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Iodoacetamide

" in MedChemExpress (MCE) Product Catalog:

31

Inhibitors & Agonists

10

Fluorescent Dye

1

Biochemical Assay Reagents

11

Peptides

1

Isotope-Labeled Compounds

3

Click Chemistry

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-34477
    2-Iodoacetamide
    2 Publications Verification

    Iodoacetamide

    DNA Alkylator/Crosslinker Others
    2-Iodoacetamide (Iodoacetamide), an alkylating agent, is a commonly used agent for alkylation of cysteine during sample preparation for proteomics .
    2-Iodoacetamide
  • HY-34477S1

    Iodoacetamide-d4

    DNA Alkylator/Crosslinker Others
    2-Iodoacetamide-d4 is the deuterium labeled 2-Iodoacetamide[1]. 2-Iodoacetamide (Iodoacetamide), an alkylating agent, is a commonly used agent for alkylation of cysteine during sample preparation for proteomics[2][3].
    2-Iodoacetamide-d4
  • HY-140857

    PROTAC Linkers Cancer
    Iodoacetamide-PEG3-azide is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs . Iodoacetamide-PEG3-azide is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
    Iodoacetamide-PEG3-azide
  • HY-134687

    PROTAC Linkers Cancer
    Iodoacetamide-PEG5-azide is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs . Iodoacetamide-PEG5-azide is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
    Iodoacetamide-PEG5-azide
  • 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-150230

    ADC Linker Others
    Desthiobiotin-Iodoacetamide can be used as an ADC Linker. Desthiobiotin-Iodoacetamide also acts as a probe used to label the the Oridonin (HY-N0004)-treated cell lysis .
    Desthiobiotin-Iodoacetamide
  • HY-123749

    5-TMRIA

    Fluorescent Dye Others
    Tetramethylrhodamine-5-iodoacetamide (5-TMRIA) is a thiol-selective reactive dye that is used to non-specifically label proteins via the cysteine residues. Tetramethylrhodamine-5-iodoacetamide (5-TMRIA) can be used to covalently label DNA fragments .
    Tetramethylrhodamine-5-iodoacetamide
  • HY-134738

    PROTAC Linkers Cancer
    Iodoacetamide-PEG5-NH-Boc is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
    Iodoacetamide-PEG5-NH-Boc
  • HY-134688

    PROTAC Linkers Cancer
    Iodoacetamide-PEG5-NH2 is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
    Iodoacetamide-PEG5-NH2
  • HY-D1921

    Fluorescent Dye Others
    ATTO 390 iodoacetamide is the iodoacetamide derivative of ATTO 390, the maximum excitation/emission wavelength: 390/476 nm.
    ATTO 390 iodoacetamide
  • HY-134718

    PROTAC Linkers Cancer
    Glycocholic acid-PEG10-iodoacetamide is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
    Glycocholic acid-PEG10-iodoacetamide
  • HY-143205

    Others Cancer
    Desthiobiotin polyethyleneoxide iodoacetamide is useful for cysteine labeling in chemoproteomic experiments .
    Desthiobiotin polyethyleneoxide iodoacetamide
  • HY-W559951

    Biochemical Assay Reagents Others
    4-(N-Iodoacetamide)benzophenone is a biochemical reagent.
    4-(N-Iodoacetamide)benzophenone
  • HY-149182

    Fluorescent Dye Others
    Lucifer yellow iodoacetamide dipotassium is a thiol-reactive fluorescent tracer.
    Lucifer yellow iodoacetamide dipotassium
  • HY-140941

    PROTAC Linkers Cancer
    Biotin-PEG2-C2-iodoacetamide is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
    Biotin-PEG2-C2-iodoacetamide
  • HY-D1981

    Fluorescent Dye Others
    ATTO 633 Iodacetamid is an iodoacetamide derivative of ATTO 594 with excitation/emission maxima at 630/651 nm.
    ATTO 633 iodacetamid
  • HY-D1945

    Fluorescent Dye Others
    ATTO 590 Iodacetamid is an iodoacetamide derivative of ATTO 590 with maximum excitation/emission wavelengths: 594/622 nm.
    ATTO 590 iodacetamid
  • HY-D2009

    Fluorescent Dye Others
    ATTO 565 iodacetamid is an iodoacetamide derivative of ATTO 565 with maximum excitation/emission wavelengths: 564/590 nm.
    ATTO 565 iodacetamid
  • HY-D2068

    Fluorescent Dye Others
    ATTO 680 iodacetamid is an iodoacetamide derivative of ATTO 680 with maximum excitation/emission wavelengths: 681/698 nm.
    ATTO 680 iodacetamid
  • HY-D2036

    Fluorescent Dye Others
    ATTO 550 iodacetamid is an iodoacetamide derivative of ATTO 550 with maximum excitation/emission wavelengths: 554/576 nm.
    ATTO 550 iodacetamid
  • HY-D2080

    Fluorescent Dye Others
    ATTO 665 iodacetamid is an iodoacetamide derivative of ATTO 665 with maximum excitation/emission wavelengths: 663/680 nm.
    ATTO 665 iodacetamid
  • HY-D2052

    Fluorescent Dye Others
    ATTO 532 iodacetamid is a new fluorescent marker based on the Rhodamine structure. It has strong absorption, high fluorescence quantum yield, high thermal stability and photochemical stability, and is suitable for single molecule detection and high-resolution microscopy. ATTO 532 iodacetamid is an iodoacetamide derivative of ATTO 532, which can be used to label proteins or antibodies.
    ATTO 532 iodacetamid
  • HY-P3567

    Melanocortin Receptor Neurological Disease
    (p-Iodo-Phe7)-ACTH (4-10) is a adrenocorticotrophic hormone (ACTH) derivative, which is produced and secreted by the anterior pituitary gland. (p-Iodo-Phe7)-ACTH (4-10) serves as a melanocortin (MC) receptor antagonist and inhibits α-melanocyte-stimulating hormone (α-MSH)-induced excessive grooming behavior in rats .
    (p-Iodo-Phe7)-ACTH (4-10)
  • HY-P4154

    ALM-488

    Fluorescent Dye Neurological Disease Cancer
    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-P2434

    Somatostatin Receptor Neurological Disease Metabolic Disease Cancer
    AP102 is a dual SSTR2/SSTR5-specific somatostatin analog (SSA). AP102 is a disulfide-bridged octapeptide SSA containing synthetic iodinated amino acids. AP102 binds with subnanomolar affinity to SSTR2 and SSTR5 (IC50: 0.63 and 0.65 nM, respectively). AP102 does not bind to SSTR1 or SSTR3. AP102 can be used for acromegaly and neuroendocrine tumors research .
    AP102
  • 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
    CTCE-9908
    1 Publications Verification

    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
    Cotadutide acetate
    1 Publications Verification

    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
    Cotadutide
    1 Publications Verification

    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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