Dimethyl 18-hydroxy-23-methoxy-11,13,20-trioxa-3,16-diazaoctacyclo[15.6.2.01,19.02,6.03,21.06,17.07,15.010,14]pentacosa-7(15),8,10(14)-triene-16,18-dicarboxylate

Details

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Internal ID 6f6e3652-99cc-46e4-b00e-f0d1c2b7d9af
Taxonomy Alkaloids and derivatives > Aspidofractine alkaloids
IUPAC Name dimethyl 18-hydroxy-23-methoxy-11,13,20-trioxa-3,16-diazaoctacyclo[15.6.2.01,19.02,6.03,21.06,17.07,15.010,14]pentacosa-7(15),8,10(14)-triene-16,18-dicarboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C25H28N2O9/c1-31-14-10-15-26-9-8-23-12-4-5-13-17(35-11-34-13)16(12)27(21(29)33-3)24(23)7-6-22(14,18(23)26)19(36-15)25(24,30)20(28)32-2/h4-5,14-15,18-19,30H,6-11H2,1-3H3
InChI Key FATPEVYALCFKAP-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C25H28N2O9
Molecular Weight 500.50 g/mol
Exact Mass 500.17948047 g/mol
Topological Polar Surface Area (TPSA) 116.00 Ų
XlogP 0.80
Atomic LogP (AlogP) 0.89
H-Bond Acceptor 10
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Dimethyl 18-hydroxy-23-methoxy-11,13,20-trioxa-3,16-diazaoctacyclo[15.6.2.01,19.02,6.03,21.06,17.07,15.010,14]pentacosa-7(15),8,10(14)-triene-16,18-dicarboxylate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9032 90.32%
Caco-2 - 0.5744 57.44%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.5313 53.13%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8747 87.47%
OATP1B3 inhibitior + 0.9300 93.00%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.8364 83.64%
P-glycoprotein inhibitior + 0.6692 66.92%
P-glycoprotein substrate + 0.6041 60.41%
CYP3A4 substrate + 0.6783 67.83%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7870 78.70%
CYP3A4 inhibition + 0.5790 57.90%
CYP2C9 inhibition - 0.8033 80.33%
CYP2C19 inhibition - 0.5633 56.33%
CYP2D6 inhibition - 0.8055 80.55%
CYP1A2 inhibition - 0.8765 87.65%
CYP2C8 inhibition + 0.5493 54.93%
CYP inhibitory promiscuity - 0.7941 79.41%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.5816 58.16%
Eye corrosion - 0.9862 98.62%
Eye irritation - 0.9127 91.27%
Skin irritation - 0.7986 79.86%
Skin corrosion - 0.9381 93.81%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3749 37.49%
Micronuclear + 0.7200 72.00%
Hepatotoxicity - 0.5322 53.22%
skin sensitisation - 0.8817 88.17%
Respiratory toxicity + 0.8000 80.00%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity + 0.4626 46.26%
Acute Oral Toxicity (c) III 0.6424 64.24%
Estrogen receptor binding + 0.8088 80.88%
Androgen receptor binding + 0.7755 77.55%
Thyroid receptor binding + 0.5511 55.11%
Glucocorticoid receptor binding + 0.7063 70.63%
Aromatase binding + 0.7055 70.55%
PPAR gamma + 0.7377 73.77%
Honey bee toxicity - 0.7134 71.34%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9158 91.58%

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 98.51% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.38% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.38% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.67% 85.14%
CHEMBL4208 P20618 Proteasome component C5 95.06% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.07% 95.56%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 92.41% 96.77%
CHEMBL5028 O14672 ADAM10 90.06% 97.50%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.60% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.18% 95.89%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 86.66% 85.30%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.47% 86.33%
CHEMBL2581 P07339 Cathepsin D 86.26% 98.95%
CHEMBL340 P08684 Cytochrome P450 3A4 85.98% 91.19%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 85.79% 89.62%
CHEMBL230 P35354 Cyclooxygenase-2 82.98% 89.63%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.57% 96.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.19% 100.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 81.50% 93.04%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.18% 92.62%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.13% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.41% 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.
Kopsia singapurensis

Cross-Links

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PubChem 163103931
LOTUS LTS0021777
wikiData Q104992424