124753
琥珀酰胺
98%
别名:
丁二酰胺
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关于此项目
线性分子式:
NH2COCH2CH2CONH2
化学文摘社编号:
分子量:
116.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-739-9
Beilstein/REAXYS Number:
1753983
MDL number:
产品名称
琥珀酰胺, 98%
InChI key
SNCZNSNPXMPCGN-UHFFFAOYSA-N
InChI
1S/C4H8N2O2/c5-3(7)1-2-4(6)8/h1-2H2,(H2,5,7)(H2,6,8)
SMILES string
NC(=O)CCC(N)=O
assay
98%
mp
260-265 °C (dec.) (lit.)
solubility
cold water: soluble 220 part
boiling water: soluble 9 part
alcohol: insoluble
diethyl ether: insoluble
functional group
amide
Quality Level
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Application
琥珀酰胺已被用于表征来自半胱氨酸水解酶超家族的一种新型双缩脲水解酶 。在斜生栅藻和绿藻的培养基中作为氮源补充。
存储类别
11 - Combustible Solids
wgk
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
法规信息
新产品
此项目有
Birgit T Priest et al.
Biochemistry, 43(30), 9866-9876 (2004-07-28)
Sodium channel blockers are used clinically to treat a number of neuropathic pain conditions, but more potent and selective agents should improve on the therapeutic index of currently used drugs. In a high-throughput functional assay, a novel sodium channel (Na(V))
T Watanabe et al.
Chemical & pharmaceutical bulletin, 45(9), 1458-1469 (1997-10-23)
A series of succinamide derivatives containing the 5,11-dihydro-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one skeleton (6a-z) was prepared and evaluated for binding affinity to muscarinic receptors in vitro and for antagonism of bradycardia and salivation in vivo in comparison with AF-DX 116 (1a). Structure-activity relationships (SAR)
Elisabeth Garanger et al.
Bioconjugate chemistry, 20(1), 170-173 (2008-12-17)
The biotin/avidin system is one of the most widely used affinity detection and affinity capture systems in biology. However, the determination of the exact number of biotin tags attached onto a substrate is complicated by the fact that biotin does
Hideki Onagi et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 9(24), 5978-5988 (2003-12-18)
Eight new [2]rotaxanes have been prepared, incorporating an alpha-cyclodextrin as the rotor, a stilbene as the axle, and trinitrophenyl substituents as capping groups. Strategies have been devised to elaborate these by linking the rotor to the axle, to produce two
Adaptable synthesis of C-glycosidic multivalent carbohydrates and succinamide-linked derivatization.
Gavin J Miller et al.
Organic letters, 12(22), 5262-5265 (2010-10-22)
A modular approach to the synthesis of trivalent C-glycosidic carbohydrates is described. The approach is illustrated employing carboxylate-terminated C-glycosidic d-mannose, d-glucose, and d-galactose derivatives with different length C1-linked spacer units and also core units with different length linker units attached.
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