71079-19-1 Usage
Description
Timegadine is an anti-inflammatory drug that possesses potent prostaglandin synthetase inhibitory properties. It effectively inhibits cyclo-oxygenase (COX) and lipo-oxygenase, making it a valuable compound in the realm of pharmaceuticals for managing inflammation and related conditions.
Uses
Used in Pharmaceutical Industry:
Timegadine is used as an anti-inflammatory agent for its ability to inhibit prostaglandin synthetase, COX, and lipo-oxygenase. This makes it a suitable candidate for the treatment of various inflammation-related conditions, providing relief and managing the symptoms effectively.
Used in Pain Management:
In the field of pain management, Timegadine is utilized as a therapeutic agent to alleviate pain by reducing the production of prostaglandins, which are known to play a significant role in the sensation of pain and inflammation.
Used in Inflammatory Disease Treatment:
Timegadine is also used in the treatment of various inflammatory diseases, where its inhibitory effects on key enzymes involved in the inflammatory process can help in reducing inflammation and managing the disease progression.
Check Digit Verification of cas no
The CAS Registry Mumber 71079-19-1 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 9 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 71079-19:
(7*7)+(6*1)+(5*0)+(4*7)+(3*9)+(2*1)+(1*9)=121
121 % 10 = 1
So 71079-19-1 is a valid CAS Registry Number.
InChI:InChI=1/C20H23N5S/c1-14-13-18(16-9-5-6-10-17(16)22-14)24-19(25-20-21-11-12-26-20)23-15-7-3-2-4-8-15/h5-6,9-13,15H,2-4,7-8H2,1H3,(H2,21,22,23,24,25)
71079-19-1Relevant articles and documents
Basic Antiinflammatory Compounds. N,N',N''-Trisubstituted Guanidines
Rachlin, Schneur,Bramm, E.,Ahnfelt-Ronne, I.,Arrigoni-Martelli, E.
, p. 13 - 20 (2007/10/02)
A variety of basic N,N',N''-trisubstituted guanidines was prepared and tested for antiinflammatory activity.Compounds with a thiazoylguanidine moiety linked to the 4 position of the 2-methylquinoline ring exhibited fairly high antiinflammatory activity.Optimal activity was associated with the presence of N-cycloalkyl substituents on N''-4-(2-methylquinolyl)-N'-2-thiazolylguanidine.Pharmalogical data on N-cyclohexyl-N''-4-(2-methylquinolyl)-N'-2-thiazolylguanidine (SR 1368, 44) are presented and discussed.