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🧪 Chemistry  ·  Coordination Compounds  ·  NEET & JEE

Cisplatin's anticancer activity is due to:

Answer: Cross-linking DNA by displacing Cl- with purine N-donors (N7 of guanine), distorting DNA helix.

  • A Cross-linking DNA by displacing Cl- with purine N-donors (N7 of guanine), distorting DNA helix
  • B Generally releasing free toxic platinum ions that poison the entire cell under most conditions encountered
  • C Directly inhibiting a specific metabolic enzyme without touching DNA as frequently observed in practice
  • D Binding to and disrupting the lipid bilayer of the cell membrane in many documented cases

Correct answer: A. Cross-linking DNA by displacing Cl- with purine N-donors (N7 of guanine), distorting DNA helix

Explanation: Cisplatin undergoes aquation (Cl- replaced by H<sub>2</sub>O), then bifunctionally binds N7 of adjacent guanines, forming 1,2-d(GpG) intrastrand cross-links that kink DNA and block replication.

Octahedralcoordination no. 6e.g. [Co(NH3)6]3+Tetrahedralcoordination no. 4e.g. [Ni(CO)4]Square Planarcoordination no. 4e.g. [Pt(NH3)2Cl2]

The three common coordination geometries: octahedral (6 ligands), tetrahedral (4 ligands), and square planar (4 ligands in one plane).

Concept context

Study of compounds where a central metal atom is bonded to surrounding ligands. Covers nomenclature, types of isomerism, bonding theories (VBT, CFT), and applications in medicine, photography, and industry.

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