GLPBio

Recombinant Proteins

Research Areas

Products Related to Recombinant Proteins(96)

  • GC73363 structure
    GC73363Antitumor agent-81
    CAS: 2765180-17-2
    Purity: >98.00%

    Antitumor agent-81 (compound 5a) is a low cytotoxicity P62-RNF168 agonist that enhances the interaction between P62 and RNF168.

  • GC73408 structure
    GC73408Tisotumab vedotin
    CAS: 1418731-10-8
    Purity: >99.00%

    Tisotumab vedotin is an ADC targeting tissue factor (TF), formed by covalently linking a fully human monoclonal antibody (TF-011) against TF with the microtubule disruptor MMAE.

  • GC73689 structure
    GC73689Depatuxizumab MMAE
    Purity: >99.00%

    Depatuxizumab MMAE is an antibody-drug conjugate (ADC) comprising an anti EGFR monoclonal antibody (Depatuxizumab) and the cytotoxic agent Monometl auristatin E (MMAE).

  • GC73838 structure
    GC73838TfR-1-IN-1
    CAS: 1643444-62-5
    Purity: >96.00%

    TfR-1-IN-1 (compound C4) is an inhibitor of transferrin receptor 1 (TfR-1) with anticancer activity.

  • GC73961 structure
    GC73961Fumagilin-105
    CAS: 2410081-58-0
    Purity: >97.00%

    Fumagilin-105 is an autophagy targeting chimera (AUTOTAC) that induces p62 self-oligomerization with DC50 values of 0.7 μM for MetAP2 in HEK293 cells.

  • GC74068 structure
    GC74068ORM-5029
    Purity: >99.00%

    ORM-5029 is a first-in-class human epidermal growth factor receptor 2 (HER2)-targeted antibody-drug conjugate (ADC) comprised of SMol006, a highly potent GSPT1 degrader, conjugated to Pertuzumab.

  • GC74451 structure
    GC74451Enfortumab vedotin-ejfv (solution)
    CAS: 1346452-25-2
    Purity: >99.00%

    Enfortumab vedotin-ejfv (solution) is an anti-Nectin-4 antibody-drug conjugate for the management of urothelial carcinoma.

  • GC74509 structure
    GC74509Azintuxizumab vedotin
    CAS: 1826819-58-2
    Purity: >98.00%

    Azintuxizumab vedotin (ABBV-838) is an antibody–drug conjugate (ADC) targeting a unique epitope of CD2 subset 1, a cell-surface glycoprotein expressed on multiple myeloma cells.

  • GC74519 structure
    GC74519Cantuzumab ravtansine
    CAS: 868747-45-9
    Purity: >98.00%

    Cantuzumab ravtansine (IMGN242; huC242-DM4), an ADC, is a humanized monoclonal antibody, huC242, covalently linked via a disulfide bond to DM4 (DM4 ).

  • GC74533 structure
    GC74533Tusamitamab ravtansine
    CAS: 2254086-60-5
    Purity: >99.00%

    Tusamitamab ravtansine (SAR-408701) is a targeted ADC against tumor cells expressing CEACAM5, composed of a humanized anti-CEACAM5 monoclonal antibody covalently linked to the potent cytotoxic agent, maytansinoid DM4 , via a cleavable linker.

  • GC74540 structure
    GC74540Sofituzumab vedotin
    CAS: 1418200-58-4
    Purity: >98.00%

    Sofituzumab vedotin (DMUC5754A) is a MMAE-containing anti-MUC16 antibody-drug conjugate (ADC) with a protease-cleavable linker.

  • GC74544 structure
    GC74544Farletuzumab ecteribulin
    CAS: 2407465-18-1
    Purity: >98.00%

    Farletuzumab ecteribulin (MORAb-202) is an ADC, consisting of the humanized anti-human FRA antibody Farletuzumab conjugated via reduced interchain disulfide bonds to Mal-PEG2-Val-Cit-PAB-eribulin.

  • GC74567 structure
    GC74567Labetuzumab govitecan
    CAS: 1469876-18-3
    Purity: >98.00%

    Labetuzumab govitecan (IMMU 130) is an Anti-CEACAM5/SN-38 antibody-drug conjugate (ADC).

  • GC74600 structure
    GC74600Cofetuzumab pelidotin
    CAS: 1869937-48-3
    Purity: >99.00%

    Cofetuzumab pelidotin (PF-06647020) is a PTK7-targeting ADC comprising a humanized anti-PTK7 mAb joined to an auristatin microtubule inhibitor payload, auristatin-0101, by a cleavable valine-citrulline (vc)-based linker.

  • GC74620 structure
    GC74620Zilovertamab vedotin
    Purity: >98.00%

    Zilovertamab vedotin (VLS-101) is a novel antibody-drug conjugate comprising the humanized monoclonal antibody zilovertamab and and the anti-microtubule cytotoxin monometl vedotin.

  • GC74702 structure
    GC74702YTK-105
    CAS: 774192-20-0
    Purity: >98.00%

    YTK-105 is a ligand of p62-ZZ domain.

  • GC78874 structure
    GC78874BMMP
    CAS: 748785-70-8
    Purity: >99.50%

    BMMP is an anti- HIV-1 agent and hnRNP M modulator.

  • GC78992 structure
    GC78992EAD1 trihydrochloride
    Purity: >98.00%

    EAD1 trihydrochloride is a Chloroquine analog with anticancer activity.

  • GC79124 structure
    GC79124CDH11-IN-1
    CAS: 1239467-61-8
    Purity: >99.50%

    CDH11-IN-1 is a CDH11 inhibitor.

  • GC79125 structure
    GC79125BAS00093476
    CAS: 300670-24-0
    Purity: >99.00%

    BAS00093476 is an E-cadherin inhibitor.

  • GC79126 structure
    GC79126BAS00602705
    CAS: 317321-89-4
    Purity: >98.50%

    BAS00602705 is an E-cadherin inhibitor.

  • GC79127 structure
    GC79127Pitstop 2c
    Purity: >98.50%

    Pitstop 2c is a clathrin terminal domain inhibitor with an IC 50 of 1.8 μM.

  • GC79128 structure
    GC79128Type IV collagen peptide acetate
    Purity: >98.00%

    Type IV collagen peptide acetate is a cell-binding ligand peptide derived from type IV collagen.

  • GC79138 structure
    GC79138CAST-calpain-2 stabilizer-1
    CAS: 3110929-05-7
    Purity: >99.50%

    CAST-calpain-2 stabilizer-1 is a blood-brain barrier permeable stabilizer of CAST-calpain-2 interaction.