1-adamantanol
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
152.23 1 1 1.95 SF_C399 None Not checked

SMILES: OC12CC3CC(CC(C3)C1)C2

Supramolecules

Namelog KSDpHT(°C)MethodRef
[NC0-b-CD](1).[1-adamantanol] 5.62 7.0 25.0 Fluorescence spectroscopy Hiroshi Ikeda 2005
[NC4-b-CD](1).[1-adamantanol] 4.20 7.0 25.0 Fluorescence spectroscopy Hiroshi Ikeda 2005
[NC0-g-CD](1).[1-adamantanol] 3.18 7.0 25.0 Fluorescence spectroscopy Hiroshi Ikeda 2005

1-adamantanol
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
152.23 1 1 1.95 SF_C527 None Not checked

SMILES: OC12CC3CC(CC(C3)C1)C2

Supramolecules

Namelog KSDpHT(°C)MethodRef
[unique helical macromolecule consisting of a chromophoric polyacetylene backbone and a b-cyclodextrin as the side group](1).[1-adamantanol] 2.39 25.0 Absorpton and circular dichroism spectroscopies Eiji Yashima 2006

1-adamantanol
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
152.23 1 1 1.95 JN_4 None Not checked

SMILES: OC12CC3CC(CC(C3)C1)C2

Supramolecules

Namelog KSDpHT(°C)MethodRef
[6-Deoxy-6-amino{2-[4-(dimethylamino)phenylazo]benzoyl}-BCD (methyl red-modified BCD, "1")](1).[1-adamantanol] 2.86 1.6 UV-vis spectroscopy, induced circular dichroism Tetsuo Kuwabara 1994
[6-Deoxy-6-amino{2-[4-(dimethylamino)phenylazo]benzoyl}-BCD (methyl red-modified BCD, "1")](1).[1-adamantanol] 3.30 UV-vis spectroscopy, induced circular dichroism Tetsuo Kuwabara 1994
[6-Deoxy-6-amino{4-[4-(dimethylamino)phenylazo]benzoyl}-BCD (p-methyl red-modified; "2")](1).[1-adamantanol] 4.55 2.52 UV-vis spectroscopy, induced circular dichroism Tetsuo Kuwabara 1994
[6-Deoxy-6-amino{4-[4-(dimethylamino)phenylazo]benzoyl}-BCD (p-methyl red-modified; "2")](1).[1-adamantanol] 3.86 7.2 UV-vis spectroscopy, induced circular dichroism Tetsuo Kuwabara 1994

1-adamantanol
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
152.23 1 1 1.95 JN_404 None Not checked

SMILES: OC12CC3CC(CC(C3)C1)C2

Supramolecules

Namelog KSDpHT(°C)MethodRef
[b-Cyclodextrin](1).[1-adamantanol] 4.00 6.4 20.0 electrochemical masurements, cyclic voltammetry Marcin Majda 2000
[g-Cyclodextrin](1).[1-adamantanol] 4.41 6.4 20.0 electrochemical masurements, cyclic voltammetry Marcin Majda 2000

1-adamantanol

MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
152.23 1 1 1.95 SF_C1022 None Not checked

SMILES: OC12CC3CC(CC(C3)C1)C2

Supramolecules

Namelog KSDpHT(°C)MethodRef
[mono[6-(p-metholxylphenylseleno)-6-deoxy]-b-cyclodextrin](1).[1-adamantanol ] 3.86 7.2 25.0 Circular dichroism spectroscopy Yu Liu 1999
[mono[6-(ptolylseleno)-6-deoxy]-b-cyclodextrin](1).[1-adamantanol ] 5.44 7.2 25.0 Circular dichroism spectroscopy Yu Liu 1999

1-adamantylammonium chloride
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
187.71 0 1 -1.80 SF_C596 None Not checked

SMILES: [Cl-].[NH3+]C12CC3CC(CC(C3)C1)C2

Supramolecules

Namelog KSDpHT(°C)MethodRef
[Mono-6-deoxy-6-N-[4-(1-methyl-4-pyridinio)-1-pyridiniooctyl]amino-b-CD](1).[1-adamantylammonium chloride] 3.81 2.85 7.0 25.0 NMR spectroscopy Joon Woo Park 2005
[Mono-6-deoxy-6-N-[4-(1-methyl-4-pyridinio)-1-pyridiniooctyl]amino-b-CD](1).[1-adamantylammonium chloride] 3.82 3.18 8.9 25.0 Induced circular dichroism Joon Woo Park 2005

1-aminomethyl-2,3-diazabicyclo[2.2.2]oct-2-ene

MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
139.20 3 1 0.66 SF_C867 None Not checked

SMILES: NCC12CCC(CC1)N=N2

Supramolecules

Namelog KSDpHT(°C)MethodRef
[b-Cyclodextrin](1).[1-aminomethyl-2,3-diazabicyclo[2.2.2]oct-2-ene ] 2.40 1.30 11.0 25.0 UV-vis spectroscopy and NMR spetroscopy Werner M. Nau 2002
[b-Cyclodextrin](1).[1-aminomethyl-2,3-diazabicyclo[2.2.2]oct-2-ene ] 1.30 1.00 5.0 25.0 Induced circular dichroism Werner M. Nau 2002

1-anilino-8-naphthalenesulfonate
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
298.34 3 1 4.64 JN_454 None Not checked

SMILES: [O-][S](=O)(=O)c1cccc2cccc(Nc3ccccc3)c12

Supramolecules

Namelog KSDpHT(°C)MethodRef
[b-Cyclodextrin](1).[1-anilino-8-naphthalenesulfonate] 1.75 Yoshihisa Inoue 1993
[modified BCD (with bridging disulfonates)](1).[1-anilino-8-naphthalenesulfonate] 3.11 Yoshihisa Inoue 1993

1-anilino-8-naphthalenesulfonate ion
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
None None JN_237 None

SMILES:

Supramolecules

Namelog KSDpHT(°C)MethodRef
[b-Cyclodextrin](1).[1-anilino-8-naphthalenesulfonate ion] 1.57 0.26 11.6 25.0 spectrofluorometry Oswald S.Tee 1996
[b-Cyclodextrin](1).[1-anilino-8-naphthalenesulfonate ion] 2.04 25.0 fluorescence spectroscopy Oswald S.Tee 1996
[b-Cyclodextrin](1).[1-anilino-8-naphthalenesulfonate ion] 1.96 25.0 Oswald S.Tee 1996
[b-Cyclodextrin](1).[1-anilino-8-naphthalenesulfonate ion] 1.82 25.0 NMR titration Oswald S.Tee 1996
[g-Cyclodextrin](1).[1-anilino-8-naphthalenesulfonate ion] 2.11 0.45 11.6 25.0 spectrofluorometry Oswald S.Tee 1996
[g-Cyclodextrin](1).[1-anilino-8-naphthalenesulfonate ion] 3.10 25.0 NMR titration Oswald S.Tee 1996
[g-Cyclodextrin](1).[1-anilino-8-naphthalenesulfonate ion] 2.44 25.0 fluorescence spectroscopy Oswald S.Tee 1996
[2-O-(2-Hydroxy)propyl-b-Cyclodextrin](1).[1-anilino-8-naphthalenesulfonate ion] 2.77 1.14 11.6 25.0 spectrofluorometry Oswald S.Tee 1996

1-anilinonaphthalene-8-sulfonate
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
298.34 3 1 4.64 NT_a0001 None Not checked

SMILES: [O-][S](=O)(=O)c1cccc2cccc(Nc3ccccc3)c12

Supramolecules

Namelog KSDpHT(°C)MethodRef
[b-Cyclodextrin](1).[1-anilinonaphthalene-8-sulfonate] 1.93 25.0 Fluorometric method PARK, J.W., 1989

1-anilinonaphthalene-8-sulfonic acid
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
299.34 4 2 4.98 SF_C1717 None Not checked

SMILES: O[S](=O)(=O)c1cccc2cccc(Nc3ccccc3)c12

Supramolecules

Namelog KSDpHT(°C)MethodRef
[Heptakis{6-deoxy-6-[12-(thiododecyl)undecanamido]}-b-cyclodextrin](1).[1-anilinonaphthalene-8-sulfonic acid] 5.46 4.11 7.0 25.0 Electrochemical impedance measurements David N. Reinhoudt 2000

1-b-D ribofuranosyl-1-H-1,2,4-triazole-3-carboxamide
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
244.20 8 4 -2.31 NT_a0069 None Not checked

SMILES: O=C(C1=NN([C@H]2[C@@H]([C@@H]([C@@H](CO)O2)O)O)C=N1)N

Supramolecules

Namelog KSDpHT(°C)MethodRef
[a-Cyclodextrin](1).[1-b-D ribofuranosyl-1-H-1,2,4-triazole-3-carboxamide] 3.17 4.6 18.0 HPLC Kedzierewicz, F. 2005
[b-Cyclodextrin](1).[1-b-D ribofuranosyl-1-H-1,2,4-triazole-3-carboxamide] 3.42 4.6 18.0 HPLC Kedzierewicz, F. 2005
[g-Cyclodextrin](1).[1-b-D ribofuranosyl-1-H-1,2,4-triazole-3-carboxamide] 3.07 4.6 18.0 HPLC Kedzierewicz, F. 2005

1-bromonaphtalene
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
207.07 0 0 3.60 SF_C1300 None Not checked

SMILES: C1=CC=C2C(=C1)C=CC=C2Br

Supramolecules

Namelog KSDpHT(°C)MethodRef
[6-O-a-D-glucosyl-b-CD](1).[1-bromonaphtalene] 3.51 7.0 22.0 Fluorescence spectroscopy Daniel G. Nocera 1993

1-bromonaphthalene
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
207.07 0 0 3.60 SF_C1368 None Not checked

SMILES: Brc1cccc2ccccc12

Supramolecules

Namelog KSDpHT(°C)MethodRef
[glucosyl modified b-yclodextrin](1).[1-bromonaphthalene] 3.13 7.0 22.0 UV-vis spectroscopy Daniel G. Nocera 1996
[glucosyl modified b-yclodextrin](1).[1-bromonaphthalene] 3.37 2.9 22.0 UV-vis spectroscopy Daniel G. Nocera 1996
[glucosyl modified b-yclodextrin](1).[1-bromonaphthalene] 3.58 9.0 22.0 UV-vis spectroscopy Daniel G. Nocera 1996