Haginin B

Details

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Internal ID 71194379-f0e1-485d-a7cf-ceef687190a4
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > O-methylated isoflavonoids > 2-O-methylated isoflavonoids
IUPAC Name 3-(4-hydroxy-2-methoxyphenyl)-2H-chromen-7-ol
SMILES (Canonical) COC1=C(C=CC(=C1)O)C2=CC3=C(C=C(C=C3)O)OC2
SMILES (Isomeric) COC1=C(C=CC(=C1)O)C2=CC3=C(C=C(C=C3)O)OC2
InChI InChI=1S/C16H14O4/c1-19-16-8-13(18)4-5-14(16)11-6-10-2-3-12(17)7-15(10)20-9-11/h2-8,17-18H,9H2,1H3
InChI Key RMENXIMFGIVCHR-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H14O4
Molecular Weight 270.28 g/mol
Exact Mass 270.08920892 g/mol
Topological Polar Surface Area (TPSA) 58.90 Ų
XlogP 2.70
Atomic LogP (AlogP) 3.04
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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7,4'-Dihydroxy-2'-methoxyisoflavene
LMPK12080063

2D Structure

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2D Structure of Haginin B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9884 98.84%
Caco-2 + 0.8891 88.91%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.8027 80.27%
OATP2B1 inhibitior - 0.8375 83.75%
OATP1B1 inhibitior + 0.9127 91.27%
OATP1B3 inhibitior + 0.9738 97.38%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.5658 56.58%
P-glycoprotein inhibitior - 0.9061 90.61%
P-glycoprotein substrate - 0.6117 61.17%
CYP3A4 substrate + 0.5094 50.94%
CYP2C9 substrate - 0.8037 80.37%
CYP2D6 substrate + 0.4028 40.28%
CYP3A4 inhibition + 0.5089 50.89%
CYP2C9 inhibition + 0.9121 91.21%
CYP2C19 inhibition + 0.9714 97.14%
CYP2D6 inhibition - 0.7731 77.31%
CYP1A2 inhibition + 0.9250 92.50%
CYP2C8 inhibition + 0.5392 53.92%
CYP inhibitory promiscuity + 0.9685 96.85%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9213 92.13%
Carcinogenicity (trinary) Non-required 0.6151 61.51%
Eye corrosion - 0.9881 98.81%
Eye irritation + 0.9046 90.46%
Skin irritation - 0.7548 75.48%
Skin corrosion - 0.9601 96.01%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6483 64.83%
Micronuclear + 0.8300 83.00%
Hepatotoxicity - 0.5466 54.66%
skin sensitisation - 0.8681 86.81%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity + 0.5138 51.38%
Acute Oral Toxicity (c) III 0.6262 62.62%
Estrogen receptor binding + 0.7836 78.36%
Androgen receptor binding + 0.8363 83.63%
Thyroid receptor binding + 0.7970 79.70%
Glucocorticoid receptor binding + 0.8130 81.30%
Aromatase binding + 0.7584 75.84%
PPAR gamma + 0.7216 72.16%
Honey bee toxicity - 0.8958 89.58%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity + 0.5051 50.51%
Fish aquatic toxicity + 0.9540 95.40%

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 96.32% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.50% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.79% 86.33%
CHEMBL2581 P07339 Cathepsin D 91.76% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.28% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.35% 95.56%
CHEMBL2535 P11166 Glucose transporter 88.01% 98.75%
CHEMBL4208 P20618 Proteasome component C5 87.51% 90.00%
CHEMBL1951 P21397 Monoamine oxidase A 86.65% 91.49%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.13% 99.17%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 84.26% 89.62%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.93% 94.00%
CHEMBL242 Q92731 Estrogen receptor beta 83.15% 98.35%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.69% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.39% 100.00%
CHEMBL3194 P02766 Transthyretin 80.52% 90.71%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 80.18% 82.67%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.11% 89.00%

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.
Lespedeza cyrtobotrya
Teucrium betonicum

Cross-Links

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PubChem 14077816
NPASS NPC191903
LOTUS LTS0113663
wikiData Q105240735