Revision as of 06:45, 27 December 2024 editBoghog (talk | contribs)Autopatrolled, Extended confirmed users, IP block exemptions, New page reviewers, Pending changes reviewers, Rollbackers, Template editors137,699 edits created drug stubTag: nowiki added | Revision as of 09:22, 27 December 2024 edit undoGraeme Bartlett (talk | contribs)Administrators249,639 edits added Category:Ethoxy compounds using HotCatNext edit → | ||
Line 123: | Line 123: | ||
] | ] | ||
] | ] | ||
] |
Revision as of 09:22, 27 December 2024
Pharmaceutical compound
Clinical data | |
---|---|
Other names | CRN04894 |
Identifiers | |
IUPAC name
| |
CAS Number | |
PubChem CID | |
IUPHAR/BPS | |
UNII | |
Chemical and physical data | |
Formula | C33H42F3N5O3 |
Molar mass | 613.726 g·mol |
3D model (JSmol) | |
SMILES
| |
InChI
|
Atumelnant (CRN04894) is an investigational new drug developed by Crinetics Pharmaceuticals for the treatment of adrenocorticotropic hormone (ACTH)-dependent endocrine disorders. It is a selective antagonist of the melanocortin type 2 receptor (MC2R), also known as the ACTH receptor, which is primarily expressed in the adrenal glands. Atumelnant is being evaluated to treat conditions such as congenital adrenal hyperplasia (CAH) and ACTH-dependent Cushing's syndrome caused for example by pituitary adenomas.
References
- "Atumelnant (CRN04894)". crinetics.com.
- Varlamov EV, Gheorghiu ML, Fleseriu M (December 2024). "Pharmacological management of pituitary adenomas - what is new on the horizon?". Expert Opinion on Pharmacotherapy. doi:10.1080/14656566.2024.2446625. PMID 39718553.
This pharmacology-related article is a stub. You can help Misplaced Pages by expanding it. |