(2S)-2-[4-[(2S,3S,4S,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxyphenyl]-5,7-dimethoxy-2,3-dihydrochromen-4-one

Details

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Internal ID dffb9c52-4dfc-4aec-b307-b34986fcfae8
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glycosides
IUPAC Name (2S)-2-[4-[(2S,3S,4S,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxyphenyl]-5,7-dimethoxy-2,3-dihydrochromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C29H36O14/c1-12-22(32)23(33)25(35)28(39-12)43-27-20(11-30)42-29(26(36)24(27)34)40-14-6-4-13(5-7-14)17-10-16(31)21-18(38-3)8-15(37-2)9-19(21)41-17/h4-9,12,17,20,22-30,32-36H,10-11H2,1-3H3/t12-,17-,20+,22-,23+,24-,25-,26-,27+,28-,29+/m0/s1
InChI Key HDSXTURQGPCWIN-UBUJWPRQSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C29H36O14
Molecular Weight 608.60 g/mol
Exact Mass 608.21050582 g/mol
Topological Polar Surface Area (TPSA) 203.00 Ų
XlogP -1.00
Atomic LogP (AlogP) -0.56
H-Bond Acceptor 14
H-Bond Donor 6
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2S)-2-[4-[(2S,3S,4S,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxyphenyl]-5,7-dimethoxy-2,3-dihydrochromen-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5254 52.54%
Caco-2 - 0.8580 85.80%
Blood Brain Barrier - 0.8250 82.50%
Human oral bioavailability - 0.8286 82.86%
Subcellular localzation Mitochondria 0.6365 63.65%
OATP2B1 inhibitior - 0.8598 85.98%
OATP1B1 inhibitior + 0.9292 92.92%
OATP1B3 inhibitior + 0.9197 91.97%
MATE1 inhibitior - 0.9212 92.12%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.6174 61.74%
P-glycoprotein inhibitior - 0.4848 48.48%
P-glycoprotein substrate - 0.6349 63.49%
CYP3A4 substrate + 0.6497 64.97%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8239 82.39%
CYP3A4 inhibition - 0.8915 89.15%
CYP2C9 inhibition - 0.9119 91.19%
CYP2C19 inhibition - 0.9389 93.89%
CYP2D6 inhibition - 0.9323 93.23%
CYP1A2 inhibition - 0.9182 91.82%
CYP2C8 inhibition - 0.5667 56.67%
CYP inhibitory promiscuity - 0.6277 62.77%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6967 69.67%
Eye corrosion - 0.9889 98.89%
Eye irritation - 0.9295 92.95%
Skin irritation - 0.8413 84.13%
Skin corrosion - 0.9645 96.45%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4505 45.05%
Micronuclear + 0.6533 65.33%
Hepatotoxicity - 0.7500 75.00%
skin sensitisation - 0.9346 93.46%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity - 0.8239 82.39%
Acute Oral Toxicity (c) III 0.6686 66.86%
Estrogen receptor binding + 0.7824 78.24%
Androgen receptor binding - 0.5938 59.38%
Thyroid receptor binding + 0.5183 51.83%
Glucocorticoid receptor binding + 0.5506 55.06%
Aromatase binding - 0.5352 53.52%
PPAR gamma + 0.7017 70.17%
Honey bee toxicity - 0.6971 69.71%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.7409 74.09%

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 98.94% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.58% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.93% 97.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.43% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.29% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.86% 94.00%
CHEMBL4208 P20618 Proteasome component C5 93.77% 90.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.48% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.23% 95.56%
CHEMBL2581 P07339 Cathepsin D 92.02% 98.95%
CHEMBL3714130 P46095 G-protein coupled receptor 6 91.47% 97.36%
CHEMBL5608 Q16288 NT-3 growth factor receptor 91.26% 95.89%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 89.14% 86.92%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.53% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.89% 96.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.60% 92.62%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 82.01% 95.89%
CHEMBL3401 O75469 Pregnane X receptor 81.81% 94.73%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 80.96% 96.21%

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.
Bauhinia variegata

Cross-Links

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PubChem 163074601
LOTUS LTS0146095
wikiData Q105026528