Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C24H30FO9P.2Na |
Molecular Weight | 558.4413 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 8 / 8 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[Na+].[Na+].[H][C@@]12C[C@@]3([H])[C@]4([H])CCC5=CC(=O)C=C[C@]5(C)[C@@]4(F)[C@@H](O)C[C@]3(C)[C@@]1(OC(C)(C)O2)C(=O)COP([O-])([O-])=O
InChI
InChIKey=XCMJCLDAGKYHPP-AREPQIRLSA-L
InChI=1S/C24H32FO9P.2Na/c1-20(2)33-19-10-16-15-6-5-13-9-14(26)7-8-21(13,3)23(15,25)17(27)11-22(16,4)24(19,34-20)18(28)12-32-35(29,30)31;;/h7-9,15-17,19,27H,5-6,10-12H2,1-4H3,(H2,29,30,31);;/q;2*+1/p-2/t15-,16-,17-,19+,21-,22-,23-,24+;;/m0../s1
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/17088419
Sources: https://www.ncbi.nlm.nih.gov/pubmed/17088419
Triamcinolone acetonide- 21-dihydrogen phosphate is the long-acting derivative of a synthetic glucocorticoid triamcinolone. Triamcinolone acetonide has eight times more potency than prednisolone. Triamcinolone acetonide- 21-dihydrogen phosphate used for intravenous injection. It is supposed to be hydrolyzed rapidly in the body to form the free corticoid alcohol.
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/17088419
Curator's Comment: Dogs data
Single injection - 0.2 mg/kg
Route of Administration:
Intravenous
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NCI_THESAURUS |
C521
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CHEMBL2111162
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100000175600
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16147
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1997-15-5
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C152734
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DTXSID30941876
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m11028
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R2MZ7K74S8
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217-878-8
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SUBSTANCE RECORD