1 total size of the pipeline 2001-2012 citeline annual review 2012 ?? adverse drug reactions (admet)...
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Total size of the pipeline 2001-2012
Citeline annual review 2012
??
Adverse drug reactions (ADMET)
Can Ayurvedic Treatment Help in Integrating with Modern Medicine?
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NCI, Specs, IBScreen Databases(888762 Compounds)
162372 Compounds162372 Compounds
(CH3)3N, Lipinski’s rule based screening
117 Compounds117 Compounds
Pharmacophore based screening, Fit value ≥ 4
In vitro HTS 56000 compounds (ChemDiv, Tripose, ChemBridge)
AChE activity < 0.35µM8 compounds
75 Compounds75 Compounds
9 Compounds9 Compounds
Docking based screening, GFS > 52
Blood Brain Barrier, Bioavailability & Toxicity based screening
2 Lead Compounds2 Lead Compounds
In vitro screening
Flow chart showing different sequential virtual screening techniques
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Finland Collaboration
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In Vitro Analysis (Finland collaboration) AChE Enzyme Assay based on Ellman’s Reagent reaction.
Data set consisted of 8 highly potent compounds (IC50 < 0.35 µM) obtained from high-throughput in vitro screening consisting of 56,000 compounds for AChE inhibitory activity.
Compounds were taken from 3 Key Databases: ChemDiv Inc (San Diego, US) , ChemBridge Corporation (San Diego, US) Tripos (US).
Selection of Compounds for Pharmacophore Identification
NN
N
O
HN N
O
S
253
S
N N
N
N
O
N
O
HN
NH
N
O
Cl
N
O N
NH
O
O
I (0.019 μM) II (0.069 μM) IV (0.204 μM)III (0.152 μM)
S
NN
NHN N
NN
N
NHN
O N
FF
NH
NO
Br
O
N
HN O
HN
ON
VI (0.236 μM)V (0.229 μM) VII (0.315 μM) VIII (0.332 μM)
#Comb. Chem. and High Throughput Screening 2010, 13, 278-284.
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Pharmacophore Model for Anti-Cholinesterase Inhibitors
D72
Y121
W279
W84
F330
F288
F331Y334
CD1
CD1 (IC50=0.019 μM)
Active binding site residues of AChE enzymein complex with CD1 molecule
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Virtually screened Lead Compounds (Specs1 and Specs2) Interaction with AChE Enzyme
IC50=3.279 μM IC50=5.986 μM
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Compound Structure (Vendor ID) Source GFS in AChEenzyme(kJ/mol)
IC50 (μM) for AChE inhibition
IC50 (μM) for BChE inhibition
(ChemDiv (CD1), (ID= C7853067)
High throughputin vitroscreening
64.60 0.019 13.27
(ChemDiv (CD2), (ID= E0170008)
61.80 0.069 23.58
(Specs (Specs1), (ID=AF-399/15128515)
Virtual screening followed by in vitro validation
55.93 3.279Less
inhibition
53.29 5.986Less
inhibition
(Specs (Specs2), (ID= AF-399/40654557)
NN
N
O
HN N
O
S
253
S
N N
N
N
O
N
O
O
S
O
O
HN
N
O
O
O
S
HN
N
O
O
Structure of the 4 lead compounds along with the AChE and BChE enzyme inhibition, and its GOLD fitness score
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Compound Toxicitya bCNS blogSb% H_O_Abs
cAlogP clogD blogBB bPSA
CD1Skin
sensitisation1 -5.64 97 3.46 1.89 -0.23 80.5
CD2 None -1 -3.53 89.6 1.23 1.23 -0.39 78.5Specs1 None 1 -3.62 100 3.85 2.36 0.18 74.3Specs2 None 1 -4.61 100 3.99 2.51 -0.11 66.1
ADMET parameters of 4 leads obtained from ChemDiv & Specs database
aToxicity prediction using DEREK software;
bPrediction using Schördinger software;
cPrediction using Discovery studio (DS2.1) ADME module software;
CNS= Predicted central nervous system activity on a -2 (inactive) to +2 (active) scale;
LogS= Predicted aqueous solubility, log S on a –6.5 to 0.5;
% H_O_Abs = Percent Human Oral Absorption;
AlogP= Log of the octanol-water partition coefficient using Ghose and Crippen's method;
LogD=The octanol-water partition coefficient calculated taking into account the ionization
states of the molecule;
LogBB= Predicted brain/blood partition coefficient on a -3 to 1.2 scale;
PSA= Van der Waals surface area of polar nitrogen and oxygen atoms. 7
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Pain Research
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Topics of Interest in Ayur Informatics• Ayurvedic Drug Designing• Biostatistics• Computational Languages• Distributed Electronic Medical Records• Emergency Communications and Remote Monitoring• Medicinal Plant Databases• Medicinal Plant Genomics• Molecular Modelling• Networking Rural Clinics with Major Medical Facilities• Pharmacogenomics• Pharmacoproteomics• Plant Datasets and Databases• Remote Analysis of Diagnostic Data• Remote Information Services & Decision Support Tools for Patient Care• Telemedicine, Telemonitoring, Telediagnostics• Use of Digital Radios and Personal Communication Services• Visualization Technology for Visualizing the Human Anatomy• Wireless Information Networks
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BIOACTIVE COMPOUNDS FROM NATURAL SOURCES(Natural Products as Lead Compounds in Drug Discovery)
Computational Approaches for the Discovery of Natural Lead Structures
Wang, S. Q., Q. S. Du, K. Zhao, A. X. Li, D. Q. Wei, and K. C. Chou. 2007. Virtual screening for finding natural inhibitor against cathepsin-L for SARS therapy. Amino Acids 33:129–135.
Natural products were often viewed as being “too complex” but then have been recognized as a valuable source of interesting and diverse structures.
Natural products show higher molecular weight than synthetic drugs, contain more oxygen atoms, fewer nitrogen atoms, three times more stereo centers, their degree of unsaturation is higher than in synthetic drugs and they incorporate less aromatic rings.
Although natural products in general contain more rings than drugs, most of them are non-aromatic and part of single fused ring system.
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Bioactive compounds from Natural Sources
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The major challenge for in silico techniques is the increased molecular weight and the higher number of saturated bonds resulting in higher molecular flexibility.
As a rule of thumb, docking and conformational sampling become slow and inaccurate when a molecule has more than seven rotatable bonds.
However, these problems are not irresolvable, but have to be addressed while setting up a virtual screening run using natural products taking into account longer computational time.
A too high degree of flexibility may also result in promiscuity, that is, a compound is fitted into a binding site in an implausible way, which stresses the need for visual inspection of virtual hits and selection of the most plausible virtual hits.
Another putative practical problem is the higher number of stereo centers whose definitions are often neglected during database construction and therefore the programs have to enumerate all stereoisomers, which unnecessarily increase the (virtual) flexibility.
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General workflow for Computer assisted strategy for Natural lead discovery (VS=Virtual screening), (NP= Natural product)
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Computational workflow for the identification of the active metabolite/s within a natural (Ayurvedic) preparation.