Allivictoside A

Details

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Internal ID 3b9a2c4e-3c99-482a-9a19-817abef1b691
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glycosides > Flavonoid-3-O-glycosides
IUPAC Name [(2S,3R,4S,5S,6R)-2-[5,7-dihydroxy-4-oxo-2-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-3-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C36H36O18/c37-13-22-26(43)29(46)31(48)35(51-22)49-19-8-4-16(5-9-19)32-33(28(45)25-20(41)11-18(40)12-21(25)50-32)54-36-34(30(47)27(44)23(14-38)52-36)53-24(42)10-3-15-1-6-17(39)7-2-15/h1-12,22-23,26-27,29-31,34-41,43-44,46-48H,13-14H2/b10-3+/t22-,23-,26-,27-,29+,30+,31-,34-,35-,36+/m1/s1
InChI Key BWJNEPWIRGMUKA-MSQUEZNUSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C36H36O18
Molecular Weight 756.70 g/mol
Exact Mass 756.19016430 g/mol
Topological Polar Surface Area (TPSA) 292.00 Ų
XlogP 1.20
Atomic LogP (AlogP) -0.80
H-Bond Acceptor 18
H-Bond Donor 10
Rotatable Bonds 10

Synonyms

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CHEMBL2206197

2D Structure

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2D Structure of Allivictoside A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5570 55.70%
Caco-2 - 0.9001 90.01%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.8143 81.43%
Subcellular localzation Mitochondria 0.5040 50.40%
OATP2B1 inhibitior - 0.5659 56.59%
OATP1B1 inhibitior + 0.8746 87.46%
OATP1B3 inhibitior + 0.9786 97.86%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.8585 85.85%
P-glycoprotein inhibitior + 0.6963 69.63%
P-glycoprotein substrate - 0.5510 55.10%
CYP3A4 substrate + 0.6823 68.23%
CYP2C9 substrate - 0.8095 80.95%
CYP2D6 substrate - 0.8711 87.11%
CYP3A4 inhibition - 0.9209 92.09%
CYP2C9 inhibition - 0.8990 89.90%
CYP2C19 inhibition - 0.8708 87.08%
CYP2D6 inhibition - 0.9370 93.70%
CYP1A2 inhibition - 0.9325 93.25%
CYP2C8 inhibition + 0.8887 88.87%
CYP inhibitory promiscuity - 0.7843 78.43%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6850 68.50%
Eye corrosion - 0.9921 99.21%
Eye irritation - 0.9005 90.05%
Skin irritation - 0.8335 83.35%
Skin corrosion - 0.9579 95.79%
Ames mutagenesis + 0.5363 53.63%
Human Ether-a-go-go-Related Gene inhibition + 0.7841 78.41%
Micronuclear + 0.6533 65.33%
Hepatotoxicity - 0.7250 72.50%
skin sensitisation - 0.8754 87.54%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.9324 93.24%
Acute Oral Toxicity (c) IV 0.4410 44.10%
Estrogen receptor binding + 0.7687 76.87%
Androgen receptor binding + 0.7106 71.06%
Thyroid receptor binding + 0.5407 54.07%
Glucocorticoid receptor binding + 0.5717 57.17%
Aromatase binding - 0.4891 48.91%
PPAR gamma + 0.7161 71.61%
Honey bee toxicity - 0.6929 69.29%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9324 93.24%

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 99.69% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 98.21% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.90% 86.33%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 95.75% 95.64%
CHEMBL3194 P02766 Transthyretin 95.57% 90.71%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.72% 99.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.66% 97.09%
CHEMBL2581 P07339 Cathepsin D 92.53% 98.95%
CHEMBL242 Q92731 Estrogen receptor beta 92.25% 98.35%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 91.04% 99.15%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 90.79% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.29% 95.56%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 90.28% 86.92%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.55% 94.45%
CHEMBL4208 P20618 Proteasome component C5 88.13% 90.00%
CHEMBL3401 O75469 Pregnane X receptor 87.81% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.72% 96.09%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 86.87% 95.78%
CHEMBL1951 P21397 Monoamine oxidase A 86.58% 91.49%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 86.16% 95.50%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.71% 94.00%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 84.59% 83.57%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 84.22% 91.71%
CHEMBL5678 P34947 G protein-coupled receptor kinase 5 84.11% 88.00%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 83.42% 95.89%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 80.57% 80.78%

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.
Allium victorialis

Cross-Links

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PubChem 71459647
LOTUS LTS0004978
wikiData Q104947277