Isoflavone, 7-hydroxy-4',6-dimethoxy-, acetate

Details

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Internal ID a12f3802-893b-41b7-a4b5-89a662d330e7
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > O-methylated isoflavonoids > 4-O-methylated isoflavonoids > 4-O-methylisoflavones
IUPAC Name [6-methoxy-3-(4-methoxyphenyl)-4-oxochromen-7-yl] acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H16O6/c1-11(20)25-18-9-16-14(8-17(18)23-3)19(21)15(10-24-16)12-4-6-13(22-2)7-5-12/h4-10H,1-3H3
InChI Key OLSFYFUZJCERJF-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C19H16O6
Molecular Weight 340.30 g/mol
Exact Mass 340.09468823 g/mol
Topological Polar Surface Area (TPSA) 71.10 Ų
XlogP 2.90
Atomic LogP (AlogP) 3.40
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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7-Hydroxy-4',6-dimethoxyisoflavone acetate
4253-19-4
DTXSID60195320
RefChem:149336
DTXCID70117811
7-O-Ac-afromosin
MLS002473152
CHEMBL446567
HMS2267B11
NCGC00247475-01
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Isoflavone, 7-hydroxy-4',6-dimethoxy-, acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9751 97.51%
Caco-2 + 0.7725 77.25%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.6549 65.49%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9468 94.68%
OATP1B3 inhibitior + 0.9806 98.06%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.7099 70.99%
P-glycoprotein inhibitior + 0.9129 91.29%
P-glycoprotein substrate - 0.7912 79.12%
CYP3A4 substrate + 0.5862 58.62%
CYP2C9 substrate - 0.8104 81.04%
CYP2D6 substrate - 0.8618 86.18%
CYP3A4 inhibition - 0.7725 77.25%
CYP2C9 inhibition - 0.9062 90.62%
CYP2C19 inhibition - 0.9025 90.25%
CYP2D6 inhibition - 0.9796 97.96%
CYP1A2 inhibition + 0.9108 91.08%
CYP2C8 inhibition + 0.5125 51.25%
CYP inhibitory promiscuity + 0.5112 51.12%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5526 55.26%
Eye corrosion - 0.9752 97.52%
Eye irritation - 0.7566 75.66%
Skin irritation - 0.8090 80.90%
Skin corrosion - 0.9780 97.80%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7342 73.42%
Micronuclear + 0.7659 76.59%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation - 0.9547 95.47%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity + 0.4826 48.26%
Acute Oral Toxicity (c) II 0.6190 61.90%
Estrogen receptor binding + 0.9107 91.07%
Androgen receptor binding + 0.9188 91.88%
Thyroid receptor binding + 0.6274 62.74%
Glucocorticoid receptor binding + 0.8256 82.56%
Aromatase binding - 0.6058 60.58%
PPAR gamma + 0.6923 69.23%
Honey bee toxicity - 0.8465 84.65%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5349 53.49%
Fish aquatic toxicity + 0.9683 96.83%

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 97.15% 91.11%
CHEMBL2581 P07339 Cathepsin D 95.81% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.71% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.63% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.56% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.10% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.84% 86.33%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 86.19% 96.47%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.97% 96.09%
CHEMBL1907 P15144 Aminopeptidase N 84.69% 93.31%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 84.45% 95.50%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.26% 85.14%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 84.09% 86.92%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.67% 96.00%
CHEMBL2535 P11166 Glucose transporter 83.35% 98.75%
CHEMBL5925 P22413 Ectonucleotide pyrophosphatase/phosphodiesterase family member 1 82.41% 92.38%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.98% 99.23%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.79% 92.62%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 80.45% 81.11%

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.
Wisteria brachybotrys
Wisteria brachybotrys

Cross-Links

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PubChem 3083840
NPASS NPC186507
LOTUS LTS0230851
wikiData Q83068209