(2S,3R,4S,5R)-3,4-dimethoxyoxane-2,5-diol

Details

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Internal ID 789a5c5e-4d31-4feb-9fcc-5c54b0dfcd30
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Monosaccharides > Pentoses
IUPAC Name (2S,3R,4S,5R)-3,4-dimethoxyoxane-2,5-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H14O5/c1-10-5-4(8)3-12-7(9)6(5)11-2/h4-9H,3H2,1-2H3/t4-,5+,6-,7+/m1/s1
InChI Key BAPQKKJFHFYDMJ-UCROKIRRSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C7H14O5
Molecular Weight 178.18 g/mol
Exact Mass 178.08412354 g/mol
Topological Polar Surface Area (TPSA) 68.20 Ų
XlogP -1.40
Atomic LogP (AlogP) -1.27
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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GlyTouCan:G18948IO
G18948IO
(2S,3R,4S,5R)-3,4-dimethoxyoxane-2,5-diol
SCHEMBL7155624

2D Structure

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2D Structure of (2S,3R,4S,5R)-3,4-dimethoxyoxane-2,5-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6541 65.41%
Caco-2 - 0.7686 76.86%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.7396 73.96%
OATP2B1 inhibitior - 0.8531 85.31%
OATP1B1 inhibitior + 0.9405 94.05%
OATP1B3 inhibitior + 0.9368 93.68%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9716 97.16%
P-glycoprotein inhibitior - 0.9669 96.69%
P-glycoprotein substrate - 0.9403 94.03%
CYP3A4 substrate - 0.5676 56.76%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8209 82.09%
CYP3A4 inhibition - 0.9835 98.35%
CYP2C9 inhibition - 0.9762 97.62%
CYP2C19 inhibition - 0.9613 96.13%
CYP2D6 inhibition - 0.9543 95.43%
CYP1A2 inhibition - 0.9501 95.01%
CYP2C8 inhibition - 0.9713 97.13%
CYP inhibitory promiscuity - 0.9687 96.87%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6973 69.73%
Eye corrosion - 0.9600 96.00%
Eye irritation - 0.6334 63.34%
Skin irritation - 0.8142 81.42%
Skin corrosion - 0.9527 95.27%
Ames mutagenesis + 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6629 66.29%
Micronuclear - 0.6000 60.00%
Hepatotoxicity - 0.7250 72.50%
skin sensitisation - 0.9039 90.39%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity - 0.5333 53.33%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity - 0.7000 70.00%
Acute Oral Toxicity (c) III 0.6918 69.18%
Estrogen receptor binding - 0.6945 69.45%
Androgen receptor binding - 0.8683 86.83%
Thyroid receptor binding - 0.5966 59.66%
Glucocorticoid receptor binding - 0.8118 81.18%
Aromatase binding - 0.7907 79.07%
PPAR gamma - 0.7958 79.58%
Honey bee toxicity - 0.8273 82.73%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.5903 59.03%
Fish aquatic toxicity - 0.9324 93.24%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.04% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.38% 91.11%
CHEMBL4040 P28482 MAP kinase ERK2 84.60% 83.82%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.87% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.30% 97.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.18% 92.94%

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.
Brassica napus

Cross-Links

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PubChem 13932295
LOTUS LTS0098480
wikiData Q104922350