BMS-708163
CAS No. 1146699-66-2
BMS-708163 ( Avagacestat )
Catalog No. M10518 CAS No. 1146699-66-2
A potent, selective and orally bioavailable inhibitor of γ-secretase with Aβ40 IC50 of 3.0 nM.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
5MG | 111 | In Stock |
|
10MG | 213 | In Stock |
|
25MG | 398 | In Stock |
|
50MG | 592 | In Stock |
|
100MG | 844 | In Stock |
|
500MG | 1701 | In Stock |
|
1G | Get Quote | In Stock |
|
Biological Information
-
Product NameBMS-708163
-
NoteResearch use only, not for human use.
-
Brief DescriptionA potent, selective and orally bioavailable inhibitor of γ-secretase with Aβ40 IC50 of 3.0 nM.
-
DescriptionA potent, selective and orally bioavailable inhibitor of γ-secretase with Aβ40 IC50 of 3.0 nM; demonstrates 193-fold selectivity against Notch; significantly reduced Aβ40 levels for sustained periods in brain, plasma, and cerebrospinal fluid in rats and dogs. Alzheimer's Disease Phase 2 Discontinued
-
SynonymsAvagacestat
-
PathwayWnt/Notch/Hedgehog
-
Targetγ-secretase
-
Recptorγsecretase(Aβ40);γsecretase(Aβ42)
-
Research AreaNeurological Disease
-
IndicationAlzheimer Disease
Chemical Information
-
CAS Number1146699-66-2
-
Formula Weight520.89
-
Molecular FormulaC20H17ClF4N4O4S
-
Purity>98% (HPLC)
-
Solubility10 mM in DMSO
-
SMILESO=C(N)[C@H](N(CC1=CC=C(C2=NOC=N2)C=C1F)S(=O)(C3=CC=C(Cl)C=C3)=O)CCC(F)(F)F
-
Chemical NamePentanamide, 2-[[(4-chlorophenyl)sulfonyl][[2-fluoro-4-(1,2,4-oxadiazol-3-yl)phenyl]methyl]amino]-5,5,5-trifluoro-, (2R)-
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Gillman KW, et al. ACS Med Chem Lett. 2010 Mar 22;1(3):120-4.
2. Albright CF, et al. J Pharmacol Exp Ther. 2013 Mar;344(3):686-95.
3. Mitani Y, et al. J Neurosci. 2012 Feb 8;32(6):2037-50.
2. Albright CF, et al. J Pharmacol Exp Ther. 2013 Mar;344(3):686-95.
3. Mitani Y, et al. J Neurosci. 2012 Feb 8;32(6):2037-50.
molnova catalog
related products
-
RO4929097
RO4929097 (RG 4733) is a potent, selective, orally active γ-secretase inhibitor with IC50 of 4 nM.
-
E-2012
A potent, second-generation γ-secretase modulator that decreases Aβ(1-39), Aβ(1-40) and A(1-42), and increases Aβ(1-37).
-
BMS-299897
A potent γ-secretase inhibitor that preferentially inhibits cleavage of the APP CTF cleavage with IC50 of 7.1 nM.