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Fmoc-(R)-2-thienylglycine. Group: Biochemicals. Alternative Names: Fmoc-L-(2-thienyl)glycine. Grades: Highly Purified. CAS No. 208259-66-9. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. US Biological Life Sciences.
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Fmoc-(R)-3-Thienylglycine
Fmoc-(R)-3-Thienylglycine. Group: Biochemicals. Alternative Names: Fmoc-D-(3-thienyl)glycine. Grades: Highly Purified. Pack Sizes: 100mg, 250mg, 500mg, 1g, 2g. US Biological Life Sciences.
Worldwide
L-α-(2-Thienyl)glycine
L-α-(2-Thienyl)glycine is a compound used in the one-pot regioselective synthesis of substituted arylglycines for kinetic resolution by penicillin G acylase. Synonyms: H-Thg(2)-OH; H-Gly(2-Thienyl)-OH. Grades: ≥ 98%. CAS No. 65058-23-3. Molecular formula: C6H7NO2S. Mole weight: 157.19.
2-(2-(Thiophene-2-carbonylsulfanyl)propanoylamino)acetic acid. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 2-[2-(thiophene-2-carbonylsulfanyl)propanoylamino]acetic acid;2-(alpha-thenoylthio)propionylglycine;bronco-plus;n-(1-oxo-2-((2-thienylcarbonyl)thio)propyl)-glycin;prostenoglycine;tiase;n-(1-oxo-2-((2-thienylcarbonyl)thio)propyl)glycine;STEPRONIN. Product Category: Heterocyclic Organic Compound. CAS No. 72324-18-6. Molecular formula: C10H11NO4S2. Mole weight: 273.32. Density: 1.428 g/cm³. Product ID: ACM72324186. Alfa Chemistry ISO 9001:2015 Certified.
Stepronin
Stepronin is a mucolytic and expectorant and it can be used for the treatment of Bronchitis and Otorhinolaryngological infections. Uses: Bronchitis; otorhinolaryngological infections. Synonyms: (2-((thiophene-2-carbonyl)thio)propanoyl)glycine; Tiofacic; Prostenoglycine; Bronco-plus; TTPG; Glycine, N-(1-oxo-2-((2-thienylcarbonyl)thio)propyl)-. Grades: 98%. CAS No. 72324-18-6. Molecular formula: C10H11NO4S2. Mole weight: 273.32.
Pelitrexol
Pelitrexol is a GARFT inhibitor, and is also a water soluble antifolate with anti-proliferative activity. Pelitrexol inhibits activity of glycinamide ribonucleotide formyltransferase (GARFT), the first folate-dependent enzyme of the de novo purine synthesis pathway essential for cell proliferation. Enzyme inhibition reduces the purine nucleotides pool required for DNA replication and RNA transcription. As a result, this agent causes cell cycle arrest in S-phase, and ultimately inhibits tumor cell proliferation. Synonyms: AG-2037; AG 2037; AG2037; L-Glutamic acid, N-((5-(2-((6S)-2-amino-1,4,5,6,7,8-hexahydro-4-oxopyrido(2,3-d)pyrimidin-6-yl)ethyl)-4-methyl-2-thienyl)carbonyl)-. Grades: >98%. CAS No. 446022-33-9. Molecular formula: C20H25N5O6S. Mole weight: 463.51.
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