Cart
sales@molnova.com
Exifone
CAS No. 52479-85-3
Exifone( NSC 680919 | NSC-680919 | NSC680919 )
Catalog No. M27224 CAS No. 52479-85-3
Exifone is a mixed, nonessential activator of HDAC1 that is capable of binding to both free and substrate-bound enzyme, resulting in an increased relative maximal rate of HDAC1-catalyzed deacetylation.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 48 | In Stock |
|
| 5MG | 48 | In Stock |
|
| 25MG | 75 | In Stock |
|
| 50MG | 111 | In Stock |
|
| 100MG | 166 | In Stock |
|
| 200MG | 248 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameExifone
-
NoteResearch use only, not for human use.
-
Brief DescriptionExifone is a mixed, nonessential activator of HDAC1 that is capable of binding to both free and substrate-bound enzyme, resulting in an increased relative maximal rate of HDAC1-catalyzed deacetylation.
-
DescriptionExifone is a mixed, nonessential activator of HDAC1 that is capable of binding to both free and substrate-bound enzyme, resulting in an increased relative maximal rate of HDAC1-catalyzed deacetylation.
-
In Vitro——
-
In Vivo——
-
SynonymsNSC 680919 | NSC-680919 | NSC680919
-
PathwayCell Cycle/DNA Damage
-
TargetHDAC
-
Recptor——
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number52479-85-3
-
Formula Weight278.216
-
Molecular FormulaC13H10O7
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESOc1ccc(C(=O)c2cc(O)c(O)c(O)c2)c(O)c1O
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Bednash JS, Weathington N, Londino J, et al. Targeting the deubiquitinase STAMBP inhibits NALP7 inflammasome activity. Nat Commun. 2017;8:15203.
molnova catalog
related products
-
Romidepsin
Romidepsin (FK228, depsipeptide) is a potent HDAC1 and HDAC2 inhibitor with IC50 of 36 nM and 47 nM, respectively.
-
ITSA-1
A small molecule suppressor that counteracts trichostatin A (TSA)-induced cell cycle arrest.
-
Pyroxamide
Pyroxamide is an histone deacetylases (HDACs) inhibitor with antineoplastic properties ( HDAC1;IC50: 0.1-0.2 μM).
