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Results for "

MSI

" in MedChemExpress (MCE) Product Catalog:

28

Inhibitors & Agonists

2

Peptides

4

Natural
Products

1

Recombinant Proteins

6

Antibodies

7

Oligonucleotides

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-105088

    MSI 78 free base

    Bacterial Infection
    Pexiganan (MSI 78 free base) is a synthetic analog of magainin 2. Pexiganan is a potent and orally active broad-spectrum antimicrobial peptide. Pexiganan can be used in the research of infections, such as diabetic foot ulcer infections .
    Pexiganan
  • HY-12219B

    Others Metabolic Disease
    MSI-1701 is an analogue of MSI-1436 which can control weight gain and blood glucose level extracted from patent US 7410959 B1.
    MSI-1701
  • HY-12219

    Trodusquemine; Aminosterol-1436

    Phosphatase Endocrinology
    MSI-1436 is a selective, non-competitive inhibitor of the enzyme protein-tyrosine phosphatase 1B (PTP1B), with an IC50 of appr 1 μM, 200-fold preference over TCPTP (IC50, 224 μM).
    MSI-1436
  • HY-RS21378

    Small Interfering RNA (siRNA) Others

    Msi2 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Msi2 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

    Msi2 Mouse Pre-designed siRNA Set A
    Msi2 Mouse Pre-designed siRNA Set A
  • HY-RS28764

    Small Interfering RNA (siRNA) Others
    Msi1 Rat Pre-designed siRNA Set A contains three designed siRNAs for Msi1 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.
    Msi1 Rat Pre-designed siRNA Set A
    Msi1 Rat Pre-designed siRNA Set A
  • HY-RS22242

    Small Interfering RNA (siRNA) Others

    Msi1 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Msi1 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

    Msi1 Mouse Pre-designed siRNA Set A
    Msi1 Mouse Pre-designed siRNA Set A
  • HY-RS27897

    Small Interfering RNA (siRNA) Others
    Msi2 Rat Pre-designed siRNA Set A contains three designed siRNAs for Msi2 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.
    Msi2 Rat Pre-designed siRNA Set A
    Msi2 Rat Pre-designed siRNA Set A
  • HY-RS08715

    Small Interfering RNA (siRNA) Others

    MSI2 Human Pre-designed siRNA Set A contains three designed siRNAs for MSI2 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

    MSI2 Human Pre-designed siRNA Set A
    MSI2 Human Pre-designed siRNA Set A
  • HY-RS08714

    Small Interfering RNA (siRNA) Others

    MSI1 Human Pre-designed siRNA Set A contains three designed siRNAs for MSI1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

    MSI1 Human Pre-designed siRNA Set A
    MSI1 Human Pre-designed siRNA Set A
  • HY-105088A

    MSI 78

    Bacterial Infection
    Pexiganan acetate (MSI 78) is the acetate salt form of Pexiganan (HY-105088). Pexiganan acetate is an orally active broad-spectrum antimicrobial peptide, which inhibits 99% gram-positive and Gram-negative aerobic bacteria through disruption of cell membrane/cells permeability. Pexiganan acetate can be used in the research of infections, such as diabetic foot ulcer infections .
    Pexiganan acetate
  • HY-12219A
    MSI-1436 lactate
    Maximum Cited Publications
    6 Publications Verification

    Trodusquemine lactate; Aminosterol-1436 lactate

    Phosphatase Endocrinology
    MSI-1436 lactate is a selective, non-competitive inhibitor of the enzyme protein-tyrosine phosphatase 1B (PTP1B), with an IC50 of 1 μM, 200-fold preference over TCPTP (IC50 of 224 μM).
    MSI-1436 lactate
  • HY-16468

    MSI-1256

    Bacterial HBV FAK Dengue Virus Infection Neurological Disease Cancer
    Squalamine (MSI-1256) is an aminosterol compound with broad-spectrum antiviral activity. Squalamine makes cells less conducive to certain viral replication by altering the electrostatic interactions in the inner membrane of host cells. Squalamine also has antibacterial and antitumor activities. Squalamine has broad-spectrum antibacterial activity against Gram-negative and Gram-positive bacteria, fungi and protozoa. Squalamine inhibits tumor-related angiogenesis and the growth of human breast cancer cells. Squalamine restores the function of enteric nervous system in Parkinson ,s disease mouse models .
    Squalamine
  • HY-16467

    MSI-1256F

    Bacterial Infection Cardiovascular Disease Cancer
    Squalamine lactate is an aminosterol compound discovered in the tissues of the dogfish shark, with antimicrobial activity, and used for the treatment of neovascular age-related macular degeneration.
    Squalamine lactate
  • HY-163941

    DNA/RNA Synthesis Cancer
    GSK_WRN2 is a potent and selective covalent WRN helicase inhibitor that suppresses replication stress caused by DNA (TA)n dinucleotide repeat expansions. GSK_WRN2 can be used to study microsatellite instability (MSI) cancers .
    GSK_WRN2
  • HY-163942

    DNA/RNA Synthesis Cancer
    GSK_WRN4 is a WRN helicase inhibitor (pIC50=7.6) with anticancer activity. GSK_WRN4 selectively inhibits the growth of MSI tumor cells in vitro and in vivo by inducing DNA double-strand breaks, particularly at expanded TA repeats and DNA damage regions .
    GSK_WRN4
  • HY-162471

    DNA/RNA Synthesis ATM/ATR Cancer
    GSK_WRN3 is selective WRN helicase inhibitor (pIC50 = 8.6). SK_WRN3 can selectively inhibit the growth of microsatellite unstable (MSI) cancer cells, induce DNA damage, and cause cell cycle arrest. GSK_WRN3 has anti-tumor activity .
    GSK_WRN3
  • HY-108466
    Ro 08-2750
    3 Publications Verification

    Apoptosis Neurological Disease Cancer
    Ro 08-2750 is a non-peptide and reversible nerve growth factor (NGF) inhibitor which binds to NGF, and with an IC50 of ~ 1 μM. Ro 08-2750 inhibits NGF binding to p75 NTR selectively over TRKA . Ro 08-2750 is a selective MSI RNA-binding activity inhibitor, with an IC50 of 2.7 μM .
    Ro 08-2750
  • HY-121515A

    Phosphatase Metabolic Disease
    DPM-1001 trihydrochloride is a potent, specific, orally active and non-competitive inhibitor of protein-tyrosine phosphatase (PTP1B) with an IC50 of 100 nM. DPM-1001 trihydrochloride is an analog of the specific PTP1B inhibitor MSI-1436. DPM-1001 trihydrochloride has anti-diabetic property .
    DPM-1001 trihydrochloride
  • HY-121515

    Phosphatase Metabolic Disease
    DPM-1001 is a potent, specific, orally active and non-competitive inhibitor of protein-tyrosine phosphatase (PTP1B) with an IC50 of 100 nM. DPM-1001 is an analog of the specific PTP1B inhibitor MSI-1436. DPM-1001 has anti-diabetic property .
    DPM-1001
  • HY-RS18892

    Small Interfering RNA (siRNA) Others

    Ebp Mouse Pre-designed siRNA Set A contains three designed siRNAs for Ebp gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

    Ebp Mouse Pre-designed siRNA Set A
    Ebp Mouse Pre-designed siRNA Set A
  • HY-119734

    DNA/RNA Synthesis Cancer
    Gossypolone is an RNA-binding protein Musashi-1 inhibitor with a Ki of 12 nM. Gossypolone disrupts the Musashi-numb RNA interaction and directly binds to the RBD1 of MSI1 protein. Gossypolone can be used for the research of cancer .
    Gossypolone
  • HY-169422

    IDE275

    DNA/RNA Synthesis Cancer
    GSK4418959 (IDE275) is a non-covalent, reversible, selective and orally active WRN helicase inhibitor. GSK4418959 inhibits ATPase and DNA unwinding functions in an ATP-competitive manner. GSK4418959 can be used for the study of microsatellite instability-high (MSI-H) cancer .
    GSK4418959
  • HY-161386

    DNA/RNA Synthesis Cancer
    WRN inhibitor 7 (Compound h6) is a WRN inhibitor. WRN inhibitor 7 effectively inhibits WRN's helicase and ATPase activity (IC50: 9.8 μM and 15.8 μM respectively). WRN inhibitor 7 can be used for research of microsatellite instable (MSI) cancers .
    WRN inhibitor 7
  • HY-156581

    DNA/RNA Synthesis Cancer
    WRN inhibitor 5, a cyclic vinyl sulfone compound, is a Wemer Syndrome ATP dependent helicase enzyme (WRN) inhibitor. WRN inhibitor 5 can be used for the research of cancer, including cancers characterized by microsatellite instability (MSI) and/or defective DNA mismatch repair system (dMMR) .
    WRN inhibitor 5
  • HY-174217

    DNA/RNA Synthesis Cancer
    WRN-IN-19 (Compound (S)-27) is a covalent WRN helicase inhibitor, with pIC50 (0 h/4 h) = 5.4/7.5 in the DNA-unwinding 5 endpoint assays. WRN-IN-19 shows synthetic lethality in MSI-H (high microsatellite instability) cancer cells .
    WRN-IN-19
  • HY-156784

    DHX9-IN-2

    DNA/RNA Synthesis Cancer
    ATX968 (example 31) is an orally active, potent and selective inhibitor of ATP-dependent RNA helicase A (DHX9), with the EC50 of 0.054 μM in circBRIP1. ATX968 results in robust and durable tumor growth inhibition or regression in mouse xenograft studies with MSI-H/dMMR colorectal cancer cell lines .
    ATX968
  • HY-168934

    DNA/RNA Synthesis Cancer
    KWR137 is a WRN degrader, with an IC50 of 8 nM. KWR137 exhibits good anti-proliferative activity against MSI-H cells, with a GI50 of 509 nM in SW48 cells and a GI50 of 824 μM in HCT116 cells. It also demonstrates anti-tumor growth effects in xenograft mouse models. KWR137 can be used for cancer research .
    KWR137
  • HY-158116

    RO7589831; VVD-133214

    DNA/RNA Synthesis Cancer
    VVD-214 is a synthetic lethal allosteric inhibitor of WRN helicase with an IC50 of 0.1316 µM. VVD-214 covalently binds to cysteine 727 of WRN and inhibits ATP hydrolysis and helicase activity. VVD-214 is potent in causing double-stranded DNA breaks, nuclear swelling, and cell death in high microsatellite instability (MSI) cancers .
    VVD-214

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