Interesting facts
Interesting Facts about [(1S,2R)-1-benzyl-3-(dimethylamino)-2-methyl-1-phenyl-propyl] propanoate; hydrochloride
This intriguing compound is a member of the class of medications known as local anesthetics. Here are some fascinating notes about its significance and applications:
- Structure-Activity Relationship: The compound features a complex molecular architecture that plays a key role in its pharmacological activity. The presence of the dimethylamino group significantly enhances the anesthetic properties, influencing its potency and duration of action.
- Target Applications: It is often explored in the context of pain management, particularly in procedures that require localized pain relief without affecting overall consciousness.
- Enantiomeric Importance: The specified stereochemistry of the compound, noted by (1S,2R), is crucial. Enantiomers can exhibit vastly different biological activities, making its stereochemical conformation a focal point in drug design.
- Synthesis and Derivatives: Chemists often develop various derivatives of this compound to enhance its efficacy and reduce potential side effects. This includes altering the propanoate group for improved solubility and absorption.
- Clinical Trials and Research: Ongoing research is essential in assessing the clinical potential and safety profile of this compound, leading to innovative applications in anesthesiology.
As we delve deeper into the world of medicinal chemistry, compounds like this one highlight the delicate balance between molecular structure and biological function. The exploration of such compounds underscores the continual advancement in therapeutic techniques, paving the way for safer and more effective medical treatments.
Synonyms
Propoxyphene hydrochloride
Algaphan
Deprancol
Propoxyphene HCl
Dextropropoxyphene hydrochloride
Develin
Dolene
Kesso-Gesic
1639-60-7
Prophene 65
Novopropoxyn
Anatalvic
Depronal
Dolotard
Doloxene
Doraphen
Prophene
Abalgin
Erantin
Liberen
Mardon
Paljin
Romidon
Zideron
Depronal retard
Margesic Improved
Dextropropofixen Dak
642 Tablets
Harmar
(+)-Propoxyphene hydrochloride
d-Propoxyphene monohydrochloride
alpha-d-Propoxyphene hydrochloride
UNII-CB2TL9PS0T
CB2TL9PS0T
EINECS 216-683-5
Propoxyphene hydrochloride 65
Propoxyphene hydrochloride cii
DTXSID6048913
CHEBI:8498
DTXCID9028839
Propoxyphene hydrochloride [USAN:USP]
DARVOCET COMPONENT PROPOXYPHENE HYDROCHLORIDE
WYGESIC COMPONENT PROPOXYPHENE HYDROCHLORIDE
DOLENE AP-65 COMPONENT PROPOXYPHENE HYDROCHLORIDE
DARVON COMPOUND COMPONENT PROPOXYPHENE HYDROCHLORIDE
Propoxyphene hydrochloride (USAN:USP)
DEXTROPROPOXYPHENE HYDROCHLORIDE (MART.)
DEXTROPROPOXYPHENE HYDROCHLORIDE [MART.]
PROPOXYPHENE HYDROCHLORIDE (USP IMPURITY)
PROPOXYPHENE HYDROCHLORIDE [USP IMPURITY]
DEXTROPROPOXYPHENE HYDROCHLORIDE (EP MONOGRAPH)
DEXTROPROPOXYPHENE HYDROCHLORIDE [EP MONOGRAPH]
Hydrochloride, Propoxyphene
PROPOXYPHENE HYDROCHLORIDE COMPONENT OF DARVOCET
PROPOXYPHENE HYDROCHLORIDE COMPONENT OF WYGESIC
PROPOXYPHENE HYDROCHLORIDE COMPONENT OF DOLENE AP-65
PROPOXYPHENE HYDROCHLORIDE COMPONENT OF DARVON COMPOUND
216-683-5
Darvon
Propoxyphene hydrochloride [USAN]
d-Propoxyphene.HCl
(2S,3R)-(+)-4-(Dimethylamino)-3-methyl-1,2-diphenyl-2-butanol propionate (ester) hydrochloride
(+)-1,2-Diphenyl-2-propionoxy-3-methyl-4-dimethylaminobutane hydrochloride
d-4-Dimethylamino-3-methyl-1,2-diphenyl-2-butanol propionate hydrochloride
Propoxyphene hydrochloride (USAN)
SK-65 Apap
Darvon (TN)
Darvon with A.S.A.
NCGC00247706-01
SCHEMBL9269
s-alpha-(2-(Dimethylamino)-1-methylethyl)-alpha-phenylbenzeneethanol propioate hydrochloride
Benzeneethanol, alpha-(2-(dimethylamino)-1-methylethyl)-alpha-phenyl-, propanoate (ester), hydrochloride, (S-(R*,S*))-
CHEMBL1237104
DEXTROPROPOXIPHENE CHLORIDE
Tox21_112860
AKOS040753628
PROPOXYPHENE HYDROCHLORIDE [MI]
DEXTRO PROPOXYPHENE HYDROCHLORIDE
Dextropropoxyphene for system suitability
2-Butanol, 4-(dimethylamino)-3-methyl-1,2-diphenyl-, propionate (ester), hydrochloride, (+)-
Benzeneethanol, alpha-((1R)-2-(dimethylamino)-1-methylethyl)-alpha-phenyl-, propanoate (ester), hydrochloride, (alphaS)-
Benzeneethanol, alpha-(2-(dimethylamino)-1-methylethyl)-alpha-phenyl-, propanoate (ester), hydrochloride, (S-(theta,S))-
PROPOXYPHENE HYDROCHLORIDE [VANDF]
CAS-1639-60-7
NS00076367
D00482
PROPOXYPHENE HYDROCHLORIDE [ORANGE BOOK]
DEXTROPROPOXYPHENE HYDROCHLORIDE [WHO-DD]
Q27108093
d-Propoxyphene.HCl, 1mg/ml in Methanol (as free base)
[(2S,3R)-4-(dimethylamino)-3-methyl-1,2-diphenylbutan-2-yl] propanoate;hydrochloride
BENZENEETHANOL, .ALPHA.-(2-(DIMETHYLAMINO)-1-METHYLETHYL)-.ALPHA.-PHENYL-, PROPANOATE (ESTER), HYDROCHLORIDE, (S-(R*,S*))-
Benzeneethanol, alpha-((1R)-2-(dimethylamino)-1-methylethyl)-alpha-phenyl-, 1-propanoate, hydrochloride (1:1), (alphaS)-
Solubility Characteristics
The solubility of [(1S,2R)-1-benzyl-3-(dimethylamino)-2-methyl-1-phenyl-propyl] propanoate; hydrochloride can be influenced by several factors including its molecular structure and the nature of its functional groups. Generally, hydrochloride salts tend to exhibit increased solubility in water compared to their free bases. Here are some key points to consider regarding solubility:
Overall, while the primary expectation is for reasonable aqueous solubility due to the hydrochloride form, empirical data and specific conditions such as solvent polarity and temperature should be assessed to understand the solubility behaviors accurately.