所有图片(2)
About This Item
经验公式（希尔记法）:
C5H11NO2
CAS号:
分子量:
117.15
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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方案
96%
沸点
81 °C/20 mmHg (lit.)
mp
34-37 °C (lit.)
官能团
ether
SMILES字符串
NOC1CCCCO1
InChI
1S/C5H11NO2/c6-8-5-3-1-2-4-7-5/h5H,1-4,6H2
InChI key
NLXXVSKHVGDQAT-UHFFFAOYSA-N
一般描述
O-(四氢-2H-吡喃-2-基)羟基胺（OTX）是一种O-取代的羟胺。据报道，OTX与碱性凝胶电泳结合，可改善检测DNA中单链断裂（SSB）的过程。
应用
O-(四氢-2H-吡喃-2-基)羟基胺可用于合成2-(5-溴噻吩-2-磺酰胺基)-N-(四氢-2H-吡喃-2-基氧基)乙酰胺。
它可用于合成以下潜在的组蛋白脱乙酰酶（HDAC）抑制剂：
它可用于合成以下潜在的组蛋白脱乙酰酶（HDAC）抑制剂：
- 2-[1-(萘-2-磺酰基)-杂环基]-嘧啶-5-羧酸(四氢吡喃-2-基氧基)-酰胺
- (E)-3-(2-苄基-1-氧代异吲哚-6-基)-N-(四氢-2H-吡喃-2-基氧基)丙烯酰胺
- 3-(1-苯磺酰基-2,3-二氢-1H-吲哚-5-基)-N-羟基丙烯酰胺
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
179.6 °F - closed cup
闪点(°C)
82 °C - closed cup
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
从最新的版本中选择一种：
分析证书(COA)
Lot/Batch Number
Elisa Nuti et al.
European journal of medicinal chemistry, 46(7), 2617-2629 (2011-04-26)
Matrix metalloproteinases (MMPs) are important factors in gliomas since these enzymes facilitate invasion into the surrounding brain and participate in neovascularization. In particular, the gelatinases (MMP-2 and MMP-9), and more recently MMP-25, have been shown to be highly expressed in
Patrick Angibaud et al.
European journal of medicinal chemistry, 40(6), 597-606 (2005-06-01)
A series of pyrimidyl-5-hydroxamic acids was prepared for evaluation as inhibitors of histone deacetylase (HDAC). Amino-2-pyrimidinyl can be used as a linker to provide HDAC inhibitors of good enzymatic potency.
Tetrahedron Letters, 45, 133-133 (2004)
Chihiro Shinji et al.
Bioorganic & medicinal chemistry, 14(22), 7625-7651 (2006-08-01)
A series of hydroxamic acid derivatives bearing a cyclic amide/imide group as a linker and/or cap structure, prepared during our structural development studies based on thalidomide, showed class-selective potent histone deacetylase (HDAC)-inhibitory activity. Structure-activity relationship studies indicated that the steric
Han-Li Huang et al.
PloS one, 7(8), e43645-e43645 (2012-08-29)
Recently, histone deacetylase (HDAC) inhibitors have emerged as a promising class of drugs for treatment of cancers, especially subcutaneous T-cell lymphoma. In this study, we demonstrated that MPT0E028, a novel N-hydroxyacrylamide-derived HDAC inhibitor, inhibited human colorectal cancer HCT116 cell growth
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