Glyurallin B

Details

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Internal ID 3369d7ec-ad96-4413-8c84-e3344196c47d
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Isoflav-2-enes > Isoflavones
IUPAC Name 3-[3,4-dihydroxy-5-(3-methylbut-2-enyl)phenyl]-5,7-dihydroxy-8-(3-methylbut-2-enyl)chromen-4-one
SMILES (Canonical) CC(=CCC1=C(C(=CC(=C1)C2=COC3=C(C(=CC(=C3C2=O)O)O)CC=C(C)C)O)O)C
SMILES (Isomeric) CC(=CCC1=C(C(=CC(=C1)C2=COC3=C(C(=CC(=C3C2=O)O)O)CC=C(C)C)O)O)C
InChI InChI=1S/C25H26O6/c1-13(2)5-7-15-9-16(10-21(28)23(15)29)18-12-31-25-17(8-6-14(3)4)19(26)11-20(27)22(25)24(18)30/h5-6,9-12,26-29H,7-8H2,1-4H3
InChI Key DPLWUTYEBRKBLI-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C25H26O6
Molecular Weight 422.50 g/mol
Exact Mass 422.17293854 g/mol
Topological Polar Surface Area (TPSA) 107.00 Ų
XlogP 6.20
Atomic LogP (AlogP) 5.30
H-Bond Acceptor 6
H-Bond Donor 4
Rotatable Bonds 5

Synonyms

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CHEMBL4068000
MEGxp0_001474
SCHEMBL12866195
ACon1_000035
CHEBI:175379
DTXSID801318034
BDBM50253186
NCGC00168855-01
199331-53-8
3-[3,4-dihydroxy-5-(3-methylbut-2-en-1-yl)phenyl]-5,7-dihydroxy-8-(3-methylbut-2-en-1-yl)-4H-chromen-4-one
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Glyurallin B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9577 95.77%
Caco-2 - 0.7298 72.98%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.5980 59.80%
OATP2B1 inhibitior + 0.5782 57.82%
OATP1B1 inhibitior + 0.8926 89.26%
OATP1B3 inhibitior + 0.9716 97.16%
MATE1 inhibitior - 0.7000 70.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.8396 83.96%
P-glycoprotein inhibitior - 0.4631 46.31%
P-glycoprotein substrate - 0.8062 80.62%
CYP3A4 substrate + 0.5365 53.65%
CYP2C9 substrate - 0.6039 60.39%
CYP2D6 substrate - 0.8389 83.89%
CYP3A4 inhibition - 0.7803 78.03%
CYP2C9 inhibition + 0.8538 85.38%
CYP2C19 inhibition + 0.7835 78.35%
CYP2D6 inhibition - 0.6554 65.54%
CYP1A2 inhibition + 0.7729 77.29%
CYP2C8 inhibition + 0.5000 50.00%
CYP inhibitory promiscuity + 0.8414 84.14%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6930 69.30%
Eye corrosion - 0.9907 99.07%
Eye irritation + 0.5560 55.60%
Skin irritation - 0.7231 72.31%
Skin corrosion - 0.9189 91.89%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6459 64.59%
Micronuclear + 0.5200 52.00%
Hepatotoxicity - 0.5427 54.27%
skin sensitisation - 0.7690 76.90%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity - 0.7145 71.45%
Acute Oral Toxicity (c) III 0.5414 54.14%
Estrogen receptor binding + 0.9439 94.39%
Androgen receptor binding + 0.7338 73.38%
Thyroid receptor binding + 0.6570 65.70%
Glucocorticoid receptor binding + 0.8342 83.42%
Aromatase binding + 0.6252 62.52%
PPAR gamma + 0.8896 88.96%
Honey bee toxicity - 0.8726 87.26%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9940 99.40%

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 99.59% 91.11%
CHEMBL2581 P07339 Cathepsin D 97.12% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 95.01% 94.73%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 94.48% 89.34%
CHEMBL1951 P21397 Monoamine oxidase A 92.25% 91.49%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.27% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.50% 86.33%
CHEMBL3038469 P24941 CDK2/Cyclin A 88.06% 91.38%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.74% 94.00%
CHEMBL3194 P02766 Transthyretin 83.71% 90.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.66% 95.56%
CHEMBL3922 P50579 Methionine aminopeptidase 2 82.42% 97.28%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.05% 99.17%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 80.98% 99.15%

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.
Glycyrrhiza glabra
Glycyrrhiza inflata
Glycyrrhiza uralensis
Glycyrrhiza uralensis
Mitracarpus hirtus

Cross-Links

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PubChem 15818599
NPASS NPC169162
LOTUS LTS0177286
wikiData Q104986575