ライフサイエンスコーパス: unreactive

1 to oxidative addition, rendering the system unreactive.

2 Hexafluorobenzene proves unreactive.

3 Aliphatic amines were unreactive.

4 ronates for reaction that would otherwise be unreactive.

5 t gas phase basicities being, in large part, unreactive.

6 eas more substituted secondary alcohols were unreactive.

7 d probe based on a warhead so far considered unreactive.

8 aromatic structure and are stable in air and unreactive.

9 ty, with the Mn(IV)(3)CaO(4) OEC model being unreactive.

10 ental P resides, is relatively insoluble and unreactive.

11 ation was attained, while anhydrite remained unreactive.

12 ive, whereas the beta-anomer was found to be unreactive.

13 of DTT thiol groups are protonated and thus unreactive.

14 ht that the interior surface of nanotubes is unreactive.

15 , which are dominant in marine systems, were unreactive.

16 alpha,beta-Unsaturated esters were unreactive.

17 ly functionalized ceramides were found to be unreactive.

18 e unable to adopt the S-cis conformation are unreactive.

19 ophiles, whereas constrained nucleotides are unreactive.

20 e spin transfer cannot occur, the species is unreactive.

21 onyl functionalities at nitrogen, are rather unreactive.

22 Esters were unfortunately found to be unreactive.

23 The other altered state is unreactive.

24 reduced form of Cys 266, which is otherwise unreactive.

25 like, acceptors were found to be essentially unreactive.

26 ntal phospholipids and alcohol analogues are unreactive.

27 e reactive than TCEP, and DTT is essentially unreactive.

28 Disulfides (cystine) are unreactive.

29 Cystine and histidine derivatives are unreactive.

30 is constrained trans to the 2'-amine is also unreactive.

31 isubstituted and trisubstituted alkenes were unreactive.

32 in, whereas the anti-beta-silyl alkoxide was unreactive.

33 lkylidenes that bear a boron substituent are unreactive.

34 ethane, and-similar to methane-is chemically unreactive.

35 n the C-H bonds, previously considered to be unreactive.

36 enging because C-C sigma-bonds are typically unreactive.

37 Of the 268 OFSs, 266 were unreactive.

38 consequence of which renders both chemically unreactive.

39 s, which in its oxidized state is relatively unreactive.

40 owed by the 3,5-positions, while the 2,6 are unreactive.

41 4.9 x 10(4) M(-1) x s(-1)) of the relatively unreactive (1)HNO into the extremely reactive (3)NO(-).

42 Inversely, with unreactive 2'-fluoro-RNA substrates, AID's deaminase act

43 trates, followed by 3, which is followed by (unreactive) 2.

44 iously reported Mn(2) -peroxides, which were unreactive, 2 proved to be a capable oxidant in aldehyde

45 tructures of these mutants complexed with an unreactive abasic site in DNA reveal these residues to a

46 ading to productive glycosylations even with unreactive acceptors.

47 rawing groups failed to glycosylate hindered unreactive acceptors.

48 formation with a reactive chiral face and an unreactive achiral face.

49 actions involving challenging and relatively unreactive acyclic diene substrates.

50 unction because it prevents the formation of unreactive acyl-enzyme intermediates, which has been a l

51 When the pupils remained dilated and unreactive after 6 mins of CPR, resuscitation efforts we

52 form alkyl iodide intermediates from simple unreactive alcohols.

53 azardous, reagents to activate the otherwise unreactive alcohols.

54 ading to higher reactivity for the otherwise unreactive aldehydes.

55 e the substitution of sulfur for hydrogen at unreactive aliphatic or electron-rich aromatic carbon at

56 his metal-free C(sp(3))-H borylation enables unreactive alkanes to be transformed into valuable organ

57 for the alkylation of amides with relatively unreactive alkyl halides (i.e., poor substrates for SN2

58 te that N-alkylation activates the otherwise unreactive amide bond towards sigma N-C cleavage by swit

59 in the presence of dihydroNADPH (NADPH3, an unreactive analogue lacking the 5,6-double bond in the n

60 nding experiments with dGCVIA peptide and an unreactive analogue of FPP, (E,E)-2-[2-oxo-2-[[(3,7,11-t

61 ynthetase, was determined in complex with an unreactive analogue of its acyl-adenylate and CoA.

62 Formamides are unreactive analogues of the aldehyde substrates of alcoh

63 ed, engineered pure-magnetite was relatively unreactive and contributed minimally to the generation o

64 and as a result, the molecule is relatively unreactive and even displays reversible electrochemical

65 resulting Au99(SPh)42 compound, however, is unreactive and highly stable in the presence of excess a

66 metals other than palladium were completely unreactive and led to recovered starting material.

67 molecule (4 or CDNB) leading to formation of unreactive and reactive complexes, respectively.

68 hydrogen bonds to the O2' atom, rendering it unreactive and thus explaining the specificity for 2'-de

69 ydrogen (C-H) bonds are typically considered unreactive and unavailable for chemical manipulation.

70 ch have been thought to be relatively inert (unreactive) and thus leach small amounts of polyaromatic

71 on paths associated with other h-e pairs are unreactive, and the moderate experimental efficiency is

72 literature but whose protons were considered unreactive are also shown for the first time to react wi

73 may be synthetically useful when relatively unreactive arene substrates such as benzene, toluene, an

74 this approach to monofluorobenzenes, highly unreactive arenes, which upon complexation become nearly

75 Secondary amines are unreactive, as is a catalyst with a single aminolyzable

76 tramethylpiperidine (TEMPO-Me) is relatively unreactive at ambient temperature in the absence of an e

77 iously difficult glycosylation with the most unreactive axial 4-OH of the rare disaccharide, and the

78 ages in [4 + 2] cycloadditions with normally unreactive azadienophiles including unactivated cyano gr

79 s the most favored one thermodynamically, is unreactive because of a high propensity for charge recom

80 tive of MDH.PQQ(NH2(+).methanol structure is unreactive because of the nonproductive means of methano

81 s for the Michael reactions of traditionally unreactive beta,beta'-enones and substituted beta,beta'-

82 also the subsequent functionalization of the unreactive beta-methylene group in an unprecedented tand

83 a powerful tool with which to convert these unreactive bonds into carbon-carbon and carbon-heteroato

84 Unreactive by itself, the Mo-dimethyl catecholate analog

85 The amination of nominally unreactive C(aryl)-H bonds via a sequential directed ort

86 one step, and in the process transforms the unreactive C-3 position to the reactive C-5 position.

87 ) may be a general strategy for cleaving the unreactive C-C bonds between adjacent sp(2)-hybridized c

88 is regard, transformation of a traditionally unreactive C-H bond, proximal to the nitrogen atom, into

89 r of synthetic challenges: the activation of unreactive C-H bonds and the need for regio- and stereos

90 nctionalize molecules directly at ostensibly unreactive C-H bonds, chemists have discovered reaction

91 t catalytic methods to cleave the relatively unreactive C-O bonds of ethers remains an important chal

92 e reaction is based on the activation of the unreactive C-OMe bond by the proximate amide directing g

93 diates capable of abstracting a hydride from unreactive carbon centers, including benzyl-, allyl-, an

94 f methane through the cleavage of the highly unreactive carbon-phosphorus bond in methyl phosphonate

95 ctivation catalysis) is employed to activate unreactive carbonyl substrates.

96 ) to undergo oxidation to Tl(III) due to the unreactive character of the 6s(2) electrons.

97 at could allow delineation of the active and unreactive clones, the sequences identified in five of t

98 entadiene isomer may be regarded as a rather unreactive closed-shell singlet species with one localiz

99 a mechanism in which each nucleotide samples unreactive (closed) and reactive (open) states.

100 teraction with the reduced Fd present in the unreactive complex.

101 predominates in the presence of practically unreactive compounds (acetone, butanol, propionic, and b

102 ion: selective preservation of biochemically unreactive compounds(4,5) and protection resulting from

103 f the triphosphate of GTP, destabilizing the unreactive conformation and thereby allowing thermal flu

104 rate processes, (b) alternative reactive and unreactive conformations, and (c) mutations within the c

105 3)Bi-7.16.4, (c) 120 muCi (213)Bi-Rituximab (unreactive control), and (d) unlabeled 7.16.4.

106 but now new substrates that were previously unreactive could be employed.

107 ust the ratio between fast reactive and slow unreactive decay channels.

108 Formation of this unreactive dimer is an important step in the mechanism o

109 efin coupling partners, including previously unreactive disubstituted terminal olefins and internal o

110 rception of the reaction by the formation of unreactive (E)-phosphazides.

111 On addition of HMBPP to an (unreactive) E126A IspH mutant, a reaction intermediate f

112 les enantioselective reactions of relatively unreactive electrophiles.

113 a new capacity, to incorporate two otherwise unreactive elements, Re and Zn, in the same structure wh

114 tially stabilize the reactive imine over the unreactive enamine tautomer.

115 FTSs can form as transient intermediates or unreactive end-products via e(aq)(-) reactions with prec

116 ing the tandem oxidation and amidation of an unreactive ethyl group.

117 active headgroup and a matrix-silane with an unreactive ethylene glycol group.

118 Thus, ostensibly unreactive excipients under certain conditions may incre

119 ys265 is absent in the homologous but oxygen-unreactive FAD site in heterotetrameric sarcosine oxidas

120 ow yield; additionally, the lactones are too unreactive for solid-phase applications.

121 cases, catalyze oxidation of the thiol to an unreactive form such as a sulfinic or sulfonic acid.

122 There was also a remnant unreactive fraction, likely attributable to Mn(III)-indu

123 The manipulation of traditionally unreactive functional groups is of paramount importance

124 Carbon-fluorine bonds are among the most unreactive functionalities in chemistry.

125 ctions is particularly pronounced in case of unreactive glycosyl donors and/or glycosyl acceptors.

126 sulted in the precipitation of insoluble and unreactive group 2 acetylides.

127 cture of RtcB in complex with Mn(II) and the unreactive GTP analogue guanosine 5'-(alpha-thio)triphos

128 The facile formation of the remarkably unreactive hemiketal 16 thwarted attempts to elaborate 1

129 generally thermodynamically and kinetically unreactive; however, we recently discovered that the tri

130 The triose binds to XI as the unreactive hydrate, but ligand binding induces metal cof

131 The selective activation of unreactive hydrocarbons by biosynthetic enzymes has insp

132 the formation of covalent bonds by oxidizing unreactive hydroquinone moieties in LHA to reactive, ele

133 plexation of an activator species to form an unreactive, immobile complex reduces the effective diffu

134 and excels at the introduction of relatively unreactive impurity ions that have not been previously a

135 Other types of cells were unreactive in both groups.

136 ediates in synthesis, they are traditionally unreactive in C(sp(3))-H activation reactions.

137 Amide N-C(O) bonds are generally unreactive in cross-coupling reactions employing low-val

138 All dyes were unreactive in the 8-position.

139 rimary C-H bonds, while methylene groups are unreactive in the absence of external ligands.

140 and also that fully saturated compounds are unreactive in the catalytic system.

141 or and a second oxidant (Ox2 ) that would be unreactive in the primary reaction.

142 eplacement for Asn245, which is inaccessible/unreactive in WT LacY, alkylates readily in the Gly-->Tr

143 coli RNAP, forming the closed, permanganate-unreactive intermediate I(1).

144 products occurs due to the epimerization of unreactive intermediates from the other two pathways, as

145 n framework confers activity on an otherwise unreactive iron-haem cofactor.

146 ssary recognition elements into an otherwise unreactive junction resulted in specific strand scission

147 talyzed Pictet-Spengler reaction (PSR) using unreactive ketone substrates is described.

148 the chemoselective reduction of an extremely unreactive lactam in the presence of a readily reduced l

149 ppears to be critical for inhibition because unreactive lipids, e.g. PGB1, PGE2, PGF2alpha, and TxB2,

150 The ratio of unreactive lithium-cationized hexose to total lithium-ca

151 zyne moiety, thereby generating a relatively unreactive meta-benzyne analogue.

152 owing to its sequestration by calcium in the unreactive mineral hydroxyapatite.

153 revealed that fungi recruit and redistribute unreactive Mn(2+) provided by fresh plant litter to prod

154 on reveals that absorption by high-frequency unreactive modes (e.g., C[double bond]C stretches) incre

155 heated in the presence of a noble gas or an unreactive molecule at 650 degrees C and 3000 atm pressu

156 reaction that consumed small amounts of the unreactive monoacetate (-)-9.

157 ds to accelerate C-H activation of otherwise unreactive monodentate substrates is crucial for outcomp

158 er reactions for a number of substituted and unreactive N-allyl-2-furfurylamines under biomimetic con

159 For example, in reaction with highly unreactive n-butyl acrylate and using only 2 equiv of MD

160 cess to reactive sites, promote formation of unreactive NH4(+), and reduce oxidant levels due to high

161 t methanol and dimethyl ether are apparently unreactive on the two most important methanol-to-hydroca

162 cyclopropane bond to give a lower energy and unreactive open triplet, has been suggested.

163 s were also easily obtained but showed to be unreactive or rearranged under these cyclization conditi

164 und for incubations of DNA/enzyme films with unreactive organic controls or hydrogen peroxide.

165 in a mixture of precursors that would remain unreactive otherwise.

166 The resting state Fe(III) is unreactive oxidatively.

167 re treated soils were dominated by dissolved unreactive P (DUP), mainly originating from manure.

168 Increased preference for the unreactive pathway upon paipai* excitation largely accou

169 ene (NHC)-induced activation of an otherwise unreactive Pd/Al2O3 catalyst.

170 ther cleaved from iridium by water or formed unreactive, phenoxide-bridged iridium dimers.

171 s of a triple C-H functionalization of three unreactive piperidine sp(3) carbons.

172 pathways: a reactive twisting pathway and an unreactive planar pathway.

173 Because hydrotalcites do not have an unreactive polymer as a structural core, their aqueous s

174 interesting biofunctionalization approach of unreactive polymers with applications in immunosensing a

175 this radical can abstract hydrogen atoms at unreactive positions, facilitating the introduction of a

176 etal complexes cleave C-H bonds at typically unreactive positions.

177 of the water adduction reaction rate or the unreactive ratio provides two separate methods for confi

178 he equilibrium constant for the formation of unreactive reactant dimers.

179 The use of well-controlled fabrics, unreactive reference materials, and a life-cycle based e

180 ted: three Ag variants and one Au used as an unreactive reference to separate mechanical from chemica

181 F3)4](-) and [(bpy)Cu(CF3)3], are stable and unreactive, remaining dead-end spectators throughout the

182 duct yield and rate of oxidation of formerly unreactive Rieske clusters.

183 ease of tethered molecules, while generating unreactive side products.

184 These thioalkyl esters are rather unreactive so the ligation reaction is catalyzed by in s

185 both catalyzing mineralization in otherwise unreactive solution and of templating nanocrystal growth

186 be fit to a model that assumed a protonated unreactive species A, a major reactive species B, and a

187 , like those obtained from biomass or highly unreactive species, such as CO2 should be transformed in

188 d positively charged, instead of the neutral unreactive state usually envisaged.

189 the open conformation possibly represents an unreactive state with Glu-288 positioned away from the c

190 of TUNEL-reactive DNA to a subsequent TUNEL-unreactive state.

191 le the racemization of traditionally static, unreactive stereocenters through the intermediacy of pro

192 ure of its complex with three Mg(2+) and the unreactive substrate analogue dimethylallyl-S-thiolodiph

193 ase complexed with three Mg(2+) ions and the unreactive substrate analogue farnesyl-S-thiolodiphospha

194 mide displacement reactions, carba-NAD is an unreactive substrate analogue for NAD-consuming enzymes.

195 The unreactive substrate analogue, maleate, is used to induc

196 ohol dehydrogenase complexed with NAD(+) and unreactive substrate analogues, 2,2,2-trifluoroethanol o

197 sing highly modified, severely minimized, or unreactive substrate analogues.

198 , which was associated with the formation of unreactive surface carbonato complexes.

199 Unreactive surface tungsta (WO(3) ) also promote the for

200 oach can be employed for a range of normally unreactive systems.

201 d to a protein target, changing an initially unreactive terminus into one that could be modified in h

202 of the approaching SO2 and makes a normally unreactive tertiary carbenium carbon susceptible to addi

203 KO(t)Bu by the selective C-C coupling of an unreactive tertiary sp(3) C-H bond.

204 in that its electrophilic carbon is rendered unreactive through steric hindrance.

205 illar inclusion pathology was diminished and unreactive to antibodies specific for the C terminus of

206 allows crosslinkers that would be otherwise unreactive to be used.

207 Ala and Gly are far too unreactive to be useful probes in typical experiments an

208 free drug, yet remain essentially stable and unreactive to in vitro DNA alkylation conditions (<0.1-0

209 cids and esters, the chromophore of pnGFP is unreactive to millimolar concentrations of hydrogen pero

210 in the presence of B(C6 F5 )3 , a Lewis acid unreactive to O2 , to generate bis(borane) peroxide.

211 This is unreactive to pinacolborane at ambient temperature, resu

212 ackground, the T cells mediating lesions are unreactive to viral Ags.

213 ctional state, in which the active sites are unreactive, to the functional proteolytic conformation.

214 s-DNA treated in buffer or buffer containing unreactive toluene resulted in no significant changes in

215 onyls and imines (pi-electrophiles), but are unreactive toward a range of other electrophiles.

216 lasses of electrophiles that were previously unreactive toward addition of alkyl-Cr reagents.

217 nce model studies showed that lactone 13 was unreactive toward amines.

218 es containing polar functionality, which are unreactive toward C-H borylation under neat conditions.

219 One-electron oxidized 2'-FdC is unreactive toward C3'* or C2'* formation.

220 ibenzofuran analogue of 1b, compound 1c, was unreactive toward CO due to the longer distance between

221 In contrast, [Zn3(OH)3L] (4) was found to be unreactive toward CO2 over the course of several days at

222 F; R = H, 1-H) were prepared and shown to be unreactive toward D(2) and alpha-olefins, leading to the

223 as independently synthesized and found to be unreactive toward dienes.

224 a high-spin, five-coordinate complex and is unreactive toward dioxygen.

225 ing to [Ar*SnH2 (PtBu3 )](+) which is rather unreactive toward further dehydrogenation.

226 While unreactive toward further oxidation, Compound RH can be

227 n CHCl3 and other nonpolar solvents, OsO4 is unreactive toward H2 over a week at ambient temperatures

228 as pi-activated alcohols, which are normally unreactive toward HCl catalysis.

229 stigations reveal that hydroxyl radicals are unreactive toward HFPO-DA, while electrochemically activ

230 lates that form on warming the solutions are unreactive toward isobutyraldehyde and undergo retroaldo

231 However, the silicon reagent is completely unreactive toward many sulfones, the tin reagent typical

232 with azide, thiocyanate, and ammonia, but is unreactive toward nitriles, NO, and butyrate.

233 Moreover, the CDO active site is essentially unreactive toward NO in the absence of substrate, sugges

234 ply that the metal centers of the oxides are unreactive toward NO(2).

235 This species is unreactive toward nucleophiles and reactive toward stron

236 l changes that render the trinuclear cluster unreactive toward O(2), demonstrating a structural role

237 (4), was prepared and found to be completely unreactive toward O(2), suggesting a critical role for F

238 rimary N-oxides, and secondary N-oxides, are unreactive toward or react predominantly by proton trans

239 by allylic oxygenation of linoleic acid, are unreactive toward oxidative fragmentation.

240 e semiquinone is highly stabilized making it unreactive toward oxygen; and 3) the Q(o) site catalyzes

241 ol(2)(eta(4)-C(4)CO)Ru(CO)(2)H](-) (13) were unreactive toward PhCHO under conditions where facile Ph

242 ive coordinate amide iodine(V) complexes are unreactive toward redox reactions due to the fact that i

243 hough B(C(6)F(5))(3) has been reported to be unreactive toward silica in the absence of a Bronsted ba

244 CsoR is unreactive toward sulfite under the same conditions.

245 otonation renders basic sites (nucleophiles) unreactive toward the N-hydroxysuccinimide ester reagent

246 alue (10.5) that makes this thiol relatively unreactive toward the target disulfide in nDsbD.

247 alts, including those substrates that remain unreactive toward the Zincke salt, which is the reagent

248 (-90 degrees C); by contrast, F(8)Cmpd-II is unreactive toward these substrates.

249 hat Mn(IV)(3)CaO(4) and Mn(IV)(3)ScO(4) were unreactive toward trimethylphosphine (PMe(3)).

250 odeled after the p53 acetylation site but is unreactive toward trypsin because all other lysine and a

251 The diradical is unreactive toward water, methanol, and chloroform; upon

252 Indeed, 1 is unreactive toward weak C-H donors and even cocrystallize

253 LS-3DCHIm is resistant to reduction, is unreactive toward weakly acidic 4-NO2-phenol, and strong

254 ular terminal metal-nitrides are notoriously unreactive towards dihydrogen, and only a few electron-r

255 -spin square planar Co(II) complex, which is unreactive towards external substrates.

256 y to cleave carbon-heteroatom bonds that are unreactive towards other transition metals.

257 Carboxamide-ligated 8 is shown to be unreactive towards oxo atom donors, in contrast to imine

258 H(2) S was unreactive towards TTP when the protein was bound to RNA

259 The complex 2 was air-stable and unreactive towards water, methanol, and other substrates

260 eful for separation of microliter amounts of unreactive trace volatile compounds from large-volume ga

261 ithin a series of g-C3N4, the yield of these unreactive trapped electrons correlates inversely with H

262 As a result, the unreactive triplet state nitrene undergoes delayed, ther

263 c acid, a compound previously reported to be unreactive under Dakin-West conditions, forms 4-phenyl-2

264 On the other hand, SA is singularly unreactive under identical reaction conditions, except f

265 hindered alpha-quaternary lactams which are unreactive under known conditions for similar transforma

266 alyzed rearrangement of precursors that were unreactive under simple thermal instigation.

267 erization into alpha-bromide that is totally unreactive under the established reaction conditions.

268 yl chlorides and aryl and vinyl halides were unreactive under the reaction conditions.

269 ng, while the 5-alkyl isomers are completely unreactive under the same conditions.

270 Although 1,5-dienes with this skeleton were unreactive under thermal conditions, they were photochem

271 ethyl, and isopropyl esters are essentially unreactive under these conditions, allowing for the sele

272 atic aldehydes, as an aliphatic aldehyde was unreactive under these conditions, and other reactive fu

273 ss of sulfur(VI) halides, that are generally unreactive unless activated by protein binding.

274 ur) is suggested to be largely insoluble and unreactive until it reacts with hydrogen sulfide.

275 were found in occluded positions, while some unreactive uracils were found in exposed positions.

276 Interestingly, trans-vinylsilanes are unreactive, whereas allylic oxidations of cis-vinylsilan

277 In this series, sulfanyl derivatives were unreactive, while sulfoxide and sulfone analogues provid

278 Sera from women and men that were unreactive with alpha-actinin (negative control sera) fa

279 Lycopene has previously been reported to be unreactive with BCO1, and our findings warrant a fresh l

280 are mutually reactive with one another, but unreactive with biopolymers and water, is challenging.

281 xy analog of the natural substrate, normally unreactive with cAOS, was thereby epoxidized stereospeci

282 Other hedgehog point mutants at D303, also unreactive with cholesterol, accepted 3HPC as a substrat

283 e, the full- and half-resonance lactams, are unreactive with DMDO.

284 4-Hydroxyphenyl isopropyl sulfone (6) is unreactive with either CCl4 or CBrCl3 in KOH-t-BuOH, its

285 ere we show that antithrombin is essentially unreactive with factor IXa in the absence of heparin (k(

286 m) of 7 microm; k(cat)) of 14 min(-1) but is unreactive with GDP, GTP, GpppA, ATP, CTP, or UTP.

287 o methylates the cap analog m(7)GpppA but is unreactive with GTP, GDP, GpppA, m2,2,7GTP, m2,2,7GDP, A

288 .26(+) OVA-specific CD4(+) T cells that were unreactive with HSV.

289 enide (TOPSe)) were surprisingly found to be unreactive with metal carboxylates and incapable of yiel

290 S esters, which would render them relatively unreactive with NHS esters.

291 This conformation of the enzyme is unreactive with oxygen.

292 d that while carboxylated SWCNTs were rather unreactive with respect to direct solar photolysis, they

293 In contrast, uracil is completely unreactive with ribose under these conditions.

294 rapidly with carbon-centered radicals but is unreactive with superoxide and lipid peroxidation produc

295 ated iron(II)-SciOPP species was found to be unreactive with the cycloheptyl bromide electrophile ove

296 d analogue of 1, [(bppppa)Ni](ClO4)2 (2), is unreactive with the hemithioacetal, thus indicating the

297 omplete V(H) and V(L )germline revertant was unreactive with the human ILD and didomain, the Escheric

298 Clones reactive with this pool but unreactive with the pool of pony antisera to organisms c

299 Complex 1 is unreactive with the thioester product, PhCH(OH)C(O)SCD3,

300 ata demonstrate that 19-substituted BQAs are unreactive with thiols, display reduced hepatotoxicity,