Aminophenols
Medchemexpress LLC BIIL-260 hydrochlori | 100MG
BIIL-260 hydrochloride is a potent and long-acting orally active leukotriene B(4) receptor LTB4 antagonist with anti-inflammatory activity BIIL-260 hydrochloride interacts with the LTB4 receptor in a saturable reversible and competitive manner has high affinity to the LTB4 receptor on isolated human neutrophil cell membranes with Ki values of 1 7 nM[1]
Medchemexpress LLC GSK 690 Hydrochlorid 100mg | 2436760-79-9 | 405.92 | C24H24ClN3O | 100 MG
GSK 690 hydrochloride is a reversible small-molecule inhibitor of lysine-specific demethylase 1 (LSD1) with a reported Kd of 9 nM and a biochemical IC50 of 37 nM. It is supplied as a light yellow to yellow solid (CAS 2436760-79-9) with reported purity of 98.58% and high solubility in DMSO.
eMolecules 548-37-8 | Medchem Express | Verbenalin | 5mg | 523883500 | HY-N2014 | MFCD00017414 | 388.369 | C17H24O10
Medchem Express | Verbenalin | 5mg | 523883500 | HY-N2014 | 548-37-8 | MFCD00017414 | 388.369 | C17H24O10
eMolecules 127818-58-0 | 3-METHYL-5-NITROPHENOL | MFCD09038591 | 1g
Ambeed | 13-Benzenedimethanamine | 25g | 600851593 | A566345 | 1477-55-0 | MFCD00008119 | 136.198 | C8H12N2
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Medchemexpress LLC UNC9994 hydrochloride | 2108826-33-9 | 99.5% | 457.84 | 100 MG
UNC9994 hydrochloride is a functionally selective, β-arrestin-biased dopamine D2 receptor (D2R) agonist that selectively activates β-arrestin recruitment and signaling. It shows a binding affinity with a Ki of 79 nM for D2R. UNC9994 hydrochloride is also an antagonist of Gi-regulated cAMP production and a partial agonist for D2R/β-arrestin-2 interactions. It demonstrates antipsychotic-like activity. It is for research use only.
- Functions as a β-arrestin-biased dopamine D2 receptor agonist.
- Selectively activates β-arrestin recruitment and signaling.
- Exhibits a binding affinity (Ki) of 79 nM for D2R.
- Acts as an antagonist of Gi-regulated cAMP production.
- Serves as a partial agonist for D2R/β-arrestin-2 interactions.
- Demonstrates antipsychotic-like activity.
Ambeed 2Methoxy6 trifluoromethoxy ph
(2-Methoxy-6-(trifluoromethoxy)phenyl)boronic acid, 309977-92-2, 95%
Ambeed 2 1HImidazol4yl ethan1amine di
2-(1H-Imidazol-4-yl)ethan-1-amine dihydrochloride, 56-92-8, 98%
Medchemexpress LLC CBL0137 hydrochloride | 1197397-89-9 | 99.7% | 372.89 g/mol | C21H25ClN2O2 | 10 MG
CBL0137 hydrochloride is a research-grade small molecule that inhibits the histone chaperone FACT, activates p53, and suppresses NF-κB signaling. It is used in preclinical studies to probe chromatin regulation and anticancer mechanisms in cell-based and biochemical assays.
- Inhibits the histone chaperone FACT.
- Activates p53 in cell-based assays (IC50 ≈ 0.37 μM).
- Inhibits NF-κB signaling in cell-based assays (IC50 ≈ 0.47 μM).
- High chemical purity, typically reported as 99.7%.
- Available as solid packs and as a DMSO solution for in vitro use.
- Suitable for mechanistic studies, pathway modulation, and preclinical cancer research.
Medchemexpress LLC Menthone | 10458-14-7 | 1000 G
Menthone is an orally active monoterpene isolated from plants and Mentha oil. It possesses antibacterial, antitumor, antioxidation, and antivirus properties, and is a main volatile component of essential oil. Menthone exhibits anti-inflammatory properties, effective in conditions such as *Schistosoma mansoni* infection and rheumatoid arthritis.
- Orally active monoterpene
- Isolated from natural sources like plants and Mentha oil
- Provides antibacterial, antitumor, antioxidation, and antivirus effects
- Acts as a main volatile component of essential oil
- Exhibits anti-inflammatory properties in *Schistosoma mansoni* infection and rheumatoid arthritis
- Inhibits proinflammatory cytokine secretion
- Modulates immune responses in allergic asthma
- Decreases Th1 and Th17 cell expression in inflammatory models