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ChemicalBook--->CAS DataBase List--->1005-24-9

1005-24-9

1005-24-9 Structure

1005-24-9 Structure
IdentificationMore
[Name]

3-CARBAMYL-1-METHYLPYRIDINIUM CHLORIDE
[CAS]

1005-24-9
[Synonyms]

1-METHYLNICOTINAMIDE CHLORIDE
1-METHYLNICOTINAMIDE CHLORIDE SALT
1-METHYLPYRIDINE-3-CARBOXYLIC ACID AMIDE CHLORIDE
3-CARBAMOYL-1-METHYLPYRIDINIUM CHLORIDE
3-CARBAMYL-1-METHYLPYRIDINIUM CHLORIDE
N1-METHYLNICOTINAMIDE CHLORIDE
NICOTINAMIDE CHLOROMETHYLATE
N-METHYLNICOTINIC ACID AMIDE CHLORIDE SALT
TRIGONELLAMIDE CHLORIDE
3-(aminocarbonyl)-1-methyl-pyridiniuchloride
3-carbamoyl-1-methyl-pyridiniuchloride
nicotinamidemethochloride
nicotinamidemethylchloride
nipecotamidemethochloride
n-methylnicotinamidechloride
n-methylnicotinic acid amide chloride
3-CARBAMYL-1-METHYLPYRIDINIUM CHLORIDE 98+%
[EINECS(EC#)]

463-670-7
[Molecular Formula]

C7H9ClN2O
[MDL Number]

MFCD00060042
[Molecular Weight]

172.61
[MOL File]

1005-24-9.mol
Chemical PropertiesBack Directory
[Melting point ]

207-209℃ (water acetone )
[storage temp. ]

room temp
[solubility ]

H2O: soluble15mg/mL, clear
[form ]

crystalline
[color ]

white
[Water Solubility ]

almost transparency
[Merck ]

9693
[CAS DataBase Reference]

1005-24-9(CAS DataBase Reference)
Safety DataBack Directory
[WGK Germany ]

3
[RTECS ]

UU1925000
[HS Code ]

2933.39.9200
Hazard InformationBack Directory
[Description]

Nicotinamide is a precursor of NAD (Item No. 16077) and NADP (Item No. 10004675), which serve essential functions in modulating cellular redox status and controlling signaling and transcriptional events. 1-Methylnicotinamide (MNA) is a primary metabolite of nicotinamide produced by the action of nicotinamide N-methyltransferase (NNMT; Item No. 15138). It demonstrates antithrombotic and anti-inflammatory properties through direct action on the endothelium by a mechanism involving the prostacyclin pathway and by improving nitric oxide bioavailability. Aggressive cancer cell lines are reported to have higher levels of MNA due to increased NNMT-directed transfer of methyl groups from S-adenosyl-L-methionine to nicotinamide, implicating a role for MNA in cancer cell metabolism.
[Uses]

1-Methylnicotinamide chloride may be used as a standard in the quantification of 1-methylnicotinamide in urine samples using ion pairing reverse-phase high performance liquid chromatography (RP-HPLC).
[Uses]

Nicotinamide is a precursor of NAD and NADP , which serve essential functions in modulating cellular redox status and controlling signaling and transcriptional events. 1-Methylnicotinamide (MNA) is a primary metabolite of nicotinamide produced by the action of nicotinamide N-methyltransferase (NNMT; ). It demonstrates antithrombotic and anti-inflammatory properties through direct action on the endothelium by a mechanism involving the prostacyclin pathway and by improving nitric oxide bioavailability. Aggressive cancer cell lines are reported to have higher levels of MNA due to increased NNMT-directed transfer of methyl groups from S-adenosyl-L-methionine to nicotinamide, implicating a role for MNA in cancer cell metabolism.
[General Description]

1-Methylnicotinamide (MNA) is a primary metabolite of nicotinamide produced mainly by nicotinamide N-methyltransferase (NNMT) and exhibits antithrombotic and anti-inflammatory effects.
[Biochem/physiol Actions]

1-Methylnicotinamide (MNA) is a primary metabolite of nicotinamide produced mainly by nicotinamide N-methyltransferase (NNMT). 1-Methylnicotinamide (MNA) has been shown to have antithrombotic and anti-inflammatory effects. A recent study indicated that MNA may exert antithrombotic and anti-inflammatory effects through direct action on the endothelium, with a vasorelaxing effect by enhancement of NO bioavailability and reduction of eNOS-dependent oxidative stress. Enhanced NNMT activity is a feature of many types of cancer. How much direct involvement MNA has in the tumorigenesis associated with overexpression of NNMT is under investigation. MNA by itself increased mitochondrial Complex I activity and increased cancer cell viability in SH-SY5Y neuroblastoma cells that do not produce NNMT.
[storage]

Store at -20°C
[Purification Methods]

Recrystallise it from MeOH. [Beilstein 22 III/IV 468, 22/2 V 80.]
Spectrum DetailBack Directory
[Spectrum Detail]

3-CARBAMYL-1-METHYLPYRIDINIUM CHLORIDE(1005-24-9)1HNMR
3-CARBAMYL-1-METHYLPYRIDINIUM CHLORIDE(1005-24-9)IR1
3-CARBAMYL-1-METHYLPYRIDINIUM CHLORIDE(1005-24-9)IR2
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

1005-24-9(sigmaaldrich)
[TCI AMERICA]

3-Carbamyl-1-methylpyridinium Chloride,>98.0%(LC)(T)(1005-24-9)
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