superbug challenger from nature - michigan state …...“superbug challenger” from nature irosha...
TRANSCRIPT
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Platensimycin “Superbug
Challenger”
from Nature
Irosha
Nayanthika
NawarathneMichigan State University02/14/07
O
O
NH
OOH
OH
HO
O
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“Infectious diseases are now the world's biggest killer of children and young adults. They account for more than 13 million deaths a year -
one in two deaths
in developing countries.
Over the next hour alone, 1 500 people will die from an infectious disease -
over half of them children
under five.”-
WHO Report on Infectious Diseases 2000
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What are antibiotics?
Molecules that stop the microbial growth (both bacteria and fungi) or kill them outright
Walsh, C., Antibiotics Actions origins and Resistance, 2003, 4
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Classification –
According to Mode of Action
GTP GHP DHF THF
dUMP dTMP
DNA
DNA or RNA synthesis
Protein synthesis
Cell wall synthesis
Folic acid metabolism
Fatty acid synthesis
Walsh, C., Antibiotics Actions origins and Resistance, 2003, 19
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Classification –
According to Mode of Action
Quinolones,Rifampin
Aminoglycosides,Macrolides,Tetracyclines,Oxazolidinones
β-lactams,Cyclosporins,Glycopeptides
Triclosan, Isoniazid, Ethionamide
Trimethoprim,Sulfonamides
GTP GHP DHF THF
dUMP dTMP
DNA
Walsh, C., Antibiotics Actions origins and Resistance, 2003, 13-18
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Superbugs-:
Resistant to multiple classes of antibiotics
Bacterial species
Common types of Antimicrobial
Types of
Infections
Resistance
Streptococcus pneumoniae β-lactams, cephalosporins, macrolides
Otitis media, pneumonia,Tetracyclines
sinusitis, meningitis Staphylococcus aureusCommunity-associated Meticillin, cephalosporins, macrolides Skin, soft tissue, sepsis
pneumonia
Healthcare-associated Meticillin, cephalosporins, quinolones,
Endocarditis, pneumonia,aminoglycosides, macrolides
sepsis
Enterococcus spp.
Ampicillin, vancomycin, aminoglycosides Sepsis, urinary tract
Furuya, E.Y., Lowy, F.D., Nature, 2006, 4, 36
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How to address the problem of resistance
•
Chemical synthesis of analogs of known natural products
Walsh, C., Antibiotics Actions origins and Resistance, 2003, 113
N
S
COOHO
O N
S
COOHO
O
N
S
COOHO
OPenicillin
Ampicillin
Carbenicillin
H2N
HOOC
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β-lactamase
N
O OH
OCO2H
H
How to address the problem of resistance
•
Development of inhibitors of resistance mechanisms
N
S
OCO2H
HN
O
R
N
S
OCO2H
HN
O
R
Clavulanate
β-lactamaseHydrolysis of the antiboitic
Stop / minimize Hydrolysis of the antiboitic
Walsh, C., Antibiotics Actions origins and Resistance, 2003, 113
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How to address the problem of resistance
•
Discovery of completely novel antibiotics with new modes of action
Inhibitors
of Fatty Acid Biosynthesis (Fab)by targeting Fab
enzymes
Platensimycin
Singh, S.B., et al, J. Am. Chem. Soc., 2006, 128, 11916
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By systematic screening of 250,000 natural product extracts, using FabF-target based RNA-mediated gene silencing technique
Antisense RNA
mRNA
5` ………ATGGCCTGGACTTCA…………3` 3` ………TACCGGACCTGAAGT…………5`
Sense DNAAntisense
DNA
Transcription
5` ………AUGGCCUGGACUUCA…………3`
Met - Ala - Trp - Thr - Ser -
Translation
Peptide
Discovery of Platensimycin
Singh, S.B., et al, J. Am. Chem. Soc., 2006, 128, 11916Forsyth, R.A., Molecular Biology, 2002, 43, 1387
Wang, J., et al, Antimicrob. Agents Chemother., 2006, 50, 519
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Reduced or No FabF
expression
5`………
AUGGCCUGGACUUCA………3`3`………
UACCGGACCTGTTGU ………5`ds
RNA
Degradation of fabF
mRNA or inhibition of translation
In Prokaryotes-
Discovery of Platensimycin
From a strain of Streptomyces platensis recovered from soil samples
Higher sensitivity towards FabF
inhibitors
Singh, S.B., et al, J. Am. Chem. Soc., 2006, 128, 11916Forsyth, R.A., Molecular Biology, 2002, 43, 1387
Wang, J., et al, Antimicrob. Agents Chemother., 2006, 50, 519
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Structure Elucidation of Platensimycin
Through Isolation followed by Determination of Structure and Stereochemistry
O
O
NH
OOH
OH
HO
O
Singh, S.B., et al, J. Am. Chem. Soc., 2006, 128, 11916
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HR-ESI-FTMSC24
H27
NO7
UV/IR/DEPT/13C, 1H, HMQC2 methyls5 methylenes7 methines
4-Aromatic/Olefinic1-Oxy
10 non protonated
C’s 1-Ketone2-Carbonyls1-Oxygen bearing sp3 C2-Oxygen bearing sp2
C’s
Structure Elucidation of Platensimycin
Singh, S.B., et al, J. AM. CHEM. SOC., 2006, 128, 11916
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Structure Elucidation of Platensimycin
TOCSY/COSY
HMBC
2
3
OH
H
6
7
HH
7̀6̀ 11 13
9
Singh, S.B., et al, J. AM. CHEM. SOC., 2006, 128, 11916
O
O
NH
OOH
OH
HO
O
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Structure Elucidation of Platensimycin
O
OOH
OHH
HO
O OHNH
1
Combining aminobenzoic
acid unit to the ketolideHMBC ESIMS
O
O0
m/z
-
273
Singh, S.B., et al, J. AM. CHEM. SOC., 2006, 128, 11916
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Stereochemistry of Platensimycin
Relative : NOESY and Scalar Couplings
Absolute : Anomalous Scattering
Synthesis of 6’-bromoplatensimycin
Singh, S.B., et al, J. Am. Chem. Soc., 2006, 128, 11916
O
O
NHOH
1. NBS, acetone, THF
rt, 2.5 h
OOH
O
O
NHOH
OOH
HO2C
Br
HO2C
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S S
R
S
S
S
Stereochemistry of Platensimycin
Absolute and RelativeCrystal structure of 6’-Bromoplatensimycin
Singh, S.B., et al, J. Am. Chem. Soc., 2006, 128, 11916
O
OO
NH
COOHOH
OH
1 4
715
10
12
Br
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Structural Similarity of Platensimycin
Similar to known terpenoid structures
O
H
O
O
O
H
HO
HRO
17 Carbons 20 Carbons 20 Carbons
ent-KaurenePierisformoside
GPlatensimycin
Habich, D., Nussbaum, F.V., ChemMedChem, 2006, 1, 951Wang, L.Q., Qin, G.W., Chen, S., Li, C., Fitoterapia, 2001, 72, 779
O-glucoside
from Pieris
formosaIn plants and fungi
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Microbiological profiles and Toxicity of Platensimycin
Potent, Broad Spectrum Gram positive activity in vitroNo cross resistance to major superbugsOrganism and genotype Platensimycin Linezolid
Antibacterial activity (MIC, µg/ml)
S. aureus (MSSA) 0.5 4S. aureus (MRSA) 0.5 2S. aureus (MRSA,
macrolideR) 0.5 2S. aureus (MRSA, linezolidR) 1 32S. aureus (VISA) 0.5 2Enterococcus faecalis (macrolideR) 1 1Enterococcus faecium (VRE) 0.1 2S. pneumoniae 1 1
Wang, J., et al, Nature, 2006, 441, 358
MIC
–
Concentration of inhibitor used to result no visible growth of the pathogens
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Microbiological profiles and Toxicity of Platensimycin
Efflux mechanism limits the activity
Organism and genotype Platensimycin Linezolid
Antibacterial activity (MIC, µg/ml)
E. coli (wild-type) >64 >64E. coli (tolC) 16 32
Wang, J., et al, Nature, 2006, 441, 358
MIC
–
Concentration of inhibitor used to result no visible growth of the pathogens
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Microbiological profiles and Toxicity of Platensimycin
Acts selectively
Organism and genotype Platensimycin Linezolid
Toxicity (µg/ml)
HeLa
MTT (IC50
) >1,000 >100Candida albicans (MIC) >64 >64
Wang, J., et al, Nature, 2006, 441, 358
IC50 –
Concentration of the inhibitor used to kill 50%
population of the living cells
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Microbiological profiles and Toxicity of Platensimycin
In vivo Studies
In a mouse model of disseminated S. aureus
infection
Wang, J., et al, Nature, 2006, 441, 358
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Fatty Acids in bacteria…
•
Synthesis of membrane lipids which regulates membrane fluidity
eg
-
Phospholipids and Glycolipids
•
Metabolic storage
eg
-
Triacylglycerols
•
Cell Signal Transduction
Nelson, D.L., Cox, M.M., Lehninger Principles of Biochemistry, 2005, 4, 787
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FAB …….. is a good target
FAB Type I-
In mammals
FAB Type II-
In bacteria
Campbell, J.W., Cronan, J.E.Jr., Annu. Rev. Microbiol., 2001, 55, 305
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SH
SH
SH
S
O
O S
OO
S
O
O O
SSH
OH O
SSH
O
SSH
O
S
SH
O
SSH
S CoAO
O
O
SCoA
O
CO2NADPH+H
NADP
H2O
NADPH+ H
NADP
CoASH
CoASH
Biosynthesis of Saturated Fatty Acids
FabD
FabH FabG
FabZ
FabI
/ K / L
Campbell, J.W., Cronan, J.E.Jr., Annu. Rev. Microbiol., 2001, 55, 305
ACP
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SH
SH
SH
S
O
O S
OO
S
O
R
R
O O
SSH
R
OH O
SSH
R
O
SSH
R
O
S
SH
R
O
SSH
S CoAO
O
O
SCoA
O
CO2NADPH+H
NADP
H2O
NADPH+ H
NADP
CoASH
CoASH
Biosynthesis of Saturated Fatty Acids
FabD
FabF FabG
FabZ
FabI
/ K / L
Campbell, J.W., Cronan, J.E.Jr., Annu. Rev. Microbiol., 2001, 55, 305
ACP
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SH
SH
SH
S
O
O S
OO
S
O
R
R
O O
SSH
R
OH O
SSH
R
O
SSH
R
O
S
SH
R
O
SSH
S CoAO
O
O
SCoA
O
CO2NADPH+H
NADP
H2O
NADPH+ H
NADP
CoASH
CoASH
Inhibitors of Fatty Acids Biosynthesis
Triclosan,Isoniazid,Ethionamide
PlatensimycinCerulenin,
Thiolactomycin
Campbell, J.W., Cronan, J.E.Jr., Annu.Rev.Microbiol., 2001, 55, 305Price, A.C., et al, The Journal of Biological Chemistry, 2001, 276, 6551
Heath, R.J., White, S.W., Rock, C.O., Progress in Lipid Research, 2001, 40, 467
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Platensimycin- Inhibitor of Fatty Acid Synthesis
DNA,RNA, Protein and Cell wall Biosynthesis
Wang, J., et al, Nature, 2006, 441, 358Kodali, S., et al, J.Biol.Chem., 2005, 280, 1669
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Mode of Action of Platensimycin
High FabF selectivityCell - free gel - elongation assay
HO
O O
SCoA HO
O O
S ACP
O O
S ACP
OH O
S ACP
O
S ACP
O
S ACP
HO
O O
S ACP
CO2 +ACPSH
ACPSH CoASH
FabD
C02 +CoASHFabH
CoA
O
NADPH
NADP
FabG
H2O
FabAFabZ
FabIFabKFabL
FabF
NADPH
NADP
Wang, J., et al, Nature, 2006, 441, 358Heath, R.J., Nat.Prod.Rep., 2002, 19, 581
Malonyl-ACPC4:1(Δ2)-ACP
C4:0-ACP
>6C-ACP
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Mode of Action of Platensimycin
Inhibits FabF by direct targetingDirect binding assay employing 3H-dihydroplatensimycin and purified recombinant enzyme
Synthesis of 3H-dihydroplatensimycin
O
O
NH
OH
OOH
O
O
NH
OH
OOH
1. 5%Pd/ C , Isoproponol
Introduce Tritiumgasfromuraniumtritide bed(2.5 ml at 740mmHg)(5 Ci,2 Ci/ml)
2. 0.2NNaOH/ MeOH Specific activityof 15.8 Ci/mol
HO2C HO2C
T
Wang, J., et al, Nature, 2006, 441, 358
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Mode of Action of Platensimycin
Inhibits FabF by direct targetingDirect binding assay employing 3H-dihydroplatensimycin and purified recombinant enzyme
Scintillation Proximity Assay
Wang, J., et al, Nature, 2006, 441, 358
Cu2+
SPA
His6Tag
FabF
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Mode of Action of Platensimycin
Inhibits FabF by direct targetingDirect binding assay employing 3H-dihydroplatensimycin and purified recombinant enzyme
Scintillation Proximity Assay
Wang, J., et al, Nature, 2006, 441, 358
SPACu2+
His6Tag
FabFDPMN
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Mode of Action of Platensimycin
Inhibits FabF by direct targetingDirect binding assay employing 3H-dihydroplatensimycin and purified recombinant enzyme
No signal of binding
1. Loss of olefin may result no binding
2. It may require co-substratesfor the binding
Wang, J., et al, Nature, 2006, 441, 358Olesen, J.G., Structure, 2001, 9, 233
Apo FabF/FabB
Acyl Enzyme Intermediate
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Mode of Action of Platensimycin
Inhibits FabF by direct targetingDirect binding assay employing 3H-dihydroplatensimycin and purified recombinant enzyme
•
Platensimycin inhibits Acyl-Enzyme Intermediate
•
Stable
Acyl-Enzyme Intermediatethrough Mutation C163Q
Wang, J., et al, Nature, 2006, 441, 358Olesen, J.G., Structure, 2001, 9, 233
McGuire, K.A., Biochemistry, 2001, 40, 9836
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Mode of Action of Platensimycin
Inhibits FabF by direct targeting
Wang, J., et al, Nature, 2006, 441, 358Olesen, J.G., Structure, 2001, 9, 233
Apo FabF/FabB
A.E.IntermediateMutated FabF/
FabB
A.E.Intermediate
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Mode of Action of Platensimycin
Inhibits FabF by direct targeting
Wang, J., et al, Nature, 2006, 441, 358Olesen, J.G., Structure, 2001, 9, 233
Mutated FabF/
FabB
A.E.Intermediate Mutated FabF
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Mode of Action of Platensimycin
Inhibits FabF by direct targetingProposed mechanism
“
ACYL BINDING SITE ”
“
MALONYL BINDING SITE ”
ACYL-ENZYME INTERMEDIATE
Brown, E.D., Nature, 2006, 441, 293Habich, D., Nussbaum, F.V., ChemMedChem, 2006, 1, 951
O
O
S
O
ACP
R S
O
ACP
S
O
OH
O
ACP
R
O
S
O
ACP
CO2
H SFabF
CLOSED
R S
O
OPEN
FabF
H SFabF
CLOSED
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Mode of Action of Platensimycin
Inhibits FabF by direct targetingProposed mechanism
R S
O
ACP
S
O
OH
O
ACP
R
O
S
O
ACP
CO2
H SFabF
CLOSED
R S
O
OPEN
O
O
S
O
ACP FabF
H SFabF
CLOSED
“
ACYL BINDING SITE ”
“
MALONYL BINDING SITE ”
ACYL-ENZYME INTERMEDIATE
Brown, E.D., Nature, 2006, 441, 293Habich, D., Nussbaum, F.V., ChemMedChem, 2006, 1, 951
PMN
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N
N
N
N His303His298
H H
O S
OO
pantetheine
Active site tunnel
Phe229
Mode of Action of Platensimycin
Inhibits FabF by direct targeting
Wang, J., et al, Nature, 2006, 441, 358Heath, R.J., Nat.Prod.Rep., 2002, 19, 581
McGuire, K.A., Biochemistry, 2001, 40, 9836
Mutated FabF FabB
A.E.IntermediateO
O
NH
OOH
OH
HO
O
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Mode of Action of Platensimycin
Inhibits FabF by direct targeting
Direct binding assay employing 3H-dihydroplatensimycin and purified recombinant enzyme
Wang, J., et al, Nature, 2006, 441, 358
• Developing resistance through mutations at active site
would be hard
O
O
NH
OOH
OH
HO
O
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O
OO
NH
COOH
OH
HO O
OO
HO
OMOM
OMOMNH2MeO2C
1 2 3
O
OO
o
O
O
O
TBSO
4567
Retrosynthesis
of Platensimycin
Amide bond formation
Double alkylation
Ketyl radical cyclizationAnd Etherification
Cycloisomerization
Nicolaou, K.C., Li, A., Edmonds, D.J., Angew. Chem. Int. Ed. 2006, 45, 7086
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O
EtO
O
EtO
OTBS
Br
OTBS1. LDA
2. LDABr
3. DIBAL-H, -78oCto-20oCthenHCl
4. TBSCl
O
TBSO
O
TBSO
CpRu(MeCN)3 PF6
cat.
6. LiHMDS, TMSCl
5.
7. 1.1eq. Pd(OAc)222oC
8. HCl aq
O
O
8 10 11
1213
O
TBSO
9
6
92%
97% 84%twosteps
92%1: 1d.r.
68%twosteps85%
Racemic Synthesis of PlatensimycinSynthesis of pentacyclic
carboxylic acid -
3
Cycloisomerization
Dehydrosilylation
Appel reaction
Nicolaou, K.C., Li, A., Edmonds, D.J., Angew. Chem. Int. Ed. 2006, 45, 7086
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O
O 6
O
OO
OH
8. 2.2 eq. SmI2 ,
HFIP, THF/HMPA-78oC
O
OO
HO
9. TFA
10. KHMDS,MeI
O
O
11. KHMDS
I
O
OBO
O
BO
O
12. Grubbs catalyst13. 5 eq. Me3NO
95%
14. 3 eq. NaClO2,2-methyl-2-buteneNa2PO4, tBuOH/H2O
15 16
1718193
46%, 2:1 d.r.
87%
88%
79%
6 eq.
85%, 6:1 E / Z95%
Racemic Synthesis of PlatensimycinSynthesis of pentacyclic
carboxylic acid -
3
Single electron reduction
Pinnick oxidation
Nicolaou, K.C., Li, A., Edmonds, D.J., Angew. Chem. Int. Ed. 2006, 45, 7086
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Racemic Synthesis of PlatensimycinSynthesis of aromatic amine -
2
OHNO2
OH
OMOMNH2
OMOM
OMOMNHR
OMOM2. H2,Pd/C cat.
1. NaH, MOMCl
OMOMNHR
OMOMCO2Me
OMOMNH2
OMOMCO2Me
3. Boc2O
MeO CN
O
R = BoC
5. 2050C, Microwave
5 min.
2
20 21 22
23
82%
99%
99%
4. 1 eq.nBuLi,1 eq. TMSCl
then 2.2 eq. nBuLi
54%
83%
Nicolaou, K.C., Li, A., Edmonds, D.J., Angew. Chem. Int. Ed. 2006, 45, 7086
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O
OO
HOOMOM
NH2OMOM
MeO2C
O
OONH
CO2MeOMOM
OMOM
1. 4 eq.HATU, Et3N
O
OO
NH
COOHOH
OH
2. LiOH
3. aq. HCl
2 3 24
1
85%
90% two steps
Racemic Synthesis of PlatensimycinCoupling of Carboxylic acid-3 with Aromatic amine-2
Nicolaou, K.C., Li, A., Edmonds, D.J., Angew. Chem. Int. Ed. 2006, 45, 7086
HATU
–
O-(7-azabenzotriazol-1-yl)-N,N,N`,N`-tetramethyluronium hexafluorophosphate
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O
OO
HOOMOM
NH2OMOM
MeO2C
O
OONH
CO2MeOMOM
OMOM
1. 4 eq.HATU, Et3N
O
OO
NH
COOHOH
OH
2. LiOH
3. aq. HCl
2 3 24
1
85%
90% two steps
Racemic Synthesis of PlatensimycinCoupling of Carboxylic acid-3 with Aromatic amine-2
Racemic PMN Nicolaou, K.C., Li, A., Edmonds, D.J., Angew. Chem. Int. Ed. 2006, 45, 7086
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Summary and The Future Goals
O
O
NH
OOH
OH
HO
OPreclinical and
clinical trials
Explore the parts of PMN that are not involved in FabF binding
Designing analoguesFor the SAR studies
Enantioselective
synthesis
Proven potency as an antibacterial against superbugs
Developing resistance will be a slow process
No mammalian cell cytoxicity
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Acknowledgement
Dr. Walker Dr. Borhan Dr. Jackson Dr. Wulf
Dr. Hausinger Dr. Arnosti
Dr. Stoltzfus
Labmates
-
Amanda, Danielle, Karin, Mark, Sanjit, Washington, Yemane
Friends
-
Aman
D., Calvin, Chandana, Samantha, Sanjukta,Sue,
Sulagna,Tharanga, Toyin, Xiaofei, Zhenjie
Dr.Sheo
B. Singh, Dr.Stephen
Soisson, Dr.Jun
Wang
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Happy Valentine’s Day!
Happy Valentine’s Dayfilled with Love and Hope !
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Few back-up slides
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Discovery of Platensimycin Relative
Steriochemistry
NOESY
18-methyl and H-11(axial) -
β-faceH-9 and H-14 (axial) -
α-face
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Discovery of Platensimycin Structure
Elucidation
HMBCAmino benzoic Acid Unit
HOHH
HO
O OHNH
6`
2`3`
7`
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Discovery of Platensimycin Structure
Elucidation
HMBCKetolide
Unit
Cyclohexenone ring
OH
H
O1
4 6
8
18
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Biosynthesis of Malonyl
CoA
Biotincarrierprotein
HNO
S
HNNH
O
RS
HNNH
O
S
HNN
O
BaseHO O
OPO
OHOH
HO O
O
HOP
ADP
O
OH
RS
HN
O
OH
O
H2C
O
SCoA
O
O O
SCoA
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Microbiological profiles and Toxicity of Platensimycin
More potent than FabF inhibitor cerulenin