10-[2-DIETHYLAMINOPROPYL]PHENOTHIAZINE structure
|
Common Name | 10-[2-DIETHYLAMINOPROPYL]PHENOTHIAZINE | ||
|---|---|---|---|---|
| CAS Number | 1094-08-2 | Molecular Weight | 348.93300 | |
| Density | N/A | Boiling Point | 430.1ºC at 760 mmHg | |
| Molecular Formula | C19H25ClN2S | Melting Point | 225 - 228 °C | |
| MSDS | Chinese USA | Flash Point | 213.9ºC | |
| Symbol |
GHS07 |
Signal Word | Warning | |
Use of 10-[2-DIETHYLAMINOPROPYL]PHENOTHIAZINEEthopropazine (Isothazine) hydrochloride is a potent, selective BChE inhibitor and a poor AChE inhibitor. Ethopropazine hydrochloride is a phenothiazine compound with anticholinergic properties. Ethopropazine hydrochloride can be used for the research of Parkinson’s disease[1][2]. |
| Name | profenamine hydrochloride |
|---|---|
| Synonym | More Synonyms |
| Description | Ethopropazine (Isothazine) hydrochloride is a potent, selective BChE inhibitor and a poor AChE inhibitor. Ethopropazine hydrochloride is a phenothiazine compound with anticholinergic properties. Ethopropazine hydrochloride can be used for the research of Parkinson’s disease[1][2]. |
|---|---|
| Related Catalog | |
| Target |
BChE, AChE[2] |
| References |
| Boiling Point | 430.1ºC at 760 mmHg |
|---|---|
| Melting Point | 225 - 228 °C |
| Molecular Formula | C19H25ClN2S |
| Molecular Weight | 348.93300 |
| Flash Point | 213.9ºC |
| Exact Mass | 348.14300 |
| PSA | 31.78000 |
| LogP | 5.88660 |
| Vapour Pressure | 1.34E-07mmHg at 25°C |
| Storage condition | 2-8°C |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
|
|
Binding to serine 65-phosphorylated ubiquitin primes Parkin for optimal PINK1-dependent phosphorylation and activation.
EMBO Rep. 16 , 939-54, (2015) Mutations in the mitochondrial protein kinase PINK1 are associated with autosomal recessive Parkinson disease (PD). We and other groups have reported that PINK1 activates Parkin E3 ligase activity bot... |
|
|
Characterization of Species Differences in Tissue Diltiazem Deacetylation Identifies Ces2a as a Rat-Specific Diltiazem Deacetylase.
Drug Metab. Dispos. 43 , 1218-25, (2015) Diltiazem, a calcium channel blocker, is mainly metabolized via demethylation or deacetylation in humans. Diltiazem demethylation is catalyzed by cytochrome P450 2D6 and 3A4. Although it was previousl... |
|
|
Linking a compound-heterozygous Parkin mutant (Q311R and A371T) to Parkinson's disease by using proteomic and molecular approaches.
Neurochem. Int. 85-86 , 1-13, (2015) Parkin is an E3-protein ubiquitin ligase, which plays an important role as a scavenger in cell metabolism. Since the discovery of the link between Parkin and Parkinson's disease, Parkin was placed in ... |
| isothazinehydrochloride |
| ProphenamineHCl |
| parsidolhydrochloride |
| EINECS 214-134-4 |
| ethopropazine hydrochloride |
| Profenaminhydrochlorid |
| 10-[2-DIETHYLAMINOPROPYL]PHENOTHIAZINE |
| parfezin |
| lysivanehydrochloride |
| ethopropazine hcl |
| MFCD00012653 |