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Volumn 43, Issue 3, 2007, Pages 1179-1184

Validation of a HPLC method for the quantification and purity determination of SK3530 in drug substance and tablet

Author keywords

Degradation products; Diode array detection; HPLC; Mass spectrometry; SK3530

Indexed keywords

2 [5 [4 (2 HYDROXYETHYL)PIPERAZIN 1 YLSULFONYL] 2 N PROPOXYPHENYL] 5 ETHYL 7 N PROPYL 3,5 DIHYDRO 4H PYRROLO[3,2 D]PYRIMIDIN 4 ONE; 3 (5 ETHYL 4,5 DIHYDRO 4 OXO 7 N PROPYL 3H PYRROLO[3,2 D]PYRIMIDIN 2 YL) 4 PROPOXYBENZENESULFONIC ACID; 5 ETHYL 2 (5 PIPERAZINYLSULFONYL 2 N PROPOXYPHENYL) 7 N PROPYL 3,5 DIHYDRO 4H PYRROLO[3,2 D]PYRIMIDIN 4 ONE; 5 ETHYL 2 [2 N PROPOXY 5 (4 N PROPYLPIPERAZIN 1 YLSULFONYL)PHENYL] 7 N PROPYL 3,5 DIHYDRO 4H PYRROLO[3,2 D]PYRIMIDIN 4 ONE; 5 ETHYL 2 [5 [4 (2 HYDROXYETHYL)PIPERAZIN 1 YLSULFONYL] 2 HYDROXYPHENYL] 7 N PROPYL 3,5 DIHYDRO 4H PYRROLO[3,2 D]PYRIMIDIN 4 ONE; DRUG METABOLITE; PHOSPHODIESTERASE V INHIBITOR; SK 3530; UNCLASSIFIED DRUG;

EID: 33846643998     PISSN: 07317085     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jpba.2006.10.011     Document Type: Article
Times cited : (6)

References (11)
  • 1
    • 33846574882 scopus 로고    scopus 로고
    • ICH Steering Committee, ICH Q3A(R) Impurities in New Drug Substances, European Agency for the Evaluation of Medicinal Products, International Commission on Harmonisation, London (CPMP/ICH/2737/99), 2002 (http://www.ich.org).
  • 2
    • 33846645565 scopus 로고    scopus 로고
    • ICH Steering Committee, ICH Q3B(R) Impurities in New Drug Products, European Agency for the Evaluation of Medicinal Products, International Commission on Harmonisation, London (CPMP/ICH/2738/99), 2002 (http://www.ich.org).
  • 3
    • 33846619345 scopus 로고    scopus 로고
    • ICH Steering Committee, ICH Q2A Text on validation of analytical procedures, European Agency for the Evaluation of Medicinal Products, International Commission on Harmonisation, London (CPMP/ICHJ/381/95), 1994 (http://www.ich.org).
  • 4
    • 33846599463 scopus 로고    scopus 로고
    • ICH Steering Committee, ICH Q2B Validation of Analytical Procedures: Methodology, European Agency for the Evaluation of Medicinal Products, International Commission on Harmonisation, London (CPMP/ICHJ/281/95), 1996 (http://www.ich.org).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.