6-O-alpha-D-ribosyl-8-O-methylasperentin

Details

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Internal ID 52f01897-0240-4b03-b6d8-3d108880eb19
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > Phenolic glycosides
IUPAC Name (3R)-6-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-8-methoxy-3-[[(2R,6S)-6-methyloxan-2-yl]methyl]-3,4-dihydroisochromen-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H30O9/c1-11-4-3-5-13(28-11)8-14-6-12-7-15(9-16(27-2)18(12)21(26)29-14)30-22-20(25)19(24)17(10-23)31-22/h7,9,11,13-14,17,19-20,22-25H,3-6,8,10H2,1-2H3/t11-,13+,14+,17+,19+,20+,22-/m0/s1
InChI Key YWXLVYJTSKDZPJ-AMUPPJPJSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C22H30O9
Molecular Weight 438.50 g/mol
Exact Mass 438.18898253 g/mol
Topological Polar Surface Area (TPSA) 124.00 Ų
XlogP 1.90
Atomic LogP (AlogP) 0.94
H-Bond Acceptor 9
H-Bond Donor 3
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6-O-alpha-D-ribosyl-8-O-methylasperentin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7367 73.67%
Caco-2 - 0.6990 69.90%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.7838 78.38%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8574 85.74%
OATP1B3 inhibitior + 0.9303 93.03%
MATE1 inhibitior - 0.8812 88.12%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.7427 74.27%
P-glycoprotein inhibitior - 0.6199 61.99%
P-glycoprotein substrate - 0.7183 71.83%
CYP3A4 substrate + 0.6373 63.73%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8558 85.58%
CYP3A4 inhibition - 0.7554 75.54%
CYP2C9 inhibition - 0.8816 88.16%
CYP2C19 inhibition - 0.7891 78.91%
CYP2D6 inhibition - 0.8809 88.09%
CYP1A2 inhibition - 0.6352 63.52%
CYP2C8 inhibition - 0.7530 75.30%
CYP inhibitory promiscuity - 0.8009 80.09%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.7087 70.87%
Eye corrosion - 0.9915 99.15%
Eye irritation - 0.9532 95.32%
Skin irritation - 0.7870 78.70%
Skin corrosion - 0.9526 95.26%
Ames mutagenesis - 0.6140 61.40%
Human Ether-a-go-go-Related Gene inhibition - 0.4241 42.41%
Micronuclear - 0.8300 83.00%
Hepatotoxicity - 0.6875 68.75%
skin sensitisation - 0.8774 87.74%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity + 0.4866 48.66%
Acute Oral Toxicity (c) III 0.4364 43.64%
Estrogen receptor binding + 0.6904 69.04%
Androgen receptor binding - 0.5525 55.25%
Thyroid receptor binding - 0.6595 65.95%
Glucocorticoid receptor binding + 0.7603 76.03%
Aromatase binding - 0.5612 56.12%
PPAR gamma - 0.5428 54.28%
Honey bee toxicity - 0.8024 80.24%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9552 95.52%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.54% 91.11%
CHEMBL2581 P07339 Cathepsin D 97.03% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.19% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.93% 95.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 93.54% 95.89%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.85% 97.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.72% 85.14%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 92.20% 96.21%
CHEMBL220 P22303 Acetylcholinesterase 91.20% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.10% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.00% 94.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.59% 96.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.29% 89.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 87.18% 91.07%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 84.82% 97.14%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 84.65% 95.89%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 84.42% 86.92%
CHEMBL3401 O75469 Pregnane X receptor 84.30% 94.73%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.99% 92.62%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.72% 92.94%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 81.36% 94.80%
CHEMBL4581 P52732 Kinesin-like protein 1 81.25% 93.18%
CHEMBL5203 P33316 dUTP pyrophosphatase 80.88% 99.18%
CHEMBL5255 O00206 Toll-like receptor 4 80.07% 92.50%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 139586584
LOTUS LTS0245305
wikiData Q77509752