Uroterpenol

Details

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Internal ID 4aa2d772-17f4-4798-9cfe-15fff8bd8eb8
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Menthane monoterpenoids
IUPAC Name 2-(4-methylcyclohex-3-en-1-yl)propane-1,2-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H18O2/c1-8-3-5-9(6-4-8)10(2,12)7-11/h3,9,11-12H,4-7H2,1-2H3
InChI Key ZJALAEQNHJQSTN-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C10H18O2
Molecular Weight 170.25 g/mol
Exact Mass 170.130679813 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 0.80
Atomic LogP (AlogP) 1.48
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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6252-35-3
2-(4-methylcyclohex-3-en-1-yl)propane-1,2-diol
4-Menth-1-ene-8,9-diol
CCRIS 7134
2-(4-Methyl-3-cyclohexen-1-yl)propane-1,2-diol
EINECS 228-373-7
P-menth-1-ene-8,9-diol
p-Mentha-1-en-8,9-diol
Para-menth-1-ene-8,9-diol
SCHEMBL8743853
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Uroterpenol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9802 98.02%
Caco-2 + 0.7383 73.83%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.5710 57.10%
OATP2B1 inhibitior - 0.8408 84.08%
OATP1B1 inhibitior + 0.9555 95.55%
OATP1B3 inhibitior + 0.9449 94.49%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.8185 81.85%
P-glycoprotein inhibitior - 0.9869 98.69%
P-glycoprotein substrate - 0.8999 89.99%
CYP3A4 substrate - 0.5774 57.74%
CYP2C9 substrate - 0.7857 78.57%
CYP2D6 substrate - 0.7985 79.85%
CYP3A4 inhibition - 0.7184 71.84%
CYP2C9 inhibition - 0.7955 79.55%
CYP2C19 inhibition - 0.8411 84.11%
CYP2D6 inhibition - 0.8770 87.70%
CYP1A2 inhibition - 0.7711 77.11%
CYP2C8 inhibition - 0.8229 82.29%
CYP inhibitory promiscuity - 0.8738 87.38%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.6744 67.44%
Eye corrosion - 0.9493 94.93%
Eye irritation - 0.5230 52.30%
Skin irritation - 0.7753 77.53%
Skin corrosion - 0.9848 98.48%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6377 63.77%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.5469 54.69%
skin sensitisation + 0.6764 67.64%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity - 0.6333 63.33%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity - 0.6599 65.99%
Acute Oral Toxicity (c) III 0.7549 75.49%
Estrogen receptor binding - 0.9384 93.84%
Androgen receptor binding - 0.8204 82.04%
Thyroid receptor binding - 0.8119 81.19%
Glucocorticoid receptor binding - 0.7887 78.87%
Aromatase binding - 0.8534 85.34%
PPAR gamma - 0.8981 89.81%
Honey bee toxicity - 0.9764 97.64%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.8218 82.18%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 98.24% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.49% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.03% 91.11%
CHEMBL2581 P07339 Cathepsin D 89.34% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.61% 97.09%
CHEMBL3401 O75469 Pregnane X receptor 81.57% 94.73%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 80.53% 90.93%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.32% 93.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.29% 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.
There are no matching plants.

Cross-Links

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PubChem 93024
LOTUS LTS0169043
wikiData Q82963451