Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/46030
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dc.contributor.authorJain, N-
dc.contributor.authorSrivastava, T S-
dc.date.accessioned2019-03-18T09:37:41Z-
dc.date.available2019-03-18T09:37:41Z-
dc.date.issued1992-02-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/46030-
dc.description102-105en_US
dc.description.abstractThe synthesis of platinum compounds of the type [Pt (daba) X2](where daba = 3,4-diaminobenzoic acid and X = Cl, Br, or I) and the analogous chloro and bromo compounds of Pd(II) has been carried out. These compounds have been characterized by molar conductance measurements, electronic absorption, and infrared, 1H NMR and X-ray photoelectron spectroscopy. The complexes are non-electrolytic in nature and have square planar geometry with two coordination positions occupied by two amino groups of 3,4- diaminobenzoic acid and remaining two positions occupied by halide ions. The sodium salts of the above compounds have been tested against P388 lymphocytic leukemia cells. [Pt(daba)Cl2] and Pt(daba)Br2l have I.D.50 ovalues less than that of cisplatin and [Pt(daba)I2] has I.D50 values comparable to that of cisplatin.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-A Vol.31A(02) [February 1992]en_US
dc.titleSynthesis, characterization and cytotoxicity of (3,4-diaminobenzoic acid)- haloplatinum(II)/palladium(II)en_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.31A(02) [February 1992]

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