From Wikipedia, the free encyclopedia
Chemical compound
LASSBio-881
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PubChem
CID | |
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ChemSpider | |
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ChEMBL | |
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Formula | C23H27N3O6 |
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Molar mass | 441.484 g·mol−1 |
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3D model (
JSmol) | |
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Oc1c(C(C)(C)C)cc(cc1C(C)(C)C)\C=N\NC(=O)c2cc3OCOc3cc2[N](=O)=O
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InChI=1S/C23H27N3O6/c1-22(2,3)15-7-13(8-16(20(15)27)23(4,5)6)11-24-25-21(28)14-9-18-19(32-12-31-18)10-17(14)26(29)30/h7-11,27H,12H2,1-6H3,(H,25,28)/b24-11+ Key:XEYZVZBNMMRXSN-BHGWPJFGSA-N
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LASSBio-881 is a drug which acts as both a non-selective
partial agonist of the
CB1 and
CB2
cannabinoid receptors, and also as an antagonist of the
TRPV1 receptor, as well as having
antioxidant effects. It has potent
anti-inflammatory and
anti-hyperalgesic effects in animal studies.
[1]
[2]
References
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^ Duarte CD, Tributino JL, Lacerda DI, Martins MV, Alexandre-Moreira MS, Dutra F, et al. (March 2007). "Synthesis, pharmacological evaluation and electrochemical studies of novel 6-nitro-3,4-methylenedioxyphenyl-N-acylhydrazone derivatives: Discovery of LASSBio-881, a new ligand of cannabinoid receptors". Bioorganic & Medicinal Chemistry. 15 (6): 2421–33.
doi:
10.1016/j.bmc.2007.01.013.
PMID
17275312.
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^ Tributino JL, Santos ML, Mesquita CM, Lima CK, Silva LL, Maia RC, et al. (April 2010).
"LASSBio-881: an N-acylhydrazone transient receptor potential vanilloid subfamily type 1 antagonist orally effective against the hypernociception induced by capsaicin or partial sciatic ligation". British Journal of Pharmacology. 159 (8): 1716–23.
doi:
10.1111/j.1476-5381.2010.00672.x.
PMC
2925494.
PMID
20401963.
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