Trigonostemine C

Details

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Internal ID 023090d8-8556-406c-a404-7412d2693bf4
Taxonomy Alkaloids and derivatives > Harmala alkaloids
IUPAC Name (2-hydroxy-1H-indol-3-yl)-(7-methoxy-9H-pyrido[3,4-b]indol-1-yl)methanone
SMILES (Canonical) COC1=CC2=C(C=C1)C3=C(N2)C(=NC=C3)C(=O)C4=C(NC5=CC=CC=C54)O
SMILES (Isomeric) COC1=CC2=C(C=C1)C3=C(N2)C(=NC=C3)C(=O)C4=C(NC5=CC=CC=C54)O
InChI InChI=1S/C21H15N3O3/c1-27-11-6-7-12-13-8-9-22-19(18(13)23-16(12)10-11)20(25)17-14-4-2-3-5-15(14)24-21(17)26/h2-10,23-24,26H,1H3
InChI Key KXSXMTWFKGXALP-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C21H15N3O3
Molecular Weight 357.40 g/mol
Exact Mass 357.11134135 g/mol
Topological Polar Surface Area (TPSA) 91.00 Ų
XlogP 4.60
Atomic LogP (AlogP) 4.14
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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CHEMBL1957110

2D Structure

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2D Structure of Trigonostemine C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9944 99.44%
Caco-2 - 0.5577 55.77%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.7864 78.64%
OATP2B1 inhibitior + 0.5654 56.54%
OATP1B1 inhibitior + 0.9023 90.23%
OATP1B3 inhibitior + 0.9623 96.23%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.8518 85.18%
P-glycoprotein inhibitior - 0.4319 43.19%
P-glycoprotein substrate - 0.6716 67.16%
CYP3A4 substrate + 0.6258 62.58%
CYP2C9 substrate - 0.7929 79.29%
CYP2D6 substrate - 0.8458 84.58%
CYP3A4 inhibition - 0.6817 68.17%
CYP2C9 inhibition - 0.8450 84.50%
CYP2C19 inhibition - 0.5290 52.90%
CYP2D6 inhibition - 0.8634 86.34%
CYP1A2 inhibition + 0.9562 95.62%
CYP2C8 inhibition + 0.7618 76.18%
CYP inhibitory promiscuity - 0.6217 62.17%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6250 62.50%
Eye corrosion - 0.9936 99.36%
Eye irritation - 0.6518 65.18%
Skin irritation - 0.8830 88.30%
Skin corrosion - 0.9697 96.97%
Ames mutagenesis + 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6626 66.26%
Micronuclear + 0.8700 87.00%
Hepatotoxicity + 0.5712 57.12%
skin sensitisation - 0.9357 93.57%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity - 0.8527 85.27%
Acute Oral Toxicity (c) III 0.6143 61.43%
Estrogen receptor binding + 0.8422 84.22%
Androgen receptor binding + 0.8570 85.70%
Thyroid receptor binding + 0.7664 76.64%
Glucocorticoid receptor binding + 0.8018 80.18%
Aromatase binding + 0.8125 81.25%
PPAR gamma + 0.9091 90.91%
Honey bee toxicity - 0.9114 91.14%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity - 0.7031 70.31%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.63% 91.11%
CHEMBL2292 Q13627 Dual-specificity tyrosine-phosphorylation regulated kinase 1A 97.19% 93.24%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.16% 96.09%
CHEMBL1951 P21397 Monoamine oxidase A 96.47% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.44% 95.56%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 94.25% 92.67%
CHEMBL2535 P11166 Glucose transporter 93.84% 98.75%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 92.47% 96.47%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.19% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.53% 94.45%
CHEMBL4208 P20618 Proteasome component C5 90.37% 90.00%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 90.15% 94.08%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 89.08% 94.62%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.03% 99.15%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 88.64% 96.00%
CHEMBL1781 P11387 DNA topoisomerase I 87.94% 97.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.49% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.23% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.47% 99.17%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.87% 85.14%
CHEMBL1907 P15144 Aminopeptidase N 85.43% 93.31%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.76% 86.33%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 84.26% 95.50%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 83.13% 93.65%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.07% 93.99%
CHEMBL211 P08172 Muscarinic acetylcholine receptor M2 80.34% 94.97%

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 136196557
LOTUS LTS0033230
wikiData Q105147500