메뉴 건너뛰기




Volumn 25, Issue 8-9, 1999, Pages 682-688

Enantioselective synthesis of (S)-suprofen ester prodrugs by lipase in cyclohexane

Author keywords

(S) suprofen ester prodrugs; Esterification; Lipase; Transesterification

Indexed keywords

ALCOHOLS; COMPOSITION EFFECTS; ENZYMES; ESTERS; HYDROCARBONS; SYNTHESIS (CHEMICAL); WATER;

EID: 0033230966     PISSN: 01410229     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0141-0229(99)00108-8     Document Type: Article
Times cited : (17)

References (13)
  • 1
    • 0021254912 scopus 로고
    • The important of stereochemistry in the clinic pharmacokinetics of the 2-arylpropionic acid nonsteroidal anti-inflammatory drugs
    • Hutt A.J., Caldwell J. The important of stereochemistry in the clinic pharmacokinetics of the 2-arylpropionic acid nonsteroidal anti-inflammatory drugs. Clin Pharmacokin. 9:1984;371-373.
    • (1984) Clin Pharmacokin , vol.9 , pp. 371-373
    • Hutt, A.J.1    Caldwell, J.2
  • 2
    • 0026567443 scopus 로고
    • Recent developments in the synthesis of optically active 2-arylpropionic acids: An important class of nonsteroidal anti-inflammatory agents
    • Sonawane R.H., Bellur N.S., Ahuja J.R. Recent developments in the synthesis of optically active 2-arylpropionic acids an important class of nonsteroidal anti-inflammatory agents . Tetrahedron Asymmetry. 3:1992;163-192.
    • (1992) Tetrahedron Asymmetry , vol.3 , pp. 163-192
    • Sonawane, R.H.1    Bellur, N.S.2    Ahuja, J.R.3
  • 3
    • 0026557715 scopus 로고
    • Ester and amide prodrugs of Ibuprofen and Naproxen: Synthesis, anti-inflammatory activity, and gastrointestinal toxicity
    • Shanbhag V.R., Crider A.M., Gokhale R., Harpalani A., Dick R.M. Ester and amide prodrugs of Ibuprofen and Naproxen synthesis, anti-inflammatory activity, and gastrointestinal toxicity . J Pharm Sci. 81:1992;149-154.
    • (1992) J Pharm Sci , vol.81 , pp. 149-154
    • Shanbhag, V.R.1    Crider, A.M.2    Gokhale, R.3    Harpalani, A.4    Dick, R.M.5
  • 4
    • 0002327694 scopus 로고
    • Design of prodrugs: Bioreversible derivatives for various functional groups and chemical entities
    • H. Bundgaard. Amsterdam: Elsevier
    • Bundgaard H. Design of prodrugs bioreversible derivatives for various functional groups and chemical entities . Bundgaard H. Design of prodrugs. 1985;1-92 Elsevier, Amsterdam.
    • (1985) Design of Prodrugs , pp. 1-92
    • Bundgaard, H.1
  • 5
    • 0023988548 scopus 로고
    • Glycolamide esters as biolabile prodrugs of carboxylic acid agents: Synthesis, stability, bioconversion, and physicochemical properties
    • Nielsen N.N., Bundgaard H. Glycolamide esters as biolabile prodrugs of carboxylic acid agents synthesis, stability, bioconversion, and physicochemical properties . J Pharm Sci. 77:1988;285-298.
    • (1988) J Pharm Sci , vol.77 , pp. 285-298
    • Nielsen, N.N.1    Bundgaard, H.2
  • 6
    • 0027200613 scopus 로고
    • Synthesis and evaluation of morpholinoalkyl ester prodrugs of indomethacin and Naproxen
    • Tammara V.K., Narurkar M.M., Crider A.M., Khan A.M. Synthesis and evaluation of morpholinoalkyl ester prodrugs of indomethacin and Naproxen. Pharm Res. 10:1993;1191-1199.
    • (1993) Pharm Res , vol.10 , pp. 1191-1199
    • Tammara, V.K.1    Narurkar, M.M.2    Crider, A.M.3    Khan, A.M.4
  • 7
    • 0031172576 scopus 로고    scopus 로고
    • A facile enzymatic process for the preparation of (S)-Naproxen ester prodrug in organic solvents
    • Chang C.S., Tsai S.W. A facile enzymatic process for the preparation of (S)-Naproxen ester prodrug in organic solvents. Enzyme Microb Technol. 20:1997;635-639.
    • (1997) Enzyme Microb Technol , vol.20 , pp. 635-639
    • Chang, C.S.1    Tsai, S.W.2
  • 8
    • 0031055056 scopus 로고    scopus 로고
    • Enzymatic synthesis of (S)-Ibuprofen ester prodrug from racemic Ibuprofen by lipase in organic solvents
    • Tsai S.W., Lin J.J., Chang C.S., Chen J.P. Enzymatic synthesis of (S)-Ibuprofen ester prodrug from racemic Ibuprofen by lipase in organic solvents. Biotechnol Prog. 13:1997;82-88.
    • (1997) Biotechnol Prog , vol.13 , pp. 82-88
    • Tsai, S.W.1    Lin, J.J.2    Chang, C.S.3    Chen, J.P.4
  • 10
    • 0026689303 scopus 로고
    • Enantioselectivity of lipase-catalyzed hydrolysis of some 2-chloroethyl 2-arylpropannoates studied by chiral reversed-phase liquid chromatography
    • Allenmark S., Ohlsson A. Enantioselectivity of lipase-catalyzed hydrolysis of some 2-chloroethyl 2-arylpropannoates studied by chiral reversed-phase liquid chromatography. Chirality. 4:1992;98-102.
    • (1992) Chirality , vol.4 , pp. 98-102
    • Allenmark, S.1    Ohlsson, A.2
  • 11
    • 0028418787 scopus 로고
    • Enantioselective esterification of racemic naproxen by lipases in organic solvent
    • Tsai S.W., Wei H.J. Enantioselective esterification of racemic naproxen by lipases in organic solvent. Enzyme Microb Technol. 16:1994;328-333.
    • (1994) Enzyme Microb Technol , vol.16 , pp. 328-333
    • Tsai, S.W.1    Wei, H.J.2
  • 12
    • 0032876076 scopus 로고    scopus 로고
    • Lipase-catalyzed enantioselective esterification of S(+)-Naproxen ester prodrug in cyclohexane
    • In press
    • Tsai SW, Lin SF, Chang CS. Lipase-catalyzed enantioselective esterification of S(+)-Naproxen ester prodrug in cyclohexane. J Chem Technol Biotechnol, In press.
    • J Chem Technol Biotechnol
    • Tsai, S.W.1    Lin, S.F.2    Chang, C.S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.