141102-07-0 Usage
Indole derivative
A compound based on the indole structure This compound is derived from the indole structure, which is a bicyclic aromatic organic compound consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring.
Propyl group attachment
At the 1-position of the indole ring A propyl group (a three-carbon alkyl chain) is attached to the first position of the indole ring in this compound.
Carboxylic acid group
At the 3-position A carboxylic acid group (a carbonyl group bonded to an oxygen atom and a hydroxyl group) is present at the third position of the compound.
Potential pharmaceutical properties
Anti-inflammatory and analgesic agent This compound has been studied for its potential to act as an anti-inflammatory and pain-relieving substance.
Applications in medicinal chemistry
Development of novel drugs The compound may have potential applications in the field of medicinal chemistry for creating new and improved drugs.
Further research needed
Pharmacological and biological properties More research is required to fully understand the properties and potential effects of 1-propyl-1H-indole-3-carboxylic acid in biological systems.
Check Digit Verification of cas no
The CAS Registry Mumber 141102-07-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,1,0 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 141102-07:
(8*1)+(7*4)+(6*1)+(5*1)+(4*0)+(3*2)+(2*0)+(1*7)=60
60 % 10 = 0
So 141102-07-0 is a valid CAS Registry Number.
141102-07-0Relevant articles and documents
Synthesis and biological evaluation of novel indole derivatives containing sulfonamide scaffold as potential tubulin inhibitor
Man, Ruo-Jun,Tang, Dan-Jie,Lu, Xiao-Yuan,Duan, Yong-Tao,Tao, Xiang-Xiang,Yang, Meng-Ru,Wang, Le-Le,Wang, Bao-Zhong,Xu, Chen,Zhu, Hai-Liang
supporting information, p. 1759 - 1767 (2016/09/23)
Microtubule-targeted drugs play a critical role in various types of cancer therapy worldwide. In our study, a series of novel indole derivatives containing a sulfonamide scaffold were designed, synthesized and biologically evaluated as potential tubulin p
Design, synthesis, and biological activity of potent and selective inhibitors of mast cell tryptase
Hopkins, Corey R.,Czekaj, Mark,Kaye, Steven S.,Gao, Zhongli,Pribish, James,Pauls, Henry,Liang, Guyan,Sides, Keith,Cramer, Dona,Cairns, Jennifer,Luo, Yongyi,Lim, Heng-Keang,Vaz, Roy,Rebello, Sam,Maignan, Sebastian,Dupuy, Alain,Mathieu, Magali,Levell, Julian
, p. 2734 - 2737 (2007/10/03)
A new series of novel mast cell tryptase inhibitors is reported, which features the use of an indole structure as the hydrophobic substituent on a m-benzylaminepiperidine template. The best members of this series display good in vitro activity and excellent selectivity against other serine proteases.
