Pleraplysillin 2

Details

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Internal ID 348d696c-817d-4e22-8a92-bad8b4ec16d5
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Aromatic monoterpenoids
IUPAC Name furan-3-ylmethyl (2E,6E)-3,7-dimethyl-8-(4-methylfuran-2-yl)octa-2,6-dienoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H24O4/c1-15(9-19-10-17(3)12-23-19)5-4-6-16(2)11-20(21)24-14-18-7-8-22-13-18/h5,7-8,10-13H,4,6,9,14H2,1-3H3/b15-5+,16-11+
InChI Key WMZXPVNHOWYKDN-SKJRKUQSSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C20H24O4
Molecular Weight 328.40 g/mol
Exact Mass 328.16745924 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 5.00
Atomic LogP (AlogP) 5.14
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 8

Synonyms

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53492-34-5
2,6-Octadienoic acid, 3,7-dimethyl-8-(4-methyl-2-furanyl)-, 3-furanylmethyl ester, (E,E)-

2D Structure

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2D Structure of Pleraplysillin 2

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9875 98.75%
Caco-2 + 0.6564 65.64%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.7184 71.84%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8300 83.00%
OATP1B3 inhibitior + 0.9212 92.12%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior + 0.9286 92.86%
P-glycoprotein inhibitior + 0.6624 66.24%
P-glycoprotein substrate - 0.8052 80.52%
CYP3A4 substrate + 0.5925 59.25%
CYP2C9 substrate - 0.5960 59.60%
CYP2D6 substrate - 0.9009 90.09%
CYP3A4 inhibition - 0.5671 56.71%
CYP2C9 inhibition - 0.6259 62.59%
CYP2C19 inhibition - 0.6364 63.64%
CYP2D6 inhibition - 0.8366 83.66%
CYP1A2 inhibition + 0.5363 53.63%
CYP2C8 inhibition + 0.5299 52.99%
CYP inhibitory promiscuity + 0.5389 53.89%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7928 79.28%
Carcinogenicity (trinary) Non-required 0.5890 58.90%
Eye corrosion - 0.9646 96.46%
Eye irritation - 0.9279 92.79%
Skin irritation - 0.7080 70.80%
Skin corrosion - 0.9724 97.24%
Ames mutagenesis - 0.5270 52.70%
Human Ether-a-go-go-Related Gene inhibition + 0.9632 96.32%
Micronuclear - 0.8000 80.00%
Hepatotoxicity + 0.6494 64.94%
skin sensitisation - 0.8471 84.71%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity - 0.5556 55.56%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity - 0.7148 71.48%
Acute Oral Toxicity (c) III 0.6946 69.46%
Estrogen receptor binding + 0.8160 81.60%
Androgen receptor binding + 0.7522 75.22%
Thyroid receptor binding + 0.5241 52.41%
Glucocorticoid receptor binding + 0.7352 73.52%
Aromatase binding + 0.5750 57.50%
PPAR gamma + 0.7264 72.64%
Honey bee toxicity - 0.8164 81.64%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5107 51.07%
Fish aquatic toxicity + 0.9928 99.28%

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
CHEMBL3401 O75469 Pregnane X receptor 95.16% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.01% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.63% 99.17%
CHEMBL2039 P27338 Monoamine oxidase B 93.86% 92.51%
CHEMBL2581 P07339 Cathepsin D 92.49% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.10% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.74% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.37% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.37% 95.56%
CHEMBL340 P08684 Cytochrome P450 3A4 86.14% 91.19%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.80% 89.00%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 82.63% 93.65%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 82.36% 93.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.35% 96.00%
CHEMBL2563 Q9UQL6 Histone deacetylase 5 81.03% 89.67%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 81.00% 92.08%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.95% 95.50%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 80.83% 94.80%

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 6442399
LOTUS LTS0079996
wikiData Q105308939