Desmethylselegiline

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Names

[ CAS No. ]:
18913-84-3

[ Name ]:
Desmethylselegiline

[Synonym ]:
EINECS 200-659-6

Chemical & Physical Properties

[ Molecular Formula ]:
C12H15N

[ Molecular Weight ]:
173.25

[ Flash Point ]:
9℃

[ Storage condition ]:
-20°C Freezer, Under Inert Atmosphere

Safety Information

[ Symbol ]:

GHS02, GHS06, GHS08

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H225-H301 + H311 + H331-H370

[ Precautionary Statements ]:
P210-P260-P280-P301 + P310-P311

[ Hazard Codes ]:
F,T

[ Risk Phrases ]:
11-23/24/25-39/23/24/25

[ Safety Phrases ]:
7-16-36/37-45

[ RIDADR ]:
UN1230 - class 3 - PG 2 - Methanol, solution

Articles

Simultaneous determination of selegiline and desmethylselegiline in human body fluids by headspace solid-phase microextraction and gas chromatography-mass spectrometry.

J. Chromatogr. B. Analyt. Technol. Biomed. Life Sci. 844(2) , 283-91, (2006)

A method for the simultaneous determination of selegiline and its metabolite, desmethylselegiline, in human whole blood and urine is presented. The method, which combines a fiber-based headspace solid...

Modulation of neuroendocrine--immune signaling by L-deprenyl and L-desmethyldeprenyl in aging and mammary cancer.

Mech. Ageing Dev. 123(8) , 1065-79, (2002)

The aging process is characterized by a decline in cellular functions of diverse systems of the body, including the neuroendocrine-immune network. One neuroendocrinological theory of aging is based on...

Pharmacokinetic studies of (-)-deprenyl and some of its metabolites in mouse.

J. Neural Transm. Suppl. (72) , 165-73, (2007)

(-)-Deprenyl is a selective irreversible inhibitor of MAO-B. The parent compound is responsible for the enzyme inhibitory effect, but its metabolites are also playing a role in the complex pharmacolog...


More Articles


Related Compounds

  • N-Desmethylselegiline
  • desmethylselegiline hydrochloride
  • desmethylselegiline hydrochloride
  • 5,7-dimethyl-3-[(1E)-{[({[(2E)-3-phenylprop-2-en-1-yl]sulfanyl}methanimidoyl)amino]imino}methyl]-4H-chromen-4-one hydrobromide
  • (1-(Aza(4-ethoxyphenyl)methylene)inden-3-yl)(4-ethoxyphenyl)amine hydrochloride
  • (3,4-Diphenyl(2,5-thiazolyl))(4-(trifluoromethoxy)phenyl)amine
  • (4-(4-(Tert-butyl)phenyl)(2,5-thiazolyl))(4-(trifluoromethoxy)phenyl)amine, chloride
  • (R)-3-(Fmoc-amino)piperidine HCl
  • 1-Piperazinecarboxylic acid, 4-[4-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)benzoyl]-, 1,1-dimethylethyl ester
  • N-alpha-t-Butyloxycarbonyl-4-chloro-L-phenylglycine dicyclohexylamine (Boc-L-Phg(4-Cl)-OH.DCHA)
  • (S)-2-Amino-5-(tert-butoxy)-5-oxopentanoic acid hydrate
  • Sodium;chlorogold;3-diphenylphosphanylbenzenesulfonate
  • tert-butyl (4-((3-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)propyl)(tert-butoxycarbonyl)amino)butyl)(3-aminopropyl)carbamate hydrochloride
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