Unifiram
CAS No. 272786-64-8
Unifiram( —— )
Catalog No. M28161 CAS No. 272786-64-8
Unifiram is a cognition-enhancer. Unifiram induces a long-lasting increase in the amplitude of field excitatory postsynaptic potentials (fEPSPs) in the rat hippocampal CA1 region (EC50= 27 nM) and increases acetylcholine (ACh) release in the rat cerebral cortex.
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 |
|
| 50MG | 28 | In Stock |
|
| 100MG | 36 | In Stock |
|
| 200MG | 53 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameUnifiram
-
NoteResearch use only, not for human use.
-
Brief DescriptionUnifiram is a cognition-enhancer. Unifiram induces a long-lasting increase in the amplitude of field excitatory postsynaptic potentials (fEPSPs) in the rat hippocampal CA1 region (EC50= 27 nM) and increases acetylcholine (ACh) release in the rat cerebral cortex.
-
DescriptionUnifiram is a cognition-enhancer. Unifiram induces a long-lasting increase in the amplitude of field excitatory postsynaptic potentials (fEPSPs) in the rat hippocampal CA1 region (EC50= 27 nM) and increases acetylcholine (ACh) release in the rat cerebral cortex.(In Vivo):Unifiram (0.1 mg kg 1 i.p.) was able to prevent amnesia induced by scopolamine (0.8 mg kg 1 i.p.) in the rat Morris watermaze test. In the rat social learning test, Unifiram (0.1 mg kg 1 i.p.) injected in adults rats reduced the duration of active exploration of the familiar partner in the second session of the test. Unifiram, similarly to piracetam, reduced the duration of hypnosis induced by pentobarbital. At the highest effective doses, the investigated compound did not impair motor coordination (rota rod test), nor modified spontaneous (Animex).
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayOthers
-
TargetOther Targets
-
Recptor15-PGDH
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number272786-64-8
-
Formula Weight298.33
-
Molecular FormulaC13H15FN2O3S
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESFc1ccc(cc1)S(=O)(=O)N1CCN2C(CCC2=O)C1
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Niesen FH, et al. High-affinity inhibitors of human NAD-dependent 15-hydroxyprostaglandin dehydrogenase: mechanisms of inhibition and structure-activity relationships. PLoS One. 2010 Nov 2;5(11):e13719.
molnova catalog
related products
-
Salvianolic acid F
The role of our hybrid molecules, an analogue of Salvianolic acid F, in compelling the glioma cells towards apoptosis by specifically perturbing the concentration of glutathione along with caspase 6.
-
Neocnidilide
Neocnidilide is an alkyl phthalate derived from Rhizoma Ligustici Chuanxiong with the ability to inhibit the growth of mycotoxin-producing fungi and to kill insects.
-
Neuropeptide W-23(hu...
Neuropeptide W-23(human) is an endogenous ligand for NPBW1 and NPBW2.
Cart
sales@molnova.com