CompChem-Database: compound details

CompChem-Database: details for selected entry

CHEMBL5196693_p0_t0 (2539502)

Formula C₁₇H₁₉ClN₆O

MW 358.83

InChIKey HUNGUHBTUFJLAZ-NPQUBYNZNA-N

Entry_Date 2023-09-01

Net_Charge 0

Number_Atoms 44

Number_Heavy_Atoms 25

Number_Rings 4

Number_Bonds 47

Rotat_Bonds 2

Unbranched_Chain 1

Chiral_Centers 0

ONatoms 7

HB_Donor 3

HB_Acceptor 2

OpenEye_HB_Donors 4

OpenEye_HB_Acceptors 4

Lipinski_HB_Donors 3

Lipinski_HB_Acceptors 7

Lipinski_Violations 0

XLogP3 0

XLogP 2.65

logP 3.0495

PSA 103.69

MR 101.957

ABS 0.55

Solubility soluble

Aggregator Pass

PM7_Heat_of_Formation_kcal_per_mol 42.31098

PM7_Total_Energy_ev -4023.16979

PM7_Electronic_Energy_ev -31536.06286

PM7_Dipole_Debye 8.73903

PM7_Point_Group C1

PM7_HOMO_Energy_ev -8.863

PM7_LUMO_Energy_ev -0.33

PM7_COSMO_Area_square_ang 354

PM7_COSMO_Volue_cubic_ang 404.59

PM7_Electron_Affinity_ev 0.33

PM7_Ionization_Energy_ev 8.863

PM7_Energy_Gap_ev 8.533

PM7_Global_Hardness_ev 4.2665

PM7_Global_Softness_ev 0.23438415563107934

PM7_Chemical_Potential_ev -4.5965

PM7_Electronigativity_ev 4.5965

PM7_Back_Donation_Energy_ev -1.066625

PM7_Electrophilicity_ev 2.4760122172741124

OPENEYE_Name 6-(4-amino-4-methyl-1-piperidyl)-3-(3-chlorophenyl)-1,5-dihydropyrazolo[3,4-d]pyrimidin-4-one

SMILES c1cc(cc(c1)Cl)c2c3c(nc([nH]c3=O)N4CCC(CC4)(C)N)[nH]n2

Canonical_SMILES Clc1cccc(c1)c1n[nH]c2c1c(=O)[nH]c(n2)N1CCC(CC1)(C)N

InChI 1/C17H19ClN6O/c1-17(19)5-7-24(8-6-17)16-20-14-12(15(25)21-16)13(22-23-14)10-3-2-4-11(18)9-10/h2-4,9H,5-8,19H2,1H3,(H2,20,21,22,23,25)/f/h21,23H

InChI_3D 1S/C17H19ClN6O/c1-17(19)5-7-24(8-6-17)16-20-14-12(15(25)21-16)13(22-23-14)10-3-2-4-11(18)9-10/h2-4,9H,5-8,19H2,1H3,(H2,20,21,22,23,25)

AuxInfo 1/1/N:17,1,2,3,12,13,14,15,4,5,7,6,8,9,10,11,16,25,23,19,21,18,20,22,24/E:(5,6)(7,8)/F:m/E:m/rA:44nCCCCCCCCCCCCCCCCCNNNNNNOClHHHHHHHHHHHHHHHHHHH/rB:d1;s1;;s2d4;;d3s4;s5s6;d6;s6;;;;s12;s13;s12s13;s16;d8;s9d11;s9s18;s10s11;s11s14s15;s16;d10;s7;s1;s2;s3;s4;s12;s12;s13;s13;s14;s14;s15;s15;s17;s17;s17;s20;s21;s23;s23;/rC:1.7717,2.4507,0;1.4668,1.4983,0;2.7547,2.6611,0;3.1178,.9645,0;2.1348,.7541,0;.868,-.5079,0;3.4327,1.9191,0;1.8258,-.1969,0;.868,-1.515,0;;-.868,-1.5137,0;-3.4773,-2.0225,0;-2.6077,-3.5239,0;-2.6075,-1.5187,0;-1.7378,-3.02,0;-3.473,-3.0226,0;-4.0708,-4.6673,0;2.4178,-1.0115,0;0,-2.0116,0;1.8258,-1.8263,0;-.868,-.5079,0;-1.7333,-2.0149,0;-5.1971,-2.7228,0;0,1,0;4.4105,2.1284,0;1.4361,2.8213,0;.9779,1.3937,0;2.9071,3.1373,0;3.4518,.5924,0;-3.9694,-2.111,0;-3.6494,-1.5531,0;-2.2861,-3.9068,0;-2.9293,-3.9067,0;-2.9301,-1.1368,0;-2.2881,-1.134,0;-1.2452,-2.9345,0;-1.5671,-3.49,0;-4.5407,-4.4965,0;-3.6009,-4.8381,0;-4.2416,-5.1372,0;1.9803,-2.3018,0;-1.3017,-.2592,0;-5.3692,-2.2533,0;-5.5176,-3.1065,0;

Duplicates CHEMBL5196693_p0_t0

mol2_Path /CCDB/ChEMBL/Database/Compound-0005150000-0005199999/Compound-0005196500-0005196749/CHEMBL5196693_p0_t0.mol2

pdbqt_Path /CCDB/ChEMBL/Database/Compound-0005150000-0005199999/Compound-0005196500-0005196749/CHEMBL5196693_p0_t0.pdbqt

sdf_Path /CCDB/ChEMBL/Database/Compound-0005150000-0005199999/Compound-0005196500-0005196749/CHEMBL5196693_p0_t0.sdf

Formula	C₁₇H₁₉ClN₆O
MW	358.83
InChIKey	HUNGUHBTUFJLAZ-NPQUBYNZNA-N
Entry_Date	2023-09-01
Net_Charge	0
Number_Atoms	44
Number_Heavy_Atoms	25
Number_Rings	4
Number_Bonds	47
Rotat_Bonds	2
Unbranched_Chain	1
Chiral_Centers	0
ONatoms	7
HB_Donor	3
HB_Acceptor	2
OpenEye_HB_Donors	4
OpenEye_HB_Acceptors	4
Lipinski_HB_Donors	3
Lipinski_HB_Acceptors	7
Lipinski_Violations	0
XLogP3	0
XLogP	2.65
logP	3.0495
PSA	103.69
MR	101.957
ABS	0.55
Solubility	soluble
Aggregator	Pass
PM7_Heat_of_Formation_kcal_per_mol	42.31098
PM7_Total_Energy_ev	-4023.16979
PM7_Electronic_Energy_ev	-31536.06286
PM7_Dipole_Debye	8.73903
PM7_Point_Group	C1
PM7_HOMO_Energy_ev	-8.863
PM7_LUMO_Energy_ev	-0.33
PM7_COSMO_Area_square_ang	354
PM7_COSMO_Volue_cubic_ang	404.59
PM7_Electron_Affinity_ev	0.33
PM7_Ionization_Energy_ev	8.863
PM7_Energy_Gap_ev	8.533
PM7_Global_Hardness_ev	4.2665
PM7_Global_Softness_ev	0.23438415563107934
PM7_Chemical_Potential_ev	-4.5965
PM7_Electronigativity_ev	4.5965
PM7_Back_Donation_Energy_ev	-1.066625
PM7_Electrophilicity_ev	2.4760122172741124
OPENEYE_Name	6-(4-amino-4-methyl-1-piperidyl)-3-(3-chlorophenyl)-1,5-dihydropyrazolo[3,4-d]pyrimidin-4-one
SMILES	c1cc(cc(c1)Cl)c2c3c(nc([nH]c3=O)N4CCC(CC4)(C)N)[nH]n2
Canonical_SMILES	Clc1cccc(c1)c1n[nH]c2c1c(=O)[nH]c(n2)N1CCC(CC1)(C)N
InChI	1/C17H19ClN6O/c1-17(19)5-7-24(8-6-17)16-20-14-12(15(25)21-16)13(22-23-14)10-3-2-4-11(18)9-10/h2-4,9H,5-8,19H2,1H3,(H2,20,21,22,23,25)/f/h21,23H
InChI_3D	1S/C17H19ClN6O/c1-17(19)5-7-24(8-6-17)16-20-14-12(15(25)21-16)13(22-23-14)10-3-2-4-11(18)9-10/h2-4,9H,5-8,19H2,1H3,(H2,20,21,22,23,25)
AuxInfo	1/1/N:17,1,2,3,12,13,14,15,4,5,7,6,8,9,10,11,16,25,23,19,21,18,20,22,24/E:(5,6)(7,8)/F:m/E:m/rA:44nCCCCCCCCCCCCCCCCCNNNNNNOClHHHHHHHHHHHHHHHHHHH/rB:d1;s1;;s2d4;;d3s4;s5s6;d6;s6;;;;s12;s13;s12s13;s16;d8;s9d11;s9s18;s10s11;s11s14s15;s16;d10;s7;s1;s2;s3;s4;s12;s12;s13;s13;s14;s14;s15;s15;s17;s17;s17;s20;s21;s23;s23;/rC:1.7717,2.4507,0;1.4668,1.4983,0;2.7547,2.6611,0;3.1178,.9645,0;2.1348,.7541,0;.868,-.5079,0;3.4327,1.9191,0;1.8258,-.1969,0;.868,-1.515,0;;-.868,-1.5137,0;-3.4773,-2.0225,0;-2.6077,-3.5239,0;-2.6075,-1.5187,0;-1.7378,-3.02,0;-3.473,-3.0226,0;-4.0708,-4.6673,0;2.4178,-1.0115,0;0,-2.0116,0;1.8258,-1.8263,0;-.868,-.5079,0;-1.7333,-2.0149,0;-5.1971,-2.7228,0;0,1,0;4.4105,2.1284,0;1.4361,2.8213,0;.9779,1.3937,0;2.9071,3.1373,0;3.4518,.5924,0;-3.9694,-2.111,0;-3.6494,-1.5531,0;-2.2861,-3.9068,0;-2.9293,-3.9067,0;-2.9301,-1.1368,0;-2.2881,-1.134,0;-1.2452,-2.9345,0;-1.5671,-3.49,0;-4.5407,-4.4965,0;-3.6009,-4.8381,0;-4.2416,-5.1372,0;1.9803,-2.3018,0;-1.3017,-.2592,0;-5.3692,-2.2533,0;-5.5176,-3.1065,0;
Duplicates	CHEMBL5196693_p0_t0
mol2_Path	/CCDB/ChEMBL/Database/Compound-0005150000-0005199999/Compound-0005196500-0005196749/CHEMBL5196693_p0_t0.mol2
pdbqt_Path	/CCDB/ChEMBL/Database/Compound-0005150000-0005199999/Compound-0005196500-0005196749/CHEMBL5196693_p0_t0.pdbqt
sdf_Path	/CCDB/ChEMBL/Database/Compound-0005150000-0005199999/Compound-0005196500-0005196749/CHEMBL5196693_p0_t0.sdf