CymitQuimica logo
IAP

IAP

Os inibidores das proteínas inibidoras da apoptose (IAP) são compostos que bloqueiam a atividade das IAPs, uma família de proteínas que previnem a apoptose, inibindo caspases e outros componentes da maquinaria apoptótica. Os inibidores de IAP promovem a apoptose em células cancerígenas ao neutralizar esses sinais de sobrevivência, tornando-os ferramentas importantes na pesquisa e terapia contra o câncer. Na CymitQuimica, oferecemos uma ampla gama de inibidores de IAP de alta qualidade para apoiar sua pesquisa em oncologia, apoptose e desenvolvimento terapêutico.

Foram encontrados 77 produtos para "IAP".

produtos por página.
  • MV1

    CAS:
    MV1 is an IAP antagonist. When combined with HaloTag ligand, MV1 causes protein knockdown of HaloTag-fused proteins.
    Fórmula:C33H44N4O5
    Pureza:99.86%
    Cor e Forma:Solid
    Peso molecular:576.7263
  • PROTAC KRAS G12C degrader-2

    CAS:
    PROTAC KRAS G12C degrader-2 (compound 432) is a targeted modulator of K-Ras protein hydrolysis that functions as a bifunctional PROTAC molecule, incorporating a cereblon inhibitor of apoptosis proteins (IAP) ligand on one terminus and a KRAS-binding moiety on the opposite end, thereby enabling selective recruitment of mutant KRAS G12C to the ubiquitin–proteasome system for controlled degradation and mechanistic investigation of KRAS-driven oncogenic signaling pathways.
    Fórmula:C51H53ClFN9O7
    Cor e Forma:Solid
    Peso molecular:958.47
  • MDM2/XIAP-IN-1


    MDM2/XIAP-IN-1 (compound 14) is an orally active dual inhibitor of MDM2 and XIAP, exhibiting anti-cancer activity with an IC50 of 0.3 μM and potential
    Cor e Forma:Odour Solid
  • SM-164 Hydrochloride


    SM-164 Hydrochloride: cell-permeable, binds to XIAP (BIR2/3 domains), IC50 of 1.39 nM, potent XIAP antagonist.
    Fórmula:C62H85ClN14O6
    Pureza:98%
    Cor e Forma:Solid
    Peso molecular:1157.88
  • SBP-0636457

    CAS:
    SBP-0636457: SMAC mimetic, IAP inhibitor, binds BIR-domains (Ki=0.27μM), potential in tumor/cancer research.
    Fórmula:C25H36N4O4
    Cor e Forma:Solid
    Peso molecular:456.5777
  • XIAP BIR2/BIR2-3 inhibitor-1

    CAS:
    XIAP BIR2/BIR2-3 inhibitor-1 (compound 3) serves as a potent dual inhibitor targeting BIR2 and BIR2-3 domains, with IC50 values of 1.9 nM and 0.8 nM, respectively. This compound is utilized in cancer research studies [1].
    Fórmula:C72H96N16O14
    Cor e Forma:Solid
    Peso molecular:1409.63
  • PROTAC TEAD1/IAP degrader-1


    PROTAC TEAD1/IAP degrader-1 (Compound A232) is a selective PROTAC-based degrader targeting TEAD1 and cIAP1, with DC50 values of 14 nM and 270 nM, respectively. This compound facilitates the ubiquitination and degradation of TEAD1 and cIAP1, and it reduces the expression of the TEAD-dependent gene CTGF. Additionally, PROTAC TEAD1/IAP degrader-1 exhibits anticancer activity against mesothelioma.
  • IAP ligand 9


    IAP ligand 9 is a SMAC mimetic and binds to the IAP (inhibitor of apoptosis protein) BIR domains, selectively targeting cIAP1-BIR3 and XIAP-BIR3, while showing minimal affinity for XIAP-BIR2, with SPR pKD values of 7.0, 8.0, and 5.0, respectively. As an IAP ligand module, it can be conjugated via linkers with degraders targeting the TEAD1 P site to form IAP-recruiting proteolysis-targeting chimeras (PROTACs/IPDs). This IPD recruits the IAPE3 ubiquitin ligase to form the TEAD1-IPD-IAP ternary complex, mediating ubiquitination and proteasome-dependent degradation of TEAD1 and inducing autodegradation of cIAP1. IAP ligand 9 and related degraders are useful in the study of solid tumors such as malignant pleural mesothelioma associated with abnormal activation of the Hippo pathway.
  • S2/IAPinh


    S2/IAPinh is a conjugate composed of an inhibitor of apoptosis proteins inhibitor (IAPinh) and a ligand of sigma 2 SW43. It demonstrates anti-proliferative and apoptosis-inducing activity by degrading inhibitor of apoptosis proteins (clAP-1).
    Fórmula:C52H75Cl2FN6O6S
    Cor e Forma:Solid
    Peso molecular:1000.48299
  • XIAP BIR2/BIR2-3 inhibitor-3

    CAS:
    XIAP BIR2/BIR2-3 Inhibitor-3 functions as a dual inhibitor targeting both BIR2 and BIR2-3 domains, exhibiting potent activity with IC50 values below 1 nM. This compound is utilized in cancer research [1].
    Fórmula:C86H106N18O16S2
    Cor e Forma:Solid
    Peso molecular:1712
  • XIAP BIR2/BIR2-3 inhibitor-2

    CAS:
    XIAP BIR2/BIR2-3 Inhibitor-2 is a dual inhibitor of BIR2 and BIR2-3 with IC50 values less than 1 nM. It can be used in the study of cancers [1].
    Fórmula:C80H96N20O12
    Peso molecular:1529.75
  • CST626

    CAS:
    CST626 is a PROTAC degrader that targets XIAP, cIAP1, and cIAP2.
    Fórmula:C61H82N8O9S
    Pureza:95.87%
    Cor e Forma:Solid
    Peso molecular:1103.42
  • PROTAC TEAD1/IAP degrader-2


    PROTAC TEAD1/IAP degrader-2 is an IAP-recruiting TEAD1 PROTAC degrader with a DC50 of 170 nM for TEAD1 in NCI-H2052 cells. It exhibits moderate antiproliferative activity in mesothelioma cells that depend on the Hippo pathway. PROTAC TEAD1/IAP degrader-2 also inhibits CTGF expression, though less effectively than the TEAD inhibitor VT-107, and is applicable for mesothelioma research.
  • Dasminapant

    CAS:
    APG-1387 inhibits IAPs, degrades cIAP1/2, XIAP, boosts chemosensitivity, and induces apoptosis in NPC.
    Fórmula:C60H72N10O10S2
    Cor e Forma:White Solid
    Peso molecular:1157.405
  • Anti-CD47 Antibody-FITC (9X161)


    Anti-CD47 Antibody-FITC (9X161) is a FITC-conjugated Mouse antibody targeting CD47. Anti-CD47 Antibody-FITC (9X161) can be used in FCM.
    Cor e Forma:Odour Liquid
  • AZD5582

    CAS:
    AZD5582 is an inhibitor of IAPs, which binds to the BIR3 domains cIAP1, cIAP2, and XIAP with IC50s of 15, 21, and 15 nM, respectively. It induces apoptosis.
    Fórmula:C60H79F3N8O10
    Pureza:98.75% - >99.99%
    Cor e Forma:Solid
    Peso molecular:1129.3121
  • CD47 Protein, Mouse, Recombinant (His)


    CD47 Protein, Mouse, Recombinant (His) is expressed in HEK293 mammalian cells with His tag.
    Pureza:SDS-PAGE: 98.3%; SEC-HPLC: 98.5%
    Cor e Forma:Lyophilized Powder
    Peso molecular:15.3 kDa (predicted); 34-44 kDa (reducing condition, due to glycosylation)
  • Anti-CD47 Antibody-PE (9X161)


    Anti-CD47 Antibody-PE (9X161) is a PE-conjugated Mouse antibody targeting CD47. Anti-CD47 Antibody-PE (9X161) can be used in FCM.
    Cor e Forma:Odour Liquid
  • Anti-CD47 Antibody (8A121)


    Anti-CD47 Antibody (8A121) is a Mouse antibody targeting CD47. Anti-CD47 Antibody (8A121) can be used in ELISA.
    Cor e Forma:Odour Liquid
  • Anti-CD47 Antibody (1F304)


    Anti-CD47 Antibody (1F304) is an antibody targeting CD47. Anti-CD47 Antibody (1F304) can be used in ELISA, FCM.
    Cor e Forma:Odour Liquid