Minovincinine, 16-methoxy-

Details

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Internal ID ad451dbc-04b4-48f9-aeef-6d53459715ef
Taxonomy Alkaloids and derivatives > Aspidospermatan-type alkaloids
IUPAC Name methyl 12-(1-hydroxyethyl)-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)O
SMILES (Isomeric) CC(C12CCCN3C1C4(CC3)C5=C(C=C(C=C5)OC)NC4=C(C2)C(=O)OC)O
InChI InChI=1S/C22H28N2O4/c1-13(25)21-7-4-9-24-10-8-22(20(21)24)16-6-5-14(27-2)11-17(16)23-18(22)15(12-21)19(26)28-3/h5-6,11,13,20,23,25H,4,7-10,12H2,1-3H3
InChI Key RFESMOWWVVPMAX-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H28N2O4
Molecular Weight 384.50 g/mol
Exact Mass 384.20490738 g/mol
Topological Polar Surface Area (TPSA) 71.00 Ų
XlogP 2.30

Synonyms

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16-Methoxyminovincinine
RFESMOWWVVPMAX-UHFFFAOYSA-N
Methyl 20-hydroxy-16-methoxy-2,3-didehydroaspidospermidine-3-carboxylate #
Aspidospermidine-3-carboxylic acid, 2,3-didehydro-20-hydroxy-16-methoxy-, methyl ester, (5.alpha.,12.beta.,19.alpha.,20R)-

2D Structure

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2D Structure of Minovincinine, 16-methoxy-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
No predicted properties yet!

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.92% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.98% 91.11%
CHEMBL4208 P20618 Proteasome component C5 96.90% 90.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.35% 85.14%
CHEMBL2581 P07339 Cathepsin D 93.84% 98.95%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 93.52% 90.71%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.25% 94.45%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 91.86% 93.03%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 91.83% 91.03%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 91.01% 91.07%
CHEMBL2535 P11166 Glucose transporter 89.00% 98.75%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.96% 95.89%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.67% 95.56%
CHEMBL240 Q12809 HERG 87.29% 89.76%
CHEMBL221 P23219 Cyclooxygenase-1 85.99% 90.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.94% 97.09%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.45% 99.15%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 85.11% 92.62%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.44% 94.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.88% 97.14%
CHEMBL340 P08684 Cytochrome P450 3A4 81.67% 91.19%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 80.71% 90.24%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 80.15% 100.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.13% 86.33%

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
Vinca minor

Cross-Links

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PubChem 587929
LOTUS LTS0072665
wikiData Q105235342