12-Methoxyvoaphylline

Details

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Internal ID d0d3c2e1-d5d0-4c39-9fa7-2fbc7f1bb103
Taxonomy Alkaloids and derivatives > Quebrachamine alkaloids
IUPAC Name (15S,16S,18R)-15-ethyl-14-methoxy-17-oxa-1,11-diazapentacyclo[13.4.1.04,12.05,10.016,18]icosa-4(12),5,7,9-tetraene
SMILES (Canonical) CCC12CN(CCC3=C(CC1OC)NC4=CC=CC=C34)CC5C2O5
SMILES (Isomeric) CC[C@]12CN(CCC3=C(CC1OC)NC4=CC=CC=C34)C[C@@H]5[C@H]2O5
InChI InChI=1S/C20H26N2O2/c1-3-20-12-22(11-17-19(20)24-17)9-8-14-13-6-4-5-7-15(13)21-16(14)10-18(20)23-2/h4-7,17-19,21H,3,8-12H2,1-2H3/t17-,18?,19-,20+/m1/s1
InChI Key SJTDSAMPXFCOBV-XUBOLADHSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C20H26N2O2
Molecular Weight 326.40 g/mol
Exact Mass 326.199428076 g/mol
Topological Polar Surface Area (TPSA) 40.80 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.76
H-Bond Acceptor 3
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 12-Methoxyvoaphylline

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9858 98.58%
Caco-2 + 0.8941 89.41%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Lysosomes 0.7648 76.48%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9053 90.53%
OATP1B3 inhibitior + 0.9393 93.93%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior + 0.5960 59.60%
P-glycoprotein inhibitior - 0.4725 47.25%
P-glycoprotein substrate + 0.6391 63.91%
CYP3A4 substrate + 0.6767 67.67%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.5000 50.00%
CYP3A4 inhibition + 0.5609 56.09%
CYP2C9 inhibition - 0.8631 86.31%
CYP2C19 inhibition - 0.7537 75.37%
CYP2D6 inhibition - 0.6013 60.13%
CYP1A2 inhibition - 0.8150 81.50%
CYP2C8 inhibition - 0.5832 58.32%
CYP inhibitory promiscuity - 0.8179 81.79%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6418 64.18%
Eye corrosion - 0.9883 98.83%
Eye irritation - 0.9917 99.17%
Skin irritation - 0.7881 78.81%
Skin corrosion - 0.9281 92.81%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9454 94.54%
Micronuclear + 0.6100 61.00%
Hepatotoxicity - 0.5163 51.63%
skin sensitisation - 0.8451 84.51%
Respiratory toxicity + 0.9222 92.22%
Reproductive toxicity + 0.9667 96.67%
Mitochondrial toxicity + 0.9125 91.25%
Nephrotoxicity - 0.6805 68.05%
Acute Oral Toxicity (c) III 0.4696 46.96%
Estrogen receptor binding + 0.7409 74.09%
Androgen receptor binding + 0.6253 62.53%
Thyroid receptor binding + 0.6856 68.56%
Glucocorticoid receptor binding - 0.5494 54.94%
Aromatase binding + 0.5749 57.49%
PPAR gamma - 0.4845 48.45%
Honey bee toxicity - 0.8456 84.56%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity - 0.4730 47.30%

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 99.30% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.13% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.65% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.99% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.47% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.09% 97.25%
CHEMBL2581 P07339 Cathepsin D 92.79% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.24% 95.56%
CHEMBL3192 Q9BY41 Histone deacetylase 8 91.51% 93.99%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 89.49% 94.08%
CHEMBL1914 P06276 Butyrylcholinesterase 88.39% 95.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.29% 95.89%
CHEMBL255 P29275 Adenosine A2b receptor 86.95% 98.59%
CHEMBL3310 Q96DB2 Histone deacetylase 11 86.48% 88.56%
CHEMBL2535 P11166 Glucose transporter 86.18% 98.75%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 85.89% 91.71%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.63% 94.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 83.55% 97.14%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 83.45% 97.50%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.39% 86.33%
CHEMBL4588 P22894 Matrix metalloproteinase 8 82.78% 94.66%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.47% 92.62%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.03% 89.00%
CHEMBL5028 O14672 ADAM10 81.50% 97.50%
CHEMBL5103 Q969S8 Histone deacetylase 10 81.10% 90.08%

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.
Tabernaemontana bovina
Tabernaemontana dichotoma

Cross-Links

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PubChem 13342867
LOTUS LTS0063806
wikiData Q104394814