(2-Methylidene-5-propan-2-ylcyclohex-3-en-1-yl) 2-phenylacetate

Details

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Internal ID 6897a681-06c9-4a3e-8309-856468ae0d3c
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Aromatic monoterpenoids
IUPAC Name (2-methylidene-5-propan-2-ylcyclohex-3-en-1-yl) 2-phenylacetate
SMILES (Canonical) CC(C)C1CC(C(=C)C=C1)OC(=O)CC2=CC=CC=C2
SMILES (Isomeric) CC(C)C1CC(C(=C)C=C1)OC(=O)CC2=CC=CC=C2
InChI InChI=1S/C18H22O2/c1-13(2)16-10-9-14(3)17(12-16)20-18(19)11-15-7-5-4-6-8-15/h4-10,13,16-17H,3,11-12H2,1-2H3
InChI Key LRIJTJALEPQHJR-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H22O2
Molecular Weight 270.40 g/mol
Exact Mass 270.161979940 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 4.30
Atomic LogP (AlogP) 3.93
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2-Methylidene-5-propan-2-ylcyclohex-3-en-1-yl) 2-phenylacetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.8855 88.55%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.8471 84.71%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9182 91.82%
OATP1B3 inhibitior + 0.9076 90.76%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.4527 45.27%
P-glycoprotein inhibitior - 0.8075 80.75%
P-glycoprotein substrate - 0.7962 79.62%
CYP3A4 substrate + 0.5113 51.13%
CYP2C9 substrate - 0.8092 80.92%
CYP2D6 substrate - 0.8671 86.71%
CYP3A4 inhibition - 0.7784 77.84%
CYP2C9 inhibition - 0.7589 75.89%
CYP2C19 inhibition + 0.7746 77.46%
CYP2D6 inhibition - 0.8513 85.13%
CYP1A2 inhibition - 0.6694 66.94%
CYP2C8 inhibition - 0.8081 80.81%
CYP inhibitory promiscuity + 0.7604 76.04%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6532 65.32%
Carcinogenicity (trinary) Non-required 0.7017 70.17%
Eye corrosion - 0.9514 95.14%
Eye irritation - 0.7308 73.08%
Skin irritation - 0.7755 77.55%
Skin corrosion - 0.9880 98.80%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7245 72.45%
Micronuclear - 0.7615 76.15%
Hepatotoxicity + 0.6056 60.56%
skin sensitisation + 0.8101 81.01%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity - 0.7574 75.74%
Acute Oral Toxicity (c) III 0.8144 81.44%
Estrogen receptor binding - 0.7836 78.36%
Androgen receptor binding - 0.7464 74.64%
Thyroid receptor binding + 0.5231 52.31%
Glucocorticoid receptor binding - 0.6576 65.76%
Aromatase binding - 0.5375 53.75%
PPAR gamma - 0.6857 68.57%
Honey bee toxicity - 0.8854 88.54%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6055 60.55%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL2581 P07339 Cathepsin D 96.69% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 96.60% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.38% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.76% 95.56%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 89.49% 95.50%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 88.57% 94.62%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.29% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.97% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.95% 94.45%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 81.79% 94.08%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.29% 86.33%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 80.25% 96.47%

Plants that contains it

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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.
Trattinnickia burserifolia

Cross-Links

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PubChem 162820445
LOTUS LTS0250755
wikiData Q104171240