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Cat. No. | Product Name | Target | Signaling Pathways |
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T81148 |
Smac-based peptide
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Smac-based peptide为具有生物活性的肽,源自SMAC与BIR3结构域的结合。 | |||
T6763 |
Xevinapant
ARRY-334543,SM-406,AT406,Debio-1143 |
IAP | Apoptosis |
Xevinapant (Debio-1143) 是一种有效的 Smac 模拟物和 IAP 的拮抗剂,能够抑制 XIAP,cIAP1 和 cIAP2 蛋白,Ki 值分别为 66.4,1.9 和 5.1 nM。 | |||
T3299 |
Xevinapant hydrochloride
AT-406 HCl,SM-406 |
Apoptosis; IAP | Apoptosis |
Xevinapant hydrochloride (AT-406 HCl) 是口服生物可利用的 Smac 模拟物,也是细胞凋亡蛋白抑制剂的拮抗剂。它在无细胞功能测定中有效拮抗 XIAP BIR3 蛋白,诱导细胞 cIAP1 蛋白的快速降解,并抑制各种人类癌细胞系中的癌细胞生长。它在诱导异种移植肿瘤细胞凋亡方面非常有效。 | |||
T20053 |
Jasmacyclen
EC 226-501-6,NSC-6598,Verdyl acetate,Greenyl acetate,NS 6598,NSC 6598 |
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Jasmacyclen is a compound in which has an aroma. | |||
T35205 |
Xylosmacin
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Xylosmacin is a biochemical. | |||
T2080 |
LCL161
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IAP | Apoptosis |
LCL161 是一种 SMAC 模拟物,可有效结合并抑制多种 IAP。它抑制 HEK293 细胞中 XIAP 和 MDA-MB-231细胞中 cIAP1的 IC50分别为 35 和 0.4 nM。 | |||
T6007 |
Birinapant
TL32711,比瑞那帕 |
Apoptosis; IAP; HIV Protease | Apoptosis; Microbiology/Virology; Proteases/Proteasome |
Birinapant (TL32711) 是一种二价 Smac 模拟物,是 XIAP 和 cIAP1的强效拮抗剂,Kd 值分别为 45 nM 和小于 1 nM。它靶向与 TRAF2 相关的 cIAP,并消除 TNF 诱导的 NF-κB 活化。 | |||
T12932L |
SM-164
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Apoptosis; IAP | Apoptosis |
SM-164 是细胞渗透性 Smac 类似物,与含有 BIR2 和 BIR3 结构域的 XIAP 蛋白结合,IC50值为 1.39 nM,它用作XIAP 的强效拮抗剂。 | |||
T26242 |
SW IV-52
SW-IV-52,SW IV52,SW IV 52,SWIV52 |
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SW IV-52 is an XIAP-inhibitor that acts as a second mitochondria-derived activator of caspases (SMAC) mimetic. | |||
T64217 | SM-433 hydrochloride | ||
SM-433 hydrochlorid 是一种 Smac 模拟物,是一种凋亡抑制蛋白(IAPs)抑制剂。SM-433 hydrochlorid 能够强力结合 XIAP BIR3 蛋白 (IC50<1 μM)。 | |||
T63969 |
SM-433
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SM-433 是 Smac 模拟物,是凋亡抑制蛋白(IAPs)的抑制剂。SM-433 对 XIAP BIR3 蛋白具有较强的亲和力 (IC50<1 μM)。 | |||
T15723 |
LBW242
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Others | Others |
LBW242 is a 3-mer and Smac mimetic and is an effective and orally active proapoptotic IAP inhibitor. LBW242 has activity against multiple myeloma and potentiates TRAIL- and anticancer drug-mediated cell death of ovarian cancer cells. LBW242 displays effec | |||
T38857 |
SBP-0636457
SBI-0636457,SB1-0636457,SBP-0636457 |
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SBP-0636457 (SB1-0636457) is a SMAC mimetic and an inhibitor of inhibitor of apoptosis (IAP) proteins. It specifically binds to the BIR-domains of IAP proteins with a Ki value of 0.27 μM. SBP-0636457 holds potential for research in the fields of solid tumors and hematologic cancers. | |||
T75243 | SM-164 Hydrochloride | ||
SM-164 Hydrochloride 是一种可渗透细胞的 Smac 类似物。SM-164 与含有 BIR2 和 BIR3 结构域的XIAP 蛋白结合,IC50值为 1.39 nM,SM-164 用作XIAP 的强效拮抗剂。 | |||
T12932 |
SM-164 Hydrochloride (957135-43-2 free base)
SM-164 Hydrochloride |
IAP | Apoptosis |
SM-164 Hydrochloride is a cell-permeable Smac mimetic compound. SM-164 binds to XIAP protein containing both the BIR2 and BIR3 domains(IC50 value of 1.39 nM) and functions as an extremely potent antagonist of XIAP. | |||
T36201 |
AZD5582 dihydrochloride
AZD 5582 dihydrochloride |
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Dimeric Smac mimetic; potent inhibitor of X-linked (XIAP) and cellular (cIAP) inhibitor of apoptosis protein (IC50 values are 15, 15 and 21 nM for XIAP, cIAP1 and cIAP2 respectively). Binds to the BIR3 domain of XIAP to prevent interaction with caspase-9. Causes degradation of cIAP1 and cIAP2 and induces apoptosis in MDA-MB-231 breast cancer cells. Causes tumor regression in MDA-MB-231 xenograft-bearing mice. Hennessy et al (2013) Discovery of a novel class of dimeric Smac mimetics as potent IAP... | |||
T69200 |
CGP74514A
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CGP74514A is a CDK1 inhibitor with potential anticancer activity. In U937 cells, CGP74514A - induced apoptosis (5 microM) became apparent within 4 hr and approached 100% by 24 hr. The pan- caspase inhibitor Boc-fmk and the caspase-8 inhibitor lETD-fmk opposed CGP74514A -induced caspase-9 activation and PARP degradation, but not cytochrome c or Smac/DIABLO release. CGP74514A -mediated apoptosis was substantially blocked by ectopic expression of full-length Bel- 2, a loop-deleted mutant Bcl-2, and... | |||
T69323 |
Dexamethasone sodium succinate
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Dexamethasone sodium succinate is the acetate salt form of dexamethasone, which is a synthetic glucocorticoid; it combines high anti-inflammatory effects with low mineralocorticoid activity. At high doses (e.g. 40 mg), it reduces the immune response. Dexamethasone acetate (NEOFORDEX®) is indicated in adults for the treatment of symptomatic multiple myeloma in combination with other medicinal products. Dexamethasone has been shown to induce multiple myeloma cell death (apoptosis) via a down-regul... |
Cat. No. | Product Name | Species | Expression System |
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TMPY-00924 |
SMAC Protein, Human, Recombinant (His)
DFNA64,diablo, IAP-binding mitochondrial protein,SMAC |
Human | E. coli |
Apoptosis is an essential processes required for normal development and homeostasis of all metazoan organisms. Second Mitochondria-Derived Activator of Caspases (Smac) or Direct IAP Binding Protein with low isoelectric point, pI (Diablo) is a proapoptogenic mitochondrial protein that is released to the cytosol in response to diverse apoptotic stimuli, including commonly used chemotherapeutic drugs. The current knowlege about structure and function of Smac/Diablo during programmed cell death, bot... | |||
TMPY-01176 |
cIAP1 Protein, Human, Recombinant (Avi)
Hiap-2,API1,HIAP2,RNF48,baculoviral IAP repeat containing 2,... |
Human | E. coli |
The cellular inhibitor of apoptosis protein-1 (cIAP1) is a member of the Inhibitor of Apoptosis family proteins are (IAP) whose members are characterized by a novel domain of about 70 amino acids termed baculoviral IAP repeats (BIRs). The BIR domains of cIAP1 and cIAP2 bind to caspases, the key effector proteases of apoptosis. The IAP protein family which can enhance cell survival are crucial regulators of programmed cell death. Both cIAP1 and cIAP2 are the E3 ubiquitin protein isopeptide ligase... |