Cart
sales@molnova.com
NSC 3852
CAS No. 3565-26-2
NSC 3852( —— )
Catalog No. M20951 CAS No. 3565-26-2
NSC 3852 is a potent inhibitor of histone deacetylase.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 28 | In Stock |
|
| 100MG | Get Quote | In Stock |
|
| 200MG | 27 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameNSC 3852
-
NoteResearch use only, not for human use.
-
Brief DescriptionNSC 3852 is a potent inhibitor of histone deacetylase.
-
DescriptionNSC 3852 is a potent inhibitor of histone deacetylase.
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayCell Cycle/DNA Damage
-
TargetHDAC
-
RecptorHDAC
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number3565-26-2
-
Formula Weight174.16
-
Molecular FormulaC9H6N2O2
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESO=Nc1ccc(O)c2ncccc12
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Jeannine S. Strobl Christopher W. Seibert Yunbo Li Rana Nagarkatti Sheila M. Mitchell Alexa C. Rosypal Dharmendar Rathore and David S. Lindsay. Inhibition of Toxoplasma gondii and Plasmodium falciparum Infections in Vitro by NSC3852 a Redox Active Antiproliferative and Tumor Cell Differentiation Agent[J]. Journal of Parasitology 2009 95(1):p.215-223.
molnova catalog
related products
-
Valproic acid
A HDAC inhibitor that selectively inhibits the catalytic activity of class I HDACs, and induces proteasomal degradation of HDAC2.
-
BRD4354
BRD4354 is a moderately potent, selective, reversible inhibitor of HDAC5 and HDAC9 with IC50 of 0.85 uM and 1.88 uM.
-
ACY-1083
ACY-1083 is a selective and brain-penetrating HDAC6 inhibitor (IC50: 3 nM). It is 260-fold more selective for HDAC6 than all other classes of HDAC isoforms.
