In vitro inhibition of rat basophilic leukaemia mast cell (RBL-2H3) degranulation by novel indane compounds

Inflammation Research

Volumn 57, Issue SUPPL. 1, 2008, Pages

  Passante, E ^a   Ehrhardt, C ^a   Sheridan, H ^a   Frankish, N ^a  

^a TRINITY COLLEGE DUBLIN   (Ireland)

Author keywords

[No Author keywords available]

Indexed keywords

2 BENZYL 2,3 DIHYDRO HYDRO 1H 1'H 2,2' BIINDEN 1 OL; BETA N ACETYLHEXOSAMINIDASE; INDAN DERIVATIVE;

ANIMAL CELL; BASOPHIL; CONFERENCE PAPER; CONTROLLED STUDY; CYTOTOXICITY TEST; ENZYME RELEASE; HISTAMINE RELEASE; LEUKEMIA; MAST CELL DEGRANULATION; NONHUMAN; RAT; STEREOCHEMISTRY;

ANIMALS; ANTIOXIDANTS; BETA-N-ACETYLHEXOSAMINIDASES; CELL DEGRANULATION; CELL LINE; DOSE-RESPONSE RELATIONSHIP, DRUG; HISTAMINE H1 ANTAGONISTS, NON-SEDATING; HISTAMINE RELEASE; INDENES; LEUKEMIA, BASOPHILIC, ACUTE; MAST CELLS; MOLECULAR STRUCTURE; QUERCETIN; RATS; TERFENADINE;

EID: 43249087204     PISSN: 10233830     EISSN: 1420908X     Source Type: Journal    
DOI: 10.1007/s00011-007-0607-1     Document Type: Conference Paper

References (6)

1. Indane dimer compounds and their pharmaceutical use-respiratory and anti-inflammatory. PCT/IE 96/00080, Granted US-09/093,060, EP-96942550, 2002.
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