o-Mentha-1(7),8-dien-3-ol

Details

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Internal ID 9a62ed2d-38d8-4804-a308-e7f42c8f381f
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Monocyclic monoterpenoids
IUPAC Name 3-methylidene-2-prop-1-en-2-ylcyclohexan-1-ol
SMILES (Canonical) CC(=C)C1C(CCCC1=C)O
SMILES (Isomeric) CC(=C)C1C(CCCC1=C)O
InChI InChI=1S/C10H16O/c1-7(2)10-8(3)5-4-6-9(10)11/h9-11H,1,3-6H2,2H3
InChI Key QUDZQFLTGZFKLG-UHFFFAOYSA-N
Popularity 0 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 1

Synonyms

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QUDZQFLTGZFKLG-UHFFFAOYSA-N
2-Isopropenyl-3-methylenecyclohexanol #

2D Structure

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2D Structure of o-Mentha-1(7),8-dien-3-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9912 99.12%
Caco-2 - 0.5751 57.51%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.5801 58.01%
OATP2B1 inhibitior - 0.8454 84.54%
OATP1B1 inhibitior + 0.9415 94.15%
OATP1B3 inhibitior + 0.9408 94.08%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.9628 96.28%
P-glycoprotein inhibitior - 0.9681 96.81%
P-glycoprotein substrate - 0.9197 91.97%
CYP3A4 substrate - 0.5829 58.29%
CYP2C9 substrate - 0.8090 80.90%
CYP2D6 substrate - 0.7021 70.21%
CYP3A4 inhibition - 0.9497 94.97%
CYP2C9 inhibition - 0.9205 92.05%
CYP2C19 inhibition - 0.8890 88.90%
CYP2D6 inhibition - 0.9389 93.89%
CYP1A2 inhibition - 0.8925 89.25%
CYP2C8 inhibition - 0.9700 97.00%
CYP inhibitory promiscuity - 0.8599 85.99%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8228 82.28%
Carcinogenicity (trinary) Non-required 0.6218 62.18%
Eye corrosion - 0.6352 63.52%
Eye irritation + 0.9567 95.67%
Skin irritation + 0.6696 66.96%
Skin corrosion - 0.8488 84.88%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6055 60.55%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation + 0.8162 81.62%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity + 0.5070 50.70%
Acute Oral Toxicity (c) III 0.7748 77.48%
Estrogen receptor binding - 0.9058 90.58%
Androgen receptor binding - 0.8170 81.70%
Thyroid receptor binding - 0.8278 82.78%
Glucocorticoid receptor binding - 0.7534 75.34%
Aromatase binding - 0.8608 86.08%
PPAR gamma - 0.7922 79.22%
Honey bee toxicity - 0.9282 92.82%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.7597 75.97%

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 94.39% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.29% 96.09%
CHEMBL1951 P21397 Monoamine oxidase A 90.62% 91.49%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.04% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.56% 97.09%
CHEMBL2581 P07339 Cathepsin D 82.69% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.64% 100.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.88% 92.94%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.65% 95.89%
CHEMBL226 P30542 Adenosine A1 receptor 81.42% 95.93%

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.
Cymbopogon schoenanthus

Cross-Links

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PubChem 564552
LOTUS LTS0114947
wikiData Q105228114