Bretazenil
CAS No. 84379-13-5
Bretazenil ( Ro 16-6028 )
Catalog No. M27608 CAS No. 84379-13-5
Bretazenil is a GABAA benzodiazepine site partial agonist. Bretazenil shows an EC50 of 10 nM for recombinant α1β1γ2.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
2MG | 66 | Get Quote |
|
5MG | 101 | Get Quote |
|
10MG | 165 | Get Quote |
|
25MG | 358 | Get Quote |
|
50MG | 533 | Get Quote |
|
100MG | 761 | Get Quote |
|
200MG | Get Quote | Get Quote |
|
500MG | Get Quote | Get Quote |
|
1G | Get Quote | Get Quote |
|
Biological Information
-
Product NameBretazenil
-
NoteResearch use only, not for human use.
-
Brief DescriptionBretazenil is a GABAA benzodiazepine site partial agonist. Bretazenil shows an EC50 of 10 nM for recombinant α1β1γ2.
-
DescriptionBretazenil is a GABAA benzodiazepine site partial agonist. Bretazenil shows an EC50 of 10 nM for recombinant α1β1γ2.(In Vitro):Bretazenil was the most potent benzodiazepine examined, exhibiting an IC50 of 6.1 nM, compared to clonazepam (7.9 nM), flunitrazepam (13.6 nM) and diazepam (91.1 nM). The rank order of potency for inhibition of [35S]TBPS binding was identical to that for inhibition of [3H]flunitrazepam binding. However, Bretazenil was less efficacious in that it produced 27% inhibition of specific [35S]TBPS binding, compared to clonazepam (34%), flunitrazepam (41%) or diazepam (49%). Bretazenil antagonized the inhibition of [35S]TBPS binding produced by 10 microM diazepam. Bretazenil was also more potent and less efficacious than diazepam in potentiating GABA-stimulated 36Cl- uptake.(In Vivo):Bretazenil, was studied in 240 rats in five age groups: age 7, 12, 18, 25 and 90 days. Motor seizures induced by metrazol (pentamethylenetetrazol, PTZ, 100 mg/kg subcutaneously (s.c.) except for 18-day-old rats which received a dose of 90 mg/kg) served as a model. Animals were pretreated with Bretazenil in doses of 0.001-0.1 mg/kg intraperitoneally 10 min before metrazol. Both types of metrazol-induced seizures, minimal (mMS, predominantly clonic with preserved righting ability) and major (MMS, generalized tonic-clonic), were suppressed by Bretazenil in a dose-dependent manner. Major seizures were always more sensitive to Bretazenil than were minimal seizures. The youngest rats exhibited maximal effects of Bretazenil against major seizures. On the other hand, this drug increased the incidence of minimal seizures in 7- and 12-day-old rats, i.e., in age groups in which this type of seizure is rare under control conditions.
-
SynonymsRo 16-6028
-
PathwayOthers
-
TargetOther Targets
-
Recptor——
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number84379-13-5
-
Formula Weight418.3
-
Molecular FormulaC19H20BrN3O3
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESBrC1=C2C(N3[C@H](C4=C(C(OC(C)(C)C)=O)N=CN4C2=CC=C1)CCC3)=O
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Zhao F, et al. [Anthraquinones from the roots of Knoxia valerianoides]. Zhongguo Zhong Yao Za Zhi. 2011 Nov;36(21):2980-6. Chinese.
molnova catalog
related products
-
1,3,5-Trimethyl-1H-P...
1,3,5-Trimethyl-1H-Pyrazole-4-Carboxylic Acid is a marine derived natural products found in Cinachyrella sp.
-
DEBIO 1143
DEBIO 1143 (AT-406, DEBIO-1143, SM406, ARRY-334543, D1143) is potent, orally active Smac mimetic that antagonizes cIAP1, cIAP2 and XIAP with Ki of 66.4, 1.9 and 5.1 nM, respectively.
-
SR11237
SR11237 is a Pan retinoid X receptor (RXR) agonist. SR11237 causes RXR/RXR homodimers to form and transactivate a reporter gene containing a RXR-response element.