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ACS Fall 2017, Washington, D.C.
comparing cahn-ingold-prelog rule implementations:
the need for an open cipJohnMayfield,DanielLowe,RogerSayle
“The Cahn–Ingold–Prelog (CIP) sequence rules … are a standard process used in organic chemistry to completely and unequivocally name a stereoisomer of a molecule.” - Wikipedia
“The Cahn–Ingold–Prelog (CIP) sequence rules … are a standard process used in organic chemistry to completely and unequivocally name a stereoisomer of a molecule.” - Wikipedia
If you are not naming stereoisomers you (probably) don’t want to use CIP
Tools can give different answers, What can we do about it?
NUMBER OF STEREOCENTRES PER ENTRY
chebi_154
chembl_23
pubchem
pubchem_substance
eMolecules170601
0 5 10 15 20 25 30 35 40 45 50 55 60 65 70 75 80 85 90 95 100% of Dataset
Dat
aset
Count0123456789
eMolecules2017-Jun-01
PubChemSubstance
PubChemCompound(Aug17)
ChEMBL23
ChEBI154
+
14milliontotal
234milliontotal
93milliontotal
1.7milliontotal
95thousandtotal
Many chemists are taught the CIP rules during their education and is deceptively simple
‣ Simple cases are easy for a human (and computers) ‣ Complex cases are hard for a
human (and computers)
IUPAC Blue Book (2013) extends recommendations but incomplete (and some mistakes)
The Sequence RULES (in essence)
Rule 1 a. Higher atomic number precedes lower b. An atom node duplicated closer to the root ranks higher than one
duplicated further Rule 2 Higher atomic mass number precedes lower Rule 3 Z precedes E and this precedes nonstereogenic (nst) double bonds Rule 4
a. Chiral stereogenic units precede pseudoasymmetric stereogenic units and these precede nonstereogenic units (R = S > r = s > nst)
b. When two ligands have different descriptor pairs, the one with the first chosen like descriptor pairs has priority over the one with a corresponding unlike descriptor pairs
c. r precedes s Rule 5 An atom or group with descriptor R has priority over its enantiomorph S
O
HH
HH
H
HH
H
H321 5
4
6
12 3
5
6 4
H
Example
1. In the sphere (i) C2 and C5 are tied O > C5 = C2 > H 2. In the sphere (ii) C2 and C5 are split C,H,H > H,H,H
and therefore C2 > C5 3. The priority is 4, 2, 5, 6 and the configuration is S
(i)
(ii)
DIGRAPHS
• Rules are applied to hierarchal directed acyclic graphs (digraphs)
• Comparison proceeds in “spheres” out from the root of the graph
• Combinatorial explosions for some structures
H
OHH
H
H
H
H
H H
H
H
1
7
6
5
(1)
(1)65234
O
O
34 2
1
6 5
7
7
PSEUDO-ASYMMETRYSome confusion of lower case r and s
• Assigned only when Rule 5 has been used • Not indication of non-constitutional
Why? Reflection is superimposable:
AUXILIARY DESCRIPTORSAuxiliary descriptors are used to split ties by symmetric molecules by labelling the asymmetric digraphs
Tieininitialdigraph
Calculateauxiliarydescriptors
R>S(Rule5)3:rPicture: May, J. W. (2015). Cheminformatics for genome-scale metabolic reconstructions (doctoral thesis).
mancude ring handling
P-92.1.4.4 Nomenclature of Organic Chemistry: IUPAC Recommendations and Preferred Names 2013
Kekulé forms can result if different digraphs
Handled using fractional atomic numbers
The Sequence RULES (in essence)
Rule 1 a. Higher atomic number precedes lower b. An atom node duplicated closer to the root ranks higher than one
duplicated further Rule 2 Higher atomic mass number precedes lower Rule 3 Z precedes E and this precedes nonstereogenic (nst) double bonds Rule 4
a. Chiral stereogenic units precede pseudoasymmetric stereogenic units and these precede nonstereogenic units (R = S > r = s > nst)
b. When two ligands have different descriptor pairs, the one with the first chosen like descriptor pairs has priority over the one with a corresponding unlike descriptor pairs
c. r precedes s Rule 5 An atom or group with descriptor R has priority over its enantiomorph S
ChEBI ChEMBL eMolecules PubChemCompound
PubChemSubstance
Rule1a 281K 99.6% 1.8M 98.6% 2.4M 97.0% 53.5M 100.0% 93.1M 98.7%
Rule1b 4 1 164 255
Rule2 14 3,565 6,789
Rule3 29 3 441 36 45
Rule4a 122 126 273 4 12,770
Rule4b 563 0.2% 4,037 0.2% 3,188 0.1% 125K 0.1%
Rule4c 19 558
Rule5 285 0.1% 23.4K 1.2% 69K 2.8% 15 1.1M 1.2%
Total 282K 1.9M 2.4M 53.5M 94.3M
MAJORITY HANDLED BY RULE 1a
Countisnumberofstereocentres,valuesofzeroandpercentagesclosetozeroremovedtoreducecomplexity
05
101520253035404550556065707580859095
100
1 2 3 4 5 6 7 8 9 10Sphere
% o
f Ste
reoc
entre
s Datasetchebi_154chembl_23eMolecules170601pubchempubchem_substance
distance from rootMajority (but not all) stereocentres labelled within first few spheres
Best to generate digraph lazily as required
Some digraphs are far too big to generate fully (e.g. fullerenes)
05
101520253035404550556065707580859095
100
1 2 3 4 5 6 7 8 9 10Sphere
% o
f Ste
reoc
entre
s Datasetchebi_154chembl_23eMolecules170601pubchempubchem_substance
comparison
Rule 1AI II
Centres 2.0 R R JMol 14.20.3 R R ACD/ChemSketch 14.05beta R R Balloon 1.6.5beta R R KnowItAll ChemWindow 2018 R R ChemDraw 16.0 R R BIOVIA Draw 2017 R R MarvinSketch 17.17 R - Indigo 1.3.0Beta.r16 - R RDKit 2017.03.03 S R DataWarrior 4.6.0 R R CACTVS (NCI Resolver Aug 17) R R OPSIN 2.3.1 R R LexiChem (OEChem) 20170613 R R ChemDoodle 7.0.2 R R CDK 2.0 - R JUMBO 6 R -
I
II
Rule 1B Centres 2.0 R JMol 14.20.3 R ACD/ChemSketch 14.05beta R Balloon 1.6.5beta R KnowItAll ChemWindow 2018 R ChemDraw 16.0 R BIOVIA Draw 2017 - MarvinSketch 17.17 - Indigo 1.3.0Beta.r16 - RDKit 2017.03.03 R DataWarrior 4.6.0 - CACTVS (NCI Resolver Aug 17) - OPSIN 2.3.1 R LexiChem (OEChem) 20170613 - ChemDoodle 7.0.2 - CDK 2.0 - JUMBO 6 -
Rule 2Jan 2015 Aug 2017
Centres R R JMol n/a R ACD/ChemSketch R R Balloon 1.6.5beta n/a R KnowItAll ChemWindow n/a R ChemDraw S S Accelrys/BIOVIA Draw S R MarvinSketch S S Indigo R R RDKit S S DataWarrior S S CACTVS S R OPSIN R R LexiChem (OEChem) S R ChemDoodle S n/a CDK S S JUMBO - -RorS?Let’sVotehttps://nextmovesoftware.com/blog/2015/01/21/r-or-s-lets-vote/
Rule 4b
SSS R
Centres 2.0 R JMol 14.20.3 R ACD/ChemSketch 14.05beta R Balloon 1.6.5beta R KnowItAll ChemWindow 2018 R ChemDraw 16.0 R BIOVIA Draw 2017 R MarvinSketch 17.17 R Indigo 1.3.0Beta.r16 R RDKit 2017.03.03 S DataWarrior 4.6.0 S CACTVS (NCI Resolver Aug 17) S OPSIN 2.3.1 - LexiChem (OEChem) 20170613 - ChemDoodle 7.0.2 s CDK 2.0 - JUMBO 6 -
MANCUDE RINGS Centres 2.0 R R JMol 14.20.3 R R ACD/ChemSketch 14.05beta R R Balloon 1.6.5beta R R KnowItAll ChemWindow 2018 R R ChemDraw 16.0 R R BIOVIA Draw 2017 R R MarvinSketch 17.17 R R Indigo 1.3.0Beta.r16 S R RDKit 2017.03.03 R R DataWarrior 4.6.0 R R CACTVS (NCI Resolver Aug 17) S R OPSIN 2.3.1 S R LexiChem (OEChem) 20170613 S R ChemDoodle 7.0.2 S R CDK 2.0 S R JUMBO 6 S S
I II
I
II
Centres 2.0 R JMol 14.20.3 R ACD/ChemSketch 14.05beta R Balloon 1.6.5beta R KnowItAll ChemWindow 2018 R ChemDraw 16.0 R BIOVIA Draw 2017 R MarvinSketch 17.17 - Indigo 1.3.0Beta.r16 - RDKit 2017.03.03 - DataWarrior 4.6.0 - CACTVS (NCI Resolver Aug 17) - OPSIN 2.3.1 - LexiChem (OEChem) 20170613 - ChemDoodle 7.0.2 - CDK 2.0 - JUMBO 6 -
AUX DESCRIPTORS
hard to implement AMarvinSketch 17.17
(S)
O
O
(S)
OH
(S)
O
O
(R)
OH
Turning aromaticity on flips stereochemistry (e.g. CHEBI:16063)
Labels depend on input order
OH1
(S)2
(r)3
OH4
(R)5
OH6
(S)7
OH8
(s)9
HO10
(R)11
HO12
(S)1
OH2
OH3
(R)4
HO5
OH6
(R)7
OH8
(S)9
(R)10 (R)11
HO12
(r)1
OH2
(s)3
HO4
(S)5
(R)6
(S)7
(R)8 OH9
OH10
HO11
OH12
hard to implement B
(R)OH
H
(CH2)2CH2HO OH
(R)OH
H
(CH2)11(CH2)10HO OH
OH
H
(CH2)17(CH2)16HO OH
Becomes undefined distance ≥ 16
ChemDraw 16.0
(R)
(s)
(CH2)2
(R)OH
(r)
(s)
(CH2)11
(R)OH
open cip?Why? • Provide a blessed implementation that can be
used directly or compared against
• Toolkit agnostic library to facilitate downstream integration
“FIX-CIP” CoLABORATIONRobert Hanson (JMol), John Mayfield (Centres)
Mikko Vainio (Balloon), Andrey Yerin (ACD/Name), Sophia Gillian Musacchio (St. Olaf College)
Goals • Discuss and resolve software inconsistencies • Generate comprehensive test set based on
BlueBook structure • Recomend rule amendments and additions
Publication in preparation
should you use CIP?Yes
Systematic nomenclature Human conversation (if no pen is handy)
Probably not (better algorithms exist) Unique labelling (see right) Compute “conversation” Finding/cleaning stereocentres
No Relative comparison, e.g. substructure search
should you use CIP?Yes
Systematic nomenclature Human conversation (if no pen is handy)
Probably not (better algorithms exist) Unique labelling (see right) Compute “conversation” Finding/cleaning stereocentres
No Relative comparison, e.g. substructure search
(S)
(S)
(R) (S)
(R)
(R)
(S)(R)
(S)
(S)
(R) (S)
(R)
(R)
(S)(R)
acknowledgements SciMix Poster
Robert Hanson (JMol) Mikko Vainio (Balloon) Andrey Yerin (ACD/Name) Sophia Gillian Musacchio (St. Olaf College) Karl Nedwed (Bio-Rad) Noel O’Boyle (NextMove Software) Shuzhe Wang (NextMove Software)
JohnMayfield,DanielLoweandRogerSayleNextMoveSoftwareLtd,Cambridge,UK.
NextMoveSoftwareLimitedInnovationCentre(Unit23)
CambridgeScienceParkMiltonRoad,Cambridge
UKCB40EY
www.nextmovesoftware.com
Introduction
Robert Hanson, Andrey Yerin, Mikko Vainio, and Sophia Gillian Musacchio for initiating and participating in the “Fix CIP” collaboration and the many in-depth technical discussions that have lead to improvements in the tools. Karl Nedwed for providing KnowItAll results. Philip Skinner for providing ChemDraw licenses. Noel O’Boyle for feedback and suggestions.
the need for open-cip
The Cahn-Ingold-Prelog (CIP) priority rules rank atoms around a stereogenic unit to assign a stereo-descriptor that is invariant to atom order and layout, for example R (right) or S (left) for tetrahedral atoms.
A directed acyclic graph (digraph) is constructed for each stereogenic unit and the out edges from the root node compared and ranked according to eight sequence rules[1]. Each rule is applied exhaustively and tested on the entire digraph before applying the next rule[2].
Acknowledgements
Results
1. P-92.1.3 Nomenclature of Organic Chemistry: IUPAC Recommendations and Preferred Names 20132. Paulina Mata. The CIP System Again: Respecting Hierarchies Is Always a Must. J. Chem. Inf. Comput. Sci., 1999,
39 (6)
Bibliography
ConclusionThe CIP sequence rules provide a standard way for chemists to effectively describe the configurations of most stereogenic units. However, beyond simple cases the complexity of the rules necessitates software is used as an aid to naming configurations. The results demonstrate even then, software implementations do not all agree on the configuration.
Through the results presented here and the on-going effort of the Fix CIP collaboration, software should aim to converge upon consistent stereochemistry naming. An Open CIP software tool could provide “blessed” stereochemistry configuration names and provide a standard algorithm implementation for other vendors to integrate or adapt.
Comparing Cahn-Ingold-Prelog Rule Implementations
Rule 1 a. Higher atomic number precedes lower b. An atom node duplicated closer to the root ranks higher than one duplicated further
Rule 2 Higher atomic mass number precedes lower Rule 3 Z precedes E and this precedes nonstereogenic (nst) double bonds Rule 4
a. Chiral stereogenic units precede pseudoasymmetric stereogenic units and these precede nonstereogenic units (R = S > r = s > nst)
b. When two ligands have different descriptor pairs, the one with the first chosen like descriptor pairs has priority over the one with a corresponding unlike descriptor pairs
c. r precedes s Rule 5 An atom or group with descriptor R has priority over its enantiomorph S
Stereochemistry in Databases
chebi_154
chembl_23
pubchem
pubchem_substance
eMolecules170601
0 5 10 15 20 25 30 35 40 45 50 55 60 65 70 75 80 85 90 95 100% of Dataset
Datase
t
Count0123456789
eMolecules(June2017)
PubChemSubstance
PubChemCompound(Aug2017)
ChEMBL23
ChEBI154
14millionrecords
234millionrecords
93millionrecords
1.7millionrecords
95thousandrecords
chebi_154
chembl_23
pubchem
pubchem_substance
eMolecules170601
0 5 10 15 20 25 30 35 40 45 50 55 60 65 70 75 80 85 90 95 100% of Dataset
Dat
aset
Count0123456789N
umbe
rofStereogen
icUnits
+
chebi_154
chembl_23
pubchem
pubchem_substance
eMolecules170601
0 5 10 15 20 25 30 35 40 45 50 55 60 65 70 75 80 85 90 95 100% of Dataset
Dat
aset
Count0123456789
The number of defined stereogenic units per molecule varies between databases.
The application of Rule 1a to the digraph for 2-butanol ranks the out edges connected to the root as giving the label S (4 > 2 > 5 are anticlockwise looking towards 6).
ChEBI ChEMBL eMolecules PubChem Compound1
PubChem Substance
Rule 1a 281K 99.6% 1.8M 98.6% 2.4M 97.0% 53.5M 100.0% 93.1M 98.7%
Rule 1b 4 1 164 255
Rule 2 14 3,565 6,789
Rule 3 29 3 441 36 45
Rule 4a 122 126 273 4 12,770
Rule 4b 563 0.2% 4,037 0.2% 3,188 0.1% 125K 0.1%
Rule 4c 19 558
Rule 5 285 0.1% 23.4K 1.2% 69K 2.8% 15 1.1M 1.2%
Total 282K 1.9M 2.4M 53.5M 94.3M
The majority of stereogenic units are constitutionally asymmetric and can be ranked using Rule 1a. However, in some datasets the number of stereogenic units requiring Rule 4b and 5 can be significant.
I II III IV V VI VII VIII IX X XIa XIb XII XIII
Centres 2.0 R R R R R R R R R r R R r R JMol 14.20.3 R R R R R R R R R r R R r R ACD/ChemSketch 14.05beta R R R R R R R R R r R R r R Balloon 1.6.5beta R R R R R R R R R r R R r R KnowItAll ChemWindow 2018 R R R R R R R R R r R R r R5
ChemDraw 16.0 R R R R S R R R R r R R r R BIOVIA Draw 2017 R R R - R R R R R -1 R R -1 R MarvinSketch 17.17 R - - - S R - R - r R R r - Indigo 1.3.0Beta.r16 -2 R - - R - R R R r S R - - RDKit 2017.03.03 S R S R S R R S R R R R - - DataWarrior 4.6.0 R R R - S R R S R R R3 R - - CACTVS (NCI Resolver Aug 17) R R S - S4 R R S R R S R - - OPSIN 2.3.1 R R R R R - - - - - S R - - LexiChem (OEChem) 20170613 R R - - R - - - - - S R - - ChemDoodle 7.0.2 R R - - S - - s - r S R - - CDK 2.0 - R R5 - S - - - - - S R - - JUMBO 6 R - S - - - - - - - S S - -
Constitutional (Rule 1a, 1b, 2)
Geometrical + Topographical (Rule 3,4a,4b,4c,5)
Special (Mancude,
Aux Descriptors)
1. Pseudoasymmetric r/s labels not displayed but must be calculated due to answers given for IX and XIII
2. Runtime error occurs3. Impossible to test as different Kekulé forms are normalised4. R in CACTVS since Feb 2015, NCI resolver is old version5. Other descriptor is assigned differently
A set of fourteen structures was collected to identify differences between software implementations. The structures were selected to cover all the sequence rules and their applications to special cases.
Eight sequence rules (in essence)
Fix CIP CollaborationSince submitting this work for presentation the developers: Centres, JMol, ACD/ChemSketch, and Balloon have begun a collaboration. We are in the process of submitting for publication an extended in-depth validation set and proposing sequence rule refinements and additions where they are required.
1As part of the PubChem Compound’s processing, non-constitutional stereochemistry is removed: for example the nine stereoisomers of inositols are all represented by CID 892.
Atoms connected by double and triple bonds as well as ring closures result in duplicated nodes in the digraph. In the structure below atoms 5 and 6 appear twice and atom 1 (the root) appears three times.
Due to this duplication, complex ring systems can generate exponentially large digraphs that are not computationally tractable. Further complexity in digraphs is caused by the use of fractional atomic numbers in mancude ring-systems and assignment of auxiliary descriptors for applying Rules 3-5.
H
OHH
H
H
H
H
H H
H
H
1
7
6
5
(1)
(1)65234
O
O
34 2
1
6 5
7
7
O
HH
HH
H
HH
H
H321 5
4
6
12 3
5
6 4
H