CompChem-Database: compound details

CompChem-Database: details for selected entry

DB04748_t0 (5078)

Formula C₃₄H₄₆N₆O₆S₂

MW 698.89

InChIKey PJLSJXTZOMOVBI-YLHGWYNBNA-N

Entry_Date 2023-09-01

Net_Charge 0

Number_Atoms 94

Number_Heavy_Atoms 48

Number_Rings 4

Number_Bonds 97

Rotat_Bonds 19

Unbranched_Chain 3

Chiral_Centers 3

ONatoms 12

HB_Donor 3

HB_Acceptor 7

OpenEye_HB_Donors 3

OpenEye_HB_Acceptors 7

Lipinski_HB_Donors 3

Lipinski_HB_Acceptors 12

Lipinski_Violations 2

XLogP3 0

XLogP 4.36

logP 5.3046

PSA 192.36

MR 194.597

ABS 0.17

Solubility soluble

Aggregator Pass

PM7_Heat_of_Formation_kcal_per_mol -162.75692

PM7_Total_Energy_ev -8038.64507

PM7_Electronic_Energy_ev -94727.7911

PM7_Dipole_Debye 9.92201

PM7_Point_Group C1

PM7_HOMO_Energy_ev -9.071

PM7_LUMO_Energy_ev -1.049

PM7_COSMO_Area_square_ang 640.13

PM7_COSMO_Volue_cubic_ang 857.6

PM7_Electron_Affinity_ev 1.049

PM7_Ionization_Energy_ev 9.071

PM7_Energy_Gap_ev 8.022

PM7_Global_Hardness_ev 4.011

PM7_Global_Softness_ev 0.2493143854400399

PM7_Chemical_Potential_ev -5.06

PM7_Electronigativity_ev 5.06

PM7_Back_Donation_Energy_ev -1.00275

PM7_Electrophilicity_ev 3.191672899526303

OPENEYE_Name (2~{S})-~{N}-[(1~{S},2~{R})-1-benzyl-2-hydroxy-3-[[4-[(~{E})-hydroxyiminomethyl]phenyl]sulfonyl-isobutyl-amino]propyl]-3-methyl-2-[3-[(2-methylthiazol-4-yl)methyl]-2-oxo-imidazolidin-1-yl]butanamide

SMILES c1ccc(cc1)CC(C(CN(CC(C)C)S(=O)(=O)c2ccc(cc2)C=NO)O)NC(=O)C(C(C)C)N3C(=O)N(CC3)Cc4csc(n4)C

Canonical_SMILES O/N=C/c1ccc(cc1)S(=O)(=O)N(C[C@H]([C@H](Cc1ccccc1)NC(=O)[C@@H](N1CCN(C1=O)Cc1csc(n1)C)C(C)C)O)CC(C)C

InChI 1/C34H46N6O6S2/c1-23(2)19-39(48(45,46)29-13-11-27(12-14-29)18-35-44)21-31(41)30(17-26-9-7-6-8-10-26)37-33(42)32(24(3)4)40-16-15-38(34(40)43)20-28-22-47-25(5)36-28/h6-14,18,22-24,30-32,41,44H,15-17,19-21H2,1-5H3,(H,37,42)/f/h37H

InChI_3D 1S/C34H46N6O6S2/c1-23(2)19-39(48(45,46)29-13-11-27(12-14-29)18-35-44)21-31(41)30(17-26-9-7-6-8-10-26)37-33(42)32(24(3)4)40-16-15-38(34(40)43)20-28-22-47-25(5)36-28/h6-14,18,22-24,30-32,41,44H,15-17,19-21H2,1-5H3,(H,37,42)/b35-18+/t30-,31+,32-/m0/s1

AuxInfo 1/1/N:22,23,24,25,21,1,2,3,6,7,4,5,8,9,19,20,26,17,28,27,29,10,31,32,15,12,11,14,13,33,34,30,18,16,36,35,39,37,40,38,45,42,41,46,43,44,47,48/E:(1,2)(3,4)(7,8)(9,10)(11,12)(13,14)(45,46)/F:m/E:m/CRV:48.6/rA:94cCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCNNNNNNOOOOOOSSHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHH/rB:d1;s1;;;s2;d3;d4;s5;;s4d5;d6s7;s8d9;d10;;;s11;;;s19;s15;;;;;s12;s14;;;s18;s22s23s28;s24s25s30;s26;s29s33;s14d15;w17;s16s19s27;s16s20s30;s18s33;s28s29;d16;d18;;;s34;s36;s10s15;s13s40d43d44;s1;s2;s3;s4;s5;s6;s7;s8;s9;s10;s17;s19;s19;s20;s20;s21;s21;s21;s22;s22;s22;s23;s23;s23;s24;s24;s24;s25;s25;s25;s26;s26;s27;s27;s28;s28;s29;s29;s30;s31;s32;s33;s34;s39;s45;s46;/rC:-1.371,-8.7892,0;-.7007,-8.0471,0;-2.35,-8.5855,0;-9.5337,-4.754,0;-8.3745,-3.4631,0;-1.0126,-7.0915,0;-2.6619,-7.6299,0;-8.7858,-5.4256,0;-7.6266,-4.1347,0;-.3065,.9519,0;-9.3243,-3.7761,0;-1.9948,-6.8781,0;-7.8285,-5.1194,0;;1.3131,.9519,0;-2.1793,-1.614,0;-10.0683,-3.108,0;-3.1306,-3.8301,0;-.8684,-2.5689,0;-1.6791,-3.1544,0;2.2646,1.2597,0;-7.732,-8.2059,0;-6.9602,-9.3909,0;-4.7018,-2.2391,0;-4.0615,-.9781,0;-2.5378,-5.2144,0;-.5889,-.8082,0;-6.547,-7.434,0;-5.3897,-6.1453,0;-3.4409,-2.8794,0;-6.7536,-8.4125,0;-3.7512,-1.9288,0;-3.4884,-5.5247,0;-4.4391,-5.835,0;1.0014,0,0;-9.8617,-2.1296,0;-1.1777,-1.6165,0;-2.4903,-2.5691,0;-3.7987,-4.5741,0;-6.3404,-6.4556,0;-2.7659,-.8041,0;-2.1522,-4.0366,0;-7.7525,-6.5315,0;-6.4163,-5.0434,0;-4.1288,-6.7857,0;-10.6058,-1.4615,0;.5007,1.5426,0;-7.0844,-5.7875,0;-1.2158,-9.2645,0;-.2116,-8.1511,0;-2.6835,-8.958,0;-10.0093,-4.9085,0;-8.2719,-2.9737,0;-.6774,-6.7205,0;-3.1514,-7.528,0;-8.8906,-5.9145,0;-7.1517,-3.9781,0;-.7821,1.1062,0;-10.5436,-3.2632,0;-.4115,-2.366,0;-.6193,-3.0024,0;-1.3449,-3.5263,0;-2.0133,-3.5264,0;2.1107,1.7354,0;2.4184,.7839,0;2.7403,1.4135,0;-7.6287,-7.7167,0;-7.8353,-8.6951,0;-8.2212,-8.1026,0;-7.4494,-9.2876,0;-6.4709,-9.4942,0;-7.0635,-9.8801,0;-4.5467,-2.7144,0;-4.857,-1.7637,0;-5.1772,-2.3942,0;-3.5862,-.823,0;-4.5368,-1.1333,0;-4.2166,-.5028,0;-2.693,-4.7391,0;-2.0625,-5.0593,0;-.1847,-1.1027,0;-.993,-.5138,0;-6.0578,-7.5373,0;-7.0362,-7.3307,0;-5.5449,-5.67,0;-5.2346,-6.6206,0;-3.9162,-3.0346,0;-6.2643,-8.5158,0;-3.2759,-1.7736,0;-3.3333,-6.0001,0;-4.5942,-5.3597,0;-4.288,-4.4708,0;-4.4629,-7.1577,0;-10.5025,-.9722,0;

Duplicates DB04748_t0

mol2_Path /CCDB/DrugBank/Database/Compound-0000000000-0000049999/Compound-0000004500-0000004749/DB04748_t0.mol2

pdbqt_Path /CCDB/DrugBank/Database/Compound-0000000000-0000049999/Compound-0000004500-0000004749/DB04748_t0.pdbqt

sdf_Path /CCDB/DrugBank/Database/Compound-0000000000-0000049999/Compound-0000004500-0000004749/DB04748_t0.sdf

Formula	C₃₄H₄₆N₆O₆S₂
MW	698.89
InChIKey	PJLSJXTZOMOVBI-YLHGWYNBNA-N
Entry_Date	2023-09-01
Net_Charge	0
Number_Atoms	94
Number_Heavy_Atoms	48
Number_Rings	4
Number_Bonds	97
Rotat_Bonds	19
Unbranched_Chain	3
Chiral_Centers	3
ONatoms	12
HB_Donor	3
HB_Acceptor	7
OpenEye_HB_Donors	3
OpenEye_HB_Acceptors	7
Lipinski_HB_Donors	3
Lipinski_HB_Acceptors	12
Lipinski_Violations	2
XLogP3	0
XLogP	4.36
logP	5.3046
PSA	192.36
MR	194.597
ABS	0.17
Solubility	soluble
Aggregator	Pass
PM7_Heat_of_Formation_kcal_per_mol	-162.75692
PM7_Total_Energy_ev	-8038.64507
PM7_Electronic_Energy_ev	-94727.7911
PM7_Dipole_Debye	9.92201
PM7_Point_Group	C1
PM7_HOMO_Energy_ev	-9.071
PM7_LUMO_Energy_ev	-1.049
PM7_COSMO_Area_square_ang	640.13
PM7_COSMO_Volue_cubic_ang	857.6
PM7_Electron_Affinity_ev	1.049
PM7_Ionization_Energy_ev	9.071
PM7_Energy_Gap_ev	8.022
PM7_Global_Hardness_ev	4.011
PM7_Global_Softness_ev	0.2493143854400399
PM7_Chemical_Potential_ev	-5.06
PM7_Electronigativity_ev	5.06
PM7_Back_Donation_Energy_ev	-1.00275
PM7_Electrophilicity_ev	3.191672899526303
OPENEYE_Name	(2~{S})-~{N}-[(1~{S},2~{R})-1-benzyl-2-hydroxy-3-[[4-[(~{E})-hydroxyiminomethyl]phenyl]sulfonyl-isobutyl-amino]propyl]-3-methyl-2-[3-[(2-methylthiazol-4-yl)methyl]-2-oxo-imidazolidin-1-yl]butanamide
SMILES	c1ccc(cc1)CC(C(CN(CC(C)C)S(=O)(=O)c2ccc(cc2)C=NO)O)NC(=O)C(C(C)C)N3C(=O)N(CC3)Cc4csc(n4)C
Canonical_SMILES	O/N=C/c1ccc(cc1)S(=O)(=O)N(C[C@H]([C@H](Cc1ccccc1)NC(=O)[C@@H](N1CCN(C1=O)Cc1csc(n1)C)C(C)C)O)CC(C)C
InChI	1/C34H46N6O6S2/c1-23(2)19-39(48(45,46)29-13-11-27(12-14-29)18-35-44)21-31(41)30(17-26-9-7-6-8-10-26)37-33(42)32(24(3)4)40-16-15-38(34(40)43)20-28-22-47-25(5)36-28/h6-14,18,22-24,30-32,41,44H,15-17,19-21H2,1-5H3,(H,37,42)/f/h37H
InChI_3D	1S/C34H46N6O6S2/c1-23(2)19-39(48(45,46)29-13-11-27(12-14-29)18-35-44)21-31(41)30(17-26-9-7-6-8-10-26)37-33(42)32(24(3)4)40-16-15-38(34(40)43)20-28-22-47-25(5)36-28/h6-14,18,22-24,30-32,41,44H,15-17,19-21H2,1-5H3,(H,37,42)/b35-18+/t30-,31+,32-/m0/s1
AuxInfo	1/1/N:22,23,24,25,21,1,2,3,6,7,4,5,8,9,19,20,26,17,28,27,29,10,31,32,15,12,11,14,13,33,34,30,18,16,36,35,39,37,40,38,45,42,41,46,43,44,47,48/E:(1,2)(3,4)(7,8)(9,10)(11,12)(13,14)(45,46)/F:m/E:m/CRV:48.6/rA:94cCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCNNNNNNOOOOOOSSHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHH/rB:d1;s1;;;s2;d3;d4;s5;;s4d5;d6s7;s8d9;d10;;;s11;;;s19;s15;;;;;s12;s14;;;s18;s22s23s28;s24s25s30;s26;s29s33;s14d15;w17;s16s19s27;s16s20s30;s18s33;s28s29;d16;d18;;;s34;s36;s10s15;s13s40d43d44;s1;s2;s3;s4;s5;s6;s7;s8;s9;s10;s17;s19;s19;s20;s20;s21;s21;s21;s22;s22;s22;s23;s23;s23;s24;s24;s24;s25;s25;s25;s26;s26;s27;s27;s28;s28;s29;s29;s30;s31;s32;s33;s34;s39;s45;s46;/rC:-1.371,-8.7892,0;-.7007,-8.0471,0;-2.35,-8.5855,0;-9.5337,-4.754,0;-8.3745,-3.4631,0;-1.0126,-7.0915,0;-2.6619,-7.6299,0;-8.7858,-5.4256,0;-7.6266,-4.1347,0;-.3065,.9519,0;-9.3243,-3.7761,0;-1.9948,-6.8781,0;-7.8285,-5.1194,0;;1.3131,.9519,0;-2.1793,-1.614,0;-10.0683,-3.108,0;-3.1306,-3.8301,0;-.8684,-2.5689,0;-1.6791,-3.1544,0;2.2646,1.2597,0;-7.732,-8.2059,0;-6.9602,-9.3909,0;-4.7018,-2.2391,0;-4.0615,-.9781,0;-2.5378,-5.2144,0;-.5889,-.8082,0;-6.547,-7.434,0;-5.3897,-6.1453,0;-3.4409,-2.8794,0;-6.7536,-8.4125,0;-3.7512,-1.9288,0;-3.4884,-5.5247,0;-4.4391,-5.835,0;1.0014,0,0;-9.8617,-2.1296,0;-1.1777,-1.6165,0;-2.4903,-2.5691,0;-3.7987,-4.5741,0;-6.3404,-6.4556,0;-2.7659,-.8041,0;-2.1522,-4.0366,0;-7.7525,-6.5315,0;-6.4163,-5.0434,0;-4.1288,-6.7857,0;-10.6058,-1.4615,0;.5007,1.5426,0;-7.0844,-5.7875,0;-1.2158,-9.2645,0;-.2116,-8.1511,0;-2.6835,-8.958,0;-10.0093,-4.9085,0;-8.2719,-2.9737,0;-.6774,-6.7205,0;-3.1514,-7.528,0;-8.8906,-5.9145,0;-7.1517,-3.9781,0;-.7821,1.1062,0;-10.5436,-3.2632,0;-.4115,-2.366,0;-.6193,-3.0024,0;-1.3449,-3.5263,0;-2.0133,-3.5264,0;2.1107,1.7354,0;2.4184,.7839,0;2.7403,1.4135,0;-7.6287,-7.7167,0;-7.8353,-8.6951,0;-8.2212,-8.1026,0;-7.4494,-9.2876,0;-6.4709,-9.4942,0;-7.0635,-9.8801,0;-4.5467,-2.7144,0;-4.857,-1.7637,0;-5.1772,-2.3942,0;-3.5862,-.823,0;-4.5368,-1.1333,0;-4.2166,-.5028,0;-2.693,-4.7391,0;-2.0625,-5.0593,0;-.1847,-1.1027,0;-.993,-.5138,0;-6.0578,-7.5373,0;-7.0362,-7.3307,0;-5.5449,-5.67,0;-5.2346,-6.6206,0;-3.9162,-3.0346,0;-6.2643,-8.5158,0;-3.2759,-1.7736,0;-3.3333,-6.0001,0;-4.5942,-5.3597,0;-4.288,-4.4708,0;-4.4629,-7.1577,0;-10.5025,-.9722,0;
Duplicates	DB04748_t0
mol2_Path	/CCDB/DrugBank/Database/Compound-0000000000-0000049999/Compound-0000004500-0000004749/DB04748_t0.mol2
pdbqt_Path	/CCDB/DrugBank/Database/Compound-0000000000-0000049999/Compound-0000004500-0000004749/DB04748_t0.pdbqt
sdf_Path	/CCDB/DrugBank/Database/Compound-0000000000-0000049999/Compound-0000004500-0000004749/DB04748_t0.sdf