Abstract
The incorporation of 2-[35S]thiouracil and 2 of its derivatives into murine melanomas [S91 aND Harding Passey], in vivo, was studied. 2-Thiouracil has a marked affinity for melanin-producing tissue and an affinity for such tissue could be sustained by 5-substituted 2-thiouracils. A series of derivatives of arotinoids and retinoids, with or without a 2-thiouracil group as a potential carrier to obtain affinity for melanomas, was examined for cytostatic activity, in vitro. None of these showed significant activity against murine melanomas.

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