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

Details

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Internal ID 8f728036-68e6-40b6-ab30-e2d1b3d930a1
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Cembrane diterpenoids
IUPAC Name (3E,7E,11E,14S)-3,7,11-trimethyl-14-prop-1-en-2-ylcyclotetradeca-3,7,11-trien-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H30O/c1-15(2)19-13-12-17(4)10-6-8-16(3)9-7-11-18(5)14-20(19)21/h8,11-12,19H,1,6-7,9-10,13-14H2,2-5H3/b16-8+,17-12+,18-11+/t19-/m0/s1
InChI Key FHFFESCITRPPTG-QPHFJTKNSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H30O
Molecular Weight 286.50 g/mol
Exact Mass 286.229665576 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 4.70
Atomic LogP (AlogP) 5.94
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9961 99.61%
Caco-2 + 0.7776 77.76%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.4349 43.49%
OATP2B1 inhibitior - 0.8543 85.43%
OATP1B1 inhibitior + 0.9667 96.67%
OATP1B3 inhibitior + 0.8303 83.03%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.6365 63.65%
P-glycoprotein inhibitior - 0.6969 69.69%
P-glycoprotein substrate - 0.9320 93.20%
CYP3A4 substrate - 0.5372 53.72%
CYP2C9 substrate - 0.8012 80.12%
CYP2D6 substrate - 0.7855 78.55%
CYP3A4 inhibition - 0.8837 88.37%
CYP2C9 inhibition - 0.8983 89.83%
CYP2C19 inhibition - 0.8061 80.61%
CYP2D6 inhibition - 0.9451 94.51%
CYP1A2 inhibition - 0.5544 55.44%
CYP2C8 inhibition - 0.9030 90.30%
CYP inhibitory promiscuity - 0.8875 88.75%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8300 83.00%
Carcinogenicity (trinary) Non-required 0.5563 55.63%
Eye corrosion - 0.8131 81.31%
Eye irritation - 0.6661 66.61%
Skin irritation + 0.6447 64.47%
Skin corrosion - 0.9598 95.98%
Ames mutagenesis - 0.8028 80.28%
Human Ether-a-go-go-Related Gene inhibition + 0.7306 73.06%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.7533 75.33%
skin sensitisation + 0.8984 89.84%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity - 0.6778 67.78%
Mitochondrial toxicity - 0.7750 77.50%
Nephrotoxicity + 0.6590 65.90%
Acute Oral Toxicity (c) III 0.6792 67.92%
Estrogen receptor binding - 0.7215 72.15%
Androgen receptor binding - 0.6865 68.65%
Thyroid receptor binding - 0.6092 60.92%
Glucocorticoid receptor binding - 0.5851 58.51%
Aromatase binding - 0.7589 75.89%
PPAR gamma + 0.6195 61.95%
Honey bee toxicity - 0.8655 86.55%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity + 0.9796 97.96%

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 95.49% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.97% 95.56%
CHEMBL2581 P07339 Cathepsin D 89.05% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.80% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.61% 96.09%
CHEMBL1951 P21397 Monoamine oxidase A 83.67% 91.49%
CHEMBL4208 P20618 Proteasome component C5 83.00% 90.00%

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 163186289
LOTUS LTS0269085
wikiData Q104995224