3,7,11,15-Tetramethyl-2,6,10,14-hexadecatetraen-1-ol

Details

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Internal ID eb69a651-114e-44f7-ba33-8cc2b17bfb42
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Acyclic diterpenoids
IUPAC Name (2E,10E)-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraen-1-ol
SMILES (Canonical) CC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C)C
SMILES (Isomeric) CC(=CCC/C(=C/CCC(=CCC/C(=C/CO)/C)C)/C)C
InChI InChI=1S/C20H34O/c1-17(2)9-6-10-18(3)11-7-12-19(4)13-8-14-20(5)15-16-21/h9,11,13,15,21H,6-8,10,12,14,16H2,1-5H3/b18-11+,19-13?,20-15+
InChI Key OJISWRZIEWCUBN-DYCNYEKWSA-N
Popularity 0 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 6.60
Atomic LogP (AlogP) 6.12
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 10

Synonyms

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OJISWRZIEWCUBN-DYCNYEKWSA-N

2D Structure

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2D Structure of 3,7,11,15-Tetramethyl-2,6,10,14-hexadecatetraen-1-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9823 98.23%
Caco-2 + 0.8857 88.57%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Lysosomes 0.5576 55.76%
OATP2B1 inhibitior - 0.8515 85.15%
OATP1B1 inhibitior + 0.9449 94.49%
OATP1B3 inhibitior + 0.9480 94.80%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.7843 78.43%
P-glycoprotein inhibitior - 0.7547 75.47%
P-glycoprotein substrate - 0.9741 97.41%
CYP3A4 substrate - 0.6422 64.22%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7450 74.50%
CYP3A4 inhibition - 0.9088 90.88%
CYP2C9 inhibition - 0.9071 90.71%
CYP2C19 inhibition - 0.9026 90.26%
CYP2D6 inhibition - 0.9230 92.30%
CYP1A2 inhibition - 0.9046 90.46%
CYP2C8 inhibition - 0.9772 97.72%
CYP inhibitory promiscuity - 0.7650 76.50%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.6600 66.00%
Carcinogenicity (trinary) Non-required 0.6507 65.07%
Eye corrosion + 0.5325 53.25%
Eye irritation + 0.7723 77.23%
Skin irritation + 0.8492 84.92%
Skin corrosion - 0.9100 91.00%
Ames mutagenesis - 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7540 75.40%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.9375 93.75%
skin sensitisation + 0.9333 93.33%
Respiratory toxicity - 0.9667 96.67%
Reproductive toxicity - 0.9812 98.12%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity + 0.6319 63.19%
Acute Oral Toxicity (c) III 0.8552 85.52%
Estrogen receptor binding - 0.7448 74.48%
Androgen receptor binding - 0.8384 83.84%
Thyroid receptor binding + 0.6001 60.01%
Glucocorticoid receptor binding - 0.6656 66.56%
Aromatase binding - 0.4863 48.63%
PPAR gamma + 0.7760 77.60%
Honey bee toxicity - 0.9445 94.45%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9500 95.00%

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
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 94.25% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.82% 96.09%
CHEMBL2581 P07339 Cathepsin D 82.45% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.91% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.90% 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.
Bixa orellana
Blepharispermum zanguebaricum
Vanda falcata

Cross-Links

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PubChem 86591503
LOTUS LTS0145273
wikiData Q103785439