The Path to Controlled Delivery of Reactive Sulfur Species

RSS 硫化氢 硫黄 计算生物学 化学 纳米技术 计算机科学 组合化学 生化工程 生物 有机化学 材料科学 工程类 万维网
作者
Xiang Ni,Shane S. Kelly,Shi Xu,Ming Xian
出处
期刊:Accounts of Chemical Research [American Chemical Society]
卷期号:54 (20): 3968-3978 被引量:57
标识
DOI:10.1021/acs.accounts.1c00506
摘要

Reactive sulfur species (RSS) play regulatory roles in many physiological and pathological processes. Since the discovery of hydrogen sulfide (H2S) as a nitric oxide (NO)-like signaling molecule, understanding the chemical biology of H2S and H2S-related RSS, such as hydropersulfides (RSSH) and polysulfides (H2Sn), has become a fast-growing research field. However, the research on these RSS has technical difficulties due to their high reactivity and instability. To solve this problem, considerable efforts have been put into the development of unique RSS releasing compounds (e.g., donors) or in situ RSS generation systems. This Account tells the story of our research group's effort to develop novel RSS donors.We began with exploring molecular entities that were stable by themselves but could be triggered by biologically relevant factors, such as pH, thiols, light, or enzymes, to release H2S in a controllable fashion. These studies led to the discovery of a series of novel H2S donors. We later expanded our interests to other RSS including RSSH, H2Sn, RSeSH, HSNO, RSOH, etc. The fundamental chemistry of these RSS was studied and applied to the development of the corresponding donors. In addition to small molecule donors, we also worked on H2S-releasing biomaterials and their applications. This Account summarizes our work and systematically explains how each RSS donor template was proposed and evaluated. The Account covers the following key points: (1) rational chemistry design of each RSS donor template, (2) evaluation and mechanistic insights of each donor template, and (3) properties and biological applications of the donors.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
1秒前
hulai发布了新的文献求助30
2秒前
shuan完成签到,获得积分10
3秒前
研友_VZG7GZ应助哇哈哈采纳,获得10
4秒前
Dong灬完成签到 ,获得积分10
4秒前
qq987490146完成签到 ,获得积分10
5秒前
5秒前
5秒前
月月子发布了新的文献求助10
6秒前
6秒前
粗暴的依秋应助skkty采纳,获得10
7秒前
7秒前
8秒前
8秒前
地瓜儿完成签到,获得积分10
9秒前
9秒前
DMUXLW完成签到,获得积分10
10秒前
科目三应助标致又夏采纳,获得10
10秒前
今后应助Anyuan采纳,获得10
11秒前
CodeCraft应助三七采纳,获得10
11秒前
taipingyang发布了新的文献求助10
11秒前
11秒前
杜晓倩发布了新的文献求助10
13秒前
嘿嘿嘿发布了新的文献求助10
14秒前
友好易梦发布了新的文献求助50
14秒前
11发布了新的文献求助10
15秒前
失眠的夜蓉完成签到,获得积分20
15秒前
灰苓完成签到,获得积分10
15秒前
jhjhmgm完成签到,获得积分20
16秒前
17秒前
18秒前
18秒前
乐空思应助cloudtrim采纳,获得50
19秒前
gxy完成签到,获得积分20
22秒前
hzwhz完成签到,获得积分10
25秒前
哇哈哈发布了新的文献求助10
25秒前
25秒前
lobster发布了新的文献求助10
25秒前
27秒前
没骨头大人完成签到 ,获得积分10
28秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Encyclopedia of Cardiovascular Research and Medicine(2e) 820
自動車の空力技術 800
Essentials of Carbohydrate Chemistry and Biochemistry, 4th Edition 800
Organizational Behavior 510
Management and the Arts 510
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 计算机科学 化学工程 工程类 有机化学 物理 复合材料 生物化学 内科学 细胞生物学 基因 遗传学 免疫学 冶金 光电子学 癌症研究
热门帖子
关注 科研通微信公众号,转发送积分 7781791
求助须知:如何正确求助?哪些是违规求助? 9321417
关于积分的说明 20382975
捐赠科研通 7369678
什么是DOI,文献DOI怎么找? 3320126
关于科研通互助平台的介绍 2467955
邀请新用户注册赠送积分活动 2336049