Oxiconazole nitrate - ≥98% , Cytochrome P450 51 inhibitor, CAS No.64211-46-7, Cytochrome P450 51 inhibitor

CAS: 64211-46-7 Cat. No.: O276152 Peso molecular: 492.14 Número EC: 264-730-3 PubChem CID: 9556529
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
Oxistat | 2',4'-dichloro-2-imidazol-1-ylacetophenone (Z)-(OO-(2,4-dichlorobenzyl)oxime) mononitrate | C08075 | CHEBI:7826 | OXICONAZOLE NITRATE [MART.] | Oxistat (TN) | alpha-Benzoyltriethylammonium chloride | HMS3714A13 | OXICONAZOLE NITRATE [USP-RS] | H
Storage
Store at -20°C,Argon charged
Shipped In
Ice chest + Ice pads
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
5mg
O276152-5mg
3

33,90US$

50,90US$
Guardar 17,00 US$ (33.40%)
10mg
O276152-10mg
3

60,90US$

91,90US$
Guardar 31,00 US$ (33.73%)
25mg
O276152-25mg
2

132,90US$

199,90US$
Guardar 67,00 US$ (33.52%)
50mg
O276152-50mg
1

201,90US$

302,90US$
Guardar 101,00 US$ (33.34%)
100mg
O276152-100mg
1

302,90US$

454,90US$
Guardar 152,00 US$ (33.41%)
Enter a quantity for the sizes you want to add.
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Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -20°C,Argon charged Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Oxiconazole nitrate (Ro 13-8996) is the nitrate salt form of oxiconazole, a broad spectrum imidazole derivative with antifungal activity. Although the exact mechanism of action has yet to be fully elucidated, oxiconazole, like other azole antifungals, most likely inhibits the cytochrome P450-dependent demethylation of lanosterol. This prevents the synthesis of ergosterol which is a crucial component of fungal cell membrane. By disrupting fungal cell membrane synthesis and integrity, oxiconazole alters fungal cell membrane permeability, promotes loss of essential intracellular components and eventually inhibits fungal cell growth.

Specifications

Sinónimos
Oxistat | 2', 4'-dichloro-2-imidazol-1-ylacetophenone (Z)-(OO-(2, 4-dichlorobenzyl)oxime) mononitrate | C08075 | CHEBI:7826 | OXICONAZOLE NITRATE [MART.] | Oxistat (TN) | alpha-Benzoyltriethylammonium chloride | HMS3714A13 | OXICONAZOLE NITRATE [USP-RS] | H
Especificaciones y pureza
≥98%
Mecanismos bioquímicos y fisiológicos
Broad-spectrum imidazole antifungal agent. Potent inducer of CYP3A4 gene expression via PXR. Active in vivo.
Condiciones de almacenamiento de almacenamiento
Store at -20°C, Argon charged
Enviado en
Ice chest + Ice pads
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Tipo de acción
INHIBITOR
Mecanismo de acción
Cytochrome P450 51 inhibitor
Nota
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Pureza
≥98%
Nombres e identificadores
Sonrisas canónicasC1=CC(=C(C=C1Cl)Cl)CON=C(CN2C=CN=C2)C3=C(C=C(C=C3)Cl)Cl.[N+](=O)(O)[O-]
IUPAC Name(Z)-1-(2,4-dichlorophenyl)-N-[(2,4-dichlorophenyl)methoxy]-2-imidazol-1-ylethanimine;nitric acid
InChIKeyWVNOAGNOIPTWPT-NDUABGMUSA-N
INCHI1S/C18H13Cl4N3O.HNO3/c19-13-2-1-12(16(21)7-13)10-26-24-18(9-25-6-5-23-11-25)15-4-3-14(20)8-17(15)22;2-1(3)4/h1-8,11H,9-10H2;(H,2,3,4)/b24-18+;
Isómeros SMILES C1=CC(=C(C=C1Cl)Cl)CO/N=C(\CN2C=CN=C2)/C3=C(C=C(C=C3)Cl)Cl.[N+](=O)(O)[O-]
PubChem CID 9556529
Peso molecular 492.14

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClaseBenzene and substituted derivatives
SubclassHalobenzenes
Intermediate Tree Nodes Chlorobenzenes
Direct ParentDichlorobenzenes
Alternative Parents N-substituted imidazoles  Aryl chlorides  Organic nitrates  Heteroaromatic compounds  Organic nitro compounds  Organic nitric acids  Azacyclic compounds  Organopnictogen compounds  Organooxygen compounds  Organonitrogen compounds  Organochlorides  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents 1,3-dichlorobenzene - Aryl chloride - Aryl halide - N-substituted imidazole - Azole - Imidazole - Heteroaromatic compound - Organic nitrate - Organic nitro compound - Organic nitric acid - Organic nitric acid or derivatives - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Allyl-type 1,3-dipolar organic compound - Organic oxygen compound - Organic nitrogen compound - Organohalogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organochloride - Organonitrogen compound - Organooxygen compound - Aromatic heteromonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as dichlorobenzenes. These are compounds containing a benzene with exactly two chlorine atoms attached to it.
External Descriptors conazole antifungal drug - organic nitrate salt - imidazole antifungal drug
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
VDR Tclin Vitamin D receptor (26531 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GBA1 Tclin Beta-glucocerebrosidase (14647 Activities)
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ALOX15B Tchem Arachidonate 15-lipoxygenase, type II (7244 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Caco-2 (12174 Activities)
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HEK293 (82097 Activities)
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ABCC2 Tchem Canalicular multispecific organic anion transporter 1 (1191 Activities)
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ABCB11 Tchem Bile salt export pump (2311 Activities)
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ABCC3 Tbio Canalicular multispecific organic anion transporter 2 (718 Activities)
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TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
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USP2 Tbio Ubiquitin carboxyl-terminal hydrolase 2 (8818 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
LMNA Tbio Prelamin-A/C (36751 Activities)
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GMNN Tbio Geminin (128009 Activities)
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PMP22 Tbio Peripheral myelin protein 22 (699 Activities)
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SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 (2672 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLCO1B3 Tchem Solute carrier organic anion transporter family member 1B3 (2517 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ABCC4 Tchem Multidrug resistance-associated protein 4 (785 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
USP1 Tchem Ubiquitin carboxyl-terminal hydrolase 1 (22556 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Mapk1 MAP kinase ERK2 (650 Activities)
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Streptococcus (3973 Activities)
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Klebsiella pneumoniae (43867 Activities)
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Staphylococcus aureus (210822 Activities)
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Acinetobacter baumannii (41033 Activities)
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Escherichia coli (133304 Activities)
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Plasmodium falciparum (966862 Activities)
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Cryptococcus neoformans (21258 Activities)
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Candida albicans (78123 Activities)
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Trypanosoma cruzi (99888 Activities)
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Streptococcus sp. 'group A' (3417 Activities)
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NIH3T3 (5395 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mapt Microtubule-associated protein tau (6 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ska Streptokinase A (5805 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rorc Nuclear receptor ROR-gamma (89407 Activities)
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Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
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.

10 results found

Lot NumberCertificate TypeFechaArticulo
F2417457Certificate of AnalysisApr 02, 2026 O276152
F2417461Certificate of AnalysisApr 02, 2026 O276152
F2417463Certificate of AnalysisApr 02, 2026 O276152
F2417465Certificate of AnalysisApr 02, 2026 O276152
F2417468Certificate of AnalysisApr 02, 2026 O276152
F2417408Certificate of AnalysisJan 20, 2026 O276152
F2417410Certificate of AnalysisJan 20, 2026 O276152
F2417415Certificate of AnalysisJan 20, 2026 O276152
F2417416Certificate of AnalysisJan 20, 2026 O276152
F2417464Certificate of AnalysisJan 20, 2026 O276152
Propiedades químicas y físicas
SolubilidadSoluble in methanol
SensibilidadMoisture sensitive
Peso molecular492.100 g/mol
XLogP3
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count6
Rotatable Bond Count6
Exact Mass491.974 Da
Monoisotopic Mass489.977 Da
Topological Polar Surface Area105.000 Ų
Heavy Atom Count30
Formal Charge0
Complexity506.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count1
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds1
Covalently-Bonded Unit Count2
Calculadoras de soluciones
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