Wattersiixanthone B

Details

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Internal ID 069466a5-9bf5-4fae-9a95-8622667a4af1
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 1-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyxanthen-9-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H20O9/c1-26-12-3-2-4-13-15(12)16(22)10-7-9(5-6-11(10)28-13)27-20-19(25)18(24)17(23)14(8-21)29-20/h2-7,14,17-21,23-25H,8H2,1H3/t14-,17-,18+,19-,20-/m1/s1
InChI Key FZIAASYHRUKXQB-LWUBGYQZSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H20O9
Molecular Weight 404.40 g/mol
Exact Mass 404.11073221 g/mol
Topological Polar Surface Area (TPSA) 135.00 Ų
XlogP 0.80
Atomic LogP (AlogP) 0.13
H-Bond Acceptor 9
H-Bond Donor 4
Rotatable Bonds 4

Synonyms

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1-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyxanthen-9-one

2D Structure

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2D Structure of Wattersiixanthone B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.6078 60.78%
Caco-2 - 0.8411 84.11%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.5812 58.12%
OATP2B1 inhibitior - 0.8419 84.19%
OATP1B1 inhibitior + 0.9248 92.48%
OATP1B3 inhibitior + 0.9777 97.77%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.6998 69.98%
P-glycoprotein inhibitior - 0.7109 71.09%
P-glycoprotein substrate - 0.7417 74.17%
CYP3A4 substrate + 0.6147 61.47%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8291 82.91%
CYP3A4 inhibition - 0.9235 92.35%
CYP2C9 inhibition - 0.9455 94.55%
CYP2C19 inhibition - 0.9300 93.00%
CYP2D6 inhibition - 0.9277 92.77%
CYP1A2 inhibition - 0.9096 90.96%
CYP2C8 inhibition - 0.6257 62.57%
CYP inhibitory promiscuity - 0.8283 82.83%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6386 63.86%
Eye corrosion - 0.9882 98.82%
Eye irritation - 0.9554 95.54%
Skin irritation - 0.8188 81.88%
Skin corrosion - 0.9671 96.71%
Ames mutagenesis + 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4095 40.95%
Micronuclear + 0.5833 58.33%
Hepatotoxicity - 0.6750 67.50%
skin sensitisation - 0.9284 92.84%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity - 0.7548 75.48%
Acute Oral Toxicity (c) III 0.7427 74.27%
Estrogen receptor binding + 0.8130 81.30%
Androgen receptor binding + 0.6120 61.20%
Thyroid receptor binding + 0.5457 54.57%
Glucocorticoid receptor binding + 0.7880 78.80%
Aromatase binding + 0.7003 70.03%
PPAR gamma + 0.7382 73.82%
Honey bee toxicity - 0.7824 78.24%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity - 0.4202 42.02%

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 98.42% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 95.99% 94.00%
CHEMBL2581 P07339 Cathepsin D 95.17% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.96% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.99% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.11% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.30% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 90.67% 96.00%
CHEMBL220 P22303 Acetylcholinesterase 90.11% 94.45%
CHEMBL5608 Q16288 NT-3 growth factor receptor 89.28% 95.89%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.70% 99.17%
CHEMBL2535 P11166 Glucose transporter 87.07% 98.75%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.32% 97.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.38% 99.23%
CHEMBL3401 O75469 Pregnane X receptor 85.13% 94.73%
CHEMBL1907 P15144 Aminopeptidase N 84.41% 93.31%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.19% 92.62%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 82.96% 86.92%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.38% 94.45%
CHEMBL3714130 P46095 G-protein coupled receptor 6 80.07% 97.36%

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.
Polygala wattersii

Cross-Links

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PubChem 10525258
LOTUS LTS0030811
wikiData Q105004954