Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C21H28O5 |
| Molecular Weight | 360.444 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 7 / 7 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C[C@]1(O)CC[C@H]2[C@@H]3CCC4=CC(=O)C(=C[C@]4(C)[C@H]3[C@@H](O)C[C@]12C)C(O)=O
InChI
InChIKey=JOFBZBDWOWPUMO-QARKFJNLSA-N
InChI=1S/C21H28O5/c1-19-9-13(18(24)25)15(22)8-11(19)4-5-12-14-6-7-21(3,26)20(14,2)10-16(23)17(12)19/h8-9,12,14,16-17,23,26H,4-7,10H2,1-3H3,(H,24,25)/t12-,14-,16-,17+,19-,20-,21-/m0/s1
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Androstane derivatives--roxibolone and decylroxibolone--devoid of any affinity for the androgenic prostate and muscle receptors. | 1986-09 |
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| Activity of a new androstane derivative on the nitrogen metabolism: antiglucocorticoid effects. | 1985-11 |
|
| Synthesis of 2-carboxy-11 beta, 17 beta-dihydroxy-17-methyl-1, 4-androstadien-3-one and related compounds. | 1984-03 |
Patents
| Name | Type | Language | ||
|---|---|---|---|---|
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Official Name | English | ||
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Preferred Name | English | ||
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Common Name | English | ||
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Common Name | English | ||
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Common Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
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NCI_THESAURUS |
C2360
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DTXSID20208728
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60023-92-9
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68795
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100000084366
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SUB10397MIG
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CHEMBL2105402
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4513
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C044300
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ROXIBOLONE
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3R7NLP419C
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C74110
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ACTIVE MOIETY