(1S)-4,8,12-trimethyl-1-prop-1-en-2-ylcyclotetradeca-3,7,11-trien-1-ol

Details

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Internal ID 6a71a661-89ed-47d6-9d05-4304f39de472
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Cembrane diterpenoids
IUPAC Name (1S)-4,8,12-trimethyl-1-prop-1-en-2-ylcyclotetradeca-3,7,11-trien-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H32O/c1-16(2)20(21)14-12-18(4)10-6-8-17(3)9-7-11-19(5)13-15-20/h8,11-12,21H,1,6-7,9-10,13-15H2,2-5H3/t20-/m1/s1
InChI Key FHZBFUJNSBTONS-HXUWFJFHSA-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 4.70
Atomic LogP (AlogP) 5.88
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1S)-4,8,12-trimethyl-1-prop-1-en-2-ylcyclotetradeca-3,7,11-trien-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 + 0.9959 99.59%
Caco-2 + 0.8872 88.72%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Lysosomes 0.5533 55.33%
OATP2B1 inhibitior - 0.8527 85.27%
OATP1B1 inhibitior + 0.9661 96.61%
OATP1B3 inhibitior + 0.9173 91.73%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.7351 73.51%
P-glycoprotein inhibitior - 0.7648 76.48%
P-glycoprotein substrate - 0.9200 92.00%
CYP3A4 substrate - 0.5628 56.28%
CYP2C9 substrate - 0.7899 78.99%
CYP2D6 substrate - 0.7511 75.11%
CYP3A4 inhibition - 0.7779 77.79%
CYP2C9 inhibition - 0.7789 77.89%
CYP2C19 inhibition - 0.8154 81.54%
CYP2D6 inhibition - 0.9417 94.17%
CYP1A2 inhibition - 0.7312 73.12%
CYP2C8 inhibition - 0.8840 88.40%
CYP inhibitory promiscuity - 0.9366 93.66%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.7928 79.28%
Carcinogenicity (trinary) Non-required 0.5849 58.49%
Eye corrosion - 0.9057 90.57%
Eye irritation + 0.7841 78.41%
Skin irritation + 0.7078 70.78%
Skin corrosion - 0.9523 95.23%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6720 67.20%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.6463 64.63%
skin sensitisation + 0.7859 78.59%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity - 0.6667 66.67%
Mitochondrial toxicity - 0.6500 65.00%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.8085 80.85%
Estrogen receptor binding - 0.7371 73.71%
Androgen receptor binding - 0.6997 69.97%
Thyroid receptor binding - 0.5360 53.60%
Glucocorticoid receptor binding + 0.5518 55.18%
Aromatase binding - 0.5433 54.33%
PPAR gamma + 0.6452 64.52%
Honey bee toxicity - 0.8685 86.85%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9304 93.04%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.00% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.12% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.85% 97.25%
CHEMBL4208 P20618 Proteasome component C5 83.94% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.66% 95.56%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 81.17% 90.93%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 162867330
LOTUS LTS0075475
wikiData Q104995533