Drugs affecting the gastrointestinal system

L -(+)-Arabinose, a five-carbon sugar found widely in nature, plays a pivotal role in biochemical research, particularly in microbiology and biomedicine. In microbial culture, it serves as a sole carbon source for various bacteria, as many bacteria

L -(+)-Arabinose, a five-carbon sugar found widely in nature, plays a pivotal role in biochemical research, particularly in microbiology and biomedicine. In microbial culture, it serves as a sole carbon source for various bacteria, as many bacteria

L -(+)-Arabinose, a five-carbon sugar found widely in nature, plays a pivotal role in biochemical research, particularly in microbiology and biomedicine. In microbial culture, it serves as a sole carbon source for various bacteria, as many bacteria

Application L -(+)-Arabinose is used as a key starting material in the total synthesis of (+)-ambruticin, zaragozic acid A, (&#8722)-radicamine B and (+)-herbarumin I. Biochem/physiol Actions L -Arabinose is the naturally occurring isomer and is a

Application L -(+)-Arabinose is used as a key starting material in the total synthesis of (+)-ambruticin, zaragozic acid A, (&#8722)-radicamine B and (+)-herbarumin I. Biochem/physiol Actions L -Arabinose is the naturally occurring isomer and is a

Application L -(+)-Arabinose is used as a key starting material in the total synthesis of (+)-ambruticin, zaragozic acid A, (&#8722)-radicamine B and (+)-herbarumin I. Biochem/physiol Actions L -Arabinose is the naturally occurring isomer and is a

Application L-Arabitol, a rare sugar alcohol, is being studied as a food additive that reduces fat deposits in the intestines. L-Arabitol is used as an inducer of xylanase expression in Hypocrea jecorina (Trichoderma reesei).

Application L-Arabitol, a rare sugar alcohol, is being studied as a food additive that reduces fat deposits in the intestines. L-Arabitol is used as an inducer of xylanase expression in Hypocrea jecorina (Trichoderma reesei).

Biochem/physiol Actions L-Galactose was shown to be a key intermediate in the molecular pathway of converting D-glucose to oxalic acid in Pistia stratiotes. Other Notes To gain a comprehensive understanding of our extensive range of Monosaccharides

Biochem/physiol Actions L-Galactose was shown to be a key intermediate in the molecular pathway of converting D-glucose to oxalic acid in Pistia stratiotes. Other Notes To gain a comprehensive understanding of our extensive range of Monosaccharides

Synonyms: L-Asp(OMe)-OH·HCl Purity Limit: 99% CAS No.: 16856-13-6 Molecular Formula: C5H9NO4·HCl Molecular Weight: 183.64 MDL No.: MFCD00038972 Appearance: White crystalline powder Storage Temperature: Store at 0-8°C

Synonyms: L-ß-HomoGly(allyl)-OH·HCl(S)-3-Amino-5-hexenoic acid hydrochloride Purity Limit: &ge 98% (NMR) CAS No.: 270263-02-0 Molecular Formula: C6H11NO2·HCl Molecular Weight: 165.