6-Methyl-3-(1-methylethyl)-2-cyclohexen-1-ol acetate

Details

Top
Internal ID 4be188d5-93ba-4f33-bf54-9e425a44edbf
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Menthane monoterpenoids
IUPAC Name (6-methyl-3-propan-2-ylcyclohex-2-en-1-yl) acetate
SMILES (Canonical) CC1CCC(=CC1OC(=O)C)C(C)C
SMILES (Isomeric) CC1CCC(=CC1OC(=O)C)C(C)C
InChI InChI=1S/C12H20O2/c1-8(2)11-6-5-9(3)12(7-11)14-10(4)13/h7-9,12H,5-6H2,1-4H3
InChI Key KLARWHVVPTTYEW-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C12H20O2
Molecular Weight 196.29 g/mol
Exact Mass 196.146329876 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.93
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

Top
KLARWHVVPTTYEW-UHFFFAOYSA-N
6-Methyl-3-(1-methylethyl)-2-cyclohexen-1-ol acetate

2D Structure

Top
2D Structure of 6-Methyl-3-(1-methylethyl)-2-cyclohexen-1-ol acetate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9974 99.74%
Caco-2 + 0.7438 74.38%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.7220 72.20%
OATP2B1 inhibitior - 0.8517 85.17%
OATP1B1 inhibitior + 0.9362 93.62%
OATP1B3 inhibitior + 0.9278 92.78%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.9405 94.05%
P-glycoprotein inhibitior - 0.9154 91.54%
P-glycoprotein substrate - 0.9145 91.45%
CYP3A4 substrate - 0.5135 51.35%
CYP2C9 substrate + 0.5955 59.55%
CYP2D6 substrate - 0.8761 87.61%
CYP3A4 inhibition - 0.9443 94.43%
CYP2C9 inhibition - 0.9065 90.65%
CYP2C19 inhibition - 0.7026 70.26%
CYP2D6 inhibition - 0.9048 90.48%
CYP1A2 inhibition - 0.6878 68.78%
CYP2C8 inhibition - 0.9582 95.82%
CYP inhibitory promiscuity - 0.7483 74.83%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7181 71.81%
Carcinogenicity (trinary) Non-required 0.5357 53.57%
Eye corrosion - 0.8946 89.46%
Eye irritation - 0.5641 56.41%
Skin irritation + 0.7058 70.58%
Skin corrosion - 0.9810 98.10%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6157 61.57%
Micronuclear - 0.9500 95.00%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation + 0.7634 76.34%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.6333 63.33%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity - 0.6714 67.14%
Acute Oral Toxicity (c) III 0.7740 77.40%
Estrogen receptor binding - 0.9523 95.23%
Androgen receptor binding - 0.8473 84.73%
Thyroid receptor binding - 0.7736 77.36%
Glucocorticoid receptor binding - 0.8774 87.74%
Aromatase binding - 0.8882 88.82%
PPAR gamma - 0.8875 88.75%
Honey bee toxicity - 0.8637 86.37%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.6055 60.55%
Fish aquatic toxicity + 0.9803 98.03%

Targets

Top

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 96.74% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.82% 91.11%
CHEMBL2581 P07339 Cathepsin D 93.07% 98.95%
CHEMBL3359 P21462 Formyl peptide receptor 1 86.85% 93.56%
CHEMBL340 P08684 Cytochrome P450 3A4 84.28% 91.19%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 82.18% 95.89%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.39% 94.45%

Plants that contains it

Top
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.
Artemisia argyi
Artemisia montana
Artemisia princeps

Cross-Links

Top
PubChem 91748679
NPASS NPC105218