6-O-R-maltosyl-b-CD
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
None None VD-0145 None

SMILES:

Supramolecules

Namelog KSDpHT(°C)MethodRef
[6-O-R-maltosyl-b-CD](1).[dansyl-branched saccharide cyclophane] 2.78 7.0 25.0 Fluorescence spectroscopy Osamu Hayashida 2002
[6-O-R-maltosyl-b-CD](1).[prednisolone] 3.48 1.88 5.5 25.0 NMR spectroscopy Kim L.Larsen 2005
[6-O-R-maltosyl-b-CD](1).[prednisolone] 3.41 25.0 Kim L.Larsen 2005
[6-O-R-maltosyl-b-CD](1).[6a-methyl prednisolone] 3.11 1.61 5.5 25.0 NMR spectroscopy Kim L.Larsen 2005

6-O-a-D-glucosyl-b-CD
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
None None VD-0058 None

SMILES:

Supramolecules

Namelog KSDpHT(°C)MethodRef
[6-O-a-D-glucosyl-b-CD](1).[1-butanol] 1.56 7.0 22.0 Fluorescence spectroscopy Daniel G. Nocera 1993
[6-O-a-D-glucosyl-b-CD](1).[1-propanol] 1.26 7.0 22.0 Fluorescence spectroscopy Daniel G. Nocera 1993
[6-O-a-D-glucosyl-b-CD](1).[2-propanol] 1.08 7.0 22.0 Fluorescence spectroscopy Daniel G. Nocera 1993
[6-O-a-D-glucosyl-b-CD](1).[2-butanol] 1.40 7.0 22.0 Fluorescence spectroscopy Daniel G. Nocera 1993
[6-O-a-D-glucosyl-b-CD](1).[tert-butyl alcohol] 1.83 7.0 22.0 Fluorescence spectroscopy Daniel G. Nocera 1993
[6-O-a-D-glucosyl-b-CD](1).[cyclohexnol] 2.11 7.0 22.0 Fluorescence spectroscopy Daniel G. Nocera 1993
[6-O-a-D-glucosyl-b-CD](1).[1-bromonaphtalene] 3.51 7.0 22.0 Fluorescence spectroscopy Daniel G. Nocera 1993
[6-O-a-D-glucosyl-b-CD](1).[Phenol] 2.41 0.30 6.9 40.0 UV-vis spectroscopy Yoshimi Sueishi 2006
[6-O-a-D-glucosyl-b-CD](1).[4-CH3-Phenol] 2.66 0.48 6.9 40.0 UV-vis spectroscopy Yoshimi Sueishi 2006
[6-O-a-D-glucosyl-b-CD](1).[4-NO2-Phenol] 2.68 0.70 6.9 40.0 UV-vis spectroscopy Yoshimi Sueishi 2006
[6-O-a-D-glucosyl-b-CD](1).[2-Naphthol] 2.70 0.70 6.9 40.0 UV-vis spectroscopy Yoshimi Sueishi 2006
[6-O-a-D-glucosyl-b-CD](1).[4-CH3(CH2)4-phenol] 3.82 1.85 6.9 40.0 UV-vis spectroscopy Yoshimi Sueishi 2006
[6-O-a-D-glucosyl-b-CD](1).[4-CH3(CH2)5-phenol] 3.98 1.95 6.9 40.0 UV-vis spectroscopy Yoshimi Sueishi 2006

6-O-phenyl-b-CD
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
None None VD-0143 None

SMILES:

Supramolecules

Namelog KSDpHT(°C)MethodRef
[6-O-phenyl-b-CD](1).[cyclopentanol] 2.59 1.46 7.2 25.0 titration microcalorimetry Yu Liu 2004
[6-O-phenyl-b-CD](1).[cyclohexanol ] 2.92 1.08 7.2 25.0 titration microcalorimetry Yu Liu 2004
[6-O-phenyl-b-CD](1).[cycloheptanol ] 3.55 1.49 7.2 25.0 titration microcalorimetry Yu Liu 2004
[6-O-phenyl-b-CD](1).[cyclooctanol ] 3.83 1.36 7.2 25.0 titration microcalorimetry Yu Liu 2004
[6-O-phenyl-b-CD](1).[(+)-camphor] 4.14 1.74 7.2 25.0 titration microcalorimetry Yu Liu 2004
[6-O-phenyl-b-CD](1).[(-)-camphor ] 3.76 2.22 7.2 25.0 titration microcalorimetry Yu Liu 2004
[6-O-phenyl-b-CD](1).[(+)-borneol ] 4.55 3.07 7.2 25.0 titration microcalorimetry Yu Liu 2004
[6-O-phenyl-b-CD](1).[(-)-borneol] 4.51 2.97 7.2 25.0 titration microcalorimetry Yu Liu 2004

6-p-toluidinylnaphthalene-2-sulfonate
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
312.36 3 1 4.95 JN_469 None Not checked

SMILES: Cc1ccc(Nc2ccc3cc(ccc3c2)[S]([O-])(=O)=O)cc1

Supramolecules

Namelog KSDpHT(°C)MethodRef
[b-Cyclodextrin](1).[6-p-toluidinylnaphthalene-2-sulfonate] 3.04 25.0 Uv-vis spectrophotometry Yannis L. Loukas 2002
[2-O-(2-Hydroxy)propyl-b-Cyclodextrin](1).[6-p-toluidinylnaphthalene-2-sulfonate] 3.17 1.88 25.0 Uv-vis spectrophotometry Yannis L. Loukas 2002

6-p-toluidinylnaphthalene-2-sulphonate
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
312.36 3 1 4.95 JN_362 None Not checked

SMILES: Cc1ccc(Nc2ccc3cc(ccc3c2)[S]([O-])(=O)=O)cc1

Supramolecules

Namelog KSDpHT(°C)MethodRef
[b-Cyclodextrin](1).[6-p-toluidinylnaphthalene-2-sulphonate] 3.04 25.0 UV-vis spectroscopy Yannis L. Loukas 2000

6-thiopurine
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
152.18 3 2 1.02 VR_C166 None Not checked

SMILES: S=C1N=CNc2nc[nH]c12

Supramolecules

Namelog KSDpHT(°C)MethodRef
[b-Cyclodextrin](1).[6-thiopurine] 2.40 1.48 25.0 UV/VIS Spectroscopy Joel B. Alderete 2003
[chitosan-b-CD](1).[6-thiopurine] 3.23 2.48 25.0 UV/VIS Spectroscopy Joel B. Alderete 2003

6-toluidino-2-naphthalenesulfonat
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
313.37 4 1 5.03 SF_C1329 None Not checked

SMILES: Cc1ccccc1NO[S](=O)(=O)c2ccc3ccccc3c2

Supramolecules

Namelog KSDpHT(°C)MethodRef
[bis-b-CD derivative 1](1).[6-toluidino-2-naphthalenesulfonat] 4.45 3.04 7.0 23.0 Fluorescence spectroscopy Russell C. Petter 1991
[bis-b-CD derivative 2](1).[6-toluidino-2-naphthalenesulfonat] 4.87 3.90 7.0 23.0 Fluorescence spectroscopy Russell C. Petter 1991

6A-(3-Aminopropylamino)-6A-deoxy-BCD
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
None None VD-0268 None

SMILES:

Supramolecules

Namelog KSDpHT(°C)MethodRef
[6A-(3-Aminopropylamino)-6A-deoxy-BCD](1).[Co2+] 4.22 0.02 25.0 pH titration Stephen F. Lincoln 1994
[6A-(3-Aminopropylamino)-6A-deoxy-BCD](1).[Ni2+] 5.20 0.10 25.0 pH titration Stephen F. Lincoln 1994
[6A-(3-Aminopropylamino)-6A-deoxy-BCD](1).[Cu2+] 7.35 0.04 25.0 pH titration Stephen F. Lincoln 1994
[6A-(3-Aminopropylamino)-6A-deoxy-BCD](1).[Zn2+] 4.96 0.08 25.0 pH titration Stephen F. Lincoln 1994

6A-(3-Aminopropylamino)-6A-deoxy-BCD complex with Cu2+
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
None None VD-0329 None

SMILES:

Supramolecules

Namelog KSDpHT(°C)MethodRef
[6A-(3-Aminopropylamino)-6A-deoxy-BCD complex with Cu2+](1).[R-tryptophan anion] 7.85 0.07 25.0 pH titration Stephen F. Lincoln 1994
[6A-(3-Aminopropylamino)-6A-deoxy-BCD complex with Cu2+](1).[S-tryptophan anion] 8.09 0.05 25.0 pH titration Stephen F. Lincoln 1994
[6A-(3-Aminopropylamino)-6A-deoxy-BCD complex with Cu2+](1).[R-tryptophan] 5.29 0.05 25.0 pH titration Stephen F. Lincoln 1994
[6A-(3-Aminopropylamino)-6A-deoxy-BCD complex with Cu2+](1).[S-tryptophan] 5.40 0.10 25.0 pH titration Stephen F. Lincoln 1994