptor (23596 Activities)
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TYR Tclin Tyrosinase (717 Activities)
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GABRA1 Tclin GABA receptor alpha-1 subunit (399 Activities)
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TSHR Tclin Thyroid stimulating hormone receptor (29986 Activities)
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MAOA Tclin Monoamine oxidase A (11911 Activities)
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CNR1 Tclin Cannabinoid CB1 receptor (20913 Activities)
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DRD1 Tclin Dopamine D1 receptor (9720 Activities)
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DRD4 Tchem Dopamine D4 receptor (7907 Activities)
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ACHE Tclin Acetylcholinesterase (18204 Activities)
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PTGS1 Tclin Cyclooxygenase-1 (9233 Activities)
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SLC6A2 Tclin Norepinephrine transporter (10102 Activities)
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HRH2 Tclin Histamine H2 receptor (5428 Activities)
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ADRA1D Tclin Alpha-1d adrenergic receptor (4171 Activities)
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HTR1B Tclin Serotonin 1b (5-HT1b) receptor (2801 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR2A Tclin Serotonin 2a (5-HT2a) receptor (14758 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR2C Tclin Serotonin 2c (5-HT2c) receptor (11471 Activities)
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AVPR2 Tclin Vasopressin V2 receptor (2912 Activities)
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ADORA1 Tclin Adenosine A1 receptor (17603 Activities)
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AGTR1 Tclin Type-1 angiotensin II receptor (5176 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CALCR Tclin Calcitonin receptor (2215 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC6A4 Tclin Serotonin transporter (12625 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA1A Tclin Alpha-1a adrenergic receptor (8359 Activities)
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PTGS2 Tclin Cyclooxygenase-2 (13999 Activities)
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HRH1 Tclin Histamine H1 receptor (7573 Activities)
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ADRA1B Tclin Alpha-1b adrenergic receptor (2912 Activities)
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OPRM1 Tclin Mu opioid receptor (19785 Activities)
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DRD3 Tclin Dopamine D3 receptor (14368 Activities)
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AVPR1A Tclin Vasopressin V1a receptor (5412 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OPRD1 Tclin Delta opioid receptor (15096 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OPRK1 Tclin Kappa opioid receptor (16155 Activities)
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HTR3A Tclin Serotonin 3a (5-HT3a) receptor (3366 Activities)
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SLC6A3 Tclin Dopamine transporter (10535 Activities)
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GRIN1 Tclin Glutamate (NMDA) receptor subunit zeta 1 (122 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KCNH2 Tclin HERG (29587 Activities)
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Obiettivi associati (non umani)
gyrB DNA gyrase subunit B (290 Activities)
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parC Topoisomerase IV subunit A (46 Activities)
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Agtr2 Angiotensin II type 2 (AT-2) receptor (803 Activities)
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Mc4r Melanocortin receptor 4 (1205 Activities)
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Ltc4s Leukotriene C4 synthase (1 Activities)
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Sigmar1 Sigma opioid receptor (160 Activities)
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Npy1r Neuropeptide Y receptor type 1 (8 Activities)
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Cckar Cholecystokinin A receptor (90 Activities)
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Pde4d Phosphodiesterase 4D (4 Activities)
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polC DNA polymerase III (243 Activities)
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Nos2 Nitric oxide synthase, inducible (3573 Activities)
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Mapk1 MAP kinase ERK2 (650 Activities)
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Hdac6 Histone deacetylase 6 (222 Activities)
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Mmp9 Matrix metalloproteinase 9 (38 Activities)
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Abcb1a P-glycoprotein 3 (492 Activities)
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recA Recombinase A (14 Activities)
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Streptococcus pneumoniae (31063 Activities)
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Salmonella typhimurium (15756 Activities)
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Shigella boydii (323 Activities)
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Plesiomonas shigelloides (58 Activities)
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Pasteurella multocida (1166 Activities)
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Bacteroides fragilis (1445 Activities)
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Micrococcus luteus (7463 Activities)
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Staphylococcus aureus (210822 Activities)
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Meccanismi d'azione
Certificati (CoA, COO, BSE/TSE e tabella di analisi)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

2 results found

Lot NumberCertificate TypeDataOggetto
D23031186D23031186Certificate of AnalysisSep 21, 2026 N114261
K1611036K1611036Certificate of AnalysisMay 12, 2022 N114261
Proprietà chimiche e fisiche
Punto di fusione (°C)227-228°C
Peso molecolare319.330 g/mol
XLogP3-1.000
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count7
Rotatable Bond Count3
Exact Mass319.133 Da
Monoisotopic Mass319.133 Da
Topological Polar Surface Area72.900 Ų
Heavy Atom Count23
Formal Charge0
Complexity519.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Domande frequenti e articoli
Citations of This Product
Calcolatori di soluzioni
Recensioni

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