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Merck
CN

SMB01381

SAICAriboside

≥95% (HPLC), from synthetic, solid

别名:

N-Succinyl-5-aminoimidazole-4-carboxamide Ribose

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关于此项目

经验公式(希尔记法):
C13H18N4O9
化学文摘社编号:
分子量:
374.30
UNSPSC Code:
12352211
NACRES:
NA.26
MDL number:
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biological source

synthetic

Quality Level

assay

≥95% (HPLC)

form

solid

color

white to beige

mp

130-135 °C

storage temp.

2-8°C

SMILES string

NC1=C(C(N[C@H](C(O)=O)CC(O)=O)=O)N=CN1[C@H]2[C@H](O)[C@H](O)[C@@H](CO)O2

InChI

1S/C13H18N4O9/c14-10-7(11(23)16-4(13(24)25)1-6(19)20)15-3-17(10)12-9(22)8(21)5(2-18)26-12/h3-5,8-9,12,18,21-22H,1-2,14H2,(H,16,23)(H,19,20)(H,24,25)/t4-,5+,8+,9+,12+/m0/s1

InChI key

XNKLTOHYNRQCLJ-ZZZDFHIKSA-N

General description

SAICAR (a ribotide) can lose its phosphate group leading to the appearance of a riboside known as succinylaminoimidazolecarboxamide riboside (SAICAriboside or SAICAr) in cerebrospinal fluid, in urine, and, to a lesser extent, in plasma. SAICAriboside is characteristic of ADSL, a heritable deficiency of the enzyme adenylosuccinate lyase (ASL or adenylosuccinase) responsible for metabolizing SAICAR (SZMP) to AICAR (ZMP) and adenylosuccinate (SAMP) to AMP. ASL deficiency causes increased SAICAR & SAMP, and their corresponding rephosphorylated products SAICAr & succinyladenosine (S-Ado).

Preparation Note

Heat sensitive


存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Study of purinosome assembly in cell-based model systems with de novo purine synthesis and salvage pathway deficiencies
Baresova, et al.
PLoS ONE, 13, e0201432-e0201432 (2018)
Roxane Marsac et al.
Genetics, 211(4), 1297-1313 (2019-02-01)
Purine homeostasis is ensured through a metabolic network widely conserved from prokaryotes to humans. Purines can either be synthesized de novo, reused, or produced by interconversion of extant metabolites using the so-called recycling pathway. Although thoroughly characterized in microorganisms, such
A mild form of adenylosuccinate lyase deficiency in absence of typical brain MRI features diagnosed by whole exome sequencing
Macchiaiolo, et al.
Italian Journal of Pediatrics, 43, 65-65 (2017)



全球贸易项目编号

货号GTIN
SMB01381-1MG04065269389491