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  2. 4-Chlorokynurenine - Wikipedia

    en.wikipedia.org/wiki/4-Chlorokynurenine

    L-4-Chlorokynurenine (4-Cl-KYN; developmental code name AV-101) is an orally active small molecule prodrug of 7-chlorokynurenic acid, a NMDA receptor antagonist. It was investigated as a potential rapid-acting antidepressant. AV-101 was discovered at Marion Merrell Dow and its biological activity was explored at University of Maryland. It ...

  3. Drugmakers to raise US prices on over 250 medicines starting ...

    www.aol.com/news/drugmakers-raise-us-prices-over...

    The median price increase of the drugs being hiked Jan. 1 is 4.5%, which is in line with the median for all price increases last year. Drugmakers to raise US prices on over 250 medicines starting ...

  4. Cysteic acid - Wikipedia

    en.wikipedia.org/wiki/Cysteic_acid

    Cysteic acid also known as 3-sulfo-l-alanine is the organic compound with the formula HO 3 SCH 2 CH(NH 2)CO 2 H. It is often referred to as cysteate, which near neutral pH takes the form − O 3 SCH 2 CH(NH 3 +)CO 2 −. It is an amino acid generated by oxidation of cysteine, whereby a thiol group is fully oxidized to a sulfonic acid/sulfonate ...

  5. Trisodium dicarboxymethyl alaninate - Wikipedia

    en.wikipedia.org/wiki/Trisodium_dicarboxymethyl...

    An obvious synthesis route to α-alaninediacetic acid is from racemic α-DL-alanine, which provides racemic α-ADA by double cyanomethylation with methanal and hydrogen cyanide, hydrolysis of the intermediately formed diacetonitrile to the trisodium salt and subsequent acidification with mineral acids in a 97.4% overall yield. [4]

  6. Aspartate 4-decarboxylase - Wikipedia

    en.wikipedia.org/wiki/Aspartate_4-decarboxylase

    L-aspartate L-alanine + CO 2. Hence, this enzyme has one substrate, L-aspartate, and two products, L-alanine and CO 2. This reaction is the basis of the industrial synthesis of L-alanine. [1] This enzyme belongs to the family of lyases, specifically the carboxy-lyases, which cleave carbon-carbon bonds.

  7. Alanine - Wikipedia

    en.wikipedia.org/wiki/Alanine

    L-alanine is second only to L-leucine in rate of occurrence, accounting for 7.8% of the primary structure in a sample of 1,150 proteins. [5] The right-handed form, D -alanine, occurs in peptides in some bacterial cell walls [ 6 ] : 131 (in peptidoglycan ) and in some peptide antibiotics , and occurs in the tissues of many crustaceans and ...

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    Get AOL Mail for FREE! Manage your email like never before with travel, photo & document views. Personalize your inbox with themes & tabs. You've Got Mail!

  9. (R)-3-amino-2-methylpropionate—pyruvate transaminase

    en.wikipedia.org/wiki/(R)-3-amino-2...

    Thus, the two substrates of this enzyme are (R)-3-amino-2-methylpropanoate and pyruvate, whereas its two products are 2-methyl-3-oxopropanoate and L-alanine. This enzyme belongs to the family of transferases , specifically the transaminases , which transfer nitrogenous groups.

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