Wikipedia

HOPO 14-1

HOPO 14-1 is an investigational drug product for removing radioactive contaminants from the body. It is an oral capsule designed to act as a defence against radioactive threats such as nuclear power plant accidents or dirty bomb attacks.[1][2] The active ingredient is the hydroxypyridinone ligand 3,4,3-LI(1,2-HOPO), which is a powerful chelating agent.[1][3] HOPO 14-1 works by selectively binding to heavy metals in the body and forming a complex that the body can naturally excrete.[4] The drug is also being studied as a treatment for other forms of heavy metal toxicity, including lead poisoning and exposure to gadolinium from MRI contrast agents.[5][6][7][8] HOPO 14-1 was developed at Lawrence Berkeley National Laboratory by actinide chemist Rebecca Abergel. Abergel and former postdoc Julian Avery Rees co-founded HOPO Therapeutics, a company commercializing HOPO 14-1 and other treatments for heavy metal poisoning.

3,4,3-LI(1,2-HOPO)
Legal status
Legal status
  • Investigational
Identifiers
  • N,N′-1,4-Butanediylbis[N-[3-[[(1,6-dihydro-1-hydroxy-6-oxo-2-pyridinyl)carbonyl]amino]propyl]-1,6-dihydro-1-hydroxy-6-oxo-2-pyridinecarboxamide]
CAS Number
PubChem CID
ChemSpider
UNII
ChEMBL
Chemical and physical data
FormulaC34H38N8O12
Molar mass750.722 g·mol−1
3D model (JSmol)
  • O=C1C=CC=C(C(=O)NCCCN(C(=O)C2=CC=CC(=O)N2O)CCCCN(C(=O)C3=CC=CC(=O)N3O)CCCNC(=O)C4=CC=CC(=O)N4O)N1O
  • InChI=1S/C34H38N8O12/c43-27-13-3-9-23(39(27)51)31(47)35-17-7-21-37(33(49)25-11-5-15-29(45)41(25)53)19-1-2-20-38(34(50)26-12-6-16-30(46)42(26)54)22-8-18-36-32(48)24-10-4-14-28(44)40(24)52/h3-6,9-16,51-54H,1-2,7-8,17-22H2,(H,35,47)(H,36,48)
  • Key:KUWKQASGHNTJAT-UHFFFAOYSA-N

References edit

  1. ^ a b "First-in-human trial of oral drug to remove radioactive contamination begins". National Institutes of Health (NIH). 2023-05-15. Retrieved 2023-05-16.
  2. ^ Roberts M (2023-05-16). "Dirty-bomb antidote: Drug trial begins in US". BBC News. Retrieved 2023-05-16.
  3. ^ Wang Q, Liu Z, Song YF, Chai Z, Wang D (March 2023). "Chelation Behaviors of 3,4,3-LI(1,2-HOPO) with Lanthanides and Actinides Implicated by Molecular Dynamics Simulations". Inorganic Chemistry. 62 (10): 4304–4313. doi:10.1021/acs.inorgchem.2c04460. PMID 36847745. S2CID 257218983.
  4. ^ Abergel RJ, Durbin PW, Kullgren B, Ebbe SN, Xu J, Chang PY, et al. (September 2010). "Biomimetic actinide chelators: an update on the preclinical development of the orally active hydroxypyridonate decorporation agents 3,4,3-LI(1,2-HOPO) and 5-LIO(Me-3,2-HOPO)". Health Physics. 99 (3): 401–407. doi:10.1097/HP.0b013e3181c21273. PMC 2921233. PMID 20699704.
  5. ^ Rees JA, Deblonde GJ, An DD, Ansoborlo C, Gauny SS, Abergel RJ (March 2018). "Evaluating the potential of chelation therapy to prevent and treat gadolinium deposition from MRI contrast agents". Scientific Reports. 8 (1): 4419. Bibcode:2018NatSR...8.4419R. doi:10.1038/s41598-018-22511-6. PMC 5849765. PMID 29535330.
  6. ^ "This Anti-Nuclear-Contimation Pill Could Also Help MRI Patients". Lawrence Berkeley National Laboratory (Berkeley Lab). 2019-09-12. Retrieved 2023-05-29.
  7. ^ "Rebecca Abergel - Bakar Fellows Program". Bakar Fellows Program, UC Berkeley. 2021-10-21. Retrieved 2023-05-29.
  8. ^ "HOPO Therapeutics". HOPO Therapeutics, Inc. 2023-05-29. Retrieved 2023-05-29.

See also edit

 

This pharmacology-related article is a stub. You can help Wikipedia by expanding it.

Retrieved from "https://en.wikipedia.org/w/index.php?title=HOPO_14-1&oldid=1157659748"