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638165-18-1

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638165-18-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 638165-18-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,8,1,6 and 5 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 638165-18:
(8*6)+(7*3)+(6*8)+(5*1)+(4*6)+(3*5)+(2*1)+(1*8)=171
171 % 10 = 1
So 638165-18-1 is a valid CAS Registry Number.

638165-18-1Downstream Products

638165-18-1Relevant articles and documents

Synthesis and characterization of new transition metal complexes containing DNA intercalators of the acridine family

Crispini, Alessandra,Pucci, Daniela,Sessa, Stefania,Cataldi, Antonella,Napoli, Anna,Valentini, Alessandra,Ghedini, Mauro

, p. 1497 - 1503 (2007/10/03)

The coordinating ability of two DNA intercalates of the acridine family, 4-hydroxyacridine (4-OH-Acrid) and acridine orange (AO), with the transition metal ions Ni(II), Pd(II) and Pt(II), are investigated. Octahedral complexes, [Ni(4-O-Acrid)2(en)] (1), and [Ni(4-O-Acrid)2(H 2O)2] (2), are obtained when the 4-OH-Acrid ligand reacts with [Ni(Cl)2(en)2] and NiCl2·6H 2O, respectively. Single crystal X-ray analysis of complex 1 has shown that two acridine molecules are bonded to nickel through their nitrogen and oxygen atoms in a chelate fashion. Moreover, when AO reacts with different Pd(II) and Pt(II) precursors, new triamine complexes of the general formula cis-[M(A)n(Cl)(AO)]+X- (M = Pd(II), Pt(II); A = en, NH3; n = 1, 2; X- = BF4-, NO3-, PF6-) (3-6) are synthesized. Full characterization by IR, 1H NMR and electrospray ionization mass spectrometry in solution has demonstrated the coordination of the AO ligand to the metal ion through the endocyclic nitrogen atom. The biological activity of these new acridine orange derivatives is conducted on complex cis-[Pt(NH 3)2Cl(AO)][NO3] (5). The cytotoxic activity of complex 5 is compared with that of cisplatin (cis-DDP) in DU145, A2780 and A2780-cp8 cancer cell lines and the results show that its activity is twice as effective as that of cisplatin in the two cis-DDP resistant cell lines DU145 and A2780-cp8, respectively.

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