trans-p-Mentha-2,8-dienol

Details

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Internal ID 0f4387c6-146a-493d-afe6-7ff291289447
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Menthane monoterpenoids
IUPAC Name (3S,6R)-3-methyl-6-prop-1-en-2-ylcyclohexen-1-ol
SMILES (Canonical) CC1CCC(C(=C1)O)C(=C)C
SMILES (Isomeric) C[C@H]1CC[C@@H](C(=C1)O)C(=C)C
InChI InChI=1S/C10H16O/c1-7(2)9-5-4-8(3)6-10(9)11/h6,8-9,11H,1,4-5H2,2-3H3/t8-,9+/m0/s1
InChI Key FXVHTIGBZHVHOB-DTWKUNHWSA-N
Popularity 12 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16O
Molecular Weight 152.23 g/mol
Exact Mass 152.120115130 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.05
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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6-Isopropenyl-3-methyl-1-cyclohexen-1-ol #
FXVHTIGBZHVHOB-DTWKUNHWSA-N

2D Structure

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2D Structure of trans-p-Mentha-2,8-dienol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9911 99.11%
Caco-2 + 0.5791 57.91%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Lysosomes 0.4218 42.18%
OATP2B1 inhibitior - 0.8451 84.51%
OATP1B1 inhibitior + 0.9041 90.41%
OATP1B3 inhibitior + 0.9276 92.76%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.9595 95.95%
P-glycoprotein inhibitior - 0.9774 97.74%
P-glycoprotein substrate - 0.9114 91.14%
CYP3A4 substrate - 0.6126 61.26%
CYP2C9 substrate + 0.6131 61.31%
CYP2D6 substrate - 0.7940 79.40%
CYP3A4 inhibition - 0.8354 83.54%
CYP2C9 inhibition - 0.8685 86.85%
CYP2C19 inhibition - 0.7752 77.52%
CYP2D6 inhibition - 0.8573 85.73%
CYP1A2 inhibition - 0.6644 66.44%
CYP2C8 inhibition - 0.9405 94.05%
CYP inhibitory promiscuity - 0.7343 73.43%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7928 79.28%
Carcinogenicity (trinary) Non-required 0.6009 60.09%
Eye corrosion - 0.6410 64.10%
Eye irritation + 0.8886 88.86%
Skin irritation + 0.7186 71.86%
Skin corrosion - 0.5956 59.56%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6225 62.25%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation + 0.8587 85.87%
Respiratory toxicity - 0.8556 85.56%
Reproductive toxicity + 0.5410 54.10%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity + 0.4805 48.05%
Acute Oral Toxicity (c) III 0.7739 77.39%
Estrogen receptor binding - 0.9450 94.50%
Androgen receptor binding - 0.9025 90.25%
Thyroid receptor binding - 0.8566 85.66%
Glucocorticoid receptor binding - 0.7651 76.51%
Aromatase binding - 0.8913 89.13%
PPAR gamma - 0.8673 86.73%
Honey bee toxicity - 0.9415 94.15%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9721 97.21%

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 96.29% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 89.76% 91.49%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.41% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.75% 100.00%
CHEMBL2581 P07339 Cathepsin D 81.43% 98.95%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.90% 92.94%

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.
Chrysanthemum indicum
Citrus × aurantium
Citrus deliciosa
Citrus maxima
Citrus trifoliata
Mentha arvensis
Mentha canadensis

Cross-Links

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PubChem 91753981
NPASS NPC173760