Trigonostemonine D

Details

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Internal ID ea883350-4e58-48ec-9a92-a21c1b88c7c9
Taxonomy Alkaloids and derivatives > Harmala alkaloids
IUPAC Name 1-(7-methoxyquinolin-4-yl)-9H-pyrido[3,4-b]indole
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H15N3O/c1-25-13-6-7-15-16(8-10-22-19(15)12-13)20-21-17(9-11-23-20)14-4-2-3-5-18(14)24-21/h2-12,24H,1H3
InChI Key LKOLZHSYTUIODN-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C21H15N3O
Molecular Weight 325.40 g/mol
Exact Mass 325.121512110 g/mol
Topological Polar Surface Area (TPSA) 50.80 Ų
XlogP 4.20
Atomic LogP (AlogP) 4.94
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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1-(7-methoxyquinolin-4-yl)-9H-pyrido(3,4-b)indole
1-(7-methoxyquinolin-4-yl)-9H-pyrido[3,4-b]indole
RefChem:191657
CHEMBL1957113

2D Structure

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2D Structure of Trigonostemonine D

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 - 0.5322 53.22%
Blood Brain Barrier + 0.8129 81.29%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.8886 88.86%
OATP2B1 inhibitior - 0.8565 85.65%
OATP1B1 inhibitior + 0.9303 93.03%
OATP1B3 inhibitior + 0.9632 96.32%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.9555 95.55%
P-glycoprotein inhibitior - 0.4441 44.41%
P-glycoprotein substrate - 0.5213 52.13%
CYP3A4 substrate + 0.6243 62.43%
CYP2C9 substrate - 0.8134 81.34%
CYP2D6 substrate + 0.3643 36.43%
CYP3A4 inhibition + 0.7877 78.77%
CYP2C9 inhibition - 0.8166 81.66%
CYP2C19 inhibition + 0.5438 54.38%
CYP2D6 inhibition + 0.8816 88.16%
CYP1A2 inhibition + 0.9690 96.90%
CYP2C8 inhibition + 0.8561 85.61%
CYP inhibitory promiscuity + 0.8133 81.33%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9723 97.23%
Carcinogenicity (trinary) Non-required 0.4710 47.10%
Eye corrosion - 0.9900 99.00%
Eye irritation + 0.6756 67.56%
Skin irritation - 0.8329 83.29%
Skin corrosion - 0.9572 95.72%
Ames mutagenesis + 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7200 72.00%
Micronuclear + 0.8200 82.00%
Hepatotoxicity + 0.5898 58.98%
skin sensitisation - 0.9324 93.24%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity - 0.7593 75.93%
Acute Oral Toxicity (c) III 0.6125 61.25%
Estrogen receptor binding + 0.9192 91.92%
Androgen receptor binding + 0.9555 95.55%
Thyroid receptor binding + 0.8633 86.33%
Glucocorticoid receptor binding + 0.9177 91.77%
Aromatase binding + 0.9078 90.78%
PPAR gamma + 0.8404 84.04%
Honey bee toxicity - 0.8899 88.99%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity + 0.7200 72.00%
Fish aquatic toxicity - 0.7292 72.92%

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
CHEMBL1951 P21397 Monoamine oxidase A 98.85% 91.49%
CHEMBL240 Q12809 HERG 97.95% 89.76%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.41% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.23% 96.09%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 95.38% 92.67%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 94.16% 96.47%
CHEMBL1907 P15144 Aminopeptidase N 93.77% 93.31%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.27% 94.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 92.71% 93.99%
CHEMBL255 P29275 Adenosine A2b receptor 92.00% 98.59%
CHEMBL5747 Q92793 CREB-binding protein 90.25% 95.12%
CHEMBL2581 P07339 Cathepsin D 88.41% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.28% 95.56%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 88.15% 85.49%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 87.86% 96.67%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.46% 89.00%
CHEMBL4208 P20618 Proteasome component C5 86.88% 90.00%
CHEMBL1781 P11387 DNA topoisomerase I 86.72% 97.00%
CHEMBL2716 Q8WUI4 Histone deacetylase 7 86.18% 89.44%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.00% 86.33%
CHEMBL2535 P11166 Glucose transporter 85.73% 98.75%
CHEMBL2292 Q13627 Dual-specificity tyrosine-phosphorylation regulated kinase 1A 84.82% 93.24%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 83.50% 94.62%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 83.44% 99.15%
CHEMBL3714130 P46095 G-protein coupled receptor 6 83.06% 97.36%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.64% 92.62%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 82.63% 91.71%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.03% 85.14%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 81.48% 96.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.06% 96.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 80.61% 94.80%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 80.46% 100.00%

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.
Trigonostemon bonianus

Cross-Links

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PubChem 57400007
LOTUS LTS0049173
wikiData Q105153177