| Weight | 316.485 g/mol |
|---|---|
| Formula | C21H32O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
CALUSTERONE (17021-26-0)
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- Calusterone (7,17-DimethyItestosterone) as Primary and Secondary Therapy of Advanced Breast Cancer (Oncology, 1973)
- Male Breast Cancer: Two Cases with Objective Regressions from Calusterone (7, 17-dimethyltestosterone) after Failure of Orchiectomy (Oncology, 1976)
- Calusterone in the therapy for advanced breast cancer. (JAMA, 1972)
- The platelet-stimulating effects of 7-beta, 17-alpha-dimethyltestosterone (calusterone). (Blood, 1972)
- 7, 17-Dimethyltestosterone (Calusterone)-Induced Changes in the Metabolism, Production Rate, and Excretion of Estrogens in Women with Breast Cancer: A Possible Mechanism of Action (The Journal of Clinical Endocrinology and Metabolism, 1976)
- Drugs Five Years Later: Calusterone (Annals of Internal Medicine, 1978)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC1CC2=CC(=O)CCC2(C3C1C4CCC(C4(CC3)C)(C)O)C
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InChIKeyIVFYLRMMHVYGJH-UHFFFAOYSA-N
- Pubchem - CALUSTERONE
- Wikipedia - calusterone
Calusterone (INN, USAN) (brand names Methosarb, Riedemil; former developmental code names NSC-88536, U-22550), also known as 7,17-dimethyltestosterone, is an orally active anabolic-androgenic steroid (AAS) that is used as an antineoplastic agent. It is a 17-alkylated AAS similar in structure to bolasterone (which is its 7-isomer).
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