Deoxyribose

d-deoxyribose
Names
	IUPAC name 2-deoxy-d-ribose
	Other names 2-deoxy-d-erythro-pentose; thyminose
Identifiers
CAS Number	533-67-5 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:28816 ;
ChemSpider	4573703 ;
EC Number	208-573-0;
PubChem CID	5460005;
UNII	LSW4H01241 ;
CompTox Dashboard (EPA)	DTXSID60190259 ;
	InChI InChI=1S/C5H10O4/c6-2-1-4(8)5(9)3-7/h2,4-5,7-9H,1,3H2/t4-,5+/m0/s1 Key: ASJSAQIRZKANQN-CRCLSJGQSA-N ; InChI=1/C5H10O4/c6-2-1-4(8)5(9)3-7/h2,4-5,7-9H,1,3H2/t4-,5+/m0/s1 Key: ASJSAQIRZKANQN-CRCLSJGQBK;
	SMILES C(C=O)[C@@H]([C@@H](CO)O)O;
Properties
Chemical formula	C5H10O4
Molar mass	134.131 g·mol−1
Appearance	White solid
Melting point	91 °C (196 °F; 364 K)
Solubility in water	Very soluble
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Deoxyribose, or more precisely 2-deoxyribose, is a monosaccharide with idealized formula H−(C=O)−(CH₂)−(CHOH)₃−H. Its name indicates that it is a deoxy sugar, meaning that it is derived from the sugar ribose by loss of a hydroxy group. Discovered in 1929 by Phoebus Levene,^[2] deoxyribose is most notable for its presence in DNA. Since the pentose sugars arabinose and ribose only differ by the stereochemistry at C2′, 2-deoxyribose and 2-deoxyarabinose are equivalent, although the latter term is rarely used because ribose, not arabinose, is the precursor to deoxyribose.

Structure

Several isomers exist with the formula H−(C=O)−(CH₂)−(CHOH)₃−H, but in deoxyribose all the hydroxyl groups are on the same side in the Fischer projection. The term "2-deoxyribose" may refer to either of two enantiomers: the biologically important d-2-deoxyribose and to the rarely encountered mirror image l-2-deoxyribose.^[3] d-2-deoxyribose is a precursor to the nucleic acid DNA. 2-deoxyribose is an aldopentose, that is, a monosaccharide with five carbon atoms and having an aldehyde functional group.

In aqueous solution, deoxyribose primarily exists as a mixture of three structures: the linear form H−(C=O)−(CH₂)−(CHOH)₃−H and two ring forms, deoxyribofuranose ("C3′-endo"), with a five-membered ring, and deoxyribopyranose ("C2′-endo"), with a six-membered ring. The latter form is predominant (whereas the C3′-endo form is favored for ribose).

Biological importance

As a component of DNA, 2-deoxyribose derivatives have an important role in biology.^[4] The DNA (deoxyribonucleic acid) molecule, which is the main repository of genetic information in life, consists of a long chain of deoxyribose-containing units called nucleotides, linked via phosphate groups. In the standard nucleic acid nomenclature, a DNA nucleotide consists of a deoxyribose molecule with an organic base (usually adenine, thymine, guanine or cytosine) attached to the 1′ ribose carbon. The 5′ hydroxyl of each deoxyribose unit is replaced by a phosphate (forming a nucleotide) that is attached to the 3′ carbon of the deoxyribose in the preceding unit.

The absence of the 2′ hydroxyl group in deoxyribose is apparently responsible for the increased mechanical flexibility of DNA compared to RNA, which allows it to assume the double-helix conformation, and also (in the eukaryotes) to be compactly coiled within the small cell nucleus. The double-stranded DNA molecules are also typically much longer than RNA molecules. The backbone of RNA and DNA are structurally similar, but RNA is single stranded, and made from ribose as opposed to deoxyribose.

Other biologically important derivatives of deoxyribose include mono-, di-, and triphosphates, as well as 3′-5′ cyclic monophosphates.

Biosynthesis

Deoxyribose is generated from ribose 5-phosphate by enzymes called ribonucleotide reductases. These enzymes catalyse the deoxygenation process.

Angiogenesis

In one study, deoxyribose was shown to have pro-angiogenic properties when applied topically in a gel to wounds in rats.^[5] In addition, this topical gel also increased Vascular Endothelial Growth Factor (VEGF), which has been implicated in hair growth.^[6] This could potentially lead to future products to treat hair loss in humans.

References

^ The Merck Index: An Encyclopedia of Chemicals, Drugs, and Biologicals (11th ed.). Merck. 1989. ISBN 091191028X., 2890
^ "Comprehensive Timeline of Biological Discoveries" (PDF). Archived from the original (PDF) on 10 September 2016. Retrieved 31 July 2017.
^ C Bernelot-Moens and B Demple (1989), Multiple DNA repair activities for 3′-deoxyribose fragments in Escherichia coli. Nucleic Acids Research, Volume 17, issue 2, p. 587–600.
^ C.Michael Hogan. 2010. Deoxyribonucleic acid. Encyclopedia of Earth. National Council for Science and the Environment. eds. S.Draggan and C.Cleveland. Washington DC
^ Serkan Dikici, Yar, M., Bullock, A. J., Shepherd, J., Roman, S., & MacNeil, S. (2021). Developing Wound Dressings Using 2-deoxy-D-Ribose to Induce Angiogenesis as a Backdoor Route for Stimulating the Production of Vascular Endothelial Growth Factor. International Journal of Molecular Sciences, 22(21), 11437–11437. https://doi.org/10.3390/ijms222111437
^ Yano, K., Brown, L. F., & Detmar, M. (2001). Control of hair growth and follicle size by VEGF-mediated angiogenesis. Journal of Clinical Investigation, 107(4), 409–417. https://doi.org/10.1172/jci11317

[1] The Merck Index: An Encyclopedia of Chemicals, Drugs, and Biologicals (11th ed.). Merck. 1989. ISBN 091191028X., 2890

[levene-2] "Comprehensive Timeline of Biological Discoveries" (PDF). Archived from the original (PDF) on 10 September 2016. Retrieved 31 July 2017.

[moens-3] C Bernelot-Moens and B Demple (1989), Multiple DNA repair activities for 3′-deoxyribose fragments in Escherichia coli. Nucleic Acids Research, Volume 17, issue 2, p. 587–600.

[4] C.Michael Hogan. 2010. Deoxyribonucleic acid. Encyclopedia of Earth. National Council for Science and the Environment. eds. S.Draggan and C.Cleveland. Washington DC

[5] Serkan Dikici, Yar, M., Bullock, A. J., Shepherd, J., Roman, S., & MacNeil, S. (2021). Developing Wound Dressings Using 2-deoxy-D-Ribose to Induce Angiogenesis as a Backdoor Route for Stimulating the Production of Vascular Endothelial Growth Factor. International Journal of Molecular Sciences, 22(21), 11437–11437. https://doi.org/10.3390/ijms222111437

[6] Yano, K., Brown, L. F., & Detmar, M. (2001). Control of hair growth and follicle size by VEGF-mediated angiogenesis. Journal of Clinical Investigation, 107(4), 409–417. https://doi.org/10.1172/jci11317

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