欢迎访问上海芮晖化工科技有限公司官方网站！
咨询电话: 021-31433387|邮箱: sales@rechemscience.com
产品分类
联系我们
| 电话： | 021-31433387 |
| 15618786686(微信) | |
| Email: | sales@rechemscience.com |
| info@rechemscience.com | |
| QQ: | 1369748377 |
| Skype: | rechem@outlook.com |
首页 > 产品展示
| 目录号 | 产品名称 | 产品描述 |
| R10802 | Nutlin-3 | MDM2 antagonist nutlin-3 is a potent inducer of apoptosis. |
| R10803 | PX478 dihydrochloride | PX-478 是有抗癌活性的缺氧诱导因子-1α (HIF-1α) 抑制剂，对一些癌细胞系 IC50 为 20-30 μM。 |
| R10805 | Elacridar HCl | Elacridar hydrochloride is a P-glycoprotein inhibitor, and has been used both in |
| R10808 | PTZ-343; phenothiazine sodium salt | PTZ-343 is a phenothiazine derivative with chemical name: sodium 3-(10H-phenothi |
| R10809 | Golotimod; SCV 07 | Golotimod is an orally bioavailable synthetic peptide containing the amino acids |
| R10810 | Uramustine | Uramustine is a chemotherapy drug which belongs to the class of alkylating agent |
| R10813 | ARRY-520 | KSP inhibitor ARRY-520 specifically inhibits KSP (kinesin-5 or Eg5) with potenti |
| R10814 | Muscimol HBr | Muscimol hydrobromide is a potent but toxic structural analog of g-aminobutyric |
| R10815 | Oprozomib (ONX 0912; PR047) | Oprozomib (ONX 0912; PR047)是口服生物相容性的抑制剂，能抑制20S proteasome（20S蛋白酶体）β5/LMP7的CT-L活性 |
| R10816 | Tretazicar (CB 1954) | Tretazicar (CB 1954) 是一种抗肿瘤前药，对 Walker 256 大鼠肿瘤细胞系具有很高的效力和选择性。Tretazicar 酶促活化后生成 |
| R10817 | Pelitrexol | Pelitrexol (AG 2037) 是甘氨酰胺核糖核苷酸甲酰转移酶 ((GARFT)) 的抑制剂。 |
| R10818 | Varlitinib; ARRY 543 | Varlitinib is a selective and potent ErbB1(EGFR) and ErbB2(HER2) inhibitor with |
| R10820 | RO08-2750 | Ro 08-2750 是一种非肽、可逆的 NGF 抑制剂，能直接结合 NGF，IC50 值为 ~ 1 µM。Ro 08-2750 |
| R10821 | (1R,2R)-2-fluorocyclopropanecarboxylic acid | |
| R10822 | PTZ-343 | PTZ-343 is a phenothiazine derivative with chemical name: sodium 3-(10H-phenothi |
| R10823 | BOC-4-HYDROXY-L-PYRROLIDINE LACTONE | |
| R10825 | Gemcitabine elaidate(CP-4126; CO-101) | Gemcitabine elaidate(CP-4126; CO-101)是吉西他滨和饱和脂肪酸结合的衍生物，具有亲脂性和强抗癌活性。 |
| R10827 | RG7112 (Synonyms: RO5045337) | RG7112 是有效的、选择性的、第一个用于临床的、可口服的、可透过血脑屏障的、 MDM2-p53 抑制剂，IC50 值为 18 nM，结合到MDM2 的KD |
| R10828 | HO-3867 | HO-3867, an analog of curcumin, is a selective STAT3 inhibitor. |
| R10829 | SCH772984 | SCH772984 是一种高选择性和 ATP 竞争性 ERK 抑制剂，对 ERK1 和 ERK2 的 IC50 分别为 |
| R10830 | Tenofovir disoproxil fumarate | Tenofovir Disoproxil Fumarate belongs to a class of antiretroviral drugs, it inh |
| R10831 | Dasatinib monohydrate | Dasatinib Monohydrate is a novel, potent and multi-targeted inhibitor that targe |
| R10833 | Lesinurad;RDEA594 | Lesinurad 是一种 URAT1 和 OAT 抑制剂，用作肾转运蛋白OAT1 和OAT3 的底物，Km值分别为 0.85 和 2 μM。 |
| R10834 | Vinpocetine | Vinpocetine is a selective inhibitor of voltage-sensitive sodium channel for the |
| R10835 | Birabresib (Synonyms: OTX-015; MK-8628) | Birabresib (OTX-015) 是一种有效的 BRD2/3/4 抑制剂，IC50 值为 92-112 nM。 |
