Page last updated: 2024-12-09

2-(4-chlorophenyl)-4-(ethylthio)-6-(1-pyrrolidinyl)pyrimidine

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

2-(4-chlorophenyl)-4-(ethylthio)-6-(1-pyrrolidinyl)pyrimidine, often shortened to **CP-47,497**, is a synthetic compound that has garnered significant attention in research, particularly in the fields of **immunology and cancer therapy**.

Here's a breakdown of its key characteristics and importance:

**Structure and Properties:**

* **Structure:** CP-47,497 is a pyrimidine derivative, a class of organic compounds with a six-membered ring containing two nitrogen atoms. Its specific structure incorporates a 4-chlorophenyl group, an ethylthio group, and a 1-pyrrolidinyl group.
* **Chemical Formula:** C17H19ClN2S
* **Molecular Weight:** 322.86 g/mol

**Biological Activity:**

* **Immunomodulatory effects:** CP-47,497 is known for its ability to **modulate the immune system**. It acts as a **selective inhibitor of the enzyme sphingosine-1-phosphate lyase (SPL)**. SPL is responsible for breaking down sphingosine-1-phosphate (S1P), a lipid mediator that plays a critical role in various immune processes, including lymphocyte trafficking and immune cell activation.
* **Anti-cancer potential:** The inhibition of SPL by CP-47,497 has shown promise in **cancer therapy**. By affecting S1P levels, CP-47,497 can potentially:
* **Reduce tumor growth:** By influencing the migration and activity of immune cells, CP-47,497 could suppress tumor development and growth.
* **Enhance anti-tumor responses:** It could improve the effectiveness of chemotherapy and other anti-cancer treatments by modulating the immune system to better recognize and attack cancer cells.

**Research Applications:**

CP-47,497 is actively being investigated in various research areas:

* **Immunotherapy:** Its potential to enhance immune responses against cancer makes it a valuable tool in developing new immunotherapeutic strategies.
* **Autoimmune diseases:** The modulation of S1P levels by CP-47,497 could be beneficial in treating autoimmune diseases, where the immune system attacks the body's own tissues.
* **Inflammation:** Its impact on immune cell trafficking and activation could offer therapeutic avenues for managing inflammatory conditions.

**Important Note:** While CP-47,497 shows promising potential, it is still in the research phase and has not been approved for clinical use. Further research is needed to fully understand its safety, efficacy, and optimal applications.

**In summary,** 2-(4-chlorophenyl)-4-(ethylthio)-6-(1-pyrrolidinyl)pyrimidine (CP-47,497) is a significant molecule in research due to its ability to modulate the immune system by inhibiting sphingosine-1-phosphate lyase. This property makes it a promising candidate for therapeutic interventions in cancer, autoimmune diseases, and inflammatory conditions. However, further research is crucial before its potential can be fully realized in clinical settings.

Cross-References

ID SourceID
PubMed CID852319
CHEMBL ID1407233
CHEBI ID92529

Synonyms (15)

Synonym
2-(4-chlorophenyl)-4-ethylsulfanyl-6-pyrrolidin-1-ylpyrimidine
2-(4-chlorophenyl)-6-(1-pyrrolidinyl)-4-pyrimidinyl ethyl sulfide
AQ-750/42238033
MLS-0390923.0001 ,
MLS002460477
smr001382692
HMS2199P22
bdbm44369
2-(4-chlorophenyl)-4-ethylsulfanyl-6-pyrrolidin-1-yl-pyrimidine
2-(4-chlorophenyl)-4-(ethylthio)-6-(1-pyrrolidinyl)pyrimidine
cid_852319
2-(4-chlorophenyl)-4-(ethylthio)-6-pyrrolidino-pyrimidine
CHEMBL1407233
CHEBI:92529
Q27164259
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
aryl sulfideAny organic sulfide in which the sulfur is attached to at least one aromatic group.
[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 Targets (5)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Chain A, MAJOR APURINIC/APYRIMIDINIC ENDONUCLEASEHomo sapiens (human)Potency0.07520.003245.467312,589.2998AID2517
USP1 protein, partialHomo sapiens (human)Potency0.25120.031637.5844354.8130AID743255
chromobox protein homolog 1Homo sapiens (human)Potency63.09570.006026.168889.1251AID540317
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
tumor necrosis factor ligand superfamily member 10 isoform 1Homo sapiens (human)IC50 (µMol)10.00000.37202.26354.8100AID1752; AID1755
Translocator proteinRattus norvegicus (Norway rat)IC50 (µMol)10.00000.00010.63934.8100AID1755
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (13)

Assay IDTitleYearJournalArticle
AID588497High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set2010Current protocols in cytometry, Oct, Volume: Chapter 13Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening.
AID588497High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set2006Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5
Microsphere-based protease assays and screening application for lethal factor and factor Xa.
AID588497High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set2010Assay and drug development technologies, Feb, Volume: 8, Issue:1
High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors.
AID588501High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set2010Current protocols in cytometry, Oct, Volume: Chapter 13Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening.
AID588501High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set2006Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5
Microsphere-based protease assays and screening application for lethal factor and factor Xa.
AID588501High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set2010Assay and drug development technologies, Feb, Volume: 8, Issue:1
High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors.
AID588499High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set2010Current protocols in cytometry, Oct, Volume: Chapter 13Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening.
AID588499High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set2006Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5
Microsphere-based protease assays and screening application for lethal factor and factor Xa.
AID588499High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set2010Assay and drug development technologies, Feb, Volume: 8, Issue:1
High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors.
AID504810Antagonists of the Thyroid Stimulating Hormone Receptor: HTS campaign2010Endocrinology, Jul, Volume: 151, Issue:7
A small molecule inverse agonist for the human thyroid-stimulating hormone receptor.
AID504812Inverse Agonists of the Thyroid Stimulating Hormone Receptor: HTS campaign2010Endocrinology, Jul, Volume: 151, Issue:7
A small molecule inverse agonist for the human thyroid-stimulating hormone receptor.
AID1745845Primary qHTS for Inhibitors of ATXN expression
AID651635Viability Counterscreen for Primary qHTS for Inhibitors of ATXN expression
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (5)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (20.00)29.6817
2010's3 (60.00)24.3611
2020's1 (20.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 12.56

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.

MetricThis Compound (vs All)
Research Demand Index12.56 (24.57)
Research Supply Index1.79 (2.92)
Research Growth Index4.36 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (12.56)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other5 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]