5-Hydroxy-2-[3-hydroxy-4-methoxy-5-(3,4,5-trihydroxyoxan-2-yl)oxyphenyl]-3-methoxy-7-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxychromen-4-one

Details

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Internal ID 50ffad28-b710-4363-b06a-aaf8ff146b49
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glycosides > Flavonoid-7-O-glycosides
IUPAC Name 5-hydroxy-2-[3-hydroxy-4-methoxy-5-(3,4,5-trihydroxyoxan-2-yl)oxyphenyl]-3-methoxy-7-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxychromen-4-one
SMILES (Canonical) CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC)C4=CC(=C(C(=C4)OC5C(C(C(CO5)O)O)O)OC)O)O)O)O)O
SMILES (Isomeric) CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC)C4=CC(=C(C(=C4)OC5C(C(C(CO5)O)O)O)OC)O)O)O)O)O
InChI InChI=1S/C28H32O16/c1-9-18(32)21(35)23(37)28(41-9)42-11-6-12(29)17-15(7-11)43-24(26(39-3)20(17)34)10-4-13(30)25(38-2)16(5-10)44-27-22(36)19(33)14(31)8-40-27/h4-7,9,14,18-19,21-23,27-33,35-37H,8H2,1-3H3
InChI Key BBQHMWSDDYSPHQ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C28H32O16
Molecular Weight 624.50 g/mol
Exact Mass 624.16903493 g/mol
Topological Polar Surface Area (TPSA) 244.00 Ų
XlogP -0.60
Atomic LogP (AlogP) -1.09
H-Bond Acceptor 16
H-Bond Donor 8
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-Hydroxy-2-[3-hydroxy-4-methoxy-5-(3,4,5-trihydroxyoxan-2-yl)oxyphenyl]-3-methoxy-7-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxychromen-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 + 0.6767 67.67%
Caco-2 - 0.8891 88.91%
Blood Brain Barrier - 0.8250 82.50%
Human oral bioavailability - 0.7286 72.86%
Subcellular localzation Mitochondria 0.5722 57.22%
OATP2B1 inhibitior - 0.5718 57.18%
OATP1B1 inhibitior + 0.9140 91.40%
OATP1B3 inhibitior + 0.9160 91.60%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.8869 88.69%
P-glycoprotein inhibitior - 0.4606 46.06%
P-glycoprotein substrate + 0.5970 59.70%
CYP3A4 substrate + 0.6574 65.74%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8527 85.27%
CYP3A4 inhibition - 0.9128 91.28%
CYP2C9 inhibition - 0.9688 96.88%
CYP2C19 inhibition - 0.9576 95.76%
CYP2D6 inhibition - 0.9071 90.71%
CYP1A2 inhibition - 0.8949 89.49%
CYP2C8 inhibition + 0.7039 70.39%
CYP inhibitory promiscuity - 0.9006 90.06%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6509 65.09%
Eye corrosion - 0.9904 99.04%
Eye irritation - 0.9108 91.08%
Skin irritation - 0.8133 81.33%
Skin corrosion - 0.9557 95.57%
Ames mutagenesis - 0.5101 51.01%
Human Ether-a-go-go-Related Gene inhibition + 0.7220 72.20%
Micronuclear + 0.7433 74.33%
Hepatotoxicity - 0.7250 72.50%
skin sensitisation - 0.9333 93.33%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.9105 91.05%
Acute Oral Toxicity (c) III 0.6780 67.80%
Estrogen receptor binding + 0.8157 81.57%
Androgen receptor binding - 0.5053 50.53%
Thyroid receptor binding + 0.5319 53.19%
Glucocorticoid receptor binding + 0.6478 64.78%
Aromatase binding + 0.5522 55.22%
PPAR gamma + 0.7244 72.44%
Honey bee toxicity - 0.7358 73.58%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5649 56.49%
Fish aquatic toxicity + 0.7980 79.80%

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 99.37% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 97.34% 89.00%
CHEMBL1951 P21397 Monoamine oxidase A 96.23% 91.49%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 95.93% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.41% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.80% 96.09%
CHEMBL2581 P07339 Cathepsin D 91.05% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.69% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.53% 95.56%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 87.31% 90.71%
CHEMBL4208 P20618 Proteasome component C5 86.13% 90.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.63% 99.17%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.03% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.88% 99.23%
CHEMBL3401 O75469 Pregnane X receptor 82.27% 94.73%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.63% 92.94%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 80.83% 99.15%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.17% 95.89%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.14% 97.14%

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.
Dacrycarpus dacrydioides

Cross-Links

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PubChem 74978441
LOTUS LTS0271100
wikiData Q104922994