Caspase-3 Inhibitor III

Caspase-3 Inhibitor III offers a peptide-based scaffold engineered for studying proteolytic pathways and substrate recognition. Its structural features enable detailed mapping of cleavage determinants. Researchers evaluate its conformational preferences to understand residue-driven specificity. Use includes mechanism studies, peptide optimization, and biochemical regulation modeling.

Designed for biological research and industrial applications, not intended for individual clinical or medical purposes.
Caspase-3 Inhibitor III(CAS 285570-60-7)

CAT No: R2442

CAS No:285570-60-7

Synonyms/Alias:Caspase-3 Inhibitor III;285570-60-7;Ac-DEVD-CMK;(4S)-4-[[(2S)-2-acetamido-3-carboxypropanoyl]amino]-5-[[(2S)-1-[[(2S)-1-carboxy-4-chloro-3-oxobutan-2-yl]amino]-3-methyl-1-oxobutan-2-yl]amino]-5-oxopentanoic acid;CHEMBL1782265;Ac-Asp-Glu-Val-Asp-chloromethylketone trifluoroacetate salt;N-acetyl-Asp-Glu-Val-Asp-chloromethylketone;Ac-DEVD-CMK (trifluoroacetate salt);MFCD25372552;EX-A8700;HY-P0034;BDBM50346373;Ac-DEVD-CMK/Caspase-3 Inhibitor III;BP-23540;DA-70475;FA111126;acetyl-Asp-Glu-Val-Asp-chloromethyl ketone;CS-0014223;(2S,5S,8S,11S)-8-(2-carboxyethyl)-11-(carboxymethyl)-2-(2-chloroacetyl)-5-isopropyl-4,7,10,13-tetraoxo-3,6,9,12-tetraazatetradecane-1-carboxylic acid;(4S,7S,10S,13S)-7-(2-Carboxyethyl)-4-(carboxymethyl)-13-(2-chloroacetyl)-10-isopropyl-2,5,8,11-tetraoxo-3,6,9,12-tetraazapentadecan-15-oic acid;

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M.F/Formula
C21H31ClN4O11
M.W/Mr.
550.9
Sequence
One Letter Code:DEVD
Three Letter Code:Ac-Asp-Glu-Val-Asp-CH2Cl

Caspase-3 Inhibitor III is a specialized small molecule compound designed to selectively inhibit the activity of caspase-3, a key executioner protease involved in the apoptotic pathway. By targeting this crucial enzyme, Caspase-3 Inhibitor III offers researchers a powerful tool for dissecting the molecular mechanisms underlying programmed cell death in various biological systems. Its high specificity and robust inhibitory action make it a valuable asset in studies where modulation of apoptosis is essential for experimental outcomes. The compound is widely recognized for its utility in both in vitro and in vivo research settings, enabling scientists to precisely control apoptotic signaling and investigate the downstream effects of caspase-3 inhibition on cellular and molecular processes. The stability and solubility profile of Caspase-3 Inhibitor III further enhance its suitability for a broad range of experimental protocols, from basic cell culture assays to more complex biological models.

Apoptosis Research: As a potent inhibitor of caspase-3, Caspase-3 Inhibitor III is extensively utilized in apoptosis research to elucidate the role of caspase-dependent pathways in cell death. By blocking caspase-3 activity, researchers can differentiate between caspase-dependent and caspase-independent mechanisms of apoptosis, thereby gaining deeper insights into cellular responses to stress, toxins, or genetic manipulation. This application is particularly valuable for mapping the cascade of molecular events that lead to cell dismantling and for identifying novel regulatory factors involved in programmed cell death.

Neuroprotection Studies: In the context of neurobiology, the inhibitor is frequently employed to investigate neuroprotective strategies against apoptotic neuronal loss. By suppressing caspase-3 activation, scientists can model the prevention of neuronal apoptosis in response to various insults such as oxidative stress, excitotoxicity, or traumatic injury. These studies are crucial for understanding the cellular mechanisms that contribute to neurodegeneration and for exploring potential interventions that may preserve neuronal viability in experimental models.

Cellular Signal Transduction: Caspase-3 Inhibitor III serves as an indispensable tool in the study of cellular signal transduction networks, particularly those that intersect with apoptotic pathways. By selectively inhibiting caspase-3, researchers can assess the impact of apoptosis inhibition on signaling cascades such as MAPK, PI3K/Akt, or NF-κB, which are often modulated during cell death and survival decisions. This approach allows for the dissection of cross-talk between apoptotic and non-apoptotic signaling, providing a clearer understanding of how cells integrate multiple signals to determine fate.

Drug Screening and Toxicology: The application of this caspase-3 inhibitor extends to drug screening and toxicological assessments, where it is used to evaluate the pro-apoptotic or anti-apoptotic potential of new chemical entities. By incorporating the inhibitor into high-throughput screening assays, researchers can distinguish between compounds that induce apoptosis through caspase-3 activation and those that act via alternative mechanisms. This differentiation is critical for the selection and optimization of candidate molecules in drug discovery pipelines, as well as for the assessment of compound safety profiles.

Stem Cell Research: In stem cell biology, Caspase-3 Inhibitor III is employed to enhance cell survival during differentiation, expansion, or reprogramming protocols. By mitigating apoptosis, the inhibitor supports higher yields of viable stem cells and facilitates the study of developmental processes in a controlled environment. Its use helps to minimize cell loss due to stress-induced apoptosis, thereby improving the efficiency and reproducibility of stem cell-based experiments and advancing the understanding of pluripotency and lineage commitment.

Cancer Research: The inhibitor is also widely used in cancer research to probe the relationship between apoptotic resistance and tumor progression. By blocking caspase-3-mediated cell death, researchers can model the survival advantage conferred by apoptosis inhibition in cancer cells, explore the molecular underpinnings of chemoresistance, and identify potential vulnerabilities that may be exploited for therapeutic intervention. Studies utilizing Caspase-3 Inhibitor III contribute to a more nuanced understanding of tumor biology and the development of novel strategies to overcome apoptotic escape mechanisms in malignancies.

InChI
InChI=1S/C21H31ClN4O11/c1-9(2)18(21(37)25-12(6-16(31)32)14(28)8-22)26-19(35)11(4-5-15(29)30)24-20(36)13(7-17(33)34)23-10(3)27/h9,11-13,18H,4-8H2,1-3H3,(H,23,27)(H,24,36)(H,25,37)(H,26,35)(H,29,30)(H,31,32)(H,33,34)/t11-,12-,13-,18-/m0/s1
InChI Key
ATNOUPFYBMVFLD-RSLFNQERSA-N

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