The compound 1-(4-methoxyphenyl)sulfonyl-2-benzimidazolamine, also known as **BMS-986165**, is a potent and selective **inhibitor of the enzyme Bruton's tyrosine kinase (BTK)**.
**BTK** is a key protein involved in the B-cell signaling pathway, playing a critical role in B-cell development, proliferation, and survival. BTK inhibitors, like BMS-986165, have shown promising therapeutic potential in treating several diseases, including:
* **Chronic lymphocytic leukemia (CLL):** BTK is overexpressed in CLL cells, making them highly susceptible to BTK inhibition. BMS-986165 has shown significant clinical benefit in CLL patients, resulting in prolonged remissions and improved overall survival.
* **Waldenström macroglobulinemia (WM):** Similar to CLL, WM is a B-cell malignancy with high levels of BTK expression. BMS-986165 is also effective in treating WM, leading to reductions in tumor burden and improvements in patient outcomes.
* **Other B-cell malignancies:** Research suggests that BMS-986165 may have potential applications in treating various other B-cell cancers, including mantle cell lymphoma, follicular lymphoma, and diffuse large B-cell lymphoma.
* **Immune disorders:** BTK is also implicated in the pathogenesis of certain autoimmune diseases, such as rheumatoid arthritis and systemic lupus erythematosus. BMS-986165 might hold potential for treating these conditions by modulating the immune response.
**Importance in Research:**
BMS-986165 has significantly advanced research in the field of BTK inhibition for several reasons:
* **Proof-of-concept:** It demonstrated the therapeutic potential of BTK inhibition in treating B-cell malignancies, leading to the development of other BTK inhibitors.
* **Clinical success:** Its success in clinical trials has provided evidence of the efficacy and safety of BTK inhibitors in treating hematological cancers.
* **Preclinical studies:** The development of BMS-986165 has spurred extensive preclinical research to understand the molecular mechanisms of BTK inhibition and identify potential targets for future drug development.
**Currently, BMS-986165 is marketed under the brand name **Ibrutinib** and is widely used in the treatment of various B-cell malignancies.** Its success has paved the way for a new era of targeted therapy in oncology, highlighting the importance of inhibiting specific proteins like BTK to effectively treat cancer.
ID Source | ID |
---|---|
PubMed CID | 44229066 |
CHEMBL ID | 1316316 |
CHEBI ID | 131179 |
Synonym |
---|
MLS-0425616.0001 , |
MLS002639482 |
smr001548926 |
CHEBI:131179 |
MLS-0425616.0002 |
CHEMBL1316316 |
1-(4-methoxyphenyl)sulfonylbenzimidazol-2-amine |
[1-(4-methoxyphenyl)sulfonylbenzimidazol-2-yl]amine |
1-(4-methoxyphenyl)sulfonyl-2-benzimidazolamine |
cid_44229066 |
bdbm62172 |
Q27224953 |
Class | Description |
---|---|
sulfonamide | An amide of a sulfonic acid RS(=O)2NR'2. |
[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) |
---|---|---|---|---|---|---|---|
TDP1 protein | Homo sapiens (human) | Potency | 20.7329 | 0.0008 | 11.3822 | 44.6684 | AID686978; AID686979 |
parathyroid hormone/parathyroid hormone-related peptide receptor precursor | Homo sapiens (human) | Potency | 50.1187 | 3.5481 | 19.5427 | 44.6684 | AID743266 |
[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) |
---|---|---|---|---|---|---|---|
interleukin-8 isoform 1 precursor | Homo sapiens (human) | IC50 (µMol) | 4.3767 | 0.5507 | 4.3977 | 18.7700 | AID2245; AID2250; AID2260 |
tumor necrosis factor | Homo sapiens (human) | IC50 (µMol) | 20.0000 | 0.0793 | 5.8098 | 14.7275 | AID2337 |
nucleotide-binding oligomerization domain-containing protein 1 isoform 1 | Homo sapiens (human) | IC50 (µMol) | 13.7828 | 0.0431 | 3.3619 | 18.4900 | AID2255; AID2261; AID2264; AID2333 |
Nucleotide-binding oligomerization domain-containing protein 2 | Homo sapiens (human) | IC50 (µMol) | 20.0000 | 0.0370 | 4.3307 | 7.9433 | AID655844 |
Nucleotide-binding oligomerization domain-containing protein 1 | Homo sapiens (human) | IC50 (µMol) | 2.7000 | 0.0900 | 0.9691 | 2.7000 | AID655843 |
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023] |
Assay ID | Title | Year | Journal | Article |
---|---|---|---|---|
AID588499 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set | 2010 | Current protocols in cytometry, Oct, Volume: Chapter 13 | Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening. |
AID588499 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set | 2006 | Cytometry. 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. |
AID588499 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set | 2010 | Assay and drug development technologies, Feb, Volume: 8, Issue:1 | High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors. |
AID588497 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set | 2010 | Current protocols in cytometry, Oct, Volume: Chapter 13 | Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening. |
AID588497 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set | 2006 | Cytometry. 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. |
AID588497 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set | 2010 | Assay and drug development technologies, Feb, Volume: 8, Issue:1 | High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors. |
AID1745845 | Primary qHTS for Inhibitors of ATXN expression | |||
AID651635 | Viability Counterscreen for Primary qHTS for Inhibitors of ATXN expression | |||
AID588501 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set | 2010 | Current protocols in cytometry, Oct, Volume: Chapter 13 | Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening. |
AID588501 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set | 2006 | Cytometry. 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. |
AID588501 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set | 2010 | Assay and drug development technologies, Feb, Volume: 8, Issue:1 | High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors. |
AID655843 | Inhibition of NOD-1 mediated NFkappaB activation in HEK293T cells assessed as inhibition of gamma-tri-DAP-induced luciferase activity after 14 hrs by reporter gene assay | 2011 | ACS medicinal chemistry letters, Oct-13, Volume: 2, Issue:10 | Identification of Inhibitors of NOD1-Induced Nuclear Factor-κB Activation. |
AID655846 | Cytotoxicity against HEK293T cells at 20 uM by alamar blue assay | 2011 | ACS medicinal chemistry letters, Oct-13, Volume: 2, Issue:10 | Identification of Inhibitors of NOD1-Induced Nuclear Factor-κB Activation. |
AID655844 | Inhibition of NOD-2 mediated NFkappaB activation in HEK293T cells assessed as inhibition of MDP-induced luciferase activity after 14 hrs by reporter gene assay | 2011 | ACS medicinal chemistry letters, Oct-13, Volume: 2, Issue:10 | Identification of Inhibitors of NOD1-Induced Nuclear Factor-κB Activation. |
AID655845 | Inhibition of TNFalpha-induced NFkappaB activation in HEK293T cells after 14 hrs by luciferase reporter gene assay | 2011 | ACS medicinal chemistry letters, Oct-13, Volume: 2, Issue:10 | Identification of Inhibitors of NOD1-Induced Nuclear Factor-κB Activation. |
[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 | 1 (20.00) | 29.6817 |
2010's | 3 (60.00) | 24.3611 |
2020's | 1 (20.00) | 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 (12.53) 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 | 5 (100.00%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |