deoxyribose

A deoxyribonucleoside is a type of nucleoside including deoxyribose as a component.

Deoxyribonucleotides are nucleotides in which the sugar is deoxyribose.

Each nucleotide has protons on the deoxyribose sugar, which can be assigned using sequential walking.

If cytosine is attached to a deoxyribose ring, it is known as a deoxycytidine.

Deoxyribose is generated from ribose 5-phosphate by enzymes called ribonucleotide reductases.

These enzymes reduce the sugar residue from ribose to deoxyribose by removing oxygen.

The related deoxyribose is a component of DNA.

These terms refer to the carbon atom in deoxyribose to which the next phosphate in the chain attaches.

Stereoselective synthesis of deoxyribonucleosides directly from deoxyribose derivatives is more difficult to achieve because neighboring group participation cannot take place.

In molecular biology, the prime is used to denote the positions of carbon on a ring of deoxyribose or ribose.

Amino acids are left-handed, nucleic acid sugars (ribose and deoxyribose) right-handed.

When guanine is attached by its N9 nitrogen to the C1 carbon of a deoxyribose ring it is known as deoxyguanosine.

The 3'hydroxyl group in the deoxyribose ring of thymidine is replaced by an azido group which gives us zidovudine.

TMP consists of a phosphate group, the pentose sugar deoxyribose, and the nucleobase thymine.

Purines and pyrimidines, ribose and deoxyribose were all well in this range, and we shall discuss the essential role they play.

Energy stored in this bond is subsequently used for the rejoining of the DNA to the corresponding deoxyribose hydroxyl group on the other site.

Thymine combined with deoxyribose creates the nucleoside deoxythymidine, which is synonymous with the term thymidine.

In its composition, deoxythymidine is a nucleoside composed of deoxyribose (a pentose sugar) joined to the pyrimidine base thymine.

Nucleosides are glycosylamines made by attaching a nucleobase (often referred to simply as bases) to a ribose or deoxyribose (sugar) ring.

Deoxyguanosine is composed of the purine nucleoside guanine linked by its N9 nitrogen to the C1 carbon of deoxyribose.

In ribonucleotides, the sugar component is ribose while in deoxyribonucleotides, the sugar component is deoxyribose.

One end of a DNA polymer contains an exposed hydroxyl group on the deoxyribose; this is known as the 3' end of the molecule.

With few exceptions (e.g., deoxyribose), monosaccharides have this chemical formula: C(HO), where conventionally x 3.

Ribose is a constituent of RNA, and the related deoxyribose of DNA.

In the backbone of DNA the 5' carbon of one deoxyribose is linked to the 3' carbon of another by a phosphate group.