5-O-Methylglovanon

Details

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Internal ID a9248b33-7206-4481-876d-6fc5827a7365
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavans > 8-prenylated flavans > 8-prenylated flavanones
IUPAC Name (2S)-2-(3-hydroxy-4-methoxyphenyl)-5,7-dimethoxy-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H26O6/c1-13(2)6-8-15-20(27-4)12-21(28-5)22-17(25)11-19(29-23(15)22)14-7-9-18(26-3)16(24)10-14/h6-7,9-10,12,19,24H,8,11H2,1-5H3/t19-/m0/s1
InChI Key UXCYCLZPAIYCPU-IBGZPJMESA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C23H26O6
Molecular Weight 398.40 g/mol
Exact Mass 398.17293854 g/mol
Topological Polar Surface Area (TPSA) 74.20 Ų
XlogP 4.40
Atomic LogP (AlogP) 4.63
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-O-Methylglovanon

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9930 99.30%
Caco-2 + 0.9030 90.30%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.7290 72.90%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8982 89.82%
OATP1B3 inhibitior + 0.9129 91.29%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.9191 91.91%
P-glycoprotein inhibitior + 0.8361 83.61%
P-glycoprotein substrate - 0.7682 76.82%
CYP3A4 substrate + 0.5848 58.48%
CYP2C9 substrate - 0.8006 80.06%
CYP2D6 substrate - 0.7235 72.35%
CYP3A4 inhibition - 0.7017 70.17%
CYP2C9 inhibition + 0.6389 63.89%
CYP2C19 inhibition + 0.9009 90.09%
CYP2D6 inhibition - 0.7582 75.82%
CYP1A2 inhibition + 0.5819 58.19%
CYP2C8 inhibition + 0.4656 46.56%
CYP inhibitory promiscuity + 0.8252 82.52%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6793 67.93%
Eye corrosion - 0.9897 98.97%
Eye irritation - 0.8543 85.43%
Skin irritation - 0.7767 77.67%
Skin corrosion - 0.9675 96.75%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4584 45.84%
Micronuclear - 0.5600 56.00%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation - 0.8025 80.25%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.6350 63.50%
Acute Oral Toxicity (c) III 0.6796 67.96%
Estrogen receptor binding + 0.8814 88.14%
Androgen receptor binding + 0.5987 59.87%
Thyroid receptor binding + 0.6081 60.81%
Glucocorticoid receptor binding + 0.7288 72.88%
Aromatase binding - 0.6463 64.63%
PPAR gamma + 0.7728 77.28%
Honey bee toxicity - 0.7482 74.82%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.9757 97.57%

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 98.35% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.29% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.97% 94.45%
CHEMBL2581 P07339 Cathepsin D 93.37% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 92.21% 91.49%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.69% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.54% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.57% 97.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.78% 85.14%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.68% 95.89%
CHEMBL3401 O75469 Pregnane X receptor 87.03% 94.73%
CHEMBL1929 P47989 Xanthine dehydrogenase 86.95% 96.12%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.77% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.42% 99.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.04% 89.00%
CHEMBL4208 P20618 Proteasome component C5 84.80% 90.00%
CHEMBL2535 P11166 Glucose transporter 83.29% 98.75%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.20% 96.95%

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.
Glycosmis craibii

Cross-Links

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PubChem 101480801
LOTUS LTS0206072
wikiData Q105280726