147 Results for "

IAPs

" in MedChemExpress (MCE) Product Catalog:
Products (147)

147 Results for "IAPs" in MCE Product Catalog:

Cat. No.: HY-P990132

Target:  

CD47

Research Areas:  

Inflammation/Immunology Cancer

Anti-Mouse/Rat/Human CD47/IAP Antibody (MIAP410) is an anti-mouse/rat/human CD47/IAP IgG1 monoclonal antibody. Anti-Mouse/Rat/Human CD47/IAP Antibody (MIAP410) can effectively block CD47 signaling and enhance macrophage phagocytic function. Anti-Mouse/Rat/Human CD47/IAP Antibody (MIAP410) can increase the infiltration of immune cells. Anti-Mouse/Rat/Human CD47/IAP Antibody (MIAP410) may interfere with wound healing. Anti-Mouse/Rat/Human CD47/IAP Antibody (MIAP410) can be used for researches on cancer and inflammation conditions such as breast cancer and intestinal mucosal repair .
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Cat. No.: HY-111844
CAS No.: 1351169-27-1
Purity:  97.91%
PROTAC RAR degrader-1 (Compound 9) is a potent and selective RAR PROTAC Degrader consisting of apoptotic protein inhibitors (IAPs) ligands. IAPs-based degraders are also known as SNIPERs. PROTAC RAR Degrader-1 reduces RARα levels in HT1080 cells in a concentration-dependent manner but is blocked by the proteasome inhibitor MG132 (HY-13259). PROTAC RAR Degrader-1 can be used in the study of nuclear receptor-related diseases. (Pink: RAR ligand 1 (HY-111843); Black: Linker (HY-140189); Blue: IAPs Ligand (HY-B0134)) .
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Cat. No.: HY-43962
CAS No.: 693227-00-8
Synonyms: Androgen receptor ligand 3
CS-1-65 is an androgen receptor (AR) ligand. CS-1-65 is linked to an IAP ligand via a linker to form an ERα PROTAC degrader.
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Cat. No.: HY-111876
Purity:  99.51%
Target:  

SNIPERs

Research Areas:  

Cancer

SNIPER(TACC3)-1 targets the TACC3 protein for degradation via the ubiquitin-proteasome pathway based on IAP ligand. SNIPER(TACC3)-1 induces cancer cell death .
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Cat. No.: HY-78144
CAS No.: 50-85-1
4-Methylsalicylic acid is a methyl derivative of Salicylic acid (HY-B0167). 4-Methylsalicylic acid derivatives inhibit the activity of alkaline phosphatases such as TNAP and IAP. 4-Methylsalicylic acid derivatives exhibit immunosuppressive activity .
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Cat. No.: HY-130991
CAS No.: 2378261-89-1
Research Areas:  

Cancer

K-Ras ligand-Linker Conjugate 6 incorporates a ligand for K-Ras recruiting moiety, and a PROTAC linker, which recruit E3 ligases (such as VHL, CRBN, MDM2, and IAP). K-Ras ligand-Linker Conjugate 6 can be used in the synthesis of PROTAC K-Ras Degrader-1 (HY-129523), which is potent PROTAC K-Ras degrader that exhibits ≥70% degradation efficacy in SW1573 cells .
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Cat. No.: HY-111857
CAS No.: 2112837-79-1
Purity:  98.04%
Synonyms: BMS-354825 carbaldehyde; PROTAC ABL binding moiety 4
Research Areas:  

Cancer

Dasatinib carbaldehyde (BMS-354825 carbaldehyde), the Dasatinib (ABL inhibitor) based moiety, binds to IAP ligand via a linker to form SNIPER .
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Cat. No.: HY-111877
Purity:  99.81%
Target:  

SNIPERs

Research Areas:  

Cancer

SNIPER(TACC3)-2 targets the TACC3 protein for degradation via the ubiquitin-proteasome pathway based on IAP ligand. SNIPER(TACC3)-2 induces cancer cell death .
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Cat. No.: HY-128809
CAS No.: 2357114-70-4
Synonyms: E3 ligase Ligand 11
Target:  

Ligands for E3 Ligase

Research Areas:  

Cancer

cIAP1 ligand 2 is the LCL161 derivative based IAP ligand. cIAP1 ligand 2 can be connected to the ABL ligand for protein by a linker to form SNIPER.
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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 .
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Cat. No.: HY-125378A
CAS No.: 1422180-61-7
Purity:  98.36%
Synonyms: (7R)-SBI-0636457; (7R)-SB1-0636457
Target:  

IAP

Research Areas:  

Cancer

(7R)-SBP-0636457 is the isomer of SBP-0636457 (HY-125378), and can be used as an experimental control. SBP-0636457 (SB1-0636457) is a SMAC mimetic, and as an IAP antagonist. SBP-0636457 binds to the BIR-domains of the IAP proteins, with a Ki of 0.27 μM. SBP-0636457 can be used for the research of solid tumors and hematologic cancers .
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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 .
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Cat. No.: HY-131188
CAS No.: 2450351-07-0
Target:  

PROTACs Bcl-2 Family

Research Areas:  

Cancer

PROTAC Bcl-xL degrader-1 is a PROTAC that comprises a Bcl-xL (Bcl-2 family member) ligand binding group, a linker and an IAP E3 ligases binding group. PROTAC Bcl-xL degrader-1 is a potent Bcl-xL degrader, and shows toxicity for human platelets and MyLa 1929 cells with IC50 values of 62 nM and 8.5 μM, respectively .
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Cat. No.: HY-111848A
Purity:  99.26%
Research Areas:  

Cancer

PROTAC AR Degrader-4 comprises a IAP ligand binding group, a linker and an Androgen Receptor (AR) binding group. PROTAC AR Degrader-4 is an AR degrader. Degradation inducers based on cIAP1 are called specific and non-genetic IAP-dependent protein erasers (SNIPERs) .
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Cat. No.: HY-111848
CAS No.: 1351169-31-7
Research Areas:  

Cancer

PROTAC AR Degrader-4 comprises a IAP ligand binding group, a linker and an Androgen Receptor (AR) binding group. PROTAC AR Degrader-4 is an AR degrader. Degradation inducers based on cIAP1 are called specific and non-genetic IAP-dependent protein erasers (SNIPERs) .
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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.
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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 .
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Cat. No.: HY-136010
CAS No.: 2126803-41-4
Target:  

RIP kinase PROTACs

Research Areas:  

Inflammation/Immunology

RIP2 Kinase Inhibitor 4 is a potent and selective RIPK2 PROTAC. RIP2 Kinase Inhibitor 4 effectively degrades RIPK2 (pIC50 of 8) and inhibits the release of related TNF-α .
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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 .
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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 .
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