The pyridazine moiety is an important structural feature of various pharmacological active compou... more The pyridazine moiety is an important structural feature of various pharmacological active compounds. Synthetic pyridazine compounds have been reported as effective antiprostaglandins (PGs), 5-lipoxygenase (5-LOX), and antiplatelet agents, that is, inhibitors of prostaglandin or cyclooxygenase (COX-I & COX-II) enzyme, platelet cAMP phosphodiesterase, and thromboxane A2 (TXA2) synthase. These compounds are selective and nonselective COX inhibitors and showed analgesic, anti-inflammatory, and antipyretic activity. Pyridazine compounds with antiplatelet agents inhibited TXA2enzyme. Pyridazines also exhibited antirheumatoid activity. These pyridazine compounds hold considerable interest relative to the preparation of organic intermediates and other anticipated biologically active compounds.
Coumarin and its derivatives are widely spread in nature. Coumarin goes to a group as benzopyrone... more Coumarin and its derivatives are widely spread in nature. Coumarin goes to a group as benzopyrones, which consists of a benzene ring connected to a pyrone moiety. Coumarins displayed a broad range of pharmacologically useful profile. Coumarins are considered as a promising group of bioactive compounds that exhibited a wide range of biological activities like anti-microbial, anti-viral, antiparasitic, anti-helmintic, analgesic, anti-inflammatory, anti-diabetic, anti-cancer, anti-oxidant, anti-proliferative, anti-convulsant, and antihypertensive activities etc. The coumarin compounds have immense interest due to their diverse pharmacological properties. In particular, these biological activities make coumarin compounds more attractive and testing as novel therapeutic compounds.
Perilla frutescens seeds are a good source of polyunsaturated fatty acids (PUFAs). The seeds of p... more Perilla frutescens seeds are a good source of polyunsaturated fatty acids (PUFAs). The seeds of perilla are small end globular weight about 4 g/1000, contained approximately 35–45% oil. However the leaves are a very poor source of oil, since they contain only 0.2%. In addition, only the seed oil contains the omega 3 fatty acid alpha-linolenic acid (ALA). In comparing to other plant oils, perilla seed oil consistently contains the one of the highest proportion of omega-3 (ALA) fatty acids, at 54–64%. The omega-6 (linoleic acid) component is usually around 14% and omega-9 (Oleic acid) is also present in perilla oil. These polyunsaturated fatty acids are most beneficial to human health and in prevention of different diseases like cardiovascular disorders, cancer, inflammatory, rheumatoid arthritis etc.
Coumarin and its derivatives are widely spread in nature. Coumarin goes to agroup as benzopyrones... more Coumarin and its derivatives are widely spread in nature. Coumarin goes to agroup as benzopyrones, which consists of a benzene ring connected to a pyronemoiety. Coumarins displayed a broad range of pharmacologically useful profile.Coumarins are considered as a promising group of bioactive compounds thatexhibited a wide range of biological activities like anti-microbial, anti-viral,antiparasitic, anti-helmintic, analgesic, anti-inflammatory, anti-diabetic, anticancer,anti-oxidant, anti-proliferative, anti-convulsant, and antihypertensiveactivities etc. The coumarin compounds have immense interest due to theirdiverse pharmacological properties. In particular, these biological activities makecoumarin compounds more attractive and testing as novel therapeuticcompounds.
Natural antioxidants inhibit the adverse effects of the reactive oxygen species produced in livin... more Natural antioxidants inhibit the adverse effects of the reactive oxygen species produced in living things and enable to survive. Depending on this principle, humans started using some plant products to cure from various diseases. Natural products have proved of great health impact on human traditionally and scientifically. Moreover, the research has so far done in the field of natural antioxidants. Therefore, antioxidants have been traditionally used as well as experimentally proved beneficial. The antioxidant components of the natural products constitute the major source of human health promotion and maintenance. The nature is still the perfect source for health promotion and for the supplementation of safe drugs. Great attention is mandatory to explore many underestimated plants with highly effective antioxidant activity. Few classes of natural products have received as much attention as phenolics and polyphenols.
International Journal of Applied Sciences and Biotechnology
Reviewing the relationships between polyunsaturated FAs (PUFAs) with inflammation and rheumatoid ... more Reviewing the relationships between polyunsaturated FAs (PUFAs) with inflammation and rheumatoid arthritis disorders, the PUFAs containing ω-3, ω-6 and ω-9, these ω-3FAs levels were correlated with ω-6: ω-3 ratios including arachidonic acid (AA), eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA). Based on previously-reports, the levels of ω-3 FAs considered being as a 'lower risk' category for inflammation and rheumatoid arthritis. Certain PUFAs ratios may aid in inflammation and rheumatoid arthritis-related risk assessment. PUFA are the most effective for the production of oil with high concentration of DHA and EPA content significantly.DOI: http://dx.doi.org/10.3126/ijasbt.v2i1.9783Int J Appl Sci Biotechnol, Vol. 2(1): 3-17
The pyridazine moiety is an important structural feature of various pharmacological active compou... more The pyridazine moiety is an important structural feature of various pharmacological active compounds. Synthetic pyridazine compounds have been reported as effective antiprostaglandins (PGs), 5-lipoxygenase (5-LOX), and antiplatelet agents, that is, inhibitors of prostaglandin or cyclooxygenase (COX-I & COX-II) enzyme, platelet cAMP phosphodiesterase, and thromboxane A2 (TXA2) synthase. These compounds are selective and nonselective COX inhibitors and showed analgesic, anti-inflammatory, and antipyretic activity. Pyridazine compounds with antiplatelet agents inhibited TXA2enzyme. Pyridazines also exhibited antirheumatoid activity. These pyridazine compounds hold considerable interest relative to the preparation of organic intermediates and other anticipated biologically active compounds.
Levosimendan is a pyridazinone-dinitrile derivative, emerged as a potent cardiotonic agent with d... more Levosimendan is a pyridazinone-dinitrile derivative, emerged as a potent cardiotonic agent with dual inotropic and vasodilator activities in higher animals. This is a calcium (Ca2+) sensitizing cardiotonic agent, which has been shown to exert positive inotropic effects without increasing intracellular Ca2+ transient. This avoids Ca2+overload that leads to arrhythmias and myocyte injuries, and do not increase the energy consumption for handling Ca2+and has shown good activity against congestive heart failure (CHF), due to its increased myocardial contractility by stabilizing the calcium bound conformation of troponin C. Levosimendan also acts as a pulmonary and systemic vasodilator. The combination of positive inotropic and vasodilator activity has been beneficial in increasing cardiac output and decreasing left ventricular end-diastolic pressure, pulmonary wedge pressure, right atrial pressure, and systemic vascular resistance in CHF patients. The cardiac target protein of levosimen...
ABSTRACT Certain dietary contents, biological supplements might influence the occurrence or treat... more ABSTRACT Certain dietary contents, biological supplements might influence the occurrence or treatment of epilepsy. Some studies have found that the supplementation with individual nutrients reduced seizure frequency or improved other aspects of health in patients with epilepsy. Potentially beneficial dietary interventions include treating blood glucose dysregulations. Identifying and avoiding allergenic foods, and avoiding suspected triggering agents such as alcohol, aspartame, and monosodium glutamate. The Atkins diet (very low in carbohydrates) is a less restrictive type diet that may be effective in some cases. Nutrients that may reduce seizure frequency include vitamin B6, magnesium, vitamin E, manganese, taurine, dimethylglycine, and omega-3 fatty acids. Administration of thiamine may improve cognitive function in patients with epilepsy. Supplementation with folic acid, vitamin B6, biotin, vitamin D, and L-carnitine may be needed to prevent or treat deficiencies resulting from the use of anticonvulsant drugs. Vitamin K1 has been recommended near the end of pregnancy for women taking anticonvulsants. Melatonin may reduce seizure frequency in some cases, and progesterone may be useful for women with cyclic exacerbations of seizures. In most cases, nutritional therapy is not a substitute for anticonvulsant medications. However, in selected cases, depending on the effectiveness of the interventions, dosage reductions or discontinuation of medications may be possible. However, nutrient supplementation may be necessary to prevent or reverse the effects of certain deficiencies that frequently result from the use of antiepileptic drugs.
Aneuploidy implies having something other than the exact multiple of haploid number of chromosome... more Aneuploidy implies having something other than the exact multiple of haploid number of chromosomes. Aneuploidy has a severe effect on normal cells resulting in decreased fitness, increased proteotoxic stress, increased energy demand, impaired cell proliferation and cell death. Paradoxically, aneuploidy becomes the hallmark of a large number of cancer types, along with their high proliferation rate. This phenomenon offers a target for an alternative treatment approach for cancer therapy. Recently some novel compounds have been identified which can specifically target aneuploid cells, increase energy stress, inhibit autophagy and thereby treat various types of cancers.
Rajiv Gandhi University of Health Sciences Journal of Pharmaceutical Sciences, 2015
ABSTRACT Purpose: In the present study, antitubercular activities and in silico physicochemical t... more ABSTRACT Purpose: In the present study, antitubercular activities and in silico physicochemical toxicities and bioactivity profile of some 3-chloro-6-arylpyridazines (3a-d) and 6-aryl-4,5-dihydropyridazine-3(2H)-thiones (4a-d) are studied. Approach: The compounds (3a-d) and (4a-d) were evaluated as antitubercular agents against Mycobacterium tuberculosis H37Rv by screening through in vitro Microplate Alamar Blue Assay (MABA) method. Findings: In silico physicochemical parameter revealed that the entire compounds follow Lipinski’s rule-of-5 to become a “drug like” molecule. ADME (absorption, distribution, metabolism and excretions) profile prediction has shown that all the compounds can be absorbed through human intestine (HIA+), Caco-2 cell (Caco-2+) and can cross blood brain barrier (BBB+), they all are non-substrate and non-inhibitor of p-glycoprotein. Compounds 4a-d are inhibitor of human microsomal enzyme like CYP 450 1A2, CYP 450 2C19 and CYP 450 3A4. Research limitations/implications: Compounds 4a-4d are better ligand for enzyme inhibition than 3a-d compounds. The MIC of compounds 4a-d and 3a is 6.25 μg/ml. They are potent than compound 3b-d with MIC 12.5 μg/ml. Originality: Toxicity prediction indicated that compounds 3a-3d and 4a-d are non-carcinogenic and non-mutagenic. Bioactivity prediction for compounds 3a-3d and 4a-d indicated better ligand as enzyme inhibitor in comparison to standard.
Mycobacterial infections are infectious diseases. Control of TB is complicated by difficulties in... more Mycobacterial infections are infectious diseases. Control of TB is complicated by difficulties in the long-course chemotherapy treatment, the inability to eliminate latent microbes, and the increasing emergence of multidrug resistant strains of M. tuberculosis. New anti-TB drugs are urgently needed, including developments of short-term treatments to minimize the emergence of drug resistance and new drugs to treat multidrug resistant tuberculosis and to eliminate the latent microbes. Many new structural anti-TB agents exhibited promising activities against susceptible and resistant strains of M. tuberculosis. The diarylquinoline with superior anti-tuberculosis activity and encouraging results of nitroimidazopyrans and oxazolidinones have generated considerable excitement. In this review study the efforts to use of drugs for treatment of tuberculosis.
The needs of newly developed antitubercular agents are required for the control of tuberculosis i... more The needs of newly developed antitubercular agents are required for the control of tuberculosis in the present time. In the discovery of new antitubercular drugs, the emergence of multidrug-resistant (MDR) and extensively drug resistant (XDR) strains of Mycobacterium tuberculosis (Mtb) has encouraged the researchers to intensify the efforts to discover novel antitubercular drugs. These novel drugs will predominantly target the persistent state of mycobacterium strains, which are resistant to conventional drugs including non resistant mycobacterium strains. In the last three to four decades no new effective drug has been developed for the treatment of resistant tuberculosis. However, in recent years, the research and development programs for the control of TB, there is a lot works is going on to enhancement of the anti-TB activity of new drugs particularly against resistant mycobacterium strains. Simultaneously, practical usefulness of some new targets is being identified and validated for the treatment of TB. Some compounds are presently in clinical trials, while others are being investigated in an attempt to explore new compounds for the target based treatment. The present review provides an overview of the new anti-TB agents with different molecular structures that are being clinically used and advanced stages of preclinical as well as clinical stages and also attempted to highlight the efforts that are being made in the development of new drug molecules as lead anti-TB agents.
The pyridazine moiety is an important structural feature of various pharmacological active compou... more The pyridazine moiety is an important structural feature of various pharmacological active compounds. Synthetic pyridazine compounds have been reported as effective antiprostaglandins (PGs), 5-lipoxygenase (5-LOX), and antiplatelet agents, that is, inhibitors of prostaglandin or cyclooxygenase (COX-I & COX-II) enzyme, platelet cAMP phosphodiesterase, and thromboxane A2 (TXA2) synthase. These compounds are selective and nonselective COX inhibitors and showed analgesic, anti-inflammatory, and antipyretic activity. Pyridazine compounds with antiplatelet agents inhibited TXA2enzyme. Pyridazines also exhibited antirheumatoid activity. These pyridazine compounds hold considerable interest relative to the preparation of organic intermediates and other anticipated biologically active compounds.
Coumarin and its derivatives are widely spread in nature. Coumarin goes to a group as benzopyrone... more Coumarin and its derivatives are widely spread in nature. Coumarin goes to a group as benzopyrones, which consists of a benzene ring connected to a pyrone moiety. Coumarins displayed a broad range of pharmacologically useful profile. Coumarins are considered as a promising group of bioactive compounds that exhibited a wide range of biological activities like anti-microbial, anti-viral, antiparasitic, anti-helmintic, analgesic, anti-inflammatory, anti-diabetic, anti-cancer, anti-oxidant, anti-proliferative, anti-convulsant, and antihypertensive activities etc. The coumarin compounds have immense interest due to their diverse pharmacological properties. In particular, these biological activities make coumarin compounds more attractive and testing as novel therapeutic compounds.
Perilla frutescens seeds are a good source of polyunsaturated fatty acids (PUFAs). The seeds of p... more Perilla frutescens seeds are a good source of polyunsaturated fatty acids (PUFAs). The seeds of perilla are small end globular weight about 4 g/1000, contained approximately 35–45% oil. However the leaves are a very poor source of oil, since they contain only 0.2%. In addition, only the seed oil contains the omega 3 fatty acid alpha-linolenic acid (ALA). In comparing to other plant oils, perilla seed oil consistently contains the one of the highest proportion of omega-3 (ALA) fatty acids, at 54–64%. The omega-6 (linoleic acid) component is usually around 14% and omega-9 (Oleic acid) is also present in perilla oil. These polyunsaturated fatty acids are most beneficial to human health and in prevention of different diseases like cardiovascular disorders, cancer, inflammatory, rheumatoid arthritis etc.
Coumarin and its derivatives are widely spread in nature. Coumarin goes to agroup as benzopyrones... more Coumarin and its derivatives are widely spread in nature. Coumarin goes to agroup as benzopyrones, which consists of a benzene ring connected to a pyronemoiety. Coumarins displayed a broad range of pharmacologically useful profile.Coumarins are considered as a promising group of bioactive compounds thatexhibited a wide range of biological activities like anti-microbial, anti-viral,antiparasitic, anti-helmintic, analgesic, anti-inflammatory, anti-diabetic, anticancer,anti-oxidant, anti-proliferative, anti-convulsant, and antihypertensiveactivities etc. The coumarin compounds have immense interest due to theirdiverse pharmacological properties. In particular, these biological activities makecoumarin compounds more attractive and testing as novel therapeuticcompounds.
Natural antioxidants inhibit the adverse effects of the reactive oxygen species produced in livin... more Natural antioxidants inhibit the adverse effects of the reactive oxygen species produced in living things and enable to survive. Depending on this principle, humans started using some plant products to cure from various diseases. Natural products have proved of great health impact on human traditionally and scientifically. Moreover, the research has so far done in the field of natural antioxidants. Therefore, antioxidants have been traditionally used as well as experimentally proved beneficial. The antioxidant components of the natural products constitute the major source of human health promotion and maintenance. The nature is still the perfect source for health promotion and for the supplementation of safe drugs. Great attention is mandatory to explore many underestimated plants with highly effective antioxidant activity. Few classes of natural products have received as much attention as phenolics and polyphenols.
International Journal of Applied Sciences and Biotechnology
Reviewing the relationships between polyunsaturated FAs (PUFAs) with inflammation and rheumatoid ... more Reviewing the relationships between polyunsaturated FAs (PUFAs) with inflammation and rheumatoid arthritis disorders, the PUFAs containing ω-3, ω-6 and ω-9, these ω-3FAs levels were correlated with ω-6: ω-3 ratios including arachidonic acid (AA), eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA). Based on previously-reports, the levels of ω-3 FAs considered being as a 'lower risk' category for inflammation and rheumatoid arthritis. Certain PUFAs ratios may aid in inflammation and rheumatoid arthritis-related risk assessment. PUFA are the most effective for the production of oil with high concentration of DHA and EPA content significantly.DOI: http://dx.doi.org/10.3126/ijasbt.v2i1.9783Int J Appl Sci Biotechnol, Vol. 2(1): 3-17
The pyridazine moiety is an important structural feature of various pharmacological active compou... more The pyridazine moiety is an important structural feature of various pharmacological active compounds. Synthetic pyridazine compounds have been reported as effective antiprostaglandins (PGs), 5-lipoxygenase (5-LOX), and antiplatelet agents, that is, inhibitors of prostaglandin or cyclooxygenase (COX-I & COX-II) enzyme, platelet cAMP phosphodiesterase, and thromboxane A2 (TXA2) synthase. These compounds are selective and nonselective COX inhibitors and showed analgesic, anti-inflammatory, and antipyretic activity. Pyridazine compounds with antiplatelet agents inhibited TXA2enzyme. Pyridazines also exhibited antirheumatoid activity. These pyridazine compounds hold considerable interest relative to the preparation of organic intermediates and other anticipated biologically active compounds.
Levosimendan is a pyridazinone-dinitrile derivative, emerged as a potent cardiotonic agent with d... more Levosimendan is a pyridazinone-dinitrile derivative, emerged as a potent cardiotonic agent with dual inotropic and vasodilator activities in higher animals. This is a calcium (Ca2+) sensitizing cardiotonic agent, which has been shown to exert positive inotropic effects without increasing intracellular Ca2+ transient. This avoids Ca2+overload that leads to arrhythmias and myocyte injuries, and do not increase the energy consumption for handling Ca2+and has shown good activity against congestive heart failure (CHF), due to its increased myocardial contractility by stabilizing the calcium bound conformation of troponin C. Levosimendan also acts as a pulmonary and systemic vasodilator. The combination of positive inotropic and vasodilator activity has been beneficial in increasing cardiac output and decreasing left ventricular end-diastolic pressure, pulmonary wedge pressure, right atrial pressure, and systemic vascular resistance in CHF patients. The cardiac target protein of levosimen...
ABSTRACT Certain dietary contents, biological supplements might influence the occurrence or treat... more ABSTRACT Certain dietary contents, biological supplements might influence the occurrence or treatment of epilepsy. Some studies have found that the supplementation with individual nutrients reduced seizure frequency or improved other aspects of health in patients with epilepsy. Potentially beneficial dietary interventions include treating blood glucose dysregulations. Identifying and avoiding allergenic foods, and avoiding suspected triggering agents such as alcohol, aspartame, and monosodium glutamate. The Atkins diet (very low in carbohydrates) is a less restrictive type diet that may be effective in some cases. Nutrients that may reduce seizure frequency include vitamin B6, magnesium, vitamin E, manganese, taurine, dimethylglycine, and omega-3 fatty acids. Administration of thiamine may improve cognitive function in patients with epilepsy. Supplementation with folic acid, vitamin B6, biotin, vitamin D, and L-carnitine may be needed to prevent or treat deficiencies resulting from the use of anticonvulsant drugs. Vitamin K1 has been recommended near the end of pregnancy for women taking anticonvulsants. Melatonin may reduce seizure frequency in some cases, and progesterone may be useful for women with cyclic exacerbations of seizures. In most cases, nutritional therapy is not a substitute for anticonvulsant medications. However, in selected cases, depending on the effectiveness of the interventions, dosage reductions or discontinuation of medications may be possible. However, nutrient supplementation may be necessary to prevent or reverse the effects of certain deficiencies that frequently result from the use of antiepileptic drugs.
Aneuploidy implies having something other than the exact multiple of haploid number of chromosome... more Aneuploidy implies having something other than the exact multiple of haploid number of chromosomes. Aneuploidy has a severe effect on normal cells resulting in decreased fitness, increased proteotoxic stress, increased energy demand, impaired cell proliferation and cell death. Paradoxically, aneuploidy becomes the hallmark of a large number of cancer types, along with their high proliferation rate. This phenomenon offers a target for an alternative treatment approach for cancer therapy. Recently some novel compounds have been identified which can specifically target aneuploid cells, increase energy stress, inhibit autophagy and thereby treat various types of cancers.
Rajiv Gandhi University of Health Sciences Journal of Pharmaceutical Sciences, 2015
ABSTRACT Purpose: In the present study, antitubercular activities and in silico physicochemical t... more ABSTRACT Purpose: In the present study, antitubercular activities and in silico physicochemical toxicities and bioactivity profile of some 3-chloro-6-arylpyridazines (3a-d) and 6-aryl-4,5-dihydropyridazine-3(2H)-thiones (4a-d) are studied. Approach: The compounds (3a-d) and (4a-d) were evaluated as antitubercular agents against Mycobacterium tuberculosis H37Rv by screening through in vitro Microplate Alamar Blue Assay (MABA) method. Findings: In silico physicochemical parameter revealed that the entire compounds follow Lipinski’s rule-of-5 to become a “drug like” molecule. ADME (absorption, distribution, metabolism and excretions) profile prediction has shown that all the compounds can be absorbed through human intestine (HIA+), Caco-2 cell (Caco-2+) and can cross blood brain barrier (BBB+), they all are non-substrate and non-inhibitor of p-glycoprotein. Compounds 4a-d are inhibitor of human microsomal enzyme like CYP 450 1A2, CYP 450 2C19 and CYP 450 3A4. Research limitations/implications: Compounds 4a-4d are better ligand for enzyme inhibition than 3a-d compounds. The MIC of compounds 4a-d and 3a is 6.25 μg/ml. They are potent than compound 3b-d with MIC 12.5 μg/ml. Originality: Toxicity prediction indicated that compounds 3a-3d and 4a-d are non-carcinogenic and non-mutagenic. Bioactivity prediction for compounds 3a-3d and 4a-d indicated better ligand as enzyme inhibitor in comparison to standard.
Mycobacterial infections are infectious diseases. Control of TB is complicated by difficulties in... more Mycobacterial infections are infectious diseases. Control of TB is complicated by difficulties in the long-course chemotherapy treatment, the inability to eliminate latent microbes, and the increasing emergence of multidrug resistant strains of M. tuberculosis. New anti-TB drugs are urgently needed, including developments of short-term treatments to minimize the emergence of drug resistance and new drugs to treat multidrug resistant tuberculosis and to eliminate the latent microbes. Many new structural anti-TB agents exhibited promising activities against susceptible and resistant strains of M. tuberculosis. The diarylquinoline with superior anti-tuberculosis activity and encouraging results of nitroimidazopyrans and oxazolidinones have generated considerable excitement. In this review study the efforts to use of drugs for treatment of tuberculosis.
The needs of newly developed antitubercular agents are required for the control of tuberculosis i... more The needs of newly developed antitubercular agents are required for the control of tuberculosis in the present time. In the discovery of new antitubercular drugs, the emergence of multidrug-resistant (MDR) and extensively drug resistant (XDR) strains of Mycobacterium tuberculosis (Mtb) has encouraged the researchers to intensify the efforts to discover novel antitubercular drugs. These novel drugs will predominantly target the persistent state of mycobacterium strains, which are resistant to conventional drugs including non resistant mycobacterium strains. In the last three to four decades no new effective drug has been developed for the treatment of resistant tuberculosis. However, in recent years, the research and development programs for the control of TB, there is a lot works is going on to enhancement of the anti-TB activity of new drugs particularly against resistant mycobacterium strains. Simultaneously, practical usefulness of some new targets is being identified and validated for the treatment of TB. Some compounds are presently in clinical trials, while others are being investigated in an attempt to explore new compounds for the target based treatment. The present review provides an overview of the new anti-TB agents with different molecular structures that are being clinically used and advanced stages of preclinical as well as clinical stages and also attempted to highlight the efforts that are being made in the development of new drug molecules as lead anti-TB agents.
The chemistry society has activated to expand new chemistry that is less destructive to the envir... more The chemistry society has activated to expand new chemistry that is less destructive to the environment and human health. This approach has extensive interest and designates as green chemistry, environmentally friendly chemistry, clean chemistry, and atom economy. Methodology: There is advancement toward involved chemistry with the facts and do not prevent the properties of the target compound or the efficacy of solvents or reagents. The use of chemistry in a way that maximizes benefits while reducing adverse effects has come to be green chemistry. Main findings: Reduce the use and formation of harmful products or by-products. Presently maximum pollution to the environment is caused by some chemical industries. So, need to design and develop synthetic methods in such a way that the waste products are lowest and have no effect on the environment and their handy disposal. Applications of the work: Green chemistry plays a vital role in pharmaceuticals for developing new drugs which are less toxic, more effective with low side effects. The novelty of the work: The industries performing manufacturing using green synthesis methods to carry out their productions have positive impacts on environmental sustainability. This review is looking ahead at longer-term challenges and prospects in research, industrial applications, and education.
Uploads
Papers by Mohammad Asif
Main findings: Reduce the use and formation of harmful products or by-products. Presently maximum pollution to the environment is caused by some chemical industries. So, need to design and develop synthetic methods in such a way that the waste products are lowest and have no effect on the environment and their handy disposal.
Applications of the work: Green chemistry plays a vital role in pharmaceuticals for developing new drugs which are less toxic, more effective with low side effects.
The novelty of the work: The industries performing manufacturing using green synthesis methods to carry out their productions have positive impacts on environmental sustainability. This review is looking ahead at longer-term challenges and prospects in research, industrial applications, and education.