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1H-Pyrido[3,4-b]indole, 1-(3,5-dimethoxyphenyl)-2,3,4,9-tetrahydro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

331978-46-2

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331978-46-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 331978-46-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,1,9,7 and 8 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 331978-46:
(8*3)+(7*3)+(6*1)+(5*9)+(4*7)+(3*8)+(2*4)+(1*6)=162
162 % 10 = 2
So 331978-46-2 is a valid CAS Registry Number.

331978-46-2Downstream Products

331978-46-2Relevant academic research and scientific papers

The preparation and evaluation of 1-substituted 1,2,3,4-tetrahydro- and 3,4-dihydro-β-carboline derivatives as potential antitumor agents

Shen, Ya-Ching,Chen, Ching-Yeu,Hsieh, Pei-Wen,Duh, Chang-Yih,Lin, Yat-Min,Ko, Chin-Lien

, p. 32 - 36 (2005)

A series of 1-substituted 1,2,3,4-tetrahydro- and 3,4-dihydro-β- carboline derivatives have been synthesized and evaluated for antitumor activity against murine P-388 and human tumor cell lines, KB-16, A-549 and HT-29. All of the compounds prepared, excep

Ultrasound Assisted Pictet-Spengler Synthesis of Tetrahydro-β-Carboline Derivatives

Muscia, Gisela C.,De Mara, Leonardo O.,Buldain, Graciela Y.,Ass, Silvia E.

, p. 647 - 650 (2016/04/19)

The synthesis of twelve tetrahydro-β-carboline derivatives 3a, 3b, 3c, 3d, 3e, 3f, 3g, 3h, 3i, 3j, 3k, 3l prepared via the Pictet-Spengler reaction is described. The reaction of tryptamine and a variety of arylaldehydes were carried out under ultrasonic irradiation and trifluoracetic acid catalysis at room temperature. These tetrahydro-β-carbolines have been synthesized in higher yields and shorter reaction times compared to the conventional method. Moreover, the reaction proceeded successfully even employing arylaldehydes with electron-donating or electron-attracting substituents which did not react under conventional method.

1-substituted 1,2,3,4-tetrahydro-beta-carboline and 3,4-dihydro-beta-carboline and analogs as antitumor agents

-

, (2008/06/13)

A composition includes a substituted dihydro- or tetrahydro-β-carboline of formula (II) or (III), wherein the aromatic ring of the carboline may include one or more substituents selected from the group consisting of hydroxy, C1-6 alkoxy, benzyloxy, C1-6 acyloxy, amino, C1-6 alkyl, C1-6 dialkylamino, halogen, and carboxy, and the C-1 position of the carboline may include a substitutent selected from the group consisting of a carbocyclic group and a heterocyclic group. The composition may include a salt or a prodrug of the substituted dihydro- or tetrahydro-β-carboline. The composition may further includes a pharmaceutically acceptable carrier, diluent, or excipient.

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