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Myxothiazol

CAS No.
76706-55-3
Chemical Name:
Myxothiazol
Synonyms
Myxothiazo;Myxothiazol;5-dimethoxy-4-methyl-;myxothiazolfrommyxobacterium;MYXOTHIAZOL, VIAL WITH 10 MG*;MYXOTHIAZOL FROM MYXOBACTERIUM 95%;MYXOTHIAZOL, FROM MYXOCOCCUS FULVUS;myxothiazol from myxobacterium*myxococcus fulvus;7-(2’-(1,6-dimethyl-2,4-heptadienyl)(2,4’-bithiazol)-4-yl)-6-heptadienamide;2,6-Heptadienamide, 7-(2'-(1,6-dimethyl-2,4-heptadienyl)(2,4'-bithiazol)-4-yl)-3,5-dimethoxy-4-methyl-
CBNumber:
CB0453976
Molecular Formula:
C25H33N3O3S2
Molecular Weight:
487.68
MDL Number:
MFCD00043397
MOL File:
76706-55-3.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-09-12 18:48:20

Myxothiazol Properties

Boiling point 679.6±65.0 °C(Predicted)
Density 1.158±0.06 g/cm3(Predicted)
storage temp. -20°C
solubility chloroform: soluble9.80 - 10.20mg/mL, clear, colorless to yellow
form Solid
pka 14.07±0.50(Predicted)
color White to off-white
biological source Myxococcus fulvus Mx f85
InChIKey XKTFQMCPGMTBMD-ZDBABOMLSA-N
SMILES CO[C@@H](\C=C\c1csc(n1)-c2csc(n2)[C@@H](C)\C=C\C=C\C(C)C)[C@@H](C)\C(OC)=C\C(N)=O
FDA UNII 6VY98BQ7NB
UNSPSC Code 51111800
NACRES NA.77

SAFETY

Risk and Safety Statements

Symbol(GHS)  Skull and Crossbones (GHS06)
GHS06
Signal word  Danger
Hazard statements  H300
Precautionary statements  P264-P270-P301+P310-P405-P501
Hazard Codes  T+
Risk Statements  28
Safety Statements  28-36/37-45
RIDADR  UN 3462 6.1/PG 1
WGK Germany  3
RTECS  QH7580000
10
HazardClass  6.1(b)
PackingGroup  III
Storage Class 6.1A - Combustible acute toxic Cat. 1 and 2
very toxic hazardous materials
Hazard Classifications Acute Tox. 2 Oral

Myxothiazol price More Price(9)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich T5580 Myxothiazol from Myxococcus fulvus Mx f85, ≥98% (HPLC) 76706-55-3 1mg $122 2026-04-30 Buy
Sigma-Aldrich T5580 Myxothiazol from Myxococcus fulvus Mx f85, ≥98% (HPLC) 76706-55-3 5mg $489 2026-04-30 Buy
ChemScene CS-0043613 Myxothiazol 99.98% 76706-55-3 1mg $422 2026-06-04 Buy
ChemScene CS-0043613 Myxothiazol 99.98% 76706-55-3 5mg $1192 2026-06-04 Buy
ApexBio Technology BA1028 Myxothiazol 76706-55-3 1mg $378 2026-05-06 Buy
Product number Packaging Price Buy
T5580 1mg $122 Buy
T5580 5mg $489 Buy
CS-0043613 1mg $422 Buy
CS-0043613 5mg $1192 Buy
BA1028 1mg $378 Buy

Myxothiazol Chemical Properties,Uses,Production

Uses

Myxothiazol has been used in as a mitochondrial electron transport chain (mETC) inhibitor in P19 murine embryonal carcinoma pluripotent cell line and to treat HeLa cells for integrated stress response activation.

Definition

ChEBI: A 2,4'-bi-1,3-thiazole substituted at the 4-position with a (1E,3S,4R,5E)-7-amino-3,5-dimethoxy-4-methyl-7-oxohepta-1,5-dien-1-yl] group and at the 2'-position with a (2S

Biochem/physiol Actions

Myxothiazol, an antibiotic with activity against fungi and insects, is a strong inhibitor of mitochondrial cytochrome b/c1-segment of respiratory chain. Myxothiazol binds to the quinol oxidation (Qo) site of the bc1 complex, blocking electron transfer to the Rieske iron-sulfur protein in the mitochondrial respiratory chain. Oxygen consumption blockage leads to a cytostatic effect that could be reversed. Myxothiazol, as other Epothilones, which are known for their anti tumor activity, contains a thiazole ring that is formed by the incorporation of cysteine into the polyketide backbone.

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[3].

Animal Model:C57Bl/J6 mice[3]
Dosage: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.

Myxothiazol Preparation Products And Raw materials

Raw materials

Preparation Products

Myxothiazol Suppliers

Global( 33)Suppliers
Supplier Tel Email Country ProdList Advantage
3B Pharmachem (Wuhan) International Co.,Ltd. 18930552037 3bsc@sina.com China 15813 69
Shanghai Macklin Biochemical Co.,Ltd. 15221275939 15221275939 shenlinxing@macklin.cn China 15775 55
Sigma-Aldrich 021-61415566 800-8193336 orderCN@merckgroup.com China 51389 80
Artis Biotech Co. Ltd. 18108108965 18108108965 sales@artisbio.com China 2503 58
Shanghai YuanYe Biotechnology Co., Ltd. 15026964105 2881489226@qq.com China 89667 60
Shanghai Hongye Biotechnology Co. Ltd 400-9205774 400-920-5774 sales@glpbio.cn China 6705 58
Guangdong wengjiang Chemical Reagent Co., Ltd. 0751-2815688 13927872512 3007421951@qq.com China 9996 58
BOC Sciences 16314854226; +8616314854226 inquiry@bocsci.com United States 19852 58
Zhejiang Huida Biotech Co., LTD 0571-89903022 18679456698 zilong@hizyme.com China 8001 58
TargetMol Chemicals Inc. 4008200310 15002144251 marketing@tsbiochem.com China 24951 58

View Lastest Price from Myxothiazol manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Myxothiazol pictures 2026-08-25 Myxothiazol
76706-55-3
$2.00-6.00 1kg 99% 100kg ZHENGZHOU JIUYI TIME NEW MATERIALS CO,.LTD
  • Myxothiazol pictures
  • Myxothiazol
    76706-55-3
  • $2.00-6.00
  • 99%
  • ZHENGZHOU JIUYI TIME NEW MATERIALS CO,.LTD
MYXOTHIAZOL, FROM MYXOCOCCUS FULVUS 5-dimethoxy-4-methyl- 7-(2’-(1,6-dimethyl-2,4-heptadienyl)(2,4’-bithiazol)-4-yl)-6-heptadienamide myxothiazol from myxobacterium*myxococcus fulvus MYXOTHIAZOL, VIAL WITH 10 MG* MYXOTHIAZOL FROM MYXOBACTERIUM 95% myxothiazolfrommyxobacterium 2,6-Heptadienamide, 7-(2'-((1S,2E,4E)-1,6-dimethyl-2,4-heptadienyl)(2,4'-bithiazol)-4-yl)-3,5-dimethoxy-4-methyl-, (2E,4R,5S,6E)- 2,6-Heptadienamide, 7-(2'-(1,6-dimethyl-2,4-heptadienyl)(2,4'-bithiazol)-4-yl)-3,5-dimethoxy-4-methyl- Myxothiazo 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)- Myxothiazol 76706-55-3 C25H33N3O3S2 Antibiotics G-M Antibiotics Antibiotics A to Z BioChemical Inhibits an EnzymeNitric Oxide and Cell Stress Mitochondrial InhibitorsAntibiotics Antibiotics Antibiotics A to Antibiotics G-MAntibiotics AntifungalAntibiotics Cell Stress Chemical Structure Class Mechanism of Action Peptides Spectrum of Activity