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indan-1-one N-(4-methylphenyl)thiosemicarbazone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58586-85-9

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58586-85-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58586-85-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,5,8 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 58586-85:
(7*5)+(6*8)+(5*5)+(4*8)+(3*6)+(2*8)+(1*5)=179
179 % 10 = 9
So 58586-85-9 is a valid CAS Registry Number.

58586-85-9Downstream Products

58586-85-9Relevant academic research and scientific papers

Synthesis, antiviral evaluation and molecular docking studies of N4-aryl substituted/unsubstituted thiosemicarbazones derived from 1-indanones as potent anti-bovine viral diarrhea virus agents

Soraires Santacruz, María C.,Fabiani, Matías,Castro, Eliana F.,Cavallaro, Lucía V.,Finkielsztein, Liliana M.

, p. 4055 - 4063 (2017/07/05)

A series of N4-arylsubstituted thiosemicarbazones derived from 1-indanones and a set of compounds lacking such substitution in the N4 position of the thiosemicarbazone moiety were synthesized and evaluated for their anti-bovine viral

Thiosemicarbazones derived from 1-indanones as new anti-Trypanosoma cruzi agents

Caputto, María E.,Fabian, Lucas E.,Benítez, Diego,Merlino, Alicia,Ríos, Natalia,Cerecetto, Hugo,Moltrasio, Graciela Y.,Moglioni, Albertina G.,González, Mercedes,Finkielsztein, Liliana M.

experimental part, p. 6818 - 6826 (2011/12/22)

In the present work, we synthesized a series of thiosemicarbazones derived from 1-indanones with good anti-Trypanosoma cruzi activity. Most of them displayed remarkable trypanosomicidal activity. All the compounds showed nonspecific cytotoxicity on human erythrocytes. The ability of the new compounds to inhibit cruzipain, the major cysteine protease of T. cruzi, was also explored. Thiosemicarbazones 12 and 24 inhibited this enzyme at the dose assayed. This interaction was also studied in terms of molecular docking.

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