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- 文献和实验
- 技术资料
- 保存条件:
Powder: -20°C, 3 years; 4°C, 2 years.In solvent: -80°C, 6 months; -20°C, 1 month.
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货期:1-2天
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MedChemExpress LLC
- 规格:
10 mM * 1 mL/1 mg/5 mg/10 mg/25 mg/50 mg/100 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥1492.0 |
|---|---|---|---|
| 规格: | 1 mg | 产品价格: | ¥460.0 |
| 规格: | 5 mg | 产品价格: | ¥1356.0 |
| 规格: | 10 mg | 产品价格: | ¥1992.0 |
| 规格: | 25 mg | 产品价格: | ¥3252.0 |
| 规格: | 50 mg | 产品价格: | ¥4464.0 |
| 规格: | 100 mg | 产品价格: | ¥5988.0 |
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S 3304
CAS No. : 203640-27-1
MCE 国际站:S 3304
产品活性:S 3304 是一个新型的基质金属蛋白酶 (MMP) 抑制剂, 且对 MMP-2 和 MMP-9 有特异的抑制活性。S 3304 是一种点击化学试剂。它含有 Alkyne 基团,可以和含有 Azide 基团的分子发生铜催化的叠氮-炔环加成反应 (CuAAc)。
研究领域:Metabolic Enzyme/Protease
作用靶点:MMP
In Vitro: S 3304 is a novel D-tryptophan derivative and a potent, orally active, noncytotoxic Matrix metalloproteinases inhibitor (MMPI). Biochemical studies show that S 3304 most potently inhibits the activities of MMP-2 and MMP-9 but does not inhibit MMP-1, MMP-3, or MMP-7 and may, therefore, lack the musculoskeletal side effects seen with nonspecific inhibitors.
In Vivo: In vivo pharmacologic studies have shown that the oral administration of S 3304, at a dose range of 20 to 200 mg/kg, inhibits angiogenesis, artificially induced in mice by the dorsal air-sac method. Similar oral doses of S 3304 result in potent inhibition of metastatic lung colonization of Lewis murine lung carcinoma injected via tail vein and liver metastasis of C-1H human colon cancer implanted into the spleen.
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文献和实验S-腺苷甲硫氨酸 S- adenosylmethionine 亦称活性甲硫氨酸,在生物体内由 ATP与甲硫氨酸在甲硫氨酸活化酶的作用下合成。甲硫键是高能键,另外其丙基胺部分也加入到多胺化合物中。当胆碱、肌酸及其它甲基化合物生成时它作为甲基供体而起作用。认为甲硫氨酸的分解也经过此物质。
Summary: Illumina's Solexa Sequencing Technology
Here I present a brief overview of Solexa's sequencing-by-synthesis chemistry. The sample prep methods used differ slightly from that used in ABI's SOLiD system, but the basic goals are the same: generate large numbers of unique "polonies
鹅〔脱氧〕胆酸 s chenodeoxycholic acid
C 24 H 40 O 4 。 3 α, 7 α - 二羟基 -5 β - 胆烷酸。胆汁酸的一种。在哺乳类、鸟类、鱼类等的胆液中含有和甘氨酸或牛磺酸结合形成的甘氨鹅(脱氧)胆酸或牛磺鹅(脱氧)胆酸。
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