3-Methoxy-6-methyloxane-2,5-diol

Details

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Internal ID a45fffa7-41ce-468b-acfe-2d4e5fd82621
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Monosaccharides > Hexoses
IUPAC Name 3-methoxy-6-methyloxane-2,5-diol
SMILES (Canonical) CC1C(CC(C(O1)O)OC)O
SMILES (Isomeric) CC1C(CC(C(O1)O)OC)O
InChI InChI=1S/C7H14O4/c1-4-5(8)3-6(10-2)7(9)11-4/h4-9H,3H2,1-2H3
InChI Key YXOVWOKTOWFVSU-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C7H14O4
Molecular Weight 162.18 g/mol
Exact Mass 162.08920892 g/mol
Topological Polar Surface Area (TPSA) 58.90 Ų
XlogP -0.60
Atomic LogP (AlogP) -0.51
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-Methoxy-6-methyloxane-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 + 0.7899 78.99%
Caco-2 - 0.7634 76.34%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.6743 67.43%
OATP2B1 inhibitior - 0.8529 85.29%
OATP1B1 inhibitior + 0.9545 95.45%
OATP1B3 inhibitior + 0.9398 93.98%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9696 96.96%
P-glycoprotein inhibitior - 0.9699 96.99%
P-glycoprotein substrate - 0.9365 93.65%
CYP3A4 substrate - 0.5515 55.15%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7859 78.59%
CYP3A4 inhibition - 0.9886 98.86%
CYP2C9 inhibition - 0.9844 98.44%
CYP2C19 inhibition - 0.9445 94.45%
CYP2D6 inhibition - 0.9386 93.86%
CYP1A2 inhibition - 0.9620 96.20%
CYP2C8 inhibition - 0.9652 96.52%
CYP inhibitory promiscuity - 0.9808 98.08%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9315 93.15%
Carcinogenicity (trinary) Non-required 0.7099 70.99%
Eye corrosion - 0.9232 92.32%
Eye irritation - 0.7834 78.34%
Skin irritation - 0.6623 66.23%
Skin corrosion - 0.9294 92.94%
Ames mutagenesis + 0.5076 50.76%
Human Ether-a-go-go-Related Gene inhibition - 0.7386 73.86%
Micronuclear - 0.6141 61.41%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation - 0.9053 90.53%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity - 0.5525 55.25%
Acute Oral Toxicity (c) III 0.6551 65.51%
Estrogen receptor binding - 0.8693 86.93%
Androgen receptor binding - 0.8907 89.07%
Thyroid receptor binding - 0.6398 63.98%
Glucocorticoid receptor binding - 0.8187 81.87%
Aromatase binding - 0.8854 88.54%
PPAR gamma - 0.8401 84.01%
Honey bee toxicity - 0.8319 83.19%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity - 0.8651 86.51%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.26% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.24% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.56% 97.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.74% 85.14%
CHEMBL241 Q14432 Phosphodiesterase 3A 82.30% 92.94%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.14% 96.95%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 162934519
LOTUS LTS0082284
wikiData Q105368031