6-HYDROXYDOPAMINE HYDROBROMIDE

Modify Date: 2024-01-04 09:58:27

6-HYDROXYDOPAMINE HYDROBROMIDE Structure
6-HYDROXYDOPAMINE HYDROBROMIDE structure
Common Name 6-HYDROXYDOPAMINE HYDROBROMIDE
CAS Number 636-00-0 Molecular Weight 250.090
Density N/A Boiling Point 406ºC at 760 mmHg
Molecular Formula C8H12BrNO3 Melting Point 216-220 °C(lit.)
MSDS Chinese USA Flash Point 199.3ºC
Symbol GHS07
GHS07
Signal Word Warning

 Use of 6-HYDROXYDOPAMINE HYDROBROMIDE


Oxidopamine hydrobromide is a selective catecholaminergic neurotoxin, depletes brain catecholamine levels via uptake and accumulation by a transport mechanism specific to these neurons. In vitro: Oxidopamine hydrobromide-induced apoptosis of PC12 cells was initiated by superoxide generation followed by caspase cascade activation, which was associated with the suppressed Akt phosphorylation and increased p38 phosphorylation. It is likely that pCPT-cAMP prevented the Oxidopamine hydrobromide-induced apoptosis via activation of the PI3-kinase/Akt pathway without any effect on superoxide generation or mitochondrial membrane depolarization. [1]In vivo the presence of sulfhydryl antioxidants protected against neuronal degeneration in the striatum, which was particularly remarkable in the case of CySH and was attributed to its capacity to remove the H2O2 produced in the autoxidation of Oxidopamine hydrobromide.

 Names

Name 6-Hydroxydopamine hydrobromide
Synonym More Synonyms

 6-HYDROXYDOPAMINE HYDROBROMIDE Biological Activity

Description Oxidopamine hydrobromide is a selective catecholaminergic neurotoxin, depletes brain catecholamine levels via uptake and accumulation by a transport mechanism specific to these neurons. In vitro: Oxidopamine hydrobromide-induced apoptosis of PC12 cells was initiated by superoxide generation followed by caspase cascade activation, which was associated with the suppressed Akt phosphorylation and increased p38 phosphorylation. It is likely that pCPT-cAMP prevented the Oxidopamine hydrobromide-induced apoptosis via activation of the PI3-kinase/Akt pathway without any effect on superoxide generation or mitochondrial membrane depolarization. [1]In vivo the presence of sulfhydryl antioxidants protected against neuronal degeneration in the striatum, which was particularly remarkable in the case of CySH and was attributed to its capacity to remove the H2O2 produced in the autoxidation of Oxidopamine hydrobromide.
Related Catalog
References

[1]. Fujita H et al. Cell-permeable cAMP analog suppresses 6-hydroxydopamine-induced apoptosis in PC12 cells through the activation of the Akt pathway. Brain Res. 2006 Oct 3;1113(1):10-23.

[2]. Soto-Otero R et al. Autoxidation and neurotoxicity of 6-hydroxydopamine in the presence of some antioxidants: potential implication in relation to the pathogenesis of Parkinson's disease. J Neurochem. 2000 Apr;74(4):1605-12.

 Chemical & Physical Properties

Boiling Point 406ºC at 760 mmHg
Melting Point 216-220 °C(lit.)
Molecular Formula C8H12BrNO3
Molecular Weight 250.090
Flash Point 199.3ºC
Exact Mass 249.000046
PSA 86.71000
LogP 1.96300
Appearance of Characters solid | tan to brown
Storage condition 2-8°C

 Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
DC4600000
CHEMICAL NAME :
1,2,4-Benzenetriol, 5-(2-aminoethyl)-, hydrobromide
CAS REGISTRY NUMBER :
636-00-0
LAST UPDATED :
198910
DATA ITEMS CITED :
1
MOLECULAR FORMULA :
C8-H11-N-O3.Br-H
MOLECULAR WEIGHT :
250.12

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Intraperitoneal
DOSE :
100 mg/kg
SEX/DURATION :
female 21-22 day(s) after conception
TOXIC EFFECTS :
Reproductive - Paternal Effects - other effects on male Reproductive - Maternal Effects - parturition
REFERENCE :
JRPFA4 Journal of Reproduction and Fertility. (Biochemical Soc. Book Depot, POB 32, Commerce Way, Colchester, Essex CO2 8HP, UK) V.1- 1960- Volume(issue)/page/year: 76,415,1986

 Safety Information

Symbol GHS07
GHS07
Signal Word Warning
Hazard Statements H315-H319-H335
Precautionary Statements P261-P305 + P351 + P338
Personal Protective Equipment dust mask type N95 (US);Eyeshields;Gloves
Hazard Codes Xi
Risk Phrases 36/37/38
Safety Phrases S26-S36
RIDADR NONH for all modes of transport
WGK Germany 3
RTECS DC4600000
HS Code 2922299090

 Precursor & DownStream

Precursor  0

DownStream  1

 Customs

HS Code 2922299090
Summary 2922299090. other amino-naphthols and other amino-phenols, other than those containing more than one kind of oxygen function, their ethers and esters; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

 Articles92

More Articles
Rho kinase inhibition by fasudil in the striatal 6-hydroxydopamine lesion mouse model of Parkinson disease.

J. Neuropathol. Exp. Neurol. 73(8) , 770-9, (2014)

Chronic degeneration of nigrostriatal projections, followed by nigral dopaminergic cell death, is a key feature of Parkinson disease (PD). This study examines the neuroprotective potential of the rho ...

Curcumin I mediates neuroprotective effect through attenuation of quinoprotein formation, p-p38 MAPK expression, and caspase-3 activation in 6-hydroxydopamine treated SH-SY5Y cells.

Phytother Res. 28(4) , 611-6, (2014)

6-Hydroxydopamine (6-OHDA) selectively enters dopaminergic neurons and undergoes auto-oxidation resulting in the generation of reactive oxygen species and dopamine quinones, subsequently leading to ap...

Ameliorating effects of curcumin on 6-OHDA-induced dopaminergic denervation, glial response, and SOD1 reduction in the striatum of hemiparkinsonian mice.

Eur. Rev. Med. Pharmacol. Sci. 17(10) , 1360-8, (2013)

Inflammation and oxidative stress are believed to contribute to neuronal degeneration of the nigrostriatal dopaminergic (DA) pathway in Parkinson's disease. Curcumin, a component of the yellow curry s...

 Synonyms

5-(2-Aminoethyl)-1,2,4-benzenetriol hydrobromide (1:1)
1,2,4-Benzenetriol, 5-(2-aminoethyl)-, hydrobromide (1:1)
5-(2-aminoethyl)benzene-1,2,4-triol,hydrobromide
5-(2-Aminoethyl)benzene-1,2,4-triol hydrobromide (1:1)
EINECS 211-247-0
MFCD00012894
Oxidopamine (hydrobromide)
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