Cart
sales@molnova.com
Oxyphencyclimine Hydrochloride
CAS No. 125-52-0
Oxyphencyclimine Hydrochloride( —— )
Catalog No. M17223 CAS No. 125-52-0
Oxyphencyclimine Hydrochloride is a synthetic tertiary amine and antimuscarinic agent with antispasmodic and antisecretory activities.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 31 | In Stock |
|
| 5MG | 48 | In Stock |
|
| 10MG | 85 | 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 NameOxyphencyclimine Hydrochloride
-
NoteResearch use only, not for human use.
-
Brief DescriptionOxyphencyclimine Hydrochloride is a synthetic tertiary amine and antimuscarinic agent with antispasmodic and antisecretory activities.
-
DescriptionOxyphencyclimine Hydrochloride is a synthetic tertiary amine and antimuscarinic agent with antispasmodic and antisecretory activities.
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayChromatin/Epigenetic
-
TargetEpigenetic Reader Domain
-
RecptorMuscarinic AChR
-
Research AreaNeurological Disease
-
Indication——
Chemical Information
-
CAS Number125-52-0
-
Formula Weight380.91
-
Molecular FormulaC20H29ClN2O3
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESCOc1cc(c(cc1CNC[C@@H](c1c2ccc(=O)[nH]c2c(cc1)O)O)Cl)NC(=O)CCN1CCC(CC1)OC(=O)Nc1ccccc1c1ccccc1
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Waelbroeck M, et al. Eur J Pharmacol. 1992 Sep 1;227(1):33-42.
molnova catalog
related products
-
Y06137
Y06137 is an effective and selective BET inhibitor with a Kd of 81 nM for BRD4(1) bromodomain. Y06137 can be used for research on the treatment of castration-resistant prostate cancer.
-
FHT-1015
FHT-1015 is a potent SMARCA4/SMARCA2 ATPase (BRG1 and BRM) inhibitor with potential anticancer activity for the study of cancer and inflammation.
-
PBRM1-BD2-IN-5
PBRM1-BD2-IN-5 is a potent inhibitor of the PBRM1 Bromodomain, with dissociation constant (Kd) values of 1.5 μM and 3.9 μM for PBRM1-BD2 and PBRM1-BD5 respectively, and an inhibitory concentration 50 (IC50) value of 0.26 μM for PBRM1-BD2.
