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Results for "

KDM1A

" in MedChemExpress (MCE) Product Catalog:

23

Inhibitors & Agonists

1

Recombinant Proteins

4

Antibodies

3

Oligonucleotides

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-12782T
    Iadademstat dihydrochloride
    5+ Cited Publications

    ORY-1001 dihydrochloride; RG6016 dihydrochloride; RO 7051790 dihydrochloride

    Histone Demethylase Cancer
    Iadademstat (ORY-1001) dihydrochloride is a selective irreversible lysine (K)-specific demethylase 1A (KDM1A/LSD1) inhibitor.
    Iadademstat dihydrochloride
  • HY-18632
    GSK2879552
    Maximum Cited Publications
    19 Publications Verification

    Histone Demethylase Cancer
    GSK2879552 an orally active, selective and irreversible inhibitor of lysine specific demethylase 1 (LSD1/ KDM1A), with potential antineoplastic activity [1] .
    GSK2879552
  • HY-109117
    Iadademstat
    5+ Cited Publications

    ORY-1001

    Histone Demethylase Apoptosis Cancer
    Iadademstat (ORY-1001) is a highly potent, orally active and selective LSD1 (KDM1A) inhibitor with antileukemic activity. Iadademstat can be used for relapsed or refractory acute myeloid leukemia research [1].
    Iadademstat
  • HY-18632A
    GSK2879552 dihydrochloride
    Maximum Cited Publications
    19 Publications Verification

    Histone Demethylase Cancer
    GSK2879552 dihydrochloride an orally active, selective and irreversible inhibitor of lysine specific demethylase 1 (LSD1/KDM1A), with potential antineoplastic activity [1] .
    GSK2879552 dihydrochloride
  • HY-103713
    Seclidemstat
    10+ Cited Publications

    SP-2577

    Histone Demethylase Cancer
    Seclidemstat is a potent noncompetitive and reversible KDM1A (LSD1) inhibitor (Ki=31 nM, IC50=13 nM). Seclidemstat promotes antitumor immunity in switch/sucrose nonfermentable (SWI/SNF) complex mutated ovarian cancer, as well as inhibit virus production, viral DNA replication, and late gene expression. Seclidemstat can be used for the research of Ewing Sarcoma [1] .
    Seclidemstat
  • HY-19612A
    DDP-38003 dihydrochloride
    1 Publications Verification

    Histone Demethylase Cancer
    DDP-38003 dihydrochloride is an novel, orally available inhibitor of histone lysine-specific demethylase 1A (KDM1A/LSD1) with an IC50 of 84 nM [1].
    DDP-38003 dihydrochloride
  • HY-138830
    TAK-418
    2 Publications Verification

    Histone Demethylase Neurological Disease
    TAK-418 is a selective, orally active LSD1 (KDM1A) enzyme inhibitor with an IC50 of 2.9 nM. TAK-418 unlocks aberrant epigenetic machinery and improves autism symptoms in neurodevelopmental disorder models [1] .
    TAK-418
  • HY-103713A
    Seclidemstat mesylate
    10+ Cited Publications

    SP-2577 mesylate

    Histone Demethylase Cancer
    Seclidemstat (SP-2577) mesylate is a potent noncompetitive and reversible KDM1A (LSD1) inhibitor (Ki=31 nM, IC50=13 nM). Seclidemstat mesylate promotes antitumor immunity in switch/sucrose nonfermentable (SWI/SNF) complex mutated ovarian cancer, as well as inhibit virus production, viral DNA replication, and late gene expression. Seclidemstat mesylate can be used for the research of Ewing Sarcoma [1] .
    Seclidemstat mesylate
  • HY-RS07205

    Small Interfering RNA (siRNA) Others

    KDM1A Human Pre-designed siRNA Set A contains three designed siRNAs for KDM1A gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

    KDM1A Human Pre-designed siRNA Set A
    KDM1A Human Pre-designed siRNA Set A
  • HY-RS07206

    Small Interfering RNA (siRNA) Others

    Kdm1a Mouse Pre-designed siRNA Set A contains three designed siRNAs for Kdm1a gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

    Kdm1a Mouse Pre-designed siRNA Set A
    Kdm1a Mouse Pre-designed siRNA Set A
  • HY-RS07207

    Small Interfering RNA (siRNA) Others

    Kdm1a Rat Pre-designed siRNA Set A contains three designed siRNAs for Kdm1a gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

    Kdm1a Rat Pre-designed siRNA Set A
    Kdm1a Rat Pre-designed siRNA Set A
  • HY-19612B

    Histone Demethylase Cancer
    DDP-38003 trihydrochloride is an novel, orally available inhibitor of histone lysine-specific demethylase 1A (KDM1A/LSD1) with an IC50 of 84 nM.
    DDP-38003 trihydrochloride
  • HY-19612

    Histone Demethylase Cancer
    DDP-38003 (Compound 15) is an orally active KDM1A/LSD1 inhibitor with an IC50 value of 84 nM. DDP-38003 exhibits anticancer activity against promyelocytic leukemia [1].
    DDP-38003
  • HY-143238

    Histone Demethylase Cancer
    FY-56 is a highly potent and selective LSD1/KDM1A inhibitor (IC50=42 nM) and exhibits high selectivity over MAO-A/B. FY-56 induces differentiation of MOLM-13 and MV4-11 cell and has the potential for AML research [1].
    FY-56
  • HY-123577

    Histone Demethylase Apoptosis Cancer
    TPC-144 is a LSD1/KDM1A inhibitor. TPC-144 inhibits LSD1, and leads to a decrease in the protein level of DNMT1, causing low methylation of the LINE-1 element. TPC-144 can also produce a synergistic effect with Decitabine (HY-A0004) (a DNMT inhibitor), jointly promoting DNA demethylation and thereby inducing differentiation and apoptosis of leukemia cells. TPC-144 has also demonstrated anti-tumor efficacy in acute myeloid leukemia (AML) models. TPC-144 can be used for the study of AML [1] .
    TPC-144
  • HY-112304

    Histone Demethylase Others
    NCD38 TFA is a LSD1-selective inhibitor [1] .
    NCD38 TFA
  • HY-112304A

    Histone Demethylase Others
    (1R,2S)-NCD38 TFA is an enantiomer of NCD38 TFA. NCD38 TFA is a LSD1-selective inhibitor [1] .
    (1R,2S)-NCD38 TFA
  • HY-186116

    Histone Demethylase Others
    LSD1-IN-49 is a Lysine-specific demethylase 1 (LSD1/KDM1A) inhibitor with a human IC50 of 29 nM. LSD1-IN-49 irreversibly inhibits LSD1 enzyme activity by forming an adduct with the flavin adenine dinucleotide (FAD) cofactor of LSD1. LSD1-IN-49 can be used as a lead compound for the development of LSD1-targeted PET imaging agents for the brain [1].
    LSD1-IN-49
  • HY-186116A

    Histone Demethylase Neurological Disease
    LSD1-IN-49 hydrochloride (Compound (±) 1) is an irreversible LSD1/KDM1A inhibitor with an IC50 of 29 nM against hLSD1. LSD1-IN-49 hydrochloride irreversibly inhibits the enzymatic activity of LSD1 by forming an adduct with flavin adenine dinucleotide (FAD) in the binding pocket of LSD1. LSD1-IN-49 hydrochloride is applicable to research related to schizophrenia, autism spectrum disorder and Huntington's disease [1].
    LSD1-IN-49 hydrochloride
  • HY-103713AR

    SP-2577 mesylate (Standard)

    Reference Standards Histone Demethylase Cancer
    Seclidemstat mesylate (Standard) is the analytical standard of Seclidemstat mesylate (HY-103713A). This product is intended for research and analytical applications. Seclidemstat (SP-2577) mesylate is a potent noncompetitive and reversible KDM1A (LSD1) inhibitor (Ki=31 nM, IC50=13 nM). Seclidemstat mesylate promotes antitumor immunity in switch/sucrose nonfermentable (SWI/SNF) complex mutated ovarian cancer, as well as inhibit virus production, viral DNA replication, and late gene expression. Seclidemstat mesylate can be used for the research of Ewing Sarcoma [1] .
    Seclidemstat mesylate (Standard)
  • HY-103713R

    SP-2577 (Standard)

    Reference Standards Histone Demethylase Cancer
    Seclidemstat (Standard) is the analytical standard of Seclidemstat (HY-103713). This product is intended for research and analytical applications. Seclidemstat is a potent noncompetitive and reversible KDM1A (LSD1) inhibitor (Ki=31 nM, IC50=13 nM). Seclidemstat promotes antitumor immunity in switch/sucrose nonfermentable (SWI/SNF) complex mutated ovarian cancer, as well as inhibit virus production, viral DNA replication, and late gene expression. Seclidemstat can be used for the research of Ewing Sarcoma [1] .
    Seclidemstat (Standard)
  • HY-183067

    Histone Demethylase TGF-beta/Smad Notch Cancer
    TAS1440 is an orally active LSD1/KDM1A inhibitor with a human IC50 of 4.8 nM. TAS1440 non-covalently binds to the histone H3-binding pocket of LSD1, inhibiting demethylase activity and disrupting repressive complexes with INSM1 and SMAD2. TAS1440 activates tumor-suppressive TGF-β and NOTCH signaling pathways via transcriptional reprogramming. TAS1440 can be used for the research of small cell lung cancer, specifically the SCLC-A subtype [1].
    TAS1440
  • HY-183067A

    Histone Demethylase TGF-beta/Smad Notch Cancer
    TAS1440 benzoate is an orally active LSD1/KDM1A inhibitor with a human IC50 of 4.8 nM. TAS1440 benzoate non-covalently binds to the histone H3-binding pocket of LSD1, inhibiting demethylase activity and disrupting repressive complexes with INSM1 and SMAD2. TAS1440 benzoate activates tumor-suppressive TGF-β and NOTCH signaling pathways via transcriptional reprogramming. TAS1440 benzoate can be used for the research of small cell lung cancer, specifically the SCLC-A subtype [1].
    TAS1440 benzoate

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