4'-O-Methylatalantoflavone

Details

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Internal ID 5d044171-d7e0-4e12-bb8e-3e0feb9e9f2d
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Pyranoflavonoids
IUPAC Name 5-hydroxy-2-(4-methoxyphenyl)-8,8-dimethylpyrano[2,3-h]chromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H18O5/c1-21(2)9-8-14-18(26-21)11-16(23)19-15(22)10-17(25-20(14)19)12-4-6-13(24-3)7-5-12/h4-11,23H,1-3H3
InChI Key ZBCMZXUJUABTJX-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C21H18O5
Molecular Weight 350.40 g/mol
Exact Mass 350.11542367 g/mol
Topological Polar Surface Area (TPSA) 65.00 Ų
XlogP 4.30
Atomic LogP (AlogP) 4.36
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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1205687-49-5
CHEMBL5570464
orb1680558
TN6184
AKOS040763238
F94032

2D Structure

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2D Structure of 4'-O-Methylatalantoflavone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9917 99.17%
Caco-2 + 0.7619 76.19%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.8357 83.57%
OATP2B1 inhibitior - 0.7155 71.55%
OATP1B1 inhibitior + 0.9090 90.90%
OATP1B3 inhibitior + 0.9762 97.62%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.8580 85.80%
P-glycoprotein inhibitior + 0.8900 89.00%
P-glycoprotein substrate - 0.7853 78.53%
CYP3A4 substrate + 0.6274 62.74%
CYP2C9 substrate - 0.6192 61.92%
CYP2D6 substrate - 0.8382 83.82%
CYP3A4 inhibition + 0.7369 73.69%
CYP2C9 inhibition + 0.5050 50.50%
CYP2C19 inhibition + 0.8237 82.37%
CYP2D6 inhibition - 0.7943 79.43%
CYP1A2 inhibition - 0.5969 59.69%
CYP2C8 inhibition + 0.6238 62.38%
CYP inhibitory promiscuity + 0.6699 66.99%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9413 94.13%
Carcinogenicity (trinary) Danger 0.5018 50.18%
Eye corrosion - 0.9842 98.42%
Eye irritation + 0.5345 53.45%
Skin irritation - 0.7920 79.20%
Skin corrosion - 0.9768 97.68%
Ames mutagenesis + 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4458 44.58%
Micronuclear + 0.6000 60.00%
Hepatotoxicity - 0.8092 80.92%
skin sensitisation - 0.8892 88.92%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity - 0.7071 70.71%
Acute Oral Toxicity (c) III 0.5216 52.16%
Estrogen receptor binding + 0.9554 95.54%
Androgen receptor binding + 0.9153 91.53%
Thyroid receptor binding + 0.8221 82.21%
Glucocorticoid receptor binding + 0.9315 93.15%
Aromatase binding + 0.7994 79.94%
PPAR gamma + 0.8900 89.00%
Honey bee toxicity - 0.8051 80.51%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9516 95.16%

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 99.42% 91.11%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 96.62% 99.15%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 96.51% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.95% 94.45%
CHEMBL2581 P07339 Cathepsin D 94.56% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.18% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.40% 95.56%
CHEMBL1907 P15144 Aminopeptidase N 92.26% 93.31%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 91.79% 85.30%
CHEMBL3192 Q9BY41 Histone deacetylase 8 91.57% 93.99%
CHEMBL5284 Q96RR4 CaM-kinase kinase beta 89.38% 89.23%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 88.94% 96.77%
CHEMBL4208 P20618 Proteasome component C5 88.92% 90.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.66% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.59% 86.33%
CHEMBL308 P06493 Cyclin-dependent kinase 1 87.34% 91.73%
CHEMBL1951 P21397 Monoamine oxidase A 87.14% 91.49%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 85.37% 95.71%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.36% 99.17%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 82.28% 86.92%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 82.16% 81.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.44% 99.23%
CHEMBL3401 O75469 Pregnane X receptor 81.35% 94.73%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.16% 95.50%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.11% 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.
Atalantia buxifolia

Cross-Links

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PubChem 154804638
LOTUS LTS0161262
wikiData Q105370467