Remoxipride hydrochloride
CAS No. 73220-03-8
Remoxipride hydrochloride( Roxiam | (S)-Remoxipride Hydrochloride | Remoxipride Hydrochloride Anhydrous )
Catalog No. M27695 CAS No. 73220-03-8
Dopamine D2 receptor antagonist.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 85 | In Stock |
|
| 10MG | 132 | In Stock |
|
| 25MG | 264 | In Stock |
|
| 50MG | 390 | In Stock |
|
| 100MG | 576 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | 1190 | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameRemoxipride hydrochloride
-
NoteResearch use only, not for human use.
-
Brief DescriptionDopamine D2 receptor antagonist.
-
DescriptionDopamine D2 receptor antagonist.(In Vivo):In male Sprague-Dawley rats, Remoxipride hydrochloride (0.1-100 μM/kg; i.p.) blockes apomorphine-induced hyperactivity and dose-dependent blockades apomorphine-induced behaviors. In beagle dogs, Remoxipride hydrochloride (0.25-5 μM/kg; gavage) blockes apomorphine-induced vomiting.
-
In Vitro(S)-Remoxipride hydrochloride (1-100 μM; 20 min) shows binding efficiency with IC50s of >100, 1.57 and 42 μM for dopamine D1, dopamine D2 and α1-Adrenoccptor, respectively.
-
In Vivo(S)-Remoxipride hydrochloride (0.1-100 μM/kg; i.p. 60 min prior to apomorphine) blockades apomorphine-induced behaviors s in rats and vomiting in dogs.(S)-Remoxipride hydrochloride (0.1-10 mg/kg; i.p. 30 min prior to apomorphine) displaces [3H]spiperone from both striatal and extra-striatal areas.
-
SynonymsRoxiam | (S)-Remoxipride Hydrochloride | Remoxipride Hydrochloride Anhydrous
-
PathwayOthers
-
TargetOther Targets
-
Recptor——
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number73220-03-8
-
Formula Weight407.73
-
Molecular FormulaC16H24BrClN2O3
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESCl.CCN1CCC[C@H]1CNC(=O)c1c(OC)ccc(Br)c1OC
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
-
[Leu8,D-Trp22,Tyr25]...
[Leu8,D-Trp22,Tyr25] Somatostatin-28 is the analog of Somatostatin-28. Somatostatin-28 is a intestinal peptide containing somatostatin in its C-terminal portion.
-
OAT-2068
OAT-2068 is a potent and selective inhibitor of mouse chitotriosidase (CHIT1) and displays a remarkable 143-fold mCHIT1 vs. mAMCase selectivity.
-
KL-50
KL-50 is a selective toxin toward tumors that lack the DNA repair protein O6-methylguanine-DNA-methyltransferase (MGMT), which reverses the formation of O6-alkylguanine lesions. KL-50 activates DNA damage response pathways and cycle arrest in MGMT-cells, independent of mismatch repair (MMR). KL-50 is promising for research of brain tumors that lack the DNA repair protein MGMT.
Cart
sales@molnova.com