rpe

WS3 是一种可促进鼠和人原代胰岛的胰腺 β 细胞增殖的增殖分子。它可用于研究 I 型糖尿病。

Ossirene (AS101) 是一种免疫调节抑制剂，是一种新型 IL-1beta 转化酶抑制剂，可用于自身免疫性疾病和某些恶性肿瘤。它通过抑制IL-10消除 STAT3 的磷酸化，有效抑制Caspase-1。

RPE65-IN-1(Compound 16e)为高效RPE65抑制剂，适用于视网膜疾病相关研究。

Prochlorperazine Maleate (Capazine) 是一种吩噻嗪类抗精神病药，主要用于治疗恶心、呕吐和眩晕。它比氯丙嗪更容易引起锥体外系疾病。

Triptonoterpene 是在 Tripterygium wilfordii 和 Tripterygium doianum 中发现的一种天然产物。Triptonoterpene 是一种双乙烷二萜。

3-O-Acetylcalliterpenone 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 T124769，CAS号为 49816-65-1。

Securiterpenoside 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 T124804，CAS号为 479677-95-7。

Calliterpenone 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 T124920，CAS号为 38602-53-8。

Artocarpesin 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 T125061。

Triptotriterpenic acid A, a natural product isolated from *Tripterygium wilfordii*,

15-Acetoxyscirpenol, a member of the acetoxyscirpenol moiety mycotoxins (ASMs), potently induces apoptosis and inhibits the growth of Jurkat T cells in a dose-dependent manner. This effect is mediated through the activation of caspases independent of caspase-3[1].

Diacetoxyscirpenol (蛇形菌素)是一种霉菌毒素和真菌次生代谢物，能够抑制HIF-1，激活caspase-8，下调和cdk4和cyclin b1，抑制多种癌细胞生长。

Arpenal is a ganglionic blocking agent which may be useful in the treatment of bronchial asthma.

Arpenal HCl is a ganglionic blocking agent which may be useful in the treatment of bronchial asthma.

Carperone is a bio-active chemical.

Lonchocarpene is a hypoglycemic agent From the Amazonian plant Deguelia rufescens var. urucu.

Monoacetoxyscirpenol is a mycotoxin produced by Fusarium roseum Gibbosum.

Sarpedobilin is a doubly cyclized bile pigment. It is found in butterflies.

Terpentecin is isolated from strain MF730-N6 and is active against leukemia L-1210 and Ehrlich ascites carcinoma.

Terpendole I is a fungal metabolite that has been found in A. yamanashiensis.1 It is a weak inhibitor of acyl-coenzyme A:cholesterol acyltransferase (ACAT; IC50 = 145 μM) and is active against the bacteria B. cereus and B. subtilis (MICs = 100 μg/ml for both) but not S. aureus, P. aeruginosa, or K. pneumoniae (MICs = >200 μg/ml for all) or the fungus C. albicans (MIC = 200 μg/ml).1,2 It is cytotoxic to HeLa cells with an IC50 value of 52.6 μM.3 |1. Tomoda, H., Tabata, N., Yang, D.-J., et al. Terpendoles, novel ACAT inhibitors produced by Albophoma yamanashiensis. III. Production, isolation and structure elucidation of new components. J. Antibiot. (Tokyo) 48(8), 793-804 (1995).|2. Zhao, J.-C., Wang, Y.-L., Zhang, T.-Y., et al. Indole diterpenoids from the endophytic fungus Drechmeria sp. as natural antimicrobial agents. Phytochemistry 148, 21-28 (2018).|3. Nagumo, Y., Motoyama, T., Hayashi, T., et al. Structure-activity relationships of terpendole E and its natural derivatives. ChemistrySelect 2(4), 1533-1536 (2017).

Terpendole C is an indole diterpene alkaloid fungal metabolite originally isolated from A. yamanashiensis and an inhibitor of acyl-coenzyme A:cholesterol acyltransferase (ACAT; IC50 = 2.1 μM in rat liver microsomes). It also inhibits ACAT in J774 macrophages (IC50 = 0.46 μM) without affecting cell growth.

Terpendole E is an atypical L5 site inhibitor.

Norartocarpetin 是一种酪氨酸酶抑制剂。Norartocarpetin 具有较强的酪氨酸酶抑制活性，其抑制活性 IC50值为 0.47 μM。Norartocarpetin 作为一种抗褐变剂可用于食品体系的研究。Norartocarpetin 对肺癌细胞 (NCI-H460) 也具有显著的抗癌活性，其 IC50值为 22 μM。Norartocarpetin 的抗增殖作用是通过靶向 Ras Raf MAPK 信号通路、线粒体介导的细胞凋亡、S 期细胞周期阻滞和抑制细胞迁移和侵袭实现的。

Sirpefenicol (ZTS-00007928) 是一种苯酚类抗菌剂。Sirpefenicol 可用于动物的细菌感染。