Fmoc-Val-Cit-PAB-PNP

目录号: PL05038 纯度: ≥98%
Fmoc-Val-Cit-PAB-PNP 是一种可降解 (cleavable) 的 ADC linker,可用于合成抗体偶联药物 (ADC)。 Fmoc-Val-Cit-PAB-PNP 的血浆稳定性优于不可降解连接剂。
CAS No. :863971-53-3
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中文名称
Fmoc-Val-Cit-PAB-PNP
中文别名
Fmoc-val-cit-pab-pnp
英文名称
Fmoc-Val-Cit-PAB-PNP
英文别名
Fmoc-val-cit-pab-pnp;(9H-fluoren-9-yl)methyl (3-methyl-1-((1-((4-((((4-nitrophenoxy)c arbonyl)oxy)methyl)phenyl)amino)-1-oxo-5-ureidopentan-2-yl)amino)-1-oxobutan-2-yl)carbamate;Fmoc-DL-Val-DL-Cit-Unk
Cas No.
863971-53-3
分子式
C40H42N6O10
分子量
766.80
包装储存
-20°C, stored under nitrogen In solvent : -80°C, 6 months; -20°C, 1 month (stored under nitrogen)
产品详情
Fmoc-Val-Cit-PAB-PNP 是一种可降解 (cleavable) 的 ADC linker,可用于合成抗体偶联药物 (ADC)。 Fmoc-Val-Cit-PAB-PNP 的血浆稳定性优于不可降解连接剂。
生物活性
Fmoc-Val-Cit-PAB-PNP is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Fmoc-Val-Cit-PAB-PNP has superior plasma stability comparable to that of non-cleavable linkers.
性状
Solid
IC50 & Target[1][2]
Protease Cleavable Cleavable
体外研究(In Vitro)
Fmoc-Val-Cit-PAB-PNP contains peptide sequence degradable by a lysosome enzyme.
Cathepsin B in the lysosome cleaves the peptide bond between Cit-PAB of dipeptide linkers containing Valine (Val)-citrulline (Cit) and p-aminobenzylalcohol (PAB). When PAB and a drug are binded covalently with carbamate bonds, the drug can be released by hydrolysis after cleavage of the peptide bond between Cit-PAB. Antibody-drug conjugates (ADCs) has been developed using this mechanism.
has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
Fmoc-Val-Cit-PAB-PNP linker stabilization in the mouse is an essential prerequisite for designing successful efficacy and safety studies in rodents during preclinical stages of ADC programs.
Conjugation site plays an important role in determining VC-PABC linker stability in mouse plasma, and that the stability of the linker positively correlates with ADC cytotoxic potency both in vitro and in vivo.
has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
-20°C, stored under nitrogen In solvent : -80°C, 6 months; -20°C, 1 month (stored under nitrogen)
SequenceShortening
Fmoc-V-Cit-PAB-PNP
参考文献
[1]. Dubowchik GM, et al. Cathepsin B-labile dipeptide linkers for lysosomal release of doxorubicin from internalizing immunoconjugates: model studies of enzymatic drug release and antigen-specific in vitro anticancer activity. Bioconjug Chem. 2002 Jul-Aug;13(4):855-69.
[2]. Yoneda Y, et al. A cell-penetrating peptidic GRP78 ligand for tumor cell-specific prodrug therapy. Bioorg Med Chem Lett. 2008 Mar 1;18(5):1632-6.
溶解度数据
In Vitro: DMSO : ≥ 40 mg/mL (52.16 mM)配制储备液
搜索质检报告(COA)

1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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