PC54419
|
(±)-WIN 55,212 (mesylate) |
137795-17-6 |
Application||Product Type|Biochemicals|Receptor Pharmacology|Agonists||Product Type|Biochemicals|Receptor Pharmacology|Antagonists||Research Area|Immunology & Inflammation|Inflammatory Lipid Mediators|Prostaglandins||Research Area|Neuroscience|Cannabinoid Research|CB1 & CB2 Receptors||Research Area|Neuroscience|Pain Research |
PC54417
|
1,2-Didocosahexaenoyl-sn-glycero-3-PC |
99296-81-8 |
Product Type|Biochemicals|Lipids|Glycerophospholipids||Research Area|Immunology & Inflammation|Innate Immunity||Research Area|Infectious Disease|Viral Diseases|HIV & AIDS||Research Area|Lipid Biochemistry|Glycerophospholipids||Research Area|Lipid-Based Drug Delivery|Neutral Phospholipids |
PC54420
|
5(Z),8(Z),11(Z)-Eicosatrienoic Acid-d6 |
2692624-12-5 |
Application|Mass Spectrometry||Product Type|Biochemicals|Analytical Standards||Product Type|Biochemicals|Isotopically Labeled Standards|Deuterium||Product Type|Biochemicals|Lipids|Fatty Acids||Research Area|Lipid Biochemistry|Fatty Acids |
PC54402
|
ABC294640 |
915385-81-8 |
Product Type|Biochemicals|Kinase Inhibitors|Other Lipid Kinases||Product Type|Biochemicals|Small Molecule Inhibitors|Kinases||Research Area|Cancer|Cell Migration & Metastasis||Research Area|Cancer|Cell Signaling||Research Area|Immunology & Inflammation|Gastric Disease|Crohn's Disease||Research Area|Lipid Biochemistry|Sphingolipids |
PC54416
|
AZD 1480 |
935666-88-9 |
AZD-1480 是一种 ATP 竞争型的 JAK1 和 JAK2 抑制剂,IC50 分别为 1.3 nM 和 0.4 nM。 |
PC54410
|
CAY10640 |
1208549-68-1 |
Product Type|Biochemicals|Small Molecule Inhibitors||Research Area|Immunology & Inflammation |
PC54414
|
CAY10641 |
1233706-89-2 |
Product Type|Biochemicals|Small Molecule Inhibitors|Phospholipases||Research Area|Immunology & Inflammation |
PC54421
|
CAY10650 |
1233706-88-1 |
CAY10650 是一种高效的胞浆磷脂酶A2α (cPLA2α) 抑制剂,IC50 值为 12 nM。CAY10650 抑制脂滴形成和 PGE2 分泌。 |
PC54423
|
CCG-100602 |
1207113-88-9 |
CCG-100602 是心肌蛋白相关转录因子 A/血清反应因子 (MRTF-A/SRF) 信号转导的特异性抑制剂。CCG-100602 特异性阻断 MRTF-A 核定位,从而抑制纤维生成转录因子 SRF。 |
PC54403
|
Cl-Amidine (hydrochloride) |
1373232-26-8 |
Cl-amidine hydrochloride 是口服有效的 PAD 抑制剂,其对 PAD1、PAD3 和 PAD4 的 IC50 值分别为0.8 μM、 6.2 μM 和 5.9 μM。Cl-amidine hydrochloride 可诱导癌细胞的凋亡。Cl-amidine hydrochloride 可诱导 miR-16 (miRNA-16, microRNA-16),引起细胞周期阻滞。Cl-Amidine hydrochloride 可阻断组蛋白 3 瓜氨酸化和中性粒细胞胞外陷阱的形成,并提高败血症小鼠的存活率。 |
PC54412
|
ent-Corey PG-Lactone Diol |
53110-06-8 |
Product Type|Biochemicals|Synthetic Intermediates & Building Blocks||Research Area|Lipid Biochemistry|Cyclooxygenase Pathway |
PC54408
|
FLLL32 |
1226895-15-3 |
FLLL32,一种姜黄素的合成类似物,是 JAK2/STAT3 的双重抑制剂,具有抗肿瘤癌活性。FLLL32 作用于乳腺癌细胞,可抑制 IFNα 和 IL-6 诱导的 STAT3 磷酸化。 |
PC54411
|
FSB |
760988-03-2 |
Application|Fluorescence||Application|Immunocytochemistry||Application|Immunofluorescence||Application|Immunohistochemistry||Product Type|Biochemicals|Labeling & Detection|Fluorescent Probes||Research Area|Neuroscience|Neurodegenerative Disorders|Alzheimer’s Disease |
PC54399
|
HAMI3379 |
1245653-57-9 |
HAMI 3379 是一种有效的选择性 CysLT2 受体拮抗剂。HAMI 3379 对急性和亚急性缺血性脑损伤具有保护作用,并减轻小胶质细胞相关炎症。 |
PC54415
|
I-BET762 |
1260907-17-2 |
Molibresib (I-BET762; GSK525762) 是 BET 溴结构域 抑制剂,IC50 为32.5-42.5 nM。 |
PC54405
|
IU1 |
314245-33-5 |
IU1 是一种特异性的 Usp14 抑制剂,IC50 为 4-5 μM。 |
PC54409
|
KM 233 |
628263-22-9 |
Product Type|Biochemicals|Receptor Pharmacology|Agonists||Research Area|Cancer||Research Area|Neuroscience|Cannabinoid Research|CB1 & CB2 Receptors |
PC54413
|
Onalespib |
912999-49-6 |
Onalespib (AT13387) 是一种长效的二代 Hsp90 抑制剂,Kd 值为 0.71 nM。 |
PC54422
|
Pifithrin-μ |
64984-31-2 |
Pifithrin-μ 是一种 p53 和 HSP70 的抑制剂,具有抗肿瘤和神经保护作用。 |
PC54406
|
PLX4032 |
918504-65-1 |
Vemurafenib (PLX4032; RG7204; RO5185426) 是首创的,有效的 B-RAF 选择性抑制剂,能够抑制 RAF<sup>V600E</sup> 和 c-RAF-1 的活性,IC50 分别为 31 nM 和 48 nM。Vemurafenib 可以诱导细胞自噬 (autophagy)。 |