維基百科

IDRA-21

化合物

IDRA-21是種AMPA受體（英語：AMPA receptor）的正別構調節劑（英語：Allosteric modulator），也是苯丙噻二嗪（英語：Benzothiadiazine）的衍生物，也是一種手性分子，(+)-IDRA-21是其活性形式。[1]

IDRA-21
法律規範狀態
法律規範
  • 美：試驗用新藥
識別資訊
  • 7-chloro-3-methyl-3,4-dihydro-2H-1,2,4-benzothiadiazine 1,1-dioxide
CAS號22503-72-6  checkY
PubChem CID
IUPHAR/BPS
ChemSpider
UNII
ChEMBL
CompTox Dashboard（英語：CompTox Chemicals Dashboard） (EPA)
化學資訊
化學式C8H9ClN2O2S
摩爾質量232.68 g·mol−1
3D模型（JSmol（英語：JSmol））
  • CC1NC2=C(C=C(C=C2)Cl)S(=O)(=O)N1
  • InChI=1S/C8H9ClN2O2S/c1-5-10-7-3-2-6(9)4-8(7)14(12,13)11-5/h2-5,10-11H,1H3 ☒N
  • Key:VZRNTCHTJRLTMU-UHFFFAOYSA-N ☒N

在動物實驗中，IDRA-21表現出了有促進學習的效果，並能明顯改善學習和記憶。在逆轉阿普唑侖或東莨菪鹼誘發的認知障礙方面，有着約比茴拉西坦10到30倍的效力，[2][3]且在單次服用後，可產生長達48小時的持續效應，[4]其作用機制，被認為是通過促進大腦突觸間的誘導LTP達到的。[5]

正常情況下，IDRA-21或許不產生神經毒性，[6]但可能會加重中風或癲癇發作後，因全身缺血所造成的神經元損傷。[7]

與安帕金（英語：Ampakine）或苯甲酰哌啶衍生的AMPA受體增效劑相比，IDRA-21藥效優於CX-516（英語：CX-516），低於CX-546（英語：CX-546）。[8]與IDRA-21相比，效力更好的苯丙噻二嗪（英語：Benzothiadiazine）類衍生物已被開發出來，[9][10]但這些衍生物，各所獲的研究程度並不一樣，苯甲酰基哌啶（benzoylpiperidine）和苯甲酰基吡咯烷CX系列（benzoylpyrrolidine CX-series）藥物，在臨床開發中更受青睞，這或是由於它們在高劑量使用時，具有更有利的毒性特徵。[11]

另見

編輯

參考文獻

編輯
  1. ^ Uzunov DP, Zivkovich I, Pirkle WH, Costa E, Guidotti A. Enantiomeric resolution with a new chiral stationary phase of 7-chloro-3-methyl-3,4-dihydro-2H-1,2,4-benzothiadiazine S,S-dioxide, a cognition-enhancing benzothiadiazine derivative. Journal of Pharmaceutical Sciences. August 1995, 84 (8): 937–42. PMID 7500277. doi:10.1002/jps.2600840807. 
  2. ^ Thompson DM, Guidotti A, DiBella M, Costa E. 7-Chloro-3-methyl-3,4-dihydro-2H-1,2,4-benzothiadiazine S,S-dioxide (IDRA 21), a congener of aniracetam, potently abates pharmacologically induced cognitive impairments in patas monkeys. Proceedings of the National Academy of Sciences of the United States of America. August 1995, 92 (17): 7667–71. Bibcode:1995PNAS...92.7667T. PMC 41206  . PMID 7644474. doi:10.1073/pnas.92.17.7667  . 
  3. ^ Zivkovic I, Thompson DM, Bertolino M, Uzunov D, DiBella M, Costa E, Guidotti A. 7-Chloro-3-methyl-3-4-dihydro-2H-1,2,4 benzothiadiazine S,S-dioxide (IDRA 21): a benzothiadiazine derivative that enhances cognition by attenuating DL-alpha-amino-2,3-dihydro-5-methyl-3-oxo-4-isoxazolepropanoic acid (AMPA) receptor desensitization. The Journal of Pharmacology and Experimental Therapeutics. January 1995, 272 (1): 300–9. PMID 7815345. 
  4. ^ Buccafusco JJ, Weiser T, Winter K, Klinder K, Terry AV. The effects of IDRA 21, a positive modulator of the AMPA receptor, on delayed matching performance by young and aged rhesus monkeys. Neuropharmacology. January 2004, 46 (1): 10–22. PMID 14654093. S2CID 26443642. doi:10.1016/j.neuropharm.2003.07.002. 
  5. ^ Arai A, Guidotti A, Costa E, Lynch G. Effect of the AMPA receptor modulator IDRA 21 on LTP in hippocampal slices. NeuroReport. September 1996, 7 (13): 2211–5. PMID 8930991. S2CID 35888339. doi:10.1097/00001756-199609020-00031. 
  6. ^ Impagnatiello F, Oberto A, Longone P, Costa E, Guidotti A. 7-Chloro-3-methyl-3,4-dihydro-2H-1,2,4-benzothiadiazine S,S-dioxide: a partial modulator of AMPA receptor desensitization devoid of neurotoxicity. Proceedings of the National Academy of Sciences of the United States of America. June 1997, 94 (13): 7053–8. Bibcode:1997PNAS...94.7053I. PMC 21283  . PMID 9192690. doi:10.1073/pnas.94.13.7053  . 
  7. ^ Yamada KA, Covey DF, Hsu CY, Hu R, Hu Y, He YY. The diazoxide derivative IDRA 21 enhances ischemic hippocampal neuron injury. Annals of Neurology. May 1998, 43 (5): 664–9. PMID 9585363. S2CID 39977647. doi:10.1002/ana.410430517. 
  8. ^ Nagarajan N, Quast C, Boxall AR, Shahid M, Rosenmund C. Mechanism and impact of allosteric AMPA receptor modulation by the ampakine CX546. Neuropharmacology. November 2001, 41 (6): 650–63. PMID 11640919. S2CID 7796112. doi:10.1016/S0028-3908(01)00133-2. 
  9. ^ Phillips D, Sonnenberg J, Arai AC, Vaswani R, Krutzik PO, Kleisli T, et al. 5'-alkyl-benzothiadiazides: a new subgroup of AMPA receptor modulators with improved affinity. Bioorganic & Medicinal Chemistry. May 2002, 10 (5): 1229–48. CiteSeerX 10.1.1.113.7845  . PMID 11886787. doi:10.1016/S0968-0896(01)00405-9. 
  10. ^ Arai AC, Xia YF, Kessler M, Phillips D, Chamberlin R, Granger R, Lynch G. Effects of 5'-alkyl-benzothiadiazides on (R,S)-alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor biophysics and synaptic responses. Molecular Pharmacology. September 2002, 62 (3): 566–77. PMID 12181433. S2CID 16182942. doi:10.1124/mol.62.3.566. 
  11. ^ Black MD. Therapeutic potential of positive AMPA modulators and their relationship to AMPA receptor subunits. A review of preclinical data. Psychopharmacology. April 2005, 179 (1): 154–63. PMID 15672275. S2CID 5869366. doi:10.1007/s00213-004-2065-6. 
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