153415-46-4 Usage
Uses
Used in Pharmaceutical Applications:
Taxcultine is used as an antineoplastic agent for the treatment of various types of cancer, including lung, ovarian, breast, head and neck, and advanced forms of Kaposi's sarcoma. It functions as a mitotic inhibitor, playing a crucial role in cancer chemotherapy.
Used in Structural Biology:
Taxcultine is also utilized in the study of the structure and function of microtubules into tubulin, providing valuable insights into cellular processes and the development of novel therapeutic strategies.
Used in Industrial Applications:
While the provided materials do not explicitly mention industrial applications for taxcultine, its ability to interact with biopolymers and macromolecules suggests potential uses in material science, chemical engineering, or other related fields. Further research and development would be necessary to explore and confirm these potential applications.
Check Digit Verification of cas no
The CAS Registry Mumber 153415-46-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,4,1 and 5 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 153415-46:
(8*1)+(7*5)+(6*3)+(5*4)+(4*1)+(3*5)+(2*4)+(1*6)=114
114 % 10 = 4
So 153415-46-4 is a valid CAS Registry Number.
InChI:InChI=1/C44H53NO14/c1-8-15-31(49)45-33(26-16-11-9-12-17-26)34(50)40(53)57-28-21-44(54)38(58-39(52)27-18-13-10-14-19-27)36-42(7,29(48)20-30-43(36,22-55-30)59-25(4)47)37(51)35(56-24(3)46)32(23(28)2)41(44,5)6/h9-14,16-19,28-30,33-36,38,48,50,54H,8,15,20-22H2,1-7H3,(H,45,49)/t28-,29-,30+,33-,34+,35+,36-,38-,42+,43-,44+/m0/s1
153415-46-4Relevant articles and documents
Paclitaxel analogues from Taxus baccata
Gabetta, Bruno,Orsini, Paolo,Peterlongo, Federico,Appendino, Giovanni
, p. 1325 - 1329 (1998)
N-Debenzoyl-N-butanoyl- and N-debenzoyl-N-propanoyl-10- deacetylpaclitaxel were identified as minor constituents of T. baccata by HPLC-MS. The structure of these compounds was confirmed by comparison with synthetic samples prepared from 7-triethylsilylbaccatin III.