Methyl 12-(1-acetyloxyethyl)-5-methoxy-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2(7),3,5,9-tetraene-10-carboxylate

Details

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Internal ID 76857334-8565-40a2-badd-727a70bdd795
Taxonomy Alkaloids and derivatives > Aspidospermatan-type alkaloids
IUPAC Name methyl 12-(1-acetyloxyethyl)-5-methoxy-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2(7),3,5,9-tetraene-10-carboxylate
SMILES (Canonical) CC(C12CCCN3C1C4(CC3)C5=C(C=C(C=C5)OC)NC4=C(C2)C(=O)OC)OC(=O)C
SMILES (Isomeric) CC(C12CCCN3C1C4(CC3)C5=C(C=C(C=C5)OC)NC4=C(C2)C(=O)OC)OC(=O)C
InChI InChI=1S/C24H30N2O5/c1-14(31-15(2)27)23-8-5-10-26-11-9-24(22(23)26)18-7-6-16(29-3)12-19(18)25-20(24)17(13-23)21(28)30-4/h6-7,12,14,22,25H,5,8-11,13H2,1-4H3
InChI Key WQLDCBFCPROBTH-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C24H30N2O5
Molecular Weight 426.50 g/mol
Exact Mass 426.21547206 g/mol
Topological Polar Surface Area (TPSA) 77.10 Ų
XlogP 2.90
Atomic LogP (AlogP) 3.00
H-Bond Acceptor 7
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Methyl 12-(1-acetyloxyethyl)-5-methoxy-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2(7),3,5,9-tetraene-10-carboxylate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9563 95.63%
Caco-2 + 0.6908 69.08%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.7491 74.91%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8906 89.06%
OATP1B3 inhibitior + 0.9133 91.33%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.9650 96.50%
P-glycoprotein inhibitior + 0.7233 72.33%
P-glycoprotein substrate + 0.7360 73.60%
CYP3A4 substrate + 0.6897 68.97%
CYP2C9 substrate - 0.6070 60.70%
CYP2D6 substrate - 0.7940 79.40%
CYP3A4 inhibition - 0.8281 82.81%
CYP2C9 inhibition - 0.7657 76.57%
CYP2C19 inhibition - 0.8533 85.33%
CYP2D6 inhibition - 0.5994 59.94%
CYP1A2 inhibition - 0.6010 60.10%
CYP2C8 inhibition + 0.4771 47.71%
CYP inhibitory promiscuity - 0.7669 76.69%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5480 54.80%
Eye corrosion - 0.9859 98.59%
Eye irritation - 0.9700 97.00%
Skin irritation - 0.7654 76.54%
Skin corrosion - 0.9309 93.09%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8418 84.18%
Micronuclear + 0.5900 59.00%
Hepatotoxicity - 0.5323 53.23%
skin sensitisation - 0.8484 84.84%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.8875 88.75%
Nephrotoxicity - 0.8638 86.38%
Acute Oral Toxicity (c) III 0.5995 59.95%
Estrogen receptor binding + 0.7624 76.24%
Androgen receptor binding + 0.7169 71.69%
Thyroid receptor binding + 0.5976 59.76%
Glucocorticoid receptor binding + 0.7985 79.85%
Aromatase binding + 0.6818 68.18%
PPAR gamma + 0.5528 55.28%
Honey bee toxicity - 0.8459 84.59%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9870 98.70%

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 98.83% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.60% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.47% 85.14%
CHEMBL2581 P07339 Cathepsin D 96.36% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.34% 94.45%
CHEMBL4208 P20618 Proteasome component C5 94.08% 90.00%
CHEMBL240 Q12809 HERG 91.24% 89.76%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 91.19% 91.03%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 90.49% 90.71%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 90.49% 91.07%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 88.28% 99.15%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.21% 95.89%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.28% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.17% 95.56%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 86.08% 93.03%
CHEMBL340 P08684 Cytochrome P450 3A4 85.85% 91.19%
CHEMBL2535 P11166 Glucose transporter 85.76% 98.75%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.84% 92.62%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.84% 97.09%
CHEMBL221 P23219 Cyclooxygenase-1 81.71% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.49% 86.33%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.70% 97.14%

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.
Alstonia mairei

Cross-Links

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PubChem 162850092
LOTUS LTS0036665
wikiData Q105310775