beta-D-Galactopyranosiduronic acid, 5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-1-benzopyran-7-yl 2-O-(6-deoxy-alpha-L-mannopyranosyl)-

Details

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Internal ID 4b5e1343-5e36-4dc2-a5f7-d73cf46e1f36
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glucuronides > Flavonoid-7-O-glucuronides
IUPAC Name (2S,3R,4S,5R,6S)-3,4-dihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxy-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxane-2-carboxylic acid
SMILES (Canonical) CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)C(=O)O)O)O)O)O)O
SMILES (Isomeric) C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)O[C@@H]2[C@H]([C@H]([C@H](O[C@H]2OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)C(=O)O)O)O)O)O)O
InChI InChI=1S/C27H28O15/c1-9-18(31)19(32)22(35)26(38-9)42-24-21(34)20(33)23(25(36)37)41-27(24)39-12-6-13(29)17-14(30)8-15(40-16(17)7-12)10-2-4-11(28)5-3-10/h2-9,18-24,26-29,31-35H,1H3,(H,36,37)/t9-,18-,19+,20+,21-,22+,23-,24+,26-,27+/m0/s1
InChI Key ONIIEJMYZDRHKM-JHUFFODMSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C27H28O15
Molecular Weight 592.50 g/mol
Exact Mass 592.14282018 g/mol
Topological Polar Surface Area (TPSA) 242.00 Ų
XlogP 0.00
Atomic LogP (AlogP) -1.01
H-Bond Acceptor 14
H-Bond Donor 8
Rotatable Bonds 6

Synonyms

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Apigenin 7-[rhamnosyl-(1->2)-galacturonide]
beta-D-Galactopyranosiduronic acid, 5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-1-benzopyran-7-yl 2-O-(6-deoxy-alpha-L-mannopyranosyl)-
DTXSID501104696
AKOS040736106
FS-8427
5-Hydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-1-benzopyran-7-yl 2-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-galactopyranosiduronic acid

2D Structure

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2D Structure of beta-D-Galactopyranosiduronic acid, 5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-1-benzopyran-7-yl 2-O-(6-deoxy-alpha-L-mannopyranosyl)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7250 72.50%
Caco-2 - 0.9033 90.33%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability - 0.8000 80.00%
Subcellular localzation Mitochondria 0.7033 70.33%
OATP2B1 inhibitior - 0.6843 68.43%
OATP1B1 inhibitior + 0.9401 94.01%
OATP1B3 inhibitior + 0.9774 97.74%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.7029 70.29%
P-glycoprotein inhibitior - 0.6563 65.63%
P-glycoprotein substrate - 0.6559 65.59%
CYP3A4 substrate + 0.6281 62.81%
CYP2C9 substrate - 0.6532 65.32%
CYP2D6 substrate - 0.8849 88.49%
CYP3A4 inhibition - 0.7716 77.16%
CYP2C9 inhibition - 0.8518 85.18%
CYP2C19 inhibition - 0.9123 91.23%
CYP2D6 inhibition - 0.9643 96.43%
CYP1A2 inhibition - 0.8370 83.70%
CYP2C8 inhibition + 0.7975 79.75%
CYP inhibitory promiscuity - 0.7986 79.86%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5368 53.68%
Eye corrosion - 0.9899 98.99%
Eye irritation - 0.9140 91.40%
Skin irritation - 0.6876 68.76%
Skin corrosion - 0.9296 92.96%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3938 39.38%
Micronuclear + 0.8600 86.00%
Hepatotoxicity - 0.7782 77.82%
skin sensitisation - 0.9297 92.97%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity - 0.9345 93.45%
Acute Oral Toxicity (c) III 0.6408 64.08%
Estrogen receptor binding + 0.7684 76.84%
Androgen receptor binding + 0.6871 68.71%
Thyroid receptor binding + 0.5404 54.04%
Glucocorticoid receptor binding + 0.6304 63.04%
Aromatase binding + 0.5474 54.74%
PPAR gamma + 0.7376 73.76%
Honey bee toxicity - 0.7105 71.05%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9477 94.77%

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
CHEMBL1951 P21397 Monoamine oxidase A 99.79% 91.49%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.06% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 97.71% 89.00%
CHEMBL2581 P07339 Cathepsin D 96.19% 98.95%
CHEMBL3194 P02766 Transthyretin 94.87% 90.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.74% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.52% 94.00%
CHEMBL3714130 P46095 G-protein coupled receptor 6 92.25% 97.36%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.63% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 90.91% 99.15%
CHEMBL3401 O75469 Pregnane X receptor 89.32% 94.73%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 88.76% 90.71%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 87.60% 83.57%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 87.14% 91.71%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 84.15% 95.78%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.52% 99.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.24% 99.23%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 81.55% 95.64%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.30% 85.14%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.28% 95.89%
CHEMBL5284 Q96RR4 CaM-kinase kinase beta 80.50% 89.23%

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.
Silybum marianum

Cross-Links

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PubChem 101428062
LOTUS LTS0086800
wikiData Q105194703