SYNTHESIS AND CALCIUM CHANNEL ANTAGONIST ACTIVITY OF NIFEDIPINE ANALOGUES WITH CHLOROINDOLYL SUBSTITUENT

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SHAFIEI A.; DEHPOUR A.R.; HADIZADEH F.; REZAEI B.

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Journal Paper

Paper Information

Journal: DARU Journal of Pharmaceutical Sciences Year:2000 | Volume:8 | Issue:3-4 Page(s): 32-36

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Information Journal Paper

Title

SYNTHESIS AND CALCIUM CHANNEL ANTAGONIST ACTIVITY OF NIFEDIPINE ANALOGUES WITH CHLOROINDOLYL SUBSTITUENT

Author(s)

SHAFIEI A. | DEHPOUR A.R. | HADIZADEH F. | REZAEI B. | Issue Writer Certificate

Keywords

CALCIUM CHANNEL BLOCKERS

DIHYDROPYRIDINE

NIFEDIPINE ANALOGUES

Abstract

Various diester analogues of nifedipine in which the ortho nitrophenyl group at position 4 were replaced by 3-chloro-1H-2-indolyl substituent, were synthesized and evaluated as calcium antagonists on guinea-pig ileal smooth muscle. Nifedipine was used as a standard. Compound 6f was found to be the most active

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APA: Copy

SHAFIEI, A., DEHPOUR, A.R., HADIZADEH, F., & REZAEI, B.. (2000). SYNTHESIS AND CALCIUM CHANNEL ANTAGONIST ACTIVITY OF NIFEDIPINE ANALOGUES WITH CHLOROINDOLYL SUBSTITUENT. DARU JOURNAL OF PHARMACEUTICAL SCIENCE, 8(3-4), 32-36. SID. https://sid.ir/paper/275304/en

Vancouver: Copy

SHAFIEI A., DEHPOUR A.R., HADIZADEH F., REZAEI B.. SYNTHESIS AND CALCIUM CHANNEL ANTAGONIST ACTIVITY OF NIFEDIPINE ANALOGUES WITH CHLOROINDOLYL SUBSTITUENT. DARU JOURNAL OF PHARMACEUTICAL SCIENCE[Internet]. 2000;8(3-4):32-36. Available from: https://sid.ir/paper/275304/en

IEEE: Copy

A. SHAFIEI, A.R. DEHPOUR, F. HADIZADEH, and B. REZAEI, “SYNTHESIS AND CALCIUM CHANNEL ANTAGONIST ACTIVITY OF NIFEDIPINE ANALOGUES WITH CHLOROINDOLYL SUBSTITUENT,” DARU JOURNAL OF PHARMACEUTICAL SCIENCE, vol. 8, no. 3-4, pp. 32–36, 2000, [Online]. Available: https://sid.ir/paper/275304/en

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