p-Menthane-1,2,3-triol

Details

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Internal ID 2094a271-38ea-400b-8f24-d6b7b2fa2df7
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Menthane monoterpenoids
IUPAC Name 1-methyl-4-propan-2-ylcyclohexane-1,2,3-triol
SMILES (Canonical) CC(C)C1CCC(C(C1O)O)(C)O
SMILES (Isomeric) CC(C)C1CCC(C(C1O)O)(C)O
InChI InChI=1S/C10H20O3/c1-6(2)7-4-5-10(3,13)9(12)8(7)11/h6-9,11-13H,4-5H2,1-3H3
InChI Key NVGQNYUHEDOFOJ-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C10H20O3
Molecular Weight 188.26 g/mol
Exact Mass 188.14124450 g/mol
Topological Polar Surface Area (TPSA) 60.70 Ų
XlogP 0.60
Atomic LogP (AlogP) 0.53
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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1,2,3-trihydroxy-p-menthane
SCHEMBL23829006
NVGQNYUHEDOFOJ-UHFFFAOYSA-N
4-Isopropyl-1-methyl-1,2,3-cyclohexanetriol #
Z2050571702

2D Structure

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2D Structure of p-Menthane-1,2,3-triol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9338 93.38%
Caco-2 - 0.8299 82.99%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.6775 67.75%
OATP2B1 inhibitior - 0.8463 84.63%
OATP1B1 inhibitior + 0.9684 96.84%
OATP1B3 inhibitior + 0.9639 96.39%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.9582 95.82%
P-glycoprotein inhibitior - 0.9694 96.94%
P-glycoprotein substrate - 0.9020 90.20%
CYP3A4 substrate - 0.5633 56.33%
CYP2C9 substrate - 0.8008 80.08%
CYP2D6 substrate - 0.7440 74.40%
CYP3A4 inhibition - 0.8789 87.89%
CYP2C9 inhibition - 0.7490 74.90%
CYP2C19 inhibition - 0.8748 87.48%
CYP2D6 inhibition - 0.9448 94.48%
CYP1A2 inhibition - 0.8332 83.32%
CYP2C8 inhibition - 0.9799 97.99%
CYP inhibitory promiscuity - 0.9622 96.22%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.6217 62.17%
Eye corrosion - 0.9552 95.52%
Eye irritation + 0.6944 69.44%
Skin irritation + 0.5965 59.65%
Skin corrosion - 0.7537 75.37%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6249 62.49%
Micronuclear - 0.9100 91.00%
Hepatotoxicity - 0.5572 55.72%
skin sensitisation + 0.5512 55.12%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity + 0.5111 51.11%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity - 0.6210 62.10%
Acute Oral Toxicity (c) III 0.7833 78.33%
Estrogen receptor binding - 0.8375 83.75%
Androgen receptor binding - 0.7327 73.27%
Thyroid receptor binding - 0.6318 63.18%
Glucocorticoid receptor binding - 0.7928 79.28%
Aromatase binding - 0.8753 87.53%
PPAR gamma - 0.8418 84.18%
Honey bee toxicity - 0.9399 93.99%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity - 0.4252 42.52%

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 94.78% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.69% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.45% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 89.66% 90.17%
CHEMBL226 P30542 Adenosine A1 receptor 87.79% 95.93%
CHEMBL2581 P07339 Cathepsin D 87.25% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.70% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.69% 95.89%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.02% 97.09%
CHEMBL1937 Q92769 Histone deacetylase 2 82.60% 94.75%

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.
Garcinia intermedia
Mentha arvensis
Mentha canadensis

Cross-Links

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PubChem 539044
NPASS NPC295631
LOTUS LTS0006099
wikiData Q105194846