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51762-05-1
  • names:

    (6R,7R)-7-((R)-2-amino-2-(cyclohexa-1,4-dien-1-yl)acetamido)-3-methoxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

  • CAS号:

    51762-05-1

    MDL Number:
  • MF(分子式): C16H19N3O5S MW(分子量): 365.404
  • EINECS: Reaxys Number:
  • Pubchem ID: Brand:BIOFOUNT
Cefroxadine
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中文别名 Cefroxadine
英文别名 CGP 9000; CGP-9000; CGP9000; BRN 0587499; CXD; Cefroxadine. Oraspor
CAS号 51762-05-1
SMILES O=C(C(N12)=C(OC)CS[C@]2([H])[C@H](NC([C@H](N)C3=CCC=CC3)=O)C1=O)O
Inchi InChI=1S/C16H19N3O5S/c1-24-9-7-25-15-11(14(21)19(15)12(9)16(22)23)18-13(20)10(17)8-5-3-2-4-6-8/h2-3,6,10-11,15H,4-5,7,17H2,1H3,(H,18,20)(H,22,23)/t10-,11-,15-/m1/s1
InchiKey RDMOROXKXONCAL-UEKVPHQBSA-N
分子式 Formula C16H19N3O5S
分子量 Molecular Weight 365.404
闪点 FP
熔点 Melting point
沸点 Boiling point
Polarizability极化度
密度 Density
蒸汽压 Vapor Pressure
溶解度Solubility
性状 Solid powder
储藏条件 Storage conditions Dry, dark and store at 0-4℃ for short term (days to weeks) or -20℃ for long term (Store correctly 2-3years).
产品说明 Cefroxadine(CAS:51762-05-1 ):仅限应用于工业或者科学研究过程中非医疗目的,不应用于人类或动物的临床诊断以及治过程疗,该产品非药用,非食用。
IntroductionCefroxadine, also known as CGP 9000, is a cephalosporin antibiotic. It is structurally related to cefalexin, and both drugs share a similar spectrum of activity. It is available in Italy. Cefroxadine (CXD), an orally active cephalosporin antibiotic, has a broad spectrum and a bactericidal action. CXD showed excellent results in the treatment of acute uncomplicated cystitis (AUC).
Application1
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警示图
危险性 Warning
危险性警示
安全声明
安全防护
备注
[1]Kang YS, Lee SY, Kim NH, Choi HM, Park JS, Kim W, Lee HJ. A specific and rapid HPLC assay for the determination of cefroxadine in human plasma and its application to pharmacokinetic study in Korean. J Pharm Biomed Anal. 2006 Feb 13;40(2):369-74. Epub 2005 Aug 30. PubMed PMID: 16137854.
[2]Kitagawa S, Takeda J, Sato S. pH-dependent inhibitory effects of angiotensin-converting enzyme inhibitors on cefroxadine uptake by rabbit small intestinal brush-border membrane vesicles and their relationship with hydrophobicity and the ratio of zwitterionic species. Biol Pharm Bull. 1999 Jul;22(7):721-4. PubMed PMID: 10443470.
[3] Kitagawa S, Takeda J, Kaseda Y, Sato S. Inhibitory effects of angiotensin-converting enzyme inhibitor on cefroxadine uptake by rabbit small intestinal brush border membrane vesicles. Biol Pharm Bull. 1997 Apr;20(4):449-51. PubMed PMID: 9145229.
[4] Kitagawa S, Sugaya Y. Characteristics of uptake of cefroxadine by rabbit small intestinal brush border membrane vesicles. Biol Pharm Bull. 1996 Feb;19(2):268-73. PubMed PMID: 8850320.
[5] Beyssac E, Ritschel WA, Aiache JM, Haberer JP. Comparison of continuous, constant rate enteral tube feeding in supine patients to bolus food intake in ambulatory, healthy subjects regarding bioavailability of perorally administered cefroxadine. Methods Find Exp Clin Pharmacol. 1991 Nov;13(9):637-42. PubMed PMID: 1787771.
6: Beyssac E, Ritschel WA, Aiache JM, Haberer JP. Peroral absorption of cefroxadine in patients within the first day after severe trauma: comparison to cefroxadine pharmacokinetics in fasted, healthy volunteers. Methods Find Exp Clin Pharmacol. 1991 Oct;13(8):565-72. PubMed PMID: 1956212.7: Mendizabal MV, Idoate I, Jordan J, Larralde J. Effects of cefroxadine on L-leucine absorption in rat jejunum. Arch Int Physiol Biochim Biophys. 1991 Jun;99(3):247-50. PubMed PMID: 1717060.8: Cadórniga R, Molina IT, Pastoriza P, Negro S, Evora CM, Gutierrez JA. Pharmacokinetics of cefroxadine after infusion to healthy volunteers. Int J Clin Pharmacol Ther Toxicol. 1990 Oct;28(10):435-9. PubMed PMID: 2258253.9: Shibl AM, Durgham SM. In-vitro evaluation of a new oral cephalosporin, cefroxadine (CGP 9000). J Chemother. 1990 Feb;2(1):8-10. PubMed PMID: 2332786.10: Scaglione F, Cattaneo G, Bianchi MM, Verdecchia P, Maresca V, Bichisao E, Fraschini F. Cefroxadine in the treatment of children affected by respiratory and ENT diseases. A multicentre study involving 1072 in-patients. Drugs Exp Clin Res. 1989;15(2):71-6. PubMed PMID: 2737082.1
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