400-0755-639
联系微信客服
最新产品
三叶新科每月上新,持续为科研人员提供新颖性研究工具,助力科研创新与突破。
首页 最新产品
3'-sulfo Galactosylsphingosine (ammonium salt)
目录号:SY-128417
3'-sulfo Galactosylsphingosine is a form of sulfatide that is lacking the fatty acyl group. It decreases migration and adhesion of B35 neuroblastoma cells and increases cell rounding when used at a concentration of 20 μM. It also inhibits PKC and cytochrome c oxidase activity when used at concentrations of 150 and 50-100 μM, respectively. 3'-sulfo Galactosylsphingosine accumulates in patients with metachromatic leukodystrophy, a lysosomal storage disorder characterized by arylsulfatase A (ASA) deficiency leading to progressive demyelination and neuromotor deficits. In mice lacking ASA, levels of 3'-sulfo galactosylsphingosine increase after one month of age followed by demyelination and neuromotor deficits. 3'-sulfo Galactosylsphingosine has been used as a standard for the quantification of 3'-sulfo galactosylsphingosine by LC-MS.
询价
查看详情
Ro 23-9358
目录号:SY-128418
Ro 23-9358 是一种具抗炎特性的强效分泌型磷脂酶 A2 抑制剂。
询价
查看详情
Pyrrophenone
目录号:SY-128419
The group IVA phospholipase A2 (PLA2), known as calcium-dependent cytosolic PLA2 (cPLA2), selectively releases arachidonic acid (AA) from membrane phospholipids, playing a central role in initiating the synthesis of prostaglandins (PGs) and leukotrienes (LTs). Pyrrophenone inhibits cPLA2α with an IC50 of 4.2 nM in enzyme assays and potently blocks the release of AA and the production of PGE2 and LTC4 in cells (IC50 = 24, 25, and 14 nM, respectively). Its action is reversible and selective, as pyrrophenone inhibits the secretory type IB and IIA PLA2s with more than a hundred-fold less potency. Pyrrophenone has also been shown to inhibit calcium ionophore (A23187)-stimulated AA release from monocytic cells, interleukin-1-induced PGE2 synthesis in mesangial cells, and the production of PGE2, LTs, and platelet-activating factor by human neutrophils, always with maximal inhibition at concentrations below 1 μM.
¥2760.00
查看详情
ASM-IN-1
目录号:SY-128420
ASM-IN-1是一种高效的口服活性ASM抑制剂,具有1.5 µM的IC50值。该化合物在减少主动脉弓及主动脉的脂质斑块方面表现出效果,并能够降低血浆中的神经酰胺以及Ox-LDL水平。ASM-IN-1展现了抗动脉粥样硬化与抗炎的活性。
¥2760.00
查看详情
SB-435495 ditartrate
目录号:SY-128421
SB-435495 ditartrate,一种口服有效的Lp-PLA2抑制剂,特点为高效、选择性、可逆且非共价,IC50值为0.06 nM。
询价
查看详情
Phospholipase D
目录号:SY-128422
PhospholipaseD (PLD) ,即磷脂酶 D,是磷脂酶超家族的一种酶,广泛存在于细菌、酵母、植物、动物和病毒中,常用于生化研究。PhospholipaseD 可以催化甘油磷脂的磷酸二酯键水解,产生磷脂酸和可溶性胆碱。PhospholipaseD 参与了多种疾病相关过程,包括糖尿病、动脉粥样硬化形成、肥胖、肿瘤发生、免疫反应和神经内分泌功能。
¥690.00
查看详情
SPK-601
目录号:SY-128423
SPK-601 is an inhibitor of phosphatidylcholine-specific phospholipase C.
¥2185.00
查看详情
MJ33-OH lithium
目录号:SY-128424
MJ33-OH lithium (carbonate 2,2',3,4,4',6-hexachlorobiphenyl) is a metabolite of MJ33.
询价
查看详情
Ochnaflavone
目录号:SY-128425
Ochnaflavone 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN5501,CAS号为 50276-96-5。
¥4750.00
查看详情