找到约 14 条 “b-AP15” 相关结果 (用时 0.166 秒)
目录号 | 产品名称 | 中文名称 | 靶点 |
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M2431
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b-AP15 | b-AP15 | Deubiquitinase |
NSC 687852 | |||
b-AP15是一种deubiquitinases(去泛素化酶)抑制剂,作用于19S蛋白酶体,抑制Ub-AMC分解, IC50为2.1 μM。*该产品在溶液状态不稳定,建议您现配现用 | |||
M13233 | ChemBridge-11557280 | ChemBridge化合物-11557280 | Screening Compounds and Building Blocks |
1-{[4-(2-chlorobenzyl)-4-(hydroxymethyl)-1-piperidinyl]methyl}-2-naphthol (11557280) | |||
ChemBridge特有类药化合物/先导化合物-11557280,由AbMole(奥默生物)独家提供。具体售价货期请咨询AbMole(奥默生物)。运费额外计算。 | |||
M28265 | Delavirdine | 地拉韦啶 | HIV Protease |
U 90152; BHAP-U 90152 | |||
Delavirdine (U 90152) 是一种有效的口服活性非核苷逆转录酶抑制剂 (NNRTI)。Delavirdine 选择性地抑制 HIV-1 逆转录酶 (HIV-1 RT) (IC50=0.26 μM),选择性超过 DNA 聚合酶 α (IC50=440 μM) 和 DNA 聚合酶 δ (IC50>550 μM)。Delavirdine 是HIV-1 病毒复制的抑制剂,可以用于艾滋病的相关研究。 | |||
M45544 | ChemBridge-5315275 | ChemBridge化合物-5315275 | Screening Compounds and Building Blocks |
1,4-phenylenebis[(4-methoxy-1-naphthyl)methanone] (5315275) | |||
ChemBridge特有类药化合物/先导化合物-5315275,由AbMole(奥默生物)独家提供。具体售价货期请咨询AbMole(奥默生物)。运费额外计算。 | |||
M45909 | ChemBridge-6433074 | ChemBridge化合物-6433074 | Screening Compounds and Building Blocks |
17-benzyl-1,8-dimethyl-17-azapentacyclo[6.6.5.0~2,7~.0~9,14~.0~15,19~]nonadeca-2,4,6,9,11,13-hexaene-16,18-dione (6433074) | |||
ChemBridge特有类药化合物/先导化合物-6433074,由AbMole(奥默生物)独家提供。具体售价货期请咨询AbMole(奥默生物)。运费额外计算。 | |||
M50076 | ChemBridge-83321511 | ChemBridge化合物-83321511 | Screening Compounds and Building Blocks |
3-(1H-benzimidazol-2-yl)-N-[(3-methyl-5,6,7,8-tetrahydro-2,7-naphthyridin-4-yl)methyl]propanamide (83321511) | |||
ChemBridge特有类药化合物/先导化合物-83321511,由AbMole(奥默生物)独家提供。具体售价货期请咨询AbMole(奥默生物)。运费额外计算。 | |||
M13405
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RIPK3-IN-1 | RIPK3-IN-1 | RIPK |
RIPK3-IN-1 是一种RIPK3 II型DFG-out抑制剂,IC50为9.1 nM。RIPK3-IN-1抑制ABL、BRAF/V599E、MAP4K3和SRC的ic50值分别为0.37、0.15、0.012和0.075 μM。 | |||
M14658
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Barbadin | Barbadin | Apoptosis |
Barbadin 是一种选择性 β-arrestin/β2-adaptin 相互作用抑制剂,β-arrestin1和 β-arrestin2 的 IC50 值分别为 19.1 μM 和 15.6 μM。Barbadin 阻断激动剂促进 β2-adrenergic, Vasopressin V2 receptor (V2R) 和 angiotensin-II type-1 受体的内吞作用。 | |||
M20662 | Demecarium Bromide | Demecarium Bromide | Others |
BC-48 | |||
Demecarium Bromide (BC-48) is a potent cholinesterase inhibitor, with an apparent affinity (Kiapp) of 0.15 μM. | |||
M20719
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Raphin1 acetate | Raphin1 acetate | Phosphatase |
Raphin1 acetate is an orally bioavailable, selective inhibitor of the regulatory phosphatase PPP1R15B (R15B). Raphin1 acetate binds strongly to the R15B-PP1c holophosphatase with Kd of 0.033 μM. | |||
M21938
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BCI-215 | BCI-215 | Phosphatase |
BCI-215 是一种高效、肿瘤细胞选择性的双重特异性磷酸酶(DUSP-MKP)抑制剂。BCI-215可通过非氧化还原依赖的方式激活MAPK信号通路,诱导细胞外信号调节激酶(ERK)、p38和c-Jun N末端激酶(JNK)的快速和持续磷酸化。BCI-215在MDA-MB-231乳腺癌细胞中表现出抑制细胞迁移、诱导细胞凋亡的活性,但对正常细胞(肝细胞)无毒性。 | |||
M29483 | anti-TNBC agent-1 | anti-TNBC agent-1 | Apoptosis |
anti-TNBC agent-1 是一种有效的抗三阴性乳腺癌 (TNBC) 试剂。anti-TNBC agent-1 对不同的乳腺癌细胞表现出有效的活性,IC50 值范围为 0.20 μM 至 0.27 μM。anti-TNBC agent-1 通过线粒体途径诱导 SUM-159 细胞凋亡 (apoptosis) 并导致 SUM-159 细胞 G1 期阻滞。 | |||
M42434 | HIF-1α-IN-2 hydrochloride | HIF-1α-IN-2 hydrochloride | HIF |
HIF-1α-IN-2 hydrochloride 是一种有效的 HIF-1α 抑制剂,具有抗癌作用,在 MDA-MB-231 和 MiaPaCa-2 细胞 IC50 中分别为 28 nM 和 15 nM。 | |||
M58183
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Recombinant Mouse IL-15 (E. coli, N-His) | 重组小鼠IL-15 (E. coli, N-His) | Cytokines and Growth Factors |
interleukin 15 | |||
Interleukin-15 (IL-15) is a 14-15 kDa glycoprotein with immune regulatory functions in many diverse cell types. As a pleiotropic cytokine, IL-15 mediates the crosstalk between innate immunity and adaptive immunity whose principal role is to kill virally infected cells. IL-15 plays a crucial role in the development, differentiation, and survival of NK cells. |