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

Details

Top
Internal ID 2d93223e-49c8-46da-a8af-a6725ad9dc40
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Biflavonoids and polyflavonoids
IUPAC Name 5-hydroxy-3-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-3-yl]-2-(4-hydroxyphenyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C42H42O20/c43-13-25-31(49)35(53)37(55)41(61-25)57-19-9-21(47)27-23(11-19)59-39(15-1-5-17(45)6-2-15)29(33(27)51)30-34(52)28-22(48)10-20(58-42-38(56)36(54)32(50)26(14-44)62-42)12-24(28)60-40(30)16-3-7-18(46)8-4-16/h1-12,25-26,29-32,35-50,53-56H,13-14H2
InChI Key RVPPNKOUWPOQRX-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C42H42O20
Molecular Weight 866.80 g/mol
Exact Mass 866.22694372 g/mol
Topological Polar Surface Area (TPSA) 332.00 Ų
XlogP 1.00
Atomic LogP (AlogP) -0.57
H-Bond Acceptor 20
H-Bond Donor 12
Rotatable Bonds 9

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 5-Hydroxy-3-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-3-yl]-2-(4-hydroxyphenyl)-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 - 0.6788 67.88%
Caco-2 - 0.8953 89.53%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.8000 80.00%
Subcellular localzation Mitochondria 0.5329 53.29%
OATP2B1 inhibitior - 0.7060 70.60%
OATP1B1 inhibitior + 0.8788 87.88%
OATP1B3 inhibitior + 0.9724 97.24%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.7754 77.54%
P-glycoprotein inhibitior + 0.6478 64.78%
P-glycoprotein substrate - 0.9136 91.36%
CYP3A4 substrate + 0.5725 57.25%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8517 85.17%
CYP3A4 inhibition - 0.9365 93.65%
CYP2C9 inhibition - 0.9171 91.71%
CYP2C19 inhibition - 0.9032 90.32%
CYP2D6 inhibition - 0.9596 95.96%
CYP1A2 inhibition - 0.9320 93.20%
CYP2C8 inhibition - 0.5584 55.84%
CYP inhibitory promiscuity - 0.8607 86.07%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6966 69.66%
Eye corrosion - 0.9927 99.27%
Eye irritation - 0.8896 88.96%
Skin irritation - 0.8466 84.66%
Skin corrosion - 0.9636 96.36%
Ames mutagenesis - 0.5654 56.54%
Human Ether-a-go-go-Related Gene inhibition + 0.8176 81.76%
Micronuclear + 0.6533 65.33%
Hepatotoxicity - 0.7750 77.50%
skin sensitisation - 0.9177 91.77%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity + 0.6991 69.91%
Acute Oral Toxicity (c) IV 0.5235 52.35%
Estrogen receptor binding + 0.7941 79.41%
Androgen receptor binding + 0.6550 65.50%
Thyroid receptor binding + 0.5531 55.31%
Glucocorticoid receptor binding - 0.6115 61.15%
Aromatase binding - 0.5120 51.20%
PPAR gamma + 0.7526 75.26%
Honey bee toxicity - 0.7677 76.77%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5950 59.50%
Fish aquatic toxicity + 0.8498 84.98%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.35% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.01% 97.09%
CHEMBL3401 O75469 Pregnane X receptor 91.29% 94.73%
CHEMBL2581 P07339 Cathepsin D 90.91% 98.95%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 90.20% 99.15%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.49% 89.00%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 89.23% 86.92%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.95% 96.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.66% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.25% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.58% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.57% 94.45%
CHEMBL4208 P20618 Proteasome component C5 82.59% 90.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.48% 99.23%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.77% 95.89%
CHEMBL226 P30542 Adenosine A1 receptor 81.61% 95.93%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.90% 86.33%

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.
Ormocarpum kirkii

Cross-Links

Top
PubChem 14633229
LOTUS LTS0036752
wikiData Q105246181