Calpain Inhibitor III

Modify Date: 2024-01-03 10:13:33

Calpain Inhibitor III Structure
Calpain Inhibitor III structure
Common Name Calpain Inhibitor III
CAS Number 88191-84-8 Molecular Weight 382.45
Density 1.2±0.1 g/cm3 Boiling Point 450.4±45.0 °C at 760 mmHg
Molecular Formula C22H26N2O4 Melting Point N/A
MSDS USA Flash Point 226.2±28.7 °C

 Use of Calpain Inhibitor III


cysteine protease inhibitor of calpain that rapidly penetrates the blood-brain barrier following systemic administration[1][2]. MDL-28170 also block γ-secretase[4].

 Names

Name Z-Val-Phe-H
Synonym More Synonyms

 Calpain Inhibitor III Biological Activity

Description cysteine protease inhibitor of calpain that rapidly penetrates the blood-brain barrier following systemic administration[1][2]. MDL-28170 also block γ-secretase[4].
Related Catalog
Target

Calpain[1].

In Vitro MDL-28170 significantly and time-dependently improves the recovery of synaptic responses in hippocampal slices following prolonged, moderate hypoxia without hypoxic depolarization[1]. MDL-28170 dose-dependently inhibits brain cysteine proteinase activity (in vitro Ki= 0.01 μM)[2].
In Vivo Treatment with MDL-28170 (50 mg/kg, i.p.) completely prevents the striatal damage in four animals in each of the two treatment groups. The numbers of necrotic neurons are reduced by 85% and 68% in animals in which MDL-28170 injections are initiated at 0.5 and 3 h of recirculation, respectively[2]. MDL-28170 (30 mg/kg, i.p.) reduces the functional and structural deterioration of corpus callosum following fluid percussion injury[3]. MDL-28170 (10 mg/kg, i.p.) significantly improves nerve function parameters in diabetic rats. MDL-28170 (3 and 10 mg/kg, i.p.) improves nociceptive behavior in diabetic rats[5].
References

[1]. Chen ZF, et al. Neuronal recovery after moderate hypoxia is improved by the calpain inhibitor MDL28170. Brain Res. 1997 Sep 19;769(1):188-92.

[2]. Li PA, et al. Postischemic treatment with calpain inhibitor MDL 28170 ameliorates brain damage in a gerbil model of global ischemia. Neurosci Lett. 1998 May 8;247(1):17-20.

[3]. Ai J, et al. Calpain inhibitor MDL-28170 reduces the functional and structural deterioration of corpus callosum following fluid percussion injury. J Neurotrauma. 2007 Jun;24(6):960-78.

[4]. De Strooper B, et al. A presenilin-1-dependent gamma-secretase-like protease mediates release of Notch intracellular domain. Nature. 1999 Apr 8;398(6727):518-22.

[5]. Kharatmal SB, et al. Calpain inhibitor, MDL 28170 confer electrophysiological, nociceptive and biochemical improvement in diabetic neuropathy. Neuropharmacology. 2015 Oct;97:113-21.

 Chemical & Physical Properties

Density 1.2±0.1 g/cm3
Boiling Point 450.4±45.0 °C at 760 mmHg
Molecular Formula C22H26N2O4
Molecular Weight 382.45
Flash Point 226.2±28.7 °C
PSA 84.50000
LogP 3.77
Vapour Pressure 0.0±1.1 mmHg at 25°C
Index of Refraction 1.571
Storage condition 2-8℃

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Safety Phrases 22-24/25
RIDADR NONH for all modes of transport

 Articles34

More Articles
Impaired Focal Adhesion Kinase-Grb2 Interaction during Elevated Activity in Hippocampal Neurons.

Int. J. Mol. Sci. 16 , 15659-69, (2015)

Excitatory/inhibitory imbalances are implicated in many neurological disorders. Previously, we showed that chronically elevated network activity induces vulnerability in neurons due to loss of signal ...

A recoverable state of axon injury persists for hours after spinal cord contusion in vivo.

Nat. Commun. 5 , 5683, (2014)

Therapeutic strategies for spinal cord injury (SCI) commonly focus on regenerating disconnected axons. An alternative approach would be to maintain continuity of damaged axons, especially after contus...

Different patterns of electrical activity lead to long-term potentiation by activating different intracellular pathways.

J. Neurosci. 35(2) , 621-33, (2015)

Deciphering and storing information coded in different firing patterns are important properties of neuronal networks, as they allow organisms to respond and adapt to external and internal events. Here...

 Synonyms

CARBOBEZOXY-VALINYL-PHENYLALANINALZ-VAL-PHE-CHO
MFCD00798796
Carbamic acid, N-[(1S)-1-[[[(1S)-1-formyl-2-phenylethyl]amino]carbonyl]-2-methylpropyl]-, phenylmethyl ester
Carbamic acid, N-[(1S)-1-formyl-2-phenylethyl]-, phenylmethyl ester
N-benzyloxycarbonyl-(S)-valinylphenylalaninal
benzyl [(2S)-1-oxo-3-phenylpropan-2-yl]carbamate
Benzyl [(2S)-3-methyl-1-oxo-1-{[(2S)-1-oxo-3-phenylpropan-2-yl]amino}butan-2-yl]carbamate
Z-Val-Phe-H
Z-VAL-PHE-CHO
(S)-(-)-2-(Benzylcarbonylamino)-3-phenylpropanal
Z-L-Val-L-Phe-OH
Benzyl [(2S)-1-oxo-3-phenyl-2-propanyl]carbamate
CARBOBENZOXY-VALINYL-PHENYLALANINAL
CALPAIN INHIBITOR III
Benzyl [(2S)-3-methyl-1-oxo-1-{[(2S)-1-oxo-3-phenyl-2-propanyl]amino}-2-butanyl]carbamate
Cbz-L-Val-L-Phe-OH
Z-VAL-PHE-ALDEHYDE
MDL 28170
MDL-28170
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