Fmoc-Cystamine-Suc

Chemical name: 4-(2-((2-(9-Fluorenylmethyloxycarbonylamino)ethyl)disulfanyl)ethylamino)-4-oxobutanoic acid // Synonyms: 1-(9H-fluoren-9-yl)-3,12-dioxo-2-oxa-7,8-dithia-4,11-diazapentadecan-15-oic acid

Product code:RL-3310
CAS No.:946849-80-5
Formula:C₂₃H₂₆N₂O₅S₂
Molecular weight:474.59 g/mol
Purity :min. 98%

Starting at $123.75

Grouped product items
Qty	Packing unit	Price	SKU
	500 mg	$123.75	RL-3310.0500
	1 g	$181.25	RL-3310.0001
	5 g	$687.50	RL-3310.0005
	25 g	$2,750.00	RL-3310.9025
Safety Data Sheets

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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