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1-Methylnicotinamide chloride

1-Methylnicotinamide chloride structure

1-Methylnicotinamide chloride 

structure
  • CAS No:

    1005-24-9

  • Formula:

    C7H9N2O.Cl

  • Chemical Name:

    1-Methylnicotinamide chloride

  • Synonyms:

    Pyridinium,3-(aminocarbonyl)-1-methyl-,chloride (1:1);3-Carbamoyl-1-methylpyridinium chloride;Pyridinium,3-carbamoyl-1-methyl-,chloride;Pyridinium,3-(aminocarbonyl)-1-methyl-,chloride;3-Carbamyl-1-methylpyridinium chloride;N1-Methylnicotinamide chloride;1-Methylnicotinamide chloride;Trigonellamide chloride;Nicotinamide methochloride;1-Methyl-3-carbamoylpyridinium chloride;3-(Aminocarbonyl)-1-methylpyridinium chloride;N-Methyl-3-carboxamidepyridinium chloride;N-Methylnicotinamide chloride;3-Carbamoyl-1-methylpyridin-1-ium chloride;776318-66-2

  • Categories:

    Cosmetic Ingredient  >  Skin Conditioning

1-Methylnicotinamide chloride Basic Attributes

172.61

172.040344

463-670-7

L54XNJ1D5G

2933399090

Characteristics

47

-2.68570

white crystalline

207-209 °C @ Solvent: Water, Acetone

H2O: soluble 15mg/mL, clear

room temp

Safety Information

NONH for all modes of transport

3

UU1925000

P264, P280, P302+P352, P305+P351+P338, P321, P332+P313, P337+P313, P362

H315

|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P264, P280, P302+P352, P305+P351+P338, P321, P332+P313, P337+P313, and P362|The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory.|H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]|P261, P264, P271, P280, P304+P340, P305+P351+P338, P312, P337+P313, P403+P233, P405, and P501

Drug Information

1-methyl-3-carbamoylpyridinium

1-Methylnicotinamide chloride Use and Manufacturing

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.

Computed Properties

Molecular Weight:172.61
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:172.0403406
Monoisotopic Mass:172.0403406
Topological Polar Surface Area:47
Heavy Atom Count:11
Complexity:136
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes

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