Z-Ile-Glu(OtBu)-Ala-Leu-aldehyde

Modify Date: 2024-01-02 20:13:44

Z-Ile-Glu(OtBu)-Ala-Leu-aldehyde Structure
Z-Ile-Glu(OtBu)-Ala-Leu-aldehyde structure
Common Name Z-Ile-Glu(OtBu)-Ala-Leu-aldehyde
CAS Number 158442-41-2 Molecular Weight 618.761
Density 1.1±0.1 g/cm3 Boiling Point 844.2±65.0 °C at 760 mmHg
Molecular Formula C32H50N4O8 Melting Point N/A
MSDS USA Flash Point 464.4±34.3 °C

 Use of Z-Ile-Glu(OtBu)-Ala-Leu-aldehyde


PSI (Proteasome Inhibitor 1) is a potent proteasome inhibitor. PSI inhibits the proliferation of primary effusion lymphoma (PEL) cells. PSI has the potential for the research of Kaposi’s sarcoma-associated herpesvirus (KSHV) infection and KSHV-associated lymphomas[1].

 Names

Name N-[(Phenylmethoxy)carbonyl]-L-isoleucyl-L-α-glutamyl-tert-butylester-N-[(1S)-1-formyl-3-methylbutyl]-L-alaninamide
Synonym More Synonyms

 Z-Ile-Glu(OtBu)-Ala-Leu-aldehyde Biological Activity

Description PSI (Proteasome Inhibitor 1) is a potent proteasome inhibitor. PSI inhibits the proliferation of primary effusion lymphoma (PEL) cells. PSI has the potential for the research of Kaposi’s sarcoma-associated herpesvirus (KSHV) infection and KSHV-associated lymphomas[1].
Related Catalog
In Vitro PSI (24 h) inhibits the proliferation of primary effusion lymphoma (PEL) cells at low nanomolar concentrations (CC50s of 205, 190, 22.0, 53.0 nM FOR BJAB, Ramos, BC3, BCBL1 cells, respectively)[1]. PSI (50 nM; 6 h) increases caspase-3/7 activity by 8-fold compared with control[1]. PSI (50 nM; 6 h) decreases the transcriptional activity of NF-κB by 52%[1]. PSI (1, 5 nM; 3 days) inhibits the growth of BC3 cells at a high concentration (5 nM)[1]. Cell Cytotoxicity Assay[1] Cell Line: BC3, BCBL1, Ramos, BJAB cells Concentration: Incubation Time: 24 h Result: Inhibited the proliferation of primary effusion lymphoma (PEL) cells at low nanomolar concentrations (CC50s of 205, 190, 22.0, 53.0 nM FOR BJAB, Ramos, BC3, BCBL1 cells, respectively). Western Blot Analysis[1] Cell Line: HBL6 cells Concentration: 50 nM Incubation Time: 6 h Result: Decreased the NF-κB activity by 52%.
References

[1]. Saji C, et al. Proteasome inhibitors induce apoptosis and reduce viral replication in primary effusion lymphoma cells. Biochem Biophys Res Commun. 2011; 415(4):573-8.

 Chemical & Physical Properties

Density 1.1±0.1 g/cm3
Boiling Point 844.2±65.0 °C at 760 mmHg
Molecular Formula C32H50N4O8
Molecular Weight 618.761
Flash Point 464.4±34.3 °C
Exact Mass 618.362854
PSA 169.00000
LogP 5.79
Vapour Pressure 0.0±3.1 mmHg at 25°C
Index of Refraction 1.510
Storage condition −20°C

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
RIDADR NONH for all modes of transport
WGK Germany 3

 Articles1

More Articles
Figueiredo-Pereira, M.E., et al.

J. Neurochem. 63 , 5433, (1994)

 Synonyms

tert-Butyl (4S)-4-{[(2S,3S)-2-{[(benzyloxy)carbonyl]amino}-3-methylpentanoyl]amino}-5-{[(2S)-1-{[(2S)-4-methyl-1-oxopentan-2-yl]amino}-1-oxopropan-2-yl]amino}-5-oxopentanoate (non-preferred name)
PROTEASOME INHIBITOR I
M.W. 618.77 C32H50N4O8
N-Cb
2-Methyl-2-propanyl (4S)-4-{[(2S,3S)-2-{[(benzyloxy)carbonyl]amino}-3-methylpentanoyl]amino}-5-{[(2S)-1-{[(2S)-4-methyl-1-oxo-2-pentanyl]amino}-1-oxo-2-propanyl]amino}-5-oxopentanoate (non-preferred name)
Top Suppliers:I want be here
  • DC Chemicals Limited
  • China
  • Product Name: PSI
  • Price: $Inquiry/100mg $Inquiry/250mg $Inquiry/1g
  • Purity: 98.0%
  • Stocking Period: 3 Day
  • Contact: Tony Cao


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