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No matches for "

79847

" within the MedChemExpress (MCE) catalog. Here are the results you might be looking for.

8

Inhibitors & Agonists

2

Peptides

9

Antibodies

4

Oligonucleotides

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-P1750
    Shepherdin (79-87)

    		HSP Survivin Cancer
    Shepherdin (79-87) is amino acids 79 to 87 fragment of Shepherdin. Shepherdin is a peptidomimetic antagonist of the complex between Hsp90 and Survivin. Anticancer activity .
    Shepherdin (79-87)
  • HY-P1750A
    Shepherdin (79-87) TFA

    		HSP Survivin Cancer
    Shepherdin (79-87) TFA is amino acids 79 to 87 fragment of Shepherdin. Shepherdin is a peptidomimetic antagonist of the complex between Hsp90 and Survivin. Anticancer activity .
    Shepherdin (79-87) TFA
  • HY-137062
    CGP-79807

    		CDK Cancer
    CGP-79807 is a purine-based CDK inhibitor. CGP-79807 can block the cell cycle by inhibiting CDK activity to suppress the proliferation of tumor cells. CGP-79807 can be used in the study of cancer .
    CGP-79807
  • HY-117831
    NSC-79887

    		Endogenous Metabolite Bacterial Infection
    NSC-79887 is a nucleoside hydrolase (NH) inhibitor with activity against Bacillus anthracis. NSC-79887 is considered a good candidate inhibitor of nucleoside hydrolases for biological testing and further development. The pharmacokinetic (ADMET) prediction of NSC-79887 showed that all physicochemical parameters were within the acceptable range for human use .
    NSC-79887
  • HY-RI02427A
    hsa-miR-7847-3p antagomir

    		MicroRNA Cancer
    hsa-miR-7847-3p antagomirs are chemically-modified oligonucleotides that hybridize with mature miRNAs. The miRNA antagomirs have 2 phosphorothioates at the 5' end, 4 phosphorothioates at the 3' end, 1 cholesterol group at the 3' end, and full-length nucleotide 2'-methoxy modification. The miRNA antagomirs strongly compete with mature miRNAs to prevent the complementary pairing of miRNAs and their target genes, thereby inhibiting miRNAs from functioning. Stability of miRNA antagomirs appears to be significantly higher than miRNA inhibitors, they exhibits enhanced cellular uptake, stability and regulatory activity in vivo.
    hsa-miR-7847-3p antagomir
    hsa-miR-7847-3p antagomir
  • HY-R02427
    hsa-miR-7847-3p mimic

    		MicroRNA Cancer
    hsa-miR-7847-3p mimics are small, chemically synthesized double-stranded RNAs that mimic endogenous miRNAs and enable miRNA functional analysis by up-regulation of miRNA activity.
    hsa-miR-7847-3p mimic
    hsa-miR-7847-3p mimic
  • HY-RI02427
    hsa-miR-7847-3p inhibitor

    		MicroRNA Cancer
    hsa-miR-7847-3p inhibitors are chemically-modified oligonucleotides that hybridize with mature miRNAs. The miRNA inhibitors have full-length nucleotide 2'-methoxy modification. The miRNA inhibitors strongly compete with mature miRNAs to prevent the complementary pairing of miRNAs and their target genes, thereby inhibiting miRNAs from functioning.
    hsa-miR-7847-3p inhibitor
    hsa-miR-7847-3p inhibitor
  • HY-R02427A
    hsa-miR-7847-3p agomir

    		MicroRNA Cancer
    hsa-miR-7847-3p agomirs are chemically-modified double-strand miRNA mimics with modified mature miRNA strand: 2 phosphorothioates at the 5' end, 4 phosphorothioates at the 3' end, 3' end cholesterol group, and full-length nucleotide 2'-methoxy modification. They are designed to mimic endogenous miRNAs and recommended for miRNA functional studies. Compared with miRNA mimics, they exhibits enhanced cellular uptake, stability and regulatory activity in vivo.
    hsa-miR-7847-3p agomir
    hsa-miR-7847-3p agomir

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