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Batimastat and Marimastat in Cancer: Summary of Early Clinical Data
Henrik Rasmussen
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ChemInform Abstract: Five‐Component Synthesis of Marimastat Analogues.
ChemInform, 1999AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
S. PATEL +4 more
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Trends in Biotechnology, 2001
Marimastat, the matrix-metalloproteinase inhibitor developed by British Biotech (Oxford, UK), produces survival rates comparable to chemotherapy in patients suffering from non-metastatic pancreatic cancer (Journal of Clinical Oncology, 1 August). When trialled against the chemotherapeutic agent gemcitabine, one-year survival rates for patients taking ...
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Marimastat, the matrix-metalloproteinase inhibitor developed by British Biotech (Oxford, UK), produces survival rates comparable to chemotherapy in patients suffering from non-metastatic pancreatic cancer (Journal of Clinical Oncology, 1 August). When trialled against the chemotherapeutic agent gemcitabine, one-year survival rates for patients taking ...
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Ras-transfection up-regulated HaCaT cell migration: Inhibition by Marimastat
Clinical & Experimental Metastasis, 1999Cell migration is an essential process in physiological and pathological conditions such as wound healing and tumor invasion. This phenomenon involves cell adhesion on the extracellular matrix mediated by integrins, and cell detachment promoted in part by metalloproteinases (MMPs). In the present study, the migration of two HaCaT-ras clones (metastatic
S, Charvat +4 more
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Batimastat and Marimastat in Cancer
1999Batimastat® and Marimastat® are broad-spectrum matrix metalloproteinase inhibitors (MMPI) with potent activity against most of the major matrix metalloproteinases (MMPs). Batimastat is the prototype MMPI, and is highly active against interstitial collagenase (MMP-1) (IC50 = 3 nM), stomelysin-1 (MMP-3) (IC50 = 20 nM), gelatinase-A (MMP-2) (IC50 = 4 nM),
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European Journal of Pharmacology, 2007
Direct instillation of a recombinant human form of MMP-12 (rhMMP-12) in mice airways elicited an early inflammatory response characterized by neutrophil influx, cytokine release and gelatinase activation followed by a delayed response, mainly characterized by macrophage recruitment.
Soazig, Nénan +6 more
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Direct instillation of a recombinant human form of MMP-12 (rhMMP-12) in mice airways elicited an early inflammatory response characterized by neutrophil influx, cytokine release and gelatinase activation followed by a delayed response, mainly characterized by macrophage recruitment.
Soazig, Nénan +6 more
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Journal of Inorganic Biochemistry, 2007
Fe(III)-salen (N,N-bis(salicylidene)-ethane-1,2-diimine) complexes of simple hydroxamic acids and the MMP (matrix metalloproteinase) inhibitor marimastat have been evaluated as hypoxia activated drug carriers. The aceto- (aha), propion- (pha), benzohydroxamato (bha), and marimastat complexes were prepared and characterised by single crystal X-ray ...
Timothy W, Failes, Trevor W, Hambley
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Fe(III)-salen (N,N-bis(salicylidene)-ethane-1,2-diimine) complexes of simple hydroxamic acids and the MMP (matrix metalloproteinase) inhibitor marimastat have been evaluated as hypoxia activated drug carriers. The aceto- (aha), propion- (pha), benzohydroxamato (bha), and marimastat complexes were prepared and characterised by single crystal X-ray ...
Timothy W, Failes, Trevor W, Hambley
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Effect of marimastat on serum tumour markers in patients with colorectal cancer.
International journal of surgical investigation, 2003Matrix metalloproteinases (MMPs) are a family of enzymes that break down extra cellular matrix proteins during tissue formation. Tumours have been shown to over-express certain matrix metalloproteinases relative to normal tissue. Matrix metalloproteinases are associated with the disruption of tissue architecture in the growth of tumours and they are ...
H, North, J, King, D L, Morris
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