10 Results for "

organic transformations

" in MedChemExpress (MCE) Product Catalog:
Products (10)

10 Results for "organic transformations" in MCE Product Catalog:

Art. -Nr.: HY-W012218
CAS. Nr.: 5872-08-2
Synonyms: (±)-10-Camphorsulfonic acid
(±)-Camphor-10-sulfonic acid is a racemate of Camphor-10-sulfonic acid. (±)-Camphor-10-sulfonic acid can be used as an organocatalyst in performing a huge array of organic transformations .
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Art. -Nr.: HY-W011579
CAS. Nr.: 4551-69-3
4-Benzoyl-3-methyl-1-phenyl-5-pyrazolone, is a heterocyclic compound with a five-membered ring structure, which can be used as a starting material for organic synthesis, a reagent for organic transformation, and a biological probe for studying biological processes. 4-Benzoyl-3-methyl-1-phenyl-5-pyrazolone is a biomaterial or organic compound that can be used as a research-related biomaterial or organic compound in life sciences .
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Art. -Nr.: HY-W583317
CAS. Nr.: 2375242-78-5
Forschungsgebiete:  

Others

sSPhos Pd G2 is a palladium catalyst with excellent cross-coupling reaction activity. sSPhos Pd G2 exhibits efficient catalytic ability in the synthesis of organic molecules and compounds. sSPhos Pd G2 can effectively promote the formation of CC bonds, optimize reaction conditions and increase yields. sSPhos Pd G2 is also used in a variety of transformation reactions, helping researchers develop new materials and compounds.
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Art. -Nr.: HY-W000808
CAS. Nr.: 123088-59-5
Forschungsgebiete:  

Others

(4-Carbamoylphenyl) boronic acid is a boronic acid derivative bearing an amide functional group, and serves as a precursor for organic transformation reactions .
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Art. -Nr.: HY-120221
CAS. Nr.: 258278-64-7
Forschungsgebiete:  

Cardiovascular Disease

SE 175 is an organic nitrate compound that acts as an NO donor in vivo following reductive transformation of the nitrate group to nitric oxide. SE 175 stimulates endothelial soluble guanylate cyclase and induces aortic vasorelaxation with an EC50 of 0.20 µM .
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Art. -Nr.: HY-W012218R
CAS. Nr.: 5872-08-2
Synonyms: (±)-10-Camphorsulfonic acid (Standard)
Forschungsgebiete:  

Others

(±)-Camphor-10-sulfonic acid (Standard) is the analytical standard of (±)-Camphor-10-sulfonic acid. This product is intended for research and analytical applications. (±)-Camphor-10-sulfonic acid is a racemate of Camphor-10-sulfonic acid. (±)-Camphor-10-sulfonic acid can be used as an organocatalyst in performing a huge array of organic transformations .
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Art. -Nr.: HY-W075731
CAS. Nr.: 2030437-90-0
(Ir[dF (F) ppy]2 (dCF3)) PF6 is a cyclometalated iridium (III) complex that is used in visible light-mediated photocatalytic organic transformations .
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Art. -Nr.: HY-W034053
CAS. Nr.: 808142-88-3
Ir[p-F (Me) ppy]2 (dtbbpy) PF6 is a cyclometalated iridium (III) complex. Ir[p-F (Me) ppy]2 (dtbbpy) PF6 absorbs visible light (460 nm) to form a long-lived charge-separated excited state. Ir[p-F (Me) ppy]2 (dtbbpy) PF6 is applicable to visible light-mediated photocatalytic organic transformation reactions .
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Art. -Nr.: HY-119417A
CAS. Nr.: 1954-81-0
Target:  

Herbicide

Forschungsgebiete:  

Others

Chloramben sodium is a herbicide with anti-growth activity against plants. Chloramben sodium can be effectively removed by photo-Fenton reaction under natural pH conditions, showing good degradation performance. The removal rate of chloramben sodium is consistent with different electrodes, mainly due to the oxidation mediated by the hydroxyl ions formed in the Fenton reaction. Chloramben sodium is almost completely mineralized using IrO2-based electrodes at high current density, indicating that it can be effectively degraded under light. Chloramben sodium leads to the formation of persistent chlorine derivatives in chlorine-containing environments, so the removal rate and mineralization rate are slightly reduced. Chloramben sodium can form intermediates with a variety of aromatic compounds and organic acids, reflecting the complexity of its transformation in the environment .
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Art. -Nr.: HY-L189
350 compounds

Amino acids, as one of the most fundamental organic compounds in living organisms, serve not only as the basic building blocks of proteins but also but also undertake the functions of energy supply, neurotransmitter synthesis, and maintenance of internal environment stability.Amino acid metabolic enzymes are a class of enzymes involved in the metabolic processes of amino acids, catalyzing their synthesis, breakdown, transformation, and interactions with other metabolic pathways. Abnormalities in amino acid metabolic enzymes can lead to various metabolic diseases, such as phenylketonuria and hyperammonemia, etc. Therefore, actively exploring and regulating the processes of amino acid metabolism is crucial for the development of drugs related to these diseases.

MCE designs a unique collection of 350 small molecules target amino acid metabolizing enzymes, which is an important tool for studying studying amino acid metabolism processes or metabolism-related drug development.