(10E)-2,6,11,15-tetramethylhexadeca-2,7,10,14-tetraen-6-ol

Details

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Internal ID 5e9a1894-f715-4b10-a4b7-3401eb84229a
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Acyclic diterpenoids
IUPAC Name (10E)-2,6,11,15-tetramethylhexadeca-2,7,10,14-tetraen-6-ol
SMILES (Canonical) CC(=CCCC(=CCC=CC(C)(CCC=C(C)C)O)C)C
SMILES (Isomeric) CC(=CCC/C(=C/CC=CC(C)(CCC=C(C)C)O)/C)C
InChI InChI=1S/C20H34O/c1-17(2)11-9-14-19(5)13-7-8-15-20(6,21)16-10-12-18(3)4/h8,11-13,15,21H,7,9-10,14,16H2,1-6H3/b15-8?,19-13+
InChI Key SYWIUZCNOUKNSM-CMQICLSVSA-N
Popularity 121 references in papers

Physical and Chemical Properties

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Molecular Formula C20H34O
Molecular Weight 290.50 g/mol
Exact Mass 290.260965704 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 6.40
Atomic LogP (AlogP) 6.12
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (10E)-2,6,11,15-tetramethylhexadeca-2,7,10,14-tetraen-6-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9891 98.91%
Caco-2 + 0.8448 84.48%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Lysosomes 0.3611 36.11%
OATP2B1 inhibitior - 0.8571 85.71%
OATP1B1 inhibitior + 0.8966 89.66%
OATP1B3 inhibitior + 0.9609 96.09%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.7460 74.60%
P-glycoprotein inhibitior - 0.8696 86.96%
P-glycoprotein substrate - 0.9329 93.29%
CYP3A4 substrate - 0.5717 57.17%
CYP2C9 substrate - 0.7948 79.48%
CYP2D6 substrate - 0.7612 76.12%
CYP3A4 inhibition - 0.9100 91.00%
CYP2C9 inhibition - 0.7941 79.41%
CYP2C19 inhibition - 0.8107 81.07%
CYP2D6 inhibition - 0.9470 94.70%
CYP1A2 inhibition - 0.6520 65.20%
CYP2C8 inhibition - 0.9122 91.22%
CYP inhibitory promiscuity - 0.7646 76.46%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Non-required 0.6452 64.52%
Eye corrosion - 0.8146 81.46%
Eye irritation - 0.6545 65.45%
Skin irritation + 0.7659 76.59%
Skin corrosion - 0.9749 97.49%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4043 40.43%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6924 69.24%
skin sensitisation + 0.8780 87.80%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.8053 80.53%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity + 0.4739 47.39%
Acute Oral Toxicity (c) III 0.7571 75.71%
Estrogen receptor binding + 0.6619 66.19%
Androgen receptor binding - 0.8586 85.86%
Thyroid receptor binding + 0.6695 66.95%
Glucocorticoid receptor binding - 0.5419 54.19%
Aromatase binding - 0.5449 54.49%
PPAR gamma + 0.7753 77.53%
Honey bee toxicity - 0.8723 87.23%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.6600 66.00%
Fish aquatic toxicity + 0.8940 89.40%

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 94.56% 94.73%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 89.52% 92.08%
CHEMBL2581 P07339 Cathepsin D 89.09% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.77% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.69% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.92% 99.17%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.24% 97.25%

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.
Morina persica
Nelumbo lutea
Picea abies
Tilia platyphyllos subsp. corinthiaca
Zingiber officinale

Cross-Links

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PubChem 129661573
LOTUS LTS0057371
wikiData Q105263827