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Cat. No. | Product Name | Target | Signaling Pathways |
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T61249 |
α-Glucosidase-IN-2
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α-Glucosidase-IN-2 (compound 5d) 是一种有效的α-Glucosidase 抑制剂,IC50of 9.48 μM。α-Glucosidase-IN-2 是一种抗糖尿病药物。 | |||
T61706 |
α-Amylase/α-Glucosidase-IN-2
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α-Amylase/α-Glucosidase-IN-2 (compound 5) exhibits strong inhibition activity towards both α-amylase and α-glucosidase enzymes, with IC 50 values of 13.02 μM and 13.09 μM, respectively. This compound shows promise for investigating diabetic complications [1]. | |||
T67898 |
α-Glucosidase-IN-22
|
Glucosidase | Metabolism |
α-Glucosidase-IN-22是一种α-葡萄糖苷酶选择性抑制剂(IC50=0.64 μM)。α-Glucosidase-IN-22有抗糖尿病的活性,在2型糖尿病(T2DM)研究中具有潜力。 | |||
T78864 |
α-Glucosidase-IN-33
|
Glucosidase | Metabolism |
α-Glucosidase-IN-33 (compound 7c) 是一种有效的α-葡萄糖苷酶抑制剂,IC50值为2.39 μM,主要用于2型糖尿病及高血糖研究。 | |||
T78865 |
α-Glucosidase-IN-34
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Glucosidase | Metabolism |
α-Glucosidase-IN-34 (compound 7f) 作为一种有效的α-葡萄糖苷酶抑制剂,具有2.90 μM的IC50值,主要用于2型糖尿病和高血糖的研究。 | |||
T79237 |
α-Glucosidase-IN-27
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Glucosidase | Metabolism |
α-Glucosidase-IN-27(化合物8l)是一种有效的α-glucosidase抑制剂,其IC50值为25.78 μM。该化合物有望用于研究2型糖尿病(D2M)。 | |||
T78731 |
α-Glucosidase-IN-26
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Glucosidase | Metabolism |
α-Glucosidase-IN-26(化合物 7i)是一种有效的α-glucosidase抑制剂,其半抑制浓度(IC50)为4.63 µM,适用于2型糖尿病(T2DM)的研究。 | |||
T79318 |
α-Glucosidase-IN-30
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Glucosidase | Metabolism |
α-Glucosidase-IN-30 (compound 8c) 是竞争性的α-glucosidase抑制剂,口服活性强,Ki值为40.0 µM,IC50值为49.0 µM。该化合物对MCF-7和HDF细胞系无细胞毒性,适合用于2型糖尿病研究。 | |||
T78881 |
α-Glucosidase-IN-36
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Glucosidase | Metabolism |
α-Glucosidase-IN-36(compound 5g)作为一种α-glucosidase抑制剂,表现出有效的抑制活性,其IC50值为6.69 ± 0.18 μM,Ki值为1.65 μM,Kis值为4.54 μM。该化合物通过与α-glucosidase的活性位点结合及可能改变其二级结构来执行其抑制功能。α-Glucosidase-IN-36在2型糖尿病(T2DM)的研究中有应用潜力。 | |||
T37843 |
Australine (hydrochloride)
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Australine is a pyrrolizidine alkaloid originally isolated fromC. australethat has enzyme inhibitory activities.1,2,3It is an inhibitor of glucoamylase (IC50= 5.8 μM) that also inhibits glucosidase I, sucrase, maltase, andA. nigerα-glucosidase (IC50s = 20, 28, 35, and 28 μM, respectively).2,3Australine is selective for these enzymes over glucosidase II, α- and β-mannosidase, and α- and β-galactosidase up to 500 μM, β-glucosidase, with only 5% inhibition at 66 μM, as well as isomaltase and trehal... |
Cat. No. | Product Name | Target | Signaling Pathways |
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TN1488 |
Chrysin 6-C-glucoside 8-C-arabinoside
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Others | Others |
Chrysin 6-C-glucoside 8-C-arabinoside 是α±-葡萄糖苷酶抑制剂,α±-葡萄糖苷酶抑制剂广泛用于2型糖尿病的治疗。 | |||
TN1487 |
Chrysin 6-C-arabinoside 8-C-glucoside
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Others | Others |
Chrysin 6-C-arabinoside 8-C-glucoside 是α±-葡萄糖苷酶抑制剂,α±-葡萄糖苷酶抑制剂广泛用于2型糖尿病的治疗。 | |||
T6S1371 |
Isovitexin
Homovitexin,Saponaretin,Apigenin-6-C-Glucoside,异牡荆黄素 |
NF-κB; JNK; Glucosidase | MAPK; Metabolism; NF-κB |
Isovitexin (Apigenin-6-C-Glucoside) 是从亚洲水稻种得到的一种黄酮,具有抗氧化和抗炎活性。它的作用与JNK1/2的抑制剂类似,抑制NF-κB 的活化。 | |||
T5690 |
7,4'-Di-O-methylapigenin
芹菜素二甲醚,4',7-DIMETHOXY-5-HYDROXYFLAVONE |
Amylase | Metabolism |
7,4'-Di-O-methylapigenin (4',7-DIMETHOXY-5-HYDROXYFLAVONE) 可能具有抗真菌c.zeyheri 的作用,是一种潜在的抗真菌药物。它还能抑制药物流出泵(IC50 = 51.64μg /毫升)。 | |||
TN3500 |
beta-Amyrone
β-Amyron,β-香树脂酮 |
COX; AChR; PPAR; Antifection | DNA Damage/DNA Repair; Immunology/Inflammation; Metabolism; Microbiology/Virology; Neuroscience |
beta-Amyrone (β-Amyron) 对基孔肯雅病毒复制具有抗真菌活性,EC50 为 86 uM。 beta-Amyrone 通过抑制 COX-2 的表达而具有抗炎活性。 beta-Amyrone 表现出抗α-葡萄糖苷酶抑制活性和中等 AChE 活性。 β-Amyrone 可用于炎症、感染和肥胖等疾病的研究。 | |||
T3851 |
Vicenin 2
Vicenin -2,维采宁 2,新西兰牡荆苷 |
RAAS | Endocrinology/Hormones |
Vicenin 2 来源于广金钱草 (Desmodium styracifolium) 的地上部分。Vicenin 2 是一种血管紧张素转换酶 (ACE) 抑制剂,IC50=43.83 μM。 | |||
TN4279 |
Isoderrone
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Tyrosinase | Proteases/Proteasome |
Isoderrone 在体外对α-葡萄糖苷酶(α-glucosidase)有抑制作用;它是一种蛋白酪氨酸磷酸酶1B(PTP1B)抑制剂,IC50值为22.7±1.7μM,表明它可能是一种治疗2型糖尿病的新药。 | |||
T75477 | Epicoccone B | ||
Epicoccone B 首次报道于C.globosum,具有清除 DPPH 自由基的能力,IC50值为10.8 μM,并具有有效的 α-葡萄糖苷酶抑制作用,IC50值为 27.3 μM。具有抗HIV 活性。 | |||
T38330 |
Collinin
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Collinin is a coumarin that has been found in Z. schinifolium and has diverse biological activities.1,2,3,4 It is active against drug-susceptible and -resistant strains of M. tuberculosis (MIC50s = 3.13-6.25 μg/ml).1 Collinin inhibits LPS-induced nitric oxide (NO) production (IC50 = 5.9 μM) and reduces COX-2 protein levels in RAW 264.7 cells.2 It completely inhibits aggregation of isolated rabbit platelets induced by arachidonic acid , collagen, or platelet activating factor (PAF) when used at a... |