Isoterpinolene

Details

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Internal ID a9858959-0bec-4fff-b14e-ebf96883807a
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Menthane monoterpenoids
IUPAC Name 3-methyl-6-propan-2-ylidenecyclohexene
SMILES (Canonical) CC1CCC(=C(C)C)C=C1
SMILES (Isomeric) CC1CCC(=C(C)C)C=C1
InChI InChI=1S/C10H16/c1-8(2)10-6-4-9(3)5-7-10/h4,6,9H,5,7H2,1-3H3
InChI Key CIPXOBMYVWRNLL-UHFFFAOYSA-N
Popularity 31 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16
Molecular Weight 136.23 g/mol
Exact Mass 136.125200510 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.50
Atomic LogP (AlogP) 3.31
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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586-63-0
p-Mentha-2,4(8)-diene
2,4(8)-p-Menthadiene
Cyclohexene, 3-methyl-6-(1-methylethylidene)-
3-Methyl-6-(1-methylethylidene)cyclohexene
3-methyl-6-propan-2-ylidenecyclohexene
VR4XVW6V2H
EINECS 209-579-6
UNII-VR4XVW6V2H
p-2,4(8)-Menthadiene
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Isoterpinolene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9928 99.28%
Caco-2 + 0.8937 89.37%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Nucleus 0.4128 41.28%
OATP2B1 inhibitior - 0.8571 85.71%
OATP1B1 inhibitior + 0.9647 96.47%
OATP1B3 inhibitior + 0.8729 87.29%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.8906 89.06%
P-glycoprotein inhibitior - 0.9890 98.90%
P-glycoprotein substrate - 0.9417 94.17%
CYP3A4 substrate - 0.6607 66.07%
CYP2C9 substrate - 0.8080 80.80%
CYP2D6 substrate - 0.7898 78.98%
CYP3A4 inhibition - 0.9581 95.81%
CYP2C9 inhibition - 0.9216 92.16%
CYP2C19 inhibition - 0.9063 90.63%
CYP2D6 inhibition - 0.9312 93.12%
CYP1A2 inhibition - 0.8015 80.15%
CYP2C8 inhibition - 0.9567 95.67%
CYP inhibitory promiscuity - 0.7336 73.36%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6200 62.00%
Carcinogenicity (trinary) Warning 0.5233 52.33%
Eye corrosion + 0.5306 53.06%
Eye irritation + 0.9238 92.38%
Skin irritation + 0.8720 87.20%
Skin corrosion - 0.9060 90.60%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5532 55.32%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.7250 72.50%
skin sensitisation + 0.9458 94.58%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity - 0.8750 87.50%
Nephrotoxicity - 0.7469 74.69%
Acute Oral Toxicity (c) III 0.8506 85.06%
Estrogen receptor binding - 0.9880 98.80%
Androgen receptor binding - 0.8472 84.72%
Thyroid receptor binding - 0.8881 88.81%
Glucocorticoid receptor binding - 0.9114 91.14%
Aromatase binding - 0.9424 94.24%
PPAR gamma - 0.9340 93.40%
Honey bee toxicity - 0.9686 96.86%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.9802 98.02%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.14% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.03% 96.09%
CHEMBL2581 P07339 Cathepsin D 83.81% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.18% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.30% 95.56%

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.
Artemisia argyi
Chrysanthemum morifolium
Cinnamomum aromaticum
Lindera aggregata
Mentha arvensis
Mentha canadensis
Myristica fragrans
Portulaca oleracea
Salvadora persica

Cross-Links

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PubChem 102443
NPASS NPC92197
LOTUS LTS0141089
wikiData Q24514387