3,7,11,15-Tetramethylhexadeca-2,6,9,11,14-pentaen-1-ol

Details

Top
Internal ID b391d53d-5ac4-4ce5-8984-27e1a6515b23
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Acyclic diterpenoids
IUPAC Name 3,7,11,15-tetramethylhexadeca-2,6,9,11,14-pentaen-1-ol
SMILES (Canonical) CC(=CCC=C(C)C=CCC(=CCCC(=CCO)C)C)C
SMILES (Isomeric) CC(=CCC=C(C)C=CCC(=CCCC(=CCO)C)C)C
InChI InChI=1S/C20H32O/c1-17(2)9-6-10-18(3)11-7-12-19(4)13-8-14-20(5)15-16-21/h7,9-11,13,15,21H,6,8,12,14,16H2,1-5H3
InChI Key GTABLEMMFSLEDL-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C20H32O
Molecular Weight 288.50 g/mol
Exact Mass 288.245315640 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 6.70
Atomic LogP (AlogP) 5.90
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 9

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 3,7,11,15-Tetramethylhexadeca-2,6,9,11,14-pentaen-1-ol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9823 98.23%
Caco-2 + 0.9231 92.31%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Lysosomes 0.5576 55.76%
OATP2B1 inhibitior - 0.8585 85.85%
OATP1B1 inhibitior + 0.9036 90.36%
OATP1B3 inhibitior + 0.9480 94.80%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.7863 78.63%
P-glycoprotein inhibitior - 0.7085 70.85%
P-glycoprotein substrate - 0.9034 90.34%
CYP3A4 substrate - 0.5307 53.07%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7664 76.64%
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 - 0.8976 89.76%
CYP inhibitory promiscuity - 0.7650 76.50%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.6600 66.00%
Carcinogenicity (trinary) Non-required 0.6507 65.07%
Eye corrosion + 0.5325 53.25%
Eye irritation + 0.5977 59.77%
Skin irritation + 0.8492 84.92%
Skin corrosion - 0.9100 91.00%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7811 78.11%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6750 67.50%
skin sensitisation + 0.9333 93.33%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity - 0.9812 98.12%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity + 0.5060 50.60%
Acute Oral Toxicity (c) III 0.8552 85.52%
Estrogen receptor binding - 0.4931 49.31%
Androgen receptor binding - 0.8299 82.99%
Thyroid receptor binding + 0.6982 69.82%
Glucocorticoid receptor binding - 0.5571 55.71%
Aromatase binding + 0.7078 70.78%
PPAR gamma + 0.7801 78.01%
Honey bee toxicity - 0.9384 93.84%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.9500 95.00%

Targets

Top

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
CHEMBL4040 P28482 MAP kinase ERK2 93.01% 83.82%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 87.39% 92.08%
CHEMBL2581 P07339 Cathepsin D 85.67% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 83.39% 94.73%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 82.90% 93.10%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.28% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.85% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.34% 99.17%

Plants that contains it

Top
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.
There are no matching plants.

Cross-Links

Top
PubChem 73815891
LOTUS LTS0179180
wikiData Q105018344