Isorhamnetin 3-apiosyl-(1->6)-glucoside-7-rhamnoside

Details

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Internal ID ff948be5-1272-4c00-b164-6ef3de5db229
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glycosides > Flavonoid-7-O-glycosides
IUPAC Name 3-[6-[[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxychromen-4-one
SMILES (Canonical) CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)COC5C(C(CO5)(CO)O)O)O)O)O)C6=CC(=C(C=C6)O)OC)O)O)O)O
SMILES (Isomeric) CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)COC5C(C(CO5)(CO)O)O)O)O)O)C6=CC(=C(C=C6)O)OC)O)O)O)O
InChI InChI=1S/C33H40O20/c1-11-20(37)23(40)25(42)30(49-11)50-13-6-15(36)19-17(7-13)51-27(12-3-4-14(35)16(5-12)46-2)28(22(19)39)53-31-26(43)24(41)21(38)18(52-31)8-47-32-29(44)33(45,9-34)10-48-32/h3-7,11,18,20-21,23-26,29-32,34-38,40-45H,8-10H2,1-2H3
InChI Key IMCHSJLXDHJNGT-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C33H40O20
Molecular Weight 756.70 g/mol
Exact Mass 756.21129366 g/mol
Topological Polar Surface Area (TPSA) 313.00 Ų
XlogP -2.40
Atomic LogP (AlogP) -3.27
H-Bond Acceptor 20
H-Bond Donor 11
Rotatable Bonds 10

Synonyms

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LMPK12112351

2D Structure

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2D Structure of Isorhamnetin 3-apiosyl-(1->6)-glucoside-7-rhamnoside

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6887 68.87%
Caco-2 - 0.9010 90.10%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.7286 72.86%
Subcellular localzation Mitochondria 0.6723 67.23%
OATP2B1 inhibitior - 0.7196 71.96%
OATP1B1 inhibitior + 0.9086 90.86%
OATP1B3 inhibitior + 0.9577 95.77%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.7520 75.20%
P-glycoprotein inhibitior + 0.6161 61.61%
P-glycoprotein substrate + 0.6910 69.10%
CYP3A4 substrate + 0.6842 68.42%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8586 85.86%
CYP3A4 inhibition - 0.8528 85.28%
CYP2C9 inhibition - 0.9101 91.01%
CYP2C19 inhibition - 0.8532 85.32%
CYP2D6 inhibition - 0.9176 91.76%
CYP1A2 inhibition - 0.9039 90.39%
CYP2C8 inhibition + 0.8218 82.18%
CYP inhibitory promiscuity - 0.8191 81.91%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6033 60.33%
Eye corrosion - 0.9912 99.12%
Eye irritation - 0.9083 90.83%
Skin irritation - 0.8219 82.19%
Skin corrosion - 0.9504 95.04%
Ames mutagenesis - 0.6292 62.92%
Human Ether-a-go-go-Related Gene inhibition + 0.7233 72.33%
Micronuclear + 0.5874 58.74%
Hepatotoxicity - 0.6698 66.98%
skin sensitisation - 0.8758 87.58%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.8863 88.63%
Acute Oral Toxicity (c) III 0.6058 60.58%
Estrogen receptor binding + 0.8063 80.63%
Androgen receptor binding + 0.5885 58.85%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.6428 64.28%
Aromatase binding + 0.6148 61.48%
PPAR gamma + 0.7449 74.49%
Honey bee toxicity - 0.7227 72.27%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.8108 81.08%

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 99.73% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 98.38% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 97.96% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 96.72% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.02% 95.56%
CHEMBL2581 P07339 Cathepsin D 94.56% 98.95%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 94.43% 99.15%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.05% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.28% 96.09%
CHEMBL3714130 P46095 G-protein coupled receptor 6 92.09% 97.36%
CHEMBL241 Q14432 Phosphodiesterase 3A 90.37% 92.94%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 89.53% 86.92%
CHEMBL1951 P21397 Monoamine oxidase A 89.12% 91.49%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.41% 94.45%
CHEMBL4940 P07195 L-lactate dehydrogenase B chain 88.38% 95.53%
CHEMBL220 P22303 Acetylcholinesterase 86.91% 94.45%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.71% 99.23%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.83% 95.89%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.58% 96.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.36% 99.17%
CHEMBL3476 O15111 Inhibitor of nuclear factor kappa B kinase alpha subunit 84.53% 95.83%
CHEMBL4208 P20618 Proteasome component C5 83.76% 90.00%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 82.62% 95.89%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 82.54% 97.14%
CHEMBL6175 Q9H3R0 Lysine-specific demethylase 4C 82.47% 96.69%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.48% 85.14%
CHEMBL3401 O75469 Pregnane X receptor 81.44% 94.73%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.95% 90.71%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 80.58% 95.78%
CHEMBL1907 P15144 Aminopeptidase N 80.35% 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.
Viscum album

Cross-Links

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PubChem 14035419
LOTUS LTS0013369
wikiData Q105115589