2,3,4-Tri-O-methylhexose

Details

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Internal ID d45483f0-a17a-45e3-b4a1-0d70559979ba
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name 5,6-dihydroxy-2,3,4-trimethoxyhexanal
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H18O6/c1-13-7(5-11)9(15-3)8(14-2)6(12)4-10/h5-10,12H,4H2,1-3H3
InChI Key LOODZAPIPITKBN-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C9H18O6
Molecular Weight 222.24 g/mol
Exact Mass 222.11033829 g/mol
Topological Polar Surface Area (TPSA) 85.20 Ų
XlogP -1.80
Atomic LogP (AlogP) -1.42
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 8

Synonyms

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LOODZAPIPITKBN-UHFFFAOYSA-N

2D Structure

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2D Structure of 2,3,4-Tri-O-methylhexose

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8759 87.59%
Caco-2 - 0.6696 66.96%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.7582 75.82%
OATP2B1 inhibitior - 0.8556 85.56%
OATP1B1 inhibitior + 0.9202 92.02%
OATP1B3 inhibitior + 0.9334 93.34%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9700 97.00%
P-glycoprotein inhibitior - 0.9520 95.20%
P-glycoprotein substrate - 0.9478 94.78%
CYP3A4 substrate - 0.6194 61.94%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8017 80.17%
CYP3A4 inhibition - 0.8501 85.01%
CYP2C9 inhibition - 0.9469 94.69%
CYP2C19 inhibition - 0.9146 91.46%
CYP2D6 inhibition - 0.9432 94.32%
CYP1A2 inhibition - 0.9188 91.88%
CYP2C8 inhibition - 0.9699 96.99%
CYP inhibitory promiscuity - 0.9577 95.77%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.6600 66.00%
Carcinogenicity (trinary) Non-required 0.7859 78.59%
Eye corrosion - 0.8717 87.17%
Eye irritation - 0.9390 93.90%
Skin irritation - 0.8526 85.26%
Skin corrosion - 0.9631 96.31%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4474 44.74%
Micronuclear - 0.9000 90.00%
Hepatotoxicity - 0.7458 74.58%
skin sensitisation - 0.8125 81.25%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity - 0.8111 81.11%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity + 0.5478 54.78%
Acute Oral Toxicity (c) III 0.5314 53.14%
Estrogen receptor binding - 0.6121 61.21%
Androgen receptor binding - 0.8070 80.70%
Thyroid receptor binding + 0.5343 53.43%
Glucocorticoid receptor binding - 0.6243 62.43%
Aromatase binding - 0.8209 82.09%
PPAR gamma - 0.8386 83.86%
Honey bee toxicity - 0.7265 72.65%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.8300 83.00%
Fish aquatic toxicity - 0.9702 97.02%

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 94.22% 96.09%
CHEMBL2581 P07339 Cathepsin D 89.15% 98.95%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 86.00% 97.29%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.54% 85.14%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 82.88% 86.92%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.47% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.51% 96.00%

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.
Betula papyrifera
Medicago sativa

Cross-Links

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PubChem 538775
LOTUS LTS0265350
wikiData Q105154830