7-Geranylformononetin

Details

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Internal ID d14a5fdc-0420-4701-9ec5-cd88000833e1
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > O-methylated isoflavonoids > 4-O-methylated isoflavonoids > 4-O-methylisoflavones
IUPAC Name 7-[(2E)-3,7-dimethylocta-2,6-dienoxy]-3-(4-methoxyphenyl)chromen-4-one
SMILES (Canonical) CC(=CCCC(=CCOC1=CC2=C(C=C1)C(=O)C(=CO2)C3=CC=C(C=C3)OC)C)C
SMILES (Isomeric) CC(=CCC/C(=C/COC1=CC2=C(C=C1)C(=O)C(=CO2)C3=CC=C(C=C3)OC)/C)C
InChI InChI=1S/C26H28O4/c1-18(2)6-5-7-19(3)14-15-29-22-12-13-23-25(16-22)30-17-24(26(23)27)20-8-10-21(28-4)11-9-20/h6,8-14,16-17H,5,7,15H2,1-4H3/b19-14+
InChI Key NIHAJZITTDENLE-XMHGGMMESA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C26H28O4
Molecular Weight 404.50 g/mol
Exact Mass 404.19875937 g/mol
Topological Polar Surface Area (TPSA) 44.80 Ų
XlogP 6.50
Atomic LogP (AlogP) 6.54
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 8

Synonyms

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4'-Methoxy-7-geranyloxyisoflavone
CHEBI:187685
LMPK12050031
7-[(2E)-3,7-dimethylocta-2,6-dienoxy]-3-(4-methoxyphenyl)chromen-4-one

2D Structure

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2D Structure of 7-Geranylformononetin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9947 99.47%
Caco-2 + 0.6384 63.84%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.8681 86.81%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9362 93.62%
OATP1B3 inhibitior + 0.9456 94.56%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.9789 97.89%
P-glycoprotein inhibitior + 0.9342 93.42%
P-glycoprotein substrate - 0.8160 81.60%
CYP3A4 substrate + 0.6314 63.14%
CYP2C9 substrate - 0.8301 83.01%
CYP2D6 substrate - 0.7491 74.91%
CYP3A4 inhibition + 0.5319 53.19%
CYP2C9 inhibition + 0.6032 60.32%
CYP2C19 inhibition + 0.8328 83.28%
CYP2D6 inhibition - 0.8039 80.39%
CYP1A2 inhibition + 0.9153 91.53%
CYP2C8 inhibition + 0.5114 51.14%
CYP inhibitory promiscuity + 0.8563 85.63%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.7554 75.54%
Eye corrosion - 0.9888 98.88%
Eye irritation - 0.9157 91.57%
Skin irritation - 0.8391 83.91%
Skin corrosion - 0.9681 96.81%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9083 90.83%
Micronuclear - 0.7700 77.00%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation - 0.8254 82.54%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity - 0.5608 56.08%
Acute Oral Toxicity (c) III 0.4933 49.33%
Estrogen receptor binding + 0.8506 85.06%
Androgen receptor binding + 0.9376 93.76%
Thyroid receptor binding + 0.6845 68.45%
Glucocorticoid receptor binding + 0.8315 83.15%
Aromatase binding - 0.4905 49.05%
PPAR gamma + 0.8248 82.48%
Honey bee toxicity - 0.8635 86.35%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 1.0000 100.00%

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 98.88% 91.11%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 96.60% 92.08%
CHEMBL2581 P07339 Cathepsin D 96.30% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 95.06% 99.17%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.70% 94.00%
CHEMBL1907 P15144 Aminopeptidase N 92.41% 93.31%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.33% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.61% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.57% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 90.20% 94.73%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 90.14% 96.00%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 88.93% 86.92%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.13% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.10% 85.14%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 86.05% 95.50%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.88% 99.15%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.24% 94.45%
CHEMBL4208 P20618 Proteasome component C5 85.11% 90.00%

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.
Millettia ferruginea
Millettia griffoniana

Cross-Links

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PubChem 14704588
LOTUS LTS0000237
wikiData Q104399007