Classified by application
All Products
Signaling Pathways
- Angiogenesis/Protein Tyrosine Kinase
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- Epigenetics
-
GPCR/G Protein
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Neuro Signaling Pathway
- Imidazoline Receptor
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Protease/Metabolic Enzyme
- COMT
- 11β HSD
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Research Areas
- Metabolic Disease
- Neurological Disease
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Nature products
Antibodies
Peptides
Catalysts
Impurities
Intermediate
- Amino acid
- Ammonia Series
- Azaindazole
- Pyridazine Series
- Nucleoside Series
- Quinazoline
- Pyrazole Series
- Boric acid
- Pyrimidine Series
- Quinoline Series
- Pyrrole Series
- Thiophene Series
- Saccharide
- Azaindole
- Indole Series
- Piperidine Series
- Indazole Series
- Heterocyclic Series
- Benzene Series
- Pyridine Series
Raw Materials
CXCR
Chemical Structure | Cat. No. | Product Name | CAS No. |
---|
BCP24003 | Vimnerixin New | 1418112-77-2 | |
Vimnerixin is a CXC chemokine receptor type 2 agonist.
|
BCP25433 | AZD8797 New | 911715-90-7 | |
AZD8797 is a non-competitive allosteric modulator of CX3CL1. It acts by binding CX3CR1 and effecting G-protein signalling and ß-arrestin recruitment in a biased way.
|
BCP32916 | Mavorixafor trihydrochloride New | 2309699-17-8 | |
Mavorixafor trihydrochloride is a potent, selective and orally available CXCR4 antagonist, with an IC50 value of 13 nM against CXCR4 125I-SDF binding. It also inhibits the replication of T-tropic HIV-1 (NL4.3 strain) in MT-4 cells and PBMCs with IC50s of 1 and 9 nM, respectively.
|
BCP46165 | ACT-1004-1239 New | 2178049-58-4 | |
ACT-1004-1239 is a potent, insurmountable antagonist.
|
BCP45761 | ML339 New | 2579689-83-9 | |
ML-339 is a potent and selective hCXCR6 antagonist (IC50 = 140 nM).
|
BCP45167 | ML 145 New | 1164500-72-4 | |
ML 145 is a selective antagonist for the GPR35 orphan receptor GPCR (IC50 = 20.1 nM). Over 1000-fold more selective for GPR35 compared to GPR55 antagonists.
|
BCP37842 | VUF11418 New | 1414376-85-4 | |
VUF11418 first reported nonpeptidomimetic agonist on The G protein-coupled chemokine receptor CXCR3.
|
BCP34887 | VUF11207 fumarate New | 1785665-61-3 | |
VUF11207 fumarate is a CXCR7 agonist and a high-potency CXCR7 (pKi of 8.1) ligand that induces recruitment of β-arrestin2 (pEC50 of 8.8) and subsequent internalization (pEC50 of 7.9) of CXCR7.
|
BCP34188 | ALX 40-4C New | 143413-49-4 | |
ALX 40-4C is a small peptide inhibitor of the chemokine receptor CXCR4, inhibits SDF-1 from binding CXCR4 with a Ki of 1 μM, and suppresses the replication of X4 strains of HIV-1; ALX 40-4C Trifluoroacetate also acts as an antagonist of the APJ receptor, with an IC50 of 2.9 μM.
|
BCP34091 | NBI-74330 New | 855527-92-3 | |
NBI-74330 is a small molecule antagonist for CXCR3
|