1. Immunology/Inflammation
  2. FLAP
  3. AM-643

AM-643 是一种 FLAP 抑制剂,对人源的 IC50 为 2 nM,具备口服活性与皮肤活性。AM-643 可选择性抑制 FLAP,减少白三烯的生物合成,并减轻炎症性耳肿胀。AM-643 可用于研究涉及白三烯生成的皮肤疾病。

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AM-643

AM-643 Chemical Structure

CAS No. : 1233114-22-1

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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

AM-643 is a FLAP inhibitor with human IC50 of 2 nM, oral activity, and dermal activity.AM-643 selectively inhibits FLAP, reduces leukotriene biosynthesis and reduces inflammatory ear swelling.AM-643 can be used for the research of skin disorders involving leukotriene production[1].

体外研究
(In Vitro)

AM-643 (compound 6) 可强效抑制 3H-配体与人多形核白细胞来源的 FLAP 膜的结合,其 IC50 为 2 nM[1]
AM-643 可强效抑制钙离子载体诱导的分离人白细胞中 LTB4 的合成,其 IC50 为 0.6 nM[1]
AM-643 (孵育 15 分钟-5 小时) 可抑制钙离子载体诱导的人全血中 LTB4 合成,预孵育 15 分钟后的 IC50 为 161 nM,预孵育 5 小时后的 IC50 为 81 nM[1]
AM-643 可抑制人源 CYP 3A4,其 IC50 为 8.8 μM;可抑制人源 CYP 2C9,其 IC50 为 4.5 μM;且在浓度高达 30 μM 时不会抑制人源 CYP 2D6[1]

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

体内研究
(In Vivo)

AM-643 (compound 6) (30 mg/kg;口服;单次给药) 可对花生四烯酸诱导的小鼠耳水肿产生 65% 的抑制作用,并使小鼠耳组织中 CysLT 浓度降低 57%[1]
AM-643 (0.01, 0.1%;局部给药;单剂量) 可在小鼠耳部组织体内实验中以浓度依赖的方式,抑制花生四烯酸诱导的耳水肿达 61%,使 CysLT 浓度降低 37%,并使 LTB4 浓度降低 55%[1]
AM-643 (10 mg/mL;经皮给药;单剂量;封闭 24 小时) 对皮肤无刺激性,且在皮肤破损的健康雄性大鼠体内可检测到全身性暴露[1]

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

624.80

Formula

C36H40N4O4S

CAS 号
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

纯度 & 产品资料
参考文献
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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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