CompChem-Database: compound details

CompChem-Database: details for selected entry

ChEBI178294_s0_p7 (94425)

Formula C₃₆H₇₀NO₈P

MW 675.92

InChIKey CXDXDDHWBHPLKU-YLHGWYNBNA-N

Entry_Date 2023-11-01

Net_Charge 0

Number_Atoms 117

Number_Heavy_Atoms 46

Number_Rings 0

Number_Bonds 116

Rotat_Bonds 38

Unbranched_Chain 15

Chiral_Centers 1

ONatoms 9

HB_Donor 2

HB_Acceptor 4

OpenEye_HB_Donors 3

OpenEye_HB_Acceptors 4

Lipinski_HB_Donors 1

Lipinski_HB_Acceptors 9

Lipinski_Violations 2

XLogP3 0

XLogP 10.16

logP 9.1654

PSA 145.81

MR 193.222

ABS 0.17

Solubility moderately

Aggregator Pass

PM7_Heat_of_Formation_kcal_per_mol -508.94383

PM7_Total_Energy_ev -8095.91321

PM7_Electronic_Energy_ev -92311.10353

PM7_Dipole_Debye 5.8879

PM7_Point_Group C1

PM7_HOMO_Energy_ev -9.19

PM7_LUMO_Energy_ev 0.302

PM7_COSMO_Area_square_ang 721.81

PM7_COSMO_Volue_cubic_ang 949.11

PM7_Electron_Affinity_ev -0.302

PM7_Ionization_Energy_ev 9.19

PM7_Energy_Gap_ev 9.492

PM7_Global_Hardness_ev 4.746

PM7_Global_Softness_ev 0.21070375052675938

PM7_Chemical_Potential_ev -4.444

PM7_Electronigativity_ev 4.444

PM7_Back_Donation_Energy_ev -1.1865

PM7_Electrophilicity_ev 2.0806085124315215

OPENEYE_Name 2-azaniumylethyl [(2~{R})-3-[(~{Z})-hexadec-11-enoyl]oxy-2-pentadecanoyloxy-propyl] phosphate

SMILES C(=CCCCCCCCCCC(=O)OCC(COP(=O)([O-])OCC[NH3+])OC(=O)CCCCCCCCCCCCCC)CCCC

Canonical_SMILES CCCCCCCCCCCCCCC(=O)O[C@@H](CO[P@](=O)(OCC[NH3+])O)COC(=O)CCCCCCCCC/C=CCCCC

InChI 1/C36H70NO8P/c1-3-5-7-9-11-13-15-17-19-20-22-24-26-28-35(38)42-32-34(33-44-46(40,41)43-31-30-37)45-36(39)29-27-25-23-21-18-16-14-12-10-8-6-4-2/h9,11,34H,3-8,10,12-33,37H2,1-2H3,(H,40,41)/f/h37H

InChI_3D 1S/C36H70NO8P/c1-3-5-7-9-11-13-15-17-19-20-22-24-26-28-35(38)42-32-34(33-44-46(40,41)43-31-30-37)45-36(39)29-27-25-23-21-18-16-14-12-10-8-6-4-2/h9,11,34H,3-8,10,12-33,37H2,1-2H3,(H,40,41)/p+1/b11-9-/t34-/m1/s1

AuxInfo 1/1/N:5,6,11,12,13,17,7,21,1,25,2,28,8,30,14,31,18,29,22,26,27,23,24,19,20,15,16,9,10,32,33,34,35,36,3,4,37,38,39,40,41,42,44,45,43,46/E:(40,41)/F:m/E:m/rA:116cCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCN+OOOO-OOOOPHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHH/rB:w1;;;;;s1;s2;s3;s4;s5;s6;s7s11;s8;s9;s10;s12;s14;s15;s16;s17;s18;s19;s20;s21;s22s23;s24;s25;s27;s28;s29s30;;s32;;;s34s35;s32;d3;d4;;;s3s34;s4s36;s33;s35;d40s41s44s45;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;s37;s37;s37;/rC:;-.5,-.866,0;-10.5,-.866,0;-12.134,-3.2321,0;-2,3.4641,0;-12.134,-17.2321,0;-.5,.866,0;-1.5,-.866,0;-9.5,-.866,0;-12.134,-4.2321,0;-1.5,2.5981,0;-12.134,-16.2321,0;-1,1.7321,0;-2.5,-.866,0;-8.5,-.866,0;-12.134,-5.2321,0;-12.134,-15.2321,0;-3.5,-.866,0;-7.5,-.866,0;-12.134,-6.2321,0;-12.134,-14.2321,0;-4.5,-.866,0;-6.5,-.866,0;-12.134,-7.2321,0;-12.134,-13.2321,0;-5.5,-.866,0;-12.134,-8.2321,0;-12.134,-12.2321,0;-12.134,-9.2321,0;-12.134,-11.2321,0;-12.134,-10.2321,0;-19,-1.7321,0;-18,-1.7321,0;-12,-1.7321,0;-14,-1.7321,0;-13,-1.7321,0;-20,-1.7321,0;-11,0,0;-11.2679,-2.7321,0;-16,-2.7321,0;-16,-.7321,0;-11,-1.7321,0;-13,-2.7321,0;-17,-1.7321,0;-15,-1.7321,0;-16,-1.7321,0;.5,0,0;-.25,-1.299,0;-1.567,3.7141,0;-2.433,3.2141,0;-2.25,3.8971,0;-11.634,-17.2321,0;-12.634,-17.2321,0;-12.134,-17.7321,0;-.067,1.116,0;-.933,.616,0;-1.5,-.366,0;-1.5,-1.366,0;-9.5,-.366,0;-9.5,-1.366,0;-11.634,-4.2321,0;-12.634,-4.2321,0;-1.933,2.3481,0;-1.067,2.8481,0;-12.634,-16.2321,0;-11.634,-16.2321,0;-.567,1.9821,0;-1.433,1.4821,0;-2.5,-.366,0;-2.5,-1.366,0;-8.5,-1.366,0;-8.5,-.366,0;-11.634,-5.2321,0;-12.634,-5.2321,0;-12.634,-15.2321,0;-11.634,-15.2321,0;-3.5,-.366,0;-3.5,-1.366,0;-7.5,-1.366,0;-7.5,-.366,0;-11.634,-6.2321,0;-12.634,-6.2321,0;-12.634,-14.2321,0;-11.634,-14.2321,0;-4.5,-.366,0;-4.5,-1.366,0;-6.5,-1.366,0;-6.5,-.366,0;-11.634,-7.2321,0;-12.634,-7.2321,0;-12.634,-13.2321,0;-11.634,-13.2321,0;-5.5,-.366,0;-5.5,-1.366,0;-11.634,-8.2321,0;-12.634,-8.2321,0;-12.634,-12.2321,0;-11.634,-12.2321,0;-11.634,-9.2321,0;-12.634,-9.2321,0;-12.634,-11.2321,0;-11.634,-11.2321,0;-11.634,-10.2321,0;-12.634,-10.2321,0;-19,-2.2321,0;-19,-1.2321,0;-18,-1.2321,0;-18,-2.2321,0;-12,-1.2321,0;-12,-2.2321,0;-14,-2.2321,0;-14,-1.2321,0;-13,-1.2321,0;-20,-2.2321,0;-20,-1.2321,0;-20.5,-1.7321,0;

Duplicates ChEBI178294_s0_p7

mol2_Path /CCDB/ChEBI/Database/Compound-0000150000-0000199999/Compound-0000178250-0000178499/ChEBI178294_s0_p7.mol2

pdbqt_Path /CCDB/ChEBI/Database/Compound-0000150000-0000199999/Compound-0000178250-0000178499/ChEBI178294_s0_p7.pdbqt

sdf_Path /CCDB/ChEBI/Database/Compound-0000150000-0000199999/Compound-0000178250-0000178499/ChEBI178294_s0_p7.sdf

Formula	C₃₆H₇₀NO₈P
MW	675.92
InChIKey	CXDXDDHWBHPLKU-YLHGWYNBNA-N
Entry_Date	2023-11-01
Net_Charge	0
Number_Atoms	117
Number_Heavy_Atoms	46
Number_Rings	0
Number_Bonds	116
Rotat_Bonds	38
Unbranched_Chain	15
Chiral_Centers	1
ONatoms	9
HB_Donor	2
HB_Acceptor	4
OpenEye_HB_Donors	3
OpenEye_HB_Acceptors	4
Lipinski_HB_Donors	1
Lipinski_HB_Acceptors	9
Lipinski_Violations	2
XLogP3	0
XLogP	10.16
logP	9.1654
PSA	145.81
MR	193.222
ABS	0.17
Solubility	moderately
Aggregator	Pass
PM7_Heat_of_Formation_kcal_per_mol	-508.94383
PM7_Total_Energy_ev	-8095.91321
PM7_Electronic_Energy_ev	-92311.10353
PM7_Dipole_Debye	5.8879
PM7_Point_Group	C1
PM7_HOMO_Energy_ev	-9.19
PM7_LUMO_Energy_ev	0.302
PM7_COSMO_Area_square_ang	721.81
PM7_COSMO_Volue_cubic_ang	949.11
PM7_Electron_Affinity_ev	-0.302
PM7_Ionization_Energy_ev	9.19
PM7_Energy_Gap_ev	9.492
PM7_Global_Hardness_ev	4.746
PM7_Global_Softness_ev	0.21070375052675938
PM7_Chemical_Potential_ev	-4.444
PM7_Electronigativity_ev	4.444
PM7_Back_Donation_Energy_ev	-1.1865
PM7_Electrophilicity_ev	2.0806085124315215
OPENEYE_Name	2-azaniumylethyl [(2~{R})-3-[(~{Z})-hexadec-11-enoyl]oxy-2-pentadecanoyloxy-propyl] phosphate
SMILES	C(=CCCCCCCCCCC(=O)OCC(COP(=O)([O-])OCC[NH3+])OC(=O)CCCCCCCCCCCCCC)CCCC
Canonical_SMILES	CCCCCCCCCCCCCCC(=O)O[C@@H](CO[P@](=O)(OCC[NH3+])O)COC(=O)CCCCCCCCC/C=CCCCC
InChI	1/C36H70NO8P/c1-3-5-7-9-11-13-15-17-19-20-22-24-26-28-35(38)42-32-34(33-44-46(40,41)43-31-30-37)45-36(39)29-27-25-23-21-18-16-14-12-10-8-6-4-2/h9,11,34H,3-8,10,12-33,37H2,1-2H3,(H,40,41)/f/h37H
InChI_3D	1S/C36H70NO8P/c1-3-5-7-9-11-13-15-17-19-20-22-24-26-28-35(38)42-32-34(33-44-46(40,41)43-31-30-37)45-36(39)29-27-25-23-21-18-16-14-12-10-8-6-4-2/h9,11,34H,3-8,10,12-33,37H2,1-2H3,(H,40,41)/p+1/b11-9-/t34-/m1/s1
AuxInfo	1/1/N:5,6,11,12,13,17,7,21,1,25,2,28,8,30,14,31,18,29,22,26,27,23,24,19,20,15,16,9,10,32,33,34,35,36,3,4,37,38,39,40,41,42,44,45,43,46/E:(40,41)/F:m/E:m/rA:116cCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCN+OOOO-OOOOPHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHH/rB:w1;;;;;s1;s2;s3;s4;s5;s6;s7s11;s8;s9;s10;s12;s14;s15;s16;s17;s18;s19;s20;s21;s22s23;s24;s25;s27;s28;s29s30;;s32;;;s34s35;s32;d3;d4;;;s3s34;s4s36;s33;s35;d40s41s44s45;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;s37;s37;s37;/rC:;-.5,-.866,0;-10.5,-.866,0;-12.134,-3.2321,0;-2,3.4641,0;-12.134,-17.2321,0;-.5,.866,0;-1.5,-.866,0;-9.5,-.866,0;-12.134,-4.2321,0;-1.5,2.5981,0;-12.134,-16.2321,0;-1,1.7321,0;-2.5,-.866,0;-8.5,-.866,0;-12.134,-5.2321,0;-12.134,-15.2321,0;-3.5,-.866,0;-7.5,-.866,0;-12.134,-6.2321,0;-12.134,-14.2321,0;-4.5,-.866,0;-6.5,-.866,0;-12.134,-7.2321,0;-12.134,-13.2321,0;-5.5,-.866,0;-12.134,-8.2321,0;-12.134,-12.2321,0;-12.134,-9.2321,0;-12.134,-11.2321,0;-12.134,-10.2321,0;-19,-1.7321,0;-18,-1.7321,0;-12,-1.7321,0;-14,-1.7321,0;-13,-1.7321,0;-20,-1.7321,0;-11,0,0;-11.2679,-2.7321,0;-16,-2.7321,0;-16,-.7321,0;-11,-1.7321,0;-13,-2.7321,0;-17,-1.7321,0;-15,-1.7321,0;-16,-1.7321,0;.5,0,0;-.25,-1.299,0;-1.567,3.7141,0;-2.433,3.2141,0;-2.25,3.8971,0;-11.634,-17.2321,0;-12.634,-17.2321,0;-12.134,-17.7321,0;-.067,1.116,0;-.933,.616,0;-1.5,-.366,0;-1.5,-1.366,0;-9.5,-.366,0;-9.5,-1.366,0;-11.634,-4.2321,0;-12.634,-4.2321,0;-1.933,2.3481,0;-1.067,2.8481,0;-12.634,-16.2321,0;-11.634,-16.2321,0;-.567,1.9821,0;-1.433,1.4821,0;-2.5,-.366,0;-2.5,-1.366,0;-8.5,-1.366,0;-8.5,-.366,0;-11.634,-5.2321,0;-12.634,-5.2321,0;-12.634,-15.2321,0;-11.634,-15.2321,0;-3.5,-.366,0;-3.5,-1.366,0;-7.5,-1.366,0;-7.5,-.366,0;-11.634,-6.2321,0;-12.634,-6.2321,0;-12.634,-14.2321,0;-11.634,-14.2321,0;-4.5,-.366,0;-4.5,-1.366,0;-6.5,-1.366,0;-6.5,-.366,0;-11.634,-7.2321,0;-12.634,-7.2321,0;-12.634,-13.2321,0;-11.634,-13.2321,0;-5.5,-.366,0;-5.5,-1.366,0;-11.634,-8.2321,0;-12.634,-8.2321,0;-12.634,-12.2321,0;-11.634,-12.2321,0;-11.634,-9.2321,0;-12.634,-9.2321,0;-12.634,-11.2321,0;-11.634,-11.2321,0;-11.634,-10.2321,0;-12.634,-10.2321,0;-19,-2.2321,0;-19,-1.2321,0;-18,-1.2321,0;-18,-2.2321,0;-12,-1.2321,0;-12,-2.2321,0;-14,-2.2321,0;-14,-1.2321,0;-13,-1.2321,0;-20,-2.2321,0;-20,-1.2321,0;-20.5,-1.7321,0;
Duplicates	ChEBI178294_s0_p7
mol2_Path	/CCDB/ChEBI/Database/Compound-0000150000-0000199999/Compound-0000178250-0000178499/ChEBI178294_s0_p7.mol2
pdbqt_Path	/CCDB/ChEBI/Database/Compound-0000150000-0000199999/Compound-0000178250-0000178499/ChEBI178294_s0_p7.pdbqt
sdf_Path	/CCDB/ChEBI/Database/Compound-0000150000-0000199999/Compound-0000178250-0000178499/ChEBI178294_s0_p7.sdf