Minovincine, 16-methoxy-

Details

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Internal ID 400fd7fb-065f-47b3-9132-5749d6acee04
Taxonomy Alkaloids and derivatives > Aspidospermatan-type alkaloids
IUPAC Name methyl 12-acetyl-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)
SMILES (Isomeric)
InChI InChI=1S/C22H26N2O4/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/h5-6,11,20,23H,4,7-10,12H2,1-3H3
InChI Key UPEIYBJSTNGANI-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C22H26N2O4
Molecular Weight 382.50 g/mol
Exact Mass 382.18925731 g/mol
Topological Polar Surface Area (TPSA) 67.90 Ų
XlogP 2.00
Atomic LogP (AlogP) 2.63
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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UPEIYBJSTNGANI-UHFFFAOYSA-N
Q15425825
Methyl 16-methoxy-20-oxo-2,3-didehydroaspidospermidine-3-carboxylate #

2D Structure

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2D Structure of Minovincine, 16-methoxy-

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 + 0.7523 75.23%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.7491 74.91%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8977 89.77%
OATP1B3 inhibitior + 0.9133 91.33%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.9481 94.81%
P-glycoprotein inhibitior - 0.5942 59.42%
P-glycoprotein substrate + 0.6692 66.92%
CYP3A4 substrate + 0.6811 68.11%
CYP2C9 substrate - 0.7965 79.65%
CYP2D6 substrate - 0.7934 79.34%
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 + 0.4515 45.15%
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 - 0.9851 98.51%
Skin irritation - 0.7654 76.54%
Skin corrosion - 0.9309 93.09%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8630 86.30%
Micronuclear + 0.5900 59.00%
Hepatotoxicity - 0.5573 55.73%
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 - 0.7703 77.03%
Acute Oral Toxicity (c) III 0.5995 59.95%
Estrogen receptor binding + 0.7280 72.80%
Androgen receptor binding + 0.7289 72.89%
Thyroid receptor binding + 0.5723 57.23%
Glucocorticoid receptor binding + 0.7267 72.67%
Aromatase binding + 0.7603 76.03%
PPAR gamma + 0.6307 63.07%
Honey bee toxicity - 0.8897 88.97%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5000 50.00%
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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.62% 96.09%
CHEMBL240 Q12809 HERG 98.13% 89.76%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.12% 91.11%
CHEMBL4208 P20618 Proteasome component C5 95.68% 90.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.50% 94.45%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 89.82% 91.07%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.88% 86.33%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 88.23% 91.03%
CHEMBL2581 P07339 Cathepsin D 88.17% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.80% 97.09%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 87.10% 93.03%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 86.86% 90.71%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.78% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.40% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.50% 95.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.97% 95.89%
CHEMBL340 P08684 Cytochrome P450 3A4 83.43% 91.19%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.30% 92.62%
CHEMBL3437 Q16853 Amine oxidase, copper containing 82.58% 94.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 82.30% 92.94%

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.
Catharanthus trichophyllus

Cross-Links

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PubChem 586568
LOTUS LTS0151028
wikiData Q15425825