Grantioidinin

Details

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Internal ID fd7d322f-d322-424d-84f3-4182314bb259
Taxonomy Phenylpropanoids and polyketides > Flavonoids > O-methylated flavonoids > 8-O-methylated flavonoids
IUPAC Name 2-(2,5-dimethoxyphenyl)-5-hydroxy-3,6,7,8-tetramethoxychromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H22O9/c1-24-10-7-8-12(25-2)11(9-10)16-18(26-3)14(22)13-15(23)19(27-4)21(29-6)20(28-5)17(13)30-16/h7-9,23H,1-6H3
InChI Key YLDLSFKRVJHNKM-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H22O9
Molecular Weight 418.40 g/mol
Exact Mass 418.12638228 g/mol
Topological Polar Surface Area (TPSA) 102.00 Ų
XlogP 3.40
Atomic LogP (AlogP) 3.22
H-Bond Acceptor 9
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

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RefChem:144322
2-(2,5-dimethoxyphenyl)-5-hydroxy-3,6,7,8-tetramethoxychromen-4-one
135755-50-9
LMPK12113290

2D Structure

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2D Structure of Grantioidinin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9823 98.23%
Caco-2 + 0.7815 78.15%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.7745 77.45%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9025 90.25%
OATP1B3 inhibitior + 0.9817 98.17%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.7216 72.16%
P-glycoprotein inhibitior + 0.8731 87.31%
P-glycoprotein substrate - 0.8143 81.43%
CYP3A4 substrate + 0.5375 53.75%
CYP2C9 substrate - 0.6401 64.01%
CYP2D6 substrate - 0.8296 82.96%
CYP3A4 inhibition - 0.5748 57.48%
CYP2C9 inhibition - 0.8861 88.61%
CYP2C19 inhibition + 0.5778 57.78%
CYP2D6 inhibition - 0.9231 92.31%
CYP1A2 inhibition + 0.8530 85.30%
CYP2C8 inhibition + 0.6500 65.00%
CYP inhibitory promiscuity + 0.6103 61.03%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5716 57.16%
Eye corrosion - 0.9793 97.93%
Eye irritation + 0.6408 64.08%
Skin irritation - 0.7150 71.50%
Skin corrosion - 0.9836 98.36%
Ames mutagenesis + 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5475 54.75%
Micronuclear + 0.8359 83.59%
Hepatotoxicity - 0.5935 59.35%
skin sensitisation - 0.9504 95.04%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity - 0.5508 55.08%
Acute Oral Toxicity (c) II 0.4982 49.82%
Estrogen receptor binding + 0.8554 85.54%
Androgen receptor binding + 0.6849 68.49%
Thyroid receptor binding + 0.7074 70.74%
Glucocorticoid receptor binding + 0.7733 77.33%
Aromatase binding + 0.6888 68.88%
PPAR gamma + 0.7670 76.70%
Honey bee toxicity - 0.9035 90.35%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5649 56.49%
Fish aquatic toxicity + 0.8902 89.02%

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 98.23% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 96.00% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.18% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.76% 86.33%
CHEMBL4208 P20618 Proteasome component C5 88.96% 90.00%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 88.33% 94.42%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.11% 89.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 87.99% 99.15%
CHEMBL2535 P11166 Glucose transporter 87.86% 98.75%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.23% 99.17%
CHEMBL2581 P07339 Cathepsin D 86.29% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.46% 99.23%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.46% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 81.39% 94.73%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.69% 96.00%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 80.16% 96.67%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.10% 95.89%

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.
Iphiona grantioides

Cross-Links

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PubChem 14861189
LOTUS LTS0174991
wikiData Q105350083