P9386
聚-L-组氨酸
mol wt 5,000-25,000
别名:
L-Histidine homopolymer
SMILES string
[N+H3][C@@H](Cc1[nH]cnc1)C(=O)[O-]
InChI
1S/C6H9N3O2/c7-5(6(10)11)1-4-2-8-3-9-4/h2-3,5H,1,7H2,(H,8,9)(H,10,11)/t5-/m0/s1
InChI key
HNDVDQJCIGZPNO-YFKPBYRVSA-N
form
powder or solid
mol wt
5,000-25,000
color
white to light yellow
application(s)
cell analysis
storage temp.
−20°C
Quality Level
General description
聚-L-组氨酸是一种两性化合物。结构中的咪唑环可进行质子化−去质子化反应。
Application
聚L-组氨酸已用于：
- 作为聚阳离子分散多壁碳纳米管(MWCNT)
- 作为多离子化合物研究其破坏细胞外包膜病毒膜的能力
- 通过在细胞水平上和在体内的抗朊毒体(prion)分析，进行其抗朊毒体活性筛选
Biochem/physiol Actions
聚L-组氨酸(Phis)共聚物具有生物相容性、pH响应性和较低的毒性。它具有逃逸内溶酶体的功能。聚L组氨酸与聚乙二醇−聚(d,l-丙交酯) (PEG-PLA)的共聚物可有效递送阿霉素。pH敏感性聚l-组氨酸共聚物胶束可在酸性微环境中递送抗癌药物。
Analysis Note
分子量 (MALLS)。
Other Notes
有关聚氨基酸的其他技术信息，请访问 聚氨基酸常见问题解答资源。
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Frank Morgner et al.
Sensors (Basel, Switzerland), 11(10), 9667-9684 (2011-12-14)
Förster resonance energy transfer (FRET) from luminescent terbium complexes (LTC) as donors to semiconductor quantum dots (QDs) as acceptors allows extraordinary large FRET efficiencies due to the long Förster distances afforded. Moreover, time-gated detection permits an efficient suppression of autofluorescent
Electrochemical determination of ascorbic acid and paracetamol in pharmaceutical formulations using a glassy carbon electrode modified with multi-wall carbon nanotubes dispersed in polyhistidine
Dalmasso PR, et al.
Sensors and Actuators B, Chemical, 173(5), 732-736 (2012)
Masaharu Kondo et al.
Biomacromolecules, 13(2), 432-438 (2012-01-14)
A polyhistidine (His) tag was fused to the C- or N-terminus of the light-harvesting (LH1)-α chain of the photosynthetic antenna core complex (LH1-RC) from Rhodobacter sphaeroides to allow immobilization of the complex on a solid substrate with defined orientation. His-tagged
Rong Liu et al.
International journal of nanomedicine, 7, 4433-4446 (2012-08-28)
Two methoxyl poly(ethylene glycol)-poly(L-histidine)-poly(L-lactide) (mPEG-PH-PLLA) triblock copolymers with different poly(L-histidine) chain lengths were synthesized. The morphology and biocompatibility of these self-assembled nanoparticles was investigated. Doxorubicin, an antitumor drug, was trapped in the nanoparticles to explore their drug-release behavior. The drug-loaded
Poly (l-histidine)-PEG block copolymer micelles and pH-induced destabilization
Lee ES, et al.
Journal of Controlled Release : Official Journal of the Controlled Release Society, 90(3), 363-374 (2003)
商品
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