欢迎访问ProbeChem中文网站,英文网站请访问www.probechem.com

首页-小分子抑制剂&激动剂-Others-PCSK9-Enlicitide
Enlicitide

Chemical Structure : Enlicitide

CAS No.: 2407527-16-4

Enlicitide (MK-0616, MK0616, Enlicitide chloride)

货号: PC-26304Not For Human Use, Lab Use Only.

Enlicitide (MK-0616) is a highly potent, orally bioavailable macrocyclic peptide inhibitor of proprotein convertase subtilisin/kexin type 9 (PCSK9) with Ki of 5 pM, binds to the LDLR binding domain of PCSK9.

规格 价格 库存 数量
1 mg ¥5880 In stock
2 mg ¥8980 In stock
5 mg Get quote
25 mg Get quote

大包装,大折扣!

E-mail: sales@probechem.com

Tech Support: tech@probechem.com

纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

生物&药学活性

Enlicitide (MK-0616) is a highly potent, orally bioavailable macrocyclic peptide inhibitor of proprotein convertase subtilisin/kexin type 9 (PCSK9) with Ki of 5 pM, binds to the LDLR binding domain of PCSK9.
Enlicitide (MK-0616) inhibitsPCSK9 with an IC50 2.5 nM in human plasma.
Enlicitide (MK-0616) has no observed off-target activity at 10 µM in 122 receptor, ion channel, enzyme radioligand binding, and cellular assays in the Eurofins Cerep Panlabs screening panel.
Enlicitide (MK-0616) is not only able to reduce LDL-cholesterol, non-HDL-cholesterol, and apoB, but can also lower Lp(a).

物理化学性质&存储条件

分子量 1586.29
分子式 C82H110ClFN14O15
外观性状 Solid
CAS No.
储存条件
固体粉末
-20°C 12 个月; 4°C 6 个月
配置液
-80°C 6 个月; -20°C 6 个月
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

Ala-{Dpr}-Phe-Trp-Pro-Thr-Tyr-Pro(Covalent bridge:Phe3-Pro5,Ala1-Trp4,Trp4-Pro8,Ala1-Pro8,D-Dpr2)

参考文献

1. Li H, et al. J Am Chem Soc. 2025 Apr 2;147(13):11036-11048.

2. Johns DG, et al. Circulation. 2023 Jul 11;148(2):144-158.

备案号:沪ICP备16042516号-1 Copyright © 2022 probechem.com. All Rights Reserved. probechem Copyright

联系我们 sales@probechem.com

Bulk Inquiry

* Indicates a Required FieldYour information is safe with us.

  • *Product name:
  • *Applicant name:
  • *Email address:
  • *Organization name:
  • *Requested quantity:
  • *Country:
  • *Additional Information:

询单

  • *产品名称:
  • *姓名:
  • *邮箱:
  • *公司名称:
  • *询单数量:
  • *国籍:
  • 询单信息: