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adenosine 5'-O-(3-thiotriphosphate) [Supplementary Concept]
RN given refers to cpd with unspecified locant for thio group; see also records for 1-thio & 2-thio-isomers
Date introduced: January 1, 1978
Affinity Labels
Analogs of those substrates or compounds which bind naturally at the active sites of proteins, enzymes, antibodies, steroids, or physiological receptors. These analogs form a stable covalent bond at the binding site, thereby acting as inhibitors of the proteins or steroids.
Year introduced: 1975
Ribonucleotides
Nucleotides in which the purine or pyrimidine base is combined with ribose. (Dorland, 28th ed)
Year introduced: 1973(1971)
Purines
A series of heterocyclic compounds that are variously substituted in nature and are known also as purine bases. They include ADENINE and GUANINE, constituents of nucleic acids, as well as many alkaloids such as CAFFEINE and THEOPHYLLINE. Uric acid is the metabolic end product of purine metabolism.
Purine Nucleotides
Purines attached to a RIBOSE and a phosphate that can polymerize to form DNA and RNA.
Year introduced: 1974(1972)
Nucleotides
The monomeric units from which DNA or RNA polymers are constructed. They consist of a purine or pyrimidine base, a pentose sugar, and a phosphate group. (From King and Stansfield, A Dictionary of Genetics, 4th ed)
Nucleic Acids, Nucleotides, and Nucleosides
Complex compounds of high molecular weight occurring in living cells. These are basically of two types, ribonucleic (RNA) and deoxyribonucleic (DNA) acids, both of which consist of nucleotides (nucleoside phosphates linked together by phosphate bridges).
Year introduced: 1998
Heterocyclic Compounds, 2-Ring
A class of heterocyclic compounds that include a two-ring fused structure. Both aromatic and non-aromatic ring structures are included in this category.
Heterocyclic Compounds
Cyclic compounds that include atoms other than carbon in their ring structure.
Adenine Nucleotides
Heterocyclic Compounds, Fused-Ring
Multiple ring heterocyclic compounds containing two or more rings that share two atoms and one bond in common.
Year introduced: 2017
Specialty Uses of Chemicals
Uses of chemicals in a research, industrial, or household setting. This does not include PHARMACOLOGIC ACTIONS.
Year introduced: 2004(1999)
Chemical Actions and Uses
A group of pharmacologic activities, effects on living systems and the environment, and modes of employment of drugs and chemicals. They are broken into actions, which describe their effects, and uses, which describe how they are employed.
Year introduced: 1999
Laboratory Chemicals
Chemicals necessary to perform experimental and/or investigative procedures and for the preparation of drugs and other chemicals.
Indicators and Reagents
Substances used for the detection, identification, analysis, etc. of chemical, biological, or pathologic processes or conditions. Indicators are substances that change in physical appearance, e.g., color, at or approaching the endpoint of a chemical titration, e.g., on the passage between acidity and alkalinity. Reagents are substances used for the detection or determination of another substance by chemical or microscopical means, especially analysis. Types of reagents are precipitants, solvents, oxidizers, reducers, fluxes, and colorimetric reagents. (From Grant and Hackh's Chemical Dictionary, 5th ed, p301, p499)