Cart
sales@molnova.com
N-0500 HCl
CAS No. 100935-99-7
N-0500 HCl( (-)-Propyl-9-hydroxynaphthoxazine Hydrochloride )
Catalog No. M28551 CAS No. 100935-99-7
N-0500 HCl is a very potent centrally acting DA receptor agonist. N-0500 HCl is a potent displacer of the specific [3H]DP_x005f5,6-ADTN binding with IC50 of 3nM.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 48 | In Stock |
|
| 5MG | 29 | In Stock |
|
| 10MG | 48 | In Stock |
|
| 100MG | Get Quote | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameN-0500 HCl
-
NoteResearch use only, not for human use.
-
Brief DescriptionN-0500 HCl is a very potent centrally acting DA receptor agonist. N-0500 HCl is a potent displacer of the specific [3H]DP_x005f5,6-ADTN binding with IC50 of 3nM.
-
DescriptionN-0500 HCl is a very potent centrally acting DA receptor agonist. N-0500 HCl is a potent displacer of the specific [3H]DP_x005f5,6-ADTN binding with IC50 of 3nM.
-
In Vitro——
-
In Vivo——
-
Synonyms(-)-Propyl-9-hydroxynaphthoxazine Hydrochloride
-
PathwayGPCR/G Protein
-
TargetDopamine Receptor
-
RecptorHuman Endogenous Metabolite|Apoptosis
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number100935-99-7
-
Formula Weight283.8
-
Molecular FormulaC15H22ClNO2
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESCl.CCCN1CCO[C@H]2[C@H]1CCc1ccc(O)cc21
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Amino Y, et al. Synthesis and evaluation of L-cystathionine as a standard for amino acid analysis. Biosci Biotechnol Biochem. 2017 Jan;81(1):95-101.
molnova catalog
related products
-
Nomifensine (maleate...
Nomifensine maleate is a selective inhibitor of dopamine uptake, used in adult attention deficit disorder.
-
Rotigotine
A non-selective agonist of the dopamine D3 receptor (Ki=0.71 nM); has 10-fold selectivity for the D3 receptor over the D2, D4, and D5 receptors and 100-fold selectivity for the D3 receptor over the D1 receptor.
-
A-437203
A-437203 (Lu201640) is A kind of based on 1 h - pyrimidin - 2 - one sca ? old, selective, new powerful d3 receptor antagonist, on D2, d3, and D4 receptor, Ki value 71, respectively 1.6 and 6220 nM.
