S 3304
CAS No. 203640-27-1
S 3304 ( —— )
产品货号. M23910 CAS No. 203640-27-1
S 3304 是一种新型基质金属蛋白酶抑制剂,对 MMP-2 和 MMP-9 具有特异性。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥1074 | 有现货 |
|
| 10MG | ¥1577 | 有现货 |
|
| 25MG | ¥2520 | 有现货 |
|
| 50MG | ¥3460 | 有现货 |
|
| 100MG | ¥4491 | 有现货 |
|
| 200MG | ¥6057 | 有现货 |
|
| 500MG | 获取报价 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
| 1 mL x 10 mM in DMSO | ¥1102 | 有现货 |
|
生物学信息
-
产品名称S 3304
-
注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
-
产品简述S 3304 是一种新型基质金属蛋白酶抑制剂,对 MMP-2 和 MMP-9 具有特异性。
-
产品描述S 3304 is a novel matrix metalloproteinases inhibitor which is specific for MMP-2 and MMP-9. (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.
-
体外实验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.
-
体内实验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.
-
同义词——
-
通路Metabolic Enzyme/Protease
-
靶点MMP
-
受体MMP-2|MMP-9
-
研究领域——
-
适应症——
化学信息
-
CAS Number203640-27-1
-
分子量464.56
-
分子式C24H20N2O4S2
-
纯度>98% (HPLC)
-
溶解度DMSO:83.3 mg/mL (179.31 mM)
-
SMILESCc(cc1)ccc1C#Cc(s1)ccc1S(N[C@H](Cc1c[nH]c2c1cccc2)C(O)=O)(=O)=O
-
化学全称——
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
稳定性≥ 2 years
参考文献
1.Chiappori AA, et al. A phase I pharmacokinetic and pharmacodynamic study of s-3304, a novel matrix metalloproteinase inhibitor, in patients with advanced and refractory solid tumors. Clin Cancer Res. 2007 Apr 1;13(7):2091-9.
产品手册
关联产品
-
MMP-9-IN-6
MMP-9-IN-6(Compound 3g)是一种 MMP-9 抑制剂,其 IC50 值为50 μM, 具有较好的抗溃疡功效。
-
Lucidenic acid C
Lucidenic acid C 是从灵芝中分离得到的天然产物,可抑制 PMA 诱导的 MMP-9 活性,对肝癌细胞具有抗侵袭作用。
-
Ilomastat
Ilomastat (GM6001, Galardin) 是一种广谱基质金属蛋白酶 (MMP) 抑制剂。
021-51111890
购物车()
sales@molnova.cn

