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Results for "

43-10

" in MedChemExpress (MCE) Product Catalog:

8

Inhibitors & Agonists

1

Peptides

1

Natural
Products

4

Oligonucleotides

Targets Recommended:
Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-N4310
    Taxifolin 7-O-rhamnoside

    Taxifolin 7-O-α-L-rhamnoside

    		 Others Others
    Taxifolin 7-O-rhamnoside (Taxifolin 7-O-α-L-rhamnoside) is a flavonoid isolated from Hypericum japonicum.
    Taxifolin 7-O-rhamnoside
  • HY-15417
    ML-7 hydrochloride
    20+ Cited Publications

    		 Myosin YAP Cancer
    ML-7 hydrochloride is a naphthalene sulphonamide derivative, potently inhibits MLCK (IC50=300 nM). ML-7 hydrochloride also inhibits YAP/TAZ.
    ML-7 hydrochloride
  • HY-P4310
    Boc-Val-Leu-Lys-AMC

    		Ser/Thr Protease Others
    Boc-Val-Leu-Lys-AMC is a sensitive, fluorogenic, and specific substrate of plasmin, as well as acrosin from the ascidian Halocynthia roretzi, porcine calpain isozymes I and II, and papain .
    Boc-Val-Leu-Lys-AMC
  • HY-122259
    AMPte-Glu-γ-Glu

    		Antifolate Others Cancer
    AMPte-Glu-γ-Glu is a substrate for folylpoly-γ-glutamate synthetase (FPGS). AMPte-Glu-γ-Glu exhibits cytotoxicity against chinese hamster ovaries cells, with IC50s of 20, 350 and 3 nM, for Pro3, R2, and 43-10, respectively .
    AMPte-Glu-γ-Glu
  • HY-R00990
    hsa-miR-4310 mimic

    		MicroRNA Cancer
    hsa-miR-4310 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-4310 mimic
    hsa-miR-4310 mimic
  • HY-RI00990
    hsa-miR-4310 inhibitor

    		MicroRNA Cancer
    hsa-miR-4310 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-4310 inhibitor
    hsa-miR-4310 inhibitor
  • HY-R00990A
    hsa-miR-4310 agomir

    		MicroRNA Cancer
    hsa-miR-4310 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-4310 agomir
    hsa-miR-4310 agomir
  • HY-RI00990A
    hsa-miR-4310 antagomir

    		MicroRNA Cancer
    hsa-miR-4310 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-4310 antagomir
    hsa-miR-4310 antagomir

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