3-Oxo-3-(((2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-methoxytetrahydro-2H-pyran-2-yl)methoxy)propanoic acid

Details

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Internal ID 2f8a6ae1-fb1f-4405-a208-015677e3eb00
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > O-glycosyl compounds
IUPAC Name 3-oxo-3-[[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-methoxyoxan-2-yl]methoxy]propanoic acid
SMILES (Canonical) COC1C(C(C(C(O1)COC(=O)CC(=O)O)O)O)O
SMILES (Isomeric) CO[C@H]1[C@@H]([C@H]([C@@H]([C@H](O1)COC(=O)CC(=O)O)O)O)O
InChI InChI=1S/C10H16O9/c1-17-10-9(16)8(15)7(14)4(19-10)3-18-6(13)2-5(11)12/h4,7-10,14-16H,2-3H2,1H3,(H,11,12)/t4-,7-,8+,9-,10-/m1/s1
InChI Key JHZXMTZJWGLQRP-PMZAMSJHSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16O9
Molecular Weight 280.23 g/mol
Exact Mass 280.07943208 g/mol
Topological Polar Surface Area (TPSA) 143.00 Ų
XlogP -2.30
Atomic LogP (AlogP) -2.54
H-Bond Acceptor 8
H-Bond Donor 4
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-Oxo-3-(((2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-methoxytetrahydro-2H-pyran-2-yl)methoxy)propanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.8929 89.29%
Caco-2 - 0.9283 92.83%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.7848 78.48%
OATP2B1 inhibitior - 0.8551 85.51%
OATP1B1 inhibitior + 0.9207 92.07%
OATP1B3 inhibitior + 0.9492 94.92%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8990 89.90%
P-glycoprotein inhibitior - 0.9132 91.32%
P-glycoprotein substrate - 0.9619 96.19%
CYP3A4 substrate - 0.5136 51.36%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8824 88.24%
CYP3A4 inhibition - 0.9541 95.41%
CYP2C9 inhibition - 0.9608 96.08%
CYP2C19 inhibition - 0.9545 95.45%
CYP2D6 inhibition - 0.9399 93.99%
CYP1A2 inhibition - 0.9674 96.74%
CYP2C8 inhibition - 0.8920 89.20%
CYP inhibitory promiscuity - 0.9878 98.78%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.7408 74.08%
Eye corrosion - 0.9798 97.98%
Eye irritation - 0.9037 90.37%
Skin irritation - 0.8479 84.79%
Skin corrosion - 0.9384 93.84%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7348 73.48%
Micronuclear - 0.5667 56.67%
Hepatotoxicity - 0.6375 63.75%
skin sensitisation - 0.9400 94.00%
Respiratory toxicity - 0.7667 76.67%
Reproductive toxicity - 0.6000 60.00%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity - 0.7620 76.20%
Acute Oral Toxicity (c) III 0.6417 64.17%
Estrogen receptor binding - 0.6571 65.71%
Androgen receptor binding - 0.8751 87.51%
Thyroid receptor binding - 0.6884 68.84%
Glucocorticoid receptor binding - 0.7265 72.65%
Aromatase binding - 0.8096 80.96%
PPAR gamma - 0.6085 60.85%
Honey bee toxicity - 0.9197 91.97%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity - 0.7421 74.21%

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 96.76% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.19% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.76% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.70% 99.17%
CHEMBL4040 P28482 MAP kinase ERK2 87.22% 83.82%
CHEMBL5255 O00206 Toll-like receptor 4 87.14% 92.50%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 85.49% 94.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.75% 96.00%
CHEMBL221 P23219 Cyclooxygenase-1 84.00% 90.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.95% 96.95%
CHEMBL2581 P07339 Cathepsin D 80.30% 98.95%
CHEMBL3437 Q16853 Amine oxidase, copper containing 80.26% 94.00%

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.
Gynostemma pentaphyllum
Rumex obtusifolius

Cross-Links

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PubChem 5319243
NPASS NPC100973
LOTUS LTS0215072
wikiData Q105128856