(2S,3R,4S,5R)-2,3,4-trihydroxy-5-methoxy-6-oxohexanoic acid

Details

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Internal ID e0352600-acd1-4766-9a3f-5b840ec15b18
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Sugar acids and derivatives > Glucuronic acid derivatives
IUPAC Name (2S,3R,4S,5R)-2,3,4-trihydroxy-5-methoxy-6-oxohexanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H12O7/c1-14-3(2-8)4(9)5(10)6(11)7(12)13/h2-6,9-11H,1H3,(H,12,13)/t3-,4+,5+,6-/m0/s1
InChI Key HCQISUFWFYMWKK-KCDKBNATSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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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

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There are no found synonyms.

2D Structure

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2D Structure of (2S,3R,4S,5R)-2,3,4-trihydroxy-5-methoxy-6-oxohexanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.4775 47.75%
Caco-2 - 0.9033 90.33%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.7682 76.82%
OATP2B1 inhibitior - 0.8612 86.12%
OATP1B1 inhibitior + 0.8928 89.28%
OATP1B3 inhibitior + 0.9641 96.41%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9747 97.47%
P-glycoprotein inhibitior - 0.9660 96.60%
P-glycoprotein substrate - 0.9753 97.53%
CYP3A4 substrate - 0.6251 62.51%
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 - 0.9425 94.25%
CYP inhibitory promiscuity - 0.9807 98.07%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) - 0.6196 61.96%
Carcinogenicity (trinary) Non-required 0.7638 76.38%
Eye corrosion - 0.9556 95.56%
Eye irritation - 0.9642 96.42%
Skin irritation - 0.6774 67.74%
Skin corrosion - 0.8302 83.02%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8278 82.78%
Micronuclear - 0.7400 74.00%
Hepatotoxicity - 0.5407 54.07%
skin sensitisation - 0.8987 89.87%
Respiratory toxicity - 0.7667 76.67%
Reproductive toxicity - 0.8444 84.44%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity + 0.5696 56.96%
Acute Oral Toxicity (c) III 0.7238 72.38%
Estrogen receptor binding - 0.7386 73.86%
Androgen receptor binding - 0.8404 84.04%
Thyroid receptor binding - 0.6518 65.18%
Glucocorticoid receptor binding - 0.6863 68.63%
Aromatase binding - 0.8189 81.89%
PPAR gamma - 0.7145 71.45%
Honey bee toxicity - 0.7719 77.19%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.8600 86.00%
Fish aquatic toxicity - 0.7256 72.56%

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 92.15% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.44% 85.14%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.33% 99.17%
CHEMBL340 P08684 Cytochrome P450 3A4 84.21% 91.19%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.56% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.75% 94.45%
CHEMBL2581 P07339 Cathepsin D 80.13% 98.95%

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.
Sterculia setigera

Cross-Links

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PubChem 87205204
LOTUS LTS0271659
wikiData Q105025919