Powder: -20°C for 3 years | In solvent: -80°C for 1 year
RS102895 is a potent CCR2 antagonist (IC50: 360 nM) and shows no effect on CCR1.
パッケージサイズ | 在庫状況 | 単価(税別) | |||
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サンプルについてお問い合わせ | |||||
2 mg | 在庫あり | ¥ 8,500 | |||
5 mg | 在庫あり | ¥ 13,500 | |||
10 mg | 在庫あり | ¥ 22,500 | |||
25 mg | 在庫あり | ¥ 41,000 | |||
50 mg | 在庫あり | ¥ 61,500 | |||
100 mg | 在庫あり | ¥ 91,500 | |||
1 mL * 10 mM (in DMSO) | 在庫あり | ¥ 17,000 |
説明 | RS102895 is a potent CCR2 antagonist (IC50: 360 nM) and shows no effect on CCR1. |
ターゲット&IC50 | 5-HT1A:470 nM, CCR2:360 nM, α1D-adrenoceptor (human):320 nM, α1A-adrenoceptor:130 nM |
In vitro | RS102895 also inhibits human α1a, α1d receptors, rat brain cortex 5HT1a receptor in cells with IC50s of 130, 320, 470 nM, respectively. RS102895 suppresses wild type and D284N mutant MCP-1 receptor (IC50, 550 nM and 568 nM, respectively), less potently inhibits D284A MCP-1 receptor (IC50, 1892 nM), and has no effects on E291A, E291Q, D284A/E291A or D284N/E291Q (IC50, >100,000?nM) [1]. RS102895 ameliorates the increased extracellular matrix protein expression by inhibition of CCR2 at 10 μM and obviously blocks fibronectin and type IV collagen protein expression in high glucose-stimulated mesangial cells (MCs) at 1 or 10 μM. RS102895 (10 μM) also abrogate the increased TGF-1 levels in MCs treated with MCP-1 [2]. |
In vivo | RS102895 at a concentration of 3 g/L progressively lowers the pain threshold in rats experiencing bone cancer pain (BCP) from days 3 to 9 post-surgery through intrathecal administration, with the threshold rising again after day 12. Additionally, RS102895 effectively alters the expression levels of NR2B, nNOS, and SIGIRR in the spinal cord. |
分子量 | 390.4 |
分子式 | C21H21F3N2O2 |
CAS No. | 300815-41-2 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
DMSO: 15 mg/mL (38.42 mM)
You can also refer to dose conversion for different animals. 詳細
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RS102895 300815-41-2 Immunology/Inflammation Microbiology/Virology CCR CC chemokine receptor Inhibitor RS 102895 RS-102895 inhibit inhibitor