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Enabling HTS Hit follow up via Chemo informatics, File Enrichment, and Outsourcing Graham F Smith Sandwich Chemistry Pfizer Global Research and Development
Overview Enabled  Hit Follow Up & Productive lead  Discovery File Enrichment Chemo informatics High Throughput Chemistry HTS
Presentation Overview ,[object Object],[object Object],[object Object],[object Object],[object Object]
HTS at Pfizer 10 years ago ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
File Enrichment – our early thoughts ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],George M Milne Jr (Pfizer), Annual Reports in Medicinal Chemistry, 2003, 38, 383-396
rationale for file enrichment ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],Gunther Wess (Aventis), Drug Discovery Today, 7 (10), 2002, 533-535.
file enrichment strategy:  consider attrition from outset ,[object Object],[object Object],[object Object],[object Object],hit lead candidate drug
Beautiful  compound concept parallel chemistry no toxicophores rule of 5 compliant pure and stable Pfizer exclusive Lipinski, C.A. Chris Lipinski Discusses Life and Chemistry after the Rule of Five.  Drug Discovery Today  2003 ,  8 , 12-16.
File Enrichment Initiative ,[object Object],[object Object],[object Object],[object Object],[object Object]
File Enrichment 1 – “the big four” ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
The Evotec ultra high throughput  screening system ,[object Object],[object Object],[object Object]
File Enrichment 2002-2006 ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],Alan Procter (Pfizer), Drug Discovery and Development, December, 2003 See various collaboration press releases ~$1 Billion FE  investment
File Enrichment – managing diversity La Jolla Groton Ann Arbor Sandwich Generation of ideas for library protocols Global Ideas overlap resolution La Jolla Groton Ann Arbor Sandwich Prioritization of ideas for development Library chemistry development Library idea  Management  Tool La Jolla Library production and purification
Enhancing Chemo-informatics ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
The Pfizer Global Virtual Library - PGVL ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
HTS Hit triage protocol – Pipeline Pilot Raw data ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],M Murcko (Vertex),  J. Med. Chem.  1999,  42,  5095-5099 A L Hopkins (Pfizer), Drug Discovery Today. 2004 May 15;9(10):430-1
Pipeline Pilot tree HTS Actives HTS Hits
HTS library output multiple lead options for most targets
Global Protocol database intranet access All Parallel Chemistry searchable in one place All 9 PGRD site use this tool All File enrichment research captured in the global database A link from compound to parallel synthesis protocol
Architecture based on Formal Reactions Protocols are associated into Formal Reactions VRXN-2-00001 Reductive amination as a family of protocols aldehydes nucleophilic amines Two protocols of broadest scope cover the largest range  of potential ----  thus potential  for re-use: Capturing these is what really builds  the asset in global Chemical  Knowledge Bases VRXN-2-00001 is defined by the  Formal Reaction  scheme  and spans the  space covered by all suitable  amines & aldehydes in the linked inventory db
Formal Reactions as Families of Protocols 21 VRXN-3-00029 4 VRXN-3-00007 2 VRXN-2-00081 3 VRXN-2-00018 7 VRXN-2-00017 9 VRXN-2-00016 8 VRXN-2-00013 15 VRXN-2-00011 39 VRXN-2-00010 12 VRXN-2-00009 9 VRXN-2-00007 16 VRXN-2-00005 4 VRXN-2-00004 11 VRXN-2-00002 13 VRXN-2-00001 Source (each color represents one of the Pfizer R&D sites) # of explicit protocols within reaction family Name of Formal Reaction (broad scope rxns)
Chemist’s Desktop ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],PGVL Hub, an internally developed application
PGVL Hub on the Chemist’s Desktop
Access to virtual libraries from the desktop Suitable monomers retrieved for each reaction protocol Properties calculated Inventory and location searched Clustering and filtering pre and post enumeration
Spotfire Design analysis
Hit Follow Up (2006…) ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
HTS at Pfizer now ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
HTS at Pfizer now – cont. ,[object Object],[object Object]
Measures of success: Sandwich ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
IKK2 inhibitors from HTS to multiple leads ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Crystal Structure of UK-411,930 bound to CDK2 - SBLD 2.3A resolution data SRS, Daresbury. Key pyrazole Donor Acceptor Donor interaction
Overview of Closed-loops for IKK Activity goes up with library iteration Number of actives increases with library iteration 0 10 20 30 40 50 60 0 1 2 3 4 5&6 Closed-loop iteration % of compounds active at 10  M  1 10 100 1000 10000 activity of most potent compound (nM)
novel low MWt PDE-5 inhibitors from closed loop chemistry on HTS hits ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Structure Based Library Design Templates Favoured monomers e.g. 2-aminopyridines  Pendant ionisable centre for solubility and SAR probe ,[object Object],[object Object],[object Object]
PDE5 Library lead: UK-469,413 12-24 hours 18, ER<1 1.9, 3.3 367 32v6, 5v10, 5v11 71nM UK-469413 >12 hours Pred. Hu T1/2 >10, ER<1 Caco abs. 1-2, <3 LogD, LogP <400 MWt >10x vs PDE’s Selectivity    50nM PDE5 IC50 Lead Target Criteria
PDE5 2 nd  generation series UK-469,413 ,[object Object],Gln817 H- bonds to C7-   aminopyridine  Mike Palmer  et al , Current Topics in Medicinal Chemistry, 2006, in press.
Profiles of selective PDE5 leads Criteria PDE5 IC50 PDE6 Sel. PDE11 Caco2 TPSA N,O count Lead 2 0.80nM  42x  10x 18, ER 1 93 9 Lead 3 0.50nM  104x  160x  2, ER>10 122 11 Great pharmacology, but… efflux problems.
Oxytocin hit–to-lead chemistry ,[object Object],[object Object],[object Object],[object Object],[object Object],Keating, T.A. & Armstrong, R.W. (1995) &quot;Molecular diversity via a convertible isocyanide in the Ugi four-component condensation,&quot;  J. Am. Chem. Soc.   117 : 7842-7843
Resolution of Oxytocin library actives ,[object Object],[object Object]
Long Acting Beta 2 agonists ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
mGluR1 antagonist ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
mGluR1 Leads optimised within PGVL ,[object Object],[object Object],[object Object],[object Object],[object Object],Dafydd Owen*  et al , Bioorganic Medicinal Chemistry Letter, 2006 In Press.
Maraviroc - Faster to CAN with parallel synthesis UK-107,543 (HTS hit)   400 nM CCR5 blocker no antiviral activity  CYP450 inhibitor UK-427,857   antiviral IC 90  1 nM  selective no CYP450 inhibition jun00 dec97 965  analogues Dorr  et al ,  Antimicrob Agents Chemother .,  2005 ,  49 ,  11  Armour & Wood,  Progress in Medicinal Chemistry ,  2005 ,  43 , 239 WO2003084954
CCR5 antagonist - Maraviroc ,[object Object],[object Object],[object Object],[object Object]
NEP Parallel Chemistry Strategy ,[object Object],[object Object],[object Object],[object Object],[object Object]
NEP inhibitor SAR ,[object Object],[object Object],[object Object],[object Object],David C. Pryde  et al , J. Med. Chem. 2005 WO2002002513  R2 dNEP (nM) MWt. LogD Caco-2 24 339 0.5 9/14 R1 6 393 -0.2 - 100 375 1.0 6/10 n Pr Me (CH 2 ) 2 OMe (CH 2 ) 2 OMe (CH 2 ) 2 OMe (CH 2 ) 2 OMe 4 333 0.8 21/21 3 379 0.5 12/17 0.5 396 1.0 12/14
Overview Enabled  Hit Follow Up & Productive lead  Discovery File Enrichment Chemo informatics High Throughput Chemistry HTS
Conclusions ,[object Object],[object Object],[object Object],[object Object]
Acknowledgements ,[object Object]
Additional Slides ,[object Object],[object Object]
Pfizer Overview ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
 
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],Pre-Clin Phase I Phase II Phase III Registration MARKET Animal Toxicity,  Chemical Stability, Superior Compound Human PK,  Toleration, Formulation Efficacy, Safety Differentiation , Dose Long-term Safety Approval?
The Attrition Curve 1 2 3 4 5 >12 years 60% 25% Ideas      Leads     Dev. Candidates     PhIIa Clin.     Products 25% 100 Projects 1 Product % Projects 25%

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Enabling HTS Hit follow up via Chemo informatics, File Enrichment, and Outsourcing

  • 1. Enabling HTS Hit follow up via Chemo informatics, File Enrichment, and Outsourcing Graham F Smith Sandwich Chemistry Pfizer Global Research and Development
  • 2. Overview Enabled Hit Follow Up & Productive lead Discovery File Enrichment Chemo informatics High Throughput Chemistry HTS
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  • 8. Beautiful compound concept parallel chemistry no toxicophores rule of 5 compliant pure and stable Pfizer exclusive Lipinski, C.A. Chris Lipinski Discusses Life and Chemistry after the Rule of Five. Drug Discovery Today 2003 , 8 , 12-16.
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  • 13. File Enrichment – managing diversity La Jolla Groton Ann Arbor Sandwich Generation of ideas for library protocols Global Ideas overlap resolution La Jolla Groton Ann Arbor Sandwich Prioritization of ideas for development Library chemistry development Library idea Management Tool La Jolla Library production and purification
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  • 17. Pipeline Pilot tree HTS Actives HTS Hits
  • 18. HTS library output multiple lead options for most targets
  • 19. Global Protocol database intranet access All Parallel Chemistry searchable in one place All 9 PGRD site use this tool All File enrichment research captured in the global database A link from compound to parallel synthesis protocol
  • 20. Architecture based on Formal Reactions Protocols are associated into Formal Reactions VRXN-2-00001 Reductive amination as a family of protocols aldehydes nucleophilic amines Two protocols of broadest scope cover the largest range of potential ---- thus potential for re-use: Capturing these is what really builds the asset in global Chemical Knowledge Bases VRXN-2-00001 is defined by the Formal Reaction scheme and spans the space covered by all suitable amines & aldehydes in the linked inventory db
  • 21. Formal Reactions as Families of Protocols 21 VRXN-3-00029 4 VRXN-3-00007 2 VRXN-2-00081 3 VRXN-2-00018 7 VRXN-2-00017 9 VRXN-2-00016 8 VRXN-2-00013 15 VRXN-2-00011 39 VRXN-2-00010 12 VRXN-2-00009 9 VRXN-2-00007 16 VRXN-2-00005 4 VRXN-2-00004 11 VRXN-2-00002 13 VRXN-2-00001 Source (each color represents one of the Pfizer R&D sites) # of explicit protocols within reaction family Name of Formal Reaction (broad scope rxns)
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  • 23. PGVL Hub on the Chemist’s Desktop
  • 24. Access to virtual libraries from the desktop Suitable monomers retrieved for each reaction protocol Properties calculated Inventory and location searched Clustering and filtering pre and post enumeration
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  • 31. Crystal Structure of UK-411,930 bound to CDK2 - SBLD 2.3A resolution data SRS, Daresbury. Key pyrazole Donor Acceptor Donor interaction
  • 32. Overview of Closed-loops for IKK Activity goes up with library iteration Number of actives increases with library iteration 0 10 20 30 40 50 60 0 1 2 3 4 5&6 Closed-loop iteration % of compounds active at 10  M 1 10 100 1000 10000 activity of most potent compound (nM)
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  • 35. PDE5 Library lead: UK-469,413 12-24 hours 18, ER<1 1.9, 3.3 367 32v6, 5v10, 5v11 71nM UK-469413 >12 hours Pred. Hu T1/2 >10, ER<1 Caco abs. 1-2, <3 LogD, LogP <400 MWt >10x vs PDE’s Selectivity  50nM PDE5 IC50 Lead Target Criteria
  • 36.
  • 37. Profiles of selective PDE5 leads Criteria PDE5 IC50 PDE6 Sel. PDE11 Caco2 TPSA N,O count Lead 2 0.80nM 42x 10x 18, ER 1 93 9 Lead 3 0.50nM 104x 160x 2, ER>10 122 11 Great pharmacology, but… efflux problems.
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  • 43. Maraviroc - Faster to CAN with parallel synthesis UK-107,543 (HTS hit) 400 nM CCR5 blocker no antiviral activity CYP450 inhibitor UK-427,857 antiviral IC 90 1 nM selective no CYP450 inhibition jun00 dec97 965 analogues Dorr et al , Antimicrob Agents Chemother ., 2005 , 49 , 11 Armour & Wood, Progress in Medicinal Chemistry , 2005 , 43 , 239 WO2003084954
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  • 47. Overview Enabled Hit Follow Up & Productive lead Discovery File Enrichment Chemo informatics High Throughput Chemistry HTS
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  • 54. The Attrition Curve 1 2 3 4 5 >12 years 60% 25% Ideas  Leads  Dev. Candidates  PhIIa Clin.  Products 25% 100 Projects 1 Product % Projects 25%