84 Results for "

IAP Inhibitor

" in MedChemExpress (MCE) Product Catalog:
Products (84)

84 Results for "IAP Inhibitor" in MCE Product Catalog:

Cat. No.: HY-15519
CAS No.: 867324-12-7
Target:  

IAP FLT3

Research Areas:  

Cancer

LBW242, a 3-mer and Smac mimetic, is a potent and orally active proapoptotic IAP inhibitor. LBW242 shows effects on mutant FLT3-expressing cells. LBW242 has activity against multiple myeloma, and potentiates TRAIL- and anticancer agent-mediated cell death of ovarian cancer cells .
loading...
    loading...
Cat. No.: HY-129619
CAS No.: 2222354-91-6
Research Areas:  

Cancer

SNIPER(ER)-87 consists of an inhibitor of apoptosis protein (IAP) ligand LCL161 derivative that is conjugated to the estrogen receptor α (ERα) ligand 4-hydroxytamoxifen by a PEG linker, and efficiently degrades the ERα protein (IC50=0.097 μM). SNIPER(ER)-87 preferentially recruits XIAP to ERα in the cells, and XIAP is the primary E3 ubiquitin ligase responsible for the SNIPER(ER)-87-induced ERα degradation .
loading...
    loading...
Cat. No.: HY-150825
CAS No.: 847137-53-5
Research Areas:  

Cancer

CST530 is an inhibitor of apoptosis protein (IAP) antagonist. CST530 is an IAP-type Ligands for E3 Ligase. CST530 binds to the BIR3 domain of IAP and interferes with its function, thereby promoting the ubiquitination and degradation of cIAP1. CST530 can be used to prepare PROTACs .
loading...
    loading...
Cat. No.: HY-120434
CAS No.: 949963-04-6
Synonyms: HGS1029
Target:  

IAP

Research Areas:  

Cancer

AEG40826 (HGS1029), a second mitochondria-derived activator of caspases (SMAC) mimetic, is an inhibitor of apoptosis (IAP) inhibitor. AEG40826 degrades cellular IAP1 (cIAP1) and blocks TNF-α pro-survival signaling. AEG40826 can be used for cancer research .
loading...
    loading...
Cat. No.: HY-139865
CAS No.: 2865171-75-9
Target:  

Apoptosis

Research Areas:  

Cancer

142I5 is a potent ML-IAP Lys-covalent inhibitor with an IC50 value of 11 nM.
loading...
    loading...
Cat. No.: HY-111872
CAS No.: 3093563-31-3
Purity:  99.79%
Target:  

SNIPERs Bcr-Abl

Research Areas:  

Cancer

SNIPER(ABL)-020, conjugating Dasatinib (ABL inhibitor) to Bestatin (IAP ligand) with a linker, induces the reduction of BCR-ABL protein .
loading...
    loading...
Cat. No.: HY-111860
Target:  

SNIPERs Bcr-Abl

Research Areas:  

Cancer

SNIPER(ABL)-013, conjugating GNF5 (ABL inhibitor) to Bestatin (IAP ligand) with a linker, induces the reduction of BCR-ABL protein with a DC50 of 20 μM .
loading...
    loading...
Cat. No.: HY-111861
CAS No.: 2222355-77-1
Target:  

SNIPERs Bcr-Abl

Research Areas:  

Cancer

SNIPER(ABL)-024, conjugating GNF5 (ABL inhibitor) to LCL161 derivative (IAP ligand) with a linker, induces the reduction of BCR-ABL protein with a DC50 of 5μM .
loading...
    loading...
Cat. No.: HY-111850
CAS No.: 339186-54-8
Synonyms: PROTAC IAP binding moiety 1
Target:  

Ligands for E3 Ligase

Research Areas:  

Cancer

Bestatin-amido-Me, the Bestatin-based IAP ligand, binds to ABL inhibitor via a linker to form SNIPER .
loading...
    loading...
Cat. No.: HY-111849
CAS No.: 1436868-85-7
Synonyms: CGP-57148B carbaldehyde; STI571 carbaldehyde; PROTAC ABL binding moiety 1
Research Areas:  

Cancer

Imatinib carbaldehyde (CGP-57148B carbaldehyde), the Imatinib (ABL inhibitor) based moiety, binds to IAP ligand via a linker to form SNIPER .
loading...
    loading...
Cat. No.: HY-131178
CAS No.: 1258391-29-5
Purity:  98.05%
HG-7-85-01-NH2 is the HG-7-85-01 (ABL inhibitor) based moiety, binds to IAP ligand via a linker to form SNIPER .
loading...
    loading...
Cat. No.: HY-138059
CAS No.: 1071992-81-8
Purity:  98.83%
Target:  

IAP Apoptosis

Research Areas:  

Cancer

SM-433, a Smac mimetic, function as inhibitor of inhibitor of apoptosis proteins (IAPs). SM-433 exhibits strong binding affinity XIAP BIR3 protein with an IC50<1 μM (patent WO2008128171A2) .
loading...
    loading...
Cat. No.: HY-111874
CAS No.: 2222354-29-0
Target:  

SNIPERs Bcr-Abl

Research Areas:  

Cancer

SNIPER(ABL)-039, conjugating Dasatinib (ABL inhibitor) to LCL161 derivative (IAP ligand) with a linker, induces the reduction of BCR-ABL protein with a DC50 of 10 nM. IC50s are 0.54 nM, 10 nM, 12 nM, and 50 nM for ABL, cIAP1, cIAP2, XIAP, respectively .
loading...
    loading...
Cat. No.: HY-155019
CAS No.: 2941243-62-3
Target:  

IAP

Research Areas:  

Cancer

Anticancer agent 128 (compound 1) is an IAP inhibitor that covalently targets the BIR3 domains of XIAP, cIAP1, and cIAP2. Anticancer agent 128 targets the BIR3 domains of XIAP, cIAP1, and cIAP2 with IC50s of 24.9 nM, 19.3 nM, and 10.3 nM, respectively .
loading...
    loading...
Cat. No.: HY-155018
CAS No.: 2410953-19-2
Target:  

IAP

Research Areas:  

Cancer

Anticancer agent 127 (142D6) is an IAP inhibitor that covalently targets the BIR3 domains of XIAP, cIAP1, and cIAP2. Anticancer agent 127 targets the BIR3 domains of XIAP, cIAP1, and cIAP2 with IC50s of 12 nM, 14 nM, and 9 nM, respectively. Anticancer agent 127 has anticancer effects .
loading...
    loading...
Cat. No.: HY-175446
Target:  

IAP Apoptosis

Research Areas:  

Cancer

GDC-0152-acetamide is a pan-inhibitor of apoptosis protein (IAP) antagonist. GDC-0152-acetamide induces cIAP1/2 autoubiquitination and degradation, activating the non-canonical NF-κB pathway to promote TNF-α secretion and tumor cell apoptosis. GDC-0152-acetamide is promising for research of ERα-positive breast cancer .
loading...
    loading...
Cat. No.: HY-176440
Research Areas:  

Infection

BP-198 is a inhibitor and a SNIPER-class degrader targeting to SARS-CoV-2 main protease (Mpro) , with antiviral activity. BP-198 recruits the IAP ubiquitin ligase complex to degrade target proteins via the ubiquitin-proteasome system. BP-198 also degrades protease mutants resistant to Nirmatrelvir (HY-138687). BP-198 can be used in studies related to COVID-19 .
loading...
    loading...
Cat. No.: HY-107738R
CAS No.: 95975-55-6
Synonyms: Z/E-Guggulsterone (Standard)
Guggulsterone (Standard) is the analytical standard of Guggulsterone (HY-107738). This product is intended for research and analytical applications. Guggulsterone is a plant sterol derived from the gum resin of the tree Commiphora wightii. Guggulsterone inhibits the growth of a wide variety of tumor cells and induces apoptosis through down regulation of antiapoptotic gene products (IAP1, xIAP, Bfl-1/A1, Bcl-2, cFLIP and survivin), modulation of cell cycle proteins (cyclin D1 and c-Myc), activation of caspases and JNK, inhibition of Akt. Guggulsterone, a farnesoid X receptor (FXR) antagonist, with IC50s of 24.06 μM and 39.05 μM for (-)-(E)-Guggulsterone (HY-N7781) and (Z)-Guggulsterone (HY-110066), respectively.
loading...
    loading...
Cat. No.: HY-111852
CAS No.: 778277-37-5
Synonyms: PROTAC ABL binding moiety 2
Research Areas:  

Cancer

GNF5-amido-Me, the GNF5 (ABL inhibitor) based moiety, binds to IAP ligand via a linker to form SNIPER .
loading...
    loading...
Cat. No.: HY-111853
CAS No.: 2095244-62-3
Synonyms: PROTAC IAP binding moiety 2
Target:  

Ligands for E3 Ligase

Research Areas:  

Cancer

MV-1-NH-Me, the MV-1 based IAP ligand, binds to ABL inhibitor via a linker to form SNIPER .
loading...
    loading...