Dihydroterpinyl acetate

Details

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Internal ID 26b4552e-dd7a-4c76-a7ff-b6669449870f
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Menthane monoterpenoids
IUPAC Name 2-(4-methylcyclohexyl)propan-2-yl acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H22O2/c1-9-5-7-11(8-6-9)12(3,4)14-10(2)13/h9,11H,5-8H2,1-4H3
InChI Key HBNHCGDYYBMKJN-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C12H22O2
Molecular Weight 198.30 g/mol
Exact Mass 198.161979940 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 3.40
Atomic LogP (AlogP) 3.15
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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p-Menthan-8-yl acetate
58985-18-5
Terpineol, dihydro-, acetate
RefChem:1083624
261-543-9
80-25-1
Dihydro-alpha-terpinyl acetate
2-(4-methylcyclohexyl)propan-2-yl acetate
p-MENTHAN-8-OL, ACETATE
Acetic acid, dihydroterpinyl ester
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Dihydroterpinyl acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9954 99.54%
Caco-2 + 0.7679 76.79%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.7344 73.44%
OATP2B1 inhibitior - 0.8465 84.65%
OATP1B1 inhibitior + 0.9677 96.77%
OATP1B3 inhibitior + 0.9408 94.08%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.9383 93.83%
P-glycoprotein inhibitior - 0.9202 92.02%
P-glycoprotein substrate - 0.9451 94.51%
CYP3A4 substrate - 0.5470 54.70%
CYP2C9 substrate + 0.5942 59.42%
CYP2D6 substrate - 0.8718 87.18%
CYP3A4 inhibition - 0.9396 93.96%
CYP2C9 inhibition - 0.7471 74.71%
CYP2C19 inhibition - 0.7995 79.95%
CYP2D6 inhibition - 0.9339 93.39%
CYP1A2 inhibition - 0.8435 84.35%
CYP2C8 inhibition - 0.9636 96.36%
CYP inhibitory promiscuity - 0.9325 93.25%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6500 65.00%
Carcinogenicity (trinary) Non-required 0.5421 54.21%
Eye corrosion + 0.6741 67.41%
Eye irritation + 0.7610 76.10%
Skin irritation + 0.5450 54.50%
Skin corrosion - 0.9968 99.68%
Ames mutagenesis - 0.8140 81.40%
Human Ether-a-go-go-Related Gene inhibition - 0.5918 59.18%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation + 0.8584 85.84%
Respiratory toxicity - 0.8333 83.33%
Reproductive toxicity - 0.8333 83.33%
Mitochondrial toxicity - 0.9500 95.00%
Nephrotoxicity + 0.4902 49.02%
Acute Oral Toxicity (c) III 0.7213 72.13%
Estrogen receptor binding - 0.7929 79.29%
Androgen receptor binding - 0.8692 86.92%
Thyroid receptor binding - 0.6842 68.42%
Glucocorticoid receptor binding - 0.8480 84.80%
Aromatase binding - 0.8158 81.58%
PPAR gamma - 0.9321 93.21%
Honey bee toxicity - 0.8407 84.07%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity + 0.9779 97.79%

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 97.44% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.52% 96.09%
CHEMBL2581 P07339 Cathepsin D 89.30% 98.95%
CHEMBL340 P08684 Cytochrome P450 3A4 87.43% 91.19%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.99% 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.
Elettaria cardamomum

Cross-Links

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PubChem 6631
NPASS NPC3285