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Basic Description
| Synonyms | 2-Deoxy-D-ribose | 533-67-5 | Thyminose | (3S,4R)-3,4,5-trihydroxypentanal | DEOXYRIBOSE | 2-Deoxyribose | 2-Deoxy-D-erythro-pentose | 2-Deoxy-erythro-pentose | 2-Deoxy-D-erythropentose | 1724-14-7 | D-dRib | 2-Deoxy-D-arabinose | D-erythro-Pentose, 2-deoxy- | aldehydo-2-deoxy-D-r |
|---|---|
| Specifications & Purity | 10mM in DMSO |
| Biochemical and Physiological Mechanisms | Reducing sugar used to study processes of oxidative stress and glycation in vivo and in vitro . Induces apoptosis by inhibiting the synthesis and increasing the efflux of glutathione. Endothelial-cell chemoattractant and angiogenesis-inducing factor |
| Storage Temp | Store at -80°C |
| Shipped In |
Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available. |
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
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Superclass
Organic oxygen compounds
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Class
Organooxygen compounds
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Subclass
Carbonyl compounds
- Level5 Aldehydes
- Level6 Beta-hydroxy aldehydes
- Level5 Aldehydes
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Subclass
Carbonyl compounds
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Class
Organooxygen compounds
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Superclass
Organic oxygen compounds
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic oxygen compounds |
| Class | Organooxygen compounds |
| Subclass | Carbonyl compounds |
| Intermediate Tree Nodes | Aldehydes |
| Direct Parent | Beta-hydroxy aldehydes |
| Alternative Parents | Alpha-hydrogen aldehydes Secondary alcohols Polyols Short-chain aldehydes Primary alcohols Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Beta-hydroxy aldehyde - Alpha-hydrogen aldehyde - Secondary alcohol - Polyol - Organic oxide - Hydrocarbon derivative - Short-chain aldehyde - Primary alcohol - Alcohol - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as beta-hydroxy aldehydes. These are organic compounds containing an aldehyde substituted with a hydroxy group on the second carbon atom. |
| External Descriptors | deoxypentose |
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Names and Identifiers
| IUPAC Name | (3S,4R)-3,4,5-trihydroxypentanal |
|---|---|
| INCHI | InChI=1S/C5H10O4/c6-2-1-4(8)5(9)3-7/h2,4-5,7-9H,1,3H2/t4-,5+/m0/s1 |
| InChIKey | ASJSAQIRZKANQN-CRCLSJGQSA-N |
| Smiles | C(C=O)C(C(CO)O)O |
| Isomeric SMILES | C(C=O)[C@@H]([C@@H](CO)O)O |
| WGK Germany | 3 |
| RTECS | SB7230000 |
| Molecular Weight | 134.13 |
| Beilstein | 1721978 |
| Reaxy-Rn | 1904591 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1904591&ln= |
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Chemical and Physical Properties
| Sensitivity | Hygroscopic |
|---|---|
| Specific Rotation[α] | -56 ° (C=1, H2O) |
| Melt Point(°C) | 91°C |
| Molecular Weight | 134.130 g/mol |
| XLogP3 | -2.300 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 4 |
| Exact Mass | 134.058 Da |
| Monoisotopic Mass | 134.058 Da |
| Topological Polar Surface Area | 77.800 Ų |
| Heavy Atom Count | 9 |
| Formal Charge | 0 |
| Complexity | 83.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 2 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
Citations of This Product
| 1. Binbin Zhang, Jiao Ma, Kaide Ou, Xin Cong, Hao Zou, Yonggui Liao, Yajiang Yang, Hong Wang. (2023) Luminescent lanthanide metallogel as a sensor array to efficiently discriminate various saccharides. JOURNAL OF MOLECULAR LIQUIDS, 376 (121447). |
| 2. Zong-Ying Li, Hong-Xia Zhang, Tian-Sheng He, Hong-Xin Jiang, Xiao-Wei Liu, Li-Na Zhu, Xiao-Zeng Li, De-Ming Kong. (2023) A multifunctional and water-stable Cd (II) coordination polymer: Sensitive detection of roxarsone, Fe3+, CrO42− and Cr2O72− in aqueous media. INORGANICA CHIMICA ACTA, 547 (121334). |
| 3. Shi Ning, Liu Qiying, Cen Hu, Ju Rongmei, He Xiong, Ma Longlong. (2020) Formation of humins during degradation of carbohydrates and furfural derivatives in various solvents. Biomass Conversion and Biorefinery, 10 (2): (277-287). |
| 4. Li-Hong Tan, Dan Zhang, Gang Wang, Bao Yu, Sheng-Ping Zhao, Jian-Wei Wang, Ling Yao, Wei-Guo Cao. (2016) Comparative analyses of flavonoids compositions and antioxidant activities of Hawk tea from six botanical origins. INDUSTRIAL CROPS AND PRODUCTS, 80 (123). |
| 5. Yuanfeng Wang, Yangyang Liu, Jianglei Huo, Tingtong Zhao, Jian Ren, Xinlin Wei. (2013) Effect of different drying methods on chemical composition and bioactivity of tea polysaccharides. INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 62 (714). |
| 6. Yuanfeng Wang, Zhiwei Yang, Xinlin Wei. (2012) Antioxidant activities potential of tea polysaccharide fractions obtained by ultra filtration. INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 50 (558). |
| 7. Luo Laipeng, Ding Chenkun, Zhu Qinting, Liu Lei, Wang Ping, Wang Qiang, Yu Yuanyuan. (2024) A Novel Cotton Scouring Using Pectinase in Combination with Fenton System. FIBERS AND POLYMERS, 25 (7): (2669-2682). |
| 8. Yanhui Wang, Huayu Fu, Bangqi Huang, Ziyang Liang, Yijun Shen, Yulan Wang, Jun Wu, Yi Zhao. (2024) Hollow mesoporous Prussian blue nanoenzymes as Rapamycin carrier for targeted treatment of ischemia/reperfusion-induced acute kidney injury through pro-mitophagy and oxidative stress alleviation. CHEMICAL ENGINEERING JOURNAL, 497 (155684). |
| 9. Yushi Wei, Jianmei Wu, Xi Peng, Xing Hu, Deming Gong, Guowen Zhang. (2024) Protein glycosylation inhibitory effects and mechanisms of phloretin and phlorizin. Food Bioscience, 61 (104971). |
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