Name: Fmoc-Cystamine-Suc
SKU: RL-3310
Availability: InStock

Grouped product items

Nombre

Unité de vente

Prix

SKU

Disponibilité

500 mg

99,00 €

RL-3310.0500

1 g

145,00 €

RL-3310.0001

5 g

550,00 €

RL-3310.0005

25 g

2 200,00 €

RL-3310.9025

Fiches de données de sécurité

description

Fmoc-cystamine-Suc is used in SPPS as a conjugation linker for various applications.

references

Synthesis and evaluation of redox-sensitive gonadotropin-releasing hormone receptor-targeting peptide conjugates; Yuxuan Dai, Na Yue, Chunxia Liu, Xingguang Cai, Xin Su, Xinzhou Bi, Qifei Li, Chengye Li, Wenlong Huang, Hai Qian; Bioorganic Chemistry 2019; 88: 102945. DOI: org/10.1016/j.bioorg.2019.102945

Tandem Molecular Self‐Assembly in Liver Cancer Cells; Jie Zhan, Yanbin Cai, Shuangshuang He, Ling Wang, Zhimou Yang; Angew. Chem. Int. Ed. 2018; 57(7): 1813-1816. DOI: org/10.1002/anie.201710237.

Chemoenzymatic Enrichment of Phosphotyrosine‐Containing Peptides; Shuwei Li, Dexing Zeng; Angew. Chem. Int. Ed. 2007; 46(25): 4751-4753. DOI: org/10.1002/anie.200700633.

Palladium-mediated bioorthogonal conjugation of dual-functionalised nanoparticles and their cellular delivery; Frank Thielbeer, Sunay V. Chankeshwara, Emma M. V. Johansson, Neil Norouzi, Mark Bradley; Chem. Sci. 2013; 4: 425-431. DOI: 10.1039/C2SC20706K.

Disulfide bond as a cleavable linker for molecular self-assembly and hydrogelation; Chunhua Ren, Zhijian Song, Wenting Zheng, Xuemei Chen, Ling Wang, Deling Kong, Zhimou Yang; Chem. Commun. 2011; 47: 1619-1621. DOI: 10.1039/C0CC04135A.

Peptide-Induced AIEgen Self-Assembly: A New Strategy to Realize Highly Sensitive Fluorescent Light-Up Probes

Aitian Han, Huaimin Wang, Ryan T. K. Kwok, Shenglu Ji, Jun Li, Deling Kong, Ben Zhong Tang, Bin Liu, Zhimou Yang, Dan Ding; Anal. Chem. 2016; 88(7): 3872-3878. DOI: org/10.1021/acs.analchem.6b00023.

Disulfide bond reduction-triggered molecular hydrogels of folic acid–Taxol conjugates; Chengbiao Yang, Dongxia Li, Qianqi Feng Zhao, Lianyong Wang, Ling Wang Zhimou Yang; Org. Biomol. Chem. 2013; 11: 6946-6951. DOI: 10.1039/C3OB40969D.

Conjugation of two complementary anti-cancer drugs confers molecular hydrogels as a co-delivery system; Lina Mao, Huaimin Wang, Ming Tan, Lailiang Ou, Deling Kong, Zhimou Yang; Chem. Commun. 2012; 48: 395-397. DOI: 10.1039/C1CC16250K.

Development of Hydrogel TentaGel Shell−Core Beads for Ultrahigh Throughput Solution-Phase Screening of Encoded OBOC Combinatorial Small Molecule Libraries; Hyoung Gee Baek, Ruiwu Liu, Kit S. Lam; J. Comb. Chem. 2009; 11(1): 91-102. DOI: org/10.1021/cc800092y.

Conjugation of two complementary anti-cancer drugs confers molecular hydrogels as a co-delivery system. Lina Mao, Huaimin Wang, Ming Tan, Lailiang Ou, Deling Kong, Zhimou Yang; Chem. Commun. 2012; 48: 395-397.DOI: org/10.1039/C1CC16250K

Peptide-Induced AIEgen Self-Assembly: A New Strategy to Realize Highly Sensitive Fluorescent Light-Up Probes. Aitian Han, Huaimin Wang, Ryan T. K. Kwok, Shenglu Ji, Jun Li, Deling Kong, Ben Zhong Tang, Bin Liu, Zhimou Yang, Dan Ding; Anal. Chem. 2016; 88(7): 3872-3878.DOI: org/10.1021/acs.analchem.6b00023

Tandem Molecular Self‐Assembly in Liver Cancer Cells. Jie Zhan, Yanbin Cai, Shuangshuang He, Ling Wang, Zhimou Yang; Angew. Chem. Int. Ed. 2018; 57(7): 1813-1816.DOI: org/10.1002/anie.201710237

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