| Weight | 362.466 g/mol |
|---|---|
| Formula | C21H30O5 |
| Hydrogen Acceptors | 5 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 3 |
18-HYDROXYCORTICOSTERONE (561-65-9)
18-Hydrocorticosterone · 18 Hydrocorticosterone · 18 Hydroxycorticosterone
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- The Significance of Elevated Levels of Plasma 18-Hydroxycorticosterone in Patients with Primary Aldosteronism* (The Journal of Clinical Endocrinology and Metabolism, 1979)
- 18-Hydroxycorticosterone: A review (Journal of Steroid Biochemistry, 1978)
- Dose-Response Relationships Between Plasma Adrenocorticotropin (ACTH), Cortisol, Aldosterone, and 18-Hydroxycorticosterone After Injection of ACTH-(139) or Human Corticotropin-Releasing Hormone in Man* (The Journal of Clinical Endocrinology and Metabolism, 1988)
- Response of aldosterone and 18-hydroxycorticosterone to angiotensin II in normal subjects and patients with essential hypertension, Conn's syndrome, and nontumorous hyperaldosteronism. (Hypertension, 1981)
- Simultaneous Measurement of Secretory Rates of Aldosterone and 18-Hydroxycorticosterone (The Journal of Clinical Endocrinology and Metabolism, 1965)
- 18-Hydroxycorticosterone, 18-Hydroxycortisol, and 18-Oxocortisol in the Diagnosis of Primary Aldosteronism and Its Subtypes (The Journal of Clinical Endocrinology and Metabolism, 2012)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 18-Hydrocorticosterone
- 18 Hydrocorticosterone
- 18 Hydroxycorticosterone
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SMILESCC12CCC(=O)C=C1CCC3C2C(CC4(C3CCC4C(=O)CO)CO)O
-
InChIKeyHFSXHZZDNDGLQN-UHFFFAOYSA-N
- Pubchem - 18-HYDROXYCORTICOSTERONE
- Wikipedia - 18-hydroxycorticosterone
18-Hydroxycorticosterone is a derivative of corticosterone. It serves as an intermediate in the synthesis of aldosterone by the enzyme aldosterone synthase in the zona glomerulosa:
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18-HYDROXYCORTICOSTERONE
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