(2E,5E,7S,10E,13R)-3,7,11,15-tetramethylhexadeca-2,5,10,14-tetraene-1,7,13-triol

Details

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Internal ID 1655b8d7-3e1a-4a8c-a108-b832f366cbe4
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Acyclic diterpenoids
IUPAC Name (2E,5E,7S,10E,13R)-3,7,11,15-tetramethylhexadeca-2,5,10,14-tetraene-1,7,13-triol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H34O3/c1-16(2)14-19(22)15-18(4)9-7-12-20(5,23)11-6-8-17(3)10-13-21/h6,9-11,14,19,21-23H,7-8,12-13,15H2,1-5H3/b11-6+,17-10+,18-9+/t19-,20+/m0/s1
InChI Key XVUHXGFVXWXCFD-HYEJLCSDSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H34O3
Molecular Weight 322.50 g/mol
Exact Mass 322.25079494 g/mol
Topological Polar Surface Area (TPSA) 60.70 Ų
XlogP 4.00
Atomic LogP (AlogP) 4.07
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2E,5E,7S,10E,13R)-3,7,11,15-tetramethylhexadeca-2,5,10,14-tetraene-1,7,13-triol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9817 98.17%
Caco-2 + 0.7170 71.70%
Blood Brain Barrier + 0.7135 71.35%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.5934 59.34%
OATP2B1 inhibitior - 0.8544 85.44%
OATP1B1 inhibitior + 0.8696 86.96%
OATP1B3 inhibitior + 0.9582 95.82%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7291 72.91%
BSEP inhibitior + 0.6690 66.90%
P-glycoprotein inhibitior - 0.7336 73.36%
P-glycoprotein substrate - 0.8133 81.33%
CYP3A4 substrate + 0.5478 54.78%
CYP2C9 substrate - 0.8105 81.05%
CYP2D6 substrate - 0.7730 77.30%
CYP3A4 inhibition - 0.7050 70.50%
CYP2C9 inhibition - 0.8279 82.79%
CYP2C19 inhibition - 0.8745 87.45%
CYP2D6 inhibition - 0.9134 91.34%
CYP1A2 inhibition - 0.8278 82.78%
CYP2C8 inhibition - 0.7832 78.32%
CYP inhibitory promiscuity - 0.7705 77.05%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7300 73.00%
Carcinogenicity (trinary) Non-required 0.6853 68.53%
Eye corrosion - 0.9167 91.67%
Eye irritation - 0.6075 60.75%
Skin irritation - 0.5967 59.67%
Skin corrosion - 0.9816 98.16%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6988 69.88%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.7299 72.99%
skin sensitisation + 0.6624 66.24%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity - 0.8778 87.78%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity + 0.4881 48.81%
Acute Oral Toxicity (c) III 0.6450 64.50%
Estrogen receptor binding + 0.5296 52.96%
Androgen receptor binding - 0.8316 83.16%
Thyroid receptor binding + 0.7260 72.60%
Glucocorticoid receptor binding + 0.5537 55.37%
Aromatase binding - 0.5583 55.83%
PPAR gamma + 0.7712 77.12%
Honey bee toxicity - 0.8217 82.17%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity + 0.8208 82.08%

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
CHEMBL2581 P07339 Cathepsin D 93.20% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.06% 99.17%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.45% 85.14%
CHEMBL3401 O75469 Pregnane X receptor 87.16% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.80% 96.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.58% 96.95%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.33% 93.56%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 81.23% 97.21%

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 162956168
LOTUS LTS0193034
wikiData Q105343163