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E 64c
Category | SARS-CoV |
CAS | 76684-89-4 |
Description | E-64c is a cysteine protease inhibitor used for detecting autophagy in plants. |
Product Information
Synonyms | Loxistatin acid |
IUPAC Name | (2S,3S)-3-[[(2S)-4-methyl-1-(3-methylbutylamino)-1-oxopentan-2-yl]carbamoyl]oxirane-2-carboxylic acid |
Molecular Weight | 314.38 |
Molecular Formula | C15H26N2O5 |
Canonical SMILES | CC(C)CCNC(=O)C(CC(C)C)NC(=O)C1C(O1)C(=O)O |
InChI | InChI=1S/C15H26N2O5/c1-8(2)5-6-16-13(18)10(7-9(3)4)17-14(19)11-12(22-11)15(20)21/h8-12H,5-7H2,1-4H3,(H,16,18)(H,17,19)(H,20,21)/t10-,11-,12-/m0/s1 |
InChIKey | SCMSYZJDIQPSDI-SRVKXCTJSA-N |
Boiling Point | 596.4±50.0 °C at 760 mmHg |
Flash Point | 314.5±30.1 °C |
Purity | 98% |
Density | 1.2±0.1 g/cm3 |
Solubility | In Vitro: DMSO : 250 mg/mL(795.22 mM;Need ultrasonic) In Vivo: 1.Add each solvent one by one:10% DMSO >> 40%PEG300 >> 5%Tween-80 >> 45% saline Solubility: ≥ 2.08 mg/mL (6.62 mM); Clear solution 2.Add each solvent one by one:10% DMSO >> 90% (20%SBE-β-CDin saline) Solubility: ≥ 2.08 mg/mL (6.62 mM); Clear solution 3.Add each solvent one by one:10% DMSO >> 90%corn oil Solubility: ≥ 2.08 mg/mL (6.62 mM); Clear solution |
Appearance | White to off-white (Solid) |
Storage | Store at 2-8°C |
Complexity | 422 |
Exact Mass | 314.18417193 |
Index Of Refraction | 1.504 |
In Vitro | E-64c, a derivative of naturally occurring epoxide inhibitor of cysteine proteases, with papain; especially with regard to the hydrogen bonding and hydrophobic interactions of the ligands with conserved residues in the catalytic binding site. E 64c (k2/Ki=140±5M-1s-1) is demonstrated to be a lead structure for the development of irreversible cathepsin C inhibitors. |
In Vivo | The t-1/2 of plasma E-64c is 0.48 hours. The hemodynamic effects of E-64c are absent at this dose. Using two way analysis of variance, the effects of reperfusion (p=0.0016) or E-64c (p=0.0226) per se on infarct size are significant. In comparing Group A with Group B and Group C with Group D, the depletion of CPK in the E-64c treated groups (Groups A and C) is slightly less than in the vehicle-injected groups (Groups B and D). The insufficient effect of E-64c alone may be explained by the early administration and relatively short t-1/2. Since the effectiveness of NCO-700 has been established,6),7) our findings might indicate a small but beneficial effect of E-64c on infarct size and CPK content. |
PSA | 108.03000 |
Target | Cysteine proteases, CANP, Cathepsin C; SARS-CoV |
Vapor Pressure | 0.0±3.6 mmHg at 25°C |
XLogP3-AA | 1.6 |