Trigonostemine F

Details

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Internal ID 9b74c752-f921-42ee-8f02-3404aca281d5
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Pyridoindoles > Pyridoindolones
IUPAC Name 1-(7-methoxyquinolin-4-yl)-2,9-dihydropyrido[3,4-b]indol-3-one
SMILES (Canonical) COC1=CC2=NC=CC(=C2C=C1)C3=C4C(=CC(=O)N3)C5=CC=CC=C5N4
SMILES (Isomeric) COC1=CC2=NC=CC(=C2C=C1)C3=C4C(=CC(=O)N3)C5=CC=CC=C5N4
InChI InChI=1S/C21H15N3O2/c1-26-12-6-7-14-15(8-9-22-18(14)10-12)20-21-16(11-19(25)24-20)13-4-2-3-5-17(13)23-21/h2-11,23H,1H3,(H,24,25)
InChI Key PPXQLIICQQDSIF-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C21H15N3O2
Molecular Weight 341.40 g/mol
Exact Mass 341.116426730 g/mol
Topological Polar Surface Area (TPSA) 63.20 Ų
XlogP 2.60
Atomic LogP (AlogP) 4.23
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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CHEMBL1957103

2D Structure

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2D Structure of Trigonostemine F

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9971 99.71%
Caco-2 + 0.5572 55.72%
Blood Brain Barrier + 0.7629 76.29%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.8458 84.58%
OATP2B1 inhibitior - 0.8509 85.09%
OATP1B1 inhibitior + 0.9169 91.69%
OATP1B3 inhibitior + 0.9601 96.01%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.9682 96.82%
P-glycoprotein inhibitior + 0.5941 59.41%
P-glycoprotein substrate - 0.6100 61.00%
CYP3A4 substrate + 0.6463 64.63%
CYP2C9 substrate - 0.7979 79.79%
CYP2D6 substrate - 0.8399 83.99%
CYP3A4 inhibition + 0.6442 64.42%
CYP2C9 inhibition - 0.6833 68.33%
CYP2C19 inhibition + 0.5973 59.73%
CYP2D6 inhibition - 0.6190 61.90%
CYP1A2 inhibition + 0.9386 93.86%
CYP2C8 inhibition + 0.7256 72.56%
CYP inhibitory promiscuity - 0.5408 54.08%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9423 94.23%
Carcinogenicity (trinary) Non-required 0.5108 51.08%
Eye corrosion - 0.9918 99.18%
Eye irritation - 0.6945 69.45%
Skin irritation - 0.8765 87.65%
Skin corrosion - 0.9704 97.04%
Ames mutagenesis + 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6410 64.10%
Micronuclear + 0.8600 86.00%
Hepatotoxicity + 0.5303 53.03%
skin sensitisation - 0.9268 92.68%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity - 0.7227 72.27%
Acute Oral Toxicity (c) III 0.6271 62.71%
Estrogen receptor binding + 0.8949 89.49%
Androgen receptor binding + 0.9567 95.67%
Thyroid receptor binding + 0.7200 72.00%
Glucocorticoid receptor binding + 0.9270 92.70%
Aromatase binding + 0.8316 83.16%
PPAR gamma + 0.8546 85.46%
Honey bee toxicity - 0.8662 86.62%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity - 0.7086 70.86%

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 98.79% 91.49%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.42% 91.11%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 96.62% 92.67%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.06% 95.56%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 95.15% 94.80%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.06% 96.09%
CHEMBL2581 P07339 Cathepsin D 95.00% 98.95%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 94.14% 96.47%
CHEMBL255 P29275 Adenosine A2b receptor 93.78% 98.59%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.69% 94.00%
CHEMBL2535 P11166 Glucose transporter 92.94% 98.75%
CHEMBL1907 P15144 Aminopeptidase N 92.41% 93.31%
CHEMBL4208 P20618 Proteasome component C5 91.38% 90.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.30% 85.14%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 89.52% 96.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.26% 89.00%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 88.36% 96.67%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.79% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.72% 99.23%
CHEMBL1781 P11387 DNA topoisomerase I 86.08% 97.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 85.45% 93.99%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 84.91% 85.49%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.79% 99.15%
CHEMBL4302 P08183 P-glycoprotein 1 84.37% 92.98%
CHEMBL2717 Q9HCR9 Phosphodiesterase 11A 82.40% 85.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.96% 96.00%
CHEMBL2424504 P29375 Lysine-specific demethylase 5A 81.76% 99.23%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.31% 92.62%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 80.21% 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 57396566
LOTUS LTS0041583
wikiData Q105213089