prednisolone

CAS:
Other names:
SMILES: C[C@]12C[C@H](O)[C@H]3[C@@H](CCC4=CC(=O)C=C[C@]34C)[C@@H]1CC[C@]2(O)C(=O)CO

Properties

MW HBA HBD LogP TPSA Rot. Comp. Fsp3C Brutto formula
360.44 5 3 1.56 94.83 2 48 0.71 C21H28O5

Availability

Suppliers Supplier IDs Storage Storage ID Quantity Class Added
JN_260 None Jan. 1, 2023

Bar codes

Plate barcode Sample barcode

PAINS

Identified PAINS
Not checked

Supramolecules

Namelog KSDpHT(°C)MethodRef
[a-Cyclodextrin](1).[prednisolone] 2.46 0.85 5.5 25.0 NMR spectroscopy Kim L.Larsen 2005
[a-Cyclodextrin](1).[prednisolone] 2.47 25.0 NMR, UV-vis spectroscopy, X-ray diffraction Kim L.Larsen 2005
[b-Cyclodextrin](1).[prednisolone] 3.54 2.14 5.5 25.0 NMR spectroscopy Kim L.Larsen 2005
[b-Cyclodextrin](1).[prednisolone] 3.48 25.0 NMR, UV-vis spectroscopy, X-ray diffraction Kim L.Larsen 2005
[g-Cyclodextrin](1).[prednisolone] 3.25 1.68 5.5 25.0 NMR spectroscopy Kim L.Larsen 2005
[g-Cyclodextrin](1).[prednisolone] 3.51 25.0 NMR, UV-vis spectroscopy, X-ray diffraction Kim L.Larsen 2005
[2-O-(2-Hydroxy)propyl-b-Cyclodextrin](1).[prednisolone] 3.39 1.75 5.5 25.0 NMR spectroscopy Kim L.Larsen 2005
[2-O-(2-Hydroxy)propyl-b-Cyclodextrin](1).[prednisolone] 3.12 25.0 UV-vis spectroscopy Kim L.Larsen 2005
[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
[sulfobutylether-b-cyclodextrin](1).[prednisolone] 3.43 1.79 5.5 25.0 NMR spectroscopy Kim L.Larsen 2005
[sulfobutylether-b-cyclodextrin](1).[prednisolone] 3.26 25.0 UV-vis spectroscopy Kim L.Larsen 2005
[sulfobutylether-g-cyclodextrin](1).[prednisolone] 3.50 1.93 5.5 25.0 NMR spectroscopy Kim L.Larsen 2005
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