3-o-Methylglucuronic acid

Details

Top
Internal ID 94d3e385-3d11-4a7c-bdb9-ab652c065264
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Sugar acids and derivatives > Glucuronic acid derivatives
IUPAC Name (2S,3R,4S,5R)-2,3,5-trihydroxy-4-methoxy-6-oxohexanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H12O7/c1-14-6(3(9)2-8)4(10)5(11)7(12)13/h2-6,9-11H,1H3,(H,12,13)/t3-,4+,5-,6+/m0/s1
InChI Key XBWZJBAVAXWBED-BGPJRJDNSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C7H12O7
Molecular Weight 208.17 g/mol
Exact Mass 208.05830272 g/mol
Topological Polar Surface Area (TPSA) 124.00 Ų
XlogP -2.00
Atomic LogP (AlogP) -2.63
H-Bond Acceptor 6
H-Bond Donor 4
Rotatable Bonds 6

Synonyms

Top
SCHEMBL3922086

2D Structure

Top
2D Structure of 3-o-Methylglucuronic acid

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.4775 47.75%
Caco-2 - 0.8960 89.60%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.7682 76.82%
OATP2B1 inhibitior - 0.8595 85.95%
OATP1B1 inhibitior + 0.9284 92.84%
OATP1B3 inhibitior + 0.9641 96.41%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9776 97.76%
P-glycoprotein inhibitior - 0.9638 96.38%
P-glycoprotein substrate - 0.9731 97.31%
CYP3A4 substrate - 0.6002 60.02%
CYP2C9 substrate + 0.5979 59.79%
CYP2D6 substrate - 0.8563 85.63%
CYP3A4 inhibition - 0.9535 95.35%
CYP2C9 inhibition - 0.8614 86.14%
CYP2C19 inhibition - 0.9442 94.42%
CYP2D6 inhibition - 0.9526 95.26%
CYP1A2 inhibition - 0.9289 92.89%
CYP2C8 inhibition - 0.9493 94.93%
CYP inhibitory promiscuity - 0.9807 98.07%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.6196 61.96%
Carcinogenicity (trinary) Non-required 0.7638 76.38%
Eye corrosion - 0.9556 95.56%
Eye irritation - 0.9108 91.08%
Skin irritation - 0.6774 67.74%
Skin corrosion - 0.8302 83.02%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7693 76.93%
Micronuclear - 0.7400 74.00%
Hepatotoxicity - 0.5200 52.00%
skin sensitisation - 0.8987 89.87%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity - 0.8444 84.44%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity + 0.6695 66.95%
Acute Oral Toxicity (c) III 0.7238 72.38%
Estrogen receptor binding - 0.6238 62.38%
Androgen receptor binding - 0.8513 85.13%
Thyroid receptor binding - 0.5071 50.71%
Glucocorticoid receptor binding - 0.5907 59.07%
Aromatase binding - 0.9180 91.80%
PPAR gamma - 0.8105 81.05%
Honey bee toxicity - 0.8388 83.88%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.9200 92.00%
Fish aquatic toxicity - 0.7256 72.56%

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 92.95% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.37% 85.14%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.12% 99.17%
CHEMBL340 P08684 Cytochrome P450 3A4 81.48% 91.19%
CHEMBL2581 P07339 Cathepsin D 81.10% 98.95%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 80.40% 94.08%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.38% 96.00%

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.
Grazielia serrata
Strychnos tomentosa

Cross-Links

Top
PubChem 87595821
NPASS NPC308527