1-Hydroxy-2,7-dimethoxy-3-(beta-D-glucopyranosyloxy)-9H-xanthene-9-one

Details

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Internal ID 385ad860-a6ac-4ca1-abf6-f65ce4d0b576
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 1-hydroxy-2,7-dimethoxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyxanthen-9-one
SMILES (Canonical) COC1=CC2=C(C=C1)OC3=CC(=C(C(=C3C2=O)O)OC)OC4C(C(C(C(O4)CO)O)O)O
SMILES (Isomeric) COC1=CC2=C(C=C1)OC3=CC(=C(C(=C3C2=O)O)OC)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O
InChI InChI=1S/C21H22O11/c1-28-8-3-4-10-9(5-8)15(23)14-11(30-10)6-12(20(29-2)17(14)25)31-21-19(27)18(26)16(24)13(7-22)32-21/h3-6,13,16,18-19,21-22,24-27H,7H2,1-2H3/t13-,16-,18+,19-,21-/m1/s1
InChI Key OUISWDCJSICGJA-GUTCHGCDSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H22O11
Molecular Weight 450.40 g/mol
Exact Mass 450.11621151 g/mol
Topological Polar Surface Area (TPSA) 164.00 Ų
XlogP 0.90
Atomic LogP (AlogP) -0.15
H-Bond Acceptor 11
H-Bond Donor 5
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-Hydroxy-2,7-dimethoxy-3-(beta-D-glucopyranosyloxy)-9H-xanthene-9-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5891 58.91%
Caco-2 - 0.7894 78.94%
Blood Brain Barrier - 0.8500 85.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.5382 53.82%
OATP2B1 inhibitior - 0.5555 55.55%
OATP1B1 inhibitior + 0.8420 84.20%
OATP1B3 inhibitior + 0.9702 97.02%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.5712 57.12%
P-glycoprotein inhibitior - 0.6005 60.05%
P-glycoprotein substrate - 0.5939 59.39%
CYP3A4 substrate + 0.6084 60.84%
CYP2C9 substrate - 0.8485 84.85%
CYP2D6 substrate - 0.8501 85.01%
CYP3A4 inhibition - 0.8887 88.87%
CYP2C9 inhibition - 0.9431 94.31%
CYP2C19 inhibition - 0.9262 92.62%
CYP2D6 inhibition - 0.9179 91.79%
CYP1A2 inhibition - 0.8804 88.04%
CYP2C8 inhibition + 0.5000 50.00%
CYP inhibitory promiscuity - 0.8059 80.59%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.7283 72.83%
Eye corrosion - 0.9891 98.91%
Eye irritation - 0.9256 92.56%
Skin irritation - 0.8272 82.72%
Skin corrosion - 0.9636 96.36%
Ames mutagenesis + 0.6936 69.36%
Human Ether-a-go-go-Related Gene inhibition - 0.4032 40.32%
Micronuclear + 0.6133 61.33%
Hepatotoxicity - 0.6375 63.75%
skin sensitisation - 0.9214 92.14%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity - 0.9436 94.36%
Acute Oral Toxicity (c) III 0.7037 70.37%
Estrogen receptor binding + 0.7901 79.01%
Androgen receptor binding + 0.5526 55.26%
Thyroid receptor binding + 0.5790 57.90%
Glucocorticoid receptor binding + 0.6483 64.83%
Aromatase binding + 0.6991 69.91%
PPAR gamma + 0.6745 67.45%
Honey bee toxicity - 0.8022 80.22%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6449 64.49%
Fish aquatic toxicity + 0.6994 69.94%

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 99.46% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 96.73% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.05% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.76% 89.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.42% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.56% 99.17%
CHEMBL2581 P07339 Cathepsin D 91.33% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 85.64% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.51% 94.45%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 85.50% 86.92%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.06% 96.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.67% 99.15%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.59% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.59% 95.89%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.80% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.61% 99.23%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.86% 92.62%
CHEMBL1951 P21397 Monoamine oxidase A 80.67% 91.49%

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.
Halenia corniculata

Cross-Links

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PubChem 100917653
LOTUS LTS0095470
wikiData Q105200174