Polyketide Acyl Intermediates

Related topic :
Reactive IntermediatesAcyl LipidsIntermediatesChiral IntermediatesAcyl Urea DerivativesAcyl GuanidineAcyl Chain SphingolipidsAcinitro IntermediatesTannin Acyl HydrolaseCriegee Intermediates

Investigations on the biosynthesis of secondary metabolites and

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investigations on the biosynthesis of secondary metabolites and biosynthetic enzymes from aspergillus species untersuchungen zur biosynthese von sekundärmetaboliten und zu biosynthetischen enzymen aus aspergillus-arten dissertation zur erlangung des doktorgrades der naturwissenschaften (dr. rer. nat.) dem fachbereich pharmazie der philipps-universität marburg vorgelegt von liujuan zheng aus shangrao, china marburg an der

Acyl-acyl carrier protein pool sizes during steady-state

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volume 146,number 1 febs letters september 1982 acyl-acyl carrierprotein pool sizes during steady-state fatty acid synthesis by isolated spinach chloroplasts jurgen soil* and grattan roughan + plant physiology division, department of scientific and industrial research, private bag, palmerston north, new zealand received 20 july 1982

Acyl Lipids, Pigments, and Gramine in Developing Leaves of

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plant physiol. (1981) 67, 646-654 0032-0889/81/67/0646/09/$00.50/0 downloaded from https://academic.oup.com/plphys/article/67/4/646/6077384 by guest on 14 june 2022 acyl lipids, pigments, and gramine in developing leaves of barley and its virescens mutant' received for publication may 16, 1980 and in revised form september 30, 1980 lawrence w. thomson and saul zalik

Guideline on the use of starting materials-intermediates

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london, 27 june 2013 ema/chmp/bwp/429241/2013 committee for medicinal products for human use (chmp) guideline on the use of starting materials and intermediates collected from different sources in the manufacturing of non-recombinant biological medicinal products draft agreed by biologics working party december 2011 adoption by committee for

Origin of the Spectral Shifts among the Early Intermediates

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article pubs.acs.org/jacs origin of the spectral shifts among the early intermediates of the rhodopsin photocycle pablo campomanes,† marilisa neri,† bruno a. c. horta,† ute f. röhrig,‡ stefano vanni,† ivano tavernelli,† and ursula rothlisberger*,† †laboratory of computational chemistry and biochemistry, ecole polytechnique fed́ eŕ ale lausanne, ch-1015 lausanne, switzerland ‡molecular

Mitigation Strategies for Reactive Intermediates in Drug

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mitigation strategies for reactive intermediates in drug discovery new perspectives in dmpk: informing drug discovery royal society of chemistry, london february 10-11, 2014 thomas a. baillie school of pharmacy university of washington seattle, wa, usa [email protected] chemically reactive drug metabolites role in liver toxicity cancer res., 7, 468-480 (1947)

Industrial Chemicals and Intermediates from 1, 3-Butadiene

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recent advances in petrochemical science issn: 2575-8578 review article volume 6 issue 5 - november 2019 doi: 10.19080/rapsci.2019.06.555698 recent adv petrochem sci copyright © all rights are reserved by vivek k srivastava industrial chemicals and intermediates from 1, 3-butadiene vivek k srivastava*, sukdeb saha, preetom sarkar, gs srinivasa

Biocatalytic Synthesis of Chiral Pharmaceutical Intermediates

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r. n. patel: biocatalytic synthesis of chiral intermediates, food technol. biotechnol. 42 (4) 305–325 (2004) udc 577.128.15:615.015.4 issn 1330-9862 (ftb-1418) 305 review biocatalytic synthesis of chiral pharmaceutical intermediates ramesh n. patel process r & d, bristol-myers squibb, new brunswick, nj 08903, usa received: july 29, 2004 revised version:

Photochemistry of Reactive Intermediates

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view metadata, citation and similar papers at core.ac.uk published in "chimia: international journal for chemistry 61(10): 645-649, 2007" which should be cited to refer to this work. brought to you by core provided by rero doc digital library photochemistry of reactive intermediates thomas bally* http://doc.rero.ch

Investigation of Highly-Reducing Polyketide Synthase

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university of alberta investigation of highly-reducing polyketide synthase enzymes that produce the fungal polyketides lovastatin, fumonisin bj, and hypothemycin by jesse w.-h li a thesis submitted to the faculty of graduate studies and research in partial fulfillment of the requirements for the degree of doctor of philosophy department of chemistry

Uncovering the structures of modular polyketide synthases

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natural product reports uncovering the structures of modular polyketide synthases journal: natural product reports manuscript id: np-rev-07-2014-000098.r1 article type: review article date submitted by the author: 11-sep-2014 complete list of authors: weissman, kira; lorraine university, molecular and structural enzymology group umr 7365 cnrs-ul : imopa page 1 of 17

Dissection of an Iterative Polyketide Synthase

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dissection of an iterative polyketide synthase alan scott squalestatin tetraketide synthase is a fungal type 1 iterative polyketide synthase. it is a large, single enzyme with six catalytic domains. some of these domains are selectively switched on or off during the elongation of the polyketide chain to control the extent

Isolation and Screening of Tannase producing fungi

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int.j.curr.microbiol.app.sci (2015) 4(7): 765-774 issn: 2319-7706 volume 4 number 7 (2015) pp. 765-774 http://www.ijcmas.com original research article isolation and screening of tannase producing fungi s.n. girdhari * and s.a.peshwe department of microbiology, government institute of science, aurangabad 431001(ms), india *corresponding author abstract keywords tannin acyl hydrolase,

N-acyl-L-homoserine lactones inter kingdom

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synthesis of isotope labelled and photoactivatable n-acyl-l-homoserine lactones – inter kingdom signalling molecules zur erlangung des akademischen grades eines doktors der naturwissenschaften (dr. rer. nat.) der fakultät für chemie und biowissenschaften des karlsruher instituts für technologie (kit) - universitätsbereich genehmigte dissertation von magister dorota jakubczyk aus trzcianka, polen

Derivatives of a benzoquinone acyl hydrazone with activity

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biology faculty publications university of nebraska at omaha [email protected] department of biology 11-10-2018 derivatives of a benzoquinone acyl hydrazone with activity against toxoplasma gondii a. g. sanford university of nebraska at omaha t. t. schulze university of nebraska at omaha l. p. potluri university of nebraska at omaha

Synthesis, Characterization of Ibuprofen N-Acyl-1,3,4

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sys rev pharm 2020; 11(4): 681 689 a multifaceted review journal in the field of pharmacy e-issn 0976-2779 p-issn 0975-8453 synthesis, characterization of ibuprofen n-acyl-1,3,4- oxadiazole derivatives and anticancer activity against mcf-7 cell line mustafa q. ali alderawy1, leaqaa a. raheem alrubaie1*, falah hassan sheri2 1department of pharmaceutical chemistry,

HAMPOSYL N-Acyl Sarcosinate Surfactants are anionic HAMPOSYL

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product information hamposyl n-acyl sarcosinate surfactants typical properties hamposyl surfactants hamposyl† n-acyl sarcosinate surfactants are anionic surfactants available in several acid and salt grades. hamposyl acids hamposyl active ingredient free fatty acid color, gardner appearance @25°c typical specific gravity @ 25°c softening point average molecular wt.

Long-chain Acyl-CoA is not primarily increased in myotubes

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core provided by elsevier - publisher connector metadata, citation and similar papers at core.ac.uk biochimica et biophysica acta 1762 (2006) 666 – 672 www.elsevier.com/locate/bbadis long-chain acyl-coa is not primarily increased in myotubes established from type 2 diabetic subjects malene just a, nils j. færgeman b, jens

Mechanistic Studies of the Long Chain Acyl-CoA Synthetase

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university of nebraska - lincoln [email protected] of nebraska - lincoln biochemistry faculty publications biochemistry, department of 2007 mechanistic studies of the long chain acyl-coa synthetase faa1p from saccharomyces cerevisiae hong li center for metabolic disease, ordway research institute elaina m. melton center for metabolic disease, ordway

Research Module 55 Multistep synthesis of an Acyl Pyrazolidinone

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research module 55 multistep synthesis of an acyl pyrazolidinone introduction we will begin a two-week research sequence in which we make a variety of novel “acyl pyrazolidinones”, see structures b and c in the figure below. most of these substances have never been synthesized previously, and are