cyclosporin a

Cyclosporin A 属于天然产物，是一种真菌的活性代谢产物，一种环状多肽。Cyclosporin A 是一种能与亲环素结合的免疫抑制剂，可以抑制 calcineurin (IC50=7 nM)。

6-[(3R,4R)-3-(Acetyloxy)-N,4-dimethyl-6-oxo-L-norleucine]cyclosporin A 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 T64488。

Cyclosporin A-Derivative 3 是 Cyclosporin A 的衍生物，具有钙调神经磷酸酶抑制作用。

Derivative 2 is A novel Derivative of Cyclosporin A.Cyclosporin A is an immunosuppressant that binds to cyclophilin and inhibits calcineurin.

Cyclosporin A-Derivative 1 (Free base) is a crystalline intermediate derived from the opening of cyclosporin A.

Cyclosporin A-Derivative 1 is a crystalline intermediate derived from the opening of cyclosporin A.

Cyclosporin E (11-Demethylcyclosporin A) 是从Trichoderma polysporum 等不完全真菌中分离得来的环状寡肽，是环孢菌素 (Cyclosporins) 家族的成员。Cyclosporin E 在环孢菌素类化合物的构效关系及分子动态特性研究中发挥作用，作为结构对照化合物，在药物化学和生物物理学领域具备重要研究价值。

Cyclosporin B is an immunosuppressant that has revolutionized organ transplantation through its use in the prevention of graft rejection. Cyclosporin B displays antiviral properties, inhibiting the entry of hepatitis B into hepatocytes. Cyclosporin B also

Cyclosporin U (SMP0V32C6L)为一种细胞免疫抑制剂，关键用于防止移植器官的排斥反应。

Cyclosporin D is a metabolite of cyclosporin A, an immunosuppressant drug that binds cyclophilin D, inhibiting the phosphatase activity of calcineurin in T cells.

Isocyclosporin A is a rearranged degradation product. It is formed by acid treatment of cyclosporin A under aqueous and non-aqueous conditions.

Dihydrocyclosporin A (Dihydrocyclosporin-A) 是 cyclosporin A 的密切相关的共同代谢物。它显着抑制前鞭毛体和细胞内无鞭毛体。

Acetyl-cyclosporin A aldehyde 是一种环孢菌素A衍生物，是神经钙调蛋白抑制剂和亲环素结合剂，具有潜在的抗炎抗肿瘤和抗病毒活性，可用于研究器官移植和自身免疫疾病。

Cyclosporin A-d4 (Major) 是 Cyclosporin A 的氘代化合物。Cyclosporin A 的 CAS 号为 59865-13-3。Cyclosporine A 是一种能与亲环素结合的抑制剂。 根据它的作用机制可作为钙调神经磷酸酶抑制剂、细胞色素 P450 3A4 抑制剂和 P-糖蛋白抑制剂。

Rioprostil is a methyl prostaglandin E1 analog that decreases gastric acid secretion and enhances the gastric mucus-bicarbonate barrier. It is effective in the treatment of gastric ulcers and gives significant protection against NSAID-induced gastric muco

Cyclosporin C (Cs-C) 是一种抗丝状植物病原真菌的真菌代谢物。 Cyclosporin C 具有抗真菌、抗病毒和免疫抑制特性。

SCY-635 作为一种基于环孢素的非免疫抑制类似物，展现出对乙型肝炎病毒 (HCV) 复制的强效抑制作用。

RJS308 是一种环孢菌素 A (cyclosporin A) 的PROTAC降解剂，具有284 nM的DC50。RJS308 抑制HIV-1和HCV的复制，从而展现出抗病毒活性。(Pink: ligand for target proteinCypA ligand-2; Black: linker; Blue: ligand for E3ligaseVHL(S,R,S)-AHPC-Me)

Cyclosporin H 是一种 FPR-1(甲酰肽受体 1) 的选择性强效抑制剂。它缺乏 Cyclosporin A 具有的免疫抑制活性。它是一种病毒转导增强剂，可使人脐带血来源的造血干细胞和祖细胞中慢病毒转导增强 10 倍。它与雷帕霉素或前列腺素 E2 联合使用时表现出累加效应。

Cyclopeptolide 1 is a novel antifungal cyclopeptolide. Cyclopeptolide 1 is similar to cyclosporin A that consists of nine S-amino acids and R-lactic acid.

NFAT:AP-1 inhibitor-10 is a novel inhibitor of the NFAT:AP-1:DNA interaction on the ARRE-2 element, binding to DNA in a sequence-selective manner and inhibiting the transcription of the Il2 gene and several other cyclosporin A-sensitive cytokine genes important for the effector immune response.

H-D-MeAla-EtVal-Val-MeLeu-AIa-D-AIa-MeLeu-MeLeu-MeVal-MeBmt(OAc)-Abu-O-CH2-CH2-NHMe 是一种非免疫抑制性的环孢菌素A衍生物，具备研究先天性肌营养不良症潜力[1]。

Pepluanin A, shows a very high activity for a jatrophane diterpene, outperforming cyclosporin A by a factor of at least 2 in the inhibition of Pgp-mediated daunomycin transport.

Phellamurin 是一种来自黄檗叶的黄酮糖苷，可诱导细胞凋亡，具有抗肿瘤活性。它抑制肠道 P-糖蛋白，还抑制凤蝶的产卵。