Paeonol-(apio-beta-furanosyl(1-6)glucopyranoside)

Details

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Internal ID 9b5b81a5-d9bb-4f46-b8c8-89fe52e12d78
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > Phenolic glycosides
IUPAC Name 1-[2-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-4-methoxyphenyl]ethanone
SMILES (Canonical) CC(=O)C1=C(C=C(C=C1)OC)OC2C(C(C(C(O2)COC3C(C(CO3)(CO)O)O)O)O)O
SMILES (Isomeric) CC(=O)C1=C(C=C(C=C1)OC)O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO[C@H]3[C@@H]([C@](CO3)(CO)O)O)O)O)O
InChI InChI=1S/C20H28O12/c1-9(22)11-4-3-10(28-2)5-12(11)31-18-16(25)15(24)14(23)13(32-18)6-29-19-17(26)20(27,7-21)8-30-19/h3-5,13-19,21,23-27H,6-8H2,1-2H3/t13-,14-,15+,16-,17+,18-,19-,20-/m1/s1
InChI Key IRLNKOAURQPXIQ-LTRJMQNCSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H28O12
Molecular Weight 460.40 g/mol
Exact Mass 460.15807632 g/mol
Topological Polar Surface Area (TPSA) 185.00 Ų
XlogP -2.40
Atomic LogP (AlogP) -2.46
H-Bond Acceptor 12
H-Bond Donor 6
Rotatable Bonds 8

Synonyms

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Paeonol-(apio-beta-furanosyl(1-6)glucopyranoside)
BDBM50310720
AKOS037514888

2D Structure

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2D Structure of Paeonol-(apio-beta-furanosyl(1-6)glucopyranoside)

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.6373 63.73%
Caco-2 - 0.8389 83.89%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.7185 71.85%
OATP2B1 inhibitior - 0.8602 86.02%
OATP1B1 inhibitior + 0.9290 92.90%
OATP1B3 inhibitior + 0.9529 95.29%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.4918 49.18%
P-glycoprotein inhibitior - 0.6367 63.67%
P-glycoprotein substrate - 0.6341 63.41%
CYP3A4 substrate + 0.6124 61.24%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8493 84.93%
CYP3A4 inhibition - 0.8643 86.43%
CYP2C9 inhibition - 0.8995 89.95%
CYP2C19 inhibition - 0.8725 87.25%
CYP2D6 inhibition - 0.9146 91.46%
CYP1A2 inhibition - 0.8826 88.26%
CYP2C8 inhibition - 0.5654 56.54%
CYP inhibitory promiscuity - 0.8401 84.01%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6440 64.40%
Eye corrosion - 0.9913 99.13%
Eye irritation - 0.9506 95.06%
Skin irritation - 0.8288 82.88%
Skin corrosion - 0.9542 95.42%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6497 64.97%
Micronuclear - 0.6126 61.26%
Hepatotoxicity - 0.6958 69.58%
skin sensitisation - 0.8353 83.53%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity + 0.4590 45.90%
Acute Oral Toxicity (c) III 0.6940 69.40%
Estrogen receptor binding + 0.8302 83.02%
Androgen receptor binding - 0.6005 60.05%
Thyroid receptor binding - 0.4933 49.33%
Glucocorticoid receptor binding + 0.5418 54.18%
Aromatase binding + 0.6764 67.64%
PPAR gamma + 0.7740 77.40%
Honey bee toxicity - 0.8519 85.19%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.7300 73.00%
Fish aquatic toxicity - 0.4321 43.21%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.27% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.83% 96.09%
CHEMBL3714130 P46095 G-protein coupled receptor 6 93.58% 97.36%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.23% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.61% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.49% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 90.01% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.23% 86.33%
CHEMBL4208 P20618 Proteasome component C5 88.95% 90.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.89% 95.89%
CHEMBL241 Q14432 Phosphodiesterase 3A 87.00% 92.94%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 86.01% 91.07%
CHEMBL226 P30542 Adenosine A1 receptor 85.57% 95.93%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 84.97% 95.89%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.61% 97.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.78% 96.95%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 83.12% 97.14%
CHEMBL4581 P52732 Kinesin-like protein 1 83.06% 93.18%
CHEMBL2581 P07339 Cathepsin D 82.63% 98.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 82.56% 97.21%
CHEMBL3401 O75469 Pregnane X receptor 82.46% 94.73%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 82.33% 94.33%
CHEMBL2535 P11166 Glucose transporter 80.98% 98.75%
CHEMBL3474 P14555 Phospholipase A2 group IIA 80.70% 94.05%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.10% 89.00%

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.
Paeonia suffruticosa

Cross-Links

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PubChem 46883331
NPASS NPC23253
ChEMBL CHEMBL1079882
LOTUS LTS0079536
wikiData Q105118940