EN106
CAS No. 757192-67-9
EN106( ZINC3888023 )
Catalog No. M28542 CAS No. 757192-67-9
EN106 is a potent inhibitor of FEMIB and is a cysteine-reactive covalent ligand. EN106 disrupts recognition of the key reductive stress substrate of FEM1B, FNIP1.
EN106 is a potent inhibitor of FEMIB and is a cysteine-reactive covalent ligand. EN106 disrupts recognition of the key reductive stress substrate of FEM1B, FNIP1.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
5MG | 42 | Get Quote |
|
10MG | 67 | Get Quote |
|
25MG | 133 | Get Quote |
|
50MG | 209 | Get Quote |
|
100MG | 337 | Get Quote |
|
200MG | Get Quote | Get Quote |
|
500MG | Get Quote | Get Quote |
|
1G | Get Quote | Get Quote |
|
Biological Information
-
Product NameEN106
-
NoteResearch use only, not for human use.
-
Brief DescriptionEN106 is a potent inhibitor of FEMIB and is a cysteine-reactive covalent ligand. EN106 disrupts recognition of the key reductive stress substrate of FEM1B, FNIP1.
-
DescriptionEN106 is a potent inhibitor of FEMIB and is a cysteine-reactive covalent ligand. EN106 disrupts recognition of the key reductive stress substrate of FEM1B, FNIP1.
-
In Vitro
-
In Vivo
-
SynonymsZINC3888023
-
PathwayOthers
-
TargetOther Targets
-
Recptor
-
Research Area
-
Indication
Chemical Information
-
CAS Number757192-67-9
-
Formula Weight280.71
-
Molecular FormulaC13H13ClN2O3
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?DMSO : 250 mg/mL (890.60 mM)
-
SMILESClCC(=O)N(CCC#N)c1ccc2OCCOc2c1
-
Chemical Name
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Przegaliński E, et al. On the central antiserotonin activity of benzoctamine and opipramol. Pol J Pharmacol Pharm. 1978;30(6):781-790.
molnova catalog
related products
-
3-Amino-5-Hydroxyben...
3-Amino-5-Hydroxybenzoic Acid is a marine derived natural products found in Salinispora arenicola.
-
1-(1-phenyltetrazol-...
1-(1-phenyltetrazol-5-yl)piperazine;hydrochloride is a chemical compound.
-
Silybin B
Silybin B is an effective inhibitor of raloxifene 4 '- and 6-glucosalylation, an effective anti-fibrinogenic and anti-oligomeric component of Silymarin, with free radical scavenging activity of 1, 1-diphenyl-2-pyridinyl hydrazine (DPPH), and a protective effect against cisplatin-induced neurotoxicity by alleviating DNA damage and apoptosis.