• 咨询热线
    客服服务热线 13671568941/15317326293
  • 在线咨询
  • 微信客服
    微信客服
  • 公众号
    扫码关注公众号

Livoletide

CAS No. 1088543-62-7

Livoletide ( AZP-531 | AZP531 )

产品货号. M10338 CAS No. 1088543-62-7

一种用于提高血糖控制并减轻体重的非格酸化生长素释放肽类似物。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥3392 有现货
10MG ¥5529 有现货
500MG 获取报价 有现货
1G 获取报价 有现货

生物学信息

  • 产品名称
    Livoletide
  • 注意事项
    本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
  • 产品简述
    一种用于提高血糖控制并减轻体重的非格酸化生长素释放肽类似物。
  • 产品描述
    A first-in-class analogue of unacylated ghrelin, and unacylated ghrelin receptor agonist; exhibits the same pharmacological profile as UAG both in vitro and in vivo, independently of AG receptor binding; prevents HFD-induced proinflammatory effects, stimulates expression of mitochondrial function markers in brown adipose tissue, and prevents development of a prediabetic metabolic state; also prevents a HFD-induced increase in acyl ghrelin levels.Diabetes Phase 1 Clinical.
  • 体外实验
    AZP-531 exerts survival effects on pancreatic b-cells and human pancreatic islets which is comparable to that of UAG, the parent molecule. AZP-531 is very stable in human plasma in vitro. No degradation is observed after 1 day of incubation at 37°C.
  • 体内实验
    The highest concentration of this peptide is 4350 ng/mL, and the majority of samples are above the limit of quantification (1 ng/mL). AZP-531 infusion prevents the increase in body weight caused by high-fat diet in mice. AZP-531 treatment prevents high-fat diet-induced proinflammatory effects, stimulates expression of mitochondrial function markers in brown adipose tissue, and prevents development of a prediabetic metabolic state. AZP-531 also prevents a high-fat diet-induced increase in acyl ghrelin levels. AZP-531 is well tolerated. Single- and multiple-dose pharmokinetic variables are similar. Maximum AZP-531 concentrations are typically reached at 1 h post-dose. Observed maximum concentration and area under the curve are dose-proportional. The mean terminal half-life is 2–3 h. AZP-531 (≥15 μg/kg) significantly improves glucose concentrations, without increasing insulin levels, suggesting an insulin-sensitizing effect. AZP-531 decreases mean body weight by 2.6 kg (vs 0.8 kg for placebo). Glucose variables improve in all groups, including placebo, suggesting a study effect in uncontrolled patients at baseline. AZP-531 60 μg/kg reduces HbA1c by 0.4% (vs 0.2% for placebo) and body weight by 2.1 kg (vs 1.3 kg for placebo).
  • 同义词
    AZP-531 | AZP531
  • 通路
    GPCR/G Protein
  • 靶点
    GHSR
  • 受体
    GHSR
  • 研究领域
    Metabolic Disease
  • 适应症
    Diabetes

化学信息

  • CAS Number
    1088543-62-7
  • 分子量
    962.036
  • 分子式
    C40H63N15O13
  • 纯度
    >98% (HPLC)
  • 溶解度
    DMSO : 100 mg/mL103.95 mM;
  • SMILES
    O=C(O)CC[C@H](N1)C(N[C@@H](CC2=CN=CN2)C(N[C@@H](CCC(N)=O)C(N[C@@H](CCCNC(N)=N)C(N[C@@H](C(C)C)C(N[C@@H](CCC(N)=O)C(N[C@@H](CO)C(N3CCC[C@@]3([H])C1=O)=O)=O)=O)=O)=O)=O)=O
  • 化学全称
    3-((3S,6S,9S,12S,15S,18S,21S,26aS)-6-((1H-imidazol-4-yl)methyl)-9,18-bis(3-amino-3-oxopropyl)-12-(3-guanidinopropyl)-21-(hydroxymethyl)-15-isopropyl-1,4,7,10,13,16,19,22-octaoxohexacosahydropyrrolo[1,2-a][1,4,7,10,13,16,19,22]octaazacyclotetracosin-3-yl)propanoic acid

运输与储存

  • 储存条件
    (-20℃)
  • 运输条件
    With Ice Pack
  • 稳定性
    ≥ 2 years

参考文献

1. Julien M, et al. Eur J Pharm Sci. 2012 Nov 20;47(4):625-35. 2. Delhanty PJ, et al. FASEB J. 2013 Apr;27(4):1690-700. 3. Callaghan B, et al. Br J Pharmacol. 2014 Mar;171(5):1275-86. 4. Allas S, et al. Diabetes Obes Metab. 2016 Sep;18(9):868-74.
产品手册
关联产品
  • NF-56-EJ40 hydrochlo...

    NF-56-EJ40 hydrochloride is a potent, high-affinity, and highly selective human SUCNR1 (GPR91) antagonist with an IC50 of 25 nM and a Ki of 33 nM, and shows almost no activity towards rat SUCNR1. NF-56-EJ40 hydrochloride has high affinity for humanized rat SUCNR1 with a Ki value of 17.4 nM.

  • PF-05190457

    一种有效的、选择性的、口服生物可利用的生长素释放肽受体 (GHSR) 反向激动剂,结合 pKi 为 8.36;在 10 uM 的 CEREP 组中显示出优异的脱靶活性,血清素 5-HT2B 除外 (IC50=3.7 uM)。

  • ONC212

    ONC212 是一种氟化 ONC201 类似物,是 GPR132 的选择性激动剂。