购物车0
产品总数：61047
| 货号 | 产品名 | Cas | 产品描述 |
|---|---|---|---|
| PC54583 | (-)-WIN 55,212-3 (mesylate) | 131543-25-4 | Product Type|Biochemicals|Receptor Pharmacology|Antagonists||Research Area|Neuroscience|Cannabinoid Research|CB1 & CB2 Receptors |
| PC54591 | 1,24-dihydroxy Vitamin D3 (hydrate) | 93129-94-3 | Product Type|Biochemicals|Receptor Pharmacology|Agonists||Research Area|Immunology & Inflammation|Adaptive Immunity||Research Area|Immunology & Inflammation|Autoimmunity |
| PC54564 | 19(R)-hydroxy Prostaglandin B2 | 211185-40-9 | Application|Mass Spectrometry||Product Type|Biochemicals|Analytical Standards||Product Type|Biochemicals|Lipids|Prostaglandins||Research Area|Lipid Biochemistry|Cyclooxygenase Pathway |
| PC54558 | 2-HBA | 131359-24-5 | 2-HBA 是一个有效的 NAD(P)H: 醌受体氧化还原酶 1 (NQO1) 诱导剂，也可以激活半胱天冬酶-3 (caspase-3) 和半胱天冬酶-10 (caspase-10)。 |
| PC54595 | 5-trans Prostaglandin D2 | 2202725-84-4 | Application|Mass Spectrometry||Product Type|Biochemicals|Analytical Standards||Product Type|Biochemicals|Lipids|Prostaglandins||Product Type|Biochemicals|Pharmaceutical Impurities||Research Area|Lipid Biochemistry|Cyclooxygenase Pathway |
| PC54585 | Acetildenafil | 831217-01-7 | Product Type|Biochemicals||Research Area |
| PC54562 | Atpenin A5 | 119509-24-9 | Atpenin A5 是一种有效且高度特异性的 complex II 抑制剂，IC50 为 ~10 nM，且是一种有效的 mKATP 通道激动剂和心脏保护剂。 |
| PC54584 | Bosutinib | 380843-75-4 | Bosutinib是一种口服Src/Abl酪氨酸激酶抑制剂，IC50分别为1.2 nM和1 nM。 |
| PC54559 | CDDO methyl ester | 218600-53-4 | Bardoxolone methyl (NSC 713200; RTA 402; CDDO Methyl ester) 是一种合成的三萜类化合物，具有潜在的抗肿瘤和抗炎活性，作为 Nrf2 通路的激活剂和 NF-κB 途径的抑制剂。 |
| PC54575 | CGP 36216 (hydrochloride) | 1781834-71-6 | Product Type|Biochemicals|Receptor Pharmacology|Antagonists||Research Area|Neuroscience |
| PC54570 | cis-2-Decenoic Acid | 15790-91-7 | Product Type|Biochemicals|Lipids|Fatty Acids||Research Area|Immunology & Inflammation||Research Area|Infectious Disease|Bacterial Diseases||Research Area|Infectious Disease|Fungal Diseases|Candidiasis||Research Area|Lipid Biochemistry|Fatty Acids |
| PC54568 | CP 945,598 (hydrochloride) | 686347-12-6 | Product Type|Biochemicals|Receptor Pharmacology|Antagonists||Research Area|Endocrinology & Metabolism||Research Area|Neuroscience|Cannabinoid Research|CB1 & CB2 Receptors |
| PC54592 | CPTH2 (hydrochloride) | 2108899-91-6 | Product Type|Biochemicals|Small Molecule Inhibitors|Acetyltransferases||Research Area|Epigenetics, Transcription, & Translation|Writers|Histone Acetylation |
| PC54593 | Cyclosporin A | 59865-13-3 | Cyclosporin A (Cyclosporine A) 是一种免疫抑制剂，能与亲环素结合，抑制 calcineurin 活性的IC50 值为 7 nM。Cyclosporin A 也抑制 CD11a/CD18 粘附分子。 |
| PC54572 | Fingolimod | 162359-55-9 | Fingolimod (FTY720 free base) 是一种 1-磷酸鞘氨醇 (sphingosine 1-phosphate，S1P) 拮抗剂，作用于 K562 和 NK 细胞，IC50 为 0.033 nM。Fingolimod 还是一种 pak1 激活剂，免疫抑制剂。 |
| PC54586 | GSK-J1 (sodium salt) | 1797832-71-3 | Product Type|Biochemicals|Small Molecule Inhibitors|Demethylases||Research Area|Epigenetics, Transcription, & Translation|Erasers|Histone Demethylation||Research Area|Immunology & Inflammation|Innate Immunity |
| PC54587 | GSK-J2 (sodium salt) | 2108665-15-0 | Product Type|Biochemicals|Small Molecule Inhibitors|Demethylases||Product Type|Biochemicals|Small Molecule Inhibitors|Negative Controls||Research Area|Epigenetics, Transcription, & Translation|Erasers|Histone Demethylation||Research Area|Immunology & Inflammation|Innate Immunity |
| PC54589 | GSK-J4 (hydrochloride) | 1797983-09-5 | GSK-J4 hydrochloride 是一种有效的 H3K27me3/me2 去甲基化酶 JMJD3/KDM6B 和 UTX/KDM6A 双抑制剂，IC50 分别为 8.6 μM 和 6.6 μM。GSK-J4 hydrochloride 抑制 LPS 诱导的人原代巨噬细胞产生 TNF-α，IC50 值为 9 μM。GSK-J4 hydrochloride 是 GSK-J1 的细胞通透性前药。 |
| PC54590 | GSK-J5 (hydrochloride) | 1797983-32-4 | Product Type|Biochemicals|Small Molecule Inhibitors|Demethylases||Product Type|Biochemicals|Small Molecule Inhibitors|Negative Controls||Research Area|Epigenetics, Transcription, & Translation|Erasers|Histone Demethylation||Research Area|Immunology & Inflammation|Innate Immunity |
| PC54563 | Hymeglusin | 29066-42-0 | Hymeglusin 作为一种真菌 β-内酯 antibiotic，是一种 HMG-CoA 合酶抑制剂 (IC50 = 0.12 μM)。 Hymeglusin 共价修饰酶的活性 Cys<sup>129</sup> 残基。 |
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