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  2. Homocysteine thiolactone - Wikipedia

    en.wikipedia.org/wiki/Homocysteine_thiolactone

    Homocysteine thiolactone (HTL) is an organosulfur compound with the formula H 2 NCHC(O)SCH 2 CH 2. It is the thiolactone (intramolecular thioester ) of homocysteine . It is produced by methionyl-tRNA synthetase in an error-editing reaction that prevents translational incorporation of homocysteine into proteins .

  3. Homocysteine - Wikipedia

    en.wikipedia.org/wiki/Homocysteine

    Homocysteine can cyclize to give homocysteine thiolactone, a five-membered heterocycle. Because of this "self-looping" reaction, homocysteine-containing peptides tend to cleave themselves by reactions generating oxidative stress. [12] Homocysteine also acts as an allosteric antagonist at Dopamine D 2 receptors. [13]

  4. Thiolactone - Wikipedia

    en.wikipedia.org/wiki/Thiolactone

    The activation of the drug clopidogrel (top left) gives a thiolactone, which ring-opens. [3] Thiolactones are intermediates in the activation of some drugs. [4] In nature, the most common thiolactone is homocysteine thiolactone. It is produced from homocysteine. It may play a role in protein damage. [5]

  5. Transsulfuration pathway - Wikipedia

    en.wikipedia.org/wiki/Transsulfuration_pathway

    Reaction 5 is catalyzed by cystathionine beta-synthase while reaction 6 is catalyzed by cystathionine gamma-lyase. The required homocysteine is synthesized from methionine in reactions 1, 2, and 3. The transsulfuration pathway is a metabolic pathway involving the interconversion of cysteine and homocysteine through the intermediate cystathionine.

  6. Transmethylation - Wikipedia

    en.wikipedia.org/wiki/Transmethylation

    Transmethylation is a biologically important organic chemical reaction in which a methyl group is transferred from one compound to another. An example of transmethylation is the recovery of methionine from homocysteine. In order to sustain sufficient reaction rates during metabolic stress, this reaction requires adequate levels of vitamin B 12 ...

  7. On-water reaction - Wikipedia

    en.wikipedia.org/wiki/On-water_reaction

    The reaction of quadricyclane with DEAD is a 2σ + 2σ + 2π cycloaddition that on water takes place within 10 minutes at room temperature with 82% yield. The same reaction in toluene takes 24 hours at 80 °C with 70% yield. An emulsion reaction in fluorinated cyclohexane takes 36 hours and the neat reaction takes even longer (48 hours).

  8. Bleomycin hydrolase - Wikipedia

    en.wikipedia.org/wiki/Bleomycin_hydrolase

    642 104184 Ensembl ENSG00000108578 ENSMUSG00000020840 UniProt Q13867 Q8R016 RefSeq (mRNA) NM_000386 NM_178645 RefSeq (protein) NP_000377 NP_848760 Location (UCSC) Chr 17: 30.25 – 30.29 Mb Chr 11: 76.82 – 76.88 Mb PubMed search Wikidata View/Edit Human View/Edit Mouse Bleomycin hydrolase is an enzyme that in humans is encoded by the BLMH gene. Bleomycin hydrolase (BMH) is a cytoplasmic ...

  9. Solvation shell - Wikipedia

    en.wikipedia.org/wiki/Solvation_shell

    The number of solvent molecules surrounding each unit of solute is called the hydration number of the solute. A classic example is when water molecules arrange around a metal ion. If the metal ion is a cation, the electronegative oxygen atom of the water molecule would be attracted electrostatically to the positive charge on the metal ion. The ...