2''-O-Rhamnosylicariside II

Details

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Internal ID 837077df-5cbc-4e86-aa9e-a32cc088f427
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glycosides > Flavonoid-3-O-glycosides
IUPAC Name 3-[(2S,3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-methoxyphenyl)-8-(3-methylbut-2-enyl)chromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C33H40O14/c1-13(2)6-11-18-19(34)12-20(35)21-24(38)30(28(45-29(18)21)16-7-9-17(42-5)10-8-16)46-33-31(26(40)23(37)15(4)44-33)47-32-27(41)25(39)22(36)14(3)43-32/h6-10,12,14-15,22-23,25-27,31-37,39-41H,11H2,1-5H3/t14-,15-,22-,23-,25+,26+,27+,31+,32-,33-/m0/s1
InChI Key TVBJKPLTBPGHDJ-ZJTKNEERSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C33H40O14
Molecular Weight 660.70 g/mol
Exact Mass 660.24180595 g/mol
Topological Polar Surface Area (TPSA) 214.00 Ų
XlogP 2.40
Atomic LogP (AlogP) 1.45
H-Bond Acceptor 14
H-Bond Donor 7
Rotatable Bonds 8

Synonyms

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3-[(2S,3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-methoxyphenyl)-8-(3-methylbut-2-enyl)chromen-4-one
3-((2S,3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl)oxy-5,7-dihydroxy-2-(4-methoxyphenyl)-8-(3-methylbut-2-enyl)chromen-4-one
RefChem:1058584
135293-13-9
2'-O-RHAMNOSYLICARISIDE II
2/'-O-RHAMNOSYLICARISIDE II
2''-O-Rhamnosyl icariside II
orb1296156
2'-O-rhamnosylicariside cento
SCHEMBL27013558
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2''-O-Rhamnosylicariside II

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9486 94.86%
Caco-2 - 0.9127 91.27%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.5770 57.70%
OATP2B1 inhibitior - 0.5725 57.25%
OATP1B1 inhibitior + 0.9037 90.37%
OATP1B3 inhibitior + 0.8170 81.70%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.9614 96.14%
P-glycoprotein inhibitior + 0.5887 58.87%
P-glycoprotein substrate + 0.5170 51.70%
CYP3A4 substrate + 0.6555 65.55%
CYP2C9 substrate - 0.6946 69.46%
CYP2D6 substrate - 0.8431 84.31%
CYP3A4 inhibition - 0.8789 87.89%
CYP2C9 inhibition + 0.5388 53.88%
CYP2C19 inhibition + 0.6785 67.85%
CYP2D6 inhibition - 0.7926 79.26%
CYP1A2 inhibition - 0.8168 81.68%
CYP2C8 inhibition + 0.6667 66.67%
CYP inhibitory promiscuity + 0.6630 66.30%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6053 60.53%
Eye corrosion - 0.9878 98.78%
Eye irritation - 0.9127 91.27%
Skin irritation - 0.7547 75.47%
Skin corrosion - 0.9456 94.56%
Ames mutagenesis - 0.5374 53.74%
Human Ether-a-go-go-Related Gene inhibition + 0.6615 66.15%
Micronuclear + 0.6000 60.00%
Hepatotoxicity - 0.5625 56.25%
skin sensitisation - 0.8435 84.35%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.8767 87.67%
Acute Oral Toxicity (c) III 0.6149 61.49%
Estrogen receptor binding + 0.8352 83.52%
Androgen receptor binding + 0.7311 73.11%
Thyroid receptor binding + 0.5852 58.52%
Glucocorticoid receptor binding + 0.7205 72.05%
Aromatase binding + 0.6114 61.14%
PPAR gamma + 0.6982 69.82%
Honey bee toxicity - 0.7256 72.56%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9916 99.16%

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 99.85% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 98.72% 91.49%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 95.69% 94.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.87% 85.14%
CHEMBL3401 O75469 Pregnane X receptor 94.78% 94.73%
CHEMBL2581 P07339 Cathepsin D 94.68% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.53% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.05% 89.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 91.67% 99.15%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.88% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.03% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.32% 94.45%
CHEMBL4208 P20618 Proteasome component C5 87.18% 90.00%
CHEMBL3714130 P46095 G-protein coupled receptor 6 86.73% 97.36%
CHEMBL240 Q12809 HERG 85.95% 89.76%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.41% 96.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.52% 95.89%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 82.27% 86.92%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.26% 92.62%

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.
Epimedium brevicornu
Epimedium grandiflorum
Epimedium koreanum
Epimedium pubescens
Epimedium sagittatum
Epimedium sempervirens
Epimedium wushanense

Cross-Links

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PubChem 5318987
NPASS NPC222048