2-Menthene

Details

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Internal ID 111e3ec1-faa4-4278-bf4c-8e1a7d0c392a
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Menthane monoterpenoids
IUPAC Name 3-methyl-6-propan-2-ylcyclohexene
SMILES (Canonical) CC1CCC(C=C1)C(C)C
SMILES (Isomeric) CC1CCC(C=C1)C(C)C
InChI InChI=1S/C10H18/c1-8(2)10-6-4-9(3)5-7-10/h4,6,8-10H,5,7H2,1-3H3
InChI Key WHNGPXQYYRWQAS-UHFFFAOYSA-N
Popularity 17 references in papers

Physical and Chemical Properties

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Molecular Formula C10H18
Molecular Weight 138.25 g/mol
Exact Mass 138.140850574 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.90
Atomic LogP (AlogP) 3.24
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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Cyclohexene, 3-methyl-6-(1-methylethyl)-
2-Menthene
5256-65-5
3-Isopropyl-6-methylcyclohexene
3-Methyl-6-(1-methylethyl)cyclohexene
2JPC122KT4
3-Methyl-6-isopropylcyclohexene
UNII-2JPC122KT4
2-Menthen
DTXSID30333757
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2-Menthene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9937 99.37%
Caco-2 + 0.8342 83.42%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Lysosomes 0.5091 50.91%
OATP2B1 inhibitior - 0.8570 85.70%
OATP1B1 inhibitior + 0.9572 95.72%
OATP1B3 inhibitior + 0.9093 90.93%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9441 94.41%
P-glycoprotein inhibitior - 0.9831 98.31%
P-glycoprotein substrate - 0.9040 90.40%
CYP3A4 substrate - 0.6930 69.30%
CYP2C9 substrate - 0.8071 80.71%
CYP2D6 substrate - 0.7561 75.61%
CYP3A4 inhibition - 0.9753 97.53%
CYP2C9 inhibition - 0.9417 94.17%
CYP2C19 inhibition - 0.9463 94.63%
CYP2D6 inhibition - 0.9568 95.68%
CYP1A2 inhibition - 0.8044 80.44%
CYP2C8 inhibition - 0.9886 98.86%
CYP inhibitory promiscuity - 0.8604 86.04%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6300 63.00%
Carcinogenicity (trinary) Non-required 0.4552 45.52%
Eye corrosion + 0.9095 90.95%
Eye irritation + 0.8973 89.73%
Skin irritation + 0.8855 88.55%
Skin corrosion - 0.9093 90.93%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5219 52.19%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.7377 73.77%
skin sensitisation + 0.9477 94.77%
Respiratory toxicity - 0.8444 84.44%
Reproductive toxicity - 0.5667 56.67%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity - 0.7936 79.36%
Acute Oral Toxicity (c) III 0.8016 80.16%
Estrogen receptor binding - 0.9677 96.77%
Androgen receptor binding - 0.9377 93.77%
Thyroid receptor binding - 0.8501 85.01%
Glucocorticoid receptor binding - 0.8520 85.20%
Aromatase binding - 0.9108 91.08%
PPAR gamma - 0.9393 93.93%
Honey bee toxicity - 0.8339 83.39%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.9710 97.10%

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 97.22% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.90% 96.09%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 83.81% 97.23%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.37% 97.09%
CHEMBL2581 P07339 Cathepsin D 81.20% 98.95%

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.
Basella alba
Zanthoxylum bungeanum
Zanthoxylum schinifolium

Cross-Links

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PubChem 517974
NPASS NPC210229
LOTUS LTS0162262
wikiData Q82099264