Oxyayanin A

Details

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Internal ID e2eaa830-49d3-472e-b543-80509900e64d
Taxonomy Phenylpropanoids and polyketides > Flavonoids > O-methylated flavonoids > 7-O-methylated flavonoids
IUPAC Name 2-(2,5-dihydroxy-4-methoxyphenyl)-5-hydroxy-3,7-dimethoxychromen-4-one
SMILES (Canonical) COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C=C3O)OC)O)O
SMILES (Isomeric) COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C=C3O)OC)O)O
InChI InChI=1S/C18H16O8/c1-23-8-4-12(21)15-14(5-8)26-17(18(25-3)16(15)22)9-6-11(20)13(24-2)7-10(9)19/h4-7,19-21H,1-3H3
InChI Key KGJTXYKKHKRNIM-UHFFFAOYSA-N
Popularity 7 references in papers

Physical and Chemical Properties

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Molecular Formula C18H16O8
Molecular Weight 360.30 g/mol
Exact Mass 360.08451746 g/mol
Topological Polar Surface Area (TPSA) 115.00 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.60
H-Bond Acceptor 8
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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Oxyanin A
549-17-7
CHEBI:7854
5,2',5'-trihydroxy-3,7,4'-trimethoxyflavone
Flavone. 2',5,5'-trihydroxy-3,4',7-trimethoxy-
OXYAYANINA
CHEMBL491989
DTXSID40415174
LMPK12112516
Q27107598
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Oxyayanin A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9711 97.11%
Caco-2 + 0.5779 57.79%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.7936 79.36%
OATP2B1 inhibitior - 0.6912 69.12%
OATP1B1 inhibitior + 0.8888 88.88%
OATP1B3 inhibitior + 0.9480 94.80%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.5534 55.34%
P-glycoprotein inhibitior + 0.6249 62.49%
P-glycoprotein substrate - 0.8514 85.14%
CYP3A4 substrate + 0.5431 54.31%
CYP2C9 substrate - 0.6401 64.01%
CYP2D6 substrate - 0.8296 82.96%
CYP3A4 inhibition - 0.7237 72.37%
CYP2C9 inhibition - 0.6863 68.63%
CYP2C19 inhibition + 0.6566 65.66%
CYP2D6 inhibition - 0.8329 83.29%
CYP1A2 inhibition + 0.8642 86.42%
CYP2C8 inhibition + 0.7071 70.71%
CYP inhibitory promiscuity + 0.7231 72.31%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5851 58.51%
Eye corrosion - 0.9825 98.25%
Eye irritation + 0.7454 74.54%
Skin irritation - 0.7275 72.75%
Skin corrosion - 0.9759 97.59%
Ames mutagenesis + 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7472 74.72%
Micronuclear + 0.8600 86.00%
Hepatotoxicity - 0.5625 56.25%
skin sensitisation - 0.9511 95.11%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.6242 62.42%
Acute Oral Toxicity (c) III 0.4741 47.41%
Estrogen receptor binding + 0.8581 85.81%
Androgen receptor binding + 0.7472 74.72%
Thyroid receptor binding + 0.6033 60.33%
Glucocorticoid receptor binding + 0.8458 84.58%
Aromatase binding + 0.6690 66.90%
PPAR gamma + 0.8528 85.28%
Honey bee toxicity - 0.9103 91.03%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5749 57.49%
Fish aquatic toxicity + 0.8969 89.69%

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 97.26% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.10% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.90% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 91.98% 99.15%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.35% 89.00%
CHEMBL3194 P02766 Transthyretin 91.24% 90.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.21% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.45% 85.14%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.03% 99.17%
CHEMBL2535 P11166 Glucose transporter 89.57% 98.75%
CHEMBL2581 P07339 Cathepsin D 89.21% 98.95%
CHEMBL4208 P20618 Proteasome component C5 88.63% 90.00%
CHEMBL3401 O75469 Pregnane X receptor 82.38% 94.73%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.27% 99.23%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 81.16% 94.42%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.02% 96.09%

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.
Apuleia leiocarpa
Berberis amurensis
Berberis fortunei
Berberis thunbergii
Crinum album
Distemonanthus benthamianus
Thalictrum lucidum
Vicia faba
Xanthorhiza simplicissima

Cross-Links

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PubChem 5281676
NPASS NPC200388
LOTUS LTS0273278
wikiData Q27107598