DL-trihexyphenidyl hydrochloride
CAS No. 58947-95-8
DL-trihexyphenidyl hydrochloride ( —— )
Catalog No. M15177 CAS No. 58947-95-8
One of the centrally acting muscarinic antagonists used for treatment of parkinsonia disorders and drug-induced extrapyramidal movement disorders and as an antispasmodic.
Purity : >98%(HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
5MG | 34 | In Stock |
|
10MG | 45 | In Stock |
|
25MG | 61 | In Stock |
|
50MG | 98 | In Stock |
|
100MG | 129 | In Stock |
|
200MG | 181 | In Stock |
|
500MG | Get Quote | In Stock |
|
1G | Get Quote | In Stock |
|
Biological Information
-
Product NameDL-trihexyphenidyl hydrochloride
-
NoteResearch use only, not for human use.
-
Brief DescriptionOne of the centrally acting muscarinic antagonists used for treatment of parkinsonia disorders and drug-induced extrapyramidal movement disorders and as an antispasmodic.
-
DescriptionOne of the centrally acting muscarinic antagonsistused for treatment of parkinsonian disorders and drug-induced extrapyramidal movement disorders and as an antispasmodic.
-
Synonyms——
-
PathwayEndocrinology/Hormones
-
TargetAChR
-
RecptormAChR
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number58947-95-8
-
Formula Weight337.93
-
Molecular FormulaC20H32ClNO
-
Purity>98%(HPLC)
-
SolubilityDMSO: 10 mM
-
SMILESCl.OC(CCN1CCCCC1)(C1CCCCC1)C1=CC=CC=C1
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Bognar IT, et al. Naunyn Schmiedebergs Arch Pharmacol. 1992 Jun;345(6):611-8.
molnova catalog
related products
-
Homatropine Bromide
Homatropine Bromide is muscarinic AChR antagonist, inhibits endothelial and smooth muscle muscarinic receptors.
-
Pirenzepine dihydroc...
An antimuscarinic agent that inhibits gastric secretion at lower doses than are required to affect gastrointestinal motility, salivary, central nervous system, cardiovascular, ocular, and urinary function.
-
GSK137647A
GSK137647A is a selective FFA4 agonist.