(8-Hydroxy-1,4,8-trimethyl-2-oxo-11-propan-2-ylcyclotrideca-4,9-dien-1-yl)methyl acetate

Details

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Internal ID 1d87f71f-63dc-4e5a-886e-ceac512f092d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (8-hydroxy-1,4,8-trimethyl-2-oxo-11-propan-2-ylcyclotrideca-4,9-dien-1-yl)methyl acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H36O4/c1-16(2)19-9-12-21(5,15-26-18(4)23)20(24)14-17(3)8-7-11-22(6,25)13-10-19/h8,10,13,16,19,25H,7,9,11-12,14-15H2,1-6H3
InChI Key BHSGVCGSYDQSIG-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C22H36O4
Molecular Weight 364.50 g/mol
Exact Mass 364.26135963 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 3.80
Atomic LogP (AlogP) 4.61
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (8-Hydroxy-1,4,8-trimethyl-2-oxo-11-propan-2-ylcyclotrideca-4,9-dien-1-yl)methyl acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9926 99.26%
Caco-2 + 0.7200 72.00%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.8908 89.08%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9091 90.91%
OATP1B3 inhibitior + 0.9272 92.72%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.5891 58.91%
BSEP inhibitior + 0.6900 69.00%
P-glycoprotein inhibitior - 0.5293 52.93%
P-glycoprotein substrate - 0.7240 72.40%
CYP3A4 substrate + 0.6181 61.81%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8899 88.99%
CYP3A4 inhibition - 0.8062 80.62%
CYP2C9 inhibition - 0.7048 70.48%
CYP2C19 inhibition - 0.8776 87.76%
CYP2D6 inhibition - 0.9492 94.92%
CYP1A2 inhibition - 0.8076 80.76%
CYP2C8 inhibition - 0.7713 77.13%
CYP inhibitory promiscuity - 0.9624 96.24%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8128 81.28%
Carcinogenicity (trinary) Non-required 0.6234 62.34%
Eye corrosion - 0.9840 98.40%
Eye irritation - 0.9315 93.15%
Skin irritation - 0.5847 58.47%
Skin corrosion - 0.9771 97.71%
Ames mutagenesis - 0.7624 76.24%
Human Ether-a-go-go-Related Gene inhibition + 0.7186 71.86%
Micronuclear - 0.8700 87.00%
Hepatotoxicity + 0.5968 59.68%
skin sensitisation - 0.7104 71.04%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity - 0.5953 59.53%
Acute Oral Toxicity (c) III 0.4524 45.24%
Estrogen receptor binding + 0.5414 54.14%
Androgen receptor binding - 0.7389 73.89%
Thyroid receptor binding + 0.5675 56.75%
Glucocorticoid receptor binding + 0.6565 65.65%
Aromatase binding - 0.6102 61.02%
PPAR gamma + 0.5661 56.61%
Honey bee toxicity - 0.8507 85.07%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5750 57.50%
Fish aquatic toxicity + 0.9874 98.74%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 99.31% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.23% 96.09%
CHEMBL2581 P07339 Cathepsin D 93.48% 98.95%
CHEMBL1937 Q92769 Histone deacetylase 2 93.03% 94.75%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.10% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.94% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.09% 97.09%
CHEMBL218 P21554 Cannabinoid CB1 receptor 86.83% 96.61%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.27% 95.56%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 85.65% 82.69%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.35% 99.23%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.69% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.17% 95.89%
CHEMBL4227 P25090 Lipoxin A4 receptor 81.68% 100.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.60% 85.14%
CHEMBL5103 Q969S8 Histone deacetylase 10 80.78% 90.08%
CHEMBL5028 O14672 ADAM10 80.39% 97.50%

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 72747549
LOTUS LTS0240013
wikiData Q105100703