Bioactivity | Almurtide (nor-MDP), a muramyl dipeptide derivative with anti-inflammatory and anti-tumor activity. Almurtide also shows protective effects against intraperitoneal Pseudomonas aeruginosa infection or intravenously Candida albicans infection in mice. Almurtide also inhibits the carcinogenic Friend leukemia virus[1][2][3]. |
In Vivo | Almurtide (80 mg/kg; 每天 1 次, 连续 4 天; 腹腔注射,静脉注射或皮下注射) 非特异性刺激巨噬细胞,对单核增生李斯特菌有抗感染活性。同时,它缺少口服活性,和庆大霉素 (HY-A0276A) 之间存在协同作用[2]。Almurtide (100 μg/mouse; 皮下注射; 2-3 个月 1 次, 共 2 次) 防止低剂量 Friend 白血病病毒引起的 SJL/J 小鼠的红白血病,延缓 RIII/Imr 小鼠自发乳腺肿瘤的发生[3]。 |
Name | Almurtide |
CAS | 61136-12-7 |
Formula | C18H30N4O11 |
Molar Mass | 478.45 |
Transport | Room temperature in continental US; may vary elsewhere. |
Storage | Please store the product under the recommended conditions in the Certificate of Analysis. |
Reference | [1]. Díaz-Eufracio BI, et al. Exploring the chemical space of peptides for drug discovery: a focus on linear and cyclic penta-peptides. Mol Divers. 2018 May;22(2):259-267. [2]. Fraser-Smith E B, et al. Protective effect of muramyl dipeptide analogs against infections of Pseudomonas aeruginosa or Candida albicans in mice. Infection and immunity, 1981, 34(3): 676-683. [3]. Acevedo H F, et al. Prevention of oncogenic viral infections in mice with CGP 11637, a synthetic muramyl dipeptide analog[J]. Antimicrobial agents and chemotherapy, 1985, 28(5): 589-596. |