Chemistry:Lorundrostat

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Short description: Chemical compound
Lorundrostat
Lorundrostat.svg
Clinical data
Other namesMLS 101
Legal status
Legal status
  • Investigational
Identifiers
CAS Number
PubChem CID
ChemSpider
UNII
KEGG
ChEMBL
Chemical and physical data
FormulaC24H33N7O2
Molar mass451.575 g·mol−1
3D model (JSmol)

Lorundrostat (developmental name MLS 101) is an aldosterone synthase inhibitor developed by Mineralys Therapeutics for high blood pressure. In clinical trials as an add-on medication for people with uncontrolled hypertension, decreased renin and elevated aldosterone it significantly reduced blood pressure. Hyperkalemia occurred in some trial participants.[1][2][3][4]

References

  1. Laffin, Luke J.; Rodman, David; Luther, James M.; Vaidya, Anand; Weir, Matthew R.; Rajicic, Natasa; Slingsby, B. T.; Nissen, Steven E. et al. (26 September 2023). "Aldosterone Synthase Inhibition With Lorundrostat for Uncontrolled Hypertension: The Target-HTN Randomized Clinical Trial" (in en). JAMA 330 (12): 1140–1150. doi:10.1001/jama.2023.16029. ISSN 0098-7484. PMID 37690061. 
  2. Rodman, David; Weir, Matthew R.; Slingsby, Bt; Laffin, Luke; Nissen, Steven E. (March 2023). "Highly Effective Blood Pressure Lowering with MLS-101, A New Aldosterone Synthase Inhibitor, in Individuals with Obesity and Raas Dysregulation" (in en). Journal of the American College of Cardiology 81 (8): 306. doi:10.1016/S0735-1097(23)00750-7. https://www.jacc.org/doi/full/10.1016/S0735-1097%2823%2900750-7. 
  3. Fujii, Aya; Hiraga, Yuki; Kawai, Mizue; Ogawa, Kei; Ohta, Yoshiyasu; Rahman, Sheikh Mohammed Ashfaq; Shimizu, Hidetoshi; Sugimoto-Kawabata, Kanami et al. (March 2023). "First-In-Human Study of MLS-101, A Potent and Highly Selective Aldosterone Synthase Inhibitor" (in en). Journal of the American College of Cardiology 81 (8): 616. doi:10.1016/S0735-1097(23)01060-4. https://www.jacc.org/doi/full/10.1016/S0735-1097%2823%2901060-4. 
  4. Irfan, Hamza; Ahmed, Aliza; Nawani, Komal Devi (January 2024). "Hypertension and Lorundrostat: Key Discoveries From the TARGET-HTN Trial". Current Problems in Cardiology 49 (1): 102144. doi:10.1016/j.cpcardiol.2023.102144. PMID 37858848.