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Thiourea, N-cyclohexyl-N'-2-thiazolyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

71071-22-2

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71071-22-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71071-22-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,0,7 and 1 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 71071-22:
(7*7)+(6*1)+(5*0)+(4*7)+(3*1)+(2*2)+(1*2)=92
92 % 10 = 2
So 71071-22-2 is a valid CAS Registry Number.

71071-22-2Downstream Products

71071-22-2Relevant academic research and scientific papers

Antimicrobial and anti-biofilm activity of thiourea derivatives incorporating a 2-aminothiazole scaffold

Stefanska, Joanna,Nowicka, Grazyna,Struga, Marta,Szulczyk, Daniel,Koziol, Anna Eugenia,Augustynowicz-Kopec, Ewa,Napiorkowska, Agnieszka,Bielenica, Anna,Filipowski, Wojciech,Filipowska, Anna,Drzewiecka, Aleksandra,Giliberti, Gabriele,Madeddu, Silvia,Boi, Stefano,Colla, Paolo La,Sanna, Giuseppina

, p. 225 - 236 (2015)

A series of new thiourea derivatives of 1,3-thiazole have been synthesized. All obtained compounds were tested in vitro against a number of microorganisms, including Gram-positive cocci, Gram-negative rods and Candida albicans . Compounds were also tested for their in vitro tuberculostatic activity against the Mycobacterium tuberculosis H37Rv strain, as well as two 'wild' strains isolated from tuberculosis patients. Compounds 3 and 9 showed significant inhibition against Gram-positive cocci (standard strains and hospital strain). The range of MIC values is 2-32 μg/mL. Products 3 and 9 effectively inhibited the biofilm formation of both methicillin-resistant and standard strains of S. epidermidis. The halogen atom, especially at the 3rd position of the phenyl group, is significantly important for this antimicrobial activity. Moreover, all obtained compounds resulted in cytotoxicity and antiviral activity on a large set of DNA and RNA viruses, including Human Immunodeficiency Virus type 1 (HIV-1) and other several important human pathogens. Compound 4 showed activity against HIV-1 and Coxsackievirus type B5. Seven compounds resulted in cytotoxicity against MT-4 cells (CC5010 μM).

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