Gnaphaliin 7-epoxymethylbutyl ether

Details

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Internal ID 07b68622-417d-44b0-a768-2ef3e2fb9325
Taxonomy Phenylpropanoids and polyketides > Flavonoids > O-methylated flavonoids > 8-O-methylated flavonoids
IUPAC Name 7-[(3,3-dimethyloxiran-2-yl)methoxy]-5-hydroxy-3,8-dimethoxy-2-phenylchromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H22O7/c1-22(2)15(29-22)11-27-14-10-13(23)16-17(24)21(26-4)18(12-8-6-5-7-9-12)28-20(16)19(14)25-3/h5-10,15,23H,11H2,1-4H3
InChI Key ZSBMVYLMXIISEC-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H22O7
Molecular Weight 398.40 g/mol
Exact Mass 398.13655304 g/mol
Topological Polar Surface Area (TPSA) 86.80 Ų
XlogP 3.80
Atomic LogP (AlogP) 3.74
H-Bond Acceptor 7
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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CHEBI:178241
LMPK12113079
7-[(3,3-dimethyloxiran-2-yl)methoxy]-5-hydroxy-3,8-dimethoxy-2-phenylchromen-4-one

2D Structure

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2D Structure of Gnaphaliin 7-epoxymethylbutyl ether

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9803 98.03%
Caco-2 + 0.6422 64.22%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.8007 80.07%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9235 92.35%
OATP1B3 inhibitior + 0.8976 89.76%
MATE1 inhibitior - 0.6400 64.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.9364 93.64%
P-glycoprotein inhibitior + 0.9027 90.27%
P-glycoprotein substrate - 0.6078 60.78%
CYP3A4 substrate + 0.5794 57.94%
CYP2C9 substrate - 0.6228 62.28%
CYP2D6 substrate - 0.8416 84.16%
CYP3A4 inhibition - 0.5830 58.30%
CYP2C9 inhibition - 0.6934 69.34%
CYP2C19 inhibition + 0.5287 52.87%
CYP2D6 inhibition - 0.8867 88.67%
CYP1A2 inhibition - 0.7224 72.24%
CYP2C8 inhibition + 0.7833 78.33%
CYP inhibitory promiscuity - 0.6844 68.44%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6503 65.03%
Eye corrosion - 0.9877 98.77%
Eye irritation - 0.7692 76.92%
Skin irritation - 0.8045 80.45%
Skin corrosion - 0.9638 96.38%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3822 38.22%
Micronuclear - 0.5200 52.00%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation - 0.7871 78.71%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.5787 57.87%
Acute Oral Toxicity (c) III 0.6416 64.16%
Estrogen receptor binding + 0.9190 91.90%
Androgen receptor binding + 0.8151 81.51%
Thyroid receptor binding + 0.7288 72.88%
Glucocorticoid receptor binding + 0.8381 83.81%
Aromatase binding + 0.7055 70.55%
PPAR gamma + 0.8923 89.23%
Honey bee toxicity - 0.8625 86.25%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.5251 52.51%
Fish aquatic toxicity + 0.8893 88.93%

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 99.61% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 96.21% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.54% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.35% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.55% 85.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.47% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.58% 99.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.50% 99.23%
CHEMBL2581 P07339 Cathepsin D 88.39% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.21% 96.09%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 87.00% 99.15%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 85.32% 95.50%
CHEMBL3401 O75469 Pregnane X receptor 84.45% 94.73%
CHEMBL1937 Q92769 Histone deacetylase 2 82.33% 94.75%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.80% 96.95%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.76% 97.14%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.12% 92.62%

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.
Achyrocline flaccida

Cross-Links

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PubChem 44259907
LOTUS LTS0234604
wikiData Q105382397