product information
(1,1-Cyclobutanedicarboxylato)diammine
CAS number: 41575-94-4
Groups: Pharmaceutical, Catalyst, All Chemicals
Information:
IUPAC Name: azane; cyclobutane-1,1-dicarboxylic acid; platinum(2+)

CAS Number: 70903-55-8

Chemical Formula: C6H14N2O4Pt+2

Synonyms: 1,1-Cyclobutanedicarboxylate diammine platinum(II), 41575-94-4, 70903-55-8, ammonia; cyclobutane-1,1-dicarboxylic acid; platinum(2+), azane; cyclobutane-1,1-dicarboxylic acid; platinum(2+), C6H14N2O4Pt+2, carboplatin, Carboplatine [French], Carboplatino [Spanish], Carboplatinum [Latin], Carboplatin [USAN:BAN:INN:JAN], Cbdca, CCRIS 3404, CHEBI:31355, cis-(1,1-Cyclobutanedicarboxylato)diammineplatinum(II), cis-Diammine(1,1-cyclobutanedicarboxylato)platinum, cis-Diammine(1,1-cyclobutanedicarboxylato)platinum(II), Diammine-1,1-cyclobutane dicarboxylate platinum II, Diammine(1,1-cyclobutanedicarboxylato)platinum (II), Diammine(cyclobutane-1,1-dicarboxylato(2-)-O,O')platinum, EINECS 255-446-0, EU-0100230, HSDB 6957, JM 8, NSC 201345, NSC 241240, NSC-241240, Paraplatin, Platinum, diammine(1,1-cyclobutanedicarboxylato(2-)-O,O')-, (SP-4-2), Platinum, diammine(1,1-cyclobutanedicarboxylato(2-))-, (SP-4-2)-, Platinum (II), (1,1-cyclobutanedicarboxylato)diammine-, cis-, Platinum(II), (1,1-cyclobutanedicarboxylato)diammine-, cis-, (SP-4-2)-diammine[cyclobutane-,1-dicarboxylato(2-)- kappa(2) O,O']platinum.

Product Info: Carboplatin, a platinum coordination compound which contains a platinum atom surrounded with two ammonia groups and two other ligands in a ring structure. Cisplatin is an analogue which has two chloride atoms instead of ring structure. Oxaliplatin contains a platinum atom complexed with 1,2-diaminocyclohexane and with an oxalate ligand as a leaving group. It is known that diaminocyclohexane group contributes greater cytotoxicity than cisplatin and carboplatin. Oxaliplatin is not generally cross-resistant to cisplatin or carboplatin. They are capable of forming platinum complexes producing inter- and intrastrand DNA crosslinks with neighboring guanine residues, resulting in DNA-mismatch repair (MMR) activity in the cancer cells. Carboplatin has less nephrotoxicity, neurotoxicity, ototoxicity and emetogenesis and more stability than cisplatin. They, platinum-based antineoplastics, have a broad spectrum of antitumor activity in the treatments of carcinomas of ovarian, testicular, bladder, small and non–small cell lung, head and neck carcinoma, and seminoma. They are synergistic with fluorouracil. They are radiation sensitive. The chemical designation of cisplatin is (SP-4-2)-diaminedichloroplatinum (II). It is a yellow crystalline powder; soluble in water and saline; administered intravenously. The chemical designation of carboplatin is (SP-4-2)-diammine [1,1-cyclobutanedicarboxylato (2-)-0, 0']- platinum (II). It is a white crystalline powder; soluble in water; insoluble in ethanol, acetone, and dimethylacetamide; administered intravenously. The chemical designation of oxaliplatin is SP-4-2-(1R-trans))- (1,2-cyclohexanediamine-N,N')- (ethanedioato(2-)-O,O') platinum (II). It is a white crystalline powder; soluble in water; very slightly soluble in methanol; insoluble in ethanol, hexane, benzene and acetone.
Alkylating agents are used in cancer chemotherapy by the substitutiopn of alkyl groups for the hydrogen atoms in biological organic compounds present in cells to inhibit tumor growth with mutagenic activity. They cross-links DNA, makes the strands unable to seperate, and induces mutations. They are cell cycle non-specific drugs. Their effects primarily occurs in proliferating tissues which don't have time to mitose DNA repair systems.
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