Cart
sales@molnova.com
PRX933 hydrochloride
CAS No. 639029-42-8
PRX933 hydrochloride( GW876167 hydrochloride | BVT-933 hydrochloride )
Catalog No. M26396 CAS No. 639029-42-8
PRX933 hydrochloride is an agonist of 5-HT2c receptor.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 653 | In Stock |
|
| 5MG | 568 | In Stock |
|
| 10MG | 906 | In Stock |
|
| 25MG | 1340 | In Stock |
|
| 50MG | 1776 | In Stock |
|
| 100MG | 2381 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NamePRX933 hydrochloride
-
NoteResearch use only, not for human use.
-
Brief DescriptionPRX933 hydrochloride is an agonist of 5-HT2c receptor.
-
DescriptionPRX933 hydrochloride is an agonist of 5-HT2c receptor.
-
In VitroPRX933 hydrochloride is a 5-HT2c receptor agonist which is useful for the acute treatment of hypertension.
-
In Vivo——
-
SynonymsGW876167 hydrochloride | BVT-933 hydrochloride
-
PathwayEndocrinology/Hormones
-
Target5-HT Receptor
-
Recptor——
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number639029-42-8
-
Formula Weight351.84
-
Molecular FormulaC16H22ClN5O2
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESCl.C[C@@H]1CNCCN1c1nccnc1OCCOc1cccnc1
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Kuczkowiak U, Petereit F, Nahrstedt A. Hydroxycinnamic Acid Derivatives Obtained from a Commercial Crataegus Extract and from Authentic Crataegus spp. Sci Pharm. 2014 Aug 21;82(4):835-46.
molnova catalog
related products
-
Rizatriptan benzoate
Rizatriptan Benzoate(Maxalt) is a?5-HT1 agonist triptan?drug for the treatment of migraine headaches.
-
NLX-204 hydrochlorid...
NLX-204 hydrochloride is a potent and selective ERK1/2 phosphorylation-preferring serotonin 5 HT1A receptor agonist(pKi = 10.19).NLX-204, displayed high selectivity in the SafetyScreen44 panel (including hERG channel), high solubility, metabolic stability, and Caco-2 penetration and did not block CYP3A4, CYP2D6 isoenzymes, or P-glycoprotein.
-
SB 742457
SB742457 is a highly selective 5-HT6 receptor antagonist with pKi of 9.63.
