chelerythrine

Chelerythrine (Broussonpapyrine) 是一种天然生物碱，为有效、选择性的 Ca2+/磷脂依赖性PKC 拮抗剂，IC50值为 0.7 μM。它具有抗肿瘤、抗糖尿病、抗炎的活性。它抑制BclXL-Bak BH3肽结合，IC50为 1.5 μM，并从 BclXL 取代了 Bax。它诱导细胞凋亡和自噬。

Chelerythrine chloride 是一种可渗透细胞的蛋白激酶 C 抑制剂，对磷酸盐受体具有竞争性，而对 ATP 是非竞争性的。它诱导细胞凋亡和自噬。

Chelerythrine hydroxide is the salt form of Chelerythrine, a benzophenanthridine alkaloid present in the plant Chelidonium majus (greater celandine). It is a potent, selective, and cell-permeable protein kinase C inhibitor in vitro. And an efficacious antagonist of G-protein-coupled CB1 receptors.]This molecule also exhibits anticancer qualities and it has served as a base for many potential novel drugs against cancer.

6-Methoxyldihydrochelerythrine chloride 是一种有用的有机化合物，可用于生命科学领域的相关研究，其产品编号为 T126454。

6-Ethoxychelerythrine (Ethoxychelerythrin) 具有抗菌活性，对烟曲霉和耐甲氧西林金黄色葡萄球菌 (MRSA) 表现出很强的活性。

Dihydrochelerythrine (12,13-Dihydrochelerythrine) 是一种从榕树叶片分离出的天然化合物，具有抗真菌活性，有潜力治疗多丝蚴引起的严重感染。

6-(1-Hydroxyethyl)-5,6-dihydrochelerythrine 显著影响细胞器特性，涉及早期内体、线粒体及自噬体（源自帕金森病患者的嗅觉细胞）。

Norchelerythrine shows significant inhibitory activity against Staphylococcus aureus ATCC 6538 with MIC values ranging from 12.5 to 50 ug/mL. It exhibits strong antifeeding activity in a concentration-dependant manner with the EC50 of 62.67 ppm.

6-Acetonyldihydrochelerythrine exhibits significant antioxidant activities, it exhibits significant anti-HIV activity in H9 lymphocytes with EC50 and TI (Therapeutic Index) values of 1.77 microg/mL and 14.6, respectively. 6-Acetonyldihydrochelerythrine is

Oxychelerythrine shows high modulatory activity enhancing the susceptibility of the S. aureus ATCC 6538 to all the tested antibiotics from two to four-fold. It also shows antifeeding activities against Tribolium castaneum adults, with the EC50 of 192.32 p

Sanguinarine chloride (Pseudochelerythrine chloride) 是一种来源于 Sanguinaria Canadensis 的生物碱，通过激活活性氧的产生，诱导细胞凋亡。

Sanguinarine (Pseudochelerythrine) 是一种来源于血根草的生物碱，具有抗微生物、抗氧化和抗炎特性。

Angoline hydrochloride (6-Methoxyldihydrochelerythrine) 是一种从 Zanthoxylum nitidum 中分离的选择性 IL-6/STAT3 信号通路抑制剂，具有抗癌活性，抑制 STAT3 信号传导，抑制 STAT3 磷酸化及其靶基因表达，抑制癌细胞增殖。

Angoline (6-Methoxyldihydrochelerythrine) 是选择性 IL6/STAT3信号通路的抑制剂，IC50为 11.56 μM。它抑制 STAT3 磷酸化及其靶基因表达，并抑制癌细胞增殖。