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R1757

D-(-)-核糖

Name: <SC>D</SC>-(-)-核糖
Brand: ALDRICH

98%

别名:

D-Ribose

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关于此项目

经验公式（希尔记法）:

C₅H₁₀O₅

化学文摘社编号:

50-69-1

分子量:

150.13

UNSPSC Code:

12352201

NACRES:

NA.22

PubChem Substance ID:

24899349

EC Number:

200-059-4

Beilstein/REAXYS Number:

1723081

MDL number:

MFCD00135453

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属性

Quality Level

100

assay

98%

optical activity

[α]20/D −19.7°, c = 4 in H₂O

mp

88-92 °C (lit.)

SMILES string

OC[C@@H](O)[C@@H](O)[C@@H](O)C([H])=O

InChI

1S/C5H10O5/c6-1-3(8)5(10)4(9)2-7/h1,3-5,7-10H,2H2/t3-,4+,5-/m0/s1

InChI key

PYMYPHUHKUWMLA-LMVFSUKVSA-N

说明

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存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

法规信息

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O-Aryl α,β-d-ribofuranosides: synthesis & highly efficient biocatalytic separation of anomers and evaluation of their Src kinase inhibitory activity.

Raman K Sharma et al.

Bioorganic & medicinal chemistry, 20(23), 6821-6830 (2012-10-27)

A series of peracetylated O-aryl α,β-d-ribofuranosides have been synthesized and an efficient biocatalytic methodology has been developed for the separation of their anomers which was otherwise almost impossible by column chromatographic or other techniques. The incubation of 2,3,5-tri-O-acetyl-1-O-aryl-α,β-d-ribofuranoside with Lipozyme®

Translating the concept of peptide labeling with 5-deoxy-5-[18F]fluororibose into preclinical practice: 18F-labeling of Siglec-9 peptide for PET imaging of inflammation.

Xiang-Guo Li et al.

Chemical communications (Cambridge, England), 49(35), 3682-3684 (2013-03-29)

Peptide glycosylation with 5-deoxy-5-[(18)F]fluororibose was translated into preclinical settings. The novel (18)F-labeled Siglec-9 peptide was produced using an automated synthesis procedure. The (18)F-labeled Siglec-9 peptide showed favorable binding in the animal model of inflammation in vivo.

The biolabile 2'-O-pivaloyloxymethyl modification in an RNA helix: an NMR solution structure.

Carine Baraguey et al.

Organic & biomolecular chemistry, 11(16), 2638-2647 (2013-03-05)

The pivaloyloxymethyl (PivOM) group is a biolabile 2'-O-ribose protection that is under development in a prodrug-based approach for siRNA applications. Besides an expected cellular uptake, nucleic acid sequences carrying PivOM showed also increased nuclease resistance and, in most cases, an

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全球贸易项目编号

货号	GTIN
R1757-100G-A	04061836694470
R1757-25G-A	04061836694494
R1757-10G-A	04061836694487