Search Results - "Henrar, R.E.C."

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  1. 1

    In vitro biocompatibility studies with the experimental anticancer agent BIBX1382BS by Nuijen, B., Bouma, M., Henrar, R.E.C., Brauns, U., Bette, P., Bult, A., Beijnen, J.H.

    Published in International journal of pharmaceutics (25-01-2000)
    “…The novel anticancer agent BIBX1382BS is a representative of the human epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors. BIBX1382BS, for…”
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    Journal Article
  2. 2

    EO9: a novel bioreductive alkylating indoloquinone with preferential solid tumour activity and lack of bone marrow toxicity in preclinical models by Hendriks, H R, Pizao, P E, Berger, D P, Kooistra, K L, Bibby, M C, Boven, E, Dreef-van der Meulen, H C, Henrar, R E, Fiebig, H H, Double, J A

    Published in European journal of cancer (1990) (1993)
    “…EO9 is a novel and fully synthetic bioreductive alkylating indoloquinone. Although structurally-related to mitomycin C, EO9 exhibits a distinct preclinical…”
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  3. 3

    Revisions of general guidelines for the preclinical toxicology of new cytotoxic anticancer agents in Europe by Buttles, S.S., Newell, D.R., Henrar, R.E.C., Connors, T.A.

    Published in European journal of cancer (1990) (1995)
    “…In 1980, the Cancer Research Campaign (CRC) defined minimal toxicology requirements for the testing of novel anticancer drugs prior to Phase I clinical trials…”
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  4. 4

    Systematic study on the chemical stability of the prodrug antitumor agent carzelesin (U-80,244) by Vries, J D, Doppenberg, W G, Henrar, R E, Bult, A, Beijnen, J H

    Published in Journal of pharmaceutical sciences (01-11-1996)
    “…The chemical stability of the novel anticancer agent carzelesin in aqueous buffer/acetonitrile (1:1, v/v) mixtures has been investigated utilizing a…”
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  5. 5

    Pharmaceutical development of a parenteral lyophilized formulation of the investigational antitumor neuropeptide antagonist [Arg6, D-Trp7,9, MePhe8]-substance P {6-11} by JONKMAN-DE VRIES, J. D, ROSING, H, TALSMA, H, HENRAR, R. E. C, KETTENES-VAN DEN BOSCH, J. J, BULT, A, BEIJNEN, J. H

    Published in Investigational new drugs (01-01-1998)
    “…The aim of this study was to develop a stable parenteral dosage form for the investigational cytotoxic drug [Arg6, D-Trp79,MePhe8]-Substance P [6-11]…”
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  6. 6

    Preclinical antitumour activity and animal toxicology studies of rhizoxin, a novel tubulin-interacting agent by Hendriks, H R, Plowman, J, Berger, D P, Paull, K D, Fiebig, H H, Fodstad, O, Dreef-van der Meulen, H C, Henrar, R E, Pinedo, H M, Schwartsmann, G

    Published in Annals of oncology (01-11-1992)
    “…Rhizoxin is a 16-membered antifungal macrocyclic lactone isolated from the plant pathogenic fungus Rhizopus chinensis. The compound binds to tubulin,…”
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  7. 7