GLPBio

Others

others

Research Areas

Products Related to Others(4260)

  • GC73839 structure
    GC73839(S,R,R)-VBY-825
    Purity: >98.00%

    (S, R, R)-VBY-825 is the isomer of VBY-825 , and can be used as an experimental control.

  • GC73847 structure
    GC73847Creatinol hemisulfate
    CAS: 50648-53-8
    Purity: >98.00%

    Creatinol (hemisulfate) is the N-etl analogue of creatine.

  • GC73851 structure
    GC73851TDP-43 degrader-1
    CAS: 2902692-25-3
    Purity: >95.00%

    TDP-43 degrader-1 (example 3) reduces the TDP-43 aggregation that can be in the research of Amyotrophic lateral sclerosis and Alzheimer's disease.

  • GC73853 structure
    GC73853Macropa
    CAS: 1128304-86-8
    Purity: >99.00%

    Macropa is a macrocyclic chelator that can be used as radionuclides to study soft tissue metastases.

  • GC73895 structure
    GC73895J9Z38
    CAS: 1414864-34-8
    Purity: >99.00%

    J9Z38 is a metabolite of Cyantraniliprole , a broad-spectrum agrochemical insecticide belonging to the anthranilic diamide insecticide class.

  • GC73898 structure
    GC73898TREX1-IN-1
    CAS: 2756594-27-9
    Purity: >98.00%

    TREX1-IN-1 (Compound 180) is a TREX1 inhibitor with an IC50 value for hTREX1 less than 0.1 μM.

  • GC73901 structure
    GC73901HKYK-0030
    CAS: 2923054-94-6
    Purity: >99.00%

    HKYK-0030 is an inhibitor for MTDH-SND1 protein-protein interaction.

  • GC73905 structure
    GC73905PQQ-trimethylester
    CAS: 74447-88-4
    Purity: >95.00%

    PQQ-trimetlester (PQQ-TME) is a synthetic compound that is a trimetlester derivative of pyrroloquinoline quinone (PQQ).

  • GC73910 structure
    GC73910Anticancer agent 208
    CAS: 894565-34-5

    Anticancer agent 208 (C014) is an anticancer agent that can be used to inhibit cancer or prevent its recurrence.

  • GC73916 structure
    GC73916Methoxy-PEG-C3-amide-C2-Mal
    CAS: 883993-35-9
    Purity: >99.00%

    Methoxy-PEG-C3-amide-C2-Mal can bind to hemoglobin through the 93Cys residue to produce di-PEGylated hemoglobin.

  • GC73931 structure
    GC73931KVS0001
    CAS: 3056394-59-0
    Purity: >99.00%

    KVS0001 is a selective SMG1 inhibitor.

  • GC73936 structure
    GC73936uPSEM792
    CAS: 2323525-19-3
    Purity: >99.50%

    uPSEM792 is a pharmacologically selective effector molecules (PSEM) agonist for PSAM4-GlyR, with an affinity of Ki of 0.7 nM.

  • GC73937 structure
    GC73937SPOP-IN-2
    CAS: 3031640-86-2

    SPOP-IN-2 (compound E1) is a Speckle-type POZ protein (SPOP) inhibitor with IC50 of 0.58 μM, which disrupt the SPOP-subtrate interaction and selectively inhibits proliferation of ccRCC.

  • GC73946 structure
    GC73946Z36-MP5
    CAS: 2839660-03-4
    Purity: >99.00%

    Z36-MP5 is an Mi-2β-targeted inhibitor, with IC50 of 0.082 μM.

  • GC73951 structure
    GC73951Antiproliferative agent-50
    CAS: 301675-59-2

    Antiproliferative agent-50 (Compd VIII-a) is an inhibitor of myeloma cell proliferation and may be used to inhibit multiple myeloma.

  • GC73952 structure
    GC73952Luciferase-IN-4
    CAS: 1020413-85-7

    Luciferase-IN-4 (Compound 6b) is an inhibitor for luciferase with IC50 of 4.1 μM.

  • GC73963 structure
    GC73963TX-2552
    CAS: 2446767-14-0
    Purity: >99.00%

    TX-2552 is an orally active tyrosine DNA phosphodiesterase 1 (TDP1) inhibitor with an IC50 value of 0.62 μM.

  • GC73964 structure
    GC73964Progranulin modulator-3
    CAS: 371116-39-1
    Purity: >99.00%

    Progranulin modulator-3 (compd C40) is a brain-penetrant and orally active progranulin (PGRN) inducer.

  • GC73969 structure
    GC73969CaMKK2-IN-1
    CAS: 3032691-65-6
    Purity: >98.00%

    CaMKK2-IN-1 is a selective, ligand-efficient inhibitor of CaMKK2, with IC50 of 7 nM.

  • GC73977 structure
    GC73977C3TD879
    CAS: 2850259-33-3
    Purity: >99.00%

    C3TD879 is an inhibitor of citron kinase (CITK), an AGC family serine/threonine kinase that regulates cytokinesis.

  • GC73978 structure
    GC73978FAZ-3532
    Purity: >99.00%

    FAZ-3532 (compound G3Ia) is an inhibitor of binding to the NTF2L domain of G3BP1/2 that binds to G3BP1 with a Kd of 0.54 μM.

  • GC73979 structure
    GC73979FAZ-3780
    Purity: >98.00%

    FAZ-3780 (compound G3Ib) is an inhibitor of binding to the NTF2L domain of G3BP1/2 that binds to G3BP1 with a Kd of 0.15 μM.

  • GC73987 structure
    GC73987CK-963
    CAS: 2851991-63-2
    Purity: >99.00%

    CK-963 is an activator for cardiac troponin (cTnC) with Ki of 11.5 μM.

  • GC73989 structure
    GC73989EBP-IN-1
    Purity: >99.00%

    EBP-IN-1 (compound 11) is an inhibitor of emopamil-binding protein (EBP), a sterol isomerase in the cholesterol biosynthetic pathway.