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Dihydrofolate reductase inhibitor

From Wikipedia, the free encyclopedia
Cellular enzyme inhibitor

Adihydrofolate reductase inhibitor (DHFR inhibitor) is a molecule that inhibits the function ofdihydrofolate reductase, and is a type ofantifolate.

Since folate is needed by rapidly dividing cells to makethymine, this effect may be used to therapeutic advantage. For example,methotrexate is used as cancer chemotherapy because it can preventneoplastic cells from dividing.[1][2] Bacteria also need DHFR to grow and multiply and hence inhibitors selective for bacterial vs. host DHFR have found application as antibacterial agents.[3]

Tetrahydrofolate synthesis pathway

Classes of small-molecules employed as inhibitors of dihydrofolate reductase include diaminoquinazoline and diaminopyrroloquinazoline, Most of the above specified inhibitors are structural analogues of the substrate dihydrofolate and bind to the active site of the enzyme. Further, it has been recently shown that, inE. coli DHFR, allosteric site binders can inhibit the enzyme either uncompetitively or non-competitively. The examples provided below are specific molecules belonging to one of the above-mentioned classes.

References

[edit]
  1. ^Huennekens FM (1994). "The methotrexate story: a paradigm for development of cancer chemotherapeutic agents".Advances in Enzyme Regulation.34:397–419.doi:10.1016/0065-2571(94)90025-6.PMID 7942284.
  2. ^McGuire JJ (2003)."Anticancer antifolates: current status and future directions".Current Pharmaceutical Design.9 (31):2593–613.doi:10.2174/1381612033453712.PMID 14529544.
  3. ^Hawser S, Lociuro S, Islam K (March 2006). "Dihydrofolate reductase inhibitors as antibacterial agents".Biochemical Pharmacology.71 (7):941–8.doi:10.1016/j.bcp.2005.10.052.PMID 16359642.
  4. ^Mui EJ, Schiehser GA, Milhous WK, Hsu H, Roberts CW, Kirisits M, Muench S, Rice D, Dubey JP, Fowble JW, Rathod PK, Queener SF, Liu SR, Jacobus DP, McLeod R (March 2008)."Novel triazine JPC-2067-B inhibits Toxoplasma gondii in vitro and in vivo".PLOS Neglected Tropical Diseases.2 (3): e190.doi:10.1371/journal.pntd.0000190.PMC 2254147.PMID 18320016.
  5. ^de Wit R, Kaye SB, Roberts JT, Stoter G, Scott J, Verweij J (February 1993)."Oral piritrexim, an effective treatment for metastatic urothelial cancer".British Journal of Cancer.67 (2):388–90.doi:10.1038/bjc.1993.71.PMC 1968166.PMID 8431372.
Class
Substrate
Oxidoreductase (EC 1)
Transferase (EC 2)
Hydrolase (EC 3)
Lyase (EC 4)
Miscellaneous
SPs/MIs
(M phase)
Blockmicrotubule assembly
Block microtubule disassembly
DNA replication
inhibitor
DNA precursors/
antimetabolites
(S phase)
Folic acid
Purine
Pyrimidine
Deoxyribonucleotide
Topoisomerase inhibitors
(S phase)
I
II
II+Intercalation
Crosslinking of DNA
(CCNS)
Alkylating
Platinum-based
Nonclassical
Intercalation
Photosensitizers/PDT
Other
Enzyme inhibitors
Receptor antagonists
Other/ungrouped
Antifolates
(inhibit bacterial
purine metabolism,
thereby inhibiting
DNA and RNA
synthesis)
DHFR inhibitor
Sulfonamides
(DHPS inhibitor)
Short-acting
Intermediate-acting
Long-acting
Other/ungrouped
Combinations
Other DHPS inhibitors
Quinolones
(inhibit bacterial
topoisomerase
and/orDNA gyrase,
thereby inhibiting
DNA replication)
1st generation
Fluoroquinolones
2nd generation
3rd generation
4th generation
Veterinary
Newer non-fluorinated
Related (DG)
Anaerobic DNA
inhibitors
Nitroimidazole derivatives
RNA synthesis
Rifamycins/
RNA polymerase
Lipiarmycins
Alveo-
late
Apicom-
plexa
Conoidasida/
(Coccidiostats)
Cryptosporidiosis
Isosporiasis
Toxoplasmosis
Aconoidasida
Malaria
Individual
agents
Hemozoin
inhibitors
Aminoquinolines
4-Methanolquinolines
Other
Antifolates
DHFR inhibitors
Sulfonamides
Co-formulation
Sesquiterpene
lactones
Other
Combi-
nations
Fixed-dose (co-formulated)ACTs
Other combinations
(not co-formulated)
  • artesunate/mefloquine
  • artesunate/SP
  • quinine/clindamycin
  • quinine/doxycycline
  • quinine/tetracycline
Babesiosis
Cilio-
phora
Stramen-
opile
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