Homoferreirin

Details

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Internal ID 877e281d-4740-4134-96e4-e3d626fd8b38
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > O-methylated isoflavonoids > 4-O-methylated isoflavonoids
IUPAC Name 3-(2,4-dimethoxyphenyl)-5,7-dihydroxy-2,3-dihydrochromen-4-one
SMILES (Canonical) COC1=CC(=C(C=C1)C2COC3=CC(=CC(=C3C2=O)O)O)OC
SMILES (Isomeric) COC1=CC(=C(C=C1)C2COC3=CC(=CC(=C3C2=O)O)O)OC
InChI InChI=1S/C17H16O6/c1-21-10-3-4-11(14(7-10)22-2)12-8-23-15-6-9(18)5-13(19)16(15)17(12)20/h3-7,12,18-19H,8H2,1-2H3
InChI Key LMLDNMHDNFCNCW-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C17H16O6
Molecular Weight 316.30 g/mol
Exact Mass 316.09468823 g/mol
Topological Polar Surface Area (TPSA) 85.20 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.47
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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482-01-9
3-(2,4-dimethoxyphenyl)-5,7-dihydroxy-2,3-dihydrochromen-4-one
3-(2,4-Dimethoxyphenyl)-5,7-dihydroxychroman-4-one
5,7-dihydroxy-2',4'-dimethoxyisoflavanone
3-(2,4-DIMETHOXYPHENYL)-5,7-DIHYDROXY-CHROMAN-4-ONE
starbld0019167
CHEBI:5754
DTXSID50331952
LMPK12050502
AKOS030553610
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Homoferreirin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9621 96.21%
Caco-2 + 0.8979 89.79%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.8220 82.20%
OATP2B1 inhibitior - 0.8598 85.98%
OATP1B1 inhibitior + 0.9487 94.87%
OATP1B3 inhibitior + 0.8673 86.73%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.7413 74.13%
P-glycoprotein inhibitior - 0.8029 80.29%
P-glycoprotein substrate - 0.7993 79.93%
CYP3A4 substrate + 0.5749 57.49%
CYP2C9 substrate - 0.8060 80.60%
CYP2D6 substrate - 0.7896 78.96%
CYP3A4 inhibition + 0.7069 70.69%
CYP2C9 inhibition + 0.7483 74.83%
CYP2C19 inhibition + 0.8502 85.02%
CYP2D6 inhibition - 0.7355 73.55%
CYP1A2 inhibition + 0.8365 83.65%
CYP2C8 inhibition + 0.5207 52.07%
CYP inhibitory promiscuity + 0.8550 85.50%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.7355 73.55%
Eye corrosion - 0.9803 98.03%
Eye irritation + 0.5294 52.94%
Skin irritation - 0.7538 75.38%
Skin corrosion - 0.9602 96.02%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5322 53.22%
Micronuclear + 0.8400 84.00%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation - 0.9398 93.98%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity + 0.4651 46.51%
Acute Oral Toxicity (c) III 0.7295 72.95%
Estrogen receptor binding + 0.9235 92.35%
Androgen receptor binding + 0.8087 80.87%
Thyroid receptor binding + 0.7107 71.07%
Glucocorticoid receptor binding + 0.7450 74.50%
Aromatase binding + 0.5661 56.61%
PPAR gamma + 0.6274 62.74%
Honey bee toxicity - 0.8536 85.36%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5851 58.51%
Fish aquatic toxicity + 0.8819 88.19%

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 99.19% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.20% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.13% 96.09%
CHEMBL2581 P07339 Cathepsin D 94.30% 98.95%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 93.43% 99.15%
CHEMBL3192 Q9BY41 Histone deacetylase 8 91.96% 93.99%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.88% 94.45%
CHEMBL4208 P20618 Proteasome component C5 91.60% 90.00%
CHEMBL1929 P47989 Xanthine dehydrogenase 90.98% 96.12%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.87% 86.33%
CHEMBL2535 P11166 Glucose transporter 90.53% 98.75%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.20% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 89.72% 95.89%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.40% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.72% 89.00%
CHEMBL240 Q12809 HERG 88.44% 89.76%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.42% 99.23%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 87.77% 94.80%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 87.26% 92.62%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.84% 99.17%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 86.31% 93.40%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 85.90% 100.00%
CHEMBL340 P08684 Cytochrome P450 3A4 83.77% 91.19%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.01% 97.14%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.60% 92.94%

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.
Cicer arietinum
Grona styracifolia
Zollernia paraensis

Cross-Links

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PubChem 442788
NPASS NPC156522
LOTUS LTS0273188
wikiData Q27106879