2,3,4,6-Tetra-O-methylhexose

Details

Top
Internal ID 495af60d-2ec7-403a-aac4-48db4812859a
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Monosaccharides > Hexoses
IUPAC Name 5-hydroxy-2,3,4,6-tetramethoxyhexanal
SMILES (Canonical) COCC(C(C(C(C=O)OC)OC)OC)O
SMILES (Isomeric) COCC(C(C(C(C=O)OC)OC)OC)O
InChI InChI=1S/C10H20O6/c1-13-6-7(12)9(15-3)10(16-4)8(5-11)14-2/h5,7-10,12H,6H2,1-4H3
InChI Key LMWNQPUYOLOJQP-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C10H20O6
Molecular Weight 236.26 g/mol
Exact Mass 236.12598835 g/mol
Topological Polar Surface Area (TPSA) 74.20 Ų
XlogP -1.30
Atomic LogP (AlogP) -0.76
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 9

Synonyms

Top
LMWNQPUYOLOJQP-UHFFFAOYSA-N
2,3,4,6-Tetra-O-methylhexose #
2,3,4,6-Tetra-O-methyl-D-mannose, >=95%

2D Structure

Top
2D Structure of 2,3,4,6-Tetra-O-methylhexose

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9465 94.65%
Caco-2 + 0.6559 65.59%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.7459 74.59%
OATP2B1 inhibitior - 0.8563 85.63%
OATP1B1 inhibitior + 0.9103 91.03%
OATP1B3 inhibitior + 0.9385 93.85%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9335 93.35%
P-glycoprotein inhibitior - 0.9228 92.28%
P-glycoprotein substrate - 0.9401 94.01%
CYP3A4 substrate - 0.5801 58.01%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7698 76.98%
CYP3A4 inhibition - 0.9198 91.98%
CYP2C9 inhibition - 0.9645 96.45%
CYP2C19 inhibition - 0.9158 91.58%
CYP2D6 inhibition - 0.9511 95.11%
CYP1A2 inhibition - 0.9355 93.55%
CYP2C8 inhibition - 0.9586 95.86%
CYP inhibitory promiscuity - 0.9712 97.12%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.6200 62.00%
Carcinogenicity (trinary) Non-required 0.7401 74.01%
Eye corrosion - 0.6109 61.09%
Eye irritation - 0.8687 86.87%
Skin irritation - 0.8577 85.77%
Skin corrosion - 0.9557 95.57%
Ames mutagenesis - 0.5000 50.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4675 46.75%
Micronuclear - 0.8926 89.26%
Hepatotoxicity - 0.7657 76.57%
skin sensitisation - 0.5744 57.44%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity - 0.7000 70.00%
Mitochondrial toxicity - 0.8750 87.50%
Nephrotoxicity + 0.5516 55.16%
Acute Oral Toxicity (c) III 0.6562 65.62%
Estrogen receptor binding - 0.5752 57.52%
Androgen receptor binding - 0.8295 82.95%
Thyroid receptor binding + 0.6278 62.78%
Glucocorticoid receptor binding - 0.6646 66.46%
Aromatase binding - 0.8617 86.17%
PPAR gamma - 0.7988 79.88%
Honey bee toxicity - 0.6602 66.02%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.8400 84.00%
Fish aquatic toxicity - 0.9381 93.81%

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 94.84% 96.09%
CHEMBL2581 P07339 Cathepsin D 88.78% 98.95%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 83.67% 89.34%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 83.03% 97.29%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.88% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.14% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 81.39% 94.73%

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.
Medicago sativa

Cross-Links

Top
PubChem 538740
LOTUS LTS0133982
wikiData Q105154167