30 Results for "

SMAC

" in MedChemExpress (MCE) Product Catalog:
Products (30)

30 Results for "SMAC" in MCE Product Catalog:

61
61 Publications Verification
Cat. No.: HY-15989
CAS No.: 957135-43-2
Target:  

IAP Apoptosis

Research Areas:  

Cancer

SM-164 is a cell-permeable Smac mimetic compound. SM-164 binds to XIAP protein containing both the BIR2 and BIR3 domains with an IC50 value of 1.39 nM and functions as an extremely potent antagonist of XIAP.
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61
61 Publications Verification
Cat. No.: HY-15989A
CAS No.: 2734174-02-6
Target:  

IAP Apoptosis

Research Areas:  

Cancer

SM-164 hydrochloride is a cell-permeable Smac mimetic compound. SM-164 binds to XIAP protein containing both the BIR2 and BIR3 domains with an IC50 value of 1.39 nM and functions as an extremely potent antagonist of XIAP.
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44
44 Cited Publications
Cat. No.: HY-16591
CAS No.: 1260251-31-7
Synonyms: TL32711
Target:  

IAP Apoptosis HIV

Research Areas:  

Cancer

Birinapant (TL32711), a bivalent Smac mimetic, is a potent antagonist for XIAP and cIAP1 with Kds of 45 nM and less than 1 nM, respectively. Birinapant (TL32711) induces the autoubiquitylation and proteasomal degradation of cIAP1 and cIAP2 in intact cells, which results in formation of a RIPK1: caspase-8 complex, caspase-8 activation, and induction of tumor cell death. Birinapant (TL32711) targets TRAF2-associated cIAPs and abrogates TNF-induced NF-κB activation.
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12
12 Cited Publications
Cat. No.: HY-15454
CAS No.: 1071992-99-8
Purity:  99.91%
Synonyms: AT-406; Debio 1143; SM-406
Target:  

IAP Apoptosis

Research Areas:  

Cancer

Xevinapant (AT-406) is a potent and orally bioavailable Smac mimetic and an antagonist of IAPs, and it binds to XIAP, cIAP1, and cIAP2 proteins with Ki of 66.4, 1.9, and 5.1 nM, respectively.
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12
12 Cited Publications
Cat. No.: HY-13208
CAS No.: 1071992-57-8
Purity:  98.01%
Synonyms: AT-406 hydrochloride; Debio 1143 hydrochloride; SM-406 hydrochloride
Target:  

IAP Apoptosis

Research Areas:  

Cancer

Xevinapant (AT-406) hydrochloride is a potent and orally bioavailable Smac mimetic and an antagonist of the inhibitor of apoptosis proteins (IAPs). Xevinapant hydrochloride binds to XIAP, cIAP1, and cIAP2 proteins with Kis of 66.4, 1.9, and 5.1 nM, respectively. Xevinapant hydrochloride effectively antagonizes XIAP BIR3 protein in a cell-free functional assay, induces rapid degradation of cellular cIAP1 protein, and inhibits cancer cell growth in various human cancer cell lines. Xevinapant hydrochloride is highly effective in induction of apoptosis in xenograft tumors .
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1
1 Cited Publications
Cat. No.: HY-N0732
CAS No.: 37905-08-1
Jolkinolide B is a bioactive diterpene isolated from the roots of Euphorbia fischeriana Steud with oral activity. Jolkinolide B downregulates XIAP, cIAP1, cIAP2, and phosphorylated Akt, upregulates Smac, activates caspase-3 and caspase-9, and inhibits NF-κB, TGFβ/smad3 and JAK/STAT3 pathways. Jolkinolide B exerts comprehensive biological effects including inducing cancer cell apoptosis, suppressing inflammatory responses, improving lung function, alleviating hepatic steatosis and eliminating intracellular Mycobacterium tuberculosis. Jolkinolide B can be used for the research of leukemia, histiocytic lymphoma, asthma, metabolic dysfunction-associated steatotic liver disease and tuberculosis .
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Cat. No.: HY-125593
CAS No.: 1570231-89-8
Purity:  99.36%
Synonyms: APG-1387
Target:  

IAP Apoptosis

Research Areas:  

Cancer

Dasminapant (APG-1387), a bivalent SMAC mimetic and an IAP antagonist, blocks the activity of IAPs family proteins (XIAP, cIAP-1, cIAP-2, and ML-IAP). Dasminapant induces degradation of cIAP-1 and XIAP proteins, as well as caspase-3 activation and PARP cleavage, which leads to apoptosis. Dasminapant can be used for the research of hepatocellular carcinoma, ovarian cancer, and nasopharyngeal carcinoma .
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Cat. No.: HY-138832
CAS No.: 1619923-32-8
Purity:  99.85%
Synonyms: APG-1252-M1
Research Areas:  

Cancer

BM-1244 (APG-1252-M1) is a Bcl-xL/Bcl-2 inhibitor with Kis of 134 nM and 450 nM. BM-1244 has anti-tumor effects by inducing apoptosis and suppressing tumor growth. BM-1244 can induce cytochrome C and Smac release from mitochondria with caspase-3 and PARP cleavage. BM-1244 exhibits synergy with chemotherapy in vivo. BM-1244 can be studied in research for colorectal cancer, acute myeloid leukemia and gastric cancer .
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Cat. No.: HY-W008235
CAS No.: 84000-07-7
Research Areas:  

Cancer

Fmoc-N-Me-Ala-OH is an Fmoc-protected N-methyl-L-alanine and also a building block for solid-phase peptide synthesis. As a building block, Fmoc-N-Me-Ala-OH is used to synthesize peptidomimetic antagonists of XIAP BIR3 derived from Smac/DIABLO .
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Cat. No.: HY-P10103
CAS No.: 401913-57-3
Target:  

Caspase

Research Areas:  

Cancer

Smac-N7 peptide, the seven N-terminal amino acid of the mitochondrial protein Smac (second mitochondria-derived activator of caspase), cannot pass through the cell membrane .
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Cat. No.: HY-125378
CAS No.: 1422180-49-1
Purity:  98.42%
Synonyms: SBI-0636457; SB1-0636457
Target:  

IAP

Research Areas:  

Cancer

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-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 .
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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-P10104
Target:  

Caspase

Research Areas:  

Cancer

Smac-N7, Penetratin conjugated is a caspase activator derived from the second mitochondria-derived activator of caspases (SMAC) .
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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) .
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Cat. No.: HY-155294
CAS No.: 874270-38-9
Target:  

IAP Apoptosis

Research Areas:  

Cancer

SM-122 is a monovalent Smac mimetic targeting cellular inhibitor of apoptosis protein (cIAP)-1/2. SM-122 can induce cIAP-1/2 degradation and weakly induce apoptosis in tumor cells. SM-122 can be used for the research of cancer, such as breast cancer .
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Cat. No.: HY-P5346
CAS No.: 411230-24-5
Target:  

Peptides

Research Areas:  

Others

Smac-based peptide is a biological active peptide. (peptide from SMAC binding to BIR3 domain)
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Cat. No.: HY-138059A
Purity:  98.57%
Target:  

IAP Apoptosis

Research Areas:  

Cancer

SM-433 hydrochlorid, a Smac mimetic, function as inhibitor of inhibitor of apoptosis proteins (IAPs). SM-433 hydrochlorid exhibits strong binding affinity XIAP BIR3 protein with an IC50<1 μM (patent WO2008128171A2) .
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Cat. No.: HY-RS25999
Research Areas:  

Others

Diablo Rat Pre-designed siRNA Set A contains three designed siRNAs for Diablo gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

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