17,18-Dihydroxy-2,6,10,14-phytatetraen-1,20-olide

Details

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Internal ID 8b7b649c-8bb4-4f7c-984a-f80d4736d60f
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones > Diterpene lactones
IUPAC Name 3-[(3E,7Z,11Z)-13-hydroxy-8-(hydroxymethyl)-4,12-dimethyltrideca-3,7,11-trienyl]-2H-furan-5-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H30O4/c1-16(7-4-11-19-12-20(23)24-15-19)6-3-9-18(14-22)10-5-8-17(2)13-21/h7-9,12,21-22H,3-6,10-11,13-15H2,1-2H3/b16-7+,17-8-,18-9-
InChI Key UVMQCFGEJNWYOG-NARCAAIFSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C20H30O4
Molecular Weight 334.40 g/mol
Exact Mass 334.21440943 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.61
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 11

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 17,18-Dihydroxy-2,6,10,14-phytatetraen-1,20-olide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9421 94.21%
Caco-2 - 0.5313 53.13%
Blood Brain Barrier + 0.6105 61.05%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.6281 62.81%
OATP2B1 inhibitior - 0.8548 85.48%
OATP1B1 inhibitior + 0.9061 90.61%
OATP1B3 inhibitior + 0.9429 94.29%
MATE1 inhibitior - 0.8212 82.12%
OCT2 inhibitior - 0.5673 56.73%
BSEP inhibitior + 0.7521 75.21%
P-glycoprotein inhibitior - 0.6071 60.71%
P-glycoprotein substrate - 0.7510 75.10%
CYP3A4 substrate + 0.5356 53.56%
CYP2C9 substrate + 0.5986 59.86%
CYP2D6 substrate - 0.9037 90.37%
CYP3A4 inhibition - 0.7543 75.43%
CYP2C9 inhibition - 0.8289 82.89%
CYP2C19 inhibition - 0.8339 83.39%
CYP2D6 inhibition - 0.8468 84.68%
CYP1A2 inhibition - 0.7150 71.50%
CYP2C8 inhibition - 0.8570 85.70%
CYP inhibitory promiscuity - 0.8815 88.15%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9328 93.28%
Carcinogenicity (trinary) Non-required 0.6673 66.73%
Eye corrosion - 0.9477 94.77%
Eye irritation - 0.6448 64.48%
Skin irritation - 0.7450 74.50%
Skin corrosion - 0.9603 96.03%
Ames mutagenesis + 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7252 72.52%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation - 0.8223 82.23%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity - 0.6000 60.00%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity + 0.5775 57.75%
Acute Oral Toxicity (c) III 0.6203 62.03%
Estrogen receptor binding + 0.6607 66.07%
Androgen receptor binding - 0.5996 59.96%
Thyroid receptor binding + 0.5859 58.59%
Glucocorticoid receptor binding - 0.4828 48.28%
Aromatase binding - 0.5315 53.15%
PPAR gamma + 0.8619 86.19%
Honey bee toxicity - 0.8438 84.38%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.9775 97.75%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.55% 91.11%
CHEMBL2581 P07339 Cathepsin D 95.13% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.10% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 87.96% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.63% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.45% 86.33%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 84.27% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.76% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.00% 100.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.52% 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.
Pteronia eenii

Cross-Links

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PubChem 14588991
LOTUS LTS0161820
wikiData Q105279968