[(2R,3S,4S,5R,6S)-6-[2,3-dihydroxy-4-[(E)-3-(3-hydroxy-4-methoxyphenyl)prop-2-enoyl]phenoxy]-3,4,5-trihydroxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate

Details

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Internal ID 8671a597-79d2-4c6b-88f5-189bb92367e9
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glycosides
IUPAC Name [(2R,3S,4S,5R,6S)-6-[2,3-dihydroxy-4-[(E)-3-(3-hydroxy-4-methoxyphenyl)prop-2-enoyl]phenoxy]-3,4,5-trihydroxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate
SMILES (Canonical) COC1=C(C=C(C=C1)C=CC(=O)C2=C(C(=C(C=C2)OC3C(C(C(C(O3)COC(=O)C=CC4=CC=C(C=C4)O)O)O)O)O)O)O
SMILES (Isomeric) COC1=C(C=C(C=C1)/C=C/C(=O)C2=C(C(=C(C=C2)O[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)COC(=O)/C=C/C4=CC=C(C=C4)O)O)O)O)O)O)O
InChI InChI=1S/C31H30O13/c1-41-22-11-5-17(14-21(22)34)4-10-20(33)19-9-12-23(27(37)26(19)36)43-31-30(40)29(39)28(38)24(44-31)15-42-25(35)13-6-16-2-7-18(32)8-3-16/h2-14,24,28-32,34,36-40H,15H2,1H3/b10-4+,13-6+/t24-,28-,29+,30-,31-/m1/s1
InChI Key JSFGLFKAAYSKDD-FCXJTQLZSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C31H30O13
Molecular Weight 610.60 g/mol
Exact Mass 610.16864101 g/mol
Topological Polar Surface Area (TPSA) 213.00 Ų
XlogP 2.70
Atomic LogP (AlogP) 1.86
H-Bond Acceptor 13
H-Bond Donor 7
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(2R,3S,4S,5R,6S)-6-[2,3-dihydroxy-4-[(E)-3-(3-hydroxy-4-methoxyphenyl)prop-2-enoyl]phenoxy]-3,4,5-trihydroxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.6680 66.80%
Caco-2 - 0.8985 89.85%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability - 0.8286 82.86%
Subcellular localzation Mitochondria 0.6272 62.72%
OATP2B1 inhibitior - 0.7010 70.10%
OATP1B1 inhibitior + 0.8849 88.49%
OATP1B3 inhibitior + 0.9475 94.75%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior + 0.8844 88.44%
P-glycoprotein inhibitior + 0.6576 65.76%
P-glycoprotein substrate - 0.6449 64.49%
CYP3A4 substrate + 0.6296 62.96%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8675 86.75%
CYP3A4 inhibition - 0.8083 80.83%
CYP2C9 inhibition - 0.7458 74.58%
CYP2C19 inhibition - 0.8240 82.40%
CYP2D6 inhibition - 0.9036 90.36%
CYP1A2 inhibition - 0.8398 83.98%
CYP2C8 inhibition + 0.8627 86.27%
CYP inhibitory promiscuity - 0.7426 74.26%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.7117 71.17%
Eye corrosion - 0.9899 98.99%
Eye irritation - 0.8974 89.74%
Skin irritation - 0.8386 83.86%
Skin corrosion - 0.9411 94.11%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7132 71.32%
Micronuclear + 0.6766 67.66%
Hepatotoxicity - 0.8625 86.25%
skin sensitisation - 0.8734 87.34%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity - 0.9039 90.39%
Acute Oral Toxicity (c) III 0.7576 75.76%
Estrogen receptor binding + 0.7857 78.57%
Androgen receptor binding + 0.6842 68.42%
Thyroid receptor binding + 0.6189 61.89%
Glucocorticoid receptor binding + 0.6819 68.19%
Aromatase binding - 0.5359 53.59%
PPAR gamma + 0.6951 69.51%
Honey bee toxicity - 0.8108 81.08%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.9308 93.08%

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 98.52% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 98.19% 86.33%
CHEMBL3194 P02766 Transthyretin 97.13% 90.71%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.52% 96.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 93.98% 96.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.45% 99.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.55% 89.00%
CHEMBL1951 P21397 Monoamine oxidase A 91.96% 91.49%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 89.01% 89.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.65% 95.56%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 87.84% 95.50%
CHEMBL4208 P20618 Proteasome component C5 86.45% 90.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.57% 97.09%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 84.67% 95.89%
CHEMBL3401 O75469 Pregnane X receptor 84.56% 94.73%
CHEMBL2581 P07339 Cathepsin D 84.34% 98.95%
CHEMBL2535 P11166 Glucose transporter 82.35% 98.75%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.02% 90.71%

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.
Bidens frondosa

Cross-Links

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PubChem 15755767
LOTUS LTS0106455
wikiData Q105134315