N-Carbethoxy-4-piperidone
CAS No. 29976-53-2
N-Carbethoxy-4-piperidone ( —— )
Catalog No. M13925 CAS No. 29976-53-2
Aminopyrimidine derivatives, processes for their preparation, compositions containing them and their use as pharmaceuticals.
Purity : >98%(HPLC)
Size | Price / USD | Stock | Quantity |
1G | 26 | In Stock |
|
Biological Information
-
Product NameN-Carbethoxy-4-piperidone
-
NoteResearch use only, not for human use.
-
Brief DescriptionAminopyrimidine derivatives, processes for their preparation, compositions containing them and their use as pharmaceuticals.
-
DescriptionAminopyrimidine derivatives, processes for their preparation, compositions containing them and their use as pharmaceuticals.
-
Synonyms——
-
PathwayOthers
-
TargetOther Targets
-
RecptorOthers
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number29976-53-2
-
Formula Weight171.19
-
Molecular FormulaC8H13NO3
-
Purity>98%(HPLC)
-
SolubilityLimited solubility
-
SMILESCCOC(=O)N1CCC(=O)CC1
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
-
Syk Inhibitor II hyd...
The impact of spleen tyrosine kinase (Syk) signaling might be prominent in lupus because (i) Syk is a shared downstream signaling molecule among circulating immune complex, LPS, and (1→3)-β-D-glucan (BG), and (ii) all of these factors are detectable in the serum of Fc gamma receptor IIb-deficient (FcgRIIb-/-) mice with sepsis. Syk inhibition downregulated several inflammatory pathways in FcgRIIb-/- macrophages activated with BG + LPS suggesting the potential anti-inflammatory impact of Syk inhibitors in lupus.
-
DL-Homocystine
Homocystine is the double-bonded form of homocysteine but it occurs only transiently before being converted to the harmless cystathionine via a vitamin B6-dependent enzyme. Homocystine and homocysteine-cysteine mixed disulfide account for >98% of total homocysteine in plasma from healthy individuals.
-
L-BUTHIONINE-(SR)-SU...
L-Buthionine-(SR)-sulfoximine is a cell-permeable and irreversible inhibitor of γ-glutamylcysteine synthetase (Ki <100 μM) that induces oxidative stress in cells by depleting GSH.