GLPBio

SCD

SCD (stearoyl-CoA desaturase) is a key enzyme in fatty acid metabolism and is responsible for forming a double bond in Stearoyl-CoA.

Products Related to SCD(19)

  • GC11681 structure
    GC11681MK-8245
    CAS: 1030612-90-8
    Purity: >99.50%

    A stearoyl-CoA desaturase inhibitor

  • GC17107 structure
    GC17107PluriSIn #1 (NSC 14613)
    CAS: 91396-88-2
    Purity: >99.50%

    A selective inhibitor of stearoyl-CoA desaturase

  • GC17354 structure
    GC17354SW203668
    CAS: 1673556-40-5
    Purity: >98%

    stearoyl CoA desaturase inhibitor

  • GC18558 structure
    GC18558CAY10566
    CAS: 944808-88-2
    Purity: >98.00%

    CAY10566 is a selective stearoyl-CoA desaturase 1 (SCD1) inhibitor (mouse: IC₅₀= 4.5nM; human: IC₅₀=4.5nM).

  • GC31447 structure
    GC31447CVT-12012
    CAS: 1018675-35-8
    Purity: >98.50%

    A stearoyl-CoA desaturase inhibitor

  • GC31521 structure
    GC31521XEN723
    CAS: 1072803-08-7
    Purity: >99.50%

    XEN723 is a novel and potent thiazolylimidazolidinone inhibitor of Stearoyl-CoA Desaturase (SCD1) with IC50s of 45 and 524 nM in mouse and HepG2 cell, respectively.

  • GC32780 structure
    GC32780GSK1940029 (SCD inhibitor 1)
    CAS: 1150701-66-8
    Purity: >99.50%

    GSK1940029 (SCD inhibitor 1) (SCD inhibitor 1) is a stearoyl-coa desaturase (SCD) inhibitor extracted from patent WO/2009060053 A1, compound example 16.

  • GC36604 structure
    GC36604MF-438
    CAS: 921605-87-0
    Purity: >99.50%

    MF-438 is a potent and orally bioavailable stearoyl-CoA desaturase 1 (SCD1) inhibitor with an IC50 of 2.3 nM for rSCD1.

  • GC36626 structure
    GC36626MK-8245 Trifluoroacetate
    CAS: 1415559-41-9
    Purity: >98%

    MK-8245 trifluoroacetate is a liver-targeting inhibitor of stearoyl-CoA desaturase (SCD) with IC50 of 1 nM for human SCD1 and 3 nM for both rat SCD1 and mouse SCD1, with anti-diabetic and anti-dyslipidemic efficacy.

  • GC37604 structure
    GC37604SCD1 inhibitor-1
    CAS: 1069094-65-0
    Purity: >99.00%

    SCD1 inhibitor-1 is a potent and liver-selective stearoyl-CoA desaturase-1 (SCD1) inhibitor.

  • GC38436 structure
    GC38436Elemicin
    CAS: 487-11-6
    Purity: >98.00%

    A trioxygenated phenylpropane

  • GC64869 structure
    GC64869YTX-465
    CAS: 2225824-53-1
    Purity: >99.00%

    YTX-465 is a stearoyl-CoA desaturase (Ole1/SCD) inhibitor.

  • GC65036 structure
    GC65036T-3764518
    CAS: 1809151-56-1
    Purity: >99.00%

    T-3764518 is a novel and potent stearoyl coenzyme A desaturase (SCD) inhibitor with an IC50 of 4.7 nM.

  • GC66005 structure
    GC66005CVT-11127
    CAS: 1018674-83-3
    Purity: >98%

    CVT-11127 is a potent SCD inhibitor. CVT-11127 induces apoposis and arrests the cell cycle at the G1/S phase. CVT-11127 has the potential for the research of lung cancer.

  • GC68445 structure
    GC68445SCD1 inhibitor-3
    CAS: 1282606-48-7
    Purity: >98.50%

    SCD1 inhibitor-3 is a safe, potent and orally active SCD1 inhibitor.

  • GC70426 structure
    GC70426Flurtamone
    CAS: 96525-23-4
    Purity: >95.00%

    Flurtamone is a chiral herbicide with acute toxicity levels to Selenastrum capricornutum.

  • GC71316 structure
    GC71316SSI-4
    CAS: 1875084-68-6
    Purity: >99.00%

    SSI-4 is an inhibitor of Stearoyl CoA desaturase 1 (SCD1) , which can be modified with 11C, used as a ligand to in vivo small animal PET/CT imaging of SCD1.

  • GC73574 structure
    GC73574SCD1/5-IN-1
    CAS: 1241494-17-6
    Purity: >99.00%

    SCD1/5-IN-1 (Compound 10) is a SCD1/5 inhibitor.

  • GC15921 structure
    GC15921A939572
    CAS: 1032229-33-6
    Purity: >99.50%

    A939572 is an orally effective and specific stearoyl-CoA desaturase 1 (SCD1) inhibitor with a reported IC₅₀ value of 6.3nM .