(-)-U-50488 hydrochloride
CAS No. 114528-79-9
(-)-U-50488 hydrochloride( U50488 | U-50488 )
Catalog No. M10515 CAS No. 114528-79-9
The more active enantiomer of (±)-U-50488, a potent, selective kappa-opioid receptor agonist with no μ-opioid antagonist effects.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 100MG | Get Quote | Get Quote |
|
| 200MG | 1319 | Get Quote |
|
| 500MG | 2507 | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
-
Product Name(-)-U-50488 hydrochloride
-
NoteResearch use only, not for human use.
-
Brief DescriptionThe more active enantiomer of (±)-U-50488, a potent, selective kappa-opioid receptor agonist with no μ-opioid antagonist effects.
-
DescriptionThe more active enantiomer of (±)-U-50488, a potent, selective kappa-opioid receptor agonist with no μ-opioid antagonist effects; shows analgesic, diuretic and antitussive effects, and reverses the memory impairment produced by anticholinergic drugs in vivo.Anxiety Discontinued.
-
In Vitro(-)-U-50488 hydrochloride (1 pM-100 nM; 7 days) exhibits a concentration-dependent inhibition of HIV-1 expression, the maximal inhibition at 10?13 M (approximately 73% suppression) in acutely infected blood monocyte-derived macrophages (MDM).(-)-U-50488 hydrochloride (10-13 M; 7-14 days) (10?13 M) markedly inhibits HIV-1 expression both at 7 and 14 days after infection, it has a sustained inhibitory effect on HIV-1 infection in MDM.
-
In Vivo(-)-U-50488 hydrochloride (intraperitoneal?injection?; 5mg/kg; 2 hrs before 4% paraformaldehyde (PFA)) acutely induced pMeCP2-S421 (phosphorylation of the methyl-DNA binding protein MeCP2 at Ser421) and Fos selectively in the nucleus accumbens (NAc) but does not alter MeCP2 levels in any brain region. Animal Model:C57BL/6J mice Dosage:5 mg/kg Administration:Intraperitoneal?injection; single dose; 2 hrs before 4% PFAResult:Induced pMeCP2-S421 in the brain acutely.
-
SynonymsU50488 | U-50488
-
PathwayEndocrinology/Hormones
-
TargetOpioid Receptor
-
RecptorOpioid Receptor
-
Research AreaNeurological Disease
-
IndicationAnxiety
Chemical Information
-
CAS Number114528-79-9
-
Formula Weight405.79
-
Molecular FormulaC19H26Cl2N2O.HCl
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?H2O : 50 mg/mL (123.22 mM)
-
SMILESCN(C1CCCCC1N2CCCC2)C(=O)CC3=CC(=C(C=C3)Cl)Cl.Cl
-
Chemical Nametrans-(-)-3,4-Dichloro-N-methyl-N-[2-(1-pyrrolidinyl)cyclohexyl]benzeneacetamide hydrochloride
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Tao PL, et al. Eur J Pharmacol. 1994 May 2;256(3):281-6.
2. Suarez-Roca H, et al. J Pharmacol Exp Ther. 1993 Feb;264(2):648-53.
3. Su MT, et al. Br J Pharmacol. 1998 Feb;123(4):625-30.
4. Vonvoigtlander PF, et al. J Pharmacol Exp Ther. 1983 Jan;224(1):7-12.
molnova catalog
related products
-
Hemorphin-7
Hemorphin-7 binds to the angiotensin IV receptor, triggering multiple effects including cellular proliferation and memory enhancement. Hemorphins are endogenous peptides belonging to the family of atypical opioid peptides released from hydrolyzed hemoglobin. Hemorphin-7 is investigated as a potential biomarker for breast cancer.
-
Trimebutine
Trimebutine is a drug with antimuscarinic and weak mu opioid agonist effects.
-
LY 2456302
LY 2456302 (CERC-501, JSPA 0658, Aticaprant) is a potent, selective, short-acting antagonist of κ-opioid receptor (KOR) with Ki of 0.81 nM.
Cart
sales@molnova.com