Fadrozole
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| Clinical data | |
|---|---|
| Routes of administration | Oral |
| ATC code | none |
| Legal status | |
| Legal status |
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| Identifiers | |
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| CAS Number |
102676-31-3 |
| PubChem (CID) | 59693 |
| ChemSpider |
53850 |
| UNII |
H3988M64PU |
| KEGG |
D02451 |
| ChEMBL |
CHEMBL9298 |
| ECHA InfoCard | 100.159.562 |
| Chemical and physical data | |
| Formula | C14H13N3 |
| Molar mass | 223.27 g/mol |
| 3D model (Jmol) | Interactive image |
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Fadrozole (INN, marketed as Afema by Novartis) is a selective[1] aromatase inhibitor[2] that has been introduced in Japan for the treatment of breast cancer.
References
- ↑ Browne LJ, Gude C, Rodriguez H, Steele RE, Bhatnager A (February 1991). "Fadrozole hydrochloride: a potent, selective, nonsteroidal inhibitor of aromatase for the treatment of estrogen-dependent disease". J. Med. Chem. 34 (2): 725–36. doi:10.1021/jm00106a038. PMID 1825337.
- ↑ Raats JI, Falkson G, Falkson HC (January 1992). "A study of fadrozole, a new aromatase inhibitor, in postmenopausal women with advanced metastatic breast cancer". J. Clin. Oncol. 10 (1): 111–6. PMID 1530798.
| AR |
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|---|---|---|---|---|---|---|---|---|---|---|---|
| GPRC6A |
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See also: Estrogenics • Glucocorticoidics • Mineralocorticoidics • Progestogenics • Steroid hormone metabolism modulators • List of androgens/anabolic steroids | |||||||||||
| ER |
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|---|---|---|---|---|---|---|---|---|---|---|---|
| GPER |
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See also: Androgenics • Glucocorticoidics • Mineralocorticoidics • Progestogenics • Steroid hormone metabolism modulators | |||||||||||
| HMGCR | |
|---|---|
| FPS | |
| 24-DHCR24 |
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| 20,22-Desmolase (P450scc) |
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| 17α-Hydroxylase, 17,20-Lyase |
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| 3α-HSD | |
| 3β-HSD | |
| 11β-HSD |
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| 21-Hydroxylase |
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| 11β-Hydroxylase |
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| 18-Hydroxylase |
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| 17β-HSD |
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| 5α-Reductase |
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| Aromatase |
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| SST/EST |
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| STS |
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| 27-Hydroxylase | |
| Others |
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See also: Androgenics • Estrogenics • Glucocorticoidics • Mineralocorticoidics • Progestogenics | |
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