p-Mentha-1(7),8(10)-dien-9-ol

Details

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Internal ID d282f8d8-3d18-4f23-b716-1d6497ba7257
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Menthane monoterpenoids
IUPAC Name 2-(4-methylidenecyclohexyl)prop-2-en-1-ol
SMILES (Canonical) C=C1CCC(CC1)C(=C)CO
SMILES (Isomeric) C=C1CCC(CC1)C(=C)CO
InChI InChI=1S/C10H16O/c1-8-3-5-10(6-4-8)9(2)7-11/h10-11H,1-7H2
InChI Key SDDQNZKSVASSFO-UHFFFAOYSA-N
Popularity 3 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 2.30
Atomic LogP (AlogP) 2.28
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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29548-13-8
BETA,4-BIS(METHYLENE)CYCLOHEXANEETHANOL
2-(4-methylidenecyclohexyl)prop-2-en-1-ol
SCHEMBL15319201
DTXSID50183731
SDDQNZKSVASSFO-UHFFFAOYSA-N
1(7),8(10)-p-Menthadien-9-ol
2-(4-Methylenecyclohexyl)-2-propen-1-ol
2-(4-Methylenecyclohexyl)-2-propen-1-ol #

2D Structure

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2D Structure of p-Mentha-1(7),8(10)-dien-9-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9746 97.46%
Caco-2 + 0.5335 53.35%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Lysosomes 0.4568 45.68%
OATP2B1 inhibitior - 0.8461 84.61%
OATP1B1 inhibitior + 0.9446 94.46%
OATP1B3 inhibitior + 0.9526 95.26%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior - 0.9186 91.86%
P-glycoprotein inhibitior - 0.9775 97.75%
P-glycoprotein substrate - 0.9717 97.17%
CYP3A4 substrate - 0.6620 66.20%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7134 71.34%
CYP3A4 inhibition - 0.7960 79.60%
CYP2C9 inhibition - 0.8762 87.62%
CYP2C19 inhibition - 0.8397 83.97%
CYP2D6 inhibition - 0.9251 92.51%
CYP1A2 inhibition - 0.8212 82.12%
CYP2C8 inhibition - 0.9230 92.30%
CYP inhibitory promiscuity - 0.6629 66.29%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.7728 77.28%
Carcinogenicity (trinary) Non-required 0.6748 67.48%
Eye corrosion + 0.8418 84.18%
Eye irritation + 0.9800 98.00%
Skin irritation + 0.5112 51.12%
Skin corrosion - 0.9399 93.99%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6028 60.28%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5021 50.21%
skin sensitisation + 0.8231 82.31%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity - 0.7667 76.67%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity - 0.6572 65.72%
Acute Oral Toxicity (c) III 0.7690 76.90%
Estrogen receptor binding - 0.9081 90.81%
Androgen receptor binding - 0.7862 78.62%
Thyroid receptor binding - 0.8483 84.83%
Glucocorticoid receptor binding - 0.7203 72.03%
Aromatase binding - 0.8105 81.05%
PPAR gamma - 0.8650 86.50%
Honey bee toxicity - 0.9651 96.51%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.9118 91.18%

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 92.91% 91.11%
CHEMBL226 P30542 Adenosine A1 receptor 90.47% 95.93%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.54% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.17% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.72% 100.00%

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.
Citrus × aurantium
Citrus deliciosa
Ixora chinensis

Cross-Links

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PubChem 34627
NPASS NPC204498