3,7,11,15-Tetramethylhexadeca-2,6,10,14-tetraene-1,5,13-triol

Details

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Internal ID 489682f7-eb2c-47d6-9e40-926786c7bd49
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Acyclic diterpenoids
IUPAC Name 3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraene-1,5,13-triol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H34O3/c1-15(2)11-19(22)12-16(3)7-6-8-17(4)13-20(23)14-18(5)9-10-21/h7,9,11,13,19-23H,6,8,10,12,14H2,1-5H3
InChI Key HBYDDKYAICOLRD-UHFFFAOYSA-N
Popularity 0 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 4.40
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 3,7,11,15-Tetramethylhexadeca-2,6,10,14-tetraene-1,5,13-triol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9787 97.87%
Caco-2 + 0.7576 75.76%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.5597 55.97%
OATP2B1 inhibitior - 0.8525 85.25%
OATP1B1 inhibitior + 0.9199 91.99%
OATP1B3 inhibitior + 0.9617 96.17%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.7403 74.03%
P-glycoprotein inhibitior - 0.6540 65.40%
P-glycoprotein substrate - 0.8878 88.78%
CYP3A4 substrate - 0.5484 54.84%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7295 72.95%
CYP3A4 inhibition - 0.6684 66.84%
CYP2C9 inhibition - 0.8804 88.04%
CYP2C19 inhibition - 0.8770 87.70%
CYP2D6 inhibition - 0.8852 88.52%
CYP1A2 inhibition - 0.8203 82.03%
CYP2C8 inhibition - 0.9248 92.48%
CYP inhibitory promiscuity - 0.7797 77.97%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7000 70.00%
Carcinogenicity (trinary) Non-required 0.7402 74.02%
Eye corrosion - 0.8595 85.95%
Eye irritation - 0.6029 60.29%
Skin irritation - 0.5236 52.36%
Skin corrosion - 0.9771 97.71%
Ames mutagenesis - 0.7154 71.54%
Human Ether-a-go-go-Related Gene inhibition + 0.6910 69.10%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.7875 78.75%
skin sensitisation + 0.7165 71.65%
Respiratory toxicity - 0.7667 76.67%
Reproductive toxicity - 0.9222 92.22%
Mitochondrial toxicity - 0.8250 82.50%
Nephrotoxicity + 0.5783 57.83%
Acute Oral Toxicity (c) III 0.7595 75.95%
Estrogen receptor binding - 0.5673 56.73%
Androgen receptor binding - 0.6955 69.55%
Thyroid receptor binding + 0.6067 60.67%
Glucocorticoid receptor binding - 0.6179 61.79%
Aromatase binding - 0.5222 52.22%
PPAR gamma + 0.6824 68.24%
Honey bee toxicity - 0.8728 87.28%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity + 0.7811 78.11%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.34% 96.09%
CHEMBL2581 P07339 Cathepsin D 91.29% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.15% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.62% 91.11%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 85.01% 92.08%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 81.93% 93.10%

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.
Ophryosporus floribundus

Cross-Links

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PubChem 162991487
LOTUS LTS0182446
wikiData Q105025537