(1S,3E,7E,11E,14R)-3,7,11-trimethyl-14-prop-1-en-2-ylcyclotetradeca-3,7,11-trien-1-ol

Details

Top
Internal ID bdfff3ee-efd1-4ae9-a242-7c72363d30cb
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Cembrane diterpenoids
IUPAC Name (1S,3E,7E,11E,14R)-3,7,11-trimethyl-14-prop-1-en-2-ylcyclotetradeca-3,7,11-trien-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H32O/c1-15(2)19-13-12-17(4)10-6-8-16(3)9-7-11-18(5)14-20(19)21/h8,11-12,19-21H,1,6-7,9-10,13-14H2,2-5H3/b16-8+,17-12+,18-11+/t19-,20+/m1/s1
InChI Key HTWXQGABXITTNW-VEELKJHVSA-N
Popularity 2 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 4.80
Atomic LogP (AlogP) 5.73
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (1S,3E,7E,11E,14R)-3,7,11-trimethyl-14-prop-1-en-2-ylcyclotetradeca-3,7,11-trien-1-ol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9964 99.64%
Caco-2 + 0.8419 84.19%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Lysosomes 0.4442 44.42%
OATP2B1 inhibitior - 0.8539 85.39%
OATP1B1 inhibitior + 0.9655 96.55%
OATP1B3 inhibitior + 0.8946 89.46%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.7341 73.41%
P-glycoprotein inhibitior - 0.6699 66.99%
P-glycoprotein substrate - 0.8291 82.91%
CYP3A4 substrate - 0.5700 57.00%
CYP2C9 substrate - 0.8090 80.90%
CYP2D6 substrate - 0.7021 70.21%
CYP3A4 inhibition - 0.7933 79.33%
CYP2C9 inhibition - 0.8986 89.86%
CYP2C19 inhibition - 0.8768 87.68%
CYP2D6 inhibition - 0.9373 93.73%
CYP1A2 inhibition - 0.7039 70.39%
CYP2C8 inhibition - 0.8676 86.76%
CYP inhibitory promiscuity - 0.9146 91.46%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8128 81.28%
Carcinogenicity (trinary) Non-required 0.6289 62.89%
Eye corrosion - 0.8826 88.26%
Eye irritation - 0.8401 84.01%
Skin irritation + 0.6562 65.62%
Skin corrosion - 0.9257 92.57%
Ames mutagenesis - 0.8854 88.54%
Human Ether-a-go-go-Related Gene inhibition + 0.7068 70.68%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.5551 55.51%
skin sensitisation + 0.7885 78.85%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity - 0.5667 56.67%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity + 0.5412 54.12%
Acute Oral Toxicity (c) III 0.6970 69.70%
Estrogen receptor binding - 0.6828 68.28%
Androgen receptor binding - 0.7462 74.62%
Thyroid receptor binding - 0.5360 53.60%
Glucocorticoid receptor binding - 0.5544 55.44%
Aromatase binding - 0.7152 71.52%
PPAR gamma + 0.6672 66.72%
Honey bee toxicity - 0.8561 85.61%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity + 0.9654 96.54%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.28% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.30% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.65% 97.25%
CHEMBL2581 P07339 Cathepsin D 88.28% 98.95%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.94% 93.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.42% 100.00%

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 163075026
LOTUS LTS0214071
wikiData Q105033668