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

CAS: 76706-55-3 Cat. No.: M648797 Summenformel: C25H33N3O3S2 Molekulargewicht: 487.68 EG-Nummer: 622-464-9 PubChem CID: 10972974
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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
Deutschland (EU)
USA*
Price
Qty
1mg
M648797-1mg
Auf Bestellung · 8–12 Wochen
729,68€
5mg
M648797-5mg
Auf Bestellung · 8–12 Wochen
1.823,03€
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.

Übersicht

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

Synonyme
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
Spezifikationen & Reinheit
≥99%
Biochemische und physiologische Mechanismen
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.
Storage
Store at -20°C
Verschickt in
Ice chest + Ice pads
Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.
Aktionsart
INHIBITOR
Reinheit
≥99%
Namen und Kennungen
Kanonisches LächelnCC(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
Isomere SMILES 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 Deutschland 3
PubChem CID 10972974
Molekulargewicht 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
KlasseAzoles
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
BeschreibungThis 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
3D-Struktur
Interaktives chemisches Strukturmodell





Zugehörige Ziele (menschlich)
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
Zugehörige Ziele (nicht menschlich)
MT-CYB Cytochrome b (0 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Wirkungsmechanismen
Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Chemische und physikalische Eigenschaften
Molekulargewicht487.700 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
Lösungsrechner
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