15
4
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T24608 |
PDI-IN-P1
PDI inhibitor P1,PDIINP1,PDI-inhibitor-P1 |
||
PDI-IN-P1 is an inhibitor of protein disulfide isomerase. | |||
T8640 |
G6PDi-1
|
Dehydrogenase | Metabolism |
G6PDi-1 是一种有效的 G6PD 抑制剂。它消耗 NADPH 并减少炎性细胞因子的产生。 | |||
T25821 |
ML359
ML-359,ML 359 |
Others | Others |
ML359 是选择性可逆的蛋白质二硫键异构酶有效抑制剂(IC50:250 nM)。它对体内血栓形成具有抑制作用。 | |||
T6800 |
CCF642
AC1LYELL |
Others | Others |
CCF642 (AC1LYELL) 是蛋白质二硫键异构酶抑制剂(IC50:2.9 μM)。它在多发性骨髓瘤细胞中引起急性内质网应激,并伴随凋亡诱导的钙释放,表现出广泛的抗多发性骨髓瘤作用。 | |||
T30473 |
Bis-hema ipdi
|
||
Bis-hema ipdi is a bioactive chemical. | |||
T5453 |
3-Methyltoxoflavin
3-methyl toxoflavin |
Others | Others |
3-Methyltoxoflavin (3-methyl toxoflavin) 是蛋白质二硫键异构酶抑制剂(IC50:170 nM)。 | |||
T5534 |
LOC14
|
Others | Others |
LOC14 是一种蛋白质二硫键异构酶抑制剂 (EC50=500 nM;Kd=62 nM)。它抑制 PDIA3 活性,降低肺上皮细胞中 HA 的分子内二硫键和随后的寡聚化。它在小鼠肝微粒体和血浆中表现出高稳定性,低内在微粒体清除率和低血浆蛋白结合。 | |||
T11141 |
E64FC26
|
Others | Others |
E64FC26 是一种有效的蛋白质二硫键异构酶 (PDI) 家族泛抑制剂,具有抗肿瘤活性,抑制 PDIA1、PDIA3、PDIA4、TXNDC5 和 PDIA6,可用于研究多发性骨髓瘤和胰腺癌。 | |||
T41277 |
PACMA 31
|
Others | Others |
PACMA 31 是一种不可逆的共价蛋白二硫键异构酶 (PDI) 抑制剂,IC50 为 10 μM。 PACMA 31 显着抑制卵巢肿瘤生长并表现出肿瘤靶向能力。 | |||
T69718 | Bacitracin F | ||
Bacitracin F is a major Bacitracin analog -- a peptide antibiotic used as an inhibitor of protein disulfide isomerase (PDI). | |||
T19505 |
PBDB-T
|
Others | Others |
PBDB-T serves as a wide-bandgap polymer donor within polymer solar cells that utilize Perylene Diimide (PDI) as the base. | |||
T35608 |
16F16
|
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16F16 is a protein disulfide isomerase (PDI) inhibitor.1It inhibits PDI reductase activity in an enzyme assay when used at concentrations ranging from 1 to 100 μg/ml.116F16 reduces PC12 cell apoptosis induced by the misfolded huntingtin protein HTTQ103. It suppresses PDI-dependent mitochondrial outer membrane permeabilization (MOMP) in isolated PC12 cell mitochondria. 16F16 (2, 3, 4, and 10 μM) reduces HTTN90Q73mutant huntingtin-induced medium spinal neuron death and MOMP in rat corticostriatal ... | |||
T69700 |
BAP2
|
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BAP2 is a novel inhibitor of protein disulfide isomerase (PDI). | |||
T71589 |
AS15
|
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AS15 is a novel covalent nanomolar inhibitor of protein disulfide isomerase (PDI). | |||
T39812 |
(E/Z)-E64FC26
(E/Z)-E64FC26 |
||
(E/Z)-E64FC26 is a mixture complex comprising E-E64FC26 and Z-E64FC26. E-E64FC26 is a highly potent pan-inhibitor of the protein disulfide isomerase (PDI) family, with IC50 values of 1.9, 20.9, 25.9, 16.3, and 25.4 μM against PDIA1, PDIA3, PDIA4, TXNDC5, and PDIA6, respectively. Furthermore, E64FC26 demonstrates anti-myeloma activity. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T4S1057 |
Tripdiolide
|
IL Receptor; TNF | Apoptosis; Immunology/Inflammation |
Tripdiolide has cytotoxic, and anti-rheumatic activities, it suppresses pro-inflammatory gene expression, may be effective therapy for lupus nephritis. | |||
T3752 |
4-Hydroxybenzyl alcohol
4-Methylolphenol,P-Methylolphenol,对羟基苯甲醇 |
Apoptosis; Endogenous Metabolite | Apoptosis; Metabolism |
4-Hydroxybenzyl alcohol (P-Methylolphenol) 是广泛分布于各种植物中的一种酚类天然产物,具有抗炎、抗氧化和抗伤害感受活性。它抑制肿瘤血管生成和生长,有神经保护作用。 | |||
T82003 | Juniferdin | ||
Juniferdin是一种抑制Protein disulfide isomerase (PDI),IC50为3.5 μM,旨在阻断HIV传播的化合物。此外,Juniferdin展现出细胞毒性并能抑制血小板聚集。 | |||
T74207 |
Ribostamycin
|
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Ribostamycin (Vistamycin) 是一种广谱氨基糖苷类抗生素 (antibiotic)。Ribostamycin 对革兰氏阴性和革兰氏阳性细菌感染有效。Ribostamycin 还抑制PDI 的伴侣活性。 |