Yahyaxanthone

Details

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Internal ID 81a472fc-a3c5-46ee-b2c6-dd5e8237abe4
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > Pyranoxanthones
IUPAC Name 6-hydroxy-5,8,10,11-tetramethoxy-3,3-dimethylpyrano[2,3-c]xanthen-7-one
SMILES (Canonical) CC1(C=CC2=C3C(=C(C(=C2O1)OC)O)C(=O)C4=C(O3)C(=C(C=C4OC)OC)OC)C
SMILES (Isomeric) CC1(C=CC2=C3C(=C(C(=C2O1)OC)O)C(=O)C4=C(O3)C(=C(C=C4OC)OC)OC)C
InChI InChI=1S/C22H22O8/c1-22(2)8-7-10-17-14(16(24)21(28-6)18(10)30-22)15(23)13-11(25-3)9-12(26-4)19(27-5)20(13)29-17/h7-9,24H,1-6H3
InChI Key BSWKVMNQZNMVIO-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H22O8
Molecular Weight 414.40 g/mol
Exact Mass 414.13146766 g/mol
Topological Polar Surface Area (TPSA) 92.70 Ų
XlogP 4.00
Atomic LogP (AlogP) 3.87
H-Bond Acceptor 8
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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6-hydroxy-5,8,10,11-tetramethoxy-3,3-dimethyl-3H,7H-pyrano[2,3-c]xanthen-7-one
CHEBI:66491
DTXSID801137335
Q27135094
1073242-96-2

2D Structure

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2D Structure of Yahyaxanthone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9847 98.47%
Caco-2 + 0.6414 64.14%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.7172 71.72%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8748 87.48%
OATP1B3 inhibitior + 0.9844 98.44%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.8622 86.22%
P-glycoprotein inhibitior + 0.7445 74.45%
P-glycoprotein substrate - 0.6456 64.56%
CYP3A4 substrate + 0.6109 61.09%
CYP2C9 substrate - 0.6192 61.92%
CYP2D6 substrate - 0.8382 83.82%
CYP3A4 inhibition + 0.7404 74.04%
CYP2C9 inhibition - 0.9287 92.87%
CYP2C19 inhibition + 0.6924 69.24%
CYP2D6 inhibition - 0.6622 66.22%
CYP1A2 inhibition + 0.6401 64.01%
CYP2C8 inhibition + 0.6195 61.95%
CYP inhibitory promiscuity + 0.5000 50.00%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Danger 0.4937 49.37%
Eye corrosion - 0.9848 98.48%
Eye irritation + 0.7162 71.62%
Skin irritation - 0.7469 74.69%
Skin corrosion - 0.9665 96.65%
Ames mutagenesis + 0.5136 51.36%
Human Ether-a-go-go-Related Gene inhibition - 0.5443 54.43%
Micronuclear + 0.6400 64.00%
Hepatotoxicity + 0.5125 51.25%
skin sensitisation - 0.8200 82.00%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity - 0.6929 69.29%
Acute Oral Toxicity (c) III 0.5517 55.17%
Estrogen receptor binding + 0.8334 83.34%
Androgen receptor binding + 0.5687 56.87%
Thyroid receptor binding + 0.8023 80.23%
Glucocorticoid receptor binding + 0.8772 87.72%
Aromatase binding + 0.7524 75.24%
PPAR gamma + 0.8617 86.17%
Honey bee toxicity - 0.7649 76.49%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5249 52.49%
Fish aquatic toxicity + 0.9509 95.09%

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 99.12% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.06% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.09% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.04% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.81% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.07% 95.56%
CHEMBL3192 Q9BY41 Histone deacetylase 8 88.25% 93.99%
CHEMBL1255126 O15151 Protein Mdm4 87.51% 90.20%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.55% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.12% 85.14%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.99% 99.17%
CHEMBL2535 P11166 Glucose transporter 83.94% 98.75%
CHEMBL4208 P20618 Proteasome component C5 81.75% 90.00%
CHEMBL2581 P07339 Cathepsin D 81.70% 98.95%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 80.52% 95.71%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 80.35% 99.15%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.20% 99.23%

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.
Garcinia rigida

Cross-Links

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PubChem 70697831
LOTUS LTS0209466
wikiData Q27135094