2-Hydroxy-4,6-dimethoxy-10-(4-methoxyphenyl)-11-phenyl-9-oxa-14,19-diazapentacyclo[10.7.0.02,10.03,8.014,18]nonadeca-1(12),3(8),4,6,18-pentaen-13-one

Details

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Internal ID 9530932d-9ca1-49d3-9696-f198a439bb48
Taxonomy Phenylpropanoids and polyketides > Stilbenes
IUPAC Name 2-hydroxy-4,6-dimethoxy-10-(4-methoxyphenyl)-11-phenyl-9-oxa-14,19-diazapentacyclo[10.7.0.02,10.03,8.014,18]nonadeca-1(12),3(8),4,6,18-pentaen-13-one
SMILES (Canonical) COC1=CC=C(C=C1)C23C(C4=C(C2(C5=C(O3)C=C(C=C5OC)OC)O)N=C6CCCN6C4=O)C7=CC=CC=C7
SMILES (Isomeric) COC1=CC=C(C=C1)C23C(C4=C(C2(C5=C(O3)C=C(C=C5OC)OC)O)N=C6CCCN6C4=O)C7=CC=CC=C7
InChI InChI=1S/C31H28N2O6/c1-36-20-13-11-19(12-14-20)31-26(18-8-5-4-6-9-18)25-28(32-24-10-7-15-33(24)29(25)34)30(31,35)27-22(38-3)16-21(37-2)17-23(27)39-31/h4-6,8-9,11-14,16-17,26,35H,7,10,15H2,1-3H3
InChI Key YCIPQJTZJGUXND-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C31H28N2O6
Molecular Weight 524.60 g/mol
Exact Mass 524.19473662 g/mol
Topological Polar Surface Area (TPSA) 89.80 Ų
XlogP 2.70
Atomic LogP (AlogP) 3.88
H-Bond Acceptor 8
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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155595-93-0

2D Structure

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2D Structure of 2-Hydroxy-4,6-dimethoxy-10-(4-methoxyphenyl)-11-phenyl-9-oxa-14,19-diazapentacyclo[10.7.0.02,10.03,8.014,18]nonadeca-1(12),3(8),4,6,18-pentaen-13-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9642 96.42%
Caco-2 - 0.6055 60.55%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.7136 71.36%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8680 86.80%
OATP1B3 inhibitior + 0.9382 93.82%
MATE1 inhibitior - 0.6600 66.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior + 0.9628 96.28%
P-glycoprotein inhibitior + 0.8981 89.81%
P-glycoprotein substrate + 0.5000 50.00%
CYP3A4 substrate + 0.6818 68.18%
CYP2C9 substrate - 0.8060 80.60%
CYP2D6 substrate - 0.8377 83.77%
CYP3A4 inhibition + 0.5298 52.98%
CYP2C9 inhibition - 0.7572 75.72%
CYP2C19 inhibition - 0.8291 82.91%
CYP2D6 inhibition - 0.8909 89.09%
CYP1A2 inhibition + 0.5311 53.11%
CYP2C8 inhibition + 0.6461 64.61%
CYP inhibitory promiscuity - 0.6338 63.38%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.6157 61.57%
Eye corrosion - 0.9890 98.90%
Eye irritation - 0.9250 92.50%
Skin irritation - 0.8228 82.28%
Skin corrosion - 0.9490 94.90%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3940 39.40%
Micronuclear + 0.7700 77.00%
Hepatotoxicity - 0.6499 64.99%
skin sensitisation - 0.8925 89.25%
Respiratory toxicity + 0.8556 85.56%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.8000 80.00%
Nephrotoxicity - 0.5767 57.67%
Acute Oral Toxicity (c) III 0.5848 58.48%
Estrogen receptor binding + 0.7683 76.83%
Androgen receptor binding + 0.7947 79.47%
Thyroid receptor binding + 0.6880 68.80%
Glucocorticoid receptor binding + 0.8397 83.97%
Aromatase binding + 0.6979 69.79%
PPAR gamma + 0.6823 68.23%
Honey bee toxicity - 0.8846 88.46%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.5451 54.51%
Fish aquatic toxicity - 0.5304 53.04%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.77% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.50% 96.09%
CHEMBL2581 P07339 Cathepsin D 96.47% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.32% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 95.43% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.06% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.75% 91.11%
CHEMBL3192 Q9BY41 Histone deacetylase 8 94.16% 93.99%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.65% 94.00%
CHEMBL5203 P33316 dUTP pyrophosphatase 92.54% 99.18%
CHEMBL5608 Q16288 NT-3 growth factor receptor 89.68% 95.89%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.99% 97.09%
CHEMBL240 Q12809 HERG 88.37% 89.76%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 88.31% 92.62%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 87.78% 99.15%
CHEMBL4208 P20618 Proteasome component C5 84.36% 90.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 84.20% 97.14%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 83.17% 100.00%
CHEMBL2535 P11166 Glucose transporter 80.97% 98.75%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 80.25% 93.40%

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.
Aglaia elaeagnoidea
Aglaia odorata

Cross-Links

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PubChem 9914764
LOTUS LTS0018545
wikiData Q105346306