3,11,15-Trimethyl-7-methylidenehexadeca-2,10,14-triene-1,6,13-triol

Details

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Internal ID c1fb8493-4896-4c34-bf8b-af4cb42e160b
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Acyclic diterpenoids
IUPAC Name 3,11,15-trimethyl-7-methylidenehexadeca-2,10,14-triene-1,6,13-triol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H34O3/c1-15(2)13-19(22)14-17(4)7-6-8-18(5)20(23)10-9-16(3)11-12-21/h7,11,13,19-23H,5-6,8-10,12,14H2,1-4H3
InChI Key DMYRJIPUYNBFRS-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 4.50
Atomic LogP (AlogP) 4.07
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 11

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3,11,15-Trimethyl-7-methylidenehexadeca-2,10,14-triene-1,6,13-triol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9802 98.02%
Caco-2 + 0.5559 55.59%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.5839 58.39%
OATP2B1 inhibitior - 0.8536 85.36%
OATP1B1 inhibitior + 0.9310 93.10%
OATP1B3 inhibitior + 0.9624 96.24%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7291 72.91%
BSEP inhibitior + 0.6023 60.23%
P-glycoprotein inhibitior - 0.7078 70.78%
P-glycoprotein substrate - 0.7768 77.68%
CYP3A4 substrate + 0.5375 53.75%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7295 72.95%
CYP3A4 inhibition - 0.5623 56.23%
CYP2C9 inhibition - 0.8521 85.21%
CYP2C19 inhibition - 0.8644 86.44%
CYP2D6 inhibition - 0.8890 88.90%
CYP1A2 inhibition - 0.7991 79.91%
CYP2C8 inhibition - 0.8318 83.18%
CYP inhibitory promiscuity - 0.8076 80.76%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7100 71.00%
Carcinogenicity (trinary) Non-required 0.7389 73.89%
Eye corrosion - 0.8905 89.05%
Eye irritation - 0.7544 75.44%
Skin irritation - 0.6483 64.83%
Skin corrosion - 0.9768 97.68%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3867 38.67%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.7466 74.66%
skin sensitisation + 0.6344 63.44%
Respiratory toxicity - 0.8222 82.22%
Reproductive toxicity - 0.9164 91.64%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity + 0.6879 68.79%
Acute Oral Toxicity (c) III 0.6654 66.54%
Estrogen receptor binding - 0.4872 48.72%
Androgen receptor binding - 0.6373 63.73%
Thyroid receptor binding + 0.6932 69.32%
Glucocorticoid receptor binding + 0.5599 55.99%
Aromatase binding - 0.5000 50.00%
PPAR gamma + 0.7977 79.77%
Honey bee toxicity - 0.8440 84.40%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity + 0.9159 91.59%

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 91.71% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.89% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.62% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.30% 91.11%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 85.78% 92.08%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 82.30% 95.89%
CHEMBL340 P08684 Cytochrome P450 3A4 80.10% 91.19%

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 73837998
LOTUS LTS0018662
wikiData Q104985403