CompChem-Database: details for selected entry

ChEBI192198_s0_p7 (105849)

FormulaC50H87NO10P
MW893.21
InChIKeyPZTAFSJLEGORGQ-KPTOPPAANA-M
Entry_Date2023-11-01
Net_Charge-1
Number_Atoms151
Number_Heavy_Atoms62
Number_Rings0
Number_Bonds150
Rotat_Bonds49
Unbranched_Chain23
Chiral_Centers2
ONatoms11
HB_Donor3
HB_Acceptor6
OpenEye_HB_Donors3
OpenEye_HB_Acceptors6
Lipinski_HB_Donors1
Lipinski_HB_Acceptors11
Lipinski_Violations3
XLogP30
XLogP11.22
logP12.7939
PSA183.11
MR260.396
ABS0.17
Solubilityinsoluble
AggregatorPass
PM7_Heat_of_Formation_kcal_per_mol-637.49273
PM7_Total_Energy_ev-10637.48053
PM7_Electronic_Energy_ev-156342.28196
PM7_Dipole_Debye24.59777
PM7_Point_GroupC1
PM7_HOMO_Energy_ev-6.013
PM7_LUMO_Energy_ev1.974
PM7_COSMO_Area_square_ang805.28
PM7_COSMO_Volue_cubic_ang1234.32
PM7_Electron_Affinity_ev-1.974
PM7_Ionization_Energy_ev6.013
PM7_Energy_Gap_ev7.987
PM7_Global_Hardness_ev3.9935
PM7_Global_Softness_ev0.25040691123075
PM7_Chemical_Potential_ev-2.0195
PM7_Electronigativity_ev2.0195
PM7_Back_Donation_Energy_ev-0.998375
PM7_Electrophilicity_ev0.5106273006134969
OPENEYE_Name(2~{S})-2-azaniumyl-3-[[(2~{R})-3-[(5~{Z},8~{Z},11~{Z},14~{Z},17~{Z})-icosa-5,8,11,14,17-pentaenoyl]oxy-2-tetracosanoyloxy-propoxy]-oxido-phosphoryl]oxy-propanoate
SMILESC(=CCC=CCC=CCCCC(=O)OCC(COP(=O)([O-])OCC(C(=O)[O-])[NH3+])OC(=O)CCCCCCCCCCCCCCCCCCCCCCC)CC=CCC=CCC
Canonical_SMILESCCCCCCCCCCCCCCCCCCCCCCCC(=O)O[C@@H](CO[P@](=O)(OC[C@@H](C(=O)O)[NH3+])O)COC(=O)CCC/C=CC/C=CC/C=CC/C=CC/C=CCC
InChI1/C50H88NO10P/c1-3-5-7-9-11-13-15-17-19-21-22-23-24-26-28-30-32-34-36-38-40-42-49(53)61-46(44-59-62(56,57)60-45-47(51)50(54)55)43-58-48(52)41-39-37-35-33-31-29-27-25-20-18-16-14-12-10-8-6-4-2/h6,8,12,14,18,20,27,29,33,35,46-47H,3-5,7,9-11,13,15-17,19,21-26,28,30-32,34,36-45,51H2,1-2H3,(H,54,55)(H,56,57)/p-1/fC50H87NO10P/h51H/q-1
InChI_3D1S/C50H88NO10P/c1-3-5-7-9-11-13-15-17-19-21-22-23-24-26-28-30-32-34-36-38-40-42-49(53)61-46(44-59-62(56,57)60-45-47(51)50(54)55)43-58-48(52)41-39-37-35-33-31-29-27-25-20-18-16-14-12-10-8-6-4-2/h6,8,12,14,18,20,27,29,33,35,46-47H,3-5,7,9-11,13,15-17,19,21-26,28,30-32,34,36-45,51H2,1-2H3,(H,54,55)(H,56,57)/p+1/b8-6-,14-12-,20-18-,29-27-,35-33-/t46-,47+/m1/s1
AuxInfo1/1/N:15,14,24,20,27,9,29,7,31,18,33,5,35,3,37,16,39,1,41,2,43,45,44,42,17,40,4,38,6,36,19,34,8,32,10,30,21,28,25,26,22,23,47,48,46,50,49,11,12,13,51,52,53,54,56,55,57,58,61,60,59,62/E:(54,55)(56,57)/F:m/E:m/rA:149cCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCN+OOOOO-O-OOOOPHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHH/rB:w1;;;w3;w4;;;w7;w8;;;;;;s1s3;s2s4;s5s7;s6s8;s9s14;s10;s11;s12;s15;s21s22;s23;s24;s26;s27;s28;s29;s30;s31;s32;s33;s34;s35;s36;s37;s38;s39;s40;s41;s42;s43s44;;;;s13s46;s47s48;s49;d11;d12;d13;;s13;;s11s47;s12s50;s46;s48;d55s57s60s61;s1;s2;s3;s4;s5;s6;s7;s8;s9;s10;s14;s14;s14;s15;s15;s15;s16;s16;s17;s17;s18;s18;s19;s19;s20;s20;s21;s21;s22;s22;s23;s23;s24;s24;s25;s25;s26;s26;s27;s27;s28;s28;s29;s29;s30;s30;s31;s31;s32;s32;s33;s33;s34;s34;s35;s35;s36;s36;s37;s37;s38;s38;s39;s39;s40;s40;s41;s41;s42;s42;s43;s43;s44;s44;s45;s45;s46;s46;s47;s47;s48;s48;s49;s50;s51;s51;s51;/rC:;-.5,-.866,0;-1,1.7321,0;-2.5,-.866,0;-.5,2.5981,0;-3,-1.7321,0;-1.5,4.3301,0;-5,-1.7321,0;-1,5.1962,0;-5.5,-2.5981,0;-9.5,-2.5981,0;-11.134,-4.9641,0;-18,-2.4641,0;-2,6.9282,0;-11.134,-27.9641,0;-.5,.866,0;-1.5,-.866,0;-1,3.4641,0;-4,-1.7321,0;-1.5,6.0622,0;-6.5,-2.5981,0;-8.5,-2.5981,0;-11.134,-5.9641,0;-11.134,-26.9641,0;-7.5,-2.5981,0;-11.134,-6.9641,0;-11.134,-25.9641,0;-11.134,-7.9641,0;-11.134,-24.9641,0;-11.134,-8.9641,0;-11.134,-23.9641,0;-11.134,-9.9641,0;-11.134,-22.9641,0;-11.134,-10.9641,0;-11.134,-21.9641,0;-11.134,-11.9641,0;-11.134,-20.9641,0;-11.134,-12.9641,0;-11.134,-19.9641,0;-11.134,-13.9641,0;-11.134,-18.9641,0;-11.134,-14.9641,0;-11.134,-17.9641,0;-11.134,-15.9641,0;-11.134,-16.9641,0;-17,-3.4641,0;-11,-3.4641,0;-13,-3.4641,0;-18,-3.4641,0;-12,-3.4641,0;-19,-3.4641,0;-10,-1.7321,0;-10.2679,-4.4641,0;-17.134,-1.9641,0;-15,-4.4641,0;-18.866,-1.9641,0;-15,-2.4641,0;-10,-3.4641,0;-12,-4.4641,0;-16,-3.4641,0;-14,-3.4641,0;-15,-3.4641,0;.5,0,0;-.25,-1.299,0;-1.5,1.7321,0;-2.75,-.433,0;0,2.5981,0;-2.75,-2.1651,0;-2,4.3301,0;-5.25,-1.299,0;-.5,5.1962,0;-5.25,-3.0311,0;-2.433,6.6782,0;-1.567,7.1782,0;-2.25,7.3612,0;-10.634,-27.9641,0;-11.634,-27.9641,0;-11.134,-28.4641,0;-.933,.616,0;-.067,1.116,0;-1.5,-.366,0;-1.5,-1.366,0;-1.433,3.2141,0;-.567,3.7141,0;-4,-1.2321,0;-4,-2.2321,0;-1.933,5.8122,0;-1.067,6.3122,0;-6.5,-3.0981,0;-6.5,-2.0981,0;-8.5,-2.0981,0;-8.5,-3.0981,0;-10.634,-5.9641,0;-11.634,-5.9641,0;-11.634,-26.9641,0;-10.634,-26.9641,0;-7.5,-3.0981,0;-7.5,-2.0981,0;-10.634,-6.9641,0;-11.634,-6.9641,0;-11.634,-25.9641,0;-10.634,-25.9641,0;-10.634,-7.9641,0;-11.634,-7.9641,0;-11.634,-24.9641,0;-10.634,-24.9641,0;-10.634,-8.9641,0;-11.634,-8.9641,0;-11.634,-23.9641,0;-10.634,-23.9641,0;-10.634,-9.9641,0;-11.634,-9.9641,0;-11.634,-22.9641,0;-10.634,-22.9641,0;-10.634,-10.9641,0;-11.634,-10.9641,0;-11.634,-21.9641,0;-10.634,-21.9641,0;-10.634,-11.9641,0;-11.634,-11.9641,0;-11.634,-20.9641,0;-10.634,-20.9641,0;-10.634,-12.9641,0;-11.634,-12.9641,0;-11.634,-19.9641,0;-10.634,-19.9641,0;-10.634,-13.9641,0;-11.634,-13.9641,0;-11.634,-18.9641,0;-10.634,-18.9641,0;-10.634,-14.9641,0;-11.634,-14.9641,0;-11.634,-17.9641,0;-10.634,-17.9641,0;-10.634,-15.9641,0;-11.634,-15.9641,0;-11.634,-16.9641,0;-10.634,-16.9641,0;-17,-2.9641,0;-17,-3.9641,0;-11,-2.9641,0;-11,-3.9641,0;-13,-3.9641,0;-13,-2.9641,0;-18,-3.9641,0;-12,-2.9641,0;-19,-3.9641,0;-19,-2.9641,0;-19.5,-3.4641,0;
DuplicatesChEBI192198_s0_p7
mol2_Path/CCDB/ChEBI/Database/Compound-0000150000-0000199999/Compound-0000192000-0000192249/ChEBI192198_s0_p7.mol2
pdbqt_Path/CCDB/ChEBI/Database/Compound-0000150000-0000199999/Compound-0000192000-0000192249/ChEBI192198_s0_p7.pdbqt
sdf_Path/CCDB/ChEBI/Database/Compound-0000150000-0000199999/Compound-0000192000-0000192249/ChEBI192198_s0_p7.sdf