CompChem-Database: compound details

CompChem-Database: details for selected entry

ChEBI178432 (94565)

Formula C₄₅H₇₆O₅

MW 697.09

InChIKey RMCPDLFPBFRAAF-UHFFFAOYNA-N

Entry_Date 2023-11-01

Net_Charge 0

Number_Atoms 126

Number_Heavy_Atoms 50

Number_Rings 0

Number_Bonds 125

Rotat_Bonds 39

Unbranched_Chain 21

Chiral_Centers 1

ONatoms 5

HB_Donor 1

HB_Acceptor 3

OpenEye_HB_Donors 1

OpenEye_HB_Acceptors 3

Lipinski_HB_Donors 1

Lipinski_HB_Acceptors 5

Lipinski_Violations 2

XLogP3 0

XLogP 13.19

logP 12.9533

PSA 72.83

MR 219.317

ABS 0.17

Solubility insoluble

Aggregator Pass

PM7_Heat_of_Formation_kcal_per_mol -284.67633

PM7_Total_Energy_ev -8030.61178

PM7_Electronic_Energy_ev -109509.6331

PM7_Dipole_Debye 4.78822

PM7_Point_Group C1

PM7_HOMO_Energy_ev -9.558

PM7_LUMO_Energy_ev 0.787

PM7_COSMO_Area_square_ang 675.77

PM7_COSMO_Volue_cubic_ang 1081.87

PM7_Electron_Affinity_ev -0.787

PM7_Ionization_Energy_ev 9.558

PM7_Energy_Gap_ev 10.345

PM7_Global_Hardness_ev 5.1725

PM7_Global_Softness_ev 0.1933301111648139

PM7_Chemical_Potential_ev -4.3855

PM7_Electronigativity_ev 4.3855

PM7_Back_Donation_Energy_ev -1.293125

PM7_Electrophilicity_ev 1.8591213388110197

OPENEYE_Name [(2~{S})-3-hydroxy-2-[(~{Z})-icos-11-enoyl]oxy-propyl] (7~{Z},10~{Z},13~{Z},16~{Z},19~{Z})-docosa-7,10,13,16,19-pentaenoate

SMILES C(=CCC=CCC=CCCCCCC(=O)OCC(CO)OC(=O)CCCCCCCCCC=CCCCCCCCC)CC=CCC=CCC

Canonical_SMILES CCCCCCCC/C=CCCCCCCCCCC(=O)O[C@H](COC(=O)CCCCC/C=CC/C=CC/C=CC/C=CC/C=CCC)CO

InChI 1/C45H76O5/c1-3-5-7-9-11-13-15-17-19-21-22-24-25-27-29-31-33-35-37-39-44(47)49-42-43(41-46)50-45(48)40-38-36-34-32-30-28-26-23-20-18-16-14-12-10-8-6-4-2/h5,7,11,13,17-20,22,24,27,29,43,46H,3-4,6,8-10,12,14-16,21,23,25-26,28,30-42H2,1-2H3

InChI_3D 1S/C45H76O5/c1-3-5-7-9-11-13-15-17-19-21-22-24-25-27-29-31-33-35-37-39-44(47)49-42-43(41-46)50-45(48)40-38-36-34-32-30-28-26-23-20-18-16-14-12-10-8-6-4-2/h5,7,11,13,17-20,22,24,27,29,43,46H,3-4,6,8-10,12,14-16,21,23,25-26,28,30-42H2,1-2H3/b7-5-,13-11-,19-17-,20-18-,24-22-,29-27-/t43-/m0/s1

AuxInfo 1/0/N:15,16,21,27,9,33,7,38,19,39,5,35,3,29,17,23,1,11,2,12,18,4,24,6,20,30,8,36,10,40,22,42,28,41,34,37,31,32,25,26,43,44,45,13,14,48,46,47,49,50/rA:126cCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCOOOOOHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHH/rB:w1;;;w3;w4;;;w7;w8;;w11;;;;;s1s3;s2s4;s5s7;s6s8;s9s15;s10;s11;s12;s13;s14;s16;s22;s23;s24;s25;s26;s27;s28s31;s29;s30;s32;s33;s35s38;s36;s37;s40s41;;;s43s44;d13;d14;s43;s13s44;s14s45;s1;s2;s3;s4;s5;s6;s7;s8;s9;s10;s11;s12;s15;s15;s15;s16;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;s48;/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;-14,-13.7321,0;-14.866,-13.2321,0;-11.5,-2.5981,0;-14.866,-3.2321,0;-2,6.9282,0;-14,-21.7321,0;-.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;-14,-14.7321,0;-14.866,-12.2321,0;-10.5,-2.5981,0;-14.866,-4.2321,0;-14,-20.7321,0;-7.5,-2.5981,0;-14,-15.7321,0;-14.866,-11.2321,0;-9.5,-2.5981,0;-14.866,-5.2321,0;-14,-19.7321,0;-8.5,-2.5981,0;-14,-16.7321,0;-14.866,-10.2321,0;-14.866,-6.2321,0;-14,-18.7321,0;-14,-17.7321,0;-14.866,-9.2321,0;-14.866,-7.2321,0;-14.866,-8.2321,0;-15,-1.7321,0;-13,-1.7321,0;-14,-1.7321,0;-12,-3.4641,0;-15.732,-2.7321,0;-16,-1.7321,0;-12,-1.7321,0;-14,-2.7321,0;.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;-13.567,-13.4821,0;-15.299,-13.4821,0;-2.433,6.6782,0;-1.567,7.1782,0;-2.25,7.3612,0;-14.5,-21.7321,0;-13.5,-21.7321,0;-14,-22.2321,0;-.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,-2.0981,0;-6.5,-3.0981,0;-14.5,-14.7321,0;-13.5,-14.7321,0;-14.366,-12.2321,0;-15.366,-12.2321,0;-10.5,-3.0981,0;-10.5,-2.0981,0;-15.366,-4.2321,0;-14.366,-4.2321,0;-13.5,-20.7321,0;-14.5,-20.7321,0;-7.5,-2.0981,0;-7.5,-3.0981,0;-14.5,-15.7321,0;-13.5,-15.7321,0;-14.366,-11.2321,0;-15.366,-11.2321,0;-9.5,-3.0981,0;-9.5,-2.0981,0;-15.366,-5.2321,0;-14.366,-5.2321,0;-13.5,-19.7321,0;-14.5,-19.7321,0;-8.5,-2.0981,0;-8.5,-3.0981,0;-14.5,-16.7321,0;-13.5,-16.7321,0;-14.366,-10.2321,0;-15.366,-10.2321,0;-15.366,-6.2321,0;-14.366,-6.2321,0;-13.5,-18.7321,0;-14.5,-18.7321,0;-14.5,-17.7321,0;-13.5,-17.7321,0;-14.366,-9.2321,0;-15.366,-9.2321,0;-15.366,-7.2321,0;-14.366,-7.2321,0;-14.366,-8.2321,0;-15.366,-8.2321,0;-15,-1.2321,0;-15,-2.2321,0;-13,-2.2321,0;-13,-1.2321,0;-14,-1.2321,0;-16.25,-1.299,0;

Duplicates ChEBI178432

mol2_Path /CCDB/ChEBI/Database/Compound-0000150000-0000199999/Compound-0000178250-0000178499/ChEBI178432.mol2

pdbqt_Path /CCDB/ChEBI/Database/Compound-0000150000-0000199999/Compound-0000178250-0000178499/ChEBI178432.pdbqt

sdf_Path /CCDB/ChEBI/Database/Compound-0000150000-0000199999/Compound-0000178250-0000178499/ChEBI178432.sdf

Formula	C₄₅H₇₆O₅
MW	697.09
InChIKey	RMCPDLFPBFRAAF-UHFFFAOYNA-N
Entry_Date	2023-11-01
Net_Charge	0
Number_Atoms	126
Number_Heavy_Atoms	50
Number_Rings	0
Number_Bonds	125
Rotat_Bonds	39
Unbranched_Chain	21
Chiral_Centers	1
ONatoms	5
HB_Donor	1
HB_Acceptor	3
OpenEye_HB_Donors	1
OpenEye_HB_Acceptors	3
Lipinski_HB_Donors	1
Lipinski_HB_Acceptors	5
Lipinski_Violations	2
XLogP3	0
XLogP	13.19
logP	12.9533
PSA	72.83
MR	219.317
ABS	0.17
Solubility	insoluble
Aggregator	Pass
PM7_Heat_of_Formation_kcal_per_mol	-284.67633
PM7_Total_Energy_ev	-8030.61178
PM7_Electronic_Energy_ev	-109509.6331
PM7_Dipole_Debye	4.78822
PM7_Point_Group	C1
PM7_HOMO_Energy_ev	-9.558
PM7_LUMO_Energy_ev	0.787
PM7_COSMO_Area_square_ang	675.77
PM7_COSMO_Volue_cubic_ang	1081.87
PM7_Electron_Affinity_ev	-0.787
PM7_Ionization_Energy_ev	9.558
PM7_Energy_Gap_ev	10.345
PM7_Global_Hardness_ev	5.1725
PM7_Global_Softness_ev	0.1933301111648139
PM7_Chemical_Potential_ev	-4.3855
PM7_Electronigativity_ev	4.3855
PM7_Back_Donation_Energy_ev	-1.293125
PM7_Electrophilicity_ev	1.8591213388110197
OPENEYE_Name	[(2~{S})-3-hydroxy-2-[(~{Z})-icos-11-enoyl]oxy-propyl] (7~{Z},10~{Z},13~{Z},16~{Z},19~{Z})-docosa-7,10,13,16,19-pentaenoate
SMILES	C(=CCC=CCC=CCCCCCC(=O)OCC(CO)OC(=O)CCCCCCCCCC=CCCCCCCCC)CC=CCC=CCC
Canonical_SMILES	CCCCCCCC/C=CCCCCCCCCCC(=O)O[C@H](COC(=O)CCCCC/C=CC/C=CC/C=CC/C=CC/C=CCC)CO
InChI	1/C45H76O5/c1-3-5-7-9-11-13-15-17-19-21-22-24-25-27-29-31-33-35-37-39-44(47)49-42-43(41-46)50-45(48)40-38-36-34-32-30-28-26-23-20-18-16-14-12-10-8-6-4-2/h5,7,11,13,17-20,22,24,27,29,43,46H,3-4,6,8-10,12,14-16,21,23,25-26,28,30-42H2,1-2H3
InChI_3D	1S/C45H76O5/c1-3-5-7-9-11-13-15-17-19-21-22-24-25-27-29-31-33-35-37-39-44(47)49-42-43(41-46)50-45(48)40-38-36-34-32-30-28-26-23-20-18-16-14-12-10-8-6-4-2/h5,7,11,13,17-20,22,24,27,29,43,46H,3-4,6,8-10,12,14-16,21,23,25-26,28,30-42H2,1-2H3/b7-5-,13-11-,19-17-,20-18-,24-22-,29-27-/t43-/m0/s1
AuxInfo	1/0/N:15,16,21,27,9,33,7,38,19,39,5,35,3,29,17,23,1,11,2,12,18,4,24,6,20,30,8,36,10,40,22,42,28,41,34,37,31,32,25,26,43,44,45,13,14,48,46,47,49,50/rA:126cCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCOOOOOHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHH/rB:w1;;;w3;w4;;;w7;w8;;w11;;;;;s1s3;s2s4;s5s7;s6s8;s9s15;s10;s11;s12;s13;s14;s16;s22;s23;s24;s25;s26;s27;s28s31;s29;s30;s32;s33;s35s38;s36;s37;s40s41;;;s43s44;d13;d14;s43;s13s44;s14s45;s1;s2;s3;s4;s5;s6;s7;s8;s9;s10;s11;s12;s15;s15;s15;s16;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;s48;/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;-14,-13.7321,0;-14.866,-13.2321,0;-11.5,-2.5981,0;-14.866,-3.2321,0;-2,6.9282,0;-14,-21.7321,0;-.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;-14,-14.7321,0;-14.866,-12.2321,0;-10.5,-2.5981,0;-14.866,-4.2321,0;-14,-20.7321,0;-7.5,-2.5981,0;-14,-15.7321,0;-14.866,-11.2321,0;-9.5,-2.5981,0;-14.866,-5.2321,0;-14,-19.7321,0;-8.5,-2.5981,0;-14,-16.7321,0;-14.866,-10.2321,0;-14.866,-6.2321,0;-14,-18.7321,0;-14,-17.7321,0;-14.866,-9.2321,0;-14.866,-7.2321,0;-14.866,-8.2321,0;-15,-1.7321,0;-13,-1.7321,0;-14,-1.7321,0;-12,-3.4641,0;-15.732,-2.7321,0;-16,-1.7321,0;-12,-1.7321,0;-14,-2.7321,0;.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;-13.567,-13.4821,0;-15.299,-13.4821,0;-2.433,6.6782,0;-1.567,7.1782,0;-2.25,7.3612,0;-14.5,-21.7321,0;-13.5,-21.7321,0;-14,-22.2321,0;-.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,-2.0981,0;-6.5,-3.0981,0;-14.5,-14.7321,0;-13.5,-14.7321,0;-14.366,-12.2321,0;-15.366,-12.2321,0;-10.5,-3.0981,0;-10.5,-2.0981,0;-15.366,-4.2321,0;-14.366,-4.2321,0;-13.5,-20.7321,0;-14.5,-20.7321,0;-7.5,-2.0981,0;-7.5,-3.0981,0;-14.5,-15.7321,0;-13.5,-15.7321,0;-14.366,-11.2321,0;-15.366,-11.2321,0;-9.5,-3.0981,0;-9.5,-2.0981,0;-15.366,-5.2321,0;-14.366,-5.2321,0;-13.5,-19.7321,0;-14.5,-19.7321,0;-8.5,-2.0981,0;-8.5,-3.0981,0;-14.5,-16.7321,0;-13.5,-16.7321,0;-14.366,-10.2321,0;-15.366,-10.2321,0;-15.366,-6.2321,0;-14.366,-6.2321,0;-13.5,-18.7321,0;-14.5,-18.7321,0;-14.5,-17.7321,0;-13.5,-17.7321,0;-14.366,-9.2321,0;-15.366,-9.2321,0;-15.366,-7.2321,0;-14.366,-7.2321,0;-14.366,-8.2321,0;-15.366,-8.2321,0;-15,-1.2321,0;-15,-2.2321,0;-13,-2.2321,0;-13,-1.2321,0;-14,-1.2321,0;-16.25,-1.299,0;
Duplicates	ChEBI178432
mol2_Path	/CCDB/ChEBI/Database/Compound-0000150000-0000199999/Compound-0000178250-0000178499/ChEBI178432.mol2
pdbqt_Path	/CCDB/ChEBI/Database/Compound-0000150000-0000199999/Compound-0000178250-0000178499/ChEBI178432.pdbqt
sdf_Path	/CCDB/ChEBI/Database/Compound-0000150000-0000199999/Compound-0000178250-0000178499/ChEBI178432.sdf