CompChem-Database: compound details

CompChem-Database: details for selected entry

ChEBI179078 (95126)

Formula C₃₇H₇₁O₈P

MW 674.94

InChIKey CVVFISQWWIYWED-IHBONYPBNA-N

Entry_Date 2023-11-01

Net_Charge 0

Number_Atoms 117

Number_Heavy_Atoms 46

Number_Rings 0

Number_Bonds 116

Rotat_Bonds 39

Unbranched_Chain 18

Chiral_Centers 1

ONatoms 8

HB_Donor 2

HB_Acceptor 5

OpenEye_HB_Donors 2

OpenEye_HB_Acceptors 3

Lipinski_HB_Donors 2

Lipinski_HB_Acceptors 8

Lipinski_Violations 2

XLogP3 0

XLogP 12.57

logP 11.0695

PSA 129.17

MR 194.141

ABS 0.17

Solubility soluble

Aggregator Pass

PM7_Heat_of_Formation_kcal_per_mol -556.24888

PM7_Total_Energy_ev -8048.02556

PM7_Electronic_Energy_ev -88436.24421

PM7_Dipole_Debye 4.54444

PM7_Point_Group C1

PM7_HOMO_Energy_ev -9.702

PM7_LUMO_Energy_ev -0.374

PM7_COSMO_Area_square_ang 742.26

PM7_COSMO_Volue_cubic_ang 951.59

PM7_Electron_Affinity_ev 0.374

PM7_Ionization_Energy_ev 9.702

PM7_Energy_Gap_ev 9.328

PM7_Global_Hardness_ev 4.664

PM7_Global_Softness_ev 0.2144082332761578

PM7_Chemical_Potential_ev -5.038

PM7_Electronigativity_ev 5.038

PM7_Back_Donation_Energy_ev -1.166

PM7_Electrophilicity_ev 2.7209952830188677

OPENEYE_Name [(2~{R})-2-pentadecanoyloxy-3-phosphonooxy-propyl] (~{Z})-nonadec-9-enoate

SMILES C(=CCCCCCCCCC)CCCCCCCC(=O)OCC(COP(=O)(O)O)OC(=O)CCCCCCCCCCCCCC

Canonical_SMILES CCCCCCCCCCCCCCC(=O)O[C@@H](COP(=O)(O)O)COC(=O)CCCCCCC/C=CCCCCCCCCC

InChI 1/C37H71O8P/c1-3-5-7-9-11-13-15-17-18-19-20-22-23-25-27-29-31-36(38)43-33-35(34-44-46(40,41)42)45-37(39)32-30-28-26-24-21-16-14-12-10-8-6-4-2/h18-19,35H,3-17,20-34H2,1-2H3,(H2,40,41,42)/f/h40-41H

InChI_3D 1S/C37H71O8P/c1-3-5-7-9-11-13-15-17-18-19-20-22-23-25-27-29-31-36(38)43-33-35(34-44-46(40,41)42)45-37(39)32-30-28-26-24-21-16-14-12-10-8-6-4-2/h18-19,35H,3-17,20-34H2,1-2H3,(H2,40,41,42)/b19-18-/t35-/m1/s1

AuxInfo 1/1/N:5,6,11,12,17,18,23,24,28,29,26,31,20,33,14,34,8,2,1,7,32,13,19,30,25,27,21,22,15,16,9,10,35,36,37,3,4,38,39,40,41,42,43,45,44,46/E:(40,41,42)/F:5,6,11,12,17,18,23,24,28,29,26,31,20,33,14,34,8,2,1,7,32,13,19,30,25,27,21,22,15,16,9,10,35,36,37,3,4,38,39,41,42,40,43,45,44,46/E:(40,41)/rA:117cCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCOOOOOOOOPHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHH/rB:w1;;;;;s1;s2;s3;s4;s5;s6;s7;s8;s9;s10;s11;s12;s13;s14;s15;s16;s17;s18;s19s21;s20;s22;s23s26;s24;s27;s29;s30;s31;s32s33;;;s35s36;d3;d4;;;;s3s35;s4s37;s36;d40s41s42s45;s1;s2;s5;s5;s5;s6;s6;s6;s7;s7;s8;s8;s9;s9;s10;s10;s11;s11;s12;s12;s13;s13;s14;s14;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;s41;s42;/rC:;-.5,-.866,0;-4,6.9282,0;-2.366,9.2942,0;4,-8.6603,0;-2.366,23.2942,0;-.5,.866,0;0,-1.7321,0;-3.5,6.0622,0;-2.366,10.2942,0;3.5,-7.7942,0;-2.366,22.2942,0;-1,1.7321,0;.5,-2.5981,0;-3,5.1962,0;-2.366,11.2942,0;3,-6.9282,0;-2.366,21.2942,0;-1.5,2.5981,0;1,-3.4641,0;-2.5,4.3301,0;-2.366,12.2942,0;2.5,-6.0622,0;-2.366,20.2942,0;-2,3.4641,0;1.5,-4.3301,0;-2.366,13.2942,0;2,-5.1962,0;-2.366,19.2942,0;-2.366,14.2942,0;-2.366,18.2942,0;-2.366,15.2942,0;-2.366,17.2942,0;-2.366,16.2942,0;-2.5,7.7942,0;-.5,7.7942,0;-1.5,7.7942,0;-5,6.9282,0;-3.2321,8.7942,0;2.5,7.7942,0;1.5,6.7942,0;1.5,8.7942,0;-3.5,7.7942,0;-1.5,8.7942,0;.5,7.7942,0;1.5,7.7942,0;.5,0,0;-1,-.866,0;4.433,-8.4103,0;3.567,-8.9103,0;4.25,-9.0933,0;-2.866,23.2942,0;-1.866,23.2942,0;-2.366,23.7942,0;-.067,1.116,0;-.933,.616,0;.433,-1.4821,0;-.433,-1.9821,0;-3.933,5.8122,0;-3.067,6.3122,0;-2.866,10.2942,0;-1.866,10.2942,0;3.067,-8.0442,0;3.933,-7.5442,0;-1.866,22.2942,0;-2.866,22.2942,0;-.567,1.9821,0;-1.433,1.4821,0;.933,-2.3481,0;.067,-2.8481,0;-3.433,4.9462,0;-2.567,5.4462,0;-2.866,11.2942,0;-1.866,11.2942,0;2.567,-7.1782,0;3.433,-6.6782,0;-1.866,21.2942,0;-2.866,21.2942,0;-1.067,2.8481,0;-1.933,2.3481,0;1.433,-3.2141,0;.567,-3.7141,0;-2.933,4.0801,0;-2.067,4.5801,0;-2.866,12.2942,0;-1.866,12.2942,0;2.067,-6.3122,0;2.933,-5.8122,0;-1.866,20.2942,0;-2.866,20.2942,0;-1.567,3.7141,0;-2.433,3.2141,0;1.933,-4.0801,0;1.067,-4.5801,0;-2.866,13.2942,0;-1.866,13.2942,0;1.567,-5.4462,0;2.433,-4.9462,0;-1.866,19.2942,0;-2.866,19.2942,0;-2.866,14.2942,0;-1.866,14.2942,0;-1.866,18.2942,0;-2.866,18.2942,0;-2.866,15.2942,0;-1.866,15.2942,0;-1.866,17.2942,0;-2.866,17.2942,0;-2.866,16.2942,0;-1.866,16.2942,0;-2.5,7.2942,0;-2.5,8.2942,0;-.5,8.2942,0;-.5,7.2942,0;-1.5,7.2942,0;1.933,6.5442,0;1.067,9.0442,0;

Duplicates ChEBI179078

mol2_Path /CCDB/ChEBI/Database/Compound-0000150000-0000199999/Compound-0000179000-0000179249/ChEBI179078.mol2

pdbqt_Path /CCDB/ChEBI/Database/Compound-0000150000-0000199999/Compound-0000179000-0000179249/ChEBI179078.pdbqt

sdf_Path /CCDB/ChEBI/Database/Compound-0000150000-0000199999/Compound-0000179000-0000179249/ChEBI179078.sdf

Formula	C₃₇H₇₁O₈P
MW	674.94
InChIKey	CVVFISQWWIYWED-IHBONYPBNA-N
Entry_Date	2023-11-01
Net_Charge	0
Number_Atoms	117
Number_Heavy_Atoms	46
Number_Rings	0
Number_Bonds	116
Rotat_Bonds	39
Unbranched_Chain	18
Chiral_Centers	1
ONatoms	8
HB_Donor	2
HB_Acceptor	5
OpenEye_HB_Donors	2
OpenEye_HB_Acceptors	3
Lipinski_HB_Donors	2
Lipinski_HB_Acceptors	8
Lipinski_Violations	2
XLogP3	0
XLogP	12.57
logP	11.0695
PSA	129.17
MR	194.141
ABS	0.17
Solubility	soluble
Aggregator	Pass
PM7_Heat_of_Formation_kcal_per_mol	-556.24888
PM7_Total_Energy_ev	-8048.02556
PM7_Electronic_Energy_ev	-88436.24421
PM7_Dipole_Debye	4.54444
PM7_Point_Group	C1
PM7_HOMO_Energy_ev	-9.702
PM7_LUMO_Energy_ev	-0.374
PM7_COSMO_Area_square_ang	742.26
PM7_COSMO_Volue_cubic_ang	951.59
PM7_Electron_Affinity_ev	0.374
PM7_Ionization_Energy_ev	9.702
PM7_Energy_Gap_ev	9.328
PM7_Global_Hardness_ev	4.664
PM7_Global_Softness_ev	0.2144082332761578
PM7_Chemical_Potential_ev	-5.038
PM7_Electronigativity_ev	5.038
PM7_Back_Donation_Energy_ev	-1.166
PM7_Electrophilicity_ev	2.7209952830188677
OPENEYE_Name	[(2~{R})-2-pentadecanoyloxy-3-phosphonooxy-propyl] (~{Z})-nonadec-9-enoate
SMILES	C(=CCCCCCCCCC)CCCCCCCC(=O)OCC(COP(=O)(O)O)OC(=O)CCCCCCCCCCCCCC
Canonical_SMILES	CCCCCCCCCCCCCCC(=O)O[C@@H](COP(=O)(O)O)COC(=O)CCCCCCC/C=CCCCCCCCCC
InChI	1/C37H71O8P/c1-3-5-7-9-11-13-15-17-18-19-20-22-23-25-27-29-31-36(38)43-33-35(34-44-46(40,41)42)45-37(39)32-30-28-26-24-21-16-14-12-10-8-6-4-2/h18-19,35H,3-17,20-34H2,1-2H3,(H2,40,41,42)/f/h40-41H
InChI_3D	1S/C37H71O8P/c1-3-5-7-9-11-13-15-17-18-19-20-22-23-25-27-29-31-36(38)43-33-35(34-44-46(40,41)42)45-37(39)32-30-28-26-24-21-16-14-12-10-8-6-4-2/h18-19,35H,3-17,20-34H2,1-2H3,(H2,40,41,42)/b19-18-/t35-/m1/s1
AuxInfo	1/1/N:5,6,11,12,17,18,23,24,28,29,26,31,20,33,14,34,8,2,1,7,32,13,19,30,25,27,21,22,15,16,9,10,35,36,37,3,4,38,39,40,41,42,43,45,44,46/E:(40,41,42)/F:5,6,11,12,17,18,23,24,28,29,26,31,20,33,14,34,8,2,1,7,32,13,19,30,25,27,21,22,15,16,9,10,35,36,37,3,4,38,39,41,42,40,43,45,44,46/E:(40,41)/rA:117cCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCOOOOOOOOPHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHH/rB:w1;;;;;s1;s2;s3;s4;s5;s6;s7;s8;s9;s10;s11;s12;s13;s14;s15;s16;s17;s18;s19s21;s20;s22;s23s26;s24;s27;s29;s30;s31;s32s33;;;s35s36;d3;d4;;;;s3s35;s4s37;s36;d40s41s42s45;s1;s2;s5;s5;s5;s6;s6;s6;s7;s7;s8;s8;s9;s9;s10;s10;s11;s11;s12;s12;s13;s13;s14;s14;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;s41;s42;/rC:;-.5,-.866,0;-4,6.9282,0;-2.366,9.2942,0;4,-8.6603,0;-2.366,23.2942,0;-.5,.866,0;0,-1.7321,0;-3.5,6.0622,0;-2.366,10.2942,0;3.5,-7.7942,0;-2.366,22.2942,0;-1,1.7321,0;.5,-2.5981,0;-3,5.1962,0;-2.366,11.2942,0;3,-6.9282,0;-2.366,21.2942,0;-1.5,2.5981,0;1,-3.4641,0;-2.5,4.3301,0;-2.366,12.2942,0;2.5,-6.0622,0;-2.366,20.2942,0;-2,3.4641,0;1.5,-4.3301,0;-2.366,13.2942,0;2,-5.1962,0;-2.366,19.2942,0;-2.366,14.2942,0;-2.366,18.2942,0;-2.366,15.2942,0;-2.366,17.2942,0;-2.366,16.2942,0;-2.5,7.7942,0;-.5,7.7942,0;-1.5,7.7942,0;-5,6.9282,0;-3.2321,8.7942,0;2.5,7.7942,0;1.5,6.7942,0;1.5,8.7942,0;-3.5,7.7942,0;-1.5,8.7942,0;.5,7.7942,0;1.5,7.7942,0;.5,0,0;-1,-.866,0;4.433,-8.4103,0;3.567,-8.9103,0;4.25,-9.0933,0;-2.866,23.2942,0;-1.866,23.2942,0;-2.366,23.7942,0;-.067,1.116,0;-.933,.616,0;.433,-1.4821,0;-.433,-1.9821,0;-3.933,5.8122,0;-3.067,6.3122,0;-2.866,10.2942,0;-1.866,10.2942,0;3.067,-8.0442,0;3.933,-7.5442,0;-1.866,22.2942,0;-2.866,22.2942,0;-.567,1.9821,0;-1.433,1.4821,0;.933,-2.3481,0;.067,-2.8481,0;-3.433,4.9462,0;-2.567,5.4462,0;-2.866,11.2942,0;-1.866,11.2942,0;2.567,-7.1782,0;3.433,-6.6782,0;-1.866,21.2942,0;-2.866,21.2942,0;-1.067,2.8481,0;-1.933,2.3481,0;1.433,-3.2141,0;.567,-3.7141,0;-2.933,4.0801,0;-2.067,4.5801,0;-2.866,12.2942,0;-1.866,12.2942,0;2.067,-6.3122,0;2.933,-5.8122,0;-1.866,20.2942,0;-2.866,20.2942,0;-1.567,3.7141,0;-2.433,3.2141,0;1.933,-4.0801,0;1.067,-4.5801,0;-2.866,13.2942,0;-1.866,13.2942,0;1.567,-5.4462,0;2.433,-4.9462,0;-1.866,19.2942,0;-2.866,19.2942,0;-2.866,14.2942,0;-1.866,14.2942,0;-1.866,18.2942,0;-2.866,18.2942,0;-2.866,15.2942,0;-1.866,15.2942,0;-1.866,17.2942,0;-2.866,17.2942,0;-2.866,16.2942,0;-1.866,16.2942,0;-2.5,7.2942,0;-2.5,8.2942,0;-.5,8.2942,0;-.5,7.2942,0;-1.5,7.2942,0;1.933,6.5442,0;1.067,9.0442,0;
Duplicates	ChEBI179078
mol2_Path	/CCDB/ChEBI/Database/Compound-0000150000-0000199999/Compound-0000179000-0000179249/ChEBI179078.mol2
pdbqt_Path	/CCDB/ChEBI/Database/Compound-0000150000-0000199999/Compound-0000179000-0000179249/ChEBI179078.pdbqt
sdf_Path	/CCDB/ChEBI/Database/Compound-0000150000-0000199999/Compound-0000179000-0000179249/ChEBI179078.sdf