(2S,3R,4R,5R)-3-(hydroxymethyl)-2,5-dimethoxyoxolane-3,4-diol

Details

Top
Internal ID 8881c96e-f60c-432e-8242-2db39eab1589
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > O-glycosyl compounds
IUPAC Name (2S,3R,4R,5R)-3-(hydroxymethyl)-2,5-dimethoxyoxolane-3,4-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H14O6/c1-11-5-4(9)7(10,3-8)6(12-2)13-5/h4-6,8-10H,3H2,1-2H3/t4-,5+,6-,7+/m0/s1
InChI Key RZWXIHZVIDLDSL-BNHYGAARSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C7H14O6
Molecular Weight 194.18 g/mol
Exact Mass 194.07903816 g/mol
Topological Polar Surface Area (TPSA) 88.40 Ų
XlogP -1.70
Atomic LogP (AlogP) -1.95
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (2S,3R,4R,5R)-3-(hydroxymethyl)-2,5-dimethoxyoxolane-3,4-diol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.6050 60.50%
Caco-2 - 0.7982 79.82%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.5789 57.89%
OATP2B1 inhibitior - 0.8551 85.51%
OATP1B1 inhibitior + 0.9224 92.24%
OATP1B3 inhibitior + 0.9448 94.48%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9691 96.91%
P-glycoprotein inhibitior - 0.9498 94.98%
P-glycoprotein substrate - 0.9437 94.37%
CYP3A4 substrate - 0.5794 57.94%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8470 84.70%
CYP3A4 inhibition - 0.9513 95.13%
CYP2C9 inhibition - 0.9321 93.21%
CYP2C19 inhibition - 0.9341 93.41%
CYP2D6 inhibition - 0.9566 95.66%
CYP1A2 inhibition - 0.8841 88.41%
CYP2C8 inhibition - 0.9471 94.71%
CYP inhibitory promiscuity - 0.9469 94.69%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6582 65.82%
Eye corrosion - 0.9866 98.66%
Eye irritation - 0.7637 76.37%
Skin irritation - 0.8223 82.23%
Skin corrosion - 0.9463 94.63%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6996 69.96%
Micronuclear - 0.7167 71.67%
Hepatotoxicity - 0.5442 54.42%
skin sensitisation - 0.8554 85.54%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity - 0.6444 64.44%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity + 0.5816 58.16%
Acute Oral Toxicity (c) III 0.5626 56.26%
Estrogen receptor binding - 0.5484 54.84%
Androgen receptor binding - 0.7441 74.41%
Thyroid receptor binding - 0.5342 53.42%
Glucocorticoid receptor binding - 0.7970 79.70%
Aromatase binding - 0.8195 81.95%
PPAR gamma - 0.6602 66.02%
Honey bee toxicity - 0.9080 90.80%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity - 0.9399 93.99%

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 94.60% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.36% 91.11%
CHEMBL226 P30542 Adenosine A1 receptor 84.40% 95.93%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.60% 96.95%
CHEMBL2996 Q05655 Protein kinase C delta 82.52% 97.79%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 80.36% 86.92%

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.
Hemerocallis fulva

Cross-Links

Top
PubChem 162851608
LOTUS LTS0150678
wikiData Q105248682