Gancaonin M

Details

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Internal ID a7829a06-42b9-4c64-b9ba-add90dfa7fac
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > O-methylated isoflavonoids > 4-O-methylated isoflavonoids > 4-O-methylisoflavones
IUPAC Name 5,7-dihydroxy-3-(4-methoxyphenyl)-8-(3-methylbut-2-enyl)chromen-4-one
SMILES (Canonical) CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C(=CO2)C3=CC=C(C=C3)OC)C
SMILES (Isomeric) CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C(=CO2)C3=CC=C(C=C3)OC)C
InChI InChI=1S/C21H20O5/c1-12(2)4-9-15-17(22)10-18(23)19-20(24)16(11-26-21(15)19)13-5-7-14(25-3)8-6-13/h4-8,10-11,22-23H,9H2,1-3H3
InChI Key DDLPIQXHEKZHQX-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C21H20O5
Molecular Weight 352.40 g/mol
Exact Mass 352.13107373 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 4.90
Atomic LogP (AlogP) 4.39
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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129145-51-3
Gancanin M
5,7-dihydroxy-3-(4-methoxyphenyl)-8-(3-methylbut-2-enyl)chromen-4-one
5,7,-Dihydroxy-4'-methoxy-8-prenylisoflavone
starbld0000824
SCHEMBL1171380
CHEBI:175516
DTXSID601318202
LMPK12050226
AKOS032962514
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Gancaonin M

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9897 98.97%
Caco-2 + 0.6967 69.67%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.7048 70.48%
OATP2B1 inhibitior - 0.5708 57.08%
OATP1B1 inhibitior + 0.9291 92.91%
OATP1B3 inhibitior + 0.8466 84.66%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.8141 81.41%
P-glycoprotein inhibitior + 0.6457 64.57%
P-glycoprotein substrate - 0.8768 87.68%
CYP3A4 substrate + 0.5577 55.77%
CYP2C9 substrate - 0.5929 59.29%
CYP2D6 substrate - 0.8145 81.45%
CYP3A4 inhibition - 0.6395 63.95%
CYP2C9 inhibition + 0.8833 88.33%
CYP2C19 inhibition + 0.9477 94.77%
CYP2D6 inhibition - 0.5417 54.17%
CYP1A2 inhibition + 0.8808 88.08%
CYP2C8 inhibition + 0.4906 49.06%
CYP inhibitory promiscuity + 0.9500 95.00%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6792 67.92%
Eye corrosion - 0.9881 98.81%
Eye irritation + 0.5565 55.65%
Skin irritation - 0.7722 77.22%
Skin corrosion - 0.9507 95.07%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6638 66.38%
Micronuclear + 0.5400 54.00%
Hepatotoxicity + 0.5052 50.52%
skin sensitisation - 0.8343 83.43%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity - 0.6636 66.36%
Acute Oral Toxicity (c) III 0.6798 67.98%
Estrogen receptor binding + 0.9677 96.77%
Androgen receptor binding + 0.9006 90.06%
Thyroid receptor binding + 0.7358 73.58%
Glucocorticoid receptor binding + 0.8850 88.50%
Aromatase binding + 0.7693 76.93%
PPAR gamma + 0.8991 89.91%
Honey bee toxicity - 0.8657 86.57%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.9903 99.03%

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 99.26% 91.11%
CHEMBL2581 P07339 Cathepsin D 97.22% 98.95%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 95.41% 86.92%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.75% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 93.15% 99.15%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.79% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.26% 95.56%
CHEMBL1929 P47989 Xanthine dehydrogenase 89.95% 96.12%
CHEMBL3401 O75469 Pregnane X receptor 89.39% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.22% 99.17%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 85.81% 91.71%
CHEMBL1951 P21397 Monoamine oxidase A 84.84% 91.49%
CHEMBL4208 P20618 Proteasome component C5 84.53% 90.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.28% 96.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.06% 89.00%
CHEMBL1907 P15144 Aminopeptidase N 80.75% 93.31%
CHEMBL3922 P50579 Methionine aminopeptidase 2 80.33% 97.28%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.04% 95.89%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.01% 85.14%

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.
Cullen corylifolium
Glycyrrhiza
Glycyrrhiza glabra
Glycyrrhiza inflata
Glycyrrhiza uralensis
Glycyrrhiza uralensis
Mitracarpus hirtus

Cross-Links

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PubChem 14604078
NPASS NPC56898
LOTUS LTS0262454
wikiData Q104976558