[(2R,3R,4S,5R,6S)-6-[3,5-dihydroxy-2-[3-(4-hydroxyphenyl)propanoyl]phenoxy]-3,4,5-trihydroxyoxan-2-yl]methyl acetate

Details

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Internal ID e9d29121-3b59-44cf-a087-0f5bfadf3b73
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glycosides
IUPAC Name [(2R,3R,4S,5R,6S)-6-[3,5-dihydroxy-2-[3-(4-hydroxyphenyl)propanoyl]phenoxy]-3,4,5-trihydroxyoxan-2-yl]methyl acetate
SMILES (Canonical) CC(=O)OCC1C(C(C(C(O1)OC2=CC(=CC(=C2C(=O)CCC3=CC=C(C=C3)O)O)O)O)O)O
SMILES (Isomeric) CC(=O)OC[C@@H]1[C@@H]([C@@H]([C@H]([C@@H](O1)OC2=CC(=CC(=C2C(=O)CCC3=CC=C(C=C3)O)O)O)O)O)O
InChI InChI=1S/C23H26O11/c1-11(24)32-10-18-20(29)21(30)22(31)23(34-18)33-17-9-14(26)8-16(28)19(17)15(27)7-4-12-2-5-13(25)6-3-12/h2-3,5-6,8-9,18,20-23,25-26,28-31H,4,7,10H2,1H3/t18-,20+,21+,22-,23-/m1/s1
InChI Key WKDMJJFSCAZJHE-YDXQKAQTSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C23H26O11
Molecular Weight 478.40 g/mol
Exact Mass 478.14751164 g/mol
Topological Polar Surface Area (TPSA) 183.00 Ų
XlogP 0.80
Atomic LogP (AlogP) 0.37
H-Bond Acceptor 11
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 [(2R,3R,4S,5R,6S)-6-[3,5-dihydroxy-2-[3-(4-hydroxyphenyl)propanoyl]phenoxy]-3,4,5-trihydroxyoxan-2-yl]methyl acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.6888 68.88%
Caco-2 - 0.8741 87.41%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.8143 81.43%
Subcellular localzation Mitochondria 0.8297 82.97%
OATP2B1 inhibitior - 0.5658 56.58%
OATP1B1 inhibitior + 0.8753 87.53%
OATP1B3 inhibitior + 0.8787 87.87%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.5000 50.00%
P-glycoprotein inhibitior - 0.4472 44.72%
P-glycoprotein substrate - 0.7306 73.06%
CYP3A4 substrate + 0.6107 61.07%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8760 87.60%
CYP3A4 inhibition - 0.8893 88.93%
CYP2C9 inhibition - 0.5837 58.37%
CYP2C19 inhibition - 0.8179 81.79%
CYP2D6 inhibition - 0.9274 92.74%
CYP1A2 inhibition - 0.7467 74.67%
CYP2C8 inhibition + 0.7448 74.48%
CYP inhibitory promiscuity - 0.8533 85.33%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.7573 75.73%
Eye corrosion - 0.9915 99.15%
Eye irritation - 0.8837 88.37%
Skin irritation - 0.8104 81.04%
Skin corrosion - 0.9366 93.66%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4114 41.14%
Micronuclear - 0.6708 67.08%
Hepatotoxicity - 0.7926 79.26%
skin sensitisation - 0.8982 89.82%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity - 0.7757 77.57%
Acute Oral Toxicity (c) III 0.7935 79.35%
Estrogen receptor binding + 0.8239 82.39%
Androgen receptor binding + 0.5392 53.92%
Thyroid receptor binding - 0.5124 51.24%
Glucocorticoid receptor binding + 0.5374 53.74%
Aromatase binding - 0.4877 48.77%
PPAR gamma + 0.6412 64.12%
Honey bee toxicity - 0.7979 79.79%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5955 59.55%
Fish aquatic toxicity + 0.9317 93.17%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.45% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.61% 91.11%
CHEMBL2581 P07339 Cathepsin D 95.05% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 94.60% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.15% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.94% 94.45%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 91.17% 96.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 90.75% 97.21%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.32% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.03% 89.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 88.40% 95.50%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.07% 94.00%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 86.37% 95.89%
CHEMBL4208 P20618 Proteasome component C5 85.90% 90.00%
CHEMBL3437 Q16853 Amine oxidase, copper containing 85.04% 94.00%
CHEMBL5852 Q96P65 Pyroglutamylated RFamide peptide receptor 84.17% 85.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.42% 95.89%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 81.67% 94.62%
CHEMBL3194 P02766 Transthyretin 80.54% 90.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.16% 95.56%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 80.06% 94.80%

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.
Kalmia procumbens

Cross-Links

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PubChem 162845750
LOTUS LTS0151403
wikiData Q105307255