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(N-(3-chloro-2-methylphenyl) quinoxalin-2-carboxamide) is a chemical compound with the molecular formula C16H11ClN4O, belonging to the quinoxaline class and featuring a carboxamide group. (N-(3-chloro-2-methylphenyl) quinoxalin-2-carboxamide) is characterized by a chloro substituent at the 3-position and a methyl substituent at the 2-position of the phenyl ring. It is widely utilized in the synthesis of pharmaceuticals and agrochemicals due to its potential biological activities, including anticancer and antimicrobial properties, which make it a significant molecule in the field of drug discovery and development.

930478-88-9

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930478-88-9 Usage

Uses

Used in Pharmaceutical Industry:
(N-(3-chloro-2-methylphenyl) quinoxalin-2-carboxamide) is used as an intermediate compound for the synthesis of various pharmaceuticals. Its unique structure and potential biological activities contribute to the development of new drugs with improved efficacy and reduced side effects.
Used in Agrochemical Industry:
In the agrochemical industry, (N-(3-chloro-2-methylphenyl) quinoxalin-2-carboxamide) is used as a building block for the creation of novel agrochemicals. Its antimicrobial properties make it a valuable component in the development of pesticides and fungicides, helping to protect crops from diseases and pests.
Used in Anticancer Research:
(N-(3-chloro-2-methylphenyl) quinoxalin-2-carboxamide) is employed as a potential anticancer agent in the field of oncology. Its biological activities suggest that it may play a role in inhibiting cancer cell growth and proliferation, making it a promising candidate for further research and development in cancer treatment.
Used in Antimicrobial Applications:
Due to its antimicrobial properties, (N-(3-chloro-2-methylphenyl) quinoxalin-2-carboxamide) is used in the development of new antimicrobial agents. These agents can be utilized in various settings, such as healthcare, agriculture, and the food industry, to combat the growth of harmful microorganisms and reduce the risk of infections.

Check Digit Verification of cas no

The CAS Registry Mumber 930478-88-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,0,4,7 and 8 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 930478-88:
(8*9)+(7*3)+(6*0)+(5*4)+(4*7)+(3*8)+(2*8)+(1*8)=189
189 % 10 = 9
So 930478-88-9 is a valid CAS Registry Number.

930478-88-9Downstream Products

930478-88-9Relevant academic research and scientific papers

Antidepressant and anti-anxiety like effects of 4i (N-(3-chloro-2- methylphenyl) quinoxalin-2-carboxamide), a novel 5-HT3 receptor antagonist in acute and chronic neurobehavioral rodent models

Gupta, Deepali,Radhakrishnan, Mahesh,Thangaraj, Devadoss,Kurhe, Yeshwant

, p. 59 - 67 (2014)

Depression and anxiety are the most debilitating mood disorders with poor therapeutic recovery rates. In the last decades, 5-HT3 receptor antagonists have been identified as potential agents for mood disorders. The current investigation focuses on evaluating the, antidepressant and anti-anxiety like effects of a novel 5-HT3 antagonist, 4i (N-(3-chloro-2- methylphenyl) quinoxalin-2-carboxamide). Preliminary, in vitro 5-HT3 receptor binding affinity was performed in isolated longitudinal muscle-myenteric plexus from the guinea pig ileum. Consequently, neurobehavioral effects of 4i in acute and chronic rodent models were evaluated. In addition, involvement of serotonergic system in the postulated effects of the compound was analyzed by in vivo assay. in vitro, 4i demonstrated high 5-HT3 receptor antagonistic activity (pA2, 7.6). in vivo acute study, 4i exhibited decreased duration of immobility in forced swim and tail suspension tests, and increased exploratory parameters as number and duration of nose-poking in hole board test and latency and time spent in aversive brightly illuminated light chamber in light-dark model. Moreover, in chronic model of depression, i.e., olfactory bulbectomy with behavioral deficits, 4i reversed depressive anhedonia in sucrose preference test and anxious hyperactive behavior in open field test in rats. Furthermore, synergistic effect of 4i with fluoxetine (a selective serotonin reuptake inhibitor) and inhibitory effect of 1-(m-chlorophenyl)- biguanide (a 5-HT3 receptor agonist) revealed serotonergic modulation by 4i mediated 5-HT3 receptor antagonism, which was further confirmed by potentiation of 5-hydroxytryptophan (a serotonin synthesis precursor) induced head twitch response. These findings suggest the potential antidepressant and anti-anxiety like effects of 4i, which may be related to the modulation of serotonergic system.

Effect of a novel 5-HT3 receptor antagonist 4i, in corticosterone-induced depression-like behavior and oxidative stress in mice

Gupta, Deepali,Radhakrishnan, Mahesh,Kurhe, Yeshwant

supporting information, p. 95 - 102 (2015/03/04)

Stress in our daily life severely affects the normal physiology of the biological system. Dysregulation of hypothalamic-pituitary-adrenal (HPA) axis has been implicated in the development of depression-like behavior, which remains under diagnosed and poorly treated. Exogenous corticosterone (CORT) administration has been demonstrated to develop a depression model, which has shown to mimic HPA-axis induced depression-like state in rodents. In the present study, the effect of a novel 5HT3 receptor, 4i was examined on CORT induced depression in mice. CORT (30 mg/kg, subcutaneously) was given for 4-weeks to mice in control group, while mice in drug treated group were given 4i (0.5-1 mg/kg, intraperitoneally)/fluoxetine (as a positive control, 10 mg/kg), for the last 2-weeks of CORT dosing. Repeated CORT dosing caused depression-like behavior in mice as indicated by increased despair effects in forced swim test (FST) and anhedonia in sucrose preference test. In addition, CORT administration induced oxidative load in the brain with significant increase in pro-oxidant (lipid peroxidation and nitrite levels) markers and a substantial decline in anti-oxidant defense (catalase and reduced glutathione levels) system, indicating a direct effect of stress hormones in the induction of the brain oxidative damage. On the other hand, 4i and fluoxetine treatment reversed the CORT induced depressive-like deficits. Furthermore, 4i and fluoxetine prevented CORT induced oxidative brain insults, which may plausibly demonstrate one of the key mechanisms for antidepressant-like effects of the compounds. Thus, the study suggests that 5HT3 antagonist; 4i may be implicated as pharmacological intervention targeting depressive-like anomaly associated with HPA-axis dysregulation.

Design, synthesis and structure-activity relationship of novel quinoxalin-2-carboxamides as 5-HT3 receptor antagonists for the management of depression

Mahesh, Radhakrishnan,Devadoss, Thangaraj,Pandey, Dilip Kumar,Bhatt, Shvetank,Yadav, Shushil Kumar

scheme or table, p. 6773 - 6776 (2010/12/20)

A novel series of quinoxalin-2-carboxamides were designed based on the ligand-based approach, employing a three-point pharmacophore model; it consists of an aromatic residue and a linking carbonyl group and a basic nitrogen. The target new chemical entities were synthesized from the key intermediate, quinoxalin-2-carboxylic acid, by coupling it with various amines in the presence of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC·HCl) and 1-hydroxybenzotriazole (HOBt). The obtained compounds' structures were confirmed by spectral data. The target new chemical entities were evaluated for their 5-HT3 receptor antagonisms in longitudinal muscle myenteric plexus preparation from guinea pig ileum against 5-HT3 agonist, 2-methyl-5-HT, which was expressed in the form of pA2 value. All the synthesized compounds showed antagonism towards 5-HT3 receptor; based on this result, a structure-activity relationship was derived, which reveals that the aromatic residue in 5-HT3 receptor antagonists may have hydrophobic interaction with 5-HT3 receptor. Regardless of their antagonistic potentials, all the synthesized molecules were screened for their anti-depressant potentials by using forced swim test in mice model; interestingly none of the tested compounds affect the locomotion of mice in the tested dose levels. Compounds with significant pA2 values exhibited good anti-depressant-like activity as compared to the vehicle-treated group.

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