(4-Hydroxy-3-methyl-6-prop-1-en-2-ylcyclohex-2-en-1-yl) acetate

Details

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Internal ID 8c28fd13-f365-4f56-a936-04d09a0ea8db
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Menthane monoterpenoids
IUPAC Name (4-hydroxy-3-methyl-6-prop-1-en-2-ylcyclohex-2-en-1-yl) acetate
SMILES (Canonical) CC1=CC(C(CC1O)C(=C)C)OC(=O)C
SMILES (Isomeric) CC1=CC(C(CC1O)C(=C)C)OC(=O)C
InChI InChI=1S/C12H18O3/c1-7(2)10-6-11(14)8(3)5-12(10)15-9(4)13/h5,10-12,14H,1,6H2,2-4H3
InChI Key OKQNBLMBMSJUFT-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C12H18O3
Molecular Weight 210.27 g/mol
Exact Mass 210.125594432 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 1.50
Atomic LogP (AlogP) 1.82
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (4-Hydroxy-3-methyl-6-prop-1-en-2-ylcyclohex-2-en-1-yl) acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9958 99.58%
Caco-2 + 0.5317 53.17%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.8297 82.97%
OATP2B1 inhibitior - 0.8539 85.39%
OATP1B1 inhibitior + 0.9470 94.70%
OATP1B3 inhibitior + 0.9635 96.35%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9707 97.07%
P-glycoprotein inhibitior - 0.9658 96.58%
P-glycoprotein substrate - 0.8237 82.37%
CYP3A4 substrate - 0.5303 53.03%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate - 0.8603 86.03%
CYP3A4 inhibition - 0.8074 80.74%
CYP2C9 inhibition - 0.9753 97.53%
CYP2C19 inhibition - 0.8558 85.58%
CYP2D6 inhibition - 0.9257 92.57%
CYP1A2 inhibition - 0.9407 94.07%
CYP2C8 inhibition - 0.9243 92.43%
CYP inhibitory promiscuity - 0.9342 93.42%
UGT catelyzed + 0.6362 63.62%
Carcinogenicity (binary) - 0.6626 66.26%
Carcinogenicity (trinary) Non-required 0.7238 72.38%
Eye corrosion - 0.9049 90.49%
Eye irritation + 0.5622 56.22%
Skin irritation + 0.6012 60.12%
Skin corrosion - 0.9650 96.50%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7161 71.61%
Micronuclear - 0.7441 74.41%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation + 0.6470 64.70%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity + 0.4832 48.32%
Acute Oral Toxicity (c) III 0.6956 69.56%
Estrogen receptor binding - 0.7489 74.89%
Androgen receptor binding - 0.8637 86.37%
Thyroid receptor binding - 0.7395 73.95%
Glucocorticoid receptor binding - 0.7653 76.53%
Aromatase binding - 0.8558 85.58%
PPAR gamma - 0.8621 86.21%
Honey bee toxicity - 0.7336 73.36%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity - 0.6855 68.55%
Fish aquatic toxicity + 0.9513 95.13%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.86% 96.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 91.29% 96.95%
CHEMBL340 P08684 Cytochrome P450 3A4 82.72% 91.19%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.95% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.11% 91.11%

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.
Mentha spicata subsp. condensata

Cross-Links

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PubChem 163031275
LOTUS LTS0242035
wikiData Q105193712