Powder: -20°C for 3 years | In solvent: -80°C for 1 year
AZD-5672 is an antagonist of CCR5 with an IC50 of 0.32 nM. AZD-5672 inhibits hERG cardiac ion channel binding and P-gp-mediated digoxin transport with IC50s of 7.3 μM and 32 μM. AZD-5672 can be used in studies about rheumatoid arthritis.
パッケージサイズ | 在庫状況 | 単価(税別) |
---|---|---|
1 mg | 在庫あり | ¥ 49,000 |
2 mg | 在庫あり | ¥ 73,000 |
5 mg | 在庫あり | ¥ 123,500 |
10 mg | 在庫あり | ¥ 178,500 |
25 mg | 在庫あり | ¥ 271,000 |
50 mg | 在庫あり | ¥ 372,000 |
100 mg | 在庫あり | ¥ 500,500 |
1 mL * 10 mM (in DMSO) | 在庫あり | ¥ 136,000 |
説明 | AZD-5672 is an antagonist of CCR5 with an IC50 of 0.32 nM. AZD-5672 inhibits hERG cardiac ion channel binding and P-gp-mediated digoxin transport with IC50s of 7.3 μM and 32 μM. AZD-5672 can be used in studies about rheumatoid arthritis. |
ターゲット&IC50 | CCR5:0.32 nM (IC50), ERG (human):7.3 μM (IC50), P-gp (human):32 μM (IC50) |
別名 | AZD 5672, AZD5672, UNII-61XQN688TW |
分子量 | 632.78 |
分子式 | C32H38F2N2O5S2 |
CAS No. | 780750-65-4 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
DMSO: 30 mg/mL (47.4 mM), Sonication and heating to 60℃ are recommended.
You can also refer to dose conversion for different animals. 詳細
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Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc.
AZD-5672 780750-65-4 Angiogenesis Immunology/Inflammation JAK/STAT signaling Membrane transporter/Ion channel Microbiology/Virology Neuroscience Tyrosine Kinase/Adaptors HER P-gp CCR AZD 5672 AZD5672 UNII-61XQN688TW Inhibitor inhibitor inhibit