ISRIB

ISRIB
Clinical data
ATC code
  • none
Identifiers
IUPAC name
  • trans-N,N′-(Cyclohexane-1,4-diyl)bis(2-(4-chlorophenoxy)acetamide)
CAS Number
PubChem CID
ChemSpider
Chemical and physical data
FormulaC22H24Cl2N2O4
Molar mass451.34 g·mol−1
3D model (JSmol)
SMILES
  • O=C(COC1=CC=C(Cl)C=C1)N[C@@H]2CC[C@@H](NC(COC3=CC=C(Cl)C=C3)=O)CC2
InChI
  • InChI=1S/C22H24Cl2N2O4/c23-15-1-9-19(10-2-15)29-13-21(27)25-17-5-7-18(8-6-17)26-22(28)14-30-20-11-3-16(24)4-12-20/h1-4,9-12,17-18H,5-8,13-14H2,(H,25,27)(H,26,28)/t17-,18-
  • Key:HJGMCDHQPXTGAV-IYARVYRRSA-N

ISRIB (integrated stress response inhibitor) is an experimental drug that reverses the effects of eIF2α phosphorylation with an IC50 of 5 nM. It was discovered in the laboratory of Peter Walter at University of California, San Francisco (UCSF) through a semi-automated screening of a large library of small molecules by Carmela Sidrauski, who decided to pursue research on it.[1][2] It has been shown to inhibit eIF2α phosphorylation-induced stress granule (SG) formation.[3] Since eIF2α phosphorylation is known to be involved in memory formation, ISRIB was tested to see whether it would be active in vivo, and was found to readily cross the blood-brain barrier, with a half-life of eight hours.

Subsequent testing in 2013 found ISRIB to produce significant nootropic effects in mice, as measured by enhancement of spatial and fear-associated learning in standard water-maze and conditioned environment tests.

The technology was licensed to Calico in 2015 and Sidrauski was hired to help find possible drugs based on ISRIB.[2] She heads the laboratory in which it is being studied.

Testing in 2017 indicated the experimental drug improved the ability of brain-injured mice to learn and form memories on memory tests, thus appearing to reverse impairments from traumatic brain injury.[4][5] ISRIB treatment also corrects spatial memory deficits and improves working memory in aged mice.[6]

Further research on the drug by Sidrauski has shown that the molecule restored memory formation in mice months after traumatic brain injuries. It also has shown potential in treating neurodegenerative diseases such as Alzheimer’s, Parkinson’s, and Lou Gehrig’s disease (also known as amyotrophic lateral sclerosis, or ALS). In mice, it has reduced age-related cognitive decline and given healthy mice improved memory.[2] Research on ISRIB by Sidrauski continues at Calico.

See also

References

  1. ↑ Sidrauski C, Acosta-Alvear D, Khoutorsky A, Vedantham P, Hearn BR, Li H, et al. (May 2013). "Pharmacological brake-release of mRNA translation enhances cognitive memory". eLife. 2: e00498. doi:10.7554/eLife.00498. PMC 3667625. PMID 23741617.
  2. 1 2 3 Piore, Adam, The miracle molecule that could treat brain injuries and boost your fading memory, MIT Technology Review, August 25, 2021 (Carmela Sidrauski interview)
  3. ↑ Sidrauski C, McGeachy AM, Ingolia NT, Walter P (February 2015). "The small molecule ISRIB reverses the effects of eIF2α phosphorylation on translation and stress granule assembly". eLife. 4. doi:10.7554/eLife.05033. PMC 4341466. PMID 25719440.
  4. ↑ Cross R (July 11, 2017). "Science". United Press International. Retrieved July 12, 2017.
  5. ↑ Gallegos J (2017-07-10). "New drug restores memories in brain-damaged mice". Washington Post. ISSN 0190-8286. Retrieved 2018-06-27.
  6. ↑ Krukowski K, Nolan A, Elma S, Frias E, Boone M, Ureta G, et al. (December 2020). "Small molecule cognitive enhancer reverses age-related memory decline in mice". eLife. 9: e62048. doi:10.7554/eLife.62048. PMC 7721440. PMID 33258451.
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