Acacetin-7-diglucuronide

Details

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Internal ID 578f274f-9644-429c-844e-9c1c6803c18e
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glucuronides > Flavonoid-7-O-glucuronides
IUPAC Name (2S,3S,4S,5R,6R)-6-[(2S,3R,4S,5S,6S)-6-carboxy-4,5-dihydroxy-2-[5-hydroxy-2-(4-methoxyphenyl)-4-oxochromen-7-yl]oxyoxan-3-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C28H28O17/c1-40-10-4-2-9(3-5-10)14-8-13(30)16-12(29)6-11(7-15(16)42-14)41-28-24(20(34)19(33)23(44-28)26(38)39)45-27-21(35)17(31)18(32)22(43-27)25(36)37/h2-8,17-24,27-29,31-35H,1H3,(H,36,37)(H,38,39)/t17-,18-,19-,20-,21+,22-,23-,24+,27-,28+/m0/s1
InChI Key JNGIOHRDWMHQEK-BBKSNKDASA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C28H28O17
Molecular Weight 636.50 g/mol
Exact Mass 636.13264942 g/mol
Topological Polar Surface Area (TPSA) 268.00 Ų
XlogP 0.10
Atomic LogP (AlogP) -1.64
H-Bond Acceptor 15
H-Bond Donor 8
Rotatable Bonds 8

Synonyms

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Acacetin 7-glucurono-(1a2)-glucuronide
29617-68-3

2D Structure

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2D Structure of Acacetin-7-diglucuronide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7236 72.36%
Caco-2 - 0.8831 88.31%
Blood Brain Barrier - 0.8500 85.00%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Mitochondria 0.6660 66.60%
OATP2B1 inhibitior - 0.6904 69.04%
OATP1B1 inhibitior + 0.9398 93.98%
OATP1B3 inhibitior + 0.9853 98.53%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.4510 45.10%
P-glycoprotein inhibitior - 0.4739 47.39%
P-glycoprotein substrate - 0.7870 78.70%
CYP3A4 substrate + 0.6316 63.16%
CYP2C9 substrate - 0.8245 82.45%
CYP2D6 substrate - 0.8736 87.36%
CYP3A4 inhibition - 0.7069 70.69%
CYP2C9 inhibition - 0.8743 87.43%
CYP2C19 inhibition - 0.8805 88.05%
CYP2D6 inhibition - 0.9390 93.90%
CYP1A2 inhibition - 0.7944 79.44%
CYP2C8 inhibition + 0.7750 77.50%
CYP inhibitory promiscuity - 0.7951 79.51%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5000 50.00%
Eye corrosion - 0.9853 98.53%
Eye irritation - 0.9037 90.37%
Skin irritation - 0.7006 70.06%
Skin corrosion - 0.9347 93.47%
Ames mutagenesis - 0.6064 60.64%
Human Ether-a-go-go-Related Gene inhibition + 0.7364 73.64%
Micronuclear + 0.8600 86.00%
Hepatotoxicity - 0.7782 77.82%
skin sensitisation - 0.9405 94.05%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity - 0.9167 91.67%
Acute Oral Toxicity (c) III 0.6872 68.72%
Estrogen receptor binding + 0.7936 79.36%
Androgen receptor binding + 0.7294 72.94%
Thyroid receptor binding + 0.5240 52.40%
Glucocorticoid receptor binding + 0.6599 65.99%
Aromatase binding - 0.5385 53.85%
PPAR gamma + 0.6925 69.25%
Honey bee toxicity - 0.7642 76.42%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.8979 89.79%

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%
CHEMBL1951 P21397 Monoamine oxidase A 99.01% 91.49%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.41% 85.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 95.04% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.76% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.01% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 93.61% 99.15%
CHEMBL2581 P07339 Cathepsin D 93.32% 98.95%
CHEMBL3194 P02766 Transthyretin 92.14% 90.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.44% 86.33%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 87.92% 81.11%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 86.83% 87.67%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.64% 99.17%
CHEMBL5284 Q96RR4 CaM-kinase kinase beta 85.43% 89.23%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 85.26% 95.50%
CHEMBL3714130 P46095 G-protein coupled receptor 6 85.23% 97.36%
CHEMBL3401 O75469 Pregnane X receptor 85.20% 94.73%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 84.28% 90.71%
CHEMBL4208 P20618 Proteasome component C5 84.28% 90.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.85% 95.89%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.45% 99.23%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.19% 94.45%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 82.51% 83.57%
CHEMBL340 P08684 Cytochrome P450 3A4 81.15% 91.19%
CHEMBL1907 P15144 Aminopeptidase N 80.82% 93.31%

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.
Scutellaria barbata

Cross-Links

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PubChem 11968442
NPASS NPC301738