6a-methyl prednisolone

CAS:
Other names:
SMILES: O=C1C=C[C@]2(C)[C@@]3([H])C(O)C[C@]4(C)[C@](C(CO)=O)(O)CC[C@@]4([H])[C@]3([H])C[C@H](C)C2=C1

Properties

MW HBA HBD LogP TPSA Rot. Comp. Fsp3C Brutto formula
374.47 8 3 1.80 94.83 2 48 0.73 C22H30O5

Availability

Suppliers Supplier IDs Storage Storage ID Quantity Class Added
JN_261 None Jan. 1, 2023

Bar codes

Plate barcode Sample barcode

PAINS

Identified PAINS
Not checked

Supramolecules

Namelog KSDpHT(°C)MethodRef
[a-Cyclodextrin](1).[6a-methyl prednisolone] 1.99 0.48 5.5 25.0 NMR spectroscopy Kim L.Larsen 2005
[b-Cyclodextrin](1).[6a-methyl prednisolone] 3.01 1.48 5.5 25.0 NMR spectroscopy Kim L.Larsen 2005
[g-Cyclodextrin](1).[6a-methyl prednisolone] 3.40 1.98 5.5 25.0 NMR spectroscopy Kim L.Larsen 2005
[2-O-(2-Hydroxy)propyl-b-Cyclodextrin](1).[6a-methyl prednisolone] 2.76 1.20 5.5 25.0 NMR spectroscopy Kim L.Larsen 2005
[2-O-(2-Hydroxy)propyl-b-Cyclodextrin](1).[6a-methyl prednisolone] 2.75 25.0 UV-vis spectroscopy Kim L.Larsen 2005
[2-O-(2-Hydroxy)propyl-b-Cyclodextrin](1).[6a-methyl prednisolone] 2.79 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
[sulfobutylether-b-cyclodextrin](1).[6a-methyl prednisolone] 2.85 1.28 5.5 25.0 NMR spectroscopy Kim L.Larsen 2005
[sulfobutylether-b-cyclodextrin](1).[6a-methyl prednisolone] 2.86 25.0 Kim L.Larsen 2005
[sulfobutylether-b-cyclodextrin](1).[6a-methyl prednisolone] 2.86 25.0 UV-vis spectroscopy Kim L.Larsen 2005
[sulfobutylether-g-cyclodextrin](1).[6a-methyl prednisolone] 3.10 1.59 5.5 25.0 NMR spectroscopy Kim L.Larsen 2005
[sulfobutylether-g-cyclodextrin](1).[6a-methyl prednisolone] 3.12 25.0 Kim L.Larsen 2005
Comment