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.TD$ED$M $ƋE^TD$t$E$NjM6TD$t$E$EMSD$t$E$EMJTD$t$E$EM|$ SD$ED$M $ƋEML$ SD$ED$M $kxEPn~4E$KMDD$TD$ $R8fLPML@MLTf@nEЋE9EU4R4$NKEt$D$$UKMMEHEMԉL$ SD$ED$M $ƋEVTD$t$E$NjMD$ SD$t$E$EMD$ SD$t$E$EMD$ SD$t$E$EMD$ SD$t$E$EM|$ SD$ED$M $UfBMED$ SD$ED$M $UfBMED$ SD$ED$M $UfBMED$ SD$ED$M $UfBMED$ SD$ED$M $UfBM TD$t$E$UĈBMTD$t$E$UĈBEԃE M9MErTD$ML$E$ËMED$\$ $lj$H@${HƉ|$$HE pU|$\$$EM fA UfQEUQ|[^_UH]u}ED$]؉\$E$1t?uȉt$$Zt$D$E$Klj4$8E$G$Z]u}UH]u}ED$]؉\$E$:1t?uȉt$$WZt$D$E$lj4$7E$;G$葈]u}UWVSL[}D$UT$<$E$F@@@ @@@$AFED$AD$$F$AFED$AD$$FEԉD$U؉T$t$ D$D$E܉$rEU܉T$UT$<$t$<$E4$FE؉$EUԉ$EED$ED$ .KD$JD$<$RpL[^_SSeHSbBrN;P;As;Sb;O;S;Se;Te;C;SiCannot create xml tag for error (structure #%ld.%s%s%s%s) Terminating. Cannot create end xml tag for structure #%ld.%s%s%s%s Terminating. 0*(),%dUnrecognized bond type:Unrecognized bond stereo:Bond to nonexistent atomAtom has a bond to itselfMultiple bonds between two atomsDuplicated bond(s) between two atomsAtom '%s' has more than %d bondsAtom '%s' has %d alternating bondsIgnored charge/radical redefinition:Parsed compound atom(s):Unknown element(s):%d->%dRadical center type replaced:Input type set to INPUT_INCHI Cannot allocate output message buffer. AuxInfoInChI=?FixedH ?RecMet ?SUU ?SLUUDFinal structure conversion failed Out of RAMCannot allocate output buffer. Terminating Cannot create end xml tag for structure #%d.%s%s%s%s Terminating. %-sGot non-normalized structureNot chiralGot non-canonicalized structureInChI generator not initializedStructure #%ldCannot interpret reversibility informationProton(s) added/removedCharges neutralized?helpTmnMNeAsiN:it:gE:E:HhN:F:I:AuxInfo=CRV:rA:R:rB:rC:/ \-+u?-+TDHInChI=1StructureABCDEFGHIJKLMNOPWarning: forced conversion to non-standard InChI for non-std input, Structure %ld Warning: ignore SaveOpt request for SaveOpt-less input, Structure %ld Warning: input created w/o RecMet - ignoring RecMet request, Structure %ld Warning: input created w/o FixedH - ignoring FixedH request, Structure %ld ; Error in detecting input InChI optionsAdd/Remove protons errorInChI compare errorInChI compare2 errorMerge Components errorDisconnected: *Conversion failed on component(s)MRD %s%s%d(%.96s)*Terminated by the user**Conversion failed*%s Wrong command line options: expected Inch2Struct or Inchi2Inchi End of file detected after structure %ld. Structure: %ld, Reconnected layer%s%.100sEnd of lineUnknown errorAllocation failedProgram errorSyntax error %s %s (%d) in %s (%d) (Metal compound)MOBILE_H_FORMULAMOBILE_H_CONNECTIONSMOBILE_HMOBILE_H_CHARGEMOBILE_H_PROTONSMOBILE_H_SP2MOBILE_H_SP3MOBILE_H_SP3_/mMOBILE_H_SP3_/sMOBILE_H_ISO_LAYER_FORKMOBILE_H_ISO_ATOMSMOBILE_H_ISO_EXCH_HMOBILE_H_ISO_SP2MOBILE_H_ISO_SP3MOBILE_H_ISO_SP3_/mMOBILE_H_ISO_SP3_/sFIXED_H_LAYER_FORKFIXED_H_FORMULAFIXED_HFIXED_H_CHARGEFIXED_H_SP2FIXED_H_SP3FIXED_H_SP3_/mFIXED_H_SP3_/sFIXED_H_PERMUTATIONFIXED_H_ISO_LAYER_FORKFIXED_H_ISO_ATOMSFIXED_H_ISO_LAYERFIXED_H_ISO_SP2FIXED_H_ISO_SP3FIXED_H_ISO_SP3_mFIXED_H_ISO_SP3_sFIXED_H_ISO_PERMUTATIONRECONNECTED_LAYER_FORKRECONNECTED_FORMULAMATERIAL_BALANCEUnknown ErrormnM... Mobile-H( Fixed-H(; Error: Hydrogens: Mobile-H groups: Isotopic: Charge(s): Proton balance: Exchangeable isotopic H: Stereo centers/allenes: Stereobonds/cumulenes: Fixed-H layer: Number of components: Conversion encountered: Wrong result Locations or number Fixed-H Number Missing Falsely present One instead of multiple Multiple instead of one Attachment points Do not match Atoms do not match Does not match for a component Does not match Falsely inverted Wrong parity Extra undefined Extra known Missing undefined Missing known Missing or extra Error Problems/mismatches:Omitted undefined stereoFatal undetermined program errorCannot allocate output data. TerminatingHDTN;P;O;S;Se;Te;Ambiguous stereo:center(s)bond(s)Cannot process free radical centerCannot process aromatic bondsARRAY OVERFLOWLENGTH_MISMATCHRANKING_ERRISOCOUNT_ERRTAUCOUNT_ERRISOTAUCOUNT_ERRMAPCOUNT_ERRTime limit exceededISO_H_ERRSTEREOCOUNT_ERRATOMCOUNT_ERRSTEREOBOND_ERRUser requested terminationREMOVE_STEREO_ERRCALC_STEREO_ERRSTEREO_CANON_ERRCANON_ERRWrong or missing chemical formulaUNKNOWN_ERRNo description(%d)UNKNOWN_ERR(%d)Accepted unusual valence(s):%ssdt,%s(%d)Warning (%s) structure #%ld.%s%s%s%s Error %d (%s) structure #%ld component %d.%s%s%s%s Cannot extract Component%s #%d structure #%ld.%s%s%s%s %s inp structure #%ld: End of file.%s%s%s%s End of file detected after structure #%ld. Cannot create start xml tag for structure #%ld.%s%s%s%s Terminating. Fatal Error %d (aborted; %s) inp structure #%ld.%s%s%s%s MolfileError %d (no %s; %s) inp structure #%ld.%s%s%s%s Warning: (%s) inp structure #%ld.%s%s%s%s <%s> ==== %s ==== Charges were rearrangedSalt was disconnected0D Parities Reconciliation failed:Metal was disconnectedCannot disconnect metal errorCannot distinguish componentsis missing =InChI ANNOTATED CONTENTS1, Software version 1.03%s ver %s%s. Usage: c%s-%s inputFile [outputFile [logFile [problemFile]]] [%coption[ %coption...]] Options: Input STDIO Use standard input/output streams InpAux Input structures in %s default aux. info format (for use with STDIO) SDF:DataHeader Read from the input SDfile the ID under this DataHeader Output AuxNone Omit auxiliary information (default: Include) SaveOpt Save custom InChI creation options (non-standard InChI) NoLabels Omit structure number, DataHeader and ID from %s output Tabbed Separate structure number, %s, and AuxInfo with tabs OutputSDF Convert %s created with default aux. info to SDfile SdfAtomsDT Output Hydrogen Isotopes to SDfile as Atoms D and T Structure perception SNon Exclude stereo (default: include absolute stereo) NEWPSOFF Both ends of wedge point to stereocenters (default: a narrow end) DoNotAddH All H are explicit (default: add H according to usual valences) Stereo perception modifiers (non-standard InChI) SRel Relative stereo SRac Racemic stereo SUCF Use Chiral Flag: On means Absolute stereo, Off - Relative Customizing InChI creation (non-standard InChI) SUU Always include omitted unknown/undefined stereo SLUUD Make labels for unknown and undefined stereo different RecMet Include reconnected metals results FixedH Include Fixed H layer KET Account for keto-enol tautomerism (experimental) 15T Account for 1,5-tautomerism (experimental) Generation Wnumber Set time-out per structure in seconds; W0 means unlimited WarnOnEmptyStructure Warn and produce empty %s for empty structure Key Generate InChIKey XHash1 Generate hash extension (to 256 bits) for 1st block of InChIKey XHash2 Generate hash extension (to 256 bits) for 2nd block of InChIKey %s ver %s%s. Usage: inchi-%s inputFile [outputFile [logFile [problemFile]]] [%coption[ %coption...]] Conversion InChI2InChI Convert %s string(s) into %s string(s) InChI2Struct Convert InChI string(s) to structure(s) in InChI aux.info format Using specific structure perception features: Stereo OFF Both ends of wedge point to stereocenters Do not add H Generating standard InChI Generating non-standard InChI with the options: (write H isotopes as D, T)Output SDfile only without stereochemical information and atom coordinates%s Mobile H Perception OFF (include FixedH layer) Mobile H Perception ON (omit FixedH layer) Mobile H ignored Undefined Mobile H mode Disabled Aggressive (De)protonation Include bonds to metals Do not reconnect metals (omit RecMet layer) Do not disconnect metals Racemic Relative Chiral Flag Absolute No AltBond Redund. Slow %s%s%s%sStereo ON Include undefined/unknown stereogenic centers and bonds Omit undefined/unknown stereogenic centers Omit undefined/unknown stereogenic bonds Omit undefined/unknown stereogenic centers and bonds Make labels for unknown and undefined stereo different Min. stereobond ring size: %d Min. stereobond ring size: NONE Account for keto-enol tautomerism Do not account for keto-enol tautomerism Account for 1,5-tautomerism Do not account for 1,5-tautomerism Generating standard InChIKey Generating InChIKey Generating hash extension (1st block) Generating hash extension (2nd block) Generating hash extension (two blocks) Saving InChI creation options suppressed for standard InChIIssue warning on empty structure MOLfileSDfileCMLfileInChI (plain identifier)InChI AuxInfo (xml)InChI AuxInfo (plain)UnknownInput format: %s (attempting to read Molfile number) SDfile data header: "%s" , tabbedPlain textXMLSDfile only (without stereochemical info and atom coordinates)SDfile onlyOutput format: %s%s Canon_numbers(branching, ring closures)Shorter alternativeRepresentation: Compressed Predecessor_numbers(closures)NumericalConnection table: %s, %s Aux. info suppressed Minimal Aux. info Full Aux. info Timeout per structure: %lu.%03lu sec No timeoutUp to %d atoms per structure Skipping %ld structure%s Terminate after structure #%ld Saving warning structures into the problem file Saving only all good structures into the problem file .mol.txt.log.prbSTDIOINPAUXSDF:START:END:NOLABELSSAVEOPTAUXNONEOUTPUTSDFSdfAtomsDTEQUSNONNEWPSOFFDONOTADDHSRELSRACSUCFChiralFlagONChiralFlagOFFSUUSLUUDFIXEDHRECMETKET15TWWarnOnEmptyStructureKeyXHash1XHash2InChI2InChIInChI2StructUnrecognized option: "%s". Terminating: generation of InChIKey is not available with 'Compress' option Terminating: generation of InChIKey is not available in InChI conversion mode Terminating: generation of InChIKey is not available with 'OutputSDF' option Hash extension(s) not generated: InChIKey not requestedNULrb#%dWrong 0D stereo descriptor(s): Missing atom dataWrong number of atomsMissing bonds dataWrong bonds dataWrong bond typeWrong number of bondsMissing atom coordinates dataWrong atom coordinates dataWrong number of coordinatesUnknown bond type in InChI aux assigned as a single bondProgram error interpreting InChI auxAtom has 1 or more than 3 aromatic bonds0D stereobond not recognizedCumulene stereo not recognized (0D)Cannot find non-metal stereobond neighor (0D)Missing reversibility infoWrong atoms dataEmpty structureToo many atoms/%s%s%s: %s="%s" %s="%s"%s<%s %s="%s">%s<%s %s="%s" %s="%s"/>"%d" %s="%s"Cannot find 0D stereobond neighboru%c%s%s%dc%d%s.%d.%si%doe%s%c%s%s%s%s %s="%d"%s??? Cannot allocate output buffer. No output for structure #%d.%s%s%s%s %s<%s %s="%s" %s="%s%s%s"%sStructure: %d%sStructure: %d.%s%s%s%s:%ldReChIInChI%s%s=%s%+d\%c%c//%s<%s>%s%s%s FATAL ERROR: %s ;* InChIversion1structurenumberid.nameid.valuetypemessagevaluefatal (aborted)error (no InChI)warningidentifiermobile-Hreconnectedversionalphanumericsctnormalcompressedbasicidentifier.auxiliary-info!-- This section is NOT a part of the identifier, it is not unique --omit_undef_dbondomit_undef_sp3<123fixed_Hfixed-Hisotopicstereoversionformula/cconnections/hH_atoms/qcharge/pprotons/bdbond/tsp3/msp3:invertedabs.inverted/stype (1=abs, 2=rel, 3=rac)type/iatomsexchangeable_HH-isotopic/fH_fixedH-fixed/otransposition/rreconnected bond(s) to metal(s) formulaabs_stereo_invertedstereo.abs.invertedreversibilitynormalization_typenorm-type/N:original_atom_numbersatom.orig-nbr/E:atom_equivalenceatom.equivalence/gE:group_equivalencegroup.equivalence/it:/iN:/CRV:charge_radical_valencecharges-rad-val/rA:/rB:bonds/rC:xyz/F:/I:/R:reconnected bond(s) to metal(s) part<&>"'hdt%02xABCDEFGHIJKLMNOPQRSTUVWXYZ InChIV10 V2000%3d%3d 0 0%3d 0 0 0 0 0%3d%s %10.4f%10.4f%10.4f %-3.3s%2d%3d 0 0%3d 0 0 0 0 %3u%3u%3u%3u 0 0 0 %3u%3u%3u 0 0 0 0 A %d +- %3d %3dM CHG%3d%s M RAD%3d%s M ISO%3d%s M END > <%s> > %s $$$$ COFClINPSiTeAtBN;P;As;Sb;O;S;Se;Te;C;SiN;P;As;Sb;O;S;Se;Te;%10.2e%10.2f%10.3f%10.4f%10.1f%10.3eh!-+u?tdhtdhitdh%02x %-.3s%-.3s%-.3s%-.3s%-.2s%-.3s%-.3s%-.2sMLKJIHGFEDCBOPQRSTUVWXYZ+-^HeLiBeNeNaMgAlArKCaScTiVCrMnFeCoNiCuZnGaGeKrRbSrYZrNbMoTcRuRhPdAgCdInSnXeCsBaLaCePrNdPmSmEuGdTbDyHoErTmYbLuHfTaReOsIrPtAuHgTlPbBiPoRnFrRaAcThPaUNpPuAmCmBkCfEsFmMdNoLrRf1.03_1java/lang/IllegalArgumentExceptionnet/sf/jniinchi/JniInchiInputnet/sf/jniinchi/JniInchiOutputnet/sf/jniinchi/JniInchiOutputStructurenet/sf/jniinchi/JniInchiOutputKeynet/sf/jniinchi/JniInchiInputDatanet/sf/jniinchi/JniInchiStructurenet/sf/jniinchi/JniInchiAtomnet/sf/jniinchi/JniInchiBondnet/sf/jniinchi/JniInchiStereo0D()IgetNumAtomsgetNumBondsgetNumStereo0D()Ljava/lang/String;getOptions(I)Lnet/sf/jniinchi/JniInchiAtom;getAtom(I)Lnet/sf/jniinchi/JniInchiBond;getBond(I)Lnet/sf/jniinchi/JniInchiStereo0D;getStereo0D(Lnet/sf/jniinchi/JniInchiAtom;)IgetAtomIndex(Lnet/sf/jniinchi/JniInchiAtom;)Lnet/sf/jniinchi/JniInchiAtom;addAtom(Lnet/sf/jniinchi/JniInchiBond;)Lnet/sf/jniinchi/JniInchiBond;addBond(Lnet/sf/jniinchi/JniInchiStereo0D;)Lnet/sf/jniinchi/JniInchiStereo0D;addStereo0D(DDDLjava/lang/String;)V(Lnet/sf/jniinchi/JniInchiAtom;Lnet/sf/jniinchi/JniInchiAtom;II)V(Lnet/sf/jniinchi/JniInchiAtom;Lnet/sf/jniinchi/JniInchiAtom;Lnet/sf/jniinchi/JniInchiAtom;Lnet/sf/jniinchi/JniInchiAtom;Lnet/sf/jniinchi/JniInchiAtom;II)VgetElementType()DgetXgetYgetZgetChargegetInchiRadicalgetImplicitHgetImplicitProtiumgetImplicitDeuteriumgetImplicitTritiumgetIsotopicMass(I)VsetChargesetInchiRadicalsetImplicitHsetImplicitProtiumsetImplicitDeuteriumsetImplicitTritiumsetIsotopicMass()Lnet/sf/jniinchi/JniInchiAtom;getOriginAtomgetTargetAtomgetInchiBondTypegetInchiBondStereogetCentralAtomgetNeighborgetInchiStereoTypegetInchiParity(ILjava/lang/String;Ljava/lang/String;Ljava/lang/String;Ljava/lang/String;)V(ILjava/lang/String;Ljava/lang/String;JJJJ)V(ILjava/lang/String;)V()V(ILnet/sf/jniinchi/JniInchiInput;ILjava/lang/String;)VElement name too long; maximum: Too many bonds from one atom; maximum: ư>?AAMbP?@@.A CSiGeCSiGeCSiGeNNNHz>@Q?-DT!@-DT! @?K`w.U@0M ??2@@433333?@>@Qffffff??Q?K7A`?-q=Y@Y"m@U7k_ @;f?q O?AAA<&>"' ꌠ9Y>)F++=$@{Gz??v/?v/??cG.lit$i@|.A{cAחA%! %! %! %! %! %! %! %! %! %! %! %! %! %! %! %! %! %! %! %! %! %! %! %! %! %! %! %! %! %! %" %" %" % " %" %" %" %" % " %$" %(" %," %0" %4" %8" %<" %@" %D" %H" h % hhhhhuhehNh@hhh#h8|hNrhdhh}^hThJh@h6h,h"hhhh$h2hhhhhhhhhh|hlh]xhNnh?dh0Zh PhFh H R \ f p z                ~ t j ` V L B 8 . $            A R g p       , @ T g w           # 3 E W !o " #     Q Q    `  a 1 i  @ !   (                       U # & & - 0 0 8 ; ; A D D H K X e h                              $ $     2 E O S i w {      D D  S i              S i  S i  $  <I &N >T "Y '` p { U { U b ` { U v U $ ? d@{ YzIp @  @ Mb@  Tt<"@ 7&@ (@ R,@ RLse/@# zZ2@( >?3@ ڏa6@  \(7@  A4F:@ };@ jhwH>@P [?@ ##]|A@ ((V/C@ ''ޓZ{C@ ((z6C@  --EB[zF@  00!lVG@ 33]hxI@ 44MbI@ 77xK@ 88䃞ͪK@ ;;HPswM@ ;:rL@ @?I.!vO@ A@IO@ FE^K=;Q@ IJ zR@ KKK=fR@R OP' AS@Z POƺS@ TTuVT@ UUcZ:U@ XX}гYU@  YYK89V@  [Z=,ԚyV@ ]] F%u:W@ `bsyX@ bbzX@ efvq yY@ ggˡEY@ jjyZ@ lk(Z@ pr6;Ny\@ ssbٹ\@ wx]@W zy9^@ Tt$<`@ S_@ c|`@ 'UH`@ ۊeyX5b@ 3ı.nb@ h"lxzc@ 8c@! Qkwc@$ /n}d@' oŝd@* oŽd@- &P6e@0 Fx e@3 ue@6 LJ~f@ 9 HVf@ Onf@< ^g@? T㥛g@B 0*h@E ?^h@H <h@K "aK?i@N H.i@Q ,D@i@T jjZ_j@W oj@ 6orbidullMaxClockndx;llZBasePathInEdgeListwAccessibleEndPoints͈Token[ToVertex_sCap&\ BlossomI{OneInChIOutOfStrFromINChI|HDeAbcNumberSC՗EqMultTautString̘ProtonComponent\aeaseteroAtomMayHaveXchgIsoHChargedNeighborAcidic"O"_N_VEquStringhsNC0n@dentLblllegalArgumentExceptionZOXNodeSetEmptySidjustTgroupsToForbiddenEdges2 RC#O$T,N-MOLfileError@BondsPosLELProtonAndIsoHBalanceToMobHStructdStCapFlowuAtom2وXmlEntityRefs܎emadicalToMetaluoveIsoProtonsInRestrStructProtonsInRestrStructIsoProtonsRestrProtonsRestr+keFS_FindTautJoNodeSetsIntersectSi_uplicateOrigAtomAlloctectInpInchiCreationOptionsbateBCNYBnForNonStereoRemoval^CSiDataStructopoc_SFNodesAreInSetRInchiToStructureeateBfsQueue{EdgeList{_INChIȒAnd ForNonStereoRemoval_CSiInit FillHillFormulaBn TCGBnStructyStruct Data)qs_ n5rErrMsgשZ_atom!atom_in_3memb_ringjbond_in_Nmax_memb_ringjcenterpoint_elemin_the_el}tom!ndCheckNextNeighborsoChargeType"RestoreInfoyMinus"Hydrogen"therExchangableH"rigInfoޒtomTypeHard#mmoniumSaltړhangedAtHChargeBNS#Groups2,i#ree_t_group_infoprint_digestšx_#nd_atoms_with_paritynspecial_bonds$odd_thingss$MaskwrRemoveExplOrImplH$neMsgdAddAcidicProtons$Remove$AcidicProtons%HplusNPO%atom%group'ond%itWsFromBnStructFlow%Properties@DonorAccAtomType&ardRemHCandidate&ullFlow&r3aPlusFromDB_N_DB_O_to_Metalr'lusMinusVertex:ermutationParitypevVertex'ocessingWarningsRadEndpoint'TCGroup{CPointsEndPointsalancedNetworkSearch(ns(reak`ondFlowMaxcapMinorderualancedNetworkSearch(nsxTestAndMarkAltBonds)AdjustFlowBondsRad)AltBns)InprC)TGroupInBnStruct,_INChI6In>NeighListmOneGroupInBnStruct*heckSymmPaths^ompfa*ystr1ight_change_other_atom_parity]ove_explicit_Hcationemicmprk_a+p_`ke_ft_type+lt_bonds_and_taut_groups/ LastGroupFromBnStruct,Rad-NPProtonsAndAcidCharges/FRCalculatedNonStereo`HalfStereoBondnOneStereonKnownNonStereoqInpAtBondBnStruct,TCGBnStruct{Groups2-oEdgeList{BnStruct-TCGBnStruct{Endpoints-FromMobileHEndpointewEdge.odeS2./ltPath.nyAltPath.ݜa.elpCommandLineParmsrd.lf^Remove/AddAcidicProtons/HplusNP/AcidicProtons/ׯT0I1Reversed3HillFormulas4LinCtStereoGOneOrigInchiToRevInChIeAlleNeighListLexlautNonIsoPartOfINChI0woPairsOfInChIep3RelRacAbs0t>ahI1HIGEN_N_SegmentAction1ToInchi_Inputތnchi1cr2Stereo1Msgsrev1ncpynpStructErrorType2NCHIA CanonNumberingCorrectness3INCHIA6MembTautRingM15TautPathM7MembTautRingM5MembTautRingMNextSymmNeighborsAndBonds^BnsConsistencyAndRefixStereobondsStereoINChI3INChI32333c263eocess4eprocessOneStructureintӂStructError4OneStructureAndCount4FormulaFromAtNumNoH55Layers525Taut5NonTaut2525VsNonTaut5˶p2spATOM6chi_Csertions_sortTitվfsOrder4CT6eltaChargeFromVFvtr7witch_ptrs]etha2_zCompDelimIdenticalValues_7icmpIso7S7Aux8FixedH_atoms9C9H:Line؏S7Atoms:tereoAbsInv7p:tereoAbsInv8p:T8I8Equ9ChargeRadVal9Numb9groupEqu8autTrans9so8nv9TgroupEqu8Equ8Numb9”ޭIsoSp39Sp39Numb9:Numb9:harge29onnections:_atoms:illFormula:Ύ2::פ3:2:3:2:M;ReMCanonEquivalenceInfoiUnkn0DStereoBonds}Sb0DParitiesFixedHRestoredStructureLessHydrogenInFormulaoity_of_mapped_^r>dINCHICereooingLength>uctFromApAtom>chi_DataCI?StAOrigBCompAtomDataBNeighListmAllINChIArrays_n?NC@p?chi_ƊAtom?InChIeDataBumImplicitH@ewRanksFromNeighLists^pAtom0DToInchiAtom@ChIbchvertStereooHIAhIArraysdINCHIArAuctFromAFromINChIdINCHIAStdINCHIAfromINCHIACKeyȚINCHIBStdINCHIBAtDataBStructOneStructureB0DParitiesConnectedComponentKeyFromINCHIΚKeyFromStdINCHIԚaxPrintfLengthCin]fDios_Dprint_nodisplayEvfprintfEsjgetsDprintfELfDTabDTabEstr_getDprintEresetEcloseEflushEinitEeprintEgetsEcEsE_nodisplayEE2EETabEFTabFF1FF   C_SameFB_SameH eFoXumberOfTies_ONExtFeds2addXmlEntityRefsЍ_SGStereoParity2TestHC_At_CanonRank2GB_At_CanonRanks2H̄ DGCarbGGbleGoubleToValuesH   AtomToValuesH  McrH1KEndpointInfoч 2S  ݖ  IsLastIReIGetPosISetPosIKeepLastAtomsOnlyJAJFreeJRankIAtomEquJȘ moveIAllocJIfLastAtomILastRankI    IfNoAtomsJÚ  seAtomForStereoJpSrmeŜ  ddJllocJAtomJRankJ  ߟ  2Yš  InARingKAltPathL 5TautInK2TautIn5MembAltRingK4TautInK6MembAltRingKAltPathL ǩ 5MembAltRingL7MembAltRingL Ŭ   re_alt_bondsLddr  ndPointLdgeFlowuxplicitDeletedHlementAndCountؕsM   CenterpointMM    storedStructureStereoMmoveExtraTautEndpoints DNResetOSetupPCreatePestroyNoN DNResetOSetupPCreatePestroyNoO CanonicalizationOSerializationONormalizationO CanonicalizationOSerializationONormalizationO          ڂ nPpdateVserActionorderedPartitionPmarkqMakeDiscretePCreateWFreeXJoinY rtitionQthsHaveIdenticalKnownParitiesoIsDiscreteQGetQSatisfiesLemma_2_25SCWFreeX FirstCellRTranspositionSMcrAndFixSet\ڃ MakeEmptyRGetSIntersectWithSetTŅ  romRixHInChIIdentical2MobHdorbiddenwNodeSetSEdgeListByw  ه Set2ToNodeSet1SsToRadEndpointsS     MinNodeTNumberOfNodesTΌ  א _TmNeighListTAT_b_AT_NUMBERSTBySymmAndCanonRankk2Tk PartUFullCoUCompareLayersGetFirstDiffUCUFillYInfinity[oUlear[mpareUpyV˓ LayersYmpareUpyV LayersU  CompareLayersVFullLinearCTi ɦ  neVtherSaltAdditionalLayerVComponentԁɫ NumHWCtWIsoSortKeysWOrigCoordƏĬ   CreateWFreeXƭ reateWoY  anspositionWeatʀCreateXFreeXGetMcrAndFixSetAndUnorderedPartition[    deSetXrmgFrXCreateXeeXomY ޱ  ɳ       pyYlorVertexY  ableYypeCreateYFreeZ VerticesZRadEndpoints[  OutZTautLinearCT2iIsotopicAtLinearCTiSingleStereoDescriptorsqAllStereoDescriptorsqAtomInvariant2[CdINChIfStereoParitiesqpStructEndpointFromInChI{OrigStructҏExtraFixedHData      non\lculatedPathsParitiesAreIdentical^Graph\icalization_stepgOneg_INChIi  ed]NeighLists_AndPrintINChITautomerGroupsAndEndpointsEquInfoToRanks]RanksToEquInfo]     NewRank^RingSizejDistDistributionĦ  ǫ  atom2^half_bond`  StereoBondParity^M  3`4`3_2_BySymmAndCanonRank_  fferentiateRanks_sconnect|Basic_2_3`4a     NeighborsTie`AllTiesm an_atom2`stereo_i 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|SEt.fA$u!A$uH8u HH8MDEDLLHǛ‰H iFHUH3t?H]LeLmLuL}UHAUATSHIIHH5q1?AUH5sL1?BT+H5gsL1?HH!uL H[A\A]?UHSHH?H{-{-DA<wqHHuHDA<wUHH uCA<wA1<Et9HH u{Et){Et#{AuCHIHH5yAHR>{1v{SDIdB<#/SM|A?ǀuHcH DD< S=uAA?/HxLHHxAH=ILhL2=H@HuAHDžH!K|-=HHHu!AHDžPHDžXL<HXHuAHDžPL<HPHu AH0H@MT$HxI4҉UHH@qHHt HuHUHAVAUATSIHIHHt>tzH5/8Hn5I1Hu6_B#B<v%B<vB< vJ؀wHtHL9uH{U4HIHL4I[A\A]A^UHAWAVAUATSHxIUHMfuHcHiD>fHcHiHHEAE1EEEMcLEIcDEHiN<E1AW\GdoEIcHiJ{fuq{\ksHUH}LxDpDh3HLxDpDht&IcfDdEACfD;utHUBc:CcuEAW\ID9eAD;U8E}D]HM1AHiBDfHD9|EHx[A\A]A^A_UHAWAVAUATSHIAHMHcHiD|8cHcHiL$>1AL$\McLEGAD\D9t9HHiJ(BcD9u#rHUH}2HtAL$\H91H[A\A]A^A_UHAUATSHIHDE1AH;?tH@L{2uD%kDH[A\A]UHHcHiH >q\E11LC8DQHiD8HHBDtD H~A AH9DUHHcHiHDN\HE1LoC/9t!9tHHiD8HHBDtAHE9|ADUHHcHiHDF\HN1L C*9tHHiD8HHBDtHD9|ѾUHHcHiHDF\HV1H5B#HiD8HHHD0t D9|عUHAVAUATSIHcHiH>C_S^S`SaD4sc@{AE1w(W1OHcHHHHH(BDlDK]GE9}ZK\11H=A6DSHiBD HHD8tDHH9A)E9uzD)v@un+u_DK]CA9uVK\11H=tA2DSHiBD HHD8tDHH9u AIDK]Dɉ[A\A]A^UHAVAUATSIHcHiH>C_S^S`SaD4sc@{AE1w(W1OHcHHHHH@DlC]EE9}_K\A111L @9DSHiBD HHBDtDHH9A)E9u|){@une*udC]AA9uWK\A111L@5DSHiBD HHBDtDHH9u )DS\Dщ[A\A]A^UHSADD vD9G1҃OHcHcH?HHHЀ|uD9tfA AAtAt IAuAE1DOH41AOIcHHHHDD)؅~9t AAu1ɉ[UHAUATSADD vD9G1҃OHcHcL->HHHB|(uD9tvA AAtE1AAEE1E1D_H41ۃAOIcHHHHBD(D)Ѕ~A9 9A9t AAu AD1ɉ[A\A]UHAWAVAUATSH8IHur,EAEE1HUHUHt TtEDEEMcO,H4E1^tNAH;?tH@H5"b"u D%[D;%[}AT$A̸ADOD%O^EE\D C^IU11)HiL1ɀx\u @1D9HD9|AE_AU^AU`AUa[A\A]A^UHHH5hVL8AUHH]LeHHIH>u/HHP0H1HtHHHI$HH$Ld$UHSHHHUH5^HUH5-_HhHVH5_HJHVH5_H,HVH5^HHVH5^HtnH*VH5^HtTH2VH5q^Ht:H5VH5_^Ht HYHHHH `THxTI4$HHXHHOHH /THTTI4$HHXHHHH SH6TI4$HHXHHHH SHTI4$HHjXHHHH SHSI4$HHAXHHHH SHSI6HHWHH[HH SHSI6HHWHH+HH tOHSI6HHIVHHHH DOHSI6HHVHHHH #SH}SI7HHUHHHH 3OH\SI7HHVHHkHH NH8SI7HHVHH;HH NHSI7HHUHH LH SH`PHMVH0HAHUHHLH SH(PH%VH0HAHUHHLH SHOHUH0HAHUHHtgHH RHOIuHHLUHHt:LH RHOHtUH0HAH UHH1H]LeLmLuL}UHSHHtHH[H[UHH]LeLmLuL}HPHuIHHHUIt$8IHIt$H8IHIt$H8IHI4$H8L|$L4$MIMHFTHH|TH0H1UH]LeLmLuL}UHAWAVAUATSHIAHHHHHM1IE1HEH@IEHPIEHXIEH`IEHhIEHpIEHxIEHEIEHEIEHEIEHEIEHEIEHEIEHEIEHEIEHEI$HH@L8H`XPHRHH#SH0LHM$MHLSHHL1AM$MH[SHHL1AM$MHSHHL1AM$MHSHHL1AM$MHRHHL1AM$MHRHHL1AM$MHRHHL1AM$HHPHHHL1AAIxE9HHMH3 t)HĘ[A\A]A^A_UHAWAVAUATSHIDH8HHHM1HE1HPH0HHPHCHXHCH`HCHhHC HpHC(HxHC0HEHC8HEHC@HEHCHHEHCPHEHCXHEHC`HEHChHEHCpHEDuEMEDHOHH8L1AHHE1AFLpH0BLbA9MEH~OHH8L1AMUH0EL@ATT$IHHHPHHSPH0L1AHMEHOHH8L1AIM9UAHxD;DtH HEH3t)Hĸ[A\A]A^A_UHAWAVAUATSHHIuILzEYAGEAGEAfEAGfEEgA_AGfu HE#MHBNHLL1AHEMHNHLL1AHEMAHMHLL1AIMMHMHLL1AHMMHMHLL1AMUˉT$UʉT$HD$H$MLEHMHNHHNH0L1AHMHGMHLL1AEI E9EHH[A\A]A^A_UHAWAVAUATSHxHHAEHHHU1HHHHDžHHHIHHxAAHLADH HfMHHMH0H1IHHDH+HLDHHLHgHLHxH H8H$DMDHLHHMH0H1AIHLHHPHLHHMH3 t Hx[A\A]A^A_UHH]LeLmLuH HIAH1LHI1E@HGkAHLLHPDH$Ld$Ll$Lt$UHH]LeLmLuH HIH1LHIHAHLLHPDH$Ld$Ll$Lt$UHH]LeLmLuL}H@IHuIIH1LHHH Hx= IHHw I$HLLPHEL(I$1LLHHHL Hx IHH) I$HLLPHELhH]LeLmLuL}UHH]LeLmLuL}HHLeLHpHPHLklHHHXLmLuL}HUH`HuH8IHHuH8Ll$Lt$L|$H`H$MIlH JHHVJH0H1XIDmDuHpHDHHpLDHHxLDHHPbH}i H}` LH]LeLmLuL}UHH]LeLmHPILeLH]HLbHL^IHbH} H} LH]LeLmUHH]LeLmLuL}H0IIH1LHIſ HHH@H@@HLAI$LLLPI$HL8IH@ M $MDHeHHHHH0L1MH]LeLmLuL}AUHAWAVAUATSHIHhH`EHHqGHH`1EIHbGHH`L1EIH8GHH`L1E}~IH3HcEHkxHV HpH1H` LpDž|HEHEHP(M|H3FHH`L1AIIHHFHLL1IIHPLLHHHExH Hv3IH|DH EH1LPpIHLLP1I}hHIHLLPIH5FHLL1HUHpD IHFHLL1H]HpDIHEHLL1AEIH,EHLL1AEwIH}EHLL1AEvIHEHLL1AEpIHDHLL1AEqIHDHLL1AErIHDHLL1AEsIHDHLL1fAEtfAEn|IxU9|E?MMHDHH`L1AHIH`DHHL1IIHjDHHL1IIHCHHL1EIHCHHL1AMH`CLHH`L1AAMLHH`L1AIcHkxHpHBn~'HIHAHBH0LQp8HfLBML@DtTfBnE]9]HcEH@HHsHXH1H}HXHEEMMH CHH`L1AIIHjBHLL1IMHB1HLL1AIMHLL1AHEMHLL1AHEMHLL1AHEMHALHH`L1AHUfBMLHH`L1AHMfAMHMHH`L1AHUfBMHMHH`L1AHMfAMHMHH`L1AH]fCIHAHLL1CIHeAHLL1CEHE E9E3IH#AHH`L1IIHULLHIHHx2HLHlHhHZILLLP]HhfYEfAHpHHXHYHĈ[A\A]A^A_UHH]LeLmLuH`ILmLE1t8H]HLwHLIHYH}ZL$LH]LeLmLuUHH]LeLmLuH`ILmLE1t8H]HL1wHLIIHXH}LULH]LeLmLuUHH]LeLmLuL}H@IHUH1HuHIǿHHH@H@@AdIƺA1HpAHIźA1HTMMHٺLBEI$LHuLPI$HL8IHLLM $MMH>HH(?H0L1MH]LeLmLuL}A%%%%%%%%% % %%%%%%%%%% %"%$%&%(%*%,%.%0%2%4%6%8%:%<%>%@%B%D%F%H%J%L%N%P%R%T%V%X%ZSSeHSbBrN;P;As;Sb;O;S;Se;Te;C;SiCannot create xml tag for error (structure #%ld.%s%s%s%s) Terminating. Cannot create end xml tag for structure #%ld.%s%s%s%s Terminating. 0*(),%dUnrecognized bond type:Unrecognized bond stereo:Bond to nonexistent atomAtom has a bond to itselfMultiple bonds between two atomsDuplicated bond(s) between two atomsAtom '%s' has more than %d bondsAtom '%s' has %d alternating bondsIgnored charge/radical redefinition:Parsed compound atom(s):Unknown element(s):%d->%dRadical center type replaced:Input type set to INPUT_INCHI Cannot allocate output message buffer. AuxInfoInChI=?FixedH ?RecMet ?SUU ?SLUUDFinal structure conversion failed Out of RAMCannot allocate output buffer. Terminating Cannot create end xml tag for structure #%d.%s%s%s%s Terminating. %-sGot non-normalized structureNot chiralGot non-canonicalized structureInChI generator not initializedStructure #%ldCannot interpret reversibility informationProton(s) added/removedCharges neutralized?helpTmnMNeAsiN:it:gE:E:HhN:F:I:AuxInfo=CRV:rA:R:rB:rC:/ \-+u?-+TDHInChI=1StructureABCDEFGHIJKLMNOPWarning: forced conversion to non-standard InChI for non-std input, Structure %ld Warning: ignore SaveOpt request for SaveOpt-less input, Structure %ld Warning: input created w/o RecMet - ignoring RecMet request, Structure %ld Warning: input created w/o FixedH - ignoring FixedH request, Structure %ld ; Error in detecting input InChI optionsAdd/Remove protons errorInChI compare errorInChI compare2 errorMerge Components errorDisconnected: *Conversion failed on component(s)MRD %s%s%d(%.96s)*Terminated by the user**Conversion failed* Wrong command line options: expected Inch2Struct or Inchi2Inchi End of file detected after structure %ld. Structure: %ld, Reconnected layer%s%.100sEnd of lineUnknown errorAllocation failedProgram errorSyntax error %s %s (%d) in %s (%d) (Metal compound)MOBILE_H_FORMULAMOBILE_H_CONNECTIONSMOBILE_HMOBILE_H_CHARGEMOBILE_H_PROTONSMOBILE_H_SP2MOBILE_H_SP3MOBILE_H_SP3_/mMOBILE_H_SP3_/sMOBILE_H_ISO_LAYER_FORKMOBILE_H_ISO_ATOMSMOBILE_H_ISO_EXCH_HMOBILE_H_ISO_SP2MOBILE_H_ISO_SP3MOBILE_H_ISO_SP3_/mMOBILE_H_ISO_SP3_/sFIXED_H_LAYER_FORKFIXED_H_FORMULAFIXED_HFIXED_H_CHARGEFIXED_H_SP2FIXED_H_SP3FIXED_H_SP3_/mFIXED_H_SP3_/sFIXED_H_PERMUTATIONFIXED_H_ISO_LAYER_FORKFIXED_H_ISO_ATOMSFIXED_H_ISO_LAYERFIXED_H_ISO_SP2FIXED_H_ISO_SP3FIXED_H_ISO_SP3_mFIXED_H_ISO_SP3_sFIXED_H_ISO_PERMUTATIONRECONNECTED_LAYER_FORKRECONNECTED_FORMULAMATERIAL_BALANCEUnknown ErrormnM... Mobile-H( Fixed-H(; Error: Hydrogens: Mobile-H groups: Isotopic: Charge(s): Proton balance: Exchangeable isotopic H: Stereo centers/allenes: Stereobonds/cumulenes: Fixed-H layer: Number of components: Conversion encountered: Wrong result Locations or number Fixed-H Number Missing Falsely present One instead of multiple Multiple instead of one Attachment points Do not match Atoms do not match Does not match for a component Does not match Falsely inverted Wrong parity Extra undefined Extra known Missing undefined Missing known Missing or extra Error Problems/mismatches:Omitted undefined stereoFatal undetermined program errorCannot allocate output data. TerminatingHDTN;P;O;S;Se;Te;Ambiguous stereo:center(s)bond(s)Cannot process free radical centerCannot process aromatic bondsARRAY OVERFLOWLENGTH_MISMATCHRANKING_ERRISOCOUNT_ERRTAUCOUNT_ERRISOTAUCOUNT_ERRMAPCOUNT_ERRTime limit exceededISO_H_ERRSTEREOCOUNT_ERRATOMCOUNT_ERRSTEREOBOND_ERRUser requested terminationREMOVE_STEREO_ERRCALC_STEREO_ERRSTEREO_CANON_ERRCANON_ERRWrong or missing chemical formulaUNKNOWN_ERRNo description(%d)UNKNOWN_ERR(%d)Accepted unusual valence(s):%ssdt,%s(%d)Warning (%s) structure #%ld.%s%s%s%s Error %d (%s) structure #%ld component %d.%s%s%s%s Cannot extract Component%s #%d structure #%ld.%s%s%s%s %s inp structure #%ld: End of file.%s%s%s%s End of file detected after structure #%ld. Cannot create start xml tag for structure #%ld.%s%s%s%s Terminating. Fatal Error %d (aborted; %s) inp structure #%ld.%s%s%s%s MolfileError %d (no %s; %s) inp structure #%ld.%s%s%s%s Warning: (%s) inp structure #%ld.%s%s%s%s <%s> ==== %s ==== Charges were rearrangedSalt was disconnected0D Parities Reconciliation failed:Metal was disconnectedCannot disconnect metal errorCannot distinguish componentsis missing =InChI ANNOTATED CONTENTSInChI, Software version 1.031%s ver %s%s. Usage: c%s-%s inputFile [outputFile [logFile [problemFile]]] [%coption[ %coption...]] Options: Input STDIO Use standard input/output streams InpAux Input structures in %s default aux. info format (for use with STDIO) SDF:DataHeader Read from the input SDfile the ID under this DataHeader Output AuxNone Omit auxiliary information (default: Include) SaveOpt Save custom InChI creation options (non-standard InChI) NoLabels Omit structure number, DataHeader and ID from %s output Tabbed Separate structure number, %s, and AuxInfo with tabs OutputSDF Convert %s created with default aux. info to SDfile SdfAtomsDT Output Hydrogen Isotopes to SDfile as Atoms D and T Structure perception SNon Exclude stereo (default: include absolute stereo) NEWPSOFF Both ends of wedge point to stereocenters (default: a narrow end) DoNotAddH All H are explicit (default: add H according to usual valences) Stereo perception modifiers (non-standard InChI) SRel Relative stereo SRac Racemic stereo SUCF Use Chiral Flag: On means Absolute stereo, Off - Relative Customizing InChI creation (non-standard InChI) SUU Always include omitted unknown/undefined stereo SLUUD Make labels for unknown and undefined stereo different RecMet Include reconnected metals results FixedH Include Fixed H layer KET Account for keto-enol tautomerism (experimental) 15T Account for 1,5-tautomerism (experimental) Generation Wnumber Set time-out per structure in seconds; W0 means unlimited WarnOnEmptyStructure Warn and produce empty %s for empty structure Key Generate InChIKey XHash1 Generate hash extension (to 256 bits) for 1st block of InChIKey XHash2 Generate hash extension (to 256 bits) for 2nd block of InChIKey %s ver %s%s. Usage: inchi-%s inputFile [outputFile [logFile [problemFile]]] [%coption[ %coption...]] Conversion InChI2InChI Convert %s string(s) into %s string(s) InChI2Struct Convert InChI string(s) to structure(s) in InChI aux.info format Using specific structure perception features: Stereo OFF Both ends of wedge point to stereocenters Do not add H Generating standard InChI Generating non-standard InChI with the options: (write H isotopes as D, T)Output SDfile only without stereochemical information and atom coordinates%s Mobile H Perception OFF (include FixedH layer) Mobile H Perception ON (omit FixedH layer) Mobile H ignored Undefined Mobile H mode Disabled Aggressive (De)protonation Include bonds to metals Do not reconnect metals (omit RecMet layer) Do not disconnect metals Racemic Relative Chiral Flag Absolute No AltBond Redund. Slow %s%s%s%sStereo ON Include undefined/unknown stereogenic centers and bonds Omit undefined/unknown stereogenic centers Omit undefined/unknown stereogenic bonds Omit undefined/unknown stereogenic centers and bonds Make labels for unknown and undefined stereo different Min. stereobond ring size: %d Min. stereobond ring size: NONE Account for keto-enol tautomerism Do not account for keto-enol tautomerism Account for 1,5-tautomerism Do not account for 1,5-tautomerism Generating standard InChIKey Generating InChIKey Generating hash extension (1st block) Generating hash extension (2nd block) Generating hash extension (two blocks) Saving InChI creation options suppressed for standard InChIIssue warning on empty structure MOLfileSDfileCMLfileInChI (plain identifier)InChI AuxInfo (xml)InChI AuxInfo (plain)UnknownInput format: %s (attempting to read Molfile number) SDfile data header: "%s" , tabbedPlain textXMLSDfile only (without stereochemical info and atom coordinates)SDfile onlyOutput format: %s%s Canon_numbers(branching, ring closures)Shorter alternativeRepresentation: Compressed Predecessor_numbers(closures)NumericalConnection table: %s, %s Aux. info suppressed Minimal Aux. info Full Aux. info Timeout per structure: %lu.%03lu sec No timeoutUp to %d atoms per structure Skipping %ld structure%s Terminate after structure #%ld Saving warning structures into the problem file Saving only all good structures into the problem file .mol.txt.log.prbSTDIOINPAUXSDF:START:END:NOLABELSSAVEOPTAUXNONEOUTPUTSDFSdfAtomsDTEQUSNONNEWPSOFFDONOTADDHSRELSRACSUCFChiralFlagONChiralFlagOFFSUUSLUUDFIXEDHRECMETKET15TWWarnOnEmptyStructureKeyXHash1XHash2InChI2InChIInChI2StructUnrecognized option: "%s". Terminating: generation of InChIKey is not available with 'Compress' option Terminating: generation of InChIKey is not available in InChI conversion mode Terminating: generation of InChIKey is not available with 'OutputSDF' option Hash extension(s) not generated: InChIKey not requestedNULrb#%dWrong 0D stereo descriptor(s): Missing atom dataWrong number of atomsMissing bonds dataWrong bonds dataWrong bond typeWrong number of bondsMissing atom coordinates dataWrong atom coordinates dataWrong number of coordinatesUnknown bond type in InChI aux assigned as a single bondProgram error interpreting InChI auxAtom has 1 or more than 3 aromatic bonds0D stereobond not recognizedCumulene stereo not recognized (0D)Cannot find non-metal stereobond neighor (0D)Missing reversibility infoWrong atoms dataEmpty structureToo many atoms/%s%s%s: %s="%s" %s="%s"%s<%s %s="%s">%s<%s %s="%s" %s="%s"/>"%d" %s="%s"Cannot find 0D stereobond neighboru%c%s%s%dc%d%s.%d.%si%doe%s%c%s%s%s%s %s="%d"%s??? Cannot allocate output buffer. No output for structure #%d.%s%s%s%s %s<%s %s="%s" %s="%s%s%s"%sStructure: %d%sStructure: %d.%s%s%s%s:%ldReChI%s%s=%s%+d\%c%c//%s<%s>%s%s%s FATAL ERROR: %s ;* InChIversion1structurenumberid.nameid.valuetypemessagevaluefatal (aborted)error (no InChI)warningidentifiermobile-Hreconnectedversionalphanumericsctnormalcompressedbasicidentifier.auxiliary-info!-- This section is NOT a part of the identifier, it is not unique --omit_undef_dbondomit_undef_sp3<123fixed_Hfixed-Hisotopicstereoversionformula/cconnections/hH_atoms/qcharge/pprotons/bdbond/tsp3/msp3:invertedabs.inverted/stype (1=abs, 2=rel, 3=rac)type/iatomsexchangeable_HH-isotopic/fH_fixedH-fixed/otransposition/rreconnected bond(s) to metal(s) formulaabs_stereo_invertedstereo.abs.invertedreversibilitynormalization_typenorm-type/N:original_atom_numbersatom.orig-nbr/E:atom_equivalenceatom.equivalence/gE:group_equivalencegroup.equivalence/it:/iN:/CRV:charge_radical_valencecharges-rad-val/rA:/rB:bonds/rC:xyz/F:/I:/R:reconnected bond(s) to metal(s) part<&>"'hdt%02xABCDEFGHIJKLMNOPQRSTUVWXYZ%s InChIV10 V2000%3d%3d 0 0%3d 0 0 0 0 0%3d%s %10.4f%10.4f%10.4f %-3.3s%2d%3d 0 0%3d 0 0 0 0 %3u%3u%3u%3u 0 0 0 %3u%3u%3u 0 0 0 0 A %d +- %3d %3dM CHG%3d%s M RAD%3d%s M ISO%3d%s M END > <%s> > %s $$$$ COFClINPSiTeAtBN;P;As;Sb;O;S;Se;Te;C;SiN;P;As;Sb;O;S;Se;Te;%10.2e%10.2f%10.3f%10.4f%10.1f%10.3eh!-+u?tdhtdhitdh%02x %-.3s%-.3s%-.3s%-.3s%-.2s%-.3s%-.3s%-.2sMLKJIHGFEDCBOPQRSTUVWXYZ+-^HeLiBeNeNaMgAlArKCaScTiVCrMnFeCoNiCuZnGaGeKrRbSrYZrNbMoTcRuRhPdAgCdInSnXeCsBaLaCePrNdPmSmEuGdTbDyHoErTmYbLuHfTaReOsIrPtAuHgTlPbBiPoRnFrRaAcThPaUNpPuAmCmBkCfEsFmMdNoLrRf1.03_1java/lang/IllegalArgumentExceptionnet/sf/jniinchi/JniInchiInputnet/sf/jniinchi/JniInchiOutputnet/sf/jniinchi/JniInchiOutputStructurenet/sf/jniinchi/JniInchiOutputKeynet/sf/jniinchi/JniInchiInputDatanet/sf/jniinchi/JniInchiStructurenet/sf/jniinchi/JniInchiAtomnet/sf/jniinchi/JniInchiBondnet/sf/jniinchi/JniInchiStereo0D()IgetNumAtomsgetNumBondsgetNumStereo0D()Ljava/lang/String;getOptions(I)Lnet/sf/jniinchi/JniInchiAtom;getAtom(I)Lnet/sf/jniinchi/JniInchiBond;getBond(I)Lnet/sf/jniinchi/JniInchiStereo0D;getStereo0D(Lnet/sf/jniinchi/JniInchiAtom;)IgetAtomIndex(Lnet/sf/jniinchi/JniInchiAtom;)Lnet/sf/jniinchi/JniInchiAtom;addAtom(Lnet/sf/jniinchi/JniInchiBond;)Lnet/sf/jniinchi/JniInchiBond;addBond(Lnet/sf/jniinchi/JniInchiStereo0D;)Lnet/sf/jniinchi/JniInchiStereo0D;addStereo0D(DDDLjava/lang/String;)V(Lnet/sf/jniinchi/JniInchiAtom;Lnet/sf/jniinchi/JniInchiAtom;II)V(Lnet/sf/jniinchi/JniInchiAtom;Lnet/sf/jniinchi/JniInchiAtom;Lnet/sf/jniinchi/JniInchiAtom;Lnet/sf/jniinchi/JniInchiAtom;Lnet/sf/jniinchi/JniInchiAtom;II)VgetElementType()DgetXgetYgetZgetChargegetInchiRadicalgetImplicitHgetImplicitProtiumgetImplicitDeuteriumgetImplicitTritiumgetIsotopicMass(I)VsetChargesetInchiRadicalsetImplicitHsetImplicitProtiumsetImplicitDeuteriumsetImplicitTritiumsetIsotopicMass()Lnet/sf/jniinchi/JniInchiAtom;getOriginAtomgetTargetAtomgetInchiBondTypegetInchiBondStereogetCentralAtomgetNeighborgetInchiStereoTypegetInchiParity(ILjava/lang/String;Ljava/lang/String;Ljava/lang/String;Ljava/lang/String;)V(ILjava/lang/String;Ljava/lang/String;JJJJ)V(ILjava/lang/String;)V()V(ILnet/sf/jniinchi/JniInchiInput;ILjava/lang/String;)VElement name too long; maximum: Too many bonds from one atom; maximum: ư>?MbP?@@.AC CSiGeCSiGeCSiGeNNNHz>@Q??-DT!@Y@Y"m@U7k_ @;f?-DT! @q O??K`w.U@0M ?2@@@ҩ*@>@Qffffff??Q?K7A`?-q=C<&>"' ++=$@{Gz??v/?v/??cG.lit$i@|.A{cAחALAS%hhhhhhhhhhh%h4xhCnhRdhbZhqPhFh@A>CDZDD^GIL,N&OO PeP$)Yc{`4aڴ[(2P$jh~ ?V\n?@y@@SAA[\̊QP]''f+uvv  1@""XYZZ[^C^^8___`b#c#h2h9jkkRllmfnuotu|C}}~Ӕ•-Ǯi;_7ĺV5d[G`6"w"$%P~~?]T4\ոEP%ɞD+wZm : U(UUNXj[<\`]]]FgjghHiii j;ѳUkYa6 6 )+ ', !- - Y. 0 1 ? 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