5-Hydroxy-2-[3-methoxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one

Details

Top
Internal ID 98025f4e-ac6e-4f50-9154-a3d81a50f959
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavonoid glycosides > Flavonoid O-glycosides > Flavonoid-7-O-glycosides
IUPAC Name 5-hydroxy-2-[3-methoxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C28H34O16/c1-39-16-4-10(2-3-14(16)42-28-26(38)24(36)22(34)19(9-30)44-28)15-7-13(32)20-12(31)5-11(6-17(20)41-15)40-27-25(37)23(35)21(33)18(8-29)43-27/h2-6,15,18-19,21-31,33-38H,7-9H2,1H3
InChI Key LDACQRLKWKLUEW-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C28H34O16
Molecular Weight 626.60 g/mol
Exact Mass 626.18468499 g/mol
Topological Polar Surface Area (TPSA) 255.00 Ų
XlogP -1.20
Atomic LogP (AlogP) -2.54
H-Bond Acceptor 16
H-Bond Donor 9
Rotatable Bonds 8

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 5-Hydroxy-2-[3-methoxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5457 54.57%
Caco-2 - 0.8987 89.87%
Blood Brain Barrier - 0.8250 82.50%
Human oral bioavailability - 0.7857 78.57%
Subcellular localzation Mitochondria 0.5961 59.61%
OATP2B1 inhibitior - 0.8525 85.25%
OATP1B1 inhibitior + 0.9285 92.85%
OATP1B3 inhibitior + 0.9786 97.86%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.6742 67.42%
P-glycoprotein inhibitior - 0.5266 52.66%
P-glycoprotein substrate - 0.7484 74.84%
CYP3A4 substrate + 0.6237 62.37%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8374 83.74%
CYP3A4 inhibition - 0.9437 94.37%
CYP2C9 inhibition - 0.9060 90.60%
CYP2C19 inhibition - 0.8926 89.26%
CYP2D6 inhibition - 0.9515 95.15%
CYP1A2 inhibition - 0.9150 91.50%
CYP2C8 inhibition + 0.5000 50.00%
CYP inhibitory promiscuity - 0.7142 71.42%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6642 66.42%
Eye corrosion - 0.9901 99.01%
Eye irritation - 0.9259 92.59%
Skin irritation - 0.8320 83.20%
Skin corrosion - 0.9606 96.06%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7486 74.86%
Micronuclear + 0.6533 65.33%
Hepatotoxicity - 0.8375 83.75%
skin sensitisation - 0.9324 93.24%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.5651 56.51%
Acute Oral Toxicity (c) III 0.6678 66.78%
Estrogen receptor binding + 0.7885 78.85%
Androgen receptor binding - 0.6709 67.09%
Thyroid receptor binding - 0.5437 54.37%
Glucocorticoid receptor binding - 0.5566 55.66%
Aromatase binding - 0.5141 51.41%
PPAR gamma + 0.7224 72.24%
Honey bee toxicity - 0.7159 71.59%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.7400 74.00%
Fish aquatic toxicity + 0.6698 66.98%

Targets

Top

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 98.58% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.50% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.44% 85.14%
CHEMBL2581 P07339 Cathepsin D 95.48% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 95.05% 97.09%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 95.00% 96.21%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.61% 94.00%
CHEMBL4208 P20618 Proteasome component C5 92.14% 90.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 91.43% 95.89%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 91.34% 86.92%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.20% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.20% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.69% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.38% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.85% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.57% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 82.28% 94.73%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 82.16% 99.15%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.29% 97.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.75% 99.23%

Plants that contains it

Top
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.
Viscum coloratum

Cross-Links

Top
PubChem 73039617
LOTUS LTS0124789
wikiData Q105150114