2-(Hydroxymethyl)-6-(1-hydroxy-2-methylpropan-2-yl)oxyoxane-3,4,5-triol

Details

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Internal ID ad0310a9-07e7-4799-baf0-9bea3fb05854
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > O-glycosyl compounds
IUPAC Name 2-(hydroxymethyl)-6-(1-hydroxy-2-methylpropan-2-yl)oxyoxane-3,4,5-triol
SMILES (Canonical) CC(C)(CO)OC1C(C(C(C(O1)CO)O)O)O
SMILES (Isomeric) CC(C)(CO)OC1C(C(C(C(O1)CO)O)O)O
InChI InChI=1S/C10H20O7/c1-10(2,4-12)17-9-8(15)7(14)6(13)5(3-11)16-9/h5-9,11-15H,3-4H2,1-2H3
InChI Key DRAGHEYLLOEQHM-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H20O7
Molecular Weight 252.26 g/mol
Exact Mass 252.12090297 g/mol
Topological Polar Surface Area (TPSA) 120.00 Ų
XlogP -2.30
Atomic LogP (AlogP) -2.43
H-Bond Acceptor 7
H-Bond Donor 5
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(Hydroxymethyl)-6-(1-hydroxy-2-methylpropan-2-yl)oxyoxane-3,4,5-triol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.9037 90.37%
Caco-2 - 0.8539 85.39%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.8012 80.12%
OATP2B1 inhibitior - 0.8553 85.53%
OATP1B1 inhibitior + 0.9276 92.76%
OATP1B3 inhibitior + 0.9535 95.35%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9581 95.81%
P-glycoprotein inhibitior - 0.9377 93.77%
P-glycoprotein substrate - 0.9738 97.38%
CYP3A4 substrate - 0.5510 55.10%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8487 84.87%
CYP3A4 inhibition - 0.9560 95.60%
CYP2C9 inhibition - 0.8904 89.04%
CYP2C19 inhibition - 0.8945 89.45%
CYP2D6 inhibition - 0.9491 94.91%
CYP1A2 inhibition - 0.9086 90.86%
CYP2C8 inhibition - 0.9399 93.99%
CYP inhibitory promiscuity - 0.9469 94.69%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6190 61.90%
Eye corrosion - 0.9857 98.57%
Eye irritation - 0.9517 95.17%
Skin irritation - 0.8853 88.53%
Skin corrosion - 0.9612 96.12%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7393 73.93%
Micronuclear - 0.8800 88.00%
Hepatotoxicity - 0.7500 75.00%
skin sensitisation - 0.8871 88.71%
Respiratory toxicity - 0.8556 85.56%
Reproductive toxicity - 0.7333 73.33%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity + 0.4670 46.70%
Acute Oral Toxicity (c) III 0.5397 53.97%
Estrogen receptor binding - 0.8078 80.78%
Androgen receptor binding - 0.6663 66.63%
Thyroid receptor binding + 0.6886 68.86%
Glucocorticoid receptor binding - 0.5809 58.09%
Aromatase binding - 0.6430 64.30%
PPAR gamma - 0.7504 75.04%
Honey bee toxicity - 0.8370 83.70%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.8900 89.00%
Fish aquatic toxicity - 0.7539 75.39%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.13% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.85% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.28% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 85.82% 94.73%
CHEMBL226 P30542 Adenosine A1 receptor 85.76% 95.93%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 83.66% 86.92%
CHEMBL2581 P07339 Cathepsin D 83.46% 98.95%
CHEMBL3589 P55263 Adenosine kinase 81.65% 98.05%
CHEMBL218 P21554 Cannabinoid CB1 receptor 80.87% 96.61%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.62% 99.17%

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.
Vachellia sieberiana var. woodii

Cross-Links

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PubChem 163035479
LOTUS LTS0242433
wikiData Q104987314