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PD-1/PD-L1

PD-1/PD-L1

Gli inibitori di PD-1/PD-L1 sono inibitori del checkpoint immunitario che bloccano l'interazione tra la proteina di morte cellulare programmata 1 (PD-1) sui linfociti T e il suo ligando PD-L1 sulle cellule tumorali. Questa interazione sopprime normalmente la risposta immunitaria e permette alle cellule tumorali di sfuggire al riconoscimento immunitario. Inibendo PD-1/PD-L1, questi inibitori potenziano la capacità del sistema immunitario di riconoscere e distruggere le cellule tumorali, inducendo apoptosi e regressione tumorale. Gli inibitori di PD-1/PD-L1 sono fondamentali nella ricerca sull'immunoterapia e nel trattamento del cancro. Presso CymitQuimica, offriamo una gamma di inibitori di PD-1/PD-L1 di alta qualità per supportare la tua ricerca in immuno-oncologia, apoptosi e terapia del cancro.

Trovati 184 prodotti per "PD-1/PD-L1".

prodotti per pagina.
  • Penpulimab

    CAS:
    Penpulimab is a monoclonal antibody targeting PD-1 with antitumor activity, used in studies of pancreatic cancer.
    Purezza:96.8% (SEC-HPLC) - 96.8% (SEC-HPLC)
    Colore e forma:Transparent Liquid
    Peso molecolare:145.14 kDa (Predicted)
  • Sintilimab

    CAS:
    Sintilimab (IBI308), an IgG4 monoclonal antibody, blocks PD-1, enhancing T-cell anti-tumor response; treats Hodgkin's, lung, and esophageal cancers.
    Purezza:> 95% - >95.0% (SDS-PAGE); 95.0% (SEC-HPLC)
    Colore e forma:Liquid
    Peso molecolare:143.78 kDa (Predicted)
  • Zimberelimab

    CAS:
    Zimberelimab (GLS-010) is a humanized antibody targeting PD-1, with anticancer activity.
    Purezza:95%
    Colore e forma:Transparent Liquid
    Peso molecolare:146.54 kDa (Predicted)
  • AUNP-12 acetate


    AUNP-12 acetate is a polypeptide inhibitor of PD-1 that is equivalent to PD-1 and PD-2 in inhibiting lymphocyte proliferation and effector fuction, in addition
    Formula:C144H230N40O50
    Purezza:95.07% - 99.29%
    Colore e forma:White Solid
    Peso molecolare:3321.61
  • Durvalumab

    CAS:
    Durvalumab is a humanized antibody for cancer, inhibiting PD-L1/PD-1 and CD80 interactions at very low concentrations.
    Purezza:97.2% (SDS-PAGE); 95.3% (SEC-HPLC) - 97.7% (SDS-PAGE); 99.59% (SEC-HPLC)
    Colore e forma:Transparent Liquid
    Peso molecolare:146.03 kDa (Predicted)
  • BMS-1001 hydrochloride

    CAS:
    BMS-1001 hydrochloride is an orally active inhibitor of human PD-1/PD-L1 immune checkpoint with low-toxicity in cells.BMS-1001 alleviates the inhibitory effect
    Formula:C35H35ClN2O7
    Purezza:97.36%
    Colore e forma:Solid
    Peso molecolare:631.115
  • Budigalimab

    CAS:
    Budigalimab (ABBV 181) is a humanized monoclonal antibody targeting PD-1 with potential antitumor activity.
    Purezza:97% (SDS-PAGE); 98.8% (SEC-HPLC) - 97% (SDS-PAGE); 98.8% (SEC-HPLC)
    Colore e forma:Transparent Liquid
    Peso molecolare:145.72 kDa (Predicted)
  • Dostarlimab

    CAS:
    Dostarlimab (TSR-042) is an immune checkpoint inhibitor targeting PD-1, blocking its interaction with its ligands PD-L1 and PD-L2.
    Purezza:>95%
    Colore e forma:Transparent Liquid
    Peso molecolare:144.18 kDa (Predicted)
  • Tislelizumab

    CAS:
    Tislelizumab, a PD-1 receptor monoclonal antibody, reduces Fcγ interaction and T cell clearance in advanced squamous NSCLC research.
    Purezza:95.07%
    Colore e forma:Transparent Liquid
    Peso molecolare:145 kDa (Predicted)
  • Ezabenlimab

    CAS:
    Ezabenlimab (BI-754091) is an anti-PD-1 mAb, Kd 6 nM, blocks PD-1/PD-Ls, boosts T-cell IFN-γ, inhibits tumors in vivo.
    Purezza:99.1% (SDS-PAGE); 96.9% (SEC-HPLC) - 99.1% (SDS-PAGE); 96.9% (SEC-HPLC)
    Colore e forma:Transparent Liquid
    Peso molecolare:145.21 kDa (Predicted)
  • Spartalizumab

    CAS:
    "Spartalizumab (PDR001), a humanized IgG4 monoclonal antibody, targets PD-1 to inhibit PD-L1/L2 interactions, useful in ATC research."
    Purezza:SDS-PAGE:95.2%;SEC-HPLC:96.3%
    Colore e forma:Transparent Liquid
    Peso molecolare:145.74 kDa (Predicted)
  • Sotiburafusp alfa

    CAS:
    Sotiburafusp alfa is a humanized bispecific fusion protein comprising a VEGFR-1 extracellular domain fragment (129-228, 1-100 in the current sequence) connected
    Purezza:98%
    Colore e forma:Solid
  • PD-1/PD-L1-IN-9

    CAS:
    PD-1/PD-L1-IN-9, with an IC50 of 3.8 nM, is a potent and orally active inhibitor of the PD-1/PD-L1 interaction.
    Formula:C22H24N2O2
    Purezza:99.92%
    Colore e forma:Solid
    Peso molecolare:348.4382
  • Eciskafusp alfa

    CAS:
    Eciskafusp alfa, a cis-targeted IL2v immunocytokine, acts on programmed cell death 1 (PDCD1, commonly known as PD-1), preferentially targeting antigen-specific
    Purezza:98%
    Colore e forma:Solid
  • Iparomlimab

    CAS:
    Iparomlimab serves as a functional therapeutic tool specifically designed to enable the precise detection and neutralization of the PD-1 protein which plays a pivotal role in the induction of peripheral tolerance and tumor immune evasion during strictly monitored laboratory observation periods and molecular investigations to evaluate the pharmacological potential of targeted checkpoint inhibition in specialized preclinical research environments to facilitate the study of cancer immunotherapies.
    Purezza:95%
    Colore e forma:Transparent Liquid
    Peso molecolare:146.70 kDa (Predicted)
  • MS1-96


    MS1-96 is an orally active PD-L1 (programmed death-ligand 1) degrader. It effectively reduces PD-L1 protein expression levels in various colorectal cancer (CRC) cell lines. The compound loses its ability to induce PD-L1 degradation upon HIP1R knockdown. MS1-96 binds directly to PD-L1 (KD= 2.58 μM) and enhances the interaction between HIP1R and PD-L1, altering PD-L1's intracellular transport in clathrin-coated vesicles. Additionally, MS1-96 induces abnormal N-glycosylation of PD-L1, leading to protein instability and accelerated lysosome-mediated degradation. MS1-96 is applicable for colorectal cancer research.
  • PD-1/PD-L1-IN-52


    PD-1/PD-L1-IN-52 (Compound Ⅲ-5) is an orally active inhibitor of PD-1/PD-L1 interaction, exhibiting an IC50 of 109.9 nM. It demonstrates antitumor activity in a C57BL/6 mouse model of MC38 colon carcinoma cells expressing human PD-1, achieving a tumor growth inhibition (TGI) rate of 49.6%.
    Colore e forma:Odour Solid
  • TPP-1 TFA


    TPP-1 TFA is a high-affinity PD-L1 inhibitor (KD=95nM) that boosts T-cell function to curb tumor growth.
    Formula:C109H151F3N34O34S2
    Colore e forma:Solid
    Peso molecolare:2602.69
  • HLX43


    HLX43 is an ADC targeting PD-L1 with DAR=8 and a cleavable linker that releases C24, possessing both immune blockade and bystander killing effects.
    Purezza:95% - 98.30% (SEC-HPLC)
    Peso molecolare:153.06 kDa (Predicted)
  • Human PD-L1 inhibitor I

    CAS:
    Human PD-L1 inhibitor I, a peptide, blocks PD-L1/PD-1 interaction with 3.39 μM affinity.
    Formula:C110H152N26O32
    Colore e forma:Solid
    Peso molecolare:2350.576