ライフサイエンスコーパス: be active against

1 epitope, our results suggest that Ig-2D1 may be active against 06HA only in the absence of glycosylat

2 dene]carbonimidic dihydrazide hydrochloride) were active against 24 clinical MRSA and MSSA isolates.

3 In the PhenoSense assay, T-1249 was active against 636 different HIV-1 Env-pseudotyped v

4 famethoxazole (TMP-SMX) and fluoroquinolones were active against 94% and 88% of isolates, respectivel

5 ecies, compounds that bind to the new target are active against a broad spectrum of bacterial species

6 c acid carbamoyl methyl amides (PACMAs) that are active against a panel of human ovarian cancer cell

7 Anti-PD-L1 antibodies are active against a variety of cancers, and combined an

8 Agents targeting topoisomerases are active against a wide range of human tumors.

9 y active neutralizing antibodies (NAbs) that are active against a wide variety of circulating strains

10 The ideal antibiotic should be active against a broad spectrum of pathogenic organis

11 ementarity to identify compounds expected to be active against a given target.

12 te broadly neutralizing antibody (bnAb) that is active against a broad range of HIV-1 primary isolate

13 can generate a potent triamino scaffold that is active against a panel of hard-to-kill epithelial can

14 actericidal lipoglycopeptide antibiotic that is active against a range of clinically relevant gram-po

15 Rebeccamycin analog (NSC 655649) is active against a variety of both solid and nonsolid t

16 SVS-1 is active against a variety of cancer cell lines such as

17 Irinotecan is active against a variety of malignancies; however, se

18 LipA is active against a wide range of fatty acid esters of p

19 Since STI571 is active against A-MuLV-transformed cells in vitro, we

20 In vivo, FdUMP[10] was active against a syngeneic AML model with a survival

21 All three drugs were active against a panel of seasonal H3N2 and laborat

22 These compounds were active against a transformed human colon cancer cel

23 These compounds were active against a variety of solid and hematological

24 acetylated substrates in vitro, only CjCE2C was active against acetylated mannan in Physcomitrella.

25 , are directly active against Ad3, and IP-10 is active against Ad5.

26 Thalidomide is active against advanced myeloma.

27 Iseganan, an antimicrobial peptide, is active against aerobic and anaerobic gram-positive an

28 The 4-nitroimidazole PA-824 is active against aerobic and anaerobic Mycobacterium tu

29 tool for risk assessment showed coumarin to be active against Aliivibrio fischeri bacteria down to 1

30 embers of the miR-34 family of miRNAs, which are active against all three viruses as well as the clos

31 Sofosbuvir (SOF) is active against all hepatitis C virus (HCV) genotypes,

32 st activity against xanthine than uracil and is active against all xanthine-containing DNA (C/X, T/X,

33 Itraconazole was active against all Candida spp. (96% of MICs were <

34 Voriconazole was active against all Candida spp. except C. glabrata (

35 In addition, MEDI3902 was active against all tested isolates.

36 LyeTxI and LyeTxI/betaCD were active against all strains tested at concentrations

37 producers, and (iii). in vitro, carbapenems are active against AmpC-producing strains of K. pneumoni

38 associated with exposure to antibiotics that are active against anaerobes.

39 terminal, glycine-rich attacin-analog region was active against any of the bacterial strains studied,

40 aryl-2-(3-indolyl)acetohydroxamic acids that are active against apoptosis- and multidrug-resistant ca

41 The echinocandins and triazoles were active against Aspergillus spp. (MIC90/minimum effe

42 HIV-1 IN), was found in the present study to be active against ASV IN as well as HIV-1 IN.

43 pecific chimeric antigen receptor (CD19.CAR) are active against B-cell malignancies, but it is unknow

44 Crenolanib was active against Ba/F3 cells harboring FLT3-ITD and se

45 , anhydrodinemasone BC, and nor-dinemasone B are active against bacteria, including Legionella pneumo

46 idinone antibiotics, linezolid, was found to be active against bacteria and against the halophilic ar

47 AcpP PPMO is active against Bcc infections in vitro and in vivo.

48 -blocking activity in rodent malaria models, are active against blood-stage field isolates of the maj

49 reased efficacy compared with bortezomib and was active against bortezomib-resistant MM cell lines an

50 ide chain [-HNCHMe(CH2)3NEt2] of chloroquine are active against both chloroquine-susceptible and -res

51 (F98Y) S. aureus DHFR and found that several are active against both enzymes and specifically that th

52 s with unprecedented chemical scaffolds that are active against both Gram-positive and Gram-negative

53 They are active against both parasite and mammalian CPs, desp

54 Therefore, new anti-TB agents, which are active against both the replicating form of Mtb (R-T

55 COMT expressed in E. coli is active against both caffeic and 5-hydroxyferulic acid

56 tdins, the mouse intestinal defensins, rHD-5 is active against both mouse-virulent wild-type Salmonel

57 l candidate 35b (vaniprevir, MK-7009), which is active against both the genotype 1 and genotype 2 NS3

58 LeAOS was active against both 13S-hydroperoxy-9(Z),11(E),15(Z)

59 Recombinant OPCL1 was active against both OPDA and OPC-8:0, as well as med

60 Chloroplast-produced BglC was active against both pure cellobiose and against toba

61 te specificity studies suggested that AGPAT6 was active against both saturated and unsaturated long-c

62 virus type 1 revealed that the heterocycle 3 was active against both viruses but also was cytotoxic.

63 However, CirB and cyclopsychotride were active against both Gram-positive and Gram-negative

64 lysis showed that the recombinant leukotoxin was active against bovine polymorphonuclear leukocytes a

65 roduced for treatment of metastatic melanoma are active against brain metastases and offer new opport

66 e-Poulenc Rorer, Antony, France) appeared to be active against breast cancer in phase I trials, we pe

67 All agents except for the echinocandins were active against C. neoformans, and the triazoles wer

68 he antiproliferative activity, all compounds were active against Caco-2 cell line, being the ones wit

69 conventional peptidic inhibitors of hTS that are active against cancer cells and do not result in the

70 Analogue 17 was active against carbapenem-resistant and polymyxin-re

71 en to identify small-molecule compounds that are active against CCAs.

72 Laulimalide was active against cell lines resistant to paclitaxel or

73 e VLY and ILY, which are human specific, INY is active against cells from a broad range of species.

74 veral human cancer cell lines, cyclostreptin was active against cells resistant to paclitaxel and epo

75 supernatants of chitin-grown strain 2-40 and was active against chitin and glycol chitin.

76 Flavopiridol is active against chronic lymphocytic leukemia (CLL) cel

77 Compounds from this series were active against clinical Mtb strains, while no cross

78 le of eliciting neutralizing antibodies that are active against clinically relevant HIV-1 strains.

79 New generation azoles that are active against clinically relevant, drug-resistant f

80 Two bisabolane derivatives were active against colon cancer cell lines and may be i

81 discovered, and the most promising compounds were active against COX-1 in intact ovarian carcinoma ce

82 ilability of powerful antifungal agents that are active against Cryptococcus neoformans, these drugs

83 enic acid and ergosterol endoperoxide, which were active against Cryptococcus neoformans and methicil

84 Thus, cotreatment with LBH589 and AMN107 is active against cultured or primary IM-resistant CML c

85 Furthermore, treatment with LBH589 was active against cultured primary Ph(-) ALL cells, inc

86 gests that these compounds have potential to be active against CWD in vivo.

87 We found that roscovitine is active against cysts originating from different parts

88 re encapsidated in HIV-1 and SIV virions and were active against Deltavif SIV(mac) and SIV(agm).

89 the parasite's replicative blood stages and is active against developing gametocytes, the forms resp

90 The isolated lipase was active against diolein, but not triolein.

91 z-423 is a novel immunomodulatory agent that is active against disease even in the context of defecti

92 ly-induced antiviral gene expression program is active against disparate human arthropod-borne viruse

93 antibiotic produced by Bacillus cereus that is active against diverse bacteria and lower eukaryotes.

94 velopment of new antituberculosis drugs that are active against dormant or persister populations of M

95 ng the first 28 days of therapy and rifampin was active against dormant bacilli after the establishme

96 We show here that AbsB is active against double-stranded RNA transcripts derive

97 P. falciparum-specific DHFR inhibitors that are active against drug-resistant parasites.

98 -1 RT can be used to identify compounds that are active against drug-resistant viruses.

99 xhibited excellent bactericidal activity and was active against drug-sensitive and resistant Mtb.

100 e used yeast strains to test whether DMP-840 is active against either topoisomerase I or II.

101 Oral MPA is active against endometrial carcinoma.

102 ous indirect photoinactivation mechanism may be active against Ent. faecalis, it is not for the sewag

103 Several panitides were shown to be active against Escherichia coli and cytotoxic to HeLa

104 Antibacterial assays confirmed that gallin was active against Escherichia coli, but no additional a

105 We conclude the following: (a) 4-HPR was active against ESFT cell lines in vitro at concentra

106 sults also demonstrate that these mechanisms are active against established tumor as well as developi

107 We verified that DMP-840 is active against eukaryotic topoisomerase II by demonst

108 cysteine proteases out of which 18 compounds were active against falcipain-2 and falcipain-3.

109 and only approximately 1% of the inhibitors are active against five or more kinases.

110 ovel TKI, demonstrates type I properties and is active against FLT3 containing ITD and/or D835- or F6

111 The preparation was active against fluorogenic substrates specific for c

112 C(27) 3beta-HSD cDNA encodes an enzyme that is active against four 7alpha-hydroxylated sterols, indi

113 We investigated whether resveratrol is active against fresh acute myeloid leukemia (AML) cel

114 S-1 plus cisplatin is active against gastric cancer and has a favorable tox

115 a series of N-lipidated peptide dimers that are active against Gram-negative bacteria, including car

116 t(M)) tetracycline-resistance mechanisms and are active against Gram-positive and Gram-negative organ

117 Previous studies have shown that ADEPs are active against Gram-positive bacteria (e.g., MRSA, V

118 The antibiotic, paenibacterin, is active against Gram-negative and Gram-positive bacter

119 Fosmidomycin, a potent DXR inhibitor, is active against Gram-negative bacteria.

120 Results show that the hydrogel surface is active against Gram-positive (Staphylococcus epidermi

121 Here we demonstrate that promysalin is active against Gram-positive and Gram-negative bacter

122 The lantibiotic NAI-107 is active against Gram-positive bacteria including vanco

123 in, a lipoglycopeptide antibiotic agent that is active against gram-positive pathogens, has a long pl

124 Pa-MAP 1.9 was active against Gram-negative planktonic bacteria and

125 ial activities showed that the date extracts were active against Gram (+) and Gram (-) bacteria, show

126 The obtained compounds were active against Gram-positive bacteria, including mu

127 The compounds were active against Gram-positive pathogens and revealed

128 cin, linezolid, tigecycline, and minocycline were active against >90% of VISA isolates, while >90% of

129 These new peptides were active against H3N2 and H1N1 strains of IAV.

130 Furthermore, several antiretroviral agents are active against HBV infection, including lamivudine,

131 Adenine analogue 14 was active against HBV (IC50 2 microM), VZV (IC50 2.5 mi

132 log (TCRB), the 5,6-dibromo ribonucleoside 3 was active against HCMV (IC50 approximately 4 microM) bu

133 ast, the 2-aza analogue of sangivamycin (30) was active against HCMV and HSV-1 but this apparent acti

134 ogues with hydrogen-bond-accepting character were active against HCMV (e.g., 3-formyl-2,5,6-trichloro

135 -dichloro series (20a,b, 7a,b, respectively) were active against HCMV (IC50's = 1-10 microM) and nonc

136 he 2-chloro but not the 2-amino heterocycles were active against HCMV (IC50's = 5-8 microM) but not H

137 In vitro studies demonstrate that 1 is active against HCT-15, AGS, PC-3, and LNCaP tumor cel

138 Preoperative trastuzumab and paclitaxel is active against HER2 overexpressing early-stage breast

139 a larger family of cytidine deaminases that are active against HIV-1 and other retroviruses.

140 CN) and triciribine-5'-monophosphate (TCN-P) are active against HIV-1 at submicromolar concentrations

141 FDA-approved HIV-1 protease inhibitors (PI) are active against HIV-2.

142 to the design of new inhibitors predicted to be active against HIV protease.

143 ino-5-arylthiobenzonitriles (1) was found to be active against HIV-1.

144 of acyclic nucleoside monophosphate prodrugs being active against HIV-1.

145 N-MCD4T is active against HIV-1 and HIV-2 in CEM, MT-2, and MT-4

146 that the cationic polypeptide fraction of SP is active against HIV-1, and that semenogelin-derived pe

147 The APIs released in vitro and in vivo were active against HIV-1ADA-M, HSV-2, and HPV16 PsV in

148 The lexitropsins also were active against HIV-2 IN.

149 sting, we found that some of these compounds were active against HIV.

150 re are currently no specific antivirals that are active against HPVs.

151 The N-acetyl derivative 3 was also shown to be active against HRV serotypes 2, 16, and 89.

152 ty testing then resulted in three leads that were active against HsFPPS with IC50 values in the range

153 RC-2 was active against HSV-1 KOS in cultures and showed prot

154 None of the nucleosides were active against HSV-1.

155 family of antiviral cytidine deaminases that are active against human immunodeficiency virus, simian

156 esence of the active-site residue Ser-529 to be active against human PGHS-1; the S529A mutant is resi

157 We also demonstrated that the drug is active against human topoisomerase II by showing that

158 's cytotoxicity screen, compounds 11a and 12 were active against human cancer cell lines derived from

159 e heterocycles, but not the difluoro analog, were active against human cytomegalovirus (HCMV) (IC50's

160 TAS-103 is a novel antineoplastic agent that is active against in vivo tumor models.

161 is a need to find new chemical entities that are active against infections of T. brucei.

162 nsights as to how targeted dsRNAs in general are active against insects.

163 e-daily adefovir therapy reduces HIV RNA and is active against isolates resistant to lamivudine or la

164 The tricyclic nucleoside 12, was active against its target virus, human immunodeficie

165 We conclude that EXEL-0862 is active against KIT activation loop mutants and is a p

166 All of the hydroxylated analogues were active against L1210 cells with 96-h IC(50) values

167 To determine whether adefovir is active against lamivudine-resistant hepatitis B virus

168 Tenofovir disoproxil fumarate (TDF) is active against lamivudine-resistant hepatitis B virus

169 previous work predicted that Tdp1p would not be active against lesions involving Top2p.

170 sensitive cells, compounds 1-6 were found to be active against leukemia K562 cells with IC50 in the n

171 tomegalovirus and along with the Z-isomer 5a was active against leukemia L1210 and solid tumors in vi

172 Notably, the dasatinib/PD184352 regimen was active against leukemic cells exhibiting various for

173 ty, we identified purine-type compounds that were active against lung small cell lung cancer (NSCLC).

174 Methotrexate (MTX) is active against lymphomas, but transport or polyglutam

175 inhibitor of LepB (MD3; a beta-aminoketone) was active against M. tuberculosis, exhibiting growth in

176 se activity; these acyldepsipeptides (ADEPs) were active against M. tuberculosis.

177 some strain-specific anti-HIV cytokines, CAF is active against many different virus isolates, includi

178 re potent against BCR-ABL than imatinib, and is active against many imatinib-resistant BCR-ABL mutant

179 Minocycline intravenous is active against many MDR strains of Acinetobacter, and

180 In vitro, the enzyme is active against many serotypes of S. pneumoniae, indep

181 beta-ketoiminato complexes has been shown to be active against MCF-7 (human breast carcinoma), HT-29

182 ne repertoire of T cells and antibodies that are active against melanoma, with recent glimpses of the

183 e phosphatidylinositol phosphate kinase that is active against membrane-bound substrates.

184 tance with marketed antibacterial agents and is active against methicillin-resistant staphylococcus a

185 hat spirohexenolide A, a spirotetronate that is active against methicillin-resistant Staphylococcus a

186 Both toxins are active against mice when administered intracerebrove

187 Aplidin is active against MM cells in the presence of proliferat

188 to inhibit IspC in a number of organisms and is active against most gram-negative bacteria but not gr

189 Although vancomycin is active against MRSA, it does not effectively kill int

190 ophenyl)methylene]carbonimidic dihydrazide), was active against MRSA and VRE with MIC's of 8.1 and 4.

191 losis, are nontoxic to human cell lines, and are active against multidrug-resistant M. tuberculosis s

192 (2) developing and evaluating regimens that are active against multidrug-resistant organisms.

193 strategies should focus on antibiotics that are active against multidrug-resistant tuberculosis and

194 e/tazobactam, a novel antimicrobial therapy, is active against multidrug-resistant Pseudomonas aerugi

195 ries of c-Met small molecule inhibitors that are active against multiple mutants previously identifie

196 onstrate that four of these crystal proteins are active against multiple nematode species and that ea

197 ifficulties in creating a vaccine that would be active against multiple clades of HIV.

198 ce from disseminated candidiasis and that it is active against multiple virulent strains of C. albica

199 de (chlorosulfaquinoxaline, CQS, NSC 339004) is active against murine and human solid tumors.

200 ntify and design inhibitors that will likely be active against mutants found in different cancers.

201 it primary FLT3-mutant AML blast growth, and is active against mutations that confer resistance to cl

202 (PZA) to ammonia and pyrazinoic acid, which is active against Mycobacterium tuberculosis.

203 (e.g., thalidomide and lenalidomide), which are active against myeloma, also block the activity of b

204 h are structurally distinct from crizotinib, are active against NB cells expressing ALK(F1174L).

205 Topotecan is active against neuroblastoma when it is administered

206 after cyclophosphamide is a combination that is active against newly diagnosed RMS, with an acceptabl

207 bitory concentrations (MIC) against R-TB and were active against NRP-TB in the low micromolar range,

208 ot an acid sphingomyelinase but unexpectedly is active against nucleotide diphosphate and triphosphat

209 In contrast 29 and 31 were active against one or both of these viruses but act

210 ) while 5-nitroimidazoles like metronidazole are active against only anaerobic Mtb.

211 ic cyanobacterium Hassallia sp. and found to be active against opportunistic human pathogenic fungi.

212 ertain E. faecalis clinical isolates, and it is active against other E. faecalis strains.

213 We also found that auranofin is active against other Gram-positive bacteria, includin

214 everal previously identified RGS4 inhibitors were active against other RGS members, such as RGS14, wi

215 ive against C. neoformans, and the triazoles were active against other yeasts (MIC90, 2 mug/ml).

216 Levofloxacin, gentamicin, and tetracycline were active against oxacillin-susceptible staphylococci

217 ary results indicated that compounds 3 and 6 are active against P. berghei, prolonged the life span o

218 r, our findings indicate that 4 human sPLA2s are active against P. falciparum in vitro and pave the w

219 Single-dose phage therapy was active against P. aeruginosa EE and highly synergist

220 teryl linoleate and cholesteryl arachidonate were active against P. aeruginosa at physiological conce

221 zylamine 12a and alpha-methylbenzylamine 12g were active against P. falciparum with IC50 values in th

222 Although the 1,4-hydrazone was active against P388 leukemia in mice, it was inactiv

223 These compounds also were active against pathogenic Staphylococcus aureus .

224 Importantly, CpdA was active against patient-derived plasma cells and both

225 epper line over-expressing functional CaCel1 was active against pepper matrix glycans in vitro, and s

226 LyeTxI and LyeTxI/betaCD are active against periodontopathic bacteria, showing ra

227 r of DUSP1, encoding a dual phosphatase that is active against phospho-ERK.

228 ophobic and positively charged clusters that are active against plant and human pathogens.

229 enzene-1,3-diamine) (dihydrochloride), which is active against Plasmodium berghei in vivo (oral ID(50

230 The N-acyl-2-amino-4-chlorophenyl sulfides were active against Plasmodium falciparum.

231 ibitors (PIs) recently have been reported to be active against Pneumocystis carinii in cell culture.

232 ithromycin in combination with sulphonamides is active against Pneumocystis carinii pneumonia (PCP) i

233 Adoptive cellular therapy is active against posttransplantation relapse and lympho

234 Finally, we demonstrated that the prodrugs are active against primary chronic lymphocytic leukemia

235 ere we show that the PI3K inhibitor GDC-0941 is active against primary T-ALLs from wild-type and Kras

236 Complexes 1-8 are active against promastigotes of Leishmania major and

237 Many inhibitors have been identified that are active against purified viral-encoded integrase prot

238 To determine whether this regimen is active against quiescent G(0)/G(1) MM cells, cells we

239 Maraviroc, a CCR5 antagonist, is active against R5 but not X4 or dual- or mixed-tropic

240 otecan administered on a protracted schedule is active against recurrent FHWT.

241 zylguanidine ((131)I-MIBG) has been shown to be active against refractory neuroblastoma.

242 e-3-carboxamide derivatives, which proved to be active against replicating Mycobacterium tuberculosis

243 Most notably, they are active against resistant bacteria such as methicilli

244 ere is currently a dearth of new agents that are active against resistant bacterial species.

245 py, and the development of novel agents that are active against resistant forms of target proteins cr

246 es with modified side chains, such as AQ-13, are active against resistant parasites, we compared AQ-1

247 Two IgA MAbs (33G2 and 35H6) were active against ricin's lectin subunit (RTB), and tw

248 ue to its nuclear localization because SENP1 is active against sentrinized RanGAP1 in vitro.

249 novel propargyl-linked DHFR inhibitors that are active against several trimethoprim-resistant enzyme

250 Our data indicate that PD180970 is active against several Bcr-Abl mutations that are res

251 as been exploited as a biocontrol agent that is active against several insect pests.

252 72) inhibits 1,3-beta-d-glucan synthesis and is active against several medically important fungi but

253 Azithromycin is a macrolide antibiotic that is active against several periodontal pathogens.

254 (IL-12) is an immunomodulatory cytokine that is active against several viruses.

255 ME1 and ME2 were active against several fungi, including Pythium irr

256 We found that M2-S31N inhibitors were active against several influenza A viruses that are

257 atives showed rapid bactericidal killing and were active against several multidrug-resistant (MDR) Gr

258 APOBEC3F was found to be active against SIV and sensitive to SIV(mac) Vif.

259 SJG-136 was active against small (150 mg) and large (250-400 mg)

260 otherapeutic agents has been identified that are active against solid tumors.

261 oreover, both phenanthrene-based derivatives were active against stage IV/V gametocytes of P. falcipa

262 The most potent leads are active against Staphylococcus aureus [minimal inhibi

263 Compound 1a was active against Staphylococcus aureus in mice (iv) an

264 ROAD-1 was active against Staphylococcus aureus, Escherichia co

265 orary naturally infected cattle in Botswana) were active against strain M375 in an in vitro growth in

266 licin M-like bacteriocin, pectocin M2, which is active against strains of Pectobacterium spp.

267 eriophages and the first virus documented to be active against streptococci.

268 receptors on the surface of mammalian cells, is active against T. gondii tachyzoites (50% effective c

269 otency of PC-1505 was sustained, and PC-1505 was active against T-20-resistant ("DIV") virus with a G

270 l-cell fusion and live virus replication and was active against T20 resistant strains.

271 and under development will almost certainly be active against the pandemic variant.

272 ine/adenosine analogues to remain intact and be active against the parasite, they need to either be r

273 Importantly, compound 12 was found to be active against the tested XDR-TB strains and orally a

274 Since the prompt institution of therapy that is active against the causative pathogen is one of the m

275 eftaroline is a new antibacterial agent that is active against the major bacterial pathogens found in

276 t/Km) is the main function of enzyme when it is active against the specific substrate.

277 e specific helicase inhibitors (compound 17) was active against the replicon and inhibited the helica

278 The compound was active against the three major schistosome species i

279 Quinolones were active against the bacterial enteropathogens in the

280 Tetrahydro-beta-carboline-3-carboxylic acids were active against the hydroxylation of 2'-deoxyguanosi

281 alpha-lyxose and 5-deoxy-alpha-lyxose series were active against the Towne strain of HCMV.

282 rug therapies and to discover new drugs that are active against these organisms.

283 nstructural protein 5A (NS5A) inhibitor that is active against these genotypes, improves efficacy and

284 TFO-5a was active against this target and inactive against the

285 All these compounds were active against three strains of gametocytes with di

286 CB2 was active against tOspB of strain B31, but not against

287 Most of the samples were active against Trypanosoma b.

288 acid, in addition to inhibiting osteoclasts, is active against tumor cells and suggest that zoledroni

289 RETRA is active against tumor cells expressing a variety of p5

290 The polyamide was active against two enzalutamide-resistant xenografts

291 was observed for compounds 2 and 5-9, but 4 was active against two herpes viruses and cytotoxic in t

292 , and when expressed in Escherichia coli, it is active against tyrosine and to a lesser extent agains

293 d glycopeptides with hydrophobic side chains are active against vancomycin-resistant enterococci and

294 ne derivatives, three compounds are found to be active against vancomycin and methicillin-resistant S

295 Acylated GPI-PLC was active against variant surface glycoprotein (VSG).

296 Pronucleotide 7a was active against varicella zoster virus with EC(50) 6.

297 Cytosine and thymine Z-isomers 11c and 11d were active against varicella zoster virus (VZV) with EC

298 While Mx2 is active against vesicular stomatitis virus (VSV), Mx3

299 AM7 is active against wild-type c-Met as well as several mut

300 nt screens, the most potent compound 9 (1C8) was active against wild-type HIV-1IIIB (subtype B, X4-tr