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  2. Sacubitril - Wikipedia

    en.wikipedia.org/wiki/Sacubitril

    Sacubitril is a prodrug that is activated to sacubitrilat (LBQ657) by de-ethylation via esterases. [2] Sacubitrilat inhibits the enzyme neprilysin, [3] which is responsible for the degradation of atrial and brain natriuretic peptide, two blood pressure–lowering peptides that work mainly by reducing blood volume. [4]

  3. Methyl isonicotinate - Wikipedia

    en.wikipedia.org/wiki/Methyl_isonicotinate

    Methyl isonicotinate is a toxic compound, which is used as a semiochemical. Other names for this compound are 4-pyridine carboxylic acid, and isonicotinic acid methyl ester. [1] [2] [3] This compound is slightly toxic to the human body. It has an irritating effect on the eyes, skin, and respiratory tract. [4]

  4. Bisphenol - Wikipedia

    en.wikipedia.org/wiki/Bisphenol

    Bisphenols A (BPA), F (BPF) and S (BPS) have been shown to be endocrine disruptors, potentially relating to adverse health effects. [3] [6] Due to its high production volumes, BPA has been characterised as a "pseudo-persistent" chemical, [7] leading to its spreading and potential accumulation in a variety of environmental matrices, even though it has a fairly short half-life.

  5. Picolinic acid - Wikipedia

    en.wikipedia.org/wiki/Picolinic_acid

    Picolinic acid is an organic compound with the formula NC 5 H 4 CO 2 H. It is a derivative of pyridine with a carboxylic acid (COOH) substituent at the 2-position. It is an isomer of nicotinic acid and isonicotinic acid, which have the carboxyl side chain at the 3- and 4-positions, respectively. It is a white solid although impure samples can ...

  6. Dioxolane - Wikipedia

    en.wikipedia.org/wiki/Dioxolane

    The ketal is produced by acid catalysed reaction with ethylene glycol, the reduction reaction carried out, and the protecting group removed by hydrolysis to produce 4-hydroxymethylcyclohexanone. NaBArF 4 can also be used for deprotection of acetal or ketal-protected carbonyl compounds. [6] [7] For example, deprotection of 2-phenyl-1,3-dioxolane ...

  7. Brequinar - Wikipedia

    en.wikipedia.org/wiki/Brequinar

    Brequinar has been investigated as an immunosuppressant for preventing rejection after organ transplant and also as an anti-cancer drug, but was not accepted for medical use in either application largely due to its narrow therapeutic dose range and severe side effects when dosed inappropriately. [3] [4] It has been researched both as part of a ...

  8. Fluorenylmethyloxycarbonyl protecting group - Wikipedia

    en.wikipedia.org/wiki/Fluorenylmethyloxycarbonyl...

    [4] Reacting with 9-fluorenylmethyloxycarbonyl azide (itself made by reacting Fmoc-Cl with sodium azide ) in sodium bicarbonate and aqueous dioxane is also a method to install Fmoc group. [ 1 ] Because the fluorenyl group is highly fluorescent , certain UV-inactive compounds may be reacted to give the Fmoc derivatives, suitable for analysis by ...

  9. DMTMM - Wikipedia

    en.wikipedia.org/wiki/DMTMM

    DMTMM (4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methyl-morpholinium chloride) is an organic triazine derivative commonly used for activation of carboxylic acids, particularly for amide synthesis. Amide coupling is one of the most common reactions in organic chemistry and DMTMM is one reagent used for that reaction.

  1. Related searches 4' methyl biphenyl 4 carboxylic acid ester side effects 5 mg

    4' methyl biphenyl 4 carboxylic acid ester side effects 5 mg per dayalcohol carboxylic acid ester