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78538-74-6

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78538-74-6 Usage

Description

N-METHYL-BETA-CARBOLINE-3-CARBOXAMIDE, also known as FG 7142, is a nonselective benzodiazepine inverse agonist with high affinity for the α1 subunit-containing GABAA receptor. It modulates GABA-induced chloride flux at GABAA receptors expressing the α1 subunit and increases tyrosine hydroxylation, leading to upregulation of β-adrenergic receptors in mouse cerebral cortex.
Used in Pharmaceutical Industry:
N-METHYL-BETA-CARBOLINE-3-CARBOXAMIDE is used as a benzodiazepine inverse agonist anxiogenic compound for its ability to modulate GABAA receptors and induce anxiogenic effects.

Biological Activity

Inverse agonist and anxiogenic agent. Increases tyrosine hydroxylation and causes upregulation of β -adrenoceptors in mouse cerebral cortex.

Biochem/physiol Actions

Benzodiazepine inverse receptor agonist; potent anxiogenic agent.

Check Digit Verification of cas no

The CAS Registry Mumber 78538-74-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,5,3 and 8 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 78538-74:
(7*7)+(6*8)+(5*5)+(4*3)+(3*8)+(2*7)+(1*4)=176
176 % 10 = 6
So 78538-74-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H11N3O/c1-14-13(17)11-6-9-8-4-2-3-5-10(8)16-12(9)7-15-11/h2-7,16H,1H3,(H,14,17)

78538-74-6 Well-known Company Product Price

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  • Sigma

  • (E006)  β-Carboline-3-carboxylic acid N-methylamide  

  • 78538-74-6

  • E006-100MG

  • 2,347.02CNY

  • Detail
  • Sigma

  • (E006)  β-Carboline-3-carboxylic acid N-methylamide  

  • 78538-74-6

  • E006-500MG

  • 8,113.95CNY

  • Detail

78538-74-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-Methyl-b-carboline-3-carboxamide

1.2 Other means of identification

Product number -
Other names B-carboline-3-carboxylic acid N-*methylamide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:78538-74-6 SDS

78538-74-6Relevant articles and documents

N-Methyl-β-carboline-3-carboxamide (FG 7142): an Anxiogenic Agent in Cigarette Smoke Condensate and its Mechanism of Formation

Manabe, Shigeo,Juan, Yuan,Wada, Osamu,Ueki, Akira,Kanai, Yoshikatsu

, p. 329 - 336 (1995)

β-Carboline-3-carboxylic acid methylamide (FG 7142), an anxiogenic agent has been found in cigarette smoke condensate, but not in the cigarette itself. When a cigarette, except its filter portion, was immersed in 20 ml of potassium phosphate buffer, pH 7.4, then heated at 60 deg C for 2 days with or without presence of methylamine, FG 7142 was detected only in the mixture containing methylamine. Furthermore, when the mixtures of β-carboline derivatives and various amounts of methylamine hydrochloride were heated at 60 deg C for 5 days, FG 7142 was formed only in the mixtures containing methylamine and 1-methyl-1,2,3,4-tetrahydro-β-carboline-3-carboxylic acid (MTCA) or 1,2,3,4-tetrahydro-β-carboline-3-carboxylic acid (TCCA). FG 7142 was also produced in the mixture of glucose, L-tryptophan and methylamine when heated at 200 deg C in a dry condition. These observations suggest that FG 7142 is formed through the smoking process and that methylamine in cigarette smoke may play an important role in the formation of FG 7142.

Some 3-carboxamides of β-carboline and tetrahydro-β-carboline

Couts, Ronald T.,Micetich, Ronald G.,Baker, Glen B,Benderly, Abraham,Dewhurst, Tim,et al.

, p. 131 - 142 (2007/10/02)

A series of tetrahydro-β-carboline-3-carboxamides (L- and D-series) was made by the interaction of the respective amine with the appriopriate methyl tetrahydro-β-carboline-3-carboxylate.The β-carboline-3-carboxamides were prepared by a similar route from methyl β-carboline-3-carboxylate or by aromatization of the respective tetrahydro-β-carboline-3-carboxamide.The diastereomers of N-sec-butyl tetrahydro-β-carboline-3-carboxamide (L- and D-series) were separated by chromatography.

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