6-ethyl-2-sulfanylidene-5-tetradecyl-1H-pyrimidin-4-one

Details

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Internal ID a4a9fbe7-b3b2-4a62-8fdf-2ba5c0d7b75e
Taxonomy Organoheterocyclic compounds > Diazines > Pyrimidines and pyrimidine derivatives > Pyrimidones
IUPAC Name 6-ethyl-2-sulfanylidene-5-tetradecyl-1H-pyrimidin-4-one
SMILES (Canonical) CCCCCCCCCCCCCCC1=C(NC(=S)NC1=O)CC
SMILES (Isomeric) CCCCCCCCCCCCCCC1=C(NC(=S)NC1=O)CC
InChI InChI=1S/C20H36N2OS/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17-18(4-2)21-20(24)22-19(17)23/h3-16H2,1-2H3,(H2,21,22,23,24)
InChI Key OHHXAUDEKUJJIA-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C20H36N2OS
Molecular Weight 352.60 g/mol
Exact Mass 352.25483495 g/mol
Topological Polar Surface Area (TPSA) 73.20 Ų
XlogP 7.70
Atomic LogP (AlogP) 6.24
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 14

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6-ethyl-2-sulfanylidene-5-tetradecyl-1H-pyrimidin-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9887 98.87%
Caco-2 + 0.6748 67.48%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.6130 61.30%
OATP2B1 inhibitior - 0.8488 84.88%
OATP1B1 inhibitior + 0.8937 89.37%
OATP1B3 inhibitior + 0.9418 94.18%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.9269 92.69%
P-glycoprotein inhibitior - 0.6029 60.29%
P-glycoprotein substrate - 0.8111 81.11%
CYP3A4 substrate - 0.5564 55.64%
CYP2C9 substrate + 0.5925 59.25%
CYP2D6 substrate - 0.8806 88.06%
CYP3A4 inhibition - 0.8851 88.51%
CYP2C9 inhibition - 0.7315 73.15%
CYP2C19 inhibition - 0.6509 65.09%
CYP2D6 inhibition - 0.8960 89.60%
CYP1A2 inhibition - 0.7669 76.69%
CYP2C8 inhibition - 0.8932 89.32%
CYP inhibitory promiscuity - 0.6654 66.54%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.5141 51.41%
Eye corrosion - 0.9828 98.28%
Eye irritation - 0.6377 63.77%
Skin irritation - 0.7638 76.38%
Skin corrosion - 0.9126 91.26%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3994 39.94%
Micronuclear + 0.6100 61.00%
Hepatotoxicity + 0.6783 67.83%
skin sensitisation - 0.8509 85.09%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity - 0.5979 59.79%
Acute Oral Toxicity (c) III 0.5931 59.31%
Estrogen receptor binding - 0.5846 58.46%
Androgen receptor binding - 0.5556 55.56%
Thyroid receptor binding + 0.5454 54.54%
Glucocorticoid receptor binding - 0.5635 56.35%
Aromatase binding - 0.7842 78.42%
PPAR gamma + 0.7064 70.64%
Honey bee toxicity - 0.9727 97.27%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.7855 78.55%
Fish aquatic toxicity + 0.9497 94.97%

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
CHEMBL230 P35354 Cyclooxygenase-2 99.33% 89.63%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 95.56% 92.08%
CHEMBL240 Q12809 HERG 94.59% 89.76%
CHEMBL2581 P07339 Cathepsin D 94.16% 98.95%
CHEMBL255 P29275 Adenosine A2b receptor 92.18% 98.59%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.98% 97.25%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 89.91% 89.34%
CHEMBL3401 O75469 Pregnane X receptor 89.52% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.10% 94.45%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 88.17% 92.86%
CHEMBL2885 P07451 Carbonic anhydrase III 86.96% 87.45%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.99% 99.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.50% 96.09%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 83.62% 91.81%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.48% 95.56%
CHEMBL1781 P11387 DNA topoisomerase I 82.98% 97.00%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 80.96% 91.71%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 80.96% 100.00%
CHEMBL2996 Q05655 Protein kinase C delta 80.91% 97.79%
CHEMBL5979 P05186 Alkaline phosphatase, tissue-nonspecific isozyme 80.56% 85.40%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.25% 99.17%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Pergularia tomentosa
Tacca chantrieri

Cross-Links

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PubChem 6324619
LOTUS LTS0038584
wikiData Q105192088