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Results for "

α-Amino-p-toluic acid

" in MedChemExpress (MCE) Product Catalog:

6

Inhibitors & Agonists

3

Peptides

1

Isotope-Labeled Compounds

Cat. No. 상품명 Target 연구분야 Chemical Structure
  • HY-B1258
    4-(Aminomethyl)benzoic acid
    1 Publications Verification

    Aminomethylbenzoic acid; α-Amino-p-toluic acid

    Amino Acid Derivatives Cancer
    4-(Aminomethyl)benzoic acid is a competitive inhibitor of PepT1 and has antifibrinolytic activity .
    4-(Aminomethyl)benzoic acid
  • HY-P10341

    GCGR Metabolic Disease
    ZP3022 is a dual agonist of glucagon-like peptide-1 (GLP-1) and gastrin that has the ability to sustainably improve glycemic control. Additionally, ZP3022 can effectively increase β-cell mass, promote β-cell proliferation, and enhance the function of pancreatic islets. ZP3022 can be used in anti-diabetic research .
    ZP3022
  • HY-B1258R

    Aminomethylbenzoic acid (Standard); α-Amino-p-toluic acid (Standard)

    Amino Acid Derivatives Reference Standards Others
    4-(Aminomethyl)benzoic acid (Standard) is the analytical standard of 4-(Aminomethyl)benzoic acid. This product is intended for research and analytical applications. 4-(Aminomethyl)benzoic acid is an unnatural amino acid derivative and an antifibrinolytic drug.
    4-(Aminomethyl)benzoic acid (Standard)
  • HY-P11243

    Ephrin Receptor Neurological Disease
    EphA4 agonist compound 23 is a novel EphA4 agonist peptide mimic. EphA4 agonist compound 23 exhibits high affinity, high selectivity, and significant receptor activation ability. EphA4 agonist compound 23 is commonly used in the study of neurodegenerative diseases .
    EphA4 agonist compound 23
  • HY-B1258S

    Aminomethylbenzoic acid-13C2,15N; α-Amino-p-toluic acid-13C2,15N

    Isotope-Labeled Compounds Amino Acid Derivatives Cancer
    Intermediate of tranexamic Acid- 13C2, 15N (Aminomethylbenzoic acid- 13C2, 15N) is 13C and 15N labeled 4-(Aminomethyl)benzoic acid. 4-(Aminomethyl)benzoic acid is a competitive inhibitor of PepT1 and has antifibrinolytic activity .
    Intermediate of tranexamic Acid-13C2,15N
  • HY-P10876

    Amyloid-β Neurological Disease
    mcK6A1 is an inhibitor for the aggregation of amyloid-β (), that selectively binds to the 16KLVFFA21 segment of Aβ42, forms an extended β-folded structure, and inhibits the formation of Aβ42 oligomers. mcK6A1 can be used in research of Alzheimer's disease and other amyloid-related diseases .
    mcK6A1

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