p-Menthane-2,5-diol

Details

Top
Internal ID ac243445-085f-4604-a170-a3a84696acee
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Menthane monoterpenoids
IUPAC Name 2-methyl-5-propan-2-ylcyclohexane-1,4-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H20O2/c1-6(2)8-5-9(11)7(3)4-10(8)12/h6-12H,4-5H2,1-3H3
InChI Key TXISQGBRDPUIBI-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C10H20O2
Molecular Weight 172.26 g/mol
Exact Mass 172.146329876 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 1.90
Atomic LogP (AlogP) 1.41
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

Top
SCHEMBL7043768

2D Structure

Top
2D Structure of p-Menthane-2,5-diol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9957 99.57%
Caco-2 - 0.5696 56.96%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.7497 74.97%
OATP2B1 inhibitior - 0.8423 84.23%
OATP1B1 inhibitior + 0.9646 96.46%
OATP1B3 inhibitior + 0.9539 95.39%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9693 96.93%
P-glycoprotein inhibitior - 0.9715 97.15%
P-glycoprotein substrate - 0.8919 89.19%
CYP3A4 substrate - 0.6455 64.55%
CYP2C9 substrate - 0.8151 81.51%
CYP2D6 substrate - 0.6696 66.96%
CYP3A4 inhibition - 0.8807 88.07%
CYP2C9 inhibition - 0.9171 91.71%
CYP2C19 inhibition - 0.9180 91.80%
CYP2D6 inhibition - 0.9261 92.61%
CYP1A2 inhibition - 0.8055 80.55%
CYP2C8 inhibition - 0.9954 99.54%
CYP inhibitory promiscuity - 0.9519 95.19%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.7313 73.13%
Carcinogenicity (trinary) Non-required 0.7076 70.76%
Eye corrosion - 0.7388 73.88%
Eye irritation + 0.7571 75.71%
Skin irritation - 0.5136 51.36%
Skin corrosion - 0.8899 88.99%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6079 60.79%
Micronuclear - 0.9300 93.00%
Hepatotoxicity + 0.6775 67.75%
skin sensitisation + 0.7981 79.81%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity - 0.5333 53.33%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity - 0.7335 73.35%
Acute Oral Toxicity (c) III 0.8462 84.62%
Estrogen receptor binding - 0.8479 84.79%
Androgen receptor binding - 0.7468 74.68%
Thyroid receptor binding - 0.7424 74.24%
Glucocorticoid receptor binding - 0.8374 83.74%
Aromatase binding - 0.9044 90.44%
PPAR gamma - 0.9131 91.31%
Honey bee toxicity - 0.8648 86.48%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.8465 84.65%

Targets

Top

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 92.97% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.19% 97.25%
CHEMBL2581 P07339 Cathepsin D 85.25% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.09% 97.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.99% 85.14%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 81.57% 97.23%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.34% 94.45%

Plants that contains it

Top
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.
Brickellia chlorolepis

Cross-Links

Top
PubChem 69968972
LOTUS LTS0242233
wikiData Q104197913