Myxothiazol - ≥99% , CAS No.76706-55-3

CAS: 76706-55-3 Cat. No.: M648797 Fórmula: C25H33N3O3S2 Peso molecular: 487.68 Número CE: 622-464-9 PubChem CID: 10972974
Disponível para encomenda
GRADE & PURITY ≥99%
Synonyms
1sqp | UNII-6VY98BQ7NB | 2,6-HEPTADIENAMIDE, 7-(2'-((1S,2E,4E)-1,6-DIMETHYL-2,4-HEPTADIEN-1-YL)(2,4'-BITHIAZOL)-4-YL)-3,5-DIMETHOXY-4-METHYL-, (2E,4R,5S,6E)- | SCHEMBL447904 | MS-29066 | 2,6-HEPTADIENAMIDE, 7-(2'-(1,6-DIMETHYL-2,4-HEPTADIENYL)(2,4'-BITHIA
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
★
Size
Alemanha (EU)
USA*
Price
Qty
1mg
M648797-1mg
Sob encomenda · 8–12 semanas
729,68€
5mg
M648797-5mg
Sob encomenda · 8–12 semanas
1823,03€
Enter a quantity for the sizes you want to add.
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Why this grade

≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

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

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Quality documents

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

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Literature proof

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

Visão geral

Myxothiazol, an antifungal antibiotic , is a mitochondrial electron transport chain complex III (bc1 complex) inhibitor. Myxothiazol inhibits the growth of many yeasts and fungi at concentrations between 0.01 and 3 μg/ml.

In Vitro

Myxothiazol inhibits the growth of many yeasts and fungi at concentrations between 0.01 and 3 μg/ml. Myxothiazol binds to the ubiquinol oxidation site Qo of complex III and blocks electron transfer from ubiquinol to cytochrome b and thus inhibits complex III activity. MCE has not independently confirmed the accuracy of these methods. They are for reference only.

In Vivo

Myxothiazol (i.p.; 0.56 mg/kg; daily for 4 days)-induced complex III inhibition can be induced in mice for four days in a row without overt hepatotoxicity or lethality. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: C57Bl/J6 miceDosage: 0.56 mg/kg Administration: I.p.; 24 hours intervals for at most 4 times Result: A reversible complex III activity decrease to 50% of control value occurred at 2 h post-injection. At 74 h only minor histological changes in the liver were found, supercomplex formation was preserved and no significant changes in the expression of genes indicating hepatotoxicity or inflammation were found.

Form:Solid

Specifications

Sinónimos
1sqp | UNII-6VY98BQ7NB | 2,6-HEPTADIENAMIDE, 7-(2'-((1S,2E,4E)-1,6-DIMETHYL-2,4-HEPTADIEN-1-YL)(2,4'-BITHIAZOL)-4-YL)-3,5-DIMETHOXY-4-METHYL-, (2E,4R,5S,6E)- | SCHEMBL447904 | MS-29066 | 2,6-HEPTADIENAMIDE, 7-(2'-(1,6-DIMETHYL-2,4-HEPTADIENYL)(2,4'-BITHIA
Especificações e pureza
≥99%
Mecanismos bioquímicos e fisiológicos
Myxothiazol, an antifungal antibiotic , is a mitochondrial electron transport chain complex III (bc1 complex) inhibitor. Myxothiazol inhibits the growth of many yeasts and fungi at concentrations between 0.01 and 3 μg/ml.
Condições de armazenamento de armazenamento
Store at -20°C
Enviado em
Ice chest + Ice pads
Este produto requer transporte de cadeia fria. Serviços terrestres e outros serviços econômicos não estão disponíveis.
Tipo de ação
INHIBITOR
Pureza
≥99%
Nomes e identificadores
Sorrisos canónicosCC(C)C=CC=CC(C)C1=NC(=CS1)C2=NC(=CS2)C=CC(C(C)C(=CC(=O)N)OC)OC
IUPAC Name(2E,4R,5S,6E)-3,5-dimethoxy-4-methyl-7-[2-[2-[(2S,3E,5E)-7-methylocta-3,5-dien-2-yl]-1,3-thiazol-4-yl]-1,3-thiazol-4-yl]hepta-2,6-dienamide
InChIKeyXKTFQMCPGMTBMD-FYHMSGCOSA-N
INCHI1S/C25H33N3O3S2/c1-16(2)9-7-8-10-17(3)24-28-20(15-33-24)25-27-19(14-32-25)11-12-21(30-5)18(4)22(31-6)13-23(26)29/h7-18,21H,1-6H3,(H2,26,29)/b9-7+,10-8+,12-11+,22-13+/t17-,18+,21-/m0/s1
SMILES isoméricas C[C@@H](/C=C/C=C/C(C)C)C1=NC(=CS1)C2=NC(=CS2)/C=C/[C@@H]([C@@H](C)/C(=C\C(=O)N)/OC)OC
WGK Alemanha 3
PubChem CID 10972974
Peso molecular 487.68

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
SuperclassOrganoheterocyclic compounds
ClasseAzoles
SubclassThiazoles
Intermediate Tree Nodes Not available
Direct Parent2,4-disubstituted thiazoles
Alternative Parents Vinylogous esters  Heteroaromatic compounds  Primary carboxylic acid amides  Dialkyl ethers  Azacyclic compounds  Organopnictogen compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents 2,4-disubstituted 1,3-thiazole - Vinylogous ester - Heteroaromatic compound - Carboxamide group - Primary carboxylic acid amide - Carboxylic acid derivative - Dialkyl ether - Ether - Azacycle - Organooxygen compound - Organonitrogen compound - Carbonyl group - Organic nitrogen compound - Organopnictogen compound - Organic oxide - Organic oxygen compound - Hydrocarbon derivative - Aromatic heteromonocyclic compound
DescriçãoThis compound belongs to the class of organic compounds known as 2,4-disubstituted thiazoles. These are compounds containing a thiazole ring substituted at the positions 2 and 3.
External Descriptors Not available
Estrutura 3D
Modelo de Estrutura Química Interativa





Alvos associados (humanos)
SK-MEL-2 (46422 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SK-OV-3 (52876 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
XF498 (12972 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
A549 (127892 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Alvos associados (não humanos)
MT-CYB Cytochrome b (0 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de ação
Certificados(CoA,COO,BSE/TSE e Mapa de Análise)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Propriedades químicas e físicas
Peso molecular487.700 g/mol
XLogP34.800
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count7
Rotatable Bond Count12
Exact Mass487.196 Da
Monoisotopic Mass487.196 Da
Topological Polar Surface Area144.000 Ų
Heavy Atom Count33
Formal Charge0
Complexity738.000
Isotope Atom Count0
Defined Atom Stereocenter Count3
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count4
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds4
Covalently-Bonded Unit Count1
Calculadoras de soluções
Revisões

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