Myxothiazol

Details

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Internal ID 97e67c79-ee37-4ba8-828c-85eaddf9c97f
Taxonomy Organoheterocyclic compounds > Azoles > Thiazoles > 2,4-disubstituted thiazoles
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
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/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
InChI Key XKTFQMCPGMTBMD-FYHMSGCOSA-N
Popularity 303 references in papers

Physical and Chemical Properties

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Molecular Formula C25H33N3O3S2
Molecular Weight 487.70 g/mol
Exact Mass 487.19633427 g/mol
Topological Polar Surface Area (TPSA) 144.00 Ų
XlogP 4.80
Atomic LogP (AlogP) 5.82
H-Bond Acceptor 7
H-Bond Donor 1
Rotatable Bonds 12

Synonyms

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76706-55-3
Myxothiazol A
6VY98BQ7NB
(+)-MYXOTHIAZOL A
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-
DTXSID10868411
(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
CHEBI:25461
(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
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Myxothiazol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9911 99.11%
Caco-2 - 0.6797 67.97%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.8010 80.10%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8949 89.49%
OATP1B3 inhibitior + 0.9418 94.18%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8321 83.21%
BSEP inhibitior + 0.8999 89.99%
P-glycoprotein inhibitior + 0.7758 77.58%
P-glycoprotein substrate - 0.5095 50.95%
CYP3A4 substrate + 0.5855 58.55%
CYP2C9 substrate - 0.5984 59.84%
CYP2D6 substrate - 0.8957 89.57%
CYP3A4 inhibition - 0.8704 87.04%
CYP2C9 inhibition - 0.5735 57.35%
CYP2C19 inhibition - 0.5595 55.95%
CYP2D6 inhibition - 0.9070 90.70%
CYP1A2 inhibition + 0.7004 70.04%
CYP2C8 inhibition + 0.6178 61.78%
CYP inhibitory promiscuity + 0.5756 57.56%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8000 80.00%
Carcinogenicity (trinary) Non-required 0.4733 47.33%
Eye corrosion - 0.9798 97.98%
Eye irritation - 0.9605 96.05%
Skin irritation - 0.8104 81.04%
Skin corrosion - 0.9419 94.19%
Ames mutagenesis - 0.5237 52.37%
Human Ether-a-go-go-Related Gene inhibition + 0.7166 71.66%
Micronuclear + 0.7800 78.00%
Hepatotoxicity + 0.6375 63.75%
skin sensitisation - 0.8786 87.86%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.6877 68.77%
Acute Oral Toxicity (c) III 0.5276 52.76%
Estrogen receptor binding + 0.8377 83.77%
Androgen receptor binding + 0.6357 63.57%
Thyroid receptor binding + 0.7444 74.44%
Glucocorticoid receptor binding + 0.7762 77.62%
Aromatase binding + 0.6661 66.61%
PPAR gamma + 0.6357 63.57%
Honey bee toxicity - 0.8086 80.86%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.6451 64.51%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.77% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.23% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.51% 91.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 94.03% 96.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 91.14% 95.50%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 89.96% 93.03%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 89.19% 87.67%
CHEMBL2581 P07339 Cathepsin D 89.13% 98.95%
CHEMBL2243 O00519 Anandamide amidohydrolase 88.54% 97.53%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.34% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.55% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 87.23% 94.73%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.88% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.62% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.61% 86.33%
CHEMBL1900 P15121 Aldose reductase 85.06% 92.38%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 82.96% 96.47%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 82.13% 100.00%
CHEMBL340 P08684 Cytochrome P450 3A4 81.55% 91.19%
CHEMBL2535 P11166 Glucose transporter 81.20% 98.75%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 81.06% 92.29%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 80.33% 85.30%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 10972974
LOTUS LTS0013527
wikiData Q27463616