Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T4280 |
Gcase activator 1
LTI-291,LTI 291,LTI291 |
Glucosidase | Metabolism |
Gcase activator 1 (LTI-291) 是葡糖脑苷脂酶 (Gcase) 的激活剂。 | |||
T78573 |
Glucocerebrosidase
GCase,Glucosylceramidase |
Endogenous Metabolite | Metabolism |
Glucocerebrosidase (Glucosylceramidase; GBA) 是溶酶体内的酶,负责催化GC中的β-糖苷键裂解,从而生成葡萄糖和神经酰胺。 | |||
T82330 |
GCase modulator-1
|
Glucosidase | Metabolism |
GCase modulator-1(compound 9g),一种Quinazoline衍生物,作为GCase(Glucosidase)的调节剂,展现出AC50值为2.23 μM。 | |||
T8986 |
ML198
|
Glucokinase | Metabolism |
ML198 是葡萄糖脑苷脂酶激活剂(EC50:0.4 μM)。它不会抑制该酶的作用,且能促进其易位至溶酶体,可用于研究戈谢病。 | |||
T0920 |
Ambroxol
氨溴索,氨溴索碱,Ambroxolum,NA-872 |
P450; Autophagy | Autophagy; Metabolism |
Ambroxol (NA-872) 是前药溴己辛的活性代谢产物,是一种分泌溶解剂,具有强效祛痰作用,用于治疗与粘液或过多粘液相关的呼吸道疾病。它可诱导肺组织细胞自噬,有用于帕金森氏病和神经性戈谢病的研究潜力。它是一种葡糖脑苷脂酶伴侣,可增加葡糖脑苷脂酶的活性。 | |||
T6234 |
Ambroxol hydrochloride
Mucosolvan,Mucoangin,盐酸氨溴索,Ambroxol HCl |
Sodium Channel; Autophagy | Autophagy; Membrane transporter/Ion channel |
Ambroxol hydrochloride (Mucosolvan) 是前药溴己辛的活性代谢产物,是一种葡糖脑苷脂酶伴侣,可增加葡糖脑苷脂酶的活性。它可刺激粘液纤毛作用并清除呼吸道中的空气通道,具有强效祛痰作用。它可诱导肺细胞自噬,有用于帕金森氏病和神经性戈谢病的研究潜力。 | |||
T75407 | Endoglycoceramidase I (EGCase I) | ||
Endoglycoceramidase I (EGCase I)为糖苷酶,广泛应用于生化研究。该酶具有催化转糖基化反应的功能,能将GSL的糖组分高效转移至多种1-烷醇的伯羟基。 | |||
T75406 | Endoglycoceramidase II (EGCase II) | ||
Endoglycoceramidase II (EGCase II) 是一种能从糖鞘脂的神经酰胺部分释放完整聚糖的内切-β-葡萄糖苷酶。该酶专门催化多种糖鞘脂中寡糖与神经酰胺之间的 β-糖苷键的水解反应。 | |||
T8990 | ML266 | Glucokinase | Metabolism |
ML266 是葡萄糖脑苷脂酶 (GCase) 分子伴侣, IC50值为 2.5 µM。ML266与 GCase 结合并将其转运至溶酶体,恢复 GCase 酶的活性。ML266 不会抑制 GCase 的活性。ML266 具有研究戈谢病的潜力。 | |||
T8989 |
NCGC 607
NCGC607 |
Others | Others |
NCGC 607 是一种葡萄糖脑苷酶的非抑制性分子伴侣。 | |||
T39518 |
PFB-FDGlu
|
Others | Others |
PFB-FDGlu 是一种溶酶体葡糖脑苷脂酶(GCase)底物,具有细胞渗透特异性,裂解后产生荧光素。PFB-FDGlu 通常与流式细胞仪结合使用,以单个细胞为基础测量活细胞中 GCase 的活性。 | |||
TQ0300 |
Conduritol B epoxide
|
Glucosidase | Metabolism |
Conduritol B epoxide 是不可逆的,β-glucosidase 共价抑制剂。 | |||
T37571 |
4-Methylumbelliferyl-β-D-Glucopyranoside
MU-GLU,4-MUG,4-MU-GLU,4-MU-β-Gluc,4-甲基伞形酮酰-Β-D-吡喃葡糖酸苷 |
Others | Others |
4-Methylumbelliferyl-β-D-Glucopyranoside (4-MU-GLU) 是β-glucosidase 的荧光底物,可用于β-glucosidase 活性的测定,期间释放出高荧光的 4-methylumbelliferyl (4-MU),发射波长为 445-454 nm。4-MU 激发波长值与 pH 值有关,在 pH 值为 4.6、7.4 和 10.4 时分别为 330、370 和 385 nm。 | |||
T35626 |
AMP-Deoxynojirimycin
AMP-DNM |
Transferase; Glucosidase | Metabolism |
AMP-Deoxynojirimycin (AMP-DNM) 是一种有效的神经酰胺葡萄糖基转移酶和 GCase 2 抑制剂。AMP-Deoxynojirimycin 是一种有效的 GlcCer 生物合成抑制剂,可用于研究帕金森和糖尿病。 | |||
T19181 |
Afegostat
D-Isofagomine,Isofagomine |
Others | Others |
Afegostat is a pharmacological chaperone that specifically and reversibly binds acid-β-glucosidase (GCase) in the endoplasmic reticulum with high affinity. | |||
T60353 |
Glucocerebrosidase-IN-1
|
||
Glucocerebrosidase-IN-1 (compound 11a) 是一种有效的选择性的GCase(葡糖脑苷脂酶)抑制剂,其IC50为 29.3 μM,Ki 为 18.5 μM。由于GCase 参与酶缺乏性病理疾病,Glucocerebrosidase-IN-1 可用于戈谢病 (GD) 和帕金森病 (PD) 的研究。 | |||
T71476 | Afegostat TFA | ||
Afegostat, aslo known as Isofagomine, and AT2101, was an experimental drug for the treatment of certain forms of Gaucher's disease. Isofagomine (IFG) is an acid β-glucosidase (GCase) active site inhibitor that acts as a pharmacological chaperone. FG inhibits GCase with K(i) ~30 nM for wild-type and mutant enzymes (N370S and V394L). Administration of IFG (30 mg/kg/day) to the mice homozygous for GCase mutations (V394L, D409H, or D409V) led to increased GCase activity in visceral tissues and brain... | |||
T23653 |
Afegostat HCl
Afegostat,AT-2101,Afegostat hydrochloride,AT2101 |
||
Afegostat is an acid β-glucosidase (GCase) active site inhibitor that acts as a pharmacological chaperone. Afegostat inhibits GCase with K(i) ~30 nM for wild-type and mutant enzymes. Afegostat was an experimental drug for the treatment of certain forms of | |||
T19182 |
Afegostat D-Tartrate
Isofagomine D-Tartrate,D-Isofagomine D-Tartrate |
Others | Others |
Afegostat D-Tartrate is a pharmacological chaperone that specifically and reversibly binds acid-β-glucosidase (GCase) in the endoplasmic reticulum with high affinity. | |||
T78671 |
Glucocerebrosidase-IN-1 hydrochloride
|
Glucosidase | Metabolism |
Glucocerebrosidase-IN-1 (compound 11a) hydrochloride,是一种针对GCase的高效选择性抑制剂,展现出了29.3 μM的IC50和18.5 μM的Ki。该化合物适用于戈谢病(GD)与帕金森病(PD)相关研究。 |