Pardoprunox
CAS No. 269718-84-5
Pardoprunox ( —— )
Catalog No. M13825 CAS No. 269718-84-5
Pardoprunox(SLV-308) is a novel partial dopamine D2 and D3 receptor agonist and serotonin 5-HT1A receptor agonist.
Purity : >98%(HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
5MG | 335 | In Stock |
|
10MG | 470 | In Stock |
|
25MG | 798 | 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 NamePardoprunox
-
NoteResearch use only, not for human use.
-
Brief DescriptionPardoprunox(SLV-308) is a novel partial dopamine D2 and D3 receptor agonist and serotonin 5-HT1A receptor agonist.
-
DescriptionPardoprunox(SLV-308) is a novel partial dopamine D2 and D3 receptor agonist and serotonin 5-HT1A receptor agonist; D2 (pKi = 8.1) and D3 receptor (pKi = 8.6) partial agonist (IA = 50% and 67%, respectively) and 5-HT1A receptor (pKi = 8.5) full agonist (IA = 100%); also binds to D4 (pKi = 7.8), α1-adrenergic (pKi = 7.8), α2-adrenergic (pKi = 7.4), and 5-HT7 receptors (pKi = 7.2) with lower affinity.
-
Synonyms——
-
PathwayEndocrinology/Hormones
-
Target5-HT Receptor
-
Recptor5-HT1A; α2-adrenergic receptor; D2; D3
-
Research AreaNeurological Disease
-
Indication——
Chemical Information
-
CAS Number269718-84-5
-
Formula Weight233.27
-
Molecular FormulaC12H15N3O2
-
Purity>98%(HPLC)
-
SolubilityDMSO: 10 mM
-
SMILESCN1CCN(CC1)C1=CC=CC2=C1OC(=O)N2
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Glennon JC, et al. Synapse. 2006 Dec 15;60(8):599-608.
molnova catalog
related products
-
Palonosetron hydroch...
Palonosetron (INN, trade name Aloxi) is a 5-HT3 antagonist used in the prevention and treatment of chemotherapy-induced nausea and vomiting (CINV).
-
Dapoxetine HCl
Dapoxetine HCl is a selectivity short-acting serotonin reuptake inhibitor used for the therapy of premature ejaculation.
-
Nelotanserin
A potent, selective 5-HT2A inverse agonist with pKi of 9.2; displays >30- and 5000-fold selectivity compared with 5-HT2C and 5-HT2B receptors.