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Kiran Light Laboratories 2012-13 Final

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PRICE LIST 2012-13 (Distributor for KEM LIGHT LABORATORIES & KEMIE LABS) www.labchemindia.com SPECIAL PRICE LIST (Distributor for KEM LIGHT LABORATORIES & KEMIE LABS) www.labchemindia.com INDIA- 2012-13 ( Product Name Grade Code Quantity D/P Rs ) ABSCISIC ACID 98% LPR A00110B03 25 mg 322 ABA * (+)-cis,trans-abscisic acid ,abscisin II; dormin; LPR A00110B04 100 mg 980 (2Z,4E)-5-[(1S)-Hydroxy-2,6,6-trimethyl-4-oxo-2-cyclohexen-1-yl]-3-methyl-2,4-pentadienoic acid LPR A00110B06 500 mg 5075 LPR A00110B07 1 gm 9205 ABSCISIC ACID 98+% APR A00110A03 25 mg 437.5 ABA * (+)-cis,trans-abscisic acid ,abscisin II; dormin; APR A00110A04 100 mg 1225 (2Z,4E)-5-[(1S)-Hydroxy-2,6,6-trimethyl-4-oxo-2-cyclohexen-1-yl]-3-methyl-2,4-pentadienoic acid APR A00110A06 500 mg 5950 APR A00110A07 1 gm 10465 ACENAPTHENE 96% EPR A00200C12 100 gm 154 (1,8-Ethylenenaphthalene) EPR A00200C14 500 gm 490 ACETANILIDE 98% EPR A00700C13 250 gm 73.5 (N-Phenylacetamide Antifebrin; Acetylaniline; Acetylaminobenzene) EPR A00700C14 500 gm 140 ACETANILIDE 98% LPR A00700B13 250 gm 98 (N-Phenylacetamide Antifebrin; Acetylaniline; Acetylaminobenzene) LPR A00700B14 500 gm 189 ACETO CARMINE See Carmine Aceto ACETYLACETONE 97% EPR A00900C13 250 ml 231 (2,4-Pentanedione, Diacetylmethane) EPR A00900C14 500 ml 451.5 ACETYLACETONE 98% LPR A00900B13 250 ml 280 (2,4-Pentanedione ,Diacetylmethane) LPR A00900B14 500 ml 525 ACETYLCHOLINE CHLORIDE 98% LPR A01250B10 25 gm 1170 (Ach ,2-(Acetyloxy)-N,N,N-trimethylethanaminium chloride) LPR A01250B12 100 gm 4050 ACETYLCHOLINE CHLORIDE 99% APR A01250A10 25 gm 1350 (Ach ,2-(Acetyloxy)-N,N,N-trimethylethanaminium chloride) APR A01250A12 100 gm 4950 N-ACETYL- L-CYSTEINE 99% EPR A01500C09 10 gm 90 (LNAC , NAC , L-alpha-acetamido-beta-mercaptopropionic acid) EPR A01500C12 100 gm 735 EPR A01500C15 1 kg 3975 N-ACETYL- L-CYSTEINE 99+% LPR A01500B09 10 gm 210 (LNAC , NAC , L-alpha-acetamido-beta-mercaptopropionic acid) LPR A01500B12 100 gm 1260 LPR A01500B15 1 kg 6600 N-ACETYL-L-GLUTAMIC ACID 99% LPR A01520B08 5 gm 240 LPR A01520B10 25 gm 825 N-ACETYL THIOZOLIDINE CARBOXYLIC ACID 98% EPR A01550C12 100 gm 495 N-ATCA* N-Acetyl-L-thioproline* (R)-3-Acetylthiazolidine-4-carboxylic acid EPR A01550C14 500 gm 1875 N-ACETYL THIOZOLIDINE CARBOXYLIC ACID 99+% LPR A01550B12 100 gm 585 N-ATCA* N-Acetyl-L-thioproline* (R)-3-Acetylthiazolidine-4-carboxylic acid LPR A01550B14 500 gm 2295 N-ACETYL-DL-TRYPTOPHANE 99% LPR A01560B08 5 gm 195 LPR A01560B10 25 gm 570 N-ACETYL-L-TYROSINE 99% LPR A01580B08 5 gm 420 LPR A01580B10 25 gm 1380 ACID RED 33 LPR A01600B10 25 gm 90 C.I.No.17200 / D&C Red #33 LPR A01600B12 100 gm 300 ACRIDINE ORANGE LPR A01650B09 10 gm 490 C.I.No.46005 / Basic Orange 14 / Acridine Orange hemi(zinc chloride) salt) LPR A01650B10 25 gm 1190 ACRIFLAVIN EPR A01750C08 5 gm 105 C.I No.46000 / Acriflavin Hydrochloride / Proflavine / Euflavine EPR A01750C10 25 gm 525 EPR A01750C12 100 gm 1455 ACRIFLAVIN LPR A01750B08 5 gm 150 C.I No.46000 / Acriflavin Hydrochloride / Proflavine / Euflavine LPR A01750B10 25 gm 690 LPR A01750B12 100 gm 1950 ACRYLAMIDE 98% EPR A02000C14 500 gm 135 ACRYLAMIDE 99% LPR A02000B14 500 gm 168.75 ACTIDIONE 98% LPR A02850B07 1 gm 577.5 (Cycloheximide) LPR A02850B08 5 gm 2467.5 www.lab5chemindia.com CONDITIONS APPLY* Page 1 SPECIAL PRICE LIST (Distributor for KEM LIGHT LABORATORIES & KEMIE LABS) www.labchemindia.com INDIA- 2012-13 ( Product Name Grade Code Quantity D/P Rs ) ACTIDIONE 98+% APR A02850A07 1 gm 630 (Cycloheximide) A PR A02850A08 5 gm 2975 ADAMS' CATALYST See Platinum Oxide ADENINE 98% LPR A03150B08 5 gm 72 (6-Aminopurine, Vitamin B4) LPR A03150B10 25 gm 260 (Strictly for Lab & Research use ,Not for any other use) LPR A03150B12 100 gm 860 LPR A03150B15 1 kg 7000 ADENINE 99% APR A03150A08 5 gm 80 (6-Aminopurine, Vitamin B4) APR A03150A10 25 gm 324 (Strictly for Lab & Research use ,Not for any other use) APR A03150A12 100 gm 980 APR A03150A15 1 kg 7800 ADENINE HEMISULPHATE See Adenine sulphate ADENINE HYDROCHLORIDE LPR A03200B08 5 gm 405 (6-Aminopurine hydrochloride) LPR A03200B10 25 gm 1305 ADENINE PHOSPHATE LPR A03240B08 5 gm 228 (6-Aminopurine phosphate) LPR A03240B10 25 gm 960 ADENINE SULPHATE 98% LPR A03270B08 5 gm 105 (Adenine hemisulphate,6-Aminopurine sulfate) LPR A03270B09 10 gm 210 LPR A03270B10 25 gm 420 LPR A03270B12 100 gm 1225 ADENINE SULPHATE 99.5% APR A03270A08 5 gm 105 (Adenine hemisulphate,6-Aminopurine sulfate) APR A03270A09 10 gm 165 APR A03270A12 100 gm 1500 ADENOSINE 99% EPR A03300C08 5 gm 87.5 (Adenine riboside,Adenine-9-â-D-ribofuranoside) EPR A03300C10 25 gm 385 (Strictly for Lab & Research use ,Not for any other use) EPR A03300C12 100 gm 1085 ADENOSINE 99+% LPR A03300B08 5 gm 105 (Adenine riboside,Adenine-9-â-D-ribofuranoside) LPR A03300B10 25 gm 420 (Strictly for Lab & Research use ,Not for any other use) LPR A03300B12 100 gm 1155 ADENOSINE 5-MONOPHOSPHATE DISODIUM SALT 95% LPR A03350B07 1 gm 60 (AMP-Na2)(Adenosine monophosphoric acid disodium salt) LPR A03350B08 5 gm 231 LPR A03350B10 25 gm 900 ADENOSINE 5-MONOPHOSPHATE MONOSODIUM SALT 95% LPR A03410B07 1 gm 247.5 (Adenosine monophosphoric acid monosodium salt) LPR A03410B08 5 gm 1080 LPR A03410B10 25 gm 2820 ADENOSINE 5-MONOPHOSPHATE FREE ACID 95% LPR A03460B07 1 gm 247.5 (Adenosine monophosphoric acid free acid) LPR A03460B08 5 gm 1080 LPR A03460B10 25 gm 2820 ADONITOL 99+% LPR A03490B08 5 gm 360 (Adonite,Ribitol) LPR A03490B09 10 gm 742.5 L-ADRENALINE 98% LPR A03520B07 1 gm 437.5 ((-)-Adrenaline,(- )-Epinephrine,L-Epinephrine) LPR A03520B08 5 gm 1925 (R)-(- )-3,4-Dihydroxy-á-(methylaminomethyl)benzyl alcohol) LPR A03520B10 25 gm 8575 (Strictly for Lab & Research use ,Not for any other use) L-ADRENALINE 99% APR A03520A07 1 gm 525 ((-)-Adrenaline,(- )-Epinephrine,L-Epinephrine) APR A03520A08 5 gm 2450 (R)-(- )-3,4-Dihydroxy-á-(methylaminomethyl)benzyl alcohol) APR A03520A10 25 gm 9975 (Strictly for Lab & Research use ,Not for any other use) ADRENALINE BITARTRATE 99% APR A03560A07 1 gm 480 (Adrenaline hydrogen tartrate,L-Epinephrine D-hydrogentartrate) APR A03560A08 5 gm 2200 L-Adrenaline (+)-bitartrate salt,(- )-Epinephrine (+)-bitartrate salt) (Strictly for Lab & Research use ,Not for any other use) AGAR AGAR POWDER EPR A04150C13 250 gm 368 (Food Grade) EPR A04150C14 500 gm 700 AGAR AGAR POWDER LPR A04150B12 100 gm 152 (Bacteriology Grade) LPR A04150B14 500 gm 880 www.lab5chemindia.com CONDITIONS APPLY* Page 2 SPECIAL PRICE LIST (Distributor for KEM LIGHT LABORATORIES & KEMIE LABS) www.labchemindia.com INDIA- 2012-13 ( Product Name Grade Code Quantity D/P Rs ) â-ALANINE 99% EPR A04850C10 25 gm 80 (3-Aminopropionic acid) EPR A04850C12 100 gm 300 EPR A04 850C15 1 kg 1940 â-ALANINE 99+% LPR A04850B10 25 gm 96 (3-Aminopropionic acid) LPR A04850B12 100 gm 368 LPR A04850B14 500 gm 1040 D-ALANINE 99% LPR A04870B07 1 gm 69 (R)-2-Aminopropionic acid) LPR A04870B08 5 gm 315 LPR A04870B10 25 gm 1545 DL-ALANINE 99% EPR A04920C10 25 gm 42 (+/-)-2-Aminopropionic acid) EPR A04920C12 100 gm 123 EPR A04920C15 1 kg 1095 DL-ALANINE 99+% LPR A04920B10 25 gm 51 (+/-)-2-Aminopropionic acid) LPR A04920B12 100 gm 180 LPR A04920B15 1 kg 1740 L-ALANINE 99% EPR A04950C10 25 gm 72 (S)-2-Aminopropionic acid) EPR A04950C12 100 gm 255 EPR A04950C14 500 gm 1065 EPR A04950C15 1 kg 1725 L-ALANINE 99+% LPR A04950B10 25 gm 120 (S)-2-Aminopropionic acid) LPR A04950B12 100 gm 390 LPR A04950B14 500 gm 1575 LPR A04950B15 1 kg 2925 ALAR (B-9) 97% EPR A05040C07 1 gm 87.5 (Daminozide)(Succinic acid 2,2-dimethyl hydrazide) EPR A05040C08 5 gm 362.5 (Succinic acid mono(2,2-dimethylhydrazide) EPR A05040C10 25 gm 1125 ALAR (B-9) 98% LPR A05040B07 1 gm 107.5 (Daminozide)(Succinic acid 2,2-dimethyl hydrazide) LPR A05040B08 5 gm 487.5 (Succinic acid mono(2,2-dimethylhydrazide) LPR A05040B10 25 gm 1675 ALAR (B-9) 99+% APR A05040A07 1 gm 175 (Daminozide)(Succinic acid 2,2-dimethyl hydrazide) APR A05040A08 5 gm 750 (Succinic acid mono(2,2-dimethylhydrazide) APR A05040A10 25 gm 2375 ALBUMINE BOVINE See Bovine Albumine ALCIAN BLUE 8GX EPR A05250C08 5 gm 412.5 C.I.No.74240 (Ingrain Blue 1,Alcian Blue) EPR A05250C09 10 gm 837.5 EPR A05250C10 25 gm 1837.5 ALCIAN BLUE 8GX LPR A05250B08 5 gm 475 C.I.No 74240 (Ingrain Blue 1,Alcian Blue) LPR A05250B09 10 gm 925 LPR A05250B10 25 gm 1975 ALIZARINE INDICATOR LPR A05600B10 25 gm 84 C.I.No.58000 (1,2-Dihydroxyanthraquinone,Mordant Red 11) LPR A05600B12 100 gm 300 ALIZARINE INDICATOR APR A05600A10 25 gm 116 C.I.No.58000 (1,2-Dihydroxyanthraquinone,Mordant Red 11) APR A05600A12 100 gm 384 ALIZARINE COMPLEXONE LPR A05610B07 1 gm 180 (Alizarin -3-methyl iminodiacetic acid)METAL INDICATOR LPR A05610B08 5 gm 705 ALIZARINE CYANINE GREEN LPR A05620B10 25 gm 117 C.I.No.61570 (Acid Green 25) LPR A05620B12 100 gm 345 ALIZARINE RED S INDICATOR LPR A05640B10 25 gm 100 C.I.No.58005 (Sodium Alizarine sulphonate) LPR A05640B12 100 gm 320 ALIZARINE RED S INDICATOR APR A05640A10 25 gm 120 C.I.No.58005 (Sodium Alizarine sulphonate) APR A05640A12 100 gm 372 ALIZARINE SULFONIC ACID SODIUM SALT See Alizarine Red S ALIZARINE YELLOW G INDICATOR LPR A05680B10 25 gm 660 C.I.No.14030 (Alizarin yellow R) ALIZARINE YELLOW GG INDICATOR LPR A05690B10 25 gm 675 C.I.No.14025 (Alizarine yellow 2 G) www.lab5chemindia.com CONDITIONS APPLY* Page 3 SPECIAL PRICE LIST (Distributor for KEM LIGHT LABORATORIES & KEMIE LABS) www.labchemindia.com INDIA- 2012-13 ( Product Name Grade Code Quantity D/P Rs ) A05700B10 ALIZARINE VIOLET LPR 25 gm 825 C.I.No.61710(Acid Violet 34) ALKALI BLUE 6B EPR A05 720C08 5 gm 210 C.I.
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    The Chemical Synthesis of the Crinine and Haemanthamine

    molecules Review The Chemical Synthesis of the Crinine and Haemanthamine Alkaloids: Biologically Active and Enantiomerically-Related Systems that Serve as Vehicles for Showcasing New Methodologies for Molecular Assembly † Nan Hu, Lorenzo V. White, Ping Lan and Martin G. Banwell * Institute for Advanced and Applied Chemical Synthesis, Jinan University, Zhuhai 519070, China; [email protected] (N.H.); [email protected] (L.V.W.); [email protected] (P.L.) * Correspondence: [email protected] † Dedicated to the memory of our friend and colleague Professor Lew Mander FAA, FRS (1939–2020). Abstract: The title alkaloids, often referred to collectively as crinines, are a prominent group of structurally distinct natural products with additional members being reported on a regular basis. As such, and because of their often notable biological properties, they have attracted attention as synthetic targets since the mid-1950s. Such efforts continue unabated and more recent studies on these alkaloids have focused on using them as vehicles for showcasing the utility of new synthetic methods. This review provides a comprehensive survey of the nearly seventy-year history of these Citation: Hu, N.; White, L.V.; Lan, P.; synthetic endeavors. Banwell, M.G. The Chemical Synthesis of the Crinine and Keywords: alkaloid; crinine; haemanthamine Haemanthamine Alkaloids: Biologically Active and Enantiomerically-Related Systems that Serve as Vehicles for Showcasing 1. Introduction New Methodologies for Molecular The alkaloids isolated from the widely distributed herbaceous and bulbous flowering Assembly . Molecules 2021, 26, 765. plants of the amaryllis (Amaryllidaceae) family number more than five hundred and about https://doi.org/10.3390/molecules 10% of these embody the 2,3,4,4a-tetrahydro-1H,6H-5,10b-ethanophenanthridine ring sys- 26030765 tem (Figure1)[ 1].
  • An Investigation of the Protein Metabolism in Healthy

    An Investigation of the Protein Metabolism in Healthy

    AN INVESTIGATION OF THE PROTEIN METABOLISM IN HEALTHY SUBJECTS AND WEIGHT-LOSING CANCER PATIENTS by DONALD CAMPBELL McMILLAN F.I.M.L.S. A THESIS SUBMITTED FOR THE DEGREE OF DOCTOR OF PHILOSOPHY to THE UNIVERSITY OF GLASGOW from RESEARCH CONDUCTED IN THE UNIVERSITY DEPARTMENT OF SURGERY, GLASGOW ROYAL INFIRMARY MARCH 1992 © DONALD C. McMILLAN 1 ProQuest Number: 11007691 All rights reserved INFORMATION TO ALL USERS The quality of this reproduction is dependent upon the quality of the copy submitted. In the unlikely event that the author did not send a com plete manuscript and there are missing pages, these will be noted. Also, if material had to be removed, a note will indicate the deletion. uest ProQuest 11007691 Published by ProQuest LLC(2018). Copyright of the Dissertation is held by the Author. All rights reserved. This work is protected against unauthorized copying under Title 17, United States C ode Microform Edition © ProQuest LLC. ProQuest LLC. 789 East Eisenhower Parkway P.O. Box 1346 Ann Arbor, Ml 48106- 1346 Glasgow UNIVERSITY LIBRARY 9 iia , 1 CONTENTS PAGE Contents 2 List of Tables 8 List of Figures 13 Acknowledgements 15 Declaration 17 Dedication 20 Summary 21 1. INTRODUCTION AND AIMS 1.1 Protein metabolism in man 24 1.2 Turnover measurements using isotope tracers 27 1.3 Measurement of stable isotopes 29 1.4 Protein turnover measurements 29 1.5 Cancer cachexia 1.5.1 Weight loss in cancer (cancer cachexia) 30 1.5.2 Body composition in cancer cachexia 32 1.5.3 Energy metabolism in cancer cachexia 33 1.5.4 Whole body protein metabolism in cancer cachexia 34 1.5.5 Tissue protein metabolism in cancer cachexia 36 1.6 Aims of the thesis 39 1.7 Plan of thesis 39 2 PAGE 2.
  • DDT-10-00042-OA Proof.Indd

    DDT-10-00042-OA Proof.Indd

    349 Drug Discoveries & Therapeutics. 2010; 4(5):349-354. Original Article Evaluation of therapeutic effects and pharmacokinetics of antibacterial chromogenic agents in a silkworm model of Staphylococcus aureus infection Tomoko Fujiyuki, Katsutoshi Imamura, Hiroshi Hamamoto, Kazuhisa Sekimizu* Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo, Japan. ABSTRACT: The therapeutic effect of dye diseases, chemical compounds with antibacterial compounds with antibacterial activity was evaluated activity in vitro are tested for their therapeutic in a silkworm model of Staphylococcus aureus efficacy in vivo in animal infection models. A serious infection. Among 13 chromogenic agents that show problem is that most of compounds that exhibit antibacterial activity against S. aureus (MIC = 0.02 antibacterial activity in vitro do not have therapeutic to 19 μg/mL), rifampicin had a therapeutic effect. effects in animal infection models due to toxicity The ED50 value in the silkworm model was consistent and pharmacokinetic issues. Thus, for efficient drug with that in a murine model. Other 12 dyes did not discovery, protocols must be established to exclude increase survival of the infected silkworms. We agents without therapeutic effects at earlier stages of examined the reason for the lack of therapeutic drug development. Evaluation of the therapeutic effects efficacy. Amidol, pyronin G, and safranin were of potential antibiotics has been performed using toxic to silkworms, which explained the lack of mammalian models, but conventional methods using a therapeutic effects. Fuchsin basic and methyl green large number of mammals are problematic due to high disappeared quickly from the hemolymph after costs and ethical concerns. Therefore, the development injection, suggesting that they are not stable in the of a non-vertebrate infection model to test drug efficacy hemolymph.
  • Kinetics and Regulation of Mitochondrial Cation Transport Systems

    Kinetics and Regulation of Mitochondrial Cation Transport Systems

    Kinetics and Regulation of Mitochondrial Cation Transport Systems Martin Jaburek B.S., Palacky University, 1992 A dissertation submitted to the faculty of the Oregon Graduate Institute of Science and Technology in partial fulfillment of the requirements for the degree Doctor of Philosophy III Biochemistry and Molecular Biology August 1999 The dissertation "Kinetics and Regulation of Mitochondrial Cation Transport Systems" by Martin Jaburek has been examined and approved by the following Examination Committee: Keith D. Garlid, Advisor Professor Gebre W~ldegi9rgis Associate Proressor /U_- /Peter A. Zuber Professor ~. -Jft~.rofessorKaple:m Oregon Health Sciences University 11 DEDICATION I would like to dedicate this thesis to my wife, Iva, my daughter, Veronika, and also to my parents, grandparents, and all the members of my large family, as an excuse for not being with them for such a long time. iii ACKNOWLEDGMENTS I would like to extend my gratitude to my major advisor, Dr. Keith Garlid. I am very fortunate to have had the opportunity to be a student in his laboratory, and I am very thankful for his support, guidance, and encouragement, without which I would not have been able to finish this degree. I would further like to thank Dr. Gebre Woldegiorgis for the many thought- provoking and valuable discussions we had. Thanks also to Drs. Peter Zuber and Jack Kaplan for their time and for serving as members of my thesis committee. My further thanks to Dr. Petr Paucek, who introduced me to the secrets of reconstitution; to Dr. Martin Modriansky, for being such a good roommate and for sharing the secrets of yeast expression of uncoupling proteins; to Dr.