AC-YVAD-CHO
Synonym(s):Caspase-1 Inhibitor I - CAS 143313-51-3 - Calbiochem;IL-1β Converting Enzyme (ICE) Inhibitor I, Ac-YVAD-CHO, L-709049
- CAS NO.:143313-51-3
- Empirical Formula: C23H32N4O8
- Molecular Weight: 492.52
- MDL number: MFCD00237123
- SAFETY DATA SHEET (SDS)
- Update Date: 2026-01-13 11:18:30
What is AC-YVAD-CHO?
Description
Ac-YVAD-CHO is an inhibitor of caspase-1/interleukin-1β converting enzyme (ICE; Ki = 0.76 nM) and an acetylated form of the caspase-1 inhibitor YVAD-CHO . It is selective for caspase-1 over caspase-4, -5, -8, -9, and -10 (Kis = 163-970 nM), as well as over caspase-2, -3, -6, and -7 (Kis = >10,000 nM for all). It inhibits activation of caspase-1 and IL-1β in a cell-free assay using LPS-treated THP-1 cell homogenates when used at a concentration of 5 μM. Ac-YVAD-CHO (12.5 μmol/kg) reduces pancreatic levels of IL-18 and serum levels of IL-1β, as well as reduces pyroptosis of pancreatic cells, in a mouse model of cerulein-induced acute pancreatitis but does not decrease pancreatic expression of NOD-like receptor protein 3 (NLRP3). It increases susceptibility to lethal E. coli infection but prevents LPS-induced death in C3H/HeN mice when administered at doses of 5 and 10 mg/kg, respectively.
The Uses of AC-YVAD-CHO
A potent, specific, and reversible inhibitor of caspases-1, -4 and -5
What are the applications of Application
Caspase-1 inhibitor I is an inhibitor of caspase-1, caspase-4, and caspase-5
Properties of AC-YVAD-CHO
| Boiling point: | 937.7±65.0 °C(Predicted) |
| Density | 1.276±0.06 g/cm3(Predicted) |
| storage temp. | −20°C |
| solubility | DMF:30.0(Max Conc. mg/mL);60.91(Max Conc. mM) DMSO:30.0(Max Conc. mg/mL);60.91(Max Conc. mM) Ethanol:30.0(Max Conc. mg/mL);60.91(Max Conc. mM) PBS (pH 7.2):5.0(Max Conc. mg/mL);10.15(Max Conc. mM) |
| form | Powder |
| pka | 4.20±0.10(Predicted) |
| color | White to off-white |
| Sensitive | Moisture Sensitive |
Safety information for AC-YVAD-CHO
Computed Descriptors for AC-YVAD-CHO
New Products
Levothyroxine Impurity-F Montelukast EP Impurity-D/Montelukast USP Related Compound C Atorvastatin FXA Impurity/Atorvastatin Cyclic 6-Hydroxy Impurity Sodium Salt Isosulfan blue Keto N-Oxide Impurity Ivermectin Impurity F N-Nitroso des Methyl Tramadol/N-Nitroso-N-Desmethyl-Tramadol DL-beta-(3-Bromophenyl)alanine Tetrabutylammonium perchlorate N,O-Dimethylhydroxylamine hydrochloride (RS)-beta-Amino-beta-(4-bromophenyl)propionic acid 2-Amino-5-bromo-4-(trifluoromethyl)pyridine(RM for Indian lab) N,N CARBONYL DIIMIDAZOLE (R)-BoroLeu-(+)-Pinanediol-CF3COOH 1,4-bis(methylsulfonyl)butane 4-(5-amino-1-methyl-1h-benzoimidazol-2-yl)-butyric acid isopropyl ester. 5-Methyl-1,3-benzenediacetonitrile 4-Fluorothiophenol 1-methyl amino-2,4-dinitro benzene CSA (DL-10-Camphorsulfonic Acid) 2-Hydroxy-4-methylnicotinic acid 3-iodo-1H-pyrazolo[3,4-d]pyrimidin-4-amine (2S)-1-((2S,3S)-3-(2-methylbutyl)-4-oxooxetan-2-yl)pentadecan-2-yl formylleucinate 1-(3,5-dichlorophenyl)-2,2,2-trifluoroethane-1-sulfonyl chloride S-(1-(3,5-dichlorophenyl)-2,2,2-trifluoroethyl) ethanethioateRelated products of tetrahydrofuran





![IL-1BETA CONVERTING ENZYME (ICE) INHIBITOR III, BIOTINYLATED,ICE INHIBITOR III, BIOTINYLATED,[DES-AC, BIOTIN] ICE INHIBITOR III](https://img.chemicalbook.in/StructureFile/ChemBookStructure3/GIF/CB7203745.gif)


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