(Q105216650)

English

2,3,4,5-tetrahydroxypentanal

group of isomers

aldehydo-arabinose

In more languages

Statements

group of stereoisomers

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150.05282342 dalton

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based on heuristic

inferred from SMILES

chemical formula

C₅H₁₀O₅

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canonical SMILES

O=CC(O)C(O)C(O)CO

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1 reference

Isolation and Structure Assignment of an Iminotetrasaccharide from a Cultured Filamentous CyanobacteriumAnabaenasp.†

Escherichia coli

1 reference

Metabolism of d-Arabinose by Escherichia coli B/r

Arabidopsis thaliana

2 references

Characterization of two novel aldo-keto reductases from Arabidopsis: expression patterns, broad substrate specificity, and an open active-site structure suggest a role in toxicant metabolism following stress

The biosynthesis of L-arabinose in plants: molecular cloning and characterization of a Golgi-localized UDP-D-xylose 4-epimerase encoded by the MUR4 gene of Arabidopsis

Athrotaxis cupressoides

1 reference

Die Chemie der Natürlichen Ordnung Cupressales. XXXII. Über die Inhaltsstoffe des Kernholzes von Athrotaxis selaginoides Don, Athrotaxis cupressoides Don und Chamaecyparis pisifera Sieb et. Zucc.

Athrotaxis selaginoides

1 reference

Die Chemie der Natürlichen Ordnung Cupressales. XXXII. Über die Inhaltsstoffe des Kernholzes von Athrotaxis selaginoides Don, Athrotaxis cupressoides Don und Chamaecyparis pisifera Sieb et. Zucc.

Streptomyces hainanensis

1 reference

Streptomyces hainanensis sp. nov., a novel member of the genus Streptomyces

Identifiers

InChI=1S/C5H10O5/c6-1-3(8)5(10)4(9)2-7/h1,3-5,7-10H,2H2

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PYMYPHUHKUWMLA-UHFFFAOYSA-N

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CAS Registry Number

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CAS Common Chemistry

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mapping relation type

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ChEBI release 2021-03-01

UniChem compound ID

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Probes And Drugs ID

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