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50844-81-0

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50844-81-0 Usage

Description

(2-METHYL-4-OXO-4H-QUINAZOLIN-3-YL)-ACETIC ACID, also known as picolinic acid, is a chemical compound with the molecular formula C11H9N4O3. It is a derivative of quinazoline and is used in the synthesis of various pharmaceuticals and organic compounds. (2-METHYL-4-OXO-4H-QUINAZOLIN-3-YL)-ACETIC ACID is a weak acid and forms salts with various metals, which can be used as chelating agents. Picolinic acid has also been studied for its potential as a treatment for various conditions, including neurodegenerative diseases and cancer. Additionally, it has been investigated for its role in the immune system and inflammation. Overall, (2-METHYL-4-OXO-4H-QUINAZOLIN-3-YL)-ACETIC ACID has diverse uses and potential therapeutic applications in the field of medicine and biochemistry.

Uses

Used in Pharmaceutical Industry:
(2-METHYL-4-OXO-4H-QUINAZOLIN-3-YL)-ACETIC ACID is used as a building block for the synthesis of various pharmaceuticals and organic compounds. Its unique chemical structure allows it to be incorporated into a wide range of molecules, making it a valuable component in drug development.
Used in Chelating Agents:
(2-METHYL-4-OXO-4H-QUINAZOLIN-3-YL)-ACETIC ACID is used as a chelating agent for various metals. Its ability to form salts with metals makes it useful in applications where metal ion sequestration is necessary, such as in water treatment or industrial processes.
Used in Neurodegenerative Disease Treatment:
(2-METHYL-4-OXO-4H-QUINAZOLIN-3-YL)-ACETIC ACID is used as a potential treatment for neurodegenerative diseases. Its ability to modulate various biological pathways and target specific cellular processes makes it a promising candidate for the development of therapies to combat these conditions.
Used in Cancer Treatment:
(2-METHYL-4-OXO-4H-QUINAZOLIN-3-YL)-ACETIC ACID is used as a potential treatment for various types of cancer. Its ability to target cancer cells and inhibit their growth and proliferation makes it a valuable compound in the development of cancer therapies.
Used in Immune System and Inflammation Research:
(2-METHYL-4-OXO-4H-QUINAZOLIN-3-YL)-ACETIC ACID is used in research to better understand its role in the immune system and inflammation. Its potential to modulate immune responses and reduce inflammation makes it an important compound for studying these processes and developing new treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 50844-81-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,8,4 and 4 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 50844-81:
(7*5)+(6*0)+(5*8)+(4*4)+(3*4)+(2*8)+(1*1)=120
120 % 10 = 0
So 50844-81-0 is a valid CAS Registry Number.

50844-81-0Relevant articles and documents

Development of 2-(4-oxoquinazolin-3(4 H)-yl)acetamide derivatives as novel enoyl-acyl carrier protein reductase (InhA) inhibitors for the treatment of tuberculosis

Pedgaonkar, Ganesh S.,Sridevi, Jonnalagadda Padma,Jeankumar, Variam Ullas,Saxena, Shalini,Devi, Parthiban Brindha,Renuka, Janupally,Yogeeswari, Perumal,Sriram, Dharmarajan

, p. 613 - 627 (2015/01/09)

InhA, the enoyl acyl carrier protein reductase of Mycobacterium tuberculosis (MTB) is an attractive target for developing novel anti-tubercular agents. Twenty eight 2-(4-oxoquinazolin-3(4H)-yl)acetamide derivatives were synthesized and evaluated for their in vitro MTB InhA inhibition. Compounds were further evaluated for their in vitro activity against drug sensitive and resistant MTB strains and cytotoxicity against RAW 264.7 cell line. Compounds were docked at the active site of InhA to understand their binding mode and differential scanning fluorimetry was performed to ascertain their protein interaction and stability.

Synthesis of thiadiazolo derivatives of 4-(3h)-quinazolinone as potential antimicrobial agents

Khalil,Habib

, p. 973 - 978 (2007/10/02)

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SYNTHESIS OF PEPTIDES CONTAINING A QUINAZOLIN-4-ONE MOIETY

El-Khawaga, Ahmed M.,Abd-Alla, Mohamed A.,Khalaf, Ali A.

, p. 441 - 442 (2007/10/02)

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