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GW-1100

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GW-1100
Identifiers
  • ethyl 4-[5-[(2-ethoxypyrimidin-5-yl)methyl]-2-[(4-fluorophenyl)methylsulfanyl]-4-oxopyrimidin-1-yl]benzoate
CAS Number
PubChem CID
IUPHAR/BPS
ChemSpider
ChEMBL
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC27H25FN4O4S
Molar mass520.58 g·mol−1
3D model (JSmol)
  • CCOC1=NC=C(C=N1)CC2=CN(C(=NC2=O)SCC3=CC=C(C=C3)F)C4=CC=C(C=C4)C(=O)OCC
  • InChI=1S/C27H25FN4O4S/c1-3-35-25(34)20-7-11-23(12-8-20)32-16-21(13-19-14-29-26(30-15-19)36-4-2)24(33)31-27(32)37-17-18-5-9-22(28)10-6-18/h5-12,14-16H,3-4,13,17H2,1-2H3
  • Key:PTPNCCWOTBBVJR-UHFFFAOYSA-N

GW-1100 (GW1100) is an experimental drug which acts as a potent and selective antagonist for the free fatty acid receptor FFAR1 (GPR40). Agonists for this receptor have potentially useful antiinflammatory and anti-fibrotic effects, and while GW-1100 does not have therapeutic effects in its own right, it is important for research into the FFAR1 receptor as it allows comparison testing to measure the effectiveness of FFAR1 agonists.[1][2][3][4][5][6][7] GW-1100 also showed inhibition of cancer cell growth in vitro, suggesting potential applications of FFAR1 antagonists in the treatment of cancer.[8][9]

References

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  1. ^ Briscoe, Celia P.; Peat, Andrew J.; McKeown, Stephen C.; Corbett, David F.; Goetz, Aaron S.; Littleton, Thomas R.; McCoy, David C.; Kenakin, Terry P.; Andrews, John L.; Ammala, Carina; Fornwald, James A.; Ignar, Diane M.; Jenkinson, Stephen (2006). "Pharmacological regulation of insulin secretion in MIN6 cells through the fatty acid receptor GPR40: Identification of agonist and antagonist small molecules". British Journal of Pharmacology. 148 (5): 619–628. doi:10.1038/sj.bjp.0706770. PMC 1751878. PMID 16702987.
  2. ^ Nakamoto, Kazuo; Nishinaka, Takashi; Sato, Naoya; Mankura, Mitsumasa; Koyama, Yutaka; Kasuya, Fumiyo; Tokuyama, Shogo (2013). "Hypothalamic GPR40 Signaling Activated by Free Long Chain Fatty Acids Suppresses CFA-Induced Inflammatory Chronic Pain". PLOS ONE. 8 (12): e81563. Bibcode:2013PLoSO...881563N. doi:10.1371/journal.pone.0081563. PMC 3865354. PMID 24349089.
  3. ^ Lin, Chao; Chao, Honglu; Li, Zheng; Xu, Xiupeng; Liu, Yinlong; Bao, Zhongyuan; Hou, Lijun; Liu, Yan; Wang, Xiaoming; You, Yongping; Liu, Ning; Ji, Jing (2017). "Omega-3 fatty acids regulate NLRP3 inflammasome activation and prevent behavior deficits after traumatic brain injury". Experimental Neurology. 290: 115–122. doi:10.1016/j.expneurol.2017.01.005. PMID 28077335.
  4. ^ Nakamoto, Kazuo; Aizawa, Fuka; Miyagi, Kei; Yamashita, Takuya; Mankura, Mitsumasa; Koyama, Yutaka; Kasuya, Fumiyo; Hirasawa, Akira; Kurihara, Takashi; Miyata, Atsuro; Tokuyama, Shogo (2017). "Dysfunctional GPR40/FFAR1 signaling exacerbates pain behavior in mice". PLOS ONE. 12 (7): e0180610. Bibcode:2017PLoSO..1280610N. doi:10.1371/journal.pone.0180610. PMC 5516985. PMID 28723961.
  5. ^ Aizawa, Fuka; Nakamoto, Kazuo; Tokuyama, Shogo (2018). "The involvement of free fatty acid-GPR40/FFAR1 signaling in chronic social defeat stress-induced pain prolongation in C57BL/6J male mice". Psychopharmacology. 235 (8): 2335–2347. doi:10.1007/s00213-018-4930-8. PMID 29931581.
  6. ^ Gong, Yuhang; Chen, Jingjing; Jin, Yongzeng; Wang, Chen; Zheng, Menglin; He, Ling (2020). "GW9508 ameliorates cognitive impairment via the cAMP-CREB and JNK pathways in APPswe/PS1dE9 mouse model of Alzheimer's disease". Neuropharmacology. 164. doi:10.1016/j.neuropharm.2019.107899. PMID 31809762.
  7. ^ Freitas, Raquel D. S.; Muradás, Thaís C.; Dagnino, Ana Paula A.; Rost, Fernanda L.; Costa, Kesiane M.; Venturin, Gianina T.; Greggio, Samuel; Da Costa, Jaderson C.; Campos, Maria M. (2020). "Targeting FFA1 and FFA4 receptors in cancer-induced cachexia". American Journal of Physiology-Endocrinology and Metabolism. 319 (5): E877 – E892. doi:10.1152/ajpendo.00509.2019. PMID 32893672.
  8. ^ Fukushima, Kaori; Takahashi, Kaede; Kusaka, Mirai; Ishimoto, Kaichi; Minami, Kanako; Otagaki, Shiho; Fukushima, Nobuyuki; Honoki, Kanya; Tsujiuchi, Toshifumi (2018). "Induction of GPR40 positively regulates cell motile and growth activities in breast cancer MCF-7 cells". Journal of Receptors and Signal Transduction. 38 (4): 311–315. doi:10.1080/10799893.2018.1494742. PMID 30111226.
  9. ^ Takahashi, Kaede; Fukushima, Kaori; Onishi, Yuka; Minami, Kanako; Otagaki, Shiho; Ishimoto, Kaichi; Fukushima, Nobuyuki; Honoki, Kanya; Tsujiuchi, Toshifumi (2018). "Involvement of FFA1 and FFA4 in the regulation of cellular functions during tumor progression in colon cancer cells". Experimental Cell Research. 369 (1): 54–60. doi:10.1016/j.yexcr.2018.05.005. PMID 29750897.