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Results for "

methyl methanesulfonate

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    6
    TargetMol | All_Pathways
  • Peptide Products
    1
    TargetMol | Peptide_Products
  • PROTAC Products
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    TargetMol | PROTAC
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    TargetMol | Cell_Research_Reagents
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    TargetMol | Standard_Products
Methyl methanesulfonate
T998566-27-3
Methyl methanesulfonate is a DNA alkylator that modifies adenine (3-methyladenine) and guanine (7-methyladenine) respectively, resulting in base mismatch and replication disorders.
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Methyl methanesulfonate (Standard)
T9985BP66-27-3
Methyl methanesulfonate (Standard) is a reference standard for research and analysis in studies involving Methyl methanesulfonate. Methyl methanesulfonate is a DNA alkylating agent that modifies adenine (to 3-methyladenine) and guanine (to 7-methylguanine), inducing base mismatches and replication errors.
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1-((2-(2,4-Difluorophenyl)oxiran-2-yl)methyl)-1H-1,2,4-triazole methanesulfonate
T6731886386-77-8
1-((2-(2,4-Difluorophenyl)oxiran-2-yl)methyl)-1H-1,2,4-triazole methanesulfonate is a useful organic compound for research related to life sciences. The catalog number is T67318 and the CAS number is 86386-77-8.
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    APE1-IN-1
    T61487524708-03-0In house
    APE1-IN-1 is a potent inhibitor of purine/pyrimidine endonuclease 1 (APE1) that crosses the blood-brain barrier, exhibits potential antitumor activity, and enhances the cytotoxicity of the alkylating agent [methyl methanesulfonate] on cancer cells.
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    SMD-3236
    T2053713033586-31-8
    SMD-3236 is a PRAOTAC degrader targeting SMARCA2, designed using SMARCA ligand and VHL-1 ligand, and exhibits prolonged anti-tumor activity in vivo. SMARCA2 acts as a synthetic lethal target in cancer cells lacking SMARCA4, with SMD-3236 showing 2000-fold selectivity for SMARCA2 over SMARCA4, having a DC50 of less than 1 nM and a Dmax of over 95%. In the human cancer xenograft models deficient in SMARCA4, notably the H838 model, SMD-3236 effectively induces loss of SMARCA2 in tumor tissue while sparing the SMARCA4 protein, thereby inhibiting tumor growth. The compound consists of a target protein ligand (red part) SMI-1074, a PROTAC linker (black part) (trans-4-Ethynylcyclohexyl)methyl methanesulfonate, and an E3 ligase ligand (blue part) SMARCA2 ligand-14, forming the E3LigaseLigand-linker Conjugate 159.
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    Boc-AEVD-CHO TFA
    TP4155
    Boc-AEVD-CHO TFA is a Caspase 8 inhibitor. By inhibiting apoptosis, Boc-AEVD-CHO TFA significantly increases the frequency of micronuclei (MN) and binucleated micro-nucleated cells (MNCB) in peripheral blood mononuclear cells (PBMC) when induced by Nocodazole or methyl methanesulfonate (MMS). This compound is useful for research in immune and inflammatory diseases.
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