32806-53-4 Usage
Description
4-(2-PIPERIDINOETHYL)-3-THIOSEMICARBAZIDE is an organic compound that serves as a key reactant in the synthesis of bis(thiosemicarbazonato) Cu(II), a potential theranostic agent for cancer treatment. It is characterized by its unique chemical structure, which allows it to form stable complexes with metal ions, particularly copper (II) ions.
Uses
Used in Pharmaceutical Industry:
4-(2-PIPERIDINOETHYL)-3-THIOSEMICARBAZIDE is used as a reactant for the preparation of bis(thiosemicarbazonato) Cu(II), a potential cancer theranostic agent. 4-(2-PIPERIDINOETHYL)-3-THIOSEMICARBAZIDE plays a crucial role in the development of this agent due to its ability to form stable complexes with copper (II) ions, which can be utilized for both diagnostic and therapeutic purposes in cancer treatment.
In Cancer Theranostics:
4-(2-PIPERIDINOETHYL)-3-THIOSEMICARBAZIDE is used as a component in the synthesis of bis(thiosemicarbazonato) Cu(II), which has potential applications in cancer theranostics. 4-(2-PIPERIDINOETHYL)-3-THIOSEMICARBAZIDE contributes to the formation of a complex that can be employed for targeted drug delivery, imaging, and therapy, providing a multifaceted approach to cancer management.
Check Digit Verification of cas no
The CAS Registry Mumber 32806-53-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,8,0 and 6 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 32806-53:
(7*3)+(6*2)+(5*8)+(4*0)+(3*6)+(2*5)+(1*3)=104
104 % 10 = 4
So 32806-53-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H18N4S/c9-11-8(13)10-4-7-12-5-2-1-3-6-12/h1-7,9H2,(H2,10,11,13)
32806-53-4Relevant articles and documents
Synthesis of new alkylaminoalkyl thiosemicarbazones of 3-acetylindole and their effect on DNA synthesis and cell proliferation
Siatra-Papastaikoudi,Tsotinis,Raptopoulou,Sambani,Thomou
, p. 107 - 114 (2007/10/02)
The preparation of a number of thiobemicarbazones of 3-acetylindole is described. These compounds were evaluated in vitro for their effect on proliferation and cell-division delays in cultured human peripheral blood lymphocytes, and their effect on DNA synthesit in T-cell leukemia Molt-4 cells.
