AT-56
CAS No. 162640-98-4
AT-56 ( AT-56; AT 56; AT56 )
Catalog No. M12406 CAS No. 162640-98-4
AT56, a specific inhibitor of prostaglandin D2 synthase enzymatic activity, blunted adipogenic aldosterone effects.
Purity : >98%(HPLC)
Size | Price / USD | Stock | Quantity |
5MG | 68 | In Stock |
|
10MG | 115 | In Stock |
|
25MG | 227 | In Stock |
|
50MG | 410 | In Stock |
|
100MG | 605 | In Stock |
|
200MG | Get Quote | In Stock |
|
500MG | Get Quote | In Stock |
|
1G | Get Quote | In Stock |
|
Biological Information
-
Product NameAT-56
-
NoteResearch use only, not for human use.
-
Brief DescriptionAT56, a specific inhibitor of prostaglandin D2 synthase enzymatic activity, blunted adipogenic aldosterone effects.
-
DescriptionAT56, a specific inhibitor of prostaglandin D2 synthase enzymatic activity, blunted adipogenic aldosterone effects.
-
SynonymsAT-56; AT 56; AT56
-
PathwayOthers
-
TargetOther Targets
-
RecptorL-PGDS
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number162640-98-4
-
Formula Weight397.52
-
Molecular FormulaC25H27N5
-
Purity>98%(HPLC)
-
SolubilityDMSO: > 10 mM
-
SMILESN1(CCCCC2=NNN=N2)CC/C(CC1)=C3C4=CC=CC=C4C=CC5=CC=CC=C/35
-
Chemical Name4-(5H-dibenzo[a,d]cyclohepten-5-ylidene)-1-[4-(2H-tetrazol-5-yl)butyl]-piperidine
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
-
PTD-p65-P1 Peptide
PTD-p65-P1 Peptide is a nuclear transcription factor NF-kappaB inhibitor, composed of a membrane-translocating peptide sequence generated from antennapedia (PTD) conjugated with p65-P1, which selectively inhibits activation induced by various inflammatory stimuli. PTD-p65-P1 suppressed NF-kappaB activation induced by lipopolysaccharide, interleukin-1, okadaic acid, phorbol 12-myristate 13-acetate, H(2)O(2), and cigarette smoke condensate as well as that induced by TNF.
-
Citronellol
Citronellol is used in insect repellents and perfumes and as a mite attractant.
-
AZD1208
AZD1208 is a novel, orally bioavailable, highly selective PIM kinase inhibitor with single nanomolar potency against all three PIM kinases.