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重要文件

N6506

Sigma-Aldrich

烟酰胺次黄嘌呤二核苷酸 钠盐

≥92%

同義詞:

脱氨基DPN, 脱氨基NAD, 脱氨基二磷酸吡啶核苷酸

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About This Item

經驗公式(希爾表示法):
C21H26N6O15P2
CAS號碼:
分子量::
664.41
MDL號碼:
分類程式碼代碼:
41106305
PubChem物質ID:
NACRES:
NA.51

化驗

≥92%

形狀

powder

儲存溫度

−20°C

SMILES 字串

[Na].NC(=O)C1=CC=C[N](=C1)C2OC(COP(O)(=O)OP(O)(=O)OCC3OC(C(O)C3O)n4cnc5C(=O)N=CNc45)C(O)C2O

InChI

1S/C21H27N6O15P2.Na.H/c22-17(32)9-2-1-3-26(4-9)20-15(30)13(28)10(40-20)5-38-43(34,35)42-44(36,37)39-6-11-14(29)16(31)21(41-11)27-8-25-12-18(27)23-7-24-19(12)33;;/h1-4,7-8,10-11,13-16,20-21,28-31H,5-6H2,(H2,22,32)(H,34,35)(H,36,37)(H,23,24,33);;

InChI 密鑰

XVDVDRZCJWZVDL-UHFFFAOYSA-N

相關類別

應用

烟酰胺次黄嘌呤二核苷酸(deamino-NAD)可用于研究NADH:泛醌氧化还原酶的特异性和动力学。

其他說明

β-NAD类似物

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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Jiwon Kang et al.
Journal of biochemistry and molecular biology, 40(1), 53-57 (2007-01-25)
The enzymatic properties of NADH:quinone oxidoreductase were examined in Triton X-100 extracts of Bacillus cereus membranes by using the artificial electron acceptors ubiquinone-1 and menadione. Membranes were prepared from B. cereus KCTC 3674 grown aerobically on a complex medium and
Kenji Kawahara et al.
Journal of biochemistry, 145(2), 229-237 (2008-12-09)
In the intraerythrocytic stages of malaria parasites, mitochondria lack obvious cristae and are assumed to derive energy through glycolysis. For understanding of parasite energy metabolism in mammalian hosts, we isolated rodent malaria mitochondria from Plasmodium yoelii yoelii grown in mice.
Jukka Pätsi et al.
The Biochemical journal, 409(1), 129-137 (2007-09-27)
LHON (Leber hereditary optic neuropathy) is a maternally inherited disease that leads to sudden loss of central vision at a young age. There are three common primary LHON mutations, occurring at positions 3460, 11778 and 14484 in the human mtDNA
Rosa Pello et al.
Human molecular genetics, 17(24), 4001-4011 (2008-09-23)
Leber's hereditary optic neuropathy (LHON), the most frequent mitochondrial disorder, is mostly due to three mitochondrial DNA (mtDNA) mutations in respiratory chain complex I subunit genes: 3460/ND1, 11778/ND4 and 14484/ND6. Despite considerable clinical evidences, a genetic modifying role of the
Pilvi Maliniemi et al.
Mitochondrion, 9(6), 394-401 (2009-07-21)
Seven of the 45 subunits of mitochondrial NADH:ubiquinone oxidoreductase (complex I) are mitochondrially encoded and have been shown to harbor pathogenic mutations. We modeled the human disease-associated mutations A4136G/ND1-Y277C, T4160C/ND1-L285P and C4171A/ND1-L289M in a highly conserved region of the fourth

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