1-adamantanammonium
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
152.26 0 1 1.20 JN_386 None Not checked

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

Supramolecules

Namelog KSDpHT(°C)MethodRef
[b-Cyclodextrin](1).[1-adamantanammonium] 3.93 25.0 spectrophotometry, pH potentiometry Joon Woo Park 2002

1-adamantane amine
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
151.25 1 1 2.61 SF_C402 None Not checked

SMILES: NC12CC3CC(CC(C3)C1)C2

Supramolecules

Namelog KSDpHT(°C)MethodRef
[NC0-b-CD](1).[1-adamantane amine] 4.81 7.0 25.0 Fluorescence spectroscopy Hiroshi Ikeda 2005
[NC4-b-CD](1).[1-adamantane amine] 3.30 7.0 25.0 Fluorescence spectroscopy Hiroshi Ikeda 2005

1-adamantane carboxylate
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
179.24 1 0 0.95 JN_406 None Not checked

SMILES: [O-]C(=O)C12CC3CC(CC(C3)C1)C2

Supramolecules

Namelog KSDpHT(°C)MethodRef
[a-Cyclodextrin](2).[1-adamantane carboxylate] 2.15 25.0 pH titration Marcin Majda 2000
[b-Cyclodextrin](1).[1-adamantane carboxylate] 4.30 25.0 pH titration Marcin Majda 2000
[g-Cyclodextrin](1).[1-adamantane carboxylate] 3.48 25.0 pH titration Marcin Majda 2000

1-adamantane carboxylate ion
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
None None JN_357 None

SMILES:

Supramolecules

Namelog KSDpHT(°C)MethodRef
[a-Cyclodextrin](1).[1-adamantane carboxylate ion] 2.06 25.0 capillary electrophoresis Wolfgang Zimmermann 1998
[a-Cyclodextrin](1).[1-adamantane carboxylate ion] 2.15 1.15 25.0 spectrophotometry Wolfgang Zimmermann 1998
[a-Cyclodextrin](1).[1-adamantane carboxylate ion] 2.15 25.0 microcalorimetry Wolfgang Zimmermann 1998
[b-Cyclodextrin](1).[1-adamantane carboxylate ion] 2.70 25.0 capillary electrophoresis Wolfgang Zimmermann 1998
[b-Cyclodextrin](1).[1-adamantane carboxylate ion] 6.00 25.0 spectrophotometry Wolfgang Zimmermann 1998
[b-Cyclodextrin](1).[1-adamantane carboxylate ion] 4.30 25.0 microcalorimetry Wolfgang Zimmermann 1998
[cyclomaltododecaose](1).[1-adamantane carboxylate ion] 0.60 25.0 capillary electrophoresis Wolfgang Zimmermann 1998
[cyclomaltononaose](1).[1-adamantane carboxylate ion] 0.90 25.0 capillary electrophoresis Wolfgang Zimmermann 1998
[cyclomaltotridecaose](1).[1-adamantane carboxylate ion] 0.90 25.0 capillary electrophoresis Wolfgang Zimmermann 1998
[cyclomaltoundecaose](1).[1-adamantane carboxylate ion] 0.60 25.0 capillary electrophoresis Wolfgang Zimmermann 1998
[g-Cyclodextrin](1).[1-adamantane carboxylate ion] 1.62 25.0 capillary electrophoresis Wolfgang Zimmermann 1998
[g-Cyclodextrin](1).[1-adamantane carboxylate ion] 3.48 25.0 microcalorimetry Wolfgang Zimmermann 1998
[g-Cyclodextrin](1).[1-adamantane carboxylate ion] 2.43 0.95 25.0 spectrophotometry Wolfgang Zimmermann 1998

1-adamantane carboxylic acid
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
180.24 2 1 2.29 SF_C401 None Not checked

SMILES: OC(=O)C12CC3CC(CC(C3)C1)C2

Supramolecules

Namelog KSDpHT(°C)MethodRef
[NC0-b-CD](1).[1-adamantane carboxylic acid] 5.77 7.0 25.0 Fluorescence spectroscopy Hiroshi Ikeda 2005
[NC4-b-CD](1).[1-adamantane carboxylic acid] 4.59 7.0 25.0 Fluorescence spectroscopy Hiroshi Ikeda 2005
[NC0-g-CD](1).[1-adamantane carboxylic acid] 2.90 7.0 25.0 Fluorescence spectroscopy Hiroshi Ikeda 2005

1-adamantane carboxylic acid
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
180.24 2 1 2.29 JN_W_4 None Not checked

SMILES: OC(=O)C12CC3CC(CC(C3)C1)C2

Supramolecules

Namelog KSDpHT(°C)MethodRef
[b-Cyclodextrin](1).[1-adamantane carboxylic acid] 5.48 flow microcalorimetry, pH potentiometric measurements, spectral displacement methods Véronique Wintgens 2005

1-adamantanecarboxylic acid
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
180.24 2 1 2.29 NT_a0028 None Not checked

SMILES: OC(=O)C12CC3CC(CC(C3)C1)C2

Supramolecules

Namelog KSDpHT(°C)MethodRef
[a-Cyclodextrin](1).[1-adamantanecarboxylic acid] 3.97 8.3 25.0 Absorption spectroscopy Ueno, Akihiko 1997

1-adamantanecarboxylic acid
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
180.24 2 1 2.29 SF_C1449 None Not checked

SMILES: OC(=O)C12CC3CC(CC(C3)C1)C2

Supramolecules

Namelog KSDpHT(°C)MethodRef
[phenolphthalein-modified b-CD](1).[1-adamantanecarboxylic acid] 4.70 9.4 25.0 Absorption and induced circular dichroism spectroscopy Tetsuo Kuwabara 1998
[alizarin yellow-modified b-cyclodextrin](1).[1-adamantanecarboxylic acid] 3.97 9.4 25.0 Absorption and induced circular dichroism spectroscopy Tetsuo Kuwabara 1998

1-adamantanecarboxylic acid
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
180.24 2 1 2.29 JN_3 None Not checked

SMILES: OC(=O)C12CC3CC(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-adamantanecarboxylic acid] 3.74 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-adamantanecarboxylic acid] 4.20 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-adamantanecarboxylic acid] 5.42 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-adamantanecarboxylic acid] 3.79 7.2 UV-vis spectroscopy, induced circular dichroism Tetsuo Kuwabara 1994

1-adamantanoic acid
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
180.24 2 1 2.29 SF_C118 None Not checked

SMILES: OC(=O)C12CC3CC(CC(C3)C1)C2

Supramolecules

Namelog KSDpHT(°C)MethodRef
[6I-(N-deoxy-b-cyclodextrin-6I-yl)-1-amido-3-substituted-7-pyridin-4-yl indolizine derivatives](1).[1-adamantanoic acid] 3.86 7.0 25.0 Fluorescence spectroscopy Franc¸ois Delattre 2005

1-adamantanol
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
152.23 1 1 1.95 NT_a0026 None Not checked

SMILES: OC12CC3CC(CC(C3)C1)C2

Supramolecules

Namelog KSDpHT(°C)MethodRef
[a-Cyclodextrin](1).[1-adamantanol] 3.91 8.3 25.0 Absorption spectroscopy Ueno, Akihiko 1997

1-adamantanol
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
152.23 1 1 1.95 NT_b0150 None Not checked

SMILES: OC12CC3CC(CC(C3)C1)C2

Supramolecules

Namelog KSDpHT(°C)MethodRef
[L-Trp-b-CD](1).[1-adamantanol] 3.67 7.2 25.0 spectrofluorometric titration Yu Liu 1999

1-adamantanol
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
152.23 1 1 1.95 SF_C1145 None Not checked

SMILES: OC12CC3CC(CC(C3)C1)C2

Supramolecules

Namelog KSDpHT(°C)MethodRef
[mono[6-benzylseleno-6-deoxy]-b-cyclodextrin](1).[1-adamantanol] 3.89 7.2 25.0 Differential circular dichroism spectroscopy Yu Liu 2001

1-adamantanol
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
152.23 1 1 1.95 SF_C117 None Not checked

SMILES: OC12CC3CC(CC(C3)C1)C2

Supramolecules

Namelog KSDpHT(°C)MethodRef
[6I-(N-deoxy-b-cyclodextrin-6I-yl)-1-amido-3-substituted-7-pyridin-4-yl indolizine derivatives](1).[1-adamantanol] 5.32 7.0 25.0 Fluorescence spectroscopy Franc¸ois Delattre 2005

1-adamantanol
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
152.23 1 1 1.95 SF_C1450 None Not checked

SMILES: OC12CC3CC(CC(C3)C1)C2

Supramolecules

Namelog KSDpHT(°C)MethodRef
[phenolphthalein-modified b-CD](1).[1-adamantanol] 4.98 9.4 25.0 Absorption and induced circular dichroism spectroscopy Tetsuo Kuwabara 1998
[alizarin yellow-modified b-cyclodextrin](1).[1-adamantanol] 3.91 9.4 25.0 Absorption and induced circular dichroism spectroscopy Tetsuo Kuwabara 1998