ID Source | ID |
---|---|
PubMed CID | 707946 |
CHEMBL ID | 1454141 |
CHEBI ID | 114831 |
Synonym |
---|
IDI1_003045 |
CHEMDIV2_004330 |
EU-0048056 |
n-(7-phenyl-[1,2,4]triazolo[1,5-a]pyrimidin-2-yl)-benzamide |
MLS000768463 |
smr000431784 |
CHEBI:114831 |
STK825268 |
n-(7-phenyl[1,2,4]triazolo[1,5-a]pyrimidin-2-yl)benzamide |
HMS1381E18 |
AKOS001665586 |
n-(7-phenyl-[1,2,4]triazolo[1,5-a]pyrimidin-2-yl)benzamide |
HMS2809B15 |
CHEMBL1454141 , |
Q27196334 |
500103-70-8 |
SR-01000084374-1 |
sr-01000084374 |
bdbm50518355 |
DTXSID201330327 |
Class | Description |
---|---|
pyrimidines | Any compound having a pyrimidine as part of its structure. |
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res] |
Protein | Taxonomy | Measurement | Average (µ) | Min (ref.) | Avg (ref.) | Max (ref.) | Bioassay(s) |
---|---|---|---|---|---|---|---|
Chain A, TYROSYL-DNA PHOSPHODIESTERASE | Homo sapiens (human) | Potency | 59.6217 | 0.0040 | 23.8416 | 100.0000 | AID485290; AID489007 |
Chain A, 2-oxoglutarate Oxygenase | Homo sapiens (human) | Potency | 28.1838 | 0.1778 | 14.3909 | 39.8107 | AID2147 |
Luciferase | Photinus pyralis (common eastern firefly) | Potency | 7.5686 | 0.0072 | 15.7588 | 89.3584 | AID588342 |
BRCA1 | Homo sapiens (human) | Potency | 1.5849 | 0.8913 | 7.7225 | 25.1189 | AID624202 |
ATAD5 protein, partial | Homo sapiens (human) | Potency | 13.2725 | 0.0041 | 10.8903 | 31.5287 | AID504466; AID504467 |
Microtubule-associated protein tau | Homo sapiens (human) | Potency | 0.2818 | 0.1800 | 13.5574 | 39.8107 | AID1460 |
NPC intracellular cholesterol transporter 1 precursor | Homo sapiens (human) | Potency | 2.8184 | 0.0126 | 2.4518 | 25.0177 | AID485313 |
chromobox protein homolog 1 | Homo sapiens (human) | Potency | 89.1251 | 0.0060 | 26.1688 | 89.1251 | AID540317 |
ras-related protein Rab-9A | Homo sapiens (human) | Potency | 2.5119 | 0.0002 | 2.6215 | 31.4954 | AID485297 |
DNA polymerase iota isoform a (long) | Homo sapiens (human) | Potency | 100.0000 | 0.0501 | 27.0736 | 89.1251 | AID588590 |
relaxin receptor 1 isoform 1 | Homo sapiens (human) | Potency | 39.8107 | 0.0388 | 14.3501 | 43.6206 | AID2676 |
Guanine nucleotide-binding protein G | Homo sapiens (human) | Potency | 50.1187 | 1.9953 | 25.5327 | 50.1187 | AID624287 |
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023] |
Protein | Taxonomy | Measurement | Average | Min (ref.) | Avg (ref.) | Max (ref.) | Bioassay(s) |
---|---|---|---|---|---|---|---|
Tyrosyl-DNA phosphodiesterase 2 | Homo sapiens (human) | IC50 (µMol) | 100.0000 | 0.9700 | 2.2160 | 4.1000 | AID1574190 |
Polymerase acidic protein | Influenza A virus (A/Puerto Rico/8/1934(H1N1)) | IC50 (µMol) | 200.0000 | 1.8800 | 4.6880 | 5.8600 | AID1778626 |
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023] |
Process | via Protein(s) | Taxonomy |
---|---|---|
double-strand break repair | Tyrosyl-DNA phosphodiesterase 2 | Homo sapiens (human) |
cell surface receptor signaling pathway | Tyrosyl-DNA phosphodiesterase 2 | Homo sapiens (human) |
negative regulation of DNA-templated transcription | Tyrosyl-DNA phosphodiesterase 2 | Homo sapiens (human) |
neuron development | Tyrosyl-DNA phosphodiesterase 2 | Homo sapiens (human) |
negative regulation of inflammatory response to antigenic stimulus | Guanine nucleotide-binding protein G | Homo sapiens (human) |
renal water homeostasis | Guanine nucleotide-binding protein G | Homo sapiens (human) |
G protein-coupled receptor signaling pathway | Guanine nucleotide-binding protein G | Homo sapiens (human) |
regulation of insulin secretion | Guanine nucleotide-binding protein G | Homo sapiens (human) |
cellular response to glucagon stimulus | Guanine nucleotide-binding protein G | Homo sapiens (human) |
[Information is prepared from geneontology information from the June-17-2024 release] |
Process | via Protein(s) | Taxonomy |
---|---|---|
magnesium ion binding | Tyrosyl-DNA phosphodiesterase 2 | Homo sapiens (human) |
single-stranded DNA binding | Tyrosyl-DNA phosphodiesterase 2 | Homo sapiens (human) |
transcription corepressor activity | Tyrosyl-DNA phosphodiesterase 2 | Homo sapiens (human) |
nuclease activity | Tyrosyl-DNA phosphodiesterase 2 | Homo sapiens (human) |
protein binding | Tyrosyl-DNA phosphodiesterase 2 | Homo sapiens (human) |
manganese ion binding | Tyrosyl-DNA phosphodiesterase 2 | Homo sapiens (human) |
tyrosyl-RNA phosphodiesterase activity | Tyrosyl-DNA phosphodiesterase 2 | Homo sapiens (human) |
5'-tyrosyl-DNA phosphodiesterase activity | Tyrosyl-DNA phosphodiesterase 2 | Homo sapiens (human) |
G protein activity | Guanine nucleotide-binding protein G | Homo sapiens (human) |
adenylate cyclase activator activity | Guanine nucleotide-binding protein G | Homo sapiens (human) |
[Information is prepared from geneontology information from the June-17-2024 release] |
Process | via Protein(s) | Taxonomy |
---|---|---|
nucleus | Tyrosyl-DNA phosphodiesterase 2 | Homo sapiens (human) |
nucleoplasm | Tyrosyl-DNA phosphodiesterase 2 | Homo sapiens (human) |
nucleolus | Tyrosyl-DNA phosphodiesterase 2 | Homo sapiens (human) |
cytoplasm | Tyrosyl-DNA phosphodiesterase 2 | Homo sapiens (human) |
aggresome | Tyrosyl-DNA phosphodiesterase 2 | Homo sapiens (human) |
nuclear body | Tyrosyl-DNA phosphodiesterase 2 | Homo sapiens (human) |
PML body | Tyrosyl-DNA phosphodiesterase 2 | Homo sapiens (human) |
PML body | Tyrosyl-DNA phosphodiesterase 2 | Homo sapiens (human) |
cytoplasm | Tyrosyl-DNA phosphodiesterase 2 | Homo sapiens (human) |
extracellular region | RNA-directed RNA polymerase catalytic subunit | Influenza A virus (A/Puerto Rico/8/1934(H1N1)) |
extracellular region | Polymerase acidic protein | Influenza A virus (A/Puerto Rico/8/1934(H1N1)) |
plasma membrane | Guanine nucleotide-binding protein G | Homo sapiens (human) |
[Information is prepared from geneontology information from the June-17-2024 release] |
Assay ID | Title | Year | Journal | Article |
---|---|---|---|---|
AID504810 | Antagonists of the Thyroid Stimulating Hormone Receptor: HTS campaign | 2010 | Endocrinology, Jul, Volume: 151, Issue:7 | A small molecule inverse agonist for the human thyroid-stimulating hormone receptor. |
AID651635 | Viability Counterscreen for Primary qHTS for Inhibitors of ATXN expression | |||
AID504812 | Inverse Agonists of the Thyroid Stimulating Hormone Receptor: HTS campaign | 2010 | Endocrinology, Jul, Volume: 151, Issue:7 | A small molecule inverse agonist for the human thyroid-stimulating hormone receptor. |
AID1745845 | Primary qHTS for Inhibitors of ATXN expression | |||
AID1778628 | Cytotoxicity against MDCK cells assessed as reduction in cell viability incubated for 48 hrs by MTT assay | 2021 | European journal of medicinal chemistry, Oct-05, Volume: 221 | 1,2,4-Triazolo[1,5-a]pyrimidines: Efficient one-step synthesis and functionalization as influenza polymerase PA-PB1 interaction disruptors. |
AID1778626 | Inhibition of Influenza A virus 6 His-tagged PA (239 to 716 residues) expressed in Escherichia coli BL21 pLysS/GST-tagged PB1 (1 to 25 residues) expressed in Escherichia coli protein-protein interaction using 3.3',5,5' tetramethyl benzidine as substrate b | 2021 | European journal of medicinal chemistry, Oct-05, Volume: 221 | 1,2,4-Triazolo[1,5-a]pyrimidines: Efficient one-step synthesis and functionalization as influenza polymerase PA-PB1 interaction disruptors. |
AID1574190 | Inhibition of humanized zebrafish TDP2 using 5'-(6-FAM-NHS) as substrate preincubated for 10 mins followed by substrate addition and measured after 60 mins by fluorescence assay | 2019 | Bioorganic & medicinal chemistry letters, 01-15, Volume: 29, Issue:2 | Triazolopyrimidine and triazolopyridine scaffolds as TDP2 inhibitors. |
AID1778627 | Antiviral activity against Influenza A virus A/PR/8/34(H1N1) infected in MDCK cells assessed as inhibition of plaque formation for 48 hrs by plaque reduction assay | 2021 | European journal of medicinal chemistry, Oct-05, Volume: 221 | 1,2,4-Triazolo[1,5-a]pyrimidines: Efficient one-step synthesis and functionalization as influenza polymerase PA-PB1 interaction disruptors. |
AID1794808 | Fluorescence-based screening to identify small molecule inhibitors of Plasmodium falciparum apicoplast DNA polymerase (Pf-apPOL). | 2014 | Journal of biomolecular screening, Jul, Volume: 19, Issue:6 | A High-Throughput Assay to Identify Inhibitors of the Apicoplast DNA Polymerase from Plasmodium falciparum. |
AID1794808 | Fluorescence-based screening to identify small molecule inhibitors of Plasmodium falciparum apicoplast DNA polymerase (Pf-apPOL). | |||
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] |
Timeframe | Studies, This Drug (%) | All Drugs % |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 3 (50.00) | 24.3611 |
2020's | 3 (50.00) | 2.80 |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |
According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be weak demand-to-supply ratio for research on this compound.
| This Compound (12.92) All Compounds (24.57) |
Publication Type | This drug (%) | All Drugs (%) |
---|---|---|
Trials | 0 (0.00%) | 5.53% |
Reviews | 0 (0.00%) | 6.00% |
Case Studies | 0 (0.00%) | 4.05% |
Observational | 0 (0.00%) | 0.25% |
Other | 6 (100.00%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |