3,7,11,15-Tetramethylhexadeca-1,6,10,13,15-pentaen-3-ol

Details

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Internal ID 2302c79a-9270-4c8f-a596-8e2e48e3a2f9
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 3,7,11,15-tetramethylhexadeca-1,6,10,13,15-pentaen-3-ol
SMILES (Canonical) CC(=C)C=CCC(=CCCC(=CCCC(C)(C=C)O)C)C
SMILES (Isomeric) CC(=C)C=CCC(=CCCC(=CCCC(C)(C=C)O)C)C
InChI InChI=1S/C20H32O/c1-7-20(6,21)16-10-15-19(5)14-9-13-18(4)12-8-11-17(2)3/h7-8,11,13,15,21H,1-2,9-10,12,14,16H2,3-6H3
InChI Key FRYUWZOFRMAVEU-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H32O
Molecular Weight 288.50 g/mol
Exact Mass 288.245315640 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 6.60
Atomic LogP (AlogP) 5.90
H-Bond Acceptor 1
H-Bond Donor 1
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-1,6,10,13,15-pentaen-3-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9903 99.03%
Caco-2 + 0.7779 77.79%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Lysosomes 0.4787 47.87%
OATP2B1 inhibitior - 0.8559 85.59%
OATP1B1 inhibitior + 0.9039 90.39%
OATP1B3 inhibitior + 0.9488 94.88%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.7409 74.09%
P-glycoprotein inhibitior - 0.8400 84.00%
P-glycoprotein substrate - 0.8605 86.05%
CYP3A4 substrate + 0.5230 52.30%
CYP2C9 substrate - 0.6141 61.41%
CYP2D6 substrate - 0.7761 77.61%
CYP3A4 inhibition - 0.8327 83.27%
CYP2C9 inhibition - 0.8121 81.21%
CYP2C19 inhibition - 0.8459 84.59%
CYP2D6 inhibition - 0.9451 94.51%
CYP1A2 inhibition - 0.6497 64.97%
CYP2C8 inhibition - 0.7229 72.29%
CYP inhibitory promiscuity - 0.8653 86.53%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.6200 62.00%
Carcinogenicity (trinary) Non-required 0.6488 64.88%
Eye corrosion - 0.8062 80.62%
Eye irritation - 0.5000 50.00%
Skin irritation + 0.6732 67.32%
Skin corrosion - 0.9752 97.52%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6842 68.42%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5924 59.24%
skin sensitisation + 0.8759 87.59%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity - 0.8830 88.30%
Mitochondrial toxicity - 0.8071 80.71%
Nephrotoxicity + 0.5760 57.60%
Acute Oral Toxicity (c) III 0.9106 91.06%
Estrogen receptor binding - 0.5637 56.37%
Androgen receptor binding - 0.7792 77.92%
Thyroid receptor binding + 0.5972 59.72%
Glucocorticoid receptor binding + 0.6946 69.46%
Aromatase binding - 0.5687 56.87%
PPAR gamma + 0.7932 79.32%
Honey bee toxicity - 0.7900 79.00%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity + 0.7300 73.00%
Fish aquatic toxicity + 0.9164 91.64%

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 91.44% 94.73%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 85.52% 92.08%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 84.37% 90.93%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.40% 99.17%
CHEMBL2581 P07339 Cathepsin D 81.37% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.99% 96.09%

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.
Geigeria burkei

Cross-Links

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PubChem 162915723
LOTUS LTS0022920
wikiData Q105000506