(3s,4s,6r)-p-menth-1-ene-3,6-diol 6-O-beta-d-glucopyranoside

Details

Top
Internal ID eefc7b1f-e20a-4902-bd60-d80ab9b6e25a
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides
IUPAC Name (2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(1R,4S,5S)-4-hydroxy-2-methyl-5-propan-2-ylcyclohex-2-en-1-yl]oxyoxane-3,4,5-triol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H28O7/c1-7(2)9-5-11(8(3)4-10(9)18)22-16-15(21)14(20)13(19)12(6-17)23-16/h4,7,9-21H,5-6H2,1-3H3/t9-,10+,11+,12+,13+,14-,15+,16+/m0/s1
InChI Key MJSBJGMRWXOXGY-GIIOKPNBSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C16H28O7
Molecular Weight 332.39 g/mol
Exact Mass 332.18350323 g/mol
Topological Polar Surface Area (TPSA) 120.00 Ų
XlogP -0.60
Atomic LogP (AlogP) -0.85
H-Bond Acceptor 7
H-Bond Donor 5
Rotatable Bonds 4

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (3s,4s,6r)-p-menth-1-ene-3,6-diol 6-O-beta-d-glucopyranoside

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5763 57.63%
Caco-2 - 0.8169 81.69%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.9000 90.00%
Subcellular localzation Mitochondria 0.7975 79.75%
OATP2B1 inhibitior - 0.8587 85.87%
OATP1B1 inhibitior + 0.8931 89.31%
OATP1B3 inhibitior + 0.9426 94.26%
MATE1 inhibitior - 0.9612 96.12%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9666 96.66%
P-glycoprotein inhibitior - 0.8732 87.32%
P-glycoprotein substrate - 0.8934 89.34%
CYP3A4 substrate + 0.5130 51.30%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8395 83.95%
CYP3A4 inhibition - 0.9237 92.37%
CYP2C9 inhibition - 0.8324 83.24%
CYP2C19 inhibition - 0.8073 80.73%
CYP2D6 inhibition - 0.8614 86.14%
CYP1A2 inhibition - 0.8309 83.09%
CYP2C8 inhibition - 0.8895 88.95%
CYP inhibitory promiscuity - 0.7019 70.19%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.7367 73.67%
Eye corrosion - 0.9889 98.89%
Eye irritation - 0.9825 98.25%
Skin irritation - 0.8190 81.90%
Skin corrosion - 0.9610 96.10%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4280 42.80%
Micronuclear - 0.7241 72.41%
Hepatotoxicity - 0.7395 73.95%
skin sensitisation - 0.8570 85.70%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity - 0.6499 64.99%
Acute Oral Toxicity (c) III 0.6102 61.02%
Estrogen receptor binding - 0.6463 64.63%
Androgen receptor binding - 0.7175 71.75%
Thyroid receptor binding + 0.5525 55.25%
Glucocorticoid receptor binding - 0.6517 65.17%
Aromatase binding - 0.6711 67.11%
PPAR gamma + 0.5899 58.99%
Honey bee toxicity - 0.8113 81.13%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity + 0.7546 75.46%

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 94.31% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.33% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.38% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.21% 97.09%
CHEMBL2581 P07339 Cathepsin D 89.66% 98.95%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 85.96% 86.92%
CHEMBL3401 O75469 Pregnane X receptor 85.81% 94.73%
CHEMBL2996 Q05655 Protein kinase C delta 83.13% 97.79%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.53% 95.89%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.41% 99.17%

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.
Ageratina tinifolia

Cross-Links

Top
PubChem 21630977
LOTUS LTS0271374
wikiData Q105165625