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Merck
CN

C121509

Sigma-Aldrich

胱胺 二盐酸盐

96%

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别名:
2,2ˊ-二乙氨基二硫 二盐酸盐, 2,2ˊ-二硫代二乙胺 二盐酸盐, 脱羧胱氨酸 二盐酸盐
线性分子式:
NH2CH2CH2SSCH2CH2NH2 · 2HCl
CAS号:
分子量:
225.20
Beilstein:
3616850
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

96%

形式

powder

mp

217-220 °C (dec.) (lit.)

SMILES字符串

Cl[H].Cl[H].NCCSSCCN

InChI

1S/C4H12N2S2.2ClH/c5-1-3-7-8-4-2-6;;/h1-6H2;2*1H

InChI key

YUFRRMZSSPQMOS-UHFFFAOYSA-N

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应用

盐酸胱胺可作为合成二硫键交联的寡脱氧核糖核苷酸 和psammaplin A 的结构单元。它还可通过引入巯基用于功能化PGMA(聚(甲基丙烯酸缩水甘油酯)微球),并进一步制备银纳米颗粒(AgNP)。
肝素拮抗剂和巯基修饰剂

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危险声明

危险分类

Acute Tox. 4 Oral

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves


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Synthesis and characterization of disulfide cross-linked oligonucleotides
Ferentz A E, et al.
Journal of the American Chemical Society, 115(20), 9006-9014 (1993)
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Molecules (Basel, Switzerland), 15(12), 8784-8795 (2010-12-04)
Psammaplin F, an unsymmetrical disulfide bromotyrosine, was isolated from the sponge Pseudoceratina purpurea in 2003. We reported here the first total synthesis of psammaplin F in 12% overall yield by employing Cleland's reagent reduction as key step. The longest linear
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Nanoscale research letters, 13(1), 152-152 (2018-05-17)
In this study, we propose a modified gold nanoparticle-graphene oxide sheet (AuNP-GO) nanocomposite to detect two different interactions between proteins and hybrid nanocomposites for use in biomedical applications. GO sheets have high bioaffinity, which facilitates the attachment of biomolecules to
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N-propionyl-4-S-cysteaminylphenol (NPr-4-S-CAP) is selectively incorporated into melanoma cells and degrades them. However, it remains unclear whether NPr-4-S-CAP can induce cell death associated with the induction of host immune responses and tumor suppression in vivo. To examine the molecular mechanism of
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Metastatic melanoma is resistant to conventional therapies. N-propionyl-4-S-cysteaminylphenol (NPrCAP), an N-protected sulfur-amine analog of tyrosine, is a good substrate for tyrosinase and is selectively incorporated into melanoma cells, causing cytotoxicity in vitro and in vivo. We have recently shown that

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