isojusticidin B

Details

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Internal ID a039a212-6d9e-4435-aadc-2e64b73e2c57
Taxonomy Lignans, neolignans and related compounds > Arylnaphthalene lignans
IUPAC Name 4-(1,3-benzodioxol-5-yl)-5,6-dimethoxy-1H-benzo[f][2]benzofuran-3-one
SMILES (Canonical) COC1=C(C2=C(C3=C(COC3=O)C=C2C=C1)C4=CC5=C(C=C4)OCO5)OC
SMILES (Isomeric) COC1=C(C2=C(C3=C(COC3=O)C=C2C=C1)C4=CC5=C(C=C4)OCO5)OC
InChI InChI=1S/C21H16O6/c1-23-15-6-4-11-7-13-9-25-21(22)19(13)17(18(11)20(15)24-2)12-3-5-14-16(8-12)27-10-26-14/h3-8H,9-10H2,1-2H3
InChI Key BBEFSDNXXNECSY-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C21H16O6
Molecular Weight 364.30 g/mol
Exact Mass 364.09468823 g/mol
Topological Polar Surface Area (TPSA) 63.20 Ų
XlogP 4.00
Atomic LogP (AlogP) 3.92
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of isojusticidin B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9927 99.27%
Caco-2 + 0.7539 75.39%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.7625 76.25%
OATP2B1 inhibitior - 0.8699 86.99%
OATP1B1 inhibitior + 0.9491 94.91%
OATP1B3 inhibitior + 0.9649 96.49%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.9591 95.91%
P-glycoprotein inhibitior + 0.7848 78.48%
P-glycoprotein substrate - 0.8752 87.52%
CYP3A4 substrate + 0.5356 53.56%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8360 83.60%
CYP3A4 inhibition + 0.9348 93.48%
CYP2C9 inhibition + 0.9716 97.16%
CYP2C19 inhibition + 0.9766 97.66%
CYP2D6 inhibition + 0.6561 65.61%
CYP1A2 inhibition + 0.5380 53.80%
CYP2C8 inhibition + 0.4498 44.98%
CYP inhibitory promiscuity + 0.9546 95.46%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Warning 0.4177 41.77%
Eye corrosion - 0.9817 98.17%
Eye irritation - 0.6838 68.38%
Skin irritation - 0.7884 78.84%
Skin corrosion - 0.9637 96.37%
Ames mutagenesis + 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4308 43.08%
Micronuclear + 0.7674 76.74%
Hepatotoxicity + 0.6750 67.50%
skin sensitisation - 0.6507 65.07%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity + 0.7225 72.25%
Acute Oral Toxicity (c) III 0.7135 71.35%
Estrogen receptor binding + 0.9333 93.33%
Androgen receptor binding + 0.8220 82.20%
Thyroid receptor binding + 0.6628 66.28%
Glucocorticoid receptor binding + 0.9544 95.44%
Aromatase binding + 0.6995 69.95%
PPAR gamma + 0.8121 81.21%
Honey bee toxicity - 0.8260 82.60%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.9709 97.09%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.44% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 96.43% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 95.82% 94.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 94.52% 96.77%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 93.82% 94.80%
CHEMBL2581 P07339 Cathepsin D 93.49% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.34% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.81% 95.56%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 91.03% 92.62%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 89.75% 80.96%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.19% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.63% 96.09%
CHEMBL240 Q12809 HERG 86.27% 89.76%
CHEMBL1951 P21397 Monoamine oxidase A 85.91% 91.49%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 84.28% 96.09%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 84.22% 95.50%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 84.14% 95.78%
CHEMBL2535 P11166 Glucose transporter 84.10% 98.75%
CHEMBL2717 Q9HCR9 Phosphodiesterase 11A 82.13% 85.00%
CHEMBL4940 P07195 L-lactate dehydrogenase B chain 80.90% 95.53%
CHEMBL3401 O75469 Pregnane X receptor 80.76% 94.73%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 80.50% 96.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.36% 89.00%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 80.33% 94.03%

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.
Linum austriacum
Linum perenne
Momordica charantia

Cross-Links

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PubChem 11122050
LOTUS LTS0022758
wikiData Q105162463