Melithiazol N

Details

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Internal ID b84ad130-2197-4932-9269-9bae01be14d6
Taxonomy Organoheterocyclic compounds > Azoles > Thiazoles > 2,4-disubstituted thiazoles
IUPAC Name methyl (2E,6E)-3,5-dimethoxy-4-methyl-7-[2-[2-(2-methyloxiran-2-yl)-1,3-thiazol-4-yl]-1,3-thiazol-4-yl]hepta-2,6-dienoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H24N2O5S2/c1-12(16(25-4)8-17(23)26-5)15(24-3)7-6-13-9-28-18(21-13)14-10-29-19(22-14)20(2)11-27-20/h6-10,12,15H,11H2,1-5H3/b7-6+,16-8+
InChI Key CSHVGXQYZMMSBE-QICXOPSUSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H24N2O5S2
Molecular Weight 436.50 g/mol
Exact Mass 436.11266422 g/mol
Topological Polar Surface Area (TPSA) 140.00 Ų
XlogP 2.40
Atomic LogP (AlogP) 3.88
H-Bond Acceptor 9
H-Bond Donor 0
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Melithiazol N

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9673 96.73%
Caco-2 - 0.7085 70.85%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Mitochondria 0.4946 49.46%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8812 88.12%
OATP1B3 inhibitior + 0.9342 93.42%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.8701 87.01%
P-glycoprotein inhibitior + 0.6577 65.77%
P-glycoprotein substrate - 0.5518 55.18%
CYP3A4 substrate + 0.6366 63.66%
CYP2C9 substrate - 0.8070 80.70%
CYP2D6 substrate - 0.9006 90.06%
CYP3A4 inhibition - 0.8091 80.91%
CYP2C9 inhibition - 0.5527 55.27%
CYP2C19 inhibition + 0.5166 51.66%
CYP2D6 inhibition - 0.8937 89.37%
CYP1A2 inhibition + 0.5239 52.39%
CYP2C8 inhibition + 0.6488 64.88%
CYP inhibitory promiscuity + 0.6572 65.72%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.5597 55.97%
Eye corrosion - 0.9781 97.81%
Eye irritation - 0.9566 95.66%
Skin irritation - 0.7686 76.86%
Skin corrosion - 0.9369 93.69%
Ames mutagenesis - 0.5437 54.37%
Human Ether-a-go-go-Related Gene inhibition + 0.7007 70.07%
Micronuclear + 0.6400 64.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation - 0.8027 80.27%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity + 0.7288 72.88%
Acute Oral Toxicity (c) III 0.5464 54.64%
Estrogen receptor binding + 0.8252 82.52%
Androgen receptor binding + 0.6340 63.40%
Thyroid receptor binding + 0.7576 75.76%
Glucocorticoid receptor binding + 0.7770 77.70%
Aromatase binding + 0.6695 66.95%
PPAR gamma + 0.6102 61.02%
Honey bee toxicity - 0.8006 80.06%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9501 95.01%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.88% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.81% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.47% 96.09%
CHEMBL2581 P07339 Cathepsin D 93.81% 98.95%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 92.17% 93.03%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.99% 99.23%
CHEMBL3401 O75469 Pregnane X receptor 91.40% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.04% 94.45%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 90.60% 96.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 90.40% 95.50%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.91% 86.33%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 89.79% 87.67%
CHEMBL230 P35354 Cyclooxygenase-2 89.64% 89.63%
CHEMBL4040 P28482 MAP kinase ERK2 86.86% 83.82%
CHEMBL2243 O00519 Anandamide amidohydrolase 85.17% 97.53%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.61% 95.56%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.99% 93.56%
CHEMBL340 P08684 Cytochrome P450 3A4 83.74% 91.19%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.66% 99.17%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 83.40% 91.24%
CHEMBL5028 O14672 ADAM10 82.55% 97.50%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.92% 91.07%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 80.20% 100.00%

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 10622791
LOTUS LTS0258216
wikiData Q75062428