Pyrimidine analogues are antimetabolites which mimic the structure of metabolic pyrimidines.
Examples
Medical uses
Pyrimidine antimetabolites are commonly used to treat cancer by interfering with DNA replication.[1]
References
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Receptor (ligands) | | P0 (adenine) | |
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P1 (adenosine) |
- Agonists: 2-(1-Hexynyl)-N-methyladenosine
- 2-Cl-IB-MECA
- 2-Chloroadenosine
- 2'-MeCCPA
- 4'-O-β-D-Glucosyl-9-O-(6''-deoxysaccharosyl)olivil
- 5'-N-ethylcarboxamidoadenosine
- Adenosine
- ADP
- AMP
- Apadenoson
- ATL-146e
- ATP
- BAY 60–6583
- Binodenoson
- Capadenoson
- CCPA
- CGS-21680
- CP-532,903
- CV-1808
- Evodenoson
- GR 79236
- HENECA
- LUF-5835
- LUF-5845
- N6-Cyclopentyladenosine
- Namodenoson
- NECA
- Neladenoson dalanate
- Piclidenoson
- Regadenoson
- SDZ WAG 994
- Selodenoson
- Sonedenoson
- Tecadenoson
- Trabodenoson
- UK-432,097
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P2 (nucleotide) | |
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Transporter (blockers) | | CNTsTooltip Concentrative nucleoside transporters | |
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| ENTsTooltip Equilibrative nucleoside transporters | |
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| PMATTooltip Plasma membrane monoamine transporter | |
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Enzyme (inhibitors) | | XOTooltip Xanthine oxidase | |
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| Others | |
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| Others | |
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See also: Receptor/signaling modulators |