W-Hydroxyxanthorin 1-O-methyl ester 8-O-

Details

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Internal ID 32812167-c73f-4508-b3ae-14a11d36c7c0
Taxonomy Benzenoids > Anthracenes > Anthraquinones
IUPAC Name 1-hydroxy-7-(hydroxymethyl)-2,5-dimethoxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyanthracene-9,10-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H24O12/c1-32-10-4-8(6-24)3-9-14(10)20(29)15-11(5-12(33-2)18(27)16(15)17(9)26)34-23-22(31)21(30)19(28)13(7-25)35-23/h3-5,13,19,21-25,27-28,30-31H,6-7H2,1-2H3
InChI Key WAQWVBSSPJYVCL-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C23H24O12
Molecular Weight 492.40 g/mol
Exact Mass 492.12677620 g/mol
Topological Polar Surface Area (TPSA) 192.00 Ų
XlogP 0.00
Atomic LogP (AlogP) -1.14
H-Bond Acceptor 12
H-Bond Donor 6
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of W-Hydroxyxanthorin 1-O-methyl ester 8-O-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.6618 66.18%
Caco-2 - 0.8532 85.32%
Blood Brain Barrier - 0.8250 82.50%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.4615 46.15%
OATP2B1 inhibitior - 0.7107 71.07%
OATP1B1 inhibitior + 0.7598 75.98%
OATP1B3 inhibitior + 0.9734 97.34%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.5508 55.08%
P-glycoprotein inhibitior - 0.5725 57.25%
P-glycoprotein substrate - 0.7280 72.80%
CYP3A4 substrate + 0.6250 62.50%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8421 84.21%
CYP3A4 inhibition - 0.9106 91.06%
CYP2C9 inhibition - 0.8864 88.64%
CYP2C19 inhibition - 0.8874 88.74%
CYP2D6 inhibition - 0.9420 94.20%
CYP1A2 inhibition - 0.8050 80.50%
CYP2C8 inhibition + 0.4601 46.01%
CYP inhibitory promiscuity - 0.8441 84.41%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.7294 72.94%
Eye corrosion - 0.9894 98.94%
Eye irritation - 0.8603 86.03%
Skin irritation - 0.8602 86.02%
Skin corrosion - 0.9598 95.98%
Ames mutagenesis + 0.5517 55.17%
Human Ether-a-go-go-Related Gene inhibition - 0.5253 52.53%
Micronuclear + 0.6033 60.33%
Hepatotoxicity - 0.7198 71.98%
skin sensitisation - 0.9145 91.45%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity - 0.5947 59.47%
Acute Oral Toxicity (c) III 0.6584 65.84%
Estrogen receptor binding + 0.8016 80.16%
Androgen receptor binding - 0.6194 61.94%
Thyroid receptor binding - 0.5845 58.45%
Glucocorticoid receptor binding + 0.7348 73.48%
Aromatase binding + 0.5312 53.12%
PPAR gamma + 0.5794 57.94%
Honey bee toxicity - 0.7784 77.84%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.6949 69.49%
Fish aquatic toxicity + 0.7797 77.97%

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
CHEMBL2581 P07339 Cathepsin D 98.39% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.11% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.06% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.86% 85.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.72% 89.00%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 92.52% 96.21%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.90% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.80% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 89.67% 94.73%
CHEMBL226 P30542 Adenosine A1 receptor 88.82% 95.93%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.55% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.42% 86.33%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 86.36% 86.92%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.36% 95.89%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 84.31% 95.89%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 80.99% 96.90%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.50% 97.25%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 85218866
LOTUS LTS0150723
wikiData Q77369942