Rosolutamide

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Rosolutamide

CAS 1039760-91-2

MF C28H32O6 MW464.5 g/mol

(1E,6E)-4-(cyclobutylmethyl)-1,7-bis(3,4-dimethoxyphenyl)hepta-1,6-diene-3,5-dione

(1E,6E)-4-(cyclobutylmethyl)-1,7-bis(3,4-dimethoxyphenyl)hepta-1,6-diene-3,5-dione
antiandrogen, ASC-JM-17, ASC-JM17, JM17, ALZ-003, ALZ003, 5VLL140BN9,

Rosolutamide (INNTooltip International Nonproprietary Name; developmental code name ASC-JM17JM17ALZ-003) is an agonist of nuclear respiratory factor 1 (NRF1), a nonsteroidal antiandrogen, and an androgen receptor degrader related to curcumin.[1][2][3][4][5] Other analogues like dimethylcurcumin (ASC-J9) are also known.[2][6]

3-hydroxy imidacloprid is an imidacloprid. It has a role as a neonicotinoid insectide and a nicotinic acetylcholine receptor agonist.

REF

SYN

https://patentscope.wipo.int/search/en/detail.jsf?docId=CN455268913&_cid=P11-MMOAAI-69206-1

SYN

https://patentscope.wipo.int/search/en/detail.jsf?docId=WO2025021236&_cid=P11-MMO9P1-52371-1

SYN

https://patentscope.wipo.int/search/en/detail.jsf?docId=US435547718&_cid=P11-MMOA3K-64182-1

COMPD B

SYN

https://patentscope.wipo.int/search/en/detail.jsf?docId=WO2025021237&_cid=P11-MMOA64-66109-1

SYN

https://patentscope.wipo.int/search/en/detail.jsf?docId=WO2022221276&_cid=P11-MMOA8S-67993-1

PAT

Compounds with (substituted phenyl)-propenal moiety, their derivatives, biological activity, and uses thereof

Publication Number: EP-2104659-B1

Priority Date: 2007-01-08

Grant Date: 2015-07-29

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Clinical data
Other namesASC-JM-17; ASC-JM17; JM17; ALZ-003; ALZ003
Identifiers
IUPAC name
CAS Number1039760-91-2
PubChem CID25183127
DrugBankDB16931
ChemSpider64854816
UNII5VLL140BN9
ChEMBLChEMBL5266600
Chemical and physical data
FormulaC28H32O6
Molar mass464.558 g·mol−1
3D model (JSmol)Interactive image
SMILES
InChI

References

  1.  “Proposed INN: List 131 International Nonproprietary Names for Pharmaceutical Substances (INN)” (PDF). WHO Drug Information38 (2): 428. 2024.
  2.  Chang KH, Chen CM (May 2024). “The Role of NRF2 in Trinucleotide Repeat Expansion Disorders”Antioxidants13 (6): 649. doi:10.3390/antiox13060649PMC 11200942PMID 38929088.
  3.  Yuan J, Zhang S, Zhang Y (December 2018). “Nrf1 is paved as a new strategic avenue to prevent and treat cancer, neurodegenerative and other diseases”. Toxicology and Applied Pharmacology360: 273–283. Bibcode:2018ToxAP.360..273Ydoi:10.1016/j.taap.2018.09.037PMID 30267745.
  4.  Bott LC, Badders NM, Chen KL, Harmison GG, Bautista E, Shih CC, et al. (May 2016). “A small-molecule Nrf1 and Nrf2 activator mitigates polyglutamine toxicity in spinal and bulbar muscular atrophy”Human Molecular Genetics25 (10): 1979–1989. doi:10.1093/hmg/ddw073PMC 5062587PMID 26962150.
  5.  Wu YL, Chang JC, Chao YC, Chan H, Hsieh M, Liu CS (July 2022). “In Vitro Efficacy and Molecular Mechanism of Curcumin Analog in Pathological Regulation of Spinocerebellar Ataxia Type 3”Antioxidants11 (7): 1389. doi:10.3390/antiox11071389PMC 9311745PMID 35883884.
  6.  Sangotra A, Lieberman AP (February 2025). “Therapeutic targeting of the polyglutamine androgen receptor in Spinal and Bulbar Muscular Atrophy”Expert Opinion on Therapeutic Targets: 1–13. doi:10.1080/14728222.2025.2464173PMID 39915972.

/////////rosolutamide, antiandrogen, ASC-JM-17, ASC-JM17, JM17, ALZ-003, ALZ003, 5VLL140BN9, ANAX

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