OpenSourceMalaria:GSK Arylpyrrole Series
- 1 The Arylpyrrole Series
- 1.1 The two known TCMDC series starting points
- 1.2 The Near-Neighbour Sub-series
- 1.3 Alternative side-chains
- 1.4 Other known incidences of these molecules/this series
The Arylpyrrole Series
These compounds are currently under study by the Todd lab at the University of Sydney and the Medicines for Malaria Venture, Geneva. As an open source project, anyone may participate:
Electronic Lab Notebooks
Undergraduate Project Report
The initial two subseries of leads have the general structure:
- TCMDC Aryl pyrrole core InChi Key: LNROIXNEIZSESG-UHFFFAOYSA-N
- Near-Neighbour core InChi Key: JZQOEGKHCXONAV-ZROIWOOFSA-N
A number of these compounds and intermediates are available for biological testing from Todd group by request.
The two known TCMDC series starting points
CAS Registry Number: 733026-12-5
The proposed resynthesis strategy for these two compounds:
The Near-Neighbour Sub-series
Known "Near Neighbours" contained in the Tres Cantos set
The original idea for investigation of the near-neighbour set came from Paul Willis and was posted on the synaptic leap.
Data/links for these compounds:
TCMDC-123563, CHEMBL546966, CHEMBL page: 637010 Cc1ccc(cc1)n2c(cc(c2C)C(=O)CN3C(=O)C(NC3=O)Cc4ccccc4)C
TCMDC-125698, CHEMBL587989, CHEMBL: 627784 Cc1cc(c(n1c2ccc(cc2)Cl)C)C=C3C(=O)N(C(=Nc4ccccc4)S3)C5CCCC5
TCMDC-125697, CHEMBL581336, CHEMBL: 640978 CCOC(=O)c1ccc(cc1)n2c(cc(c2C)C=C3C(=O)N(C(=Nc4ccccc4)S3)C5CCCC5)C
TCMDC-125659, CHEMBL528140, CHEMBL: 626220 Cc1ccnc(c1)n2c(cc(c2C)C=C3C(=O)N(C(=Nc4ccccc4)S3)Cc5ccco5)C
TCMDC-124103, CHEMBL588465, CHEMBL: 643107 Cc1cc(cc(c1)n2c(cc(c2C)C=C3C(=O)NC(=Nc4ccc(cc4)Cl)S3)C)C
TCMDC-124456, CHEMBL548395, CHEMBL: 640006 CCn1c(cc(c1C)C=C2C(=O)NC(=Nc3ccccc3)S2)C
Initial synthesis strategy toward near-neighbours
Current synthesis strategy toward near-neighbours
Synthesis method taken from this paper.
Some alternative heterocyclic side-chain ideas have been proposed here at the Synaptic Leap.
The  side chain would target ester isosteres (see TCMDC-123812) but with greater biological stability.
Other known incidences of these molecules/this series
Related compounds are known to inhibit the proteasome, according to this Nature paper.
According to this paper, similar compounds are agonists of the sphingosine-1-phosphate receptor subtypes 1-5, which have a role in immune system function.
A new class of antimalarial was recently published by Novartis, Imidazolopiperazines.
Misc papers to digest/assimilate regarding antimycobacterial/tuberculosis activity: Antimycobacterial 1,5-diphenyl pyrroles, 10.1016/j.ejmech.2009.06.005, 10.1016/j.bmc.2010.09.006, 10.1002/cmdc.201000526
Scifinder Search: 2,4,5-alkyl-1-aryl-pyrrole: 77552 hits, 905 biological studies:
Obesity/diabetes GIP receptor inhibitor JP 2011184298 (A)
Proteasome WO 2011094545 (A2)
WO2006076202 Steroid nuclear receptor ligands
WO 2009137133 (A2) 5-Substituted-2-Imino-Thiazolidinone Compounds And Their Use As Inhibitors Of Bacterial Infection