Assay ID | Title | Year | Journal | Article |
AID245079 | Minimum inhibitory concentration against Streptococcus pyogenes 930 (erythromycin-resistant strain) | 2005 | Bioorganic & medicinal chemistry letters, May-16, Volume: 15, Issue:10
| Design, synthesis and structure-activity relationships of 6-O-arylpropargyl diazalides with potent activity against multidrug-resistant Streptococcus pneumoniae. |
AID518962 | Induction of erm(C) expression in Escherichia coli JM109 harboring Staphylococcus aureus erm(C)-containing pERMZ7 lacking codons 2 to 4 with additional mutations leader peptide cistrons reporter plasmid at 25 mg/ml after 36 hrs at 37 degC by disc-based be | 2008 | Antimicrobial agents and chemotherapy, Mar, Volume: 52, Issue:3
| Induction of erm(C) expression by noninducing antibiotics. |
AID206748 | In vitro antibacterial activity against Staphylococcus aureus strain A 5278. | 2000 | Journal of medicinal chemistry, Mar-23, Volume: 43, Issue:6
| Design, synthesis, and antimicrobial activity of 6-O-substituted ketolides active against resistant respiratory tract pathogens. |
AID1169031 | Antibacterial activity against efflux-resistant Streptococcus pneumoniae by agar microdilution method | 2014 | ACS medicinal chemistry letters, Oct-09, Volume: 5, Issue:10
| Synthesis and Structure-Activity Relationships of α-Amino-γ-lactone Ketolides: A Novel Class of Macrolide Antibiotics. |
AID208288 | Minimum inhibitory concentration against Streptococcus pneumoniae 5649 efflux | 2001 | Journal of medicinal chemistry, Nov-22, Volume: 44, Issue:24
| Novel erythromycin derivatives with aryl groups tethered to the C-6 position are potent protein synthesis inhibitors and active against multidrug-resistant respiratory pathogens. |
AID1169029 | Antibacterial activity against erythromycin-susceptible Streptococcus pneumoniae by agar microdilution method | 2014 | ACS medicinal chemistry letters, Oct-09, Volume: 5, Issue:10
| Synthesis and Structure-Activity Relationships of α-Amino-γ-lactone Ketolides: A Novel Class of Macrolide Antibiotics. |
AID1169035 | Antibacterial activity against Haemophilus influenzae by agar microdilution method | 2014 | ACS medicinal chemistry letters, Oct-09, Volume: 5, Issue:10
| Synthesis and Structure-Activity Relationships of α-Amino-γ-lactone Ketolides: A Novel Class of Macrolide Antibiotics. |
AID1278826 | Antibacterial activity against constitutive macrolide-lincosamide-streptogramin B resistant Streptococcus pneumoniae by agar microdilution method | 2016 | Bioorganic & medicinal chemistry, Mar-15, Volume: 24, Issue:6
| Synthesis and antibacterial evaluation of novel 4″-glycyl linked quinolyl-azithromycins with potent activity against macrolide-resistant pathogens. |
AID499558 | Antibacterial activity against constitutive macrolide-lincosamide-streptogramin B-resistant Streptococcus pyogenes B0544 by agar microdilution method | 2010 | Journal of medicinal chemistry, Aug-12, Volume: 53, Issue:15
| Synthesis and structure-activity relationships of novel 8a-aza-8a-homoerythromycin A ketolides. |
AID1459110 | Antibacterial activity against inducibly macrolide/lincosamide/streptogramin B-resistant Staphylococcus aureus by agar microdilution method | 2017 | European journal of medicinal chemistry, Jan-05, Volume: 125 | Synthesis of novel 15-membered 8a-azahomoerythromycin A acylides: Consequences of structural modification at the C-3 and C-6 position on antibacterial activity. |
AID518966 | Induction of erm(C) expression in Escherichia coli JM109 harboring Staphylococcus aureus erm(C)-containing pERMZalpha reporter plasmid after 36 hrs at 37 degC by disc-based beta-galactosidase reporter gene assay | 2008 | Antimicrobial agents and chemotherapy, Mar, Volume: 52, Issue:3
| Induction of erm(C) expression by noninducing antibiotics. |
AID499560 | Antibacterial activity against Moraxella catarrhalis B0324 by agar microdilution method | 2010 | Journal of medicinal chemistry, Aug-12, Volume: 53, Issue:15
| Synthesis and structure-activity relationships of novel 8a-aza-8a-homoerythromycin A ketolides. |
AID642863 | Antibacterial activity against efflux mediated macrolide resistant Streptococcus pyogenes by agar microdilution method | 2011 | ACS medicinal chemistry letters, May-12, Volume: 2, Issue:5
| Discovery of 4''-ether linked azithromycin-quinolone hybrid series: influence of the central linker on the antibacterial activity. |
AID1278829 | Antibacterial activity against inducibly macrolide-lincosamide-streptogramin B resistant Streptococcus pyogenes by agar microdilution method | 2016 | Bioorganic & medicinal chemistry, Mar-15, Volume: 24, Issue:6
| Synthesis and antibacterial evaluation of novel 4″-glycyl linked quinolyl-azithromycins with potent activity against macrolide-resistant pathogens. |
AID210221 | In vitro antibacterial activity against Streptococcus pneumoniae 5979 (MLSB resistant stain bearing an erm (B) gene) | 2004 | Bioorganic & medicinal chemistry letters, Jul-16, Volume: 14, Issue:14
| Synthesis and antibacterial activity of novel bifunctional macrolides. |
AID210389 | In vitro antibacterial activity against Streptococcus pneumoniae strain ATCC 6303. | 2000 | Journal of medicinal chemistry, Mar-23, Volume: 43, Issue:6
| Design, synthesis, and antimicrobial activity of 6-O-substituted ketolides active against resistant respiratory tract pathogens. |
AID642857 | Antibacterial activity against erythromycin-susceptible Streptococcus pneumoniae by agar microdilution method | 2011 | ACS medicinal chemistry letters, May-12, Volume: 2, Issue:5
| Discovery of 4''-ether linked azithromycin-quinolone hybrid series: influence of the central linker on the antibacterial activity. |
AID209608 | In vitro antibacterial activity against Streptococcus pyogenes strain EES 61. | 2000 | Journal of medicinal chemistry, Mar-23, Volume: 43, Issue:6
| Design, synthesis, and antimicrobial activity of 6-O-substituted ketolides active against resistant respiratory tract pathogens. |
AID499552 | Antibacterial activity against efflux-resistant Staphylococcus aureus B0331 by agar microdilution method | 2010 | Journal of medicinal chemistry, Aug-12, Volume: 53, Issue:15
| Synthesis and structure-activity relationships of novel 8a-aza-8a-homoerythromycin A ketolides. |
AID209609 | In vitro antibacterial activity against Streptococcus pyogenes strain PIU 2548. | 2000 | Journal of medicinal chemistry, Mar-23, Volume: 43, Issue:6
| Design, synthesis, and antimicrobial activity of 6-O-substituted ketolides active against resistant respiratory tract pathogens. |
AID674452 | Antibacterial activity against macrolide-susceptible Staphylococcus aureus ATCC 29213 | 2012 | Bioorganic & medicinal chemistry letters, Jul-15, Volume: 22, Issue:14
| Synthesis and antibacterial activity of desosamine-modified macrolide derivatives. |
AID539514 | Antibacterial activity against Haemophilus influenzae B0529 by agar microdilution method | 2010 | Bioorganic & medicinal chemistry, Dec-15, Volume: 18, Issue:24
| Novel hybrids of 15-membered 8a- and 9a-azahomoerythromycin A ketolides and quinolones as potent antibacterials. |
AID539504 | Antibacterial activity against efflux-resistant Streptococcus pneumoniae B0326 by agar microdilution method | 2010 | Bioorganic & medicinal chemistry, Dec-15, Volume: 18, Issue:24
| Novel hybrids of 15-membered 8a- and 9a-azahomoerythromycin A ketolides and quinolones as potent antibacterials. |
AID674453 | Antibacterial activity against macrolide-resistant Staphylococcus aureus ATCC 33591 constitutively expressing ermA | 2012 | Bioorganic & medicinal chemistry letters, Jul-15, Volume: 22, Issue:14
| Synthesis and antibacterial activity of desosamine-modified macrolide derivatives. |
AID1459107 | Antibacterial activity against constitutively macrolide/lincosamide/streptogramin B-resistant Streptococcus pyogenes by agar microdilution method | 2017 | European journal of medicinal chemistry, Jan-05, Volume: 125 | Synthesis of novel 15-membered 8a-azahomoerythromycin A acylides: Consequences of structural modification at the C-3 and C-6 position on antibacterial activity. |
AID539503 | Antibacterial activity against erythromycin A-susceptible Streptococcus pyogenes B0542 by agar microdilution method | 2010 | Bioorganic & medicinal chemistry, Dec-15, Volume: 18, Issue:24
| Novel hybrids of 15-membered 8a- and 9a-azahomoerythromycin A ketolides and quinolones as potent antibacterials. |
AID1278828 | Antibacterial activity against erythromycin-susceptible Streptococcus pyogenes by agar microdilution method | 2016 | Bioorganic & medicinal chemistry, Mar-15, Volume: 24, Issue:6
| Synthesis and antibacterial evaluation of novel 4″-glycyl linked quinolyl-azithromycins with potent activity against macrolide-resistant pathogens. |
AID245078 | Minimum inhibitory concentration against Staphylococcus aureus A5177 (erythromycin-resistant strain | 2005 | Bioorganic & medicinal chemistry letters, May-16, Volume: 15, Issue:10
| Design, synthesis and structure-activity relationships of 6-O-arylpropargyl diazalides with potent activity against multidrug-resistant Streptococcus pneumoniae. |
AID86120 | In vitro antibacterial activity against Haemophilus influenzae strain DILL. | 2000 | Journal of medicinal chemistry, Mar-23, Volume: 43, Issue:6
| Design, synthesis, and antimicrobial activity of 6-O-substituted ketolides active against resistant respiratory tract pathogens. |
AID642859 | Antibacterial activity against efflux mediated macrolide resistant Streptococcus pneumoniae by agar microdilution method | 2011 | ACS medicinal chemistry letters, May-12, Volume: 2, Issue:5
| Discovery of 4''-ether linked azithromycin-quinolone hybrid series: influence of the central linker on the antibacterial activity. |
AID1169028 | Antibacterial activity against macrolide lincosamide- streptogramin B-resistant Staphylococcus aureus by agar microdilution method | 2014 | ACS medicinal chemistry letters, Oct-09, Volume: 5, Issue:10
| Synthesis and Structure-Activity Relationships of α-Amino-γ-lactone Ketolides: A Novel Class of Macrolide Antibiotics. |
AID539502 | Antibacterial activity against inducible macrolide-lincosamide-streptogramin B-resistant Streptococcus pyogenes B0543 by agar microdilution method | 2010 | Bioorganic & medicinal chemistry, Dec-15, Volume: 18, Issue:24
| Novel hybrids of 15-membered 8a- and 9a-azahomoerythromycin A ketolides and quinolones as potent antibacterials. |
AID1459115 | Antibacterial activity against Mef-mediated macrolide efflux resistant Streptococcus pyogenes by agar microdilution method | 2017 | European journal of medicinal chemistry, Jan-05, Volume: 125 | Synthesis of novel 15-membered 8a-azahomoerythromycin A acylides: Consequences of structural modification at the C-3 and C-6 position on antibacterial activity. |
AID206298 | In vitro antibacterial activity against Staphylococcus aureus NCTC 10649 (erythromycin-susceptible strain) | 2004 | Bioorganic & medicinal chemistry letters, Jul-16, Volume: 14, Issue:14
| Synthesis and antibacterial activity of novel bifunctional macrolides. |
AID1549405 | Inhibition of CYP3A4 (unknown origin) | 2019 | European journal of medicinal chemistry, May-01, Volume: 169 | Design, synthesis and structure-activity relationships of novel macrolones: Hybrids of 2-fluoro 9-oxime ketolides and carbamoyl quinolones with highly improved activity against resistant pathogens. |
AID499550 | Antibacterial activity against inducible macrolide-lincosamide-streptogramin B-resistant Staphylococcus aureus B0538 by agar microdilution method | 2010 | Journal of medicinal chemistry, Aug-12, Volume: 53, Issue:15
| Synthesis and structure-activity relationships of novel 8a-aza-8a-homoerythromycin A ketolides. |
AID210388 | In vitro antibacterial activity against Streptococcus pneumoniae strain 5737. | 2000 | Journal of medicinal chemistry, Mar-23, Volume: 43, Issue:6
| Design, synthesis, and antimicrobial activity of 6-O-substituted ketolides active against resistant respiratory tract pathogens. |
AID499549 | Antibacterial activity against erythromycin A-resistant Staphylococcus aureus B0329 by agar microdilution method | 2010 | Journal of medicinal chemistry, Aug-12, Volume: 53, Issue:15
| Synthesis and structure-activity relationships of novel 8a-aza-8a-homoerythromycin A ketolides. |
AID1278823 | Antibacterial activity against constitutive macrolide-lincosamide-streptogramin B resistant Staphylococcus aureus by agar microdilution method | 2016 | Bioorganic & medicinal chemistry, Mar-15, Volume: 24, Issue:6
| Synthesis and antibacterial evaluation of novel 4″-glycyl linked quinolyl-azithromycins with potent activity against macrolide-resistant pathogens. |
AID155562 | Minimum inhibitory concentration against Streptococcus pyogenes PIU2548 efflux | 2001 | Journal of medicinal chemistry, Nov-22, Volume: 44, Issue:24
| Novel erythromycin derivatives with aryl groups tethered to the C-6 position are potent protein synthesis inhibitors and active against multidrug-resistant respiratory pathogens. |
AID1459116 | Antibacterial activity against Haemophilus influenzae by agar microdilution method | 2017 | European journal of medicinal chemistry, Jan-05, Volume: 125 | Synthesis of novel 15-membered 8a-azahomoerythromycin A acylides: Consequences of structural modification at the C-3 and C-6 position on antibacterial activity. |
AID642852 | Antibacterial activity against ciprofloxacin-resistant Staphylococcus aureus by agar microdilution method | 2011 | ACS medicinal chemistry letters, May-12, Volume: 2, Issue:5
| Discovery of 4''-ether linked azithromycin-quinolone hybrid series: influence of the central linker on the antibacterial activity. |
AID206750 | In vitro antibacterial activity against Staphylococcus aureus strain ATCC 6538P. | 2000 | Journal of medicinal chemistry, Mar-23, Volume: 43, Issue:6
| Design, synthesis, and antimicrobial activity of 6-O-substituted ketolides active against resistant respiratory tract pathogens. |
AID642855 | Antibacterial activity against constitutive MLS resistant Staphylococcus aureus by agar microdilution method | 2011 | ACS medicinal chemistry letters, May-12, Volume: 2, Issue:5
| Discovery of 4''-ether linked azithromycin-quinolone hybrid series: influence of the central linker on the antibacterial activity. |
AID1459108 | Antibacterial activity against constitutively macrolide/lincosamide/streptogramin B-resistant Streptococcus pneumoniae by agar microdilution method | 2017 | European journal of medicinal chemistry, Jan-05, Volume: 125 | Synthesis of novel 15-membered 8a-azahomoerythromycin A acylides: Consequences of structural modification at the C-3 and C-6 position on antibacterial activity. |
AID1278822 | Antibacterial activity against inducibly macrolide-lincosamide-streptogramin B resistant Staphylococcus aureus by agar microdilution method | 2016 | Bioorganic & medicinal chemistry, Mar-15, Volume: 24, Issue:6
| Synthesis and antibacterial evaluation of novel 4″-glycyl linked quinolyl-azithromycins with potent activity against macrolide-resistant pathogens. |
AID642858 | Antibacterial activity against constitutive MLS resistant Streptococcus pneumoniae by agar microdilution method | 2011 | ACS medicinal chemistry letters, May-12, Volume: 2, Issue:5
| Discovery of 4''-ether linked azithromycin-quinolone hybrid series: influence of the central linker on the antibacterial activity. |
AID539510 | Antibacterial activity against erythromycin A-susceptible Staphylococcus aureus B0329 by agar microdilution method | 2010 | Bioorganic & medicinal chemistry, Dec-15, Volume: 18, Issue:24
| Novel hybrids of 15-membered 8a- and 9a-azahomoerythromycin A ketolides and quinolones as potent antibacterials. |
AID642862 | Antibacterial activity against constitutive MLS resistant Streptococcus pyogenes by agar microdilution method | 2011 | ACS medicinal chemistry letters, May-12, Volume: 2, Issue:5
| Discovery of 4''-ether linked azithromycin-quinolone hybrid series: influence of the central linker on the antibacterial activity. |
AID208290 | Minimum inhibitory concentration against Streptococcus pneumoniae ATCC 6303 Ery-S | 2001 | Journal of medicinal chemistry, Nov-22, Volume: 44, Issue:24
| Novel erythromycin derivatives with aryl groups tethered to the C-6 position are potent protein synthesis inhibitors and active against multidrug-resistant respiratory pathogens. |
AID53775 | Minimum inhibitory concentration against Haemophilus influenzae DILL Amp-R | 2001 | Journal of medicinal chemistry, Nov-22, Volume: 44, Issue:24
| Novel erythromycin derivatives with aryl groups tethered to the C-6 position are potent protein synthesis inhibitors and active against multidrug-resistant respiratory pathogens. |
AID1278821 | Antibacterial activity against erythromycin-susceptible Staphylococcus aureus by agar microdilution method | 2016 | Bioorganic & medicinal chemistry, Mar-15, Volume: 24, Issue:6
| Synthesis and antibacterial evaluation of novel 4″-glycyl linked quinolyl-azithromycins with potent activity against macrolide-resistant pathogens. |
AID1278832 | Antibacterial activity against Haemophilus influenzae by agar microdilution method | 2016 | Bioorganic & medicinal chemistry, Mar-15, Volume: 24, Issue:6
| Synthesis and antibacterial evaluation of novel 4″-glycyl linked quinolyl-azithromycins with potent activity against macrolide-resistant pathogens. |
AID1459111 | Antibacterial activity against constitutively macrolide/lincosamide/streptogramin B-resistant Staphylococcus aureus by agar microdilution method | 2017 | European journal of medicinal chemistry, Jan-05, Volume: 125 | Synthesis of novel 15-membered 8a-azahomoerythromycin A acylides: Consequences of structural modification at the C-3 and C-6 position on antibacterial activity. |
AID518975 | Induction of erm(C) expression in Escherichia coli ZK796 harboring Staphylococcus aureus erm(C)-containing pERMCT plasmid assessed as increase in A2058 dimethylation in 23S rRNA at 25% MIC after 4 hrs by primer extension assay | 2008 | Antimicrobial agents and chemotherapy, Mar, Volume: 52, Issue:3
| Induction of erm(C) expression by noninducing antibiotics. |
AID539513 | Antibacterial activity against Moraxella catarrhalis B0324 by agar microdilution method | 2010 | Bioorganic & medicinal chemistry, Dec-15, Volume: 18, Issue:24
| Novel hybrids of 15-membered 8a- and 9a-azahomoerythromycin A ketolides and quinolones as potent antibacterials. |
AID499561 | Antibacterial activity against Haemophilus influenzae B0529 by agar microdilution method | 2010 | Journal of medicinal chemistry, Aug-12, Volume: 53, Issue:15
| Synthesis and structure-activity relationships of novel 8a-aza-8a-homoerythromycin A ketolides. |
AID1169032 | Antibacterial activity against erythromycin-susceptible Streptococcus pyogenes by agar microdilution method | 2014 | ACS medicinal chemistry letters, Oct-09, Volume: 5, Issue:10
| Synthesis and Structure-Activity Relationships of α-Amino-γ-lactone Ketolides: A Novel Class of Macrolide Antibiotics. |
AID210387 | In vitro antibacterial activity against Streptococcus pneumoniae strain 5649. | 2000 | Journal of medicinal chemistry, Mar-23, Volume: 43, Issue:6
| Design, synthesis, and antimicrobial activity of 6-O-substituted ketolides active against resistant respiratory tract pathogens. |
AID674454 | Ratio of MIC for macrolide-resistant Staphylococcus aureus ATCC 33591 to MIC for macrolide-susceptible Staphylococcus aureus ATCC 29213 | 2012 | Bioorganic & medicinal chemistry letters, Jul-15, Volume: 22, Issue:14
| Synthesis and antibacterial activity of desosamine-modified macrolide derivatives. |
AID1169026 | Antibacterial activity against erythromycin-susceptible Staphylococcus aureus by agar microdilution method | 2014 | ACS medicinal chemistry letters, Oct-09, Volume: 5, Issue:10
| Synthesis and Structure-Activity Relationships of α-Amino-γ-lactone Ketolides: A Novel Class of Macrolide Antibiotics. |
AID245232 | Minimum inhibitory concentration against Streptococcus pneumoniae ATCC 6303 (erythromycin-susceptible strain) | 2005 | Bioorganic & medicinal chemistry letters, May-16, Volume: 15, Issue:10
| Design, synthesis and structure-activity relationships of 6-O-arylpropargyl diazalides with potent activity against multidrug-resistant Streptococcus pneumoniae. |
AID499553 | Antibacterial activity against erythromycin A-resistant Streptococcus pneumoniae B0541 by agar microdilution method | 2010 | Journal of medicinal chemistry, Aug-12, Volume: 53, Issue:15
| Synthesis and structure-activity relationships of novel 8a-aza-8a-homoerythromycin A ketolides. |
AID518973 | Antimicrobial activity against Escherichia coli ZK796 harboring empty plasmid | 2008 | Antimicrobial agents and chemotherapy, Mar, Volume: 52, Issue:3
| Induction of erm(C) expression by noninducing antibiotics. |
AID539508 | Antibacterial activity against constitutive macrolide-lincosamide-streptogramin B-resistant Staphylococcus aureus B0330 by agar microdilution method | 2010 | Bioorganic & medicinal chemistry, Dec-15, Volume: 18, Issue:24
| Novel hybrids of 15-membered 8a- and 9a-azahomoerythromycin A ketolides and quinolones as potent antibacterials. |
AID1169033 | Antibacterial activity against macrolide lincosamide- streptogramin B inducibly-resistant Streptococcus pyogenes by agar microdilution method | 2014 | ACS medicinal chemistry letters, Oct-09, Volume: 5, Issue:10
| Synthesis and Structure-Activity Relationships of α-Amino-γ-lactone Ketolides: A Novel Class of Macrolide Antibiotics. |
AID131225 | Mouse protection tests for effective dose against Staphylococcus aureus 10649 ((erythromycin susceptible strain)) infected mice | 2001 | Journal of medicinal chemistry, Nov-22, Volume: 44, Issue:24
| Novel erythromycin derivatives with aryl groups tethered to the C-6 position are potent protein synthesis inhibitors and active against multidrug-resistant respiratory pathogens. |
AID8441 | Minimum inhibitory concentration against Streptococcus pyogenes 930MLSB | 2001 | Journal of medicinal chemistry, Nov-22, Volume: 44, Issue:24
| Novel erythromycin derivatives with aryl groups tethered to the C-6 position are potent protein synthesis inhibitors and active against multidrug-resistant respiratory pathogens. |
AID539512 | Antibacterial activity against efflux-resistant Streptococcus pyogenes B0545 by agar microdilution method | 2010 | Bioorganic & medicinal chemistry, Dec-15, Volume: 18, Issue:24
| Novel hybrids of 15-membered 8a- and 9a-azahomoerythromycin A ketolides and quinolones as potent antibacterials. |
AID518974 | Antimicrobial activity against Escherichia coli ZK796 harboring Staphylococcus aureus erm(C)-containing pERMCT plasmid | 2008 | Antimicrobial agents and chemotherapy, Mar, Volume: 52, Issue:3
| Induction of erm(C) expression by noninducing antibiotics. |
AID499559 | Antibacterial activity against efflux-resistant Streptococcus pyogenes B0545 by agar microdilution method | 2010 | Journal of medicinal chemistry, Aug-12, Volume: 53, Issue:15
| Synthesis and structure-activity relationships of novel 8a-aza-8a-homoerythromycin A ketolides. |
AID1278825 | Antibacterial activity against erythromycin-susceptible Streptococcus pneumoniae by agar microdilution method | 2016 | Bioorganic & medicinal chemistry, Mar-15, Volume: 24, Issue:6
| Synthesis and antibacterial evaluation of novel 4″-glycyl linked quinolyl-azithromycins with potent activity against macrolide-resistant pathogens. |
AID210219 | In vitro antibacterial activity against Streptococcus pneumoniae 5649 (efflux-resistant strain bearing a mef (E) gene) | 2004 | Bioorganic & medicinal chemistry letters, Jul-16, Volume: 14, Issue:14
| Synthesis and antibacterial activity of novel bifunctional macrolides. |
AID1459109 | Antibacterial activity against erythromycin susceptible Streptococcus pneumoniae by agar microdilution method | 2017 | European journal of medicinal chemistry, Jan-05, Volume: 125 | Synthesis of novel 15-membered 8a-azahomoerythromycin A acylides: Consequences of structural modification at the C-3 and C-6 position on antibacterial activity. |
AID1169034 | Antibacterial activity against efflux-resistant Streptococcus pyogenes by agar microdilution method | 2014 | ACS medicinal chemistry letters, Oct-09, Volume: 5, Issue:10
| Synthesis and Structure-Activity Relationships of α-Amino-γ-lactone Ketolides: A Novel Class of Macrolide Antibiotics. |
AID1278824 | Antibacterial activity against efflux mediated macrolide resistant Staphylococcus aureus by agar microdilution method | 2016 | Bioorganic & medicinal chemistry, Mar-15, Volume: 24, Issue:6
| Synthesis and antibacterial evaluation of novel 4″-glycyl linked quinolyl-azithromycins with potent activity against macrolide-resistant pathogens. |
AID245131 | Minimum inhibitory concentration against Streptococcus pyogenes EES61 (erythromycin-susceptible strain) | 2005 | Bioorganic & medicinal chemistry letters, May-16, Volume: 15, Issue:10
| Design, synthesis and structure-activity relationships of 6-O-arylpropargyl diazalides with potent activity against multidrug-resistant Streptococcus pneumoniae. |
AID1278833 | Antibacterial activity against Moraxella catarrhalis by agar microdilution method | 2016 | Bioorganic & medicinal chemistry, Mar-15, Volume: 24, Issue:6
| Synthesis and antibacterial evaluation of novel 4″-glycyl linked quinolyl-azithromycins with potent activity against macrolide-resistant pathogens. |
AID1459114 | Antibacterial activity against erythromycin susceptible Staphylococcus aureus by agar microdilution method | 2017 | European journal of medicinal chemistry, Jan-05, Volume: 125 | Synthesis of novel 15-membered 8a-azahomoerythromycin A acylides: Consequences of structural modification at the C-3 and C-6 position on antibacterial activity. |
AID642856 | Antibacterial activity against efflux mediated macrolide resistant Staphylococcus aureus by agar microdilution method | 2011 | ACS medicinal chemistry letters, May-12, Volume: 2, Issue:5
| Discovery of 4''-ether linked azithromycin-quinolone hybrid series: influence of the central linker on the antibacterial activity. |
AID8627 | Minimum inhibitory concentration against Staphylococcus aureus A 5177 MLSB-i | 2001 | Journal of medicinal chemistry, Nov-22, Volume: 44, Issue:24
| Novel erythromycin derivatives with aryl groups tethered to the C-6 position are potent protein synthesis inhibitors and active against multidrug-resistant respiratory pathogens. |
AID539509 | Antibacterial activity against inducible macrolide-lincosamide-streptogramin B-resistant Staphylococcus aureus B0538 by agar microdilution method | 2010 | Bioorganic & medicinal chemistry, Dec-15, Volume: 18, Issue:24
| Novel hybrids of 15-membered 8a- and 9a-azahomoerythromycin A ketolides and quinolones as potent antibacterials. |
AID208280 | Minimum inhibitory concentration against Streptococcus pneumoniae 6303 (erythromycin susceptible strain) | 2001 | Journal of medicinal chemistry, Nov-22, Volume: 44, Issue:24
| Novel erythromycin derivatives with aryl groups tethered to the C-6 position are potent protein synthesis inhibitors and active against multidrug-resistant respiratory pathogens. |
AID245097 | Minimum inhibitory concentration against Staphylococcus aureus 6538P (erythromycin-susceptible strain) | 2005 | Bioorganic & medicinal chemistry letters, May-16, Volume: 15, Issue:10
| Design, synthesis and structure-activity relationships of 6-O-arylpropargyl diazalides with potent activity against multidrug-resistant Streptococcus pneumoniae. |
AID642860 | Antibacterial activity against erythromycin-susceptible Streptococcus pyogenes by agar microdilution method | 2011 | ACS medicinal chemistry letters, May-12, Volume: 2, Issue:5
| Discovery of 4''-ether linked azithromycin-quinolone hybrid series: influence of the central linker on the antibacterial activity. |
AID209607 | In vitro antibacterial activity against Streptococcus pyogenes strain 930. | 2000 | Journal of medicinal chemistry, Mar-23, Volume: 43, Issue:6
| Design, synthesis, and antimicrobial activity of 6-O-substituted ketolides active against resistant respiratory tract pathogens. |
AID1459113 | Antibacterial activity against Mef-mediated macrolide efflux resistant Streptococcus pneumoniae by agar microdilution method | 2017 | European journal of medicinal chemistry, Jan-05, Volume: 125 | Synthesis of novel 15-membered 8a-azahomoerythromycin A acylides: Consequences of structural modification at the C-3 and C-6 position on antibacterial activity. |
AID206747 | In vitro antibacterial activity against Staphylococcus aureus strain A 5177. | 2000 | Journal of medicinal chemistry, Mar-23, Volume: 43, Issue:6
| Design, synthesis, and antimicrobial activity of 6-O-substituted ketolides active against resistant respiratory tract pathogens. |
AID499555 | Antibacterial activity against efflux-resistant Streptococcus pneumoniae B0326 by agar microdilution method | 2010 | Journal of medicinal chemistry, Aug-12, Volume: 53, Issue:15
| Synthesis and structure-activity relationships of novel 8a-aza-8a-homoerythromycin A ketolides. |
AID499557 | Antibacterial activity against inducible macrolide-lincosamide-streptogramin B-resistant Streptococcus pyogenes B0543 by agar microdilution method | 2010 | Journal of medicinal chemistry, Aug-12, Volume: 53, Issue:15
| Synthesis and structure-activity relationships of novel 8a-aza-8a-homoerythromycin A ketolides. |
AID642853 | Antibacterial activity against erythromycin-susceptible Staphylococcus aureus by agar microdilution method | 2011 | ACS medicinal chemistry letters, May-12, Volume: 2, Issue:5
| Discovery of 4''-ether linked azithromycin-quinolone hybrid series: influence of the central linker on the antibacterial activity. |
AID206282 | In vitro antibacterial activity against Staphylococcus aureus 1775 (methicillin-resistant strain(MRSA)) | 2004 | Bioorganic & medicinal chemistry letters, Jul-16, Volume: 14, Issue:14
| Synthesis and antibacterial activity of novel bifunctional macrolides. |
AID642865 | Antibacterial activity against Moraxella catarrhalis by agar microdilution method | 2011 | ACS medicinal chemistry letters, May-12, Volume: 2, Issue:5
| Discovery of 4''-ether linked azithromycin-quinolone hybrid series: influence of the central linker on the antibacterial activity. |
AID1278831 | Antibacterial activity against efflux mediated macrolide resistant Streptococcus pyogenes by agar microdilution method | 2016 | Bioorganic & medicinal chemistry, Mar-15, Volume: 24, Issue:6
| Synthesis and antibacterial evaluation of novel 4″-glycyl linked quinolyl-azithromycins with potent activity against macrolide-resistant pathogens. |
AID539511 | Antibacterial activity against constitutive macrolide-lincosamide-streptogramin B-resistant Streptococcus pyogenes B0544 by agar microdilution method | 2010 | Bioorganic & medicinal chemistry, Dec-15, Volume: 18, Issue:24
| Novel hybrids of 15-membered 8a- and 9a-azahomoerythromycin A ketolides and quinolones as potent antibacterials. |
AID642864 | Antibacterial activity against Haemophilus influenzae B0529 by agar microdilution method | 2011 | ACS medicinal chemistry letters, May-12, Volume: 2, Issue:5
| Discovery of 4''-ether linked azithromycin-quinolone hybrid series: influence of the central linker on the antibacterial activity. |
AID67271 | Minimum inhibitory concentration against Streptococcus pyogenes EES 61 Ery-S | 2001 | Journal of medicinal chemistry, Nov-22, Volume: 44, Issue:24
| Novel erythromycin derivatives with aryl groups tethered to the C-6 position are potent protein synthesis inhibitors and active against multidrug-resistant respiratory pathogens. |
AID642861 | Antibacterial activity against Streptococcus pyogenes with inducible resistance to MLS by agar microdilution method | 2011 | ACS medicinal chemistry letters, May-12, Volume: 2, Issue:5
| Discovery of 4''-ether linked azithromycin-quinolone hybrid series: influence of the central linker on the antibacterial activity. |
AID85978 | In vitro antibacterial activity against Haemophilus influenzae GYR1435 (fully susceptible strain) | 2004 | Bioorganic & medicinal chemistry letters, Jul-16, Volume: 14, Issue:14
| Synthesis and antibacterial activity of novel bifunctional macrolides. |
AID8629 | Minimum inhibitory concentration against Staphylococcus aureus A 5278 MLSB-c | 2001 | Journal of medicinal chemistry, Nov-22, Volume: 44, Issue:24
| Novel erythromycin derivatives with aryl groups tethered to the C-6 position are potent protein synthesis inhibitors and active against multidrug-resistant respiratory pathogens. |
AID539505 | Antibacterial activity against constitutive macrolide-lincosamide-streptogramin B-resistant Streptococcus pneumoniae B0627 by agar microdilution method | 2010 | Bioorganic & medicinal chemistry, Dec-15, Volume: 18, Issue:24
| Novel hybrids of 15-membered 8a- and 9a-azahomoerythromycin A ketolides and quinolones as potent antibacterials. |
AID539507 | Antibacterial activity against efflux-resistant Staphylococcus aureus B0331 by agar microdilution method | 2010 | Bioorganic & medicinal chemistry, Dec-15, Volume: 18, Issue:24
| Novel hybrids of 15-membered 8a- and 9a-azahomoerythromycin A ketolides and quinolones as potent antibacterials. |
AID1169030 | Antibacterial activity against macrolide lincosamide- streptogramin B inducibly-resistant Streptococcus pneumoniae by agar microdilution method | 2014 | ACS medicinal chemistry letters, Oct-09, Volume: 5, Issue:10
| Synthesis and Structure-Activity Relationships of α-Amino-γ-lactone Ketolides: A Novel Class of Macrolide Antibiotics. |
AID197857 | Minimum inhibitory concentration against Staphylococcus aureus 10649 (erythromycin susceptible strain) | 2001 | Journal of medicinal chemistry, Nov-22, Volume: 44, Issue:24
| Novel erythromycin derivatives with aryl groups tethered to the C-6 position are potent protein synthesis inhibitors and active against multidrug-resistant respiratory pathogens. |
AID499551 | Antibacterial activity against constitutive macrolide-lincosamide-streptogramin B-resistant Staphylococcus aureus B0330 by agar microdilution method | 2010 | Journal of medicinal chemistry, Aug-12, Volume: 53, Issue:15
| Synthesis and structure-activity relationships of novel 8a-aza-8a-homoerythromycin A ketolides. |
AID1278827 | Antibacterial activity against efflux mediated macrolide resistant Streptococcus pneumoniae by agar microdilution method | 2016 | Bioorganic & medicinal chemistry, Mar-15, Volume: 24, Issue:6
| Synthesis and antibacterial evaluation of novel 4″-glycyl linked quinolyl-azithromycins with potent activity against macrolide-resistant pathogens. |
AID499554 | Antibacterial activity against constitutive macrolide-lincosamide-streptogramin B-resistant Streptococcus pneumoniae B0627 by agar microdilution method | 2010 | Journal of medicinal chemistry, Aug-12, Volume: 53, Issue:15
| Synthesis and structure-activity relationships of novel 8a-aza-8a-homoerythromycin A ketolides. |
AID642854 | Antibacterial activity against Staphylococcus aureus with inducible resistance to MLS by agar microdilution method | 2011 | ACS medicinal chemistry letters, May-12, Volume: 2, Issue:5
| Discovery of 4''-ether linked azithromycin-quinolone hybrid series: influence of the central linker on the antibacterial activity. |
AID539506 | Antibacterial activity against erythromycin A-susceptible Streptococcus pneumoniae B0541 by agar microdilution method | 2010 | Bioorganic & medicinal chemistry, Dec-15, Volume: 18, Issue:24
| Novel hybrids of 15-membered 8a- and 9a-azahomoerythromycin A ketolides and quinolones as potent antibacterials. |
AID210222 | In vitro antibacterial activity against Streptococcus pneumoniae ATCC 6303 (an erythromycin-susceptible strain) | 2004 | Bioorganic & medicinal chemistry letters, Jul-16, Volume: 14, Issue:14
| Synthesis and antibacterial activity of novel bifunctional macrolides. |
AID245166 | Minimum inhibitory concentration against Haemophilus influenzae GYR1435 (erythromycin susceptible strain) | 2005 | Bioorganic & medicinal chemistry letters, May-16, Volume: 15, Issue:10
| Design, synthesis and structure-activity relationships of 6-O-arylpropargyl diazalides with potent activity against multidrug-resistant Streptococcus pneumoniae. |
AID244850 | Minimum inhibitory concentration against Streptococcus pneumoniae 5649 strain | 2005 | Bioorganic & medicinal chemistry letters, May-16, Volume: 15, Issue:10
| Design, synthesis and structure-activity relationships of 6-O-arylpropargyl diazalides with potent activity against multidrug-resistant Streptococcus pneumoniae. |
AID1278830 | Antibacterial activity against constitutive macrolide-lincosamide-streptogramin B resistant Streptococcus pyogenes by agar microdilution method | 2016 | Bioorganic & medicinal chemistry, Mar-15, Volume: 24, Issue:6
| Synthesis and antibacterial evaluation of novel 4″-glycyl linked quinolyl-azithromycins with potent activity against macrolide-resistant pathogens. |
AID1459112 | Antibacterial activity against erythromycin susceptible Streptococcus pyogenes by agar microdilution method | 2017 | European journal of medicinal chemistry, Jan-05, Volume: 125 | Synthesis of novel 15-membered 8a-azahomoerythromycin A acylides: Consequences of structural modification at the C-3 and C-6 position on antibacterial activity. |
AID518970 | Induction of erm(C) expression in Escherichia coli JM109 harboring Staphylococcus aureus erm(C)-containing pERMZdelta2-4 mutant leader peptide cistrons reporter plasmid at 25 mg/ml after 36 hrs at 37 degC by disc-based beta-galactosidase reporter gene ass | 2008 | Antimicrobial agents and chemotherapy, Mar, Volume: 52, Issue:3
| Induction of erm(C) expression by noninducing antibiotics. |
AID208289 | Minimum inhibitory concentration against Streptococcus pneumoniae 5737 MLSB | 2001 | Journal of medicinal chemistry, Nov-22, Volume: 44, Issue:24
| Novel erythromycin derivatives with aryl groups tethered to the C-6 position are potent protein synthesis inhibitors and active against multidrug-resistant respiratory pathogens. |
AID244851 | Minimum inhibitory concentration against Streptococcus pneumoniae 5979 strain | 2005 | Bioorganic & medicinal chemistry letters, May-16, Volume: 15, Issue:10
| Design, synthesis and structure-activity relationships of 6-O-arylpropargyl diazalides with potent activity against multidrug-resistant Streptococcus pneumoniae. |
AID499556 | Antibacterial activity against erythromycin A-resistant Streptococcus pyogenes B0542 by agar microdilution method | 2010 | Journal of medicinal chemistry, Aug-12, Volume: 53, Issue:15
| Synthesis and structure-activity relationships of novel 8a-aza-8a-homoerythromycin A ketolides. |
AID131226 | Mouse protection tests for effective dose against Streptococcus pneumoniae 6303 ((erythromycin susceptible strain)) infected mice | 2001 | Journal of medicinal chemistry, Nov-22, Volume: 44, Issue:24
| Novel erythromycin derivatives with aryl groups tethered to the C-6 position are potent protein synthesis inhibitors and active against multidrug-resistant respiratory pathogens. |
AID209881 | Cell free inhibiting activity against erythromycin-susceptible strain Streptococcus pneumoniae 1813 (Wild type ribosomes for transcription/translation assay) | 2001 | Journal of medicinal chemistry, Nov-22, Volume: 44, Issue:24
| Novel erythromycin derivatives with aryl groups tethered to the C-6 position are potent protein synthesis inhibitors and active against multidrug-resistant respiratory pathogens. |
AID31895 | Minimum inhibitory concentration against Staphylococcus aureus ATCC 6538PEry-S | 2001 | Journal of medicinal chemistry, Nov-22, Volume: 44, Issue:24
| Novel erythromycin derivatives with aryl groups tethered to the C-6 position are potent protein synthesis inhibitors and active against multidrug-resistant respiratory pathogens. |
AID209882 | Cell free inhibiting activity against erythromycin-susceptible strain Streptococcus pneumoniae 1813 (methylated ribosomes for transcription/translation assay) | 2001 | Journal of medicinal chemistry, Nov-22, Volume: 44, Issue:24
| Novel erythromycin derivatives with aryl groups tethered to the C-6 position are potent protein synthesis inhibitors and active against multidrug-resistant respiratory pathogens. |
AID1169027 | Antibacterial activity against macrolide lincosamide- streptogramin B inducibly-resistant Staphylococcus aureus by agar microdilution method | 2014 | ACS medicinal chemistry letters, Oct-09, Volume: 5, Issue:10
| Synthesis and Structure-Activity Relationships of α-Amino-γ-lactone Ketolides: A Novel Class of Macrolide Antibiotics. |
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] |