Chemistry:Elinzanetant
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| Other names | BAY-3427080; GSK-1144814; NT-814 |
| Routes of administration | Oral administration |
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| Formula | C33H35F7N4O3 |
| Molar mass | 668.657 g·mol−1 |
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Elinzanetant (developmental code names BAY-3427080 GSK-1144814, NT-814) is an orally active small-molecule neurokinin/tachykinin NK1 receptor and NK3 receptor antagonist which is under development by Bayer, GlaxoSmithKline, and NeRRe Therapeutics for the treatment of hot flashes and "sex hormone disorders".[1][2] It has been found to relieve hot flashes in postmenopausal women and to dose-dependently suppress luteinizing hormone, estradiol, and progesterone levels in premenopausal women.[2][3] As of August 2021, elinzanetant is in phase 2 clinical trials for hot flashes and "sex hormone disorders".[1] It was also under development for the treatment of schizophrenia and opioid-related disorders, but development was discontinued for these uses.[1]
See also
References
- ↑ 1.0 1.1 1.2 "Elinzanetant - Bayer". Adis Insight. Springer Nature Switzerland AG. https://adisinsight.springer.com/drugs/800044912.
- ↑ 2.0 2.1 "Fezolinetant in the treatment of vasomotor symptoms associated with menopause". Expert Opinion on Investigational Drugs 30 (7): 681–694. July 2021. doi:10.1080/13543784.2021.1893305. PMID 33724119.
- ↑ "Elinzanetant (NT-814), a Neurokinin 1,3 Receptor Antagonist, Reduces Estradiol and Progesterone in Healthy Women". The Journal of Clinical Endocrinology and Metabolism 106 (8): e3221–e3234. July 2021. doi:10.1210/clinem/dgab108. PMID 33624806.
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