CompChem-Database: compound details

CompChem-Database: details for selected entry

DB07330_p0_t0 (6753)

Formula C₁₆H₂₂N₄O

MW 286.38

InChIKey KXSIHXHEHABEJX-HWHDIUAINA-N

Entry_Date 2023-09-01

Net_Charge 0

Number_Atoms 43

Number_Heavy_Atoms 21

Number_Rings 3

Number_Bonds 45

Rotat_Bonds 4

Unbranched_Chain 3

Chiral_Centers 0

ONatoms 5

HB_Donor 2

HB_Acceptor 2

OpenEye_HB_Donors 3

OpenEye_HB_Acceptors 3

Lipinski_HB_Donors 2

Lipinski_HB_Acceptors 5

Lipinski_Violations 0

XLogP3 0

XLogP 2.26

logP 2.8894

PSA 75.01

MR 87.5006

ABS 0.55

Solubility soluble

Aggregator Pass

PM7_Heat_of_Formation_kcal_per_mol -5.32868

PM7_Total_Energy_ev -3302.5564

PM7_Electronic_Energy_ev -24466.95969

PM7_Dipole_Debye 3.42306

PM7_Point_Group C1

PM7_HOMO_Energy_ev -8.614

PM7_LUMO_Energy_ev -0.824

PM7_COSMO_Area_square_ang 322.17

PM7_COSMO_Volue_cubic_ang 352.84

PM7_Electron_Affinity_ev 0.824

PM7_Ionization_Energy_ev 8.614

PM7_Energy_Gap_ev 7.79

PM7_Global_Hardness_ev 3.895

PM7_Global_Softness_ev 0.25673940949935814

PM7_Chemical_Potential_ev -4.719

PM7_Electronigativity_ev 4.719

PM7_Back_Donation_Energy_ev -0.97375

PM7_Electrophilicity_ev 2.858659948652118

OPENEYE_Name 2-(1-propyl-4-piperidyl)-3~{H}-benzimidazole-4-carboxamide

SMILES c1cc(c2c(c1)nc([nH]2)C3CCN(CC3)CCC)C(=O)N

Canonical_SMILES CCCN1CCC(CC1)c1nc2c([nH]1)c(ccc2)C(=O)N

InChI 1/C16H22N4O/c1-2-8-20-9-6-11(7-10-20)16-18-13-5-3-4-12(15(17)21)14(13)19-16/h3-5,11H,2,6-10H2,1H3,(H2,17,21)(H,18,19)/f/h19H,17H2

InChI_3D 1S/C16H22N4O/c1-2-8-20-9-6-11(7-10-20)16-18-13-5-3-4-12(15(17)21)14(13)19-16/h3-5,11H,2,6-10H2,1H3,(H2,17,21)(H,18,19)

AuxInfo 1/1/N:14,15,1,2,3,9,10,16,11,12,13,4,5,6,8,7,20,17,18,19,21/E:(6,7)(9,10)/F:m/E:m/rA:43nCCCCCCCCCCCCCCCCNNNNOHHHHHHHHHHHHHHHHHHHHHH/rB:d1;s1;s2;d3;d4s5;;s4;;;s9;s10;s7s9s10;;s14;s15;s5d7;s6s7;s11s12s16;s8;d8;s1;s2;s3;s9;s9;s10;s10;s11;s11;s12;s12;s13;s14;s14;s14;s15;s15;s16;s16;s18;s20;s20;/rC:;0,1.0058,0;.868,-.4979,0;.868,1.5137,0;1.736,-.0013,0;1.736,1.0058,0;3.2858,.5022,0;.868,2.5137,0;5.9742,.848,0;4.8603,-.4822,0;6.7449,.2027,0;5.631,-1.1276,0;5.0358,.5023,0;8.8773,-2.7144,0;8.1106,-2.0724,0;7.3439,-1.4304,0;2.6938,-.3126,0;2.6938,1.3168,0;6.5772,-.7884,0;1.734,3.0137,0;.002,3.0137,0;-.4327,-.2506,0;-.4337,1.2545,0;.8677,-.9979,0;5.7229,1.2803,0;6.3566,1.1702,0;4.6103,-.9152,0;4.3906,-.3108,0;6.9936,.6364,0;7.2155,.034,0;5.8797,-1.5613,0;5.2477,-1.4486,0;4.948,.9945,0;9.1983,-2.331,0;8.5563,-3.0977,0;9.2606,-3.0354,0;7.7896,-2.4557,0;8.4316,-1.689,0;7.0229,-1.8137,0;7.6649,-1.047,0;2.8483,1.7923,0;2.167,2.7637,0;1.734,3.5137,0;

Duplicates DB07330_p0_t0

mol2_Path /CCDB/DrugBank/Database/Compound-0000000000-0000049999/Compound-0000007250-0000007499/DB07330_p0_t0.mol2

pdbqt_Path /CCDB/DrugBank/Database/Compound-0000000000-0000049999/Compound-0000007250-0000007499/DB07330_p0_t0.pdbqt

sdf_Path /CCDB/DrugBank/Database/Compound-0000000000-0000049999/Compound-0000007250-0000007499/DB07330_p0_t0.sdf

Formula	C₁₆H₂₂N₄O
MW	286.38
InChIKey	KXSIHXHEHABEJX-HWHDIUAINA-N
Entry_Date	2023-09-01
Net_Charge	0
Number_Atoms	43
Number_Heavy_Atoms	21
Number_Rings	3
Number_Bonds	45
Rotat_Bonds	4
Unbranched_Chain	3
Chiral_Centers	0
ONatoms	5
HB_Donor	2
HB_Acceptor	2
OpenEye_HB_Donors	3
OpenEye_HB_Acceptors	3
Lipinski_HB_Donors	2
Lipinski_HB_Acceptors	5
Lipinski_Violations	0
XLogP3	0
XLogP	2.26
logP	2.8894
PSA	75.01
MR	87.5006
ABS	0.55
Solubility	soluble
Aggregator	Pass
PM7_Heat_of_Formation_kcal_per_mol	-5.32868
PM7_Total_Energy_ev	-3302.5564
PM7_Electronic_Energy_ev	-24466.95969
PM7_Dipole_Debye	3.42306
PM7_Point_Group	C1
PM7_HOMO_Energy_ev	-8.614
PM7_LUMO_Energy_ev	-0.824
PM7_COSMO_Area_square_ang	322.17
PM7_COSMO_Volue_cubic_ang	352.84
PM7_Electron_Affinity_ev	0.824
PM7_Ionization_Energy_ev	8.614
PM7_Energy_Gap_ev	7.79
PM7_Global_Hardness_ev	3.895
PM7_Global_Softness_ev	0.25673940949935814
PM7_Chemical_Potential_ev	-4.719
PM7_Electronigativity_ev	4.719
PM7_Back_Donation_Energy_ev	-0.97375
PM7_Electrophilicity_ev	2.858659948652118
OPENEYE_Name	2-(1-propyl-4-piperidyl)-3~{H}-benzimidazole-4-carboxamide
SMILES	c1cc(c2c(c1)nc([nH]2)C3CCN(CC3)CCC)C(=O)N
Canonical_SMILES	CCCN1CCC(CC1)c1nc2c([nH]1)c(ccc2)C(=O)N
InChI	1/C16H22N4O/c1-2-8-20-9-6-11(7-10-20)16-18-13-5-3-4-12(15(17)21)14(13)19-16/h3-5,11H,2,6-10H2,1H3,(H2,17,21)(H,18,19)/f/h19H,17H2
InChI_3D	1S/C16H22N4O/c1-2-8-20-9-6-11(7-10-20)16-18-13-5-3-4-12(15(17)21)14(13)19-16/h3-5,11H,2,6-10H2,1H3,(H2,17,21)(H,18,19)
AuxInfo	1/1/N:14,15,1,2,3,9,10,16,11,12,13,4,5,6,8,7,20,17,18,19,21/E:(6,7)(9,10)/F:m/E:m/rA:43nCCCCCCCCCCCCCCCCNNNNOHHHHHHHHHHHHHHHHHHHHHH/rB:d1;s1;s2;d3;d4s5;;s4;;;s9;s10;s7s9s10;;s14;s15;s5d7;s6s7;s11s12s16;s8;d8;s1;s2;s3;s9;s9;s10;s10;s11;s11;s12;s12;s13;s14;s14;s14;s15;s15;s16;s16;s18;s20;s20;/rC:;0,1.0058,0;.868,-.4979,0;.868,1.5137,0;1.736,-.0013,0;1.736,1.0058,0;3.2858,.5022,0;.868,2.5137,0;5.9742,.848,0;4.8603,-.4822,0;6.7449,.2027,0;5.631,-1.1276,0;5.0358,.5023,0;8.8773,-2.7144,0;8.1106,-2.0724,0;7.3439,-1.4304,0;2.6938,-.3126,0;2.6938,1.3168,0;6.5772,-.7884,0;1.734,3.0137,0;.002,3.0137,0;-.4327,-.2506,0;-.4337,1.2545,0;.8677,-.9979,0;5.7229,1.2803,0;6.3566,1.1702,0;4.6103,-.9152,0;4.3906,-.3108,0;6.9936,.6364,0;7.2155,.034,0;5.8797,-1.5613,0;5.2477,-1.4486,0;4.948,.9945,0;9.1983,-2.331,0;8.5563,-3.0977,0;9.2606,-3.0354,0;7.7896,-2.4557,0;8.4316,-1.689,0;7.0229,-1.8137,0;7.6649,-1.047,0;2.8483,1.7923,0;2.167,2.7637,0;1.734,3.5137,0;
Duplicates	DB07330_p0_t0
mol2_Path	/CCDB/DrugBank/Database/Compound-0000000000-0000049999/Compound-0000007250-0000007499/DB07330_p0_t0.mol2
pdbqt_Path	/CCDB/DrugBank/Database/Compound-0000000000-0000049999/Compound-0000007250-0000007499/DB07330_p0_t0.pdbqt
sdf_Path	/CCDB/DrugBank/Database/Compound-0000000000-0000049999/Compound-0000007250-0000007499/DB07330_p0_t0.sdf