Lalistat 1
CAS No. 501104-16-1
Lalistat 1( ZINC795230 )
Catalog No. M28175 CAS No. 501104-16-1
Lalistat 1 is an inhibitor of lysosomal acid lipase (LAL, IC50 = 68 nM) and IgA1 protease for H. influenzae.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
5MG | 69 | Get Quote |
|
10MG | 95 | Get Quote |
|
25MG | 152 | Get Quote |
|
50MG | 222 | Get Quote |
|
100MG | 327 | Get Quote |
|
500MG | 786 | Get Quote |
|
1G | Get Quote | Get Quote |
|
Biological Information
-
Product NameLalistat 1
-
NoteResearch use only, not for human use.
-
Brief DescriptionLalistat 1 is an inhibitor of lysosomal acid lipase (LAL, IC50 = 68 nM) and IgA1 protease for H. influenzae.
-
DescriptionLalistat 1 is an inhibitor of lysosomal acid lipase (LAL, IC50 = 68 nM) and IgA1 protease for H. influenzae. Lalistat 1 can be used in studies about niemann-pick type C diseases.(In Vitro):Lalistat 1 (0-100 μM) dose-dependently inhibits IgA1P B1 and B2, almost completely at 50 μM and completely at 100 μM .Lalistat 1 reduces cholesterol accumulation in lysosome-like reservoirs of GM03123 human fibroblasts lacking NPC1 .
-
In Vitro——
-
In Vivo——
-
SynonymsZINC795230
-
PathwayGPCR/G Protein
-
TargetAntibacterial
-
RecptorMMP-12
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number501104-16-1
-
Formula Weight298.36
-
Molecular FormulaC12H18N4O3S
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?DMSO : 20 mg/mL (67.03 mM)
-
SMILESO=C(Oc1nsnc1N1CCCCC1)N1CCOCC1
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Morales R, et al. Crystal structures of novel non-peptidic, non-zinc chelating inhibitors bound to MMP-12. J Mol Biol. 2004 Aug 20;341(4):1063-76.
molnova catalog
related products
-
Sanggenone C
Sanggenone C inhibits tumor cellular proteasomal activity and cell viability, via induction of cell cycle arrest and cell death , inhibiting the proteasome function.
-
Sulfamoxole
Sulfamoxole is an antibacterial belonging to sulfonamide.
-
BM212
A novel antitubercular agent that possesses strong inhibitory activity against both Mycobacterium tuberculosis (MIC=0.7-1.5 ug/ml) and some nontuberculosis mycobacteria, inhibits transport activity of MmpL3.