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度洛西汀杂质

度洛西汀杂质 相关产品(40)
货号 产品名 Cas 产品描述
PC54626 13,14-dihydro-15-keto-tetranor Prostaglandin D2 1204116-69-7 Product Type|Biochemicals|Lipids|Prostaglandins||Research Area|Lipid Biochemistry|Cyclooxygenase Pathway
PC54627 13,14-dihydro-15-keto-tetranor Prostaglandin E2 20675-85-8 Product Type|Biochemicals|Lipids|Prostaglandins||Research Area|Lipid Biochemistry|Cyclooxygenase Pathway
PC54621 16(R)-Iloprost 74843-13-3 Product Type|Biochemicals|Receptor Pharmacology|Agonists||Research Area|Cardiovascular System|Blood|Coagulation & Hemostasis||Research Area|Lipid Biochemistry|Cyclooxygenase Pathway
PC54622 16(S)-Iloprost 74843-14-4 Product Type|Biochemicals|Receptor Pharmacology|Agonists||Research Area|Cardiovascular System|Blood|Coagulation & Hemostasis||Research Area|Lipid Biochemistry|Cyclooxygenase Pathway
PC54618 17(R)-Resolvin D1 528583-91-7 Product Type|Biochemicals|Lipids|Docosanoids||Research Area|Immunology & Inflammation|Inflammatory Lipid Mediators|Specialized Pro-Resolving Mediators||Research Area|Immunology & Inflammation|Innate Immunity||Research Area|Lipid Biochemistry|Fatty Acids||Research Area|Lipid Biochemistry|Lipoxygenase Pathways
PC54617 1a,1b-dihomo Prostaglandin E1 23452-98-4 Product Type|Biochemicals|Lipids|Prostaglandins||Research Area|Cardiovascular System||Research Area|Lipid Biochemistry|Cyclooxygenase Pathway
PC54610 2-Methoxyestradiol 362-07-2 2-Methoxyestradiol (2-ME2),具有口服活性的 17β-雌二醇 (E2) 的内源性代谢产物,是凋亡 (apoptosis) 诱导剂和血管生成 (angiogenesis) 抑制剂,具有有效的抗肿瘤活性。2-Methoxyestradiol 也可破坏微管 (microtubules) 的稳定。2-Methoxyestradiol 是一种有效的超氧化物歧化酶 (SOD) 抑制剂和活性氧生成剂,可诱导转化细胞系 HEK293、癌细胞系 U87 和 HeLa 的自噬 (autophagy)。
PC54615 Alkynyl-biotin 1011268-28-2 Application|Click Chemistry||Product Type|Biochemicals|Labeling & Detection|Reactive Probes||Research Area
PC54616 Biotin-azide 908007-17-0 Biotin-azide (N-(3-Azidopropyl)biotinamide) 是具有末端叠氮基团的生物素的一种形式。Biotin-azide 用于通过 Click Chemistry 制备各种生物素化的缀合物。
PC54625 MPI-0441138 827030-33-1 Product Type|Biochemicals||Research Area|Cancer|Cell Death|Apoptosis
PC54611 N-3-oxo-butyryl-L-Homoserine lactone 148433-27-6 Product Type|Biochemicals|Homoserine Lactones||Research Area|Immunology & Inflammation||Research Area|Infectious Disease|Quorum Sensing||Research Area|Plant Biology
PC54612 N-3-oxo-decanoyl-L-Homoserine lactone 147795-40-2 Product Type|Biochemicals|Homoserine Lactones||Research Area|Immunology & Inflammation||Research Area|Infectious Disease|Bacterial Diseases||Research Area|Infectious Disease|Quorum Sensing
PC54619 N-3-oxo-hexadecanoyl-L-Homoserine lactone 925448-37-9 Product Type|Biochemicals|Homoserine Lactones||Research Area|Immunology & Inflammation||Research Area|Infectious Disease|Bacterial Diseases||Research Area|Infectious Disease|Quorum Sensing||Research Area|Plant Biology
PC54614 PD 0325901 391210-10-9 Mirdametinib (PD0325901) 是一种具有口服活性,选择性和非 ATP 竞争性的 MEK 抑制剂,IC50 为 0.33 nM。Mirdametinib 对活化的 MEK1 和 MEK2 的 Ki<sup>app</sup> 值为 1 nM。Mirdametinib 抑制 p-ERK1/2 的表达并诱导细胞凋亡 (apoptosis)。Mirdametinib 对多种人类肿瘤异种移植物具有抗癌活性。
PC54609 Prostaglandin E1 Alcohol 21562-57-2 Product Type|Biochemicals|Lipids|Prostaglandins||Product Type|Biochemicals|Receptor Pharmacology||Research Area|Immunology & Inflammation|Allergy||Research Area|Immunology & Inflammation|Inflammatory Lipid Mediators|Prostaglandins||Research Area|Immunology & Inflammation|Pulmonary Diseases|Asthma||Research Area|Lipid Biochemistry|Cyclooxygenase Pathway
PC54620 SB 203580 152121-47-6 Adezmapimod (SB 203580) 是一种选择性的,ATP 竞争性的 p38 MAPK 抑制剂,对 SAPK2a/p38 和 SAPK2b/p38β2 的 IC50 分别为 50 nM 和 500 nM。Adezmapimod 抑制 LCK,GSK3β 和 PKBα,IC50 比 SAPK2a/p38 高 100-500 倍。Adezmapimod 不抑制 JNK 活性,是一种自噬 (autophagy) 和线粒体自噬 (mitophagy) 激活剂。
PC54628 Skyrin 602-06-2 Product Type|Biochemicals|Natural Products|Anthraquinones||Product Type|Biochemicals|Natural Products|Microbial Metabolites||Research Area|Cell Biology|Cell Signaling|cAMP Signaling||Research Area|Endocrinology & Metabolism|Carbohydrate Metabolism
PC54623 Tenovin-1 380315-80-0 Tenovin-1 是 sirtuin 1 和 sirtuin 2 的抑制剂,同时可激活 p53,具有潜在的癌症研究的潜力。
PC54624 Tenovin-6 (hydrochloride) 1011301-29-3 Tenovin-6 Hydrochloride 是 Tenovin-1 (HY-13423) 的类似物,是一种 p53 转录活性的激活剂。Tenovin-6 Hydrochloride 抑制纯化人 SIRT1、SIRT2 和 SIRT3 蛋白脱乙酰酶活性,IC50 分别为 21 μM、10 μM 和 67 μM。Tenovin-6 Hydrochloride 也能抑制二氢乳清酸脱氢酶 (DHODH)。
PC54613 Valproic Acid (sodium salt) 1069-66-5 Valproic acid (Sodium Valproate) sodium 是一种具有口服活性的 HDAC 抑制剂,IC50 值为 0.5-2 mM,抑制 HDAC1 的活性,(IC50,400 μM),同时可诱导 HDAC2 的降解。Valproic acid sodium 激活 Notch1 信号并抑制小细胞肺癌 (SCLC) 细胞的增殖。Valproic acid sodium 可用于癫痫、双相情感障碍、代谢疾病、HIV 感染和偏头痛等的研究。