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acetamide

" in MedChemExpress (MCE) Product Catalog:

32

Inhibitors & Agonists

1

Fluorescent Dye

1

Biochemical Assay Reagents

10

Peptides

5

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Products

8

Isotope-Labeled Compounds

1

Click Chemistry

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-Y0946

    Biochemical Assay Reagents Inflammation/Immunology Cancer
    Acetamide is used as an intermediate in the synthesis of methylamine, thioacetamide, and insecticides, and as a plasticizer in leather, cloth and coatings. Acetamide has carcinogenicity. Acetamide derivatives may has antioxidant activity and potential anti-inflammatory activity .
    <em>Acetamide</em>
  • HY-Y0946S

    Isotope-Labeled Compounds Cancer
    Acetamide- 15N is the 15N-labeled Acetamide. Acetamide is used as an intermediate in the synthesis of methylamine, thioacetamide, and insecticides, and as a plasticizer in leather, cloth and coatings. Acetamide has carcinogenicity[1][2].
    <em>Acetamide</em>-15N
  • HY-157360

    Biochemical Assay Reagents Others
    Acetamide Agar is a solid culture media for non-fermenting bacteria. Acetamide Agar helps differentiate P. acidovorans from other non-sugar-soluble or weakly sugar-soluble Pseudomonas species. Acetamide Agar can be used to test the ability of microorganisms such as Pseudomonas aeruginosa to utilize acetamide through deamination .
    <em>Acetamide</em> Agar
  • HY-Y0946S2

    Isotope-Labeled Compounds Cancer
    Acetamide-d5 is the deuterium labeled Acetamide[1]. Acetamide is used as an intermediate in the synthesis of methylamine, thioacetamide, and insecticides, and as a plasticizer in leather, cloth and coatings. Acetamide has carcinogenicity[2][3].
    <em>Acetamide</em>-d5
  • HY-W243217

    trideuteroacetamide

    Isotope-Labeled Compounds Others
    Acetamide-2,2,2-d3 is the deuterium labeled Acetamide-2,2,2-d3[1].
    <em>Acetamide</em>-2,2,2-d3
  • HY-W016784S

    Endogenous Metabolite Others
    Indole-3-acetamide-d5 is the deuterium labeled Indole-3-acetamide[1]. Indole-3-acetamide is a biosynthesis intermediate of indole-3-acetic acid (HY-18569). Indole-3-acetic acid is the most common natural plant growth hormone of the auxin class[2].
    Indole-3-<em>acetamide</em>-d5
  • HY-W016784
    Indole-3-acetamide
    1 Publications Verification

    Endogenous Metabolite Others
    Indole-3-acetamide is a biosynthesis intermediate of indole-3-acetic acid (HY-18569). Indole-3-acetic acid is the most common natural plant growth hormone of the auxin class .
    Indole-3-<em>acetamide</em>
  • HY-W087930S

    N1-(4-nitrophenyl)acetamide-d4

    Isotope-Labeled Compounds Others
    N-(4-Nitrophenyl)acetamide-d4 is the deuterium labeled N-(4-Nitrophenyl)acetamide[1].
    N-(4-Nitrophenyl)<em>acetamide</em>-d4
  • HY-146712S

    Isotope-Labeled Compounds
    N-(4-Hydroxyphenyl)acetamide sulfate-d3 (sodium) is the deuterium labeled N-(4-Hydroxyphenyl)acetamide sulfate.
    N-(4-Hydroxyphenyl)<em>acetamide</em> sulfate-d3 sodium
  • HY-101403

    Monoacetylcadaverine

    Endogenous Metabolite Cancer
    N-(5-Aminopentyl)acetamide is the acetylated form of the polyamine cadaverine.
    N-(5-Aminopentyl)<em>acetamide</em>
  • HY-W164451

    Fungal Infection
    N-(2-hydroxy-2-phenylethyl)acetamide is isolated from the solid rice cultures of the endophytic fungus Diaporthe eucalyptorum KY-9. N-(2-hydroxy-2-phenylethyl)acetamide exhibits antifungal activities against Alternaria solani .
    N-(2-hydroxy-2-phenylethyl)<em>acetamide</em>
  • HY-153263

    Drug-Linker Conjugates for ADC Cancer
    (Aminooxy)acetamide-Val-Cit-PAB-MMAE (MMAE 5) is an intermediate used in the synthetic preparation of drug-linker conjugates for ADC. (Aminooxy)acetamide-Val-Cit-PAB-MMAE is conjugated to polyamide via oxime bond formation to form MMAE polyamide conjugate. Then MMAE polyamide conjugate can be conjugated to Trastuzumab, to make ADC .
    (Aminooxy)<em>acetamide</em>-Val-Cit-PAB-MMAE
  • HY-W140566S

    Isotope-Labeled Compounds Others
    N-(2-Aminoethyl)-2-(naphthalen-1-yl)acetamide-d4 is deuterium labeled N-(2-Aminoethyl)-2-(naphthalen-1-yl)acetamide.
    N-(2-Aminoethyl)-2-(naphthalen-1-yl)<em>acetamide</em>-d4
  • HY-101424

    Fungal Infection
    2-Chloro-N-(2-methyl-4-bromophenyl)acetamide is an antifungal compound .
    2-Chloro-N-(2-methyl-4-bromophenyl)<em>acetamide</em>
  • HY-W009512S

    Isotope-Labeled Compounds Others
    N-(2,6-Dimethylphenyl)-2-(piperazin-1-yl)acetamide-d8 is the deuterium labeled N-(2,6-Dimethylphenyl)-2-(piperazin-1-yl)acetamide[1].
    N-(2,6-Dimethylphenyl)-2-(piperazin-1-yl)<em>acetamide</em>-d8
  • HY-106947

    Endogenous Metabolite Metabolic Disease
    SY-640 is an Acetamide derivative and has potent hepatoprotective effect. SY-640 reduces Propionibacterium acnes and Lipopolysaccharide-induced liver injury in mice .
    SY-640
  • HY-D0532

    Fluorescent Dye Others
    N-[5-2-[Azo]phenyl]acetamide is a multifunctional dye. Dyes are important tools in biological experiments. They can help researchers observe and analyze cell structures, track biomolecules, evaluate cell functions, distinguish cell types, detect biomolecules, study tissue pathology and monitor microorganisms. Their applications range from basic scientific research to clinical A wide range of diagnostics. Dyes are also widely used in traditional fields such as textile dyeing, as well as in emerging fields such as functional textile processing, food pigments and dye-sensitized solar cells.
    N-[5-2-[Azo]phenyl]<em>acetamide</em>
  • HY-136205

    Iodoacetamide-alkyne; N-Hex-5-ynyl-2-iodo-acetamide

    TRP Channel Infection Inflammation/Immunology
    IA-Alkyne (Iodoacetamide-alkyne; N-Hex-5-ynyl-2-iodo-acetamide) is a TRP channel (TRPC) agonist and has the potential for the study of respiratory infection . IA-Alkyne can be used to develop an isotopically tagged probe for quantitative cysteine-reactivity profiling . IA-Alkyne is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
    IA-Alkyne
  • HY-150408

    AUTACs Cancer
    FBnG-(Cys-acetamide)-CH2-PEG3-CH2-CH2-CH2-NH2 is a linker of AUTAC4. AUTAC4 contains an p-fluorobenzylguanine (FBnG) and a phenylindole moiety, which can induce K63-linked polyubiquitination and degradation of mitochondria in HeLa cells .
    FBnG-(Cys-<em>acetamide</em>)-CH2-PEG3-CH2-CH2-CH2-NH2
  • HY-109573

    Phospholipase Cancer
    hnps-PLA-IN-1 (compound 5aa), a indole-3-acetamide, is a hnps-PLA2 inhibitor (IC50=0.124 μM) .
    hnps-PLA-IN-1
  • HY-18594

    Others Others
    NSC-41589 is an N-[2-(methylsulfanyl) phenyl]acetamide.
    NSC-41589
  • HY-144426

    Influenza Virus Infection
    Neuraminidase-IN-6 (Compound 5c) is a potent inhibitor of neuraminidase with an IC50 of 0.11 μM. Neuraminidase-IN-6 is a 1,3,4-triazole-3-acetamide derivative. Neuraminidase (NA) is an ideal target for the development of anti-influenza agents .
    Neuraminidase-IN-6
  • HY-124175

    Others Endocrinology
    16-Phenoxy prostaglandin F2α ethyl amide is a metabolically stable PGF2α analogue containing a acetamide structure .
    16-Phenoxy prostaglandin F2α ethyl <em>amide</em>
  • HY-47876

    Others Others
    2-(((Benzo[d][1,3]dioxol-5-ylmethylene)amino)oxy)-N-(m-tolyl)acetamide is an active molecule.
    WAY-659590
  • HY-146373

    Bacterial Infection
    The minimum inhibitory concentration (MIC) of a new 2- (quinoline-4-methoxy) acetamide antituberculotic agent against the reference strain of Mycobacterium tuberculosis H37Rv was as low as 0.3 μ M. It also inhibited the growth of Mycobacterium tuberculosis in the macrophage model of tuberculosis infection.
    Antibacterial agent 95
  • HY-P4154

    ALM-488

    Fluorescent Dye Neurological Disease
    Bevonescein (ALM-488) is a novel, intravenously-administrated fluorescein-conjugated peptide that binds nerve-associated connective tissue, labels peripheral nerves under real-time fluorescence imaging (FL) in living mice and human ex vivo nerve tissue. Bevonescein is a peptide-linked tracer which fluorescently labeled both intact and degenerated nerves .
    Bevonescein
  • HY-P1103A

    CXCR Cancer
    CTCE-9908 TFA is a potent and selective CXCR4 antagonist. CTCE-9908 TFA induces mitotic catastrophe, cytotoxicity and inhibits migration in CXCR4-expressing ovarian cancer cells .
    CTCE-9908 TFA
  • HY-P1103

    CXCR Cancer
    CTCE-9908 is a potent and selective CXCR4 antagonist. CTCE-9908 induces mitotic catastrophe, cytotoxicity and inhibits migration in CXCR4-expressing ovarian cancer cells .
    CTCE-9908
  • HY-P2231A

    MEDI0382 acetate

    GCGR Metabolic Disease
    Cotadutide (MEDI0382) acetate is a potent dual agonist of glucagon-like peptide-1 (GLP-1) and GCGR with EC50 values of 6.9 pM and 10.2 pM, respectively. Cotadutide acetate exhibits ability to facilitate both weight loss and glycaemic control, and alleviate fibrosis. Cotadutide acetate can be used in the research of obesity and type 2 diabetes (T2D) .
    Cotadutide acetate
  • HY-P2231

    MEDI0382

    GCGR Metabolic Disease
    Cotadutide (MEDI0382) is a potent dual agonist of glucagon-like peptide-1 (GLP-1) and GCGR with EC50 values of 6.9 pM and 10.2 pM, respectively. Cotadutide exhibits ability to facilitate both weight loss and glycaemic control, and alleviate fibrosis. Cotadutide can be used in the research of obesity and type 2 diabetes (T2D) .
    Cotadutide
  • HY-P1321

    1229U91; GW1229

    Neuropeptide Y Receptor Neurological Disease
    GR231118, an analogue of the C-terminus of neuropeptide Y, is a potent , competitive and relative seletive antagonist at human neuropeptide Y Y receptor with a pKi of 10.4. GR231118 a potent agonist at the human neuropeptide Y Y4 receptor (pEC50=8.6; pKi=9.6) and a weak agonist at the human and rat neuropeptide YY2 and Y5 receptors. GR231118 also has high affinity for the mouse neuropeptide Y Y6 receptor (pKi= 8.8) .
    GR231118
  • HY-P1321A

    1229U91 TFA; GW1229 TFA

    Neuropeptide Y Receptor Neurological Disease
    GR231118 TFA, an analogue of the C-terminus of neuropeptide Y, is a potent , competitive and relative seletive antagonist at human neuropeptide YY receptor with a pKi of 10.4. GR231118 a potent agonist at the human neuropeptide YY4 receptor (pEC50=8.6; pKi=9.6) and a weak agonist at the human and rat neuropeptide Y Y2 and Y5 receptors. GR231118 also has high affinity for the mouse neuropeptide YY6 receptor (pKi= 8.8) .
    GR231118 TFA

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