Journal- Indian Chemical Society (J INDIAN CHEM SOC)

Publisher: Indian Chemical Society

Journal description

Current impact factor: 0.17

Impact Factor Rankings

2015 Impact Factor Available summer 2016
2014 Impact Factor 0.173
2012 Impact Factor 0.251
2011 Impact Factor 0.359
2010 Impact Factor 0.301
2009 Impact Factor 0.382
2008 Impact Factor 0.384
2007 Impact Factor 0.33
2006 Impact Factor 0.34
2005 Impact Factor 0.34
2004 Impact Factor 0.36
2003 Impact Factor 0.275
2002 Impact Factor 0.437
2001 Impact Factor 0.413
2000 Impact Factor 0.248
1999 Impact Factor 0.192
1998 Impact Factor 0.191
1997 Impact Factor 0.129
1996 Impact Factor 0.141
1995 Impact Factor 0.104
1994 Impact Factor 0.09
1993 Impact Factor 0.114
1992 Impact Factor 0.085

Impact factor over time

Impact factor

Additional details

5-year impact 0.19
Cited half-life >10.0
Immediacy index 0.06
Eigenfactor 0.00
Article influence 0.03
Website Journal of the Indian Chemical Society website
Other titles Journal of the Indian Chemical Society
ISSN 0019-4522
OCLC 1029434
Material type Periodical
Document type Journal / Magazine / Newspaper

Publications in this journal

  • [Show abstract] [Hide abstract]
    ABSTRACT: A new triterpenoid, identified as 24,25-dihydrolimocinol, has been isolated from fresh fruits of Melia azadirachta. Zafaral, which was earlier reported from its leaves, has also been isolated from fruits, this time along with several known limonoids. Their structures were elucidated on the basis of spectroscopic evidences and chemical transformations.
    Journal- Indian Chemical Society 10/2015; 92(1):111-114. DOI:10.1002/chin.201541217
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    ABSTRACT: A new chelating ligand [4-Methyl-2,6-bis-(pyridin-2-yl-hydrazonomethyl)-phenol] (1) was prepared by the condensation of 2-hydrazinylpyridine with 2,6-diformyl-p-cresol. Compound 1 exhibits weak fluorescence due to intramolecular photoinduced electron transfer (PET). The sensor (1) demonstrates Zn2+-specific emission enhancement due to “PET off” process through a 1:1 binding mode with the metal ion. The fluorescence quantum yield of the chemosensor 1 is only 0.020, and it increases more than 14-fold (0.280) in the presence of one equivalent of the zinc ion. Interestingly, the introduction of other metal ions causes the fluorescence intensity to remain either unchanged or weakened except for Cd2+. Ratiometric displacement of Cd2+ ion from the complex by Zn2+ ion supports the formation of more stable sensor-Zn2+ complex over the sensor-Cd2+ complex. The experimental findings have been correlated with theoretical results using B3LYP functional and 6−31G (d, p), LANL2DZ basis set for Cd2+(2) and Zn2+(3) complex, respectively, by Density Functional Theory (DFT) method. Moreover, the ability of probe 1 to sense Zn2+ within human melanoma cancer cells has been explored, and the Zn2+-probing process in living cells was reversible. [Mn2(PHMP)2](ClO4)2(4) and [Ni2(PHMP)(H2O)5](NO3)3(5) have been also synthesized and characterized crystallographically and spectroscopically to understand the ligating behavior of the ligand PHMP.
    Journal- Indian Chemical Society 08/2015;
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    ABSTRACT: I n this s tudy, a se ries of 2-c hloro-qui noli ne-3-c arbaldehydes (1 a-g) and (2-c hloro-quinolin- 3-yl)-me thanols (2 a-g) were tested for t heir ant idermatophyt ic studies ag ainst four s pecies of de rmatophytes : T. rubrum, E. fl occosum, T. ment agrophytes and M. gypseum by we ll diffusio n method. Compounds 1c, 1e and 2a s ho wed g ood acti vi ty where as c ompound 2d exhibit mode rate acti vi ty whe n c ompared with that of st andard fluc onazole. Keywords : 2- Chloro-3-formyl -quinoline, (2-c hloro-quinolin-3-yl)-met hanol, antide rmatophytic activity.
    Journal- Indian Chemical Society 06/2015; 92(June):851-853.
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    ABSTRACT: An extensive literature review reveals that various NSAIDs, their analogues and hybrids possess anticancer and antioxidant properties. The present study aims at designing, docking studies and synthesis of drug hybrids of NSAIDs with other amino compounds linked through dipeptide spacers, which are known for their anticancer as well as cellular penetrating properties. The synthesis was carried out by solution phase method using 1-ethyl-3-(3- dimethylaminopropyl) carbodiimide (EDC) or o- (benzo triazol-1-yl)-N, N, N′, N′-tetramethyluronium tetrafluoroborate (TBTU) as coupling reagent and triethyl amine (TEA) as a base in chloroform. Antioxidant studies showed that the synthesized NSAID derivatives showed moderate antioxidant activity as compared to the standard, ascorbic acid.
    Journal- Indian Chemical Society 06/2015; 92(June 2015):863-866.
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    ABSTRACT: Abstract : Amino acids are biologically active organic compounds that combine together to form peptides and proteins. Peptides can have various important functions such as antioxidant, anthelmintic, anti-insecticidal activity etc. A novel linear tetrapeptide L-(Ile-Ala-Leu-Leu) was synthesized using 1-ethyl-3-(3 dimethylaminopropyl)carbodiimide (EDC) by solution phase peptide synthesis. The compound was characterized by 1H NMR. T he compound was tested for different biological activities i.e. anti-oxidant and anthelmintic activity. The tetrapeptide showed poor antioxidant activity compared to standard ascorbic acid and potent antihelmintic activity compared to standard Mebendazole tablets. Keywords : Tetrape ptide, ethyl-3-(3-dimethylaminopropyl)carbodiimi de, anti oxidant activity, anthel mintic activity.
    Journal- Indian Chemical Society 06/2015; 92:929-932.
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    ABSTRACT: A series of novel bioactive mononuclear N3O type mixed ligand complexes (1–4) of MAB type [M(II) = Co(II), Ni(II), Cu(II) and Zn(II); A = 5–Fluorouracil (5–FU); B = L–histamine (hist)] were synthesized and structurally characterized by various physico–chemical and spectral studies. Elemental analyses, low molar conductance and 1H NMR spectral values of the complexes are well agreed with their proposed structure having 1:1:1 (metal;5–FU:hist) stoichiometry with non–electrolytic in nature. Magnetic moment data coupled with electronic spectral data suggest octahedral environment around the central metal(II) ion. Thermogravimetric analysis show loss of coordinated water and acetate molecules in initial stage followed by decomposition of organic residues subsequently and form metal oxide as final residue. Micro–crystalline nature with homogeneous morphology of the complexes is confirmed from Powder XRD and SEM analysis. Moreover, all the complexes show more effective in vitro microbial and antioxidant activities.
    Journal- Indian Chemical Society 06/2015; 92:970-973.
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    ABSTRACT: In this paper, an economical and improved Bischler indole method to obtain 2-arylindoles in a single step without any catalyst under thermal condition is described. Reaction between α-bromoarylethanones(1equi.) and aniline(2equi.) on reflux in dimethylformamide afforded 2-arylindoles in 85-90% yield within 20minutes. All the synthesized 2-aryl indoles were characterized by spectral analyses such as FT-IR, GC-MS and NMR techniques.
    Journal- Indian Chemical Society 06/2015; 92:843-846.
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    ABSTRACT: A new series of benzimidazoles were prepared by treating o-phenylenediamine and formic acid under reflux conditions. Further 1-substituted derivatives of benzimidazoles were synthesized by reaction with chloroacetic acid followed by condensation with amino containing compounds. The structural elucidation of the compounds was performed by FT-IR, 1H-NMR and MASS spectroscopy. The synthesized compounds were subjected to anthelmintic activity studies against Eudrilus species. The title compounds exhibited moderate to good anthelmintic activity.
    Journal- Indian Chemical Society 06/2015; 92(06):908-910.
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    ABSTRACT: In the present work novel 5-((2 -chloroquinol in-3-yl)methylene)-di hydro-2-thioxopyrimidine-4,6(1H,5H)-dione derivatives were synthesized by K noevenagel condensation of 2-chloroquinoline-3-carbaldehyde with thiobarbituric acid. The synthesized compounds were successfully characterized by FTIR, 1 H NMR and 13C NMR. Further comparative docking studies were carried out to find out the effective binding affinity of thiobarbituric acid derivatives with Peroxisome Proliferator Activated Receptor-Gamma (PPAR-γ) and aldose reductase receptors with to that of standard, Rosiglitazone and Epalrestat. The results obtained have clearly sho wn that 5-((2-chloroquinolin-3-yl )methylene)-dihydro-2-thi oxopyrimidine-4,6(1H,5H)-dione possess good binding affinity with PPAR-γ, aldose reductase receptors on par with the standard.
    Journal- Indian Chemical Society 06/2015; 92:918-920.
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    ABSTRACT: Abstract : Non-steroidal anti-inflammatory drugs exert analgesic, antipyretic, and anti-inflammatory effects. But the use of these drugs has several side effects and these side effects may be reduced by coupling them with amino acids. The coupling blocks the carboxyl group and reduces acidity. A series of NSAID derivatives of amino acids were synthesized and characterized by IR, NMR and Mass spectroscopy. Docking studies of the compounds were carried out using Hex software and the receptor taken was 3LAF (colon cancer receptor). The compounds were tested for anticancer and antioxidant activities. Anticancer activity was tested on HT-29 Cells. Antioxidant activity was tested using DPPH. Ascorbic acid was taken as standard and the absorbance was measured at 517 nm. Majority of the compounds showed good antioxidant activity. Keywords : NSAID, amino acids, Hex software, anticancer, antioxidant.
    Journal- Indian Chemical Society 06/2015; 92:963-966.
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    ABSTRACT: The bas ic aim of this st udy is to present t he ro om tempe rature synthesis of ZnSe thin f i lm by varying doping concent rat ion of seleni um oxi de on ITO plate us i ng a rel at ive ly simple and low c os t t radit ional elect rodeposi t ion technique. X-Ray di f f rac t ion c onf irms the format ion of s ingle cubic ZnSe phase wi th a pref erred orientat ion along (111) direct ion wi th an average value of the c rys tal l i te s ize around 37 nm. Opt ical s tudies re veal a t ra nsmit tance above 80% for lower SeO2 concent rat ion (< 3%) then drop up to 60% for hig he r c oncent rat ion (> 5%) wi th an energ y bandg ap around 2.75 eV. Photoluminescence anal ys i s shows the presence of mainly 2 bands, narrow PL band cente red at 487 nm and broad photoemiss ion band cente red at 531 nm. Scanning elect ron mic roscopy obse rvat ions re veal t he format ion of dense nanost ruc tured f i lms.
    Journal- Indian Chemical Society 05/2015; 92(may 2015):747 - 754.
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    ABSTRACT: A series of spinel fe rri te nanopa rt ic les viz. mang ane se fe rri te (MnFe2O4 ) , zinc ferrite (ZnFe2O4 ) , cobalt ferrite (CoFe2O4 ) and nickel ferrite (NiFe2O4 ) were prepared by solvothermal process. X-Ray diff raction patterns show that the synthesized ferrite samples are pure without any impurities. The as-prepared ferrites were further used as a precursor catalyst for the growth of CNTs using thermal chemical vapor deposition (CVD) technique . Results show that these ferrites acted as effective catalysts for the growth of carbon nanotubes. The as-g rown nanotubes were studied by electron microscope (FE-SEM) . Further studies like Raman spectroscopy and VSM analysis were also done to evaluate the properties of the as-prepared catalyst and the as-grown carbon nanotubes.
    Journal- Indian Chemical Society 05/2015; Vol. 92(2015):pp. 800-803.