6'-Hydroxyjusticidin A

Details

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Internal ID a7256cff-ab87-4c81-8950-b2227ee80588
Taxonomy Lignans, neolignans and related compounds > Arylnaphthalene lignans
IUPAC Name 9-(6-hydroxy-1,3-benzodioxol-5-yl)-4,6,7-trimethoxy-3H-benzo[f][2]benzofuran-1-one
SMILES (Canonical) COC1=C(C=C2C(=C1)C(=C3C(=C2OC)COC3=O)C4=CC5=C(C=C4O)OCO5)OC
SMILES (Isomeric) COC1=C(C=C2C(=C1)C(=C3C(=C2OC)COC3=O)C4=CC5=C(C=C4O)OCO5)OC
InChI InChI=1S/C22H18O8/c1-25-15-4-10-11(5-16(15)26-2)21(27-3)13-8-28-22(24)20(13)19(10)12-6-17-18(7-14(12)23)30-9-29-17/h4-7,23H,8-9H2,1-3H3
InChI Key DFVZQTUMRRMHEL-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C22H18O8
Molecular Weight 410.40 g/mol
Exact Mass 410.10016753 g/mol
Topological Polar Surface Area (TPSA) 92.70 Ų
XlogP 3.60
Atomic LogP (AlogP) 3.64
H-Bond Acceptor 8
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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145971-08-0
Justicidin G (justicia procumbens)
UNII-2L279513IW
JUSTICIDIN G(SH)
2L279513IW
Naphtho(2,3-c)furan-1(3H)-one, 9-(6-hydroxy-1,3-benzodioxol-5-yl)-4,6,7-trimethoxy-
9-(6-hydroxy-1,3-benzodioxol-5-yl)-4,6,7-trimethoxy-3H-benzo[f][2]benzofuran-1-one
SCHEMBL17041878
DTXSID70163217
Q27254883

2D Structure

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2D Structure of 6'-Hydroxyjusticidin A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9810 98.10%
Caco-2 + 0.8683 86.83%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.7563 75.63%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9427 94.27%
OATP1B3 inhibitior + 0.9420 94.20%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.8537 85.37%
P-glycoprotein inhibitior + 0.6834 68.34%
P-glycoprotein substrate - 0.8569 85.69%
CYP3A4 substrate + 0.5662 56.62%
CYP2C9 substrate - 0.8012 80.12%
CYP2D6 substrate - 0.8332 83.32%
CYP3A4 inhibition + 0.8019 80.19%
CYP2C9 inhibition + 0.8832 88.32%
CYP2C19 inhibition + 0.8585 85.85%
CYP2D6 inhibition - 0.8601 86.01%
CYP1A2 inhibition - 0.8339 83.39%
CYP2C8 inhibition - 0.5864 58.64%
CYP inhibitory promiscuity + 0.8490 84.90%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.3935 39.35%
Eye corrosion - 0.9892 98.92%
Eye irritation - 0.6036 60.36%
Skin irritation - 0.8168 81.68%
Skin corrosion - 0.9700 97.00%
Ames mutagenesis + 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5147 51.47%
Micronuclear + 0.7900 79.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation - 0.7568 75.68%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity + 0.5428 54.28%
Acute Oral Toxicity (c) III 0.3539 35.39%
Estrogen receptor binding + 0.9040 90.40%
Androgen receptor binding + 0.5828 58.28%
Thyroid receptor binding + 0.6734 67.34%
Glucocorticoid receptor binding + 0.9345 93.45%
Aromatase binding - 0.4945 49.45%
PPAR gamma + 0.7490 74.90%
Honey bee toxicity - 0.8600 86.00%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5749 57.49%
Fish aquatic toxicity + 0.9566 95.66%

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 99.14% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.52% 95.56%
CHEMBL2535 P11166 Glucose transporter 95.47% 98.75%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 95.28% 96.77%
CHEMBL2581 P07339 Cathepsin D 95.26% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 93.52% 91.49%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.02% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.31% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.60% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.05% 94.00%
CHEMBL2002 P12268 Inosine-5'-monophosphate dehydrogenase 2 89.75% 98.21%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 89.69% 92.62%
CHEMBL4208 P20618 Proteasome component C5 87.89% 90.00%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 87.65% 82.67%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 86.47% 93.40%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.04% 99.23%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 83.19% 99.15%
CHEMBL3192 Q9BY41 Histone deacetylase 8 82.74% 93.99%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.65% 96.09%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 82.19% 96.21%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.23% 99.17%

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.
Justicia procumbens

Cross-Links

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PubChem 71587520
LOTUS LTS0028208
wikiData Q27254883