Fadrozole
Clinical data | |
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Routes of administration | Oral |
ATC code | none |
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Identifiers | |
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CAS Number | 102676-31-3 Y |
PubChem (CID) | 59693 |
ChemSpider | 53850 N |
UNII | H3988M64PU N |
KEGG | D02451 Y |
ChEMBL | CHEMBL9298 N |
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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NY (what is this?) (verify) |
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 | |
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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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