p-Menth-4(8)-en-7-ol

Details

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Internal ID f24e6f56-d7f2-41fd-9cc9-cc7e41dd06d7
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Menthane monoterpenoids
IUPAC Name (4-propan-2-ylidenecyclohexyl)methanol
SMILES (Canonical) CC(=C1CCC(CC1)CO)C
SMILES (Isomeric) CC(=C1CCC(CC1)CO)C
InChI InChI=1S/C10H18O/c1-8(2)10-5-3-9(7-11)4-6-10/h9,11H,3-7H2,1-2H3
InChI Key MBYRPVJKSJEKLH-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C10H18O
Molecular Weight 154.25 g/mol
Exact Mass 154.135765193 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.51
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of p-Menth-4(8)-en-7-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9919 99.19%
Caco-2 + 0.6944 69.44%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Lysosomes 0.6266 62.66%
OATP2B1 inhibitior - 0.8405 84.05%
OATP1B1 inhibitior + 0.9357 93.57%
OATP1B3 inhibitior + 0.9286 92.86%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.5500 55.00%
BSEP inhibitior - 0.8852 88.52%
P-glycoprotein inhibitior - 0.9784 97.84%
P-glycoprotein substrate - 0.9385 93.85%
CYP3A4 substrate - 0.6621 66.21%
CYP2C9 substrate - 0.6591 65.91%
CYP2D6 substrate - 0.7543 75.43%
CYP3A4 inhibition - 0.8838 88.38%
CYP2C9 inhibition - 0.8129 81.29%
CYP2C19 inhibition - 0.8657 86.57%
CYP2D6 inhibition - 0.8739 87.39%
CYP1A2 inhibition - 0.8383 83.83%
CYP2C8 inhibition - 0.9629 96.29%
CYP inhibitory promiscuity - 0.7270 72.70%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8128 81.28%
Carcinogenicity (trinary) Non-required 0.6700 67.00%
Eye corrosion - 0.6238 62.38%
Eye irritation + 0.9433 94.33%
Skin irritation - 0.6052 60.52%
Skin corrosion - 0.9391 93.91%
Ames mutagenesis - 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6079 60.79%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.5604 56.04%
skin sensitisation + 0.9321 93.21%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity - 0.7778 77.78%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity + 0.4738 47.38%
Acute Oral Toxicity (c) III 0.7612 76.12%
Estrogen receptor binding - 0.9744 97.44%
Androgen receptor binding - 0.7957 79.57%
Thyroid receptor binding - 0.8249 82.49%
Glucocorticoid receptor binding - 0.8858 88.58%
Aromatase binding - 0.8745 87.45%
PPAR gamma - 0.8846 88.46%
Honey bee toxicity - 0.9759 97.59%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity - 0.8100 81.00%
Fish aquatic toxicity + 0.9671 96.71%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.73% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.96% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.54% 97.25%
CHEMBL226 P30542 Adenosine A1 receptor 85.72% 95.93%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.71% 97.09%
CHEMBL2581 P07339 Cathepsin D 85.46% 98.95%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 80.59% 95.50%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.16% 95.89%

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.
Agathosma betulina

Cross-Links

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PubChem 71322201
LOTUS LTS0210845
wikiData Q105161043