OpenSourceMalaria:GSK Arylpyrrole Series
(→Other known incidences of these molecules/this series: transfer of proteasome stuff)
(→Other known incidences of these molecules/this series)
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[http://worldwide.espacenet.com/publicationDetails/biblio?DB=EPODOC&II=0&adjacent=true&locale=en_EP&FT=D&date=20110804&CC=WO&NR=2011094545A2&KC=A2 WO 2011094545 (A2)]
Revision as of 08:32, 12 July 2013
The Arylpyrrole Series
This page contains a summary of all the data associated with arylpyrrole series ("Series 1") of the Open Source Malaria project. A more human-readable summary is available. For higher-level information, see the OSM Landing Page
The two subseries 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 by request (contact information on the Landing Page). If you would like to contribute new analogs, please check the list of desired compounds.
The Two Known TCMDC Series Starting Points
Compounds are commercially-available
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
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
Searches on ChEMBL-NTD reveal:
- 19 iminothiazolidinones
- 55 2,5-dialkylpyrroles
- 58 rhodanines. These do not contain any biological data, presumably omitted due to promiscuity/PAINS issues.
Scifinder Search: 2,4,5-alkyl-1-aryl-pyrrole: 77552 hits, 905 biological studies:
Obesity/diabetes GIP receptor inhibitor JP 2011184298 (A)
Related compounds are known to inhibit the proteasome, according to this Nature paper. There is a related set of slides from a company, Progenra. The lead compound (IU1, CAS 314245-33-5) is commercially available. Related patent 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
Synthetic Routes to Analogs Proposed By Others
The CRO Asclepia, via Frederik Doroose, contributed these synthetic routes to the project:
Current tested compounds and their biological activities are summarised on a Google spreadsheet
The results are collected on malaria.ourexperiment.org.
TCMDC-123812, TCMDC-123794 and near neighbour ZYH 3-1 have been submitted for study oral in vivo mouse model. Unfortunately it was found that the compounds possess zero oral efficacy (Results available here) in this initial trial.
Mode of action
In silico prediction
In silico prediction of targets has been carried out by Iain Wallace and summarised by Mat on the synaptic leap. Detail on the procedure is given on the ELN. The following targets were identified from data derived from the ChEMBL database:
- Carboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 1
- Dihydroorotate dehydrogenase (DHODH)[in progress at GSK Tres Cantos]
- SUMO-activating enzyme subunit 2
- SUMO-activating enzyme subunit 1
- Cyclin-dependent kinase 1
Collaborators are invited to investigate these targets to confirm if these are targeted by our compounds.
GSK Tres Cantos have offered to assay our compounds against dihydroorotate dehydrogenase (DHODH).