Cart
sales@molnova.com
Diacetazotol
CAS No. 83-63-6
Diacetazotol( Diacetotoluide )
Catalog No. M26560 CAS No. 83-63-6
Diacetazotol has activity against dioxin-induced ethoxyisochromamide-O-deethylase (EROD,IC50 = 75±4 nM).
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 49 | Get Quote |
|
| 100MG | Get Quote | Get Quote |
|
| 200MG | Get Quote | Get Quote |
|
| 500MG | Get Quote | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
-
Product NameDiacetazotol
-
NoteResearch use only, not for human use.
-
Brief DescriptionDiacetazotol has activity against dioxin-induced ethoxyisochromamide-O-deethylase (EROD,IC50 = 75±4 nM).
-
DescriptionDiacetazotol has activity against dioxin-induced ethoxyisochromamide-O-deethylase (EROD,IC50 = 75±4 nM).(In Vitro):Diacetazotol can inhibit dioxin toxicity.
-
In VitroDiacetazotol has activity for inhibiting dioxin toxicity.
-
In Vivo——
-
SynonymsDiacetotoluide
-
PathwayOthers
-
TargetOther Targets
-
RecptorDihydroorotate Dehydrogenase| Parasite
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number83-63-6
-
Formula Weight309.369
-
Molecular FormulaC18H19N3O2
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?DMSO : 100 mg/mL (323.25 mM)
-
SMILESCC(=O)N(C(C)=O)c1ccc(cc1C)\N=N\c1ccccc1C
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Li SL, et al. 3D-QSAR studies on a series of dihydroorotate dehydrogenase inhibitors: analogues of the active metabolite of leflunomide. Int J Mol Sci. 2011;12(5):2982-93.
molnova catalog
related products
-
Angiogenin (108-122)...
Angiogenin (108-122) TFA is an angiogenin peptide.Angiogenin (108-122) acts as a therapeutic agent for the prophylaxis and/or treatment of cancer, an infectious disease, a fibrotic disease, an inflammatory disease, a neurodegenerative disease, an autoimmune disease, or a heart and vascular disease.
-
Itaconate-alkyne
Itaconate-alkyne is a bioorthogonal probe for quantitative and site-specific chemoproteomic profiling of itaconate in inflammatory macrophages and enables biochemical evaluation and proteomic analysis of its direct targets.
-
ZLD1039
ZLD1039 is a potent, orally bioavailable EZH2 (Enhancer of Zeste Homolog 2) inhibitor with high selectivity.
