8-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]-2-(3,4-dihydroxyphenyl)-5-hydroxychromen-4-one

Details

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Internal ID 4c86d557-98a2-4e89-9d8a-cb8bcf9ef93d
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid C-glycosides > Flavonoid 8-C-glycosides
IUPAC Name 8-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]-2-(3,4-dihydroxyphenyl)-5-hydroxychromen-4-one
SMILES (Canonical) C1=CC(=C(C=C1C2=CC(=O)C3=C(C=CC(=C3O2)C4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O)O
SMILES (Isomeric) C1=CC(=C(C=C1C2=CC(=O)C3=C(C=CC(=C3O2)[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O[C@H]5[C@@H]([C@H]([C@@H]([C@H](O5)CO)O)O)O)O)O)O
InChI InChI=1S/C27H30O15/c28-7-16-20(35)22(37)26(42-27-23(38)21(36)19(34)17(8-29)41-27)25(40-16)10-2-4-12(31)18-14(33)6-15(39-24(10)18)9-1-3-11(30)13(32)5-9/h1-6,16-17,19-23,25-32,34-38H,7-8H2/t16-,17-,19-,20-,21+,22+,23-,25+,26-,27+/m1/s1
InChI Key KZMBFFIKMXEATO-JOTPJZSTSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C27H30O15
Molecular Weight 594.50 g/mol
Exact Mass 594.15847025 g/mol
Topological Polar Surface Area (TPSA) 256.00 Ų
XlogP -1.40
Atomic LogP (AlogP) -2.08
H-Bond Acceptor 15
H-Bond Donor 10
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 8-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]-2-(3,4-dihydroxyphenyl)-5-hydroxychromen-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 - 0.5736 57.36%
Caco-2 - 0.9326 93.26%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.8286 82.86%
Subcellular localzation Mitochondria 0.5848 58.48%
OATP2B1 inhibitior - 0.5591 55.91%
OATP1B1 inhibitior + 0.8967 89.67%
OATP1B3 inhibitior + 0.9434 94.34%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.7236 72.36%
P-glycoprotein inhibitior - 0.6309 63.09%
P-glycoprotein substrate - 0.7606 76.06%
CYP3A4 substrate + 0.6305 63.05%
CYP2C9 substrate - 0.6621 66.21%
CYP2D6 substrate - 0.8575 85.75%
CYP3A4 inhibition - 0.9390 93.90%
CYP2C9 inhibition - 0.9315 93.15%
CYP2C19 inhibition - 0.9047 90.47%
CYP2D6 inhibition - 0.9458 94.58%
CYP1A2 inhibition - 0.9180 91.80%
CYP2C8 inhibition + 0.6793 67.93%
CYP inhibitory promiscuity - 0.7526 75.26%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6848 68.48%
Eye corrosion - 0.9930 99.30%
Eye irritation - 0.9106 91.06%
Skin irritation - 0.8255 82.55%
Skin corrosion - 0.9691 96.91%
Ames mutagenesis + 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4048 40.48%
Micronuclear + 0.6433 64.33%
Hepatotoxicity - 0.8446 84.46%
skin sensitisation - 0.9132 91.32%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.7485 74.85%
Acute Oral Toxicity (c) IV 0.4763 47.63%
Estrogen receptor binding + 0.8149 81.49%
Androgen receptor binding + 0.7446 74.46%
Thyroid receptor binding + 0.5557 55.57%
Glucocorticoid receptor binding - 0.4940 49.40%
Aromatase binding + 0.6491 64.91%
PPAR gamma + 0.7600 76.00%
Honey bee toxicity - 0.6520 65.20%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5650 56.50%
Fish aquatic toxicity + 0.7958 79.58%

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 99.51% 91.11%
CHEMBL2581 P07339 Cathepsin D 97.23% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 94.30% 91.49%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.09% 89.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 94.09% 99.15%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.18% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 91.01% 94.73%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 90.99% 86.92%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.58% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.93% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.19% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.58% 97.09%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 83.34% 96.21%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 83.22% 83.57%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.82% 95.89%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.79% 99.17%

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.
Podocarpus nivalis

Cross-Links

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PubChem 162983390
LOTUS LTS0233407
wikiData Q105148326