p-nitrophenol
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
139.11 2 1 1.82 JN_451 None Not checked

SMILES: Oc1ccc(cc1)[N+]([O-])=O

Supramolecules

Namelog KSDpHT(°C)MethodRef
[DIMEA](1).[p-nitrophenol] 2.87 25.0 circular dichroism Yoshihisa Inoue 1993

p-nitrophenolate
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
138.10 1 0 2.26 SF_C1331 None Not checked

SMILES: [O-]c1ccc(cc1)[N+]([O-])=O

Supramolecules

Namelog KSDpHT(°C)MethodRef
[a-Cyclodextrin](1).[p-nitrophenolate] 2.52 13.5 20.0 Pulse Voltammetry Janet G. Osteryoung 1991
[a-Cyclodextrin](1).[p-nitrophenolate] 2.26 13.5 25.0 UV-vis spectroscopy Janet G. Osteryoung 1991
[a-Cyclodextrin](1).[p-nitrophenolate] 3.30 2.30 11.0 24.5 Gradient flow injection spectrophotometric technique Michael A. Koupparis 1995

p-nitrophenolate ion
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
138.10 1 0 2.26 JN_O_3 None Not checked

SMILES: C1=CC(=CC=C1[N+](=O)[O-])[O-]

Supramolecules

Namelog KSDpHT(°C)MethodRef
[a-Cyclodextrin](1).[p-nitrophenolate ion] 3.27 1.30 10.4 25.0 UV and NMR spectroscopy Yoshihisa Matsui 1994
[a-Cyclodextrin](1).[p-nitrophenolate ion] 3.20 25.0 optical rotation method Yannis L. Loukas 1997
[a-Cyclodextrin](1).[p-nitrophenolate ion] 3.55 gel chromatography Yannis L. Loukas 1997

p-nitrophenyl a-D-mannose
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
301.25 7 4 -0.70 SF_C1325 None Not checked

SMILES: O[C@@H]([C@H]([C@@H]([C@@H](CO)O1)O)O)[C@H]1OC2=CC=C([N+]([O-])=O)C=C2

Supramolecules

Namelog KSDpHT(°C)MethodRef
[a-Cyclodextrin](1).[p-nitrophenyl a-D-mannose] 2.28 7.0 30.0 NMR spectroscopy Soledad Penades 1993
[b-Cyclodextrin](1).[p-nitrophenyl a-D-mannose] 2.42 7.0 30.0 NMR spectroscopy Soledad Penades 1993

p-nitrophenyl b-D-mannose
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
301.25 7 4 -0.70 SF_C1326 None Not checked

SMILES: O[C@@H]([C@H]([C@@H]([C@@H](CO)O1)O)O)[C@@H]1OC2=CC=C([N+]([O-])=O)C=C2

Supramolecules

Namelog KSDpHT(°C)MethodRef
[a-Cyclodextrin](1).[p-nitrophenyl b-D-mannose] 2.52 7.0 30.0 NMR spectroscopy Soledad Penades 1993
[b-Cyclodextrin](1).[p-nitrophenyl b-D-mannose] 2.27 7.0 30.0 NMR spectroscopy Soledad Penades 1993

p-nitrophenyl isonicotinate
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
244.20 4 0 2.73 JN_61 None Not checked

SMILES: [O-][N+](=O)c1ccc(OC(=O)c2ccncc2)cc1

Supramolecules

Namelog KSDpHT(°C)MethodRef
[a-Cyclodextrin](1).[p-nitrophenyl isonicotinate] 2.04 9.5 25.0 NMR spectroscopy Paolo Scrimin 1997
[b-Cyclodextrin](1).[p-nitrophenyl isonicotinate] 2.23 9.5 25.0 NMR spectroscopy Paolo Scrimin 1997

p-nitrophenyl nicotinate
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
244.20 4 0 2.73 JN_62 None Not checked

SMILES: [O-][N+](=O)c1ccc(OC(=O)c2cccnc2)cc1

Supramolecules

Namelog KSDpHT(°C)MethodRef
[a-Cyclodextrin](1).[p-nitrophenyl nicotinate] 1.95 9.5 25.0 NMR spectroscopy Paolo Scrimin 1997
[b-Cyclodextrin](1).[p-nitrophenyl nicotinate] 2.23 9.5 25.0 NMR spectroscopy Paolo Scrimin 1997

p-nitrophenyl urocanoate
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
259.22 4 1 2.46 JN_63 None Not checked

SMILES: O=C(OC1=CC=C([N+]([O-])=O)C=C1)C=CC2=CNC=N2

Supramolecules

Namelog KSDpHT(°C)MethodRef
[a-Cyclodextrin](1).[p-nitrophenyl urocanoate] 1.95 10.5 25.0 NMR spectroscopy Paolo Scrimin 1997
[b-Cyclodextrin](1).[p-nitrophenyl urocanoate] 2.32 10.5 25.0 NMR spectroscopy Paolo Scrimin 1997

p-nitrophenyl-phthalamic acid
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
286.24 5 2 3.28 SF_C793 None Not checked

SMILES: NC(=O)c1c(ccc(c1c2ccccc2)[N+]([O-])=O)C(O)=O

Supramolecules

Namelog KSDpHT(°C)MethodRef
[2-O-(2-Hydroxy)propyl-b-Cyclodextrin](1).[p-nitrophenyl-phthalamic acid] 1.95 1.30 2.0 25.0 UV-vis spectroscopy Rita H. de Rossi 2001