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84652-33-5

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84652-33-5 Usage

General Description

Decinnamoyltaxinine J is a chemical compound derived from the bark of the yew tree, Taxus species. It belongs to the taxane class of compounds, which are known for their anticancer properties. Decinnamoyltaxinine J has been found to have potent cytotoxic effects against certain cancer cell lines, making it a promising candidate for the development of new cancer treatments. Additionally, research has also shown that this compound may have anti-inflammatory and antioxidant properties, further enhancing its potential for use in therapeutic applications. Through further studies and clinical trials, decinnamoyltaxinine J may prove to be a valuable addition to the arsenal of drugs available for the treatment of cancer and other diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 84652-33-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,6,5 and 2 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 84652-33:
(7*8)+(6*4)+(5*6)+(4*5)+(3*2)+(2*3)+(1*3)=145
145 % 10 = 5
So 84652-33-5 is a valid CAS Registry Number.

84652-33-5Downstream Products

84652-33-5Relevant articles and documents

Plantes de Nouvelle-Caledonie. 124. Taxanes isoles des ecorces de tronc d'Austrotaxus spicata Compton (Taxacees)

Ettouati, Laurent,Ahond, Alain,Convert, Odile,Poupat, Christiane,Potier, Pierre

, p. 687 - 694 (2007/10/02)

Eighteen taxane-type diterpenes have been isolated from the trunk bark of Austrotaxus spicata: thirteen are alkaloids.Eight compounds have an exocyclic-4(20) methylene group: austrospicatine, 2'-desacetyl-austrospicatine, 2'-desacetoxyaustrospicatine, already found in the leaves of the same plant, comptonine, spicaledonine, 7β,9α,10β-triacetoxy 2α,5α,13α-trihydroxy 4(20),11-taxadiene, 2',13α,14β-tridesacetylaustrotaxine and 7β,9α-diacetoxy 5α,13α,14β-trihydroxy 10-oxo 4(20),11-taxadiene which are described here for the first time.The ten other compounds have an epoxide group in position 4(20): spicataxine, 9α-acetyl 10β-desacetylspicataxine, spicatine, 9α-acetyl 10β-desacetylspicatine, 10β-desacetylspicatine, nicaustrine, N-demethylnicaustrine, nicotaxine, 5α-O-(3'-methylamino 3'-phenylpropionyl)nicotaxine and 5α-O-(3'-amino 3'-phenylpropionyl)nicotaxine: all these products are new, the last five are original by owning a nicotinic substituent.The structures have been established from the spectral data, mainly from MS, 1H and 13C NMR spectra.

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