124753
Succinamide
98%
Sinônimo(s):
Succinic diamide
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About This Item
Fórmula linear:
NH2COCH2CH2CONH2
Número CAS:
Peso molecular:
116.12
Beilstein:
1753983
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22
Produtos recomendados
Nível de qualidade
Ensaio
98%
pf
260-265 °C (dec.) (lit.)
solubilidade
cold water: soluble 220 part
boiling water: soluble 9 part
alcohol: insoluble
diethyl ether: insoluble
grupo funcional
amide
cadeia de caracteres SMILES
NC(=O)CCC(N)=O
InChI
1S/C4H8N2O2/c5-3(7)1-2-4(6)8/h1-2H2,(H2,5,7)(H2,6,8)
chave InChI
SNCZNSNPXMPCGN-UHFFFAOYSA-N
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Categorias relacionadas
Aplicação
Succinamide has been used in the characterization of a novel biuret hydrolase from the cysteine hydrolase superfamily. It was used as nitrogen supplement in the culture medium of Scenedesmus obliquus and green algae.
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
Equipamento de proteção individual
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
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Modulation of mitochondrial respiratory chain, dehydrogenase, and nucleotide-metabolizing enzyme activities is fundamental to cellular protection. Here, we demonstrate that the potassium channel opener diazoxide, within its cardioprotective concentration range, modulated the activity of flavin adenine dinucleotide-dependent succinate dehydrogenase with an
T Watanabe et al.
Chemical & pharmaceutical bulletin, 45(6), 996-1007 (1997-06-01)
A series of 5,11-dihydro-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one derivatives containing the succinamide skeleton has been synthesized and evaluated for M1, M2 and M3 muscarinic receptor binding affinities (in vitro) and M2 and M3 muscarinic receptor antagonistic activities (in vivo). Some of them showed higher
Xiaobin Zhang et al.
Drug delivery, 11(5), 301-309 (2005-03-04)
To investigate the effect of RMP-7 and its derivative on drug transport across blood brain barrier (BBB), RMP-7 and DSPE-PEG-NHS [1,2-dioleoyl-sn-glycero-3-phosphoethanolamine-n-[poly(ethyleneglycol)]-hydroxy succinamide, PEG M 3400] were conjugated under mild conditions and the reaction ratio was determined using MALDI-TOF-MS (matrix-assisted laser
Olaf F A Larsen et al.
Proceedings of the National Academy of Sciences of the United States of America, 102(38), 13378-13382 (2005-09-10)
Femtosecond 2D-IR spectroscopy has been used to study the structure of a [2]rotaxane composed of a benzylic amide macrocycle that is mechanically interlocked onto a succinamide-based thread. Both the macrocycle and the thread contain carbonyl groups, and by determining the
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