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24164-13-4

Epitulipinolide, a natural product derived from the marine sponge Epitrix ciconiae, is recognized as a potent inhibitor of the protein kinase Cepsilon (PKCepsilon). Epitulipinolide is involved in a range of cellular processes such as cell growth, proliferation, and apoptosis. Its antiproliferative activity against various cancer cell lines, along with its anti-inflammatory and analgesic properties, positions Epitulipinolide as a promising candidate for pharmaceutical development and cancer therapy.
Used in Pharmaceutical Industry:
Epitulipinolide is used as a potential cancer therapeutic agent for its antiproliferative activity against several cancer cell lines. Its ability to inhibit PKCepsilon suggests a role in controlling cell growth and proliferation, making it a candidate for further research and development in oncology.
Used in Anti-inflammatory Applications:
Epitulipinolide is used as an anti-inflammatory agent due to its demonstrated properties in reducing inflammation, which could be beneficial in treating conditions characterized by excessive inflammation.
Used in Analgesic Applications:
Epitulipinolide is used as an analgesic agent for its pain-relieving properties, offering potential in the development of new treatments for pain management.
Further research into the therapeutic applications of Epitulipinolide is ongoing, with the aim of exploring its full potential in various medical fields.

24164-13-4

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    Cas No: 24164-13-4

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24164-13-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24164-13-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,1,6 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 24164-13:
(7*2)+(6*4)+(5*1)+(4*6)+(3*4)+(2*1)+(1*3)=84
84 % 10 = 4
So 24164-13-4 is a valid CAS Registry Number.
InChI:InChI=1/C17H22O4/c1-10-6-5-7-11(2)9-15-16(12(3)17(19)21-15)14(8-10)20-13(4)18/h6,9,14-16H,3,5,7-8H2,1-2,4H3/b10-6+,11-9+/t14-,15-,16-/m1/s1

24164-13-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Tulipinolide

1.2 Other means of identification

Product number -
Other names acetate of eupatolide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:24164-13-4 SDS

24164-13-4Downstream Products

24164-13-4Relevant articles and documents

Acid Cyclization and Other Products of the Germacranolide Epoxide Lipiferolide

Wilton, John H.,Doskotch, Raymond W.

, p. 4251 - 4256 (2007/10/02)

A comparison was made of the products generated from lipiferolide (2) upon treatment with SOCl2, HCl, and BF3*Et2O.SOCl2 formed three epoxide-opened compounds, chlorhydrin 3 and two allylic alcohols, 4 and 5, three cyclization products of the guaianolide type, chloro compound 9 and olefins 1 and 10, as well as three novel bicyclodecanes, 6, 7, and 8.HCl generated the epoxide-opened substances 3, 4, and 5 and guaianolides 1, 9, and 10, but no cyclobutane products.BF3*Et2O gave fluorohydrin 11 as the major component and ketone 12, xanthanolide 13, and epitulipinolide (4,5-deoxylipiferolide) as compounds not observed from the other reagents, along with small yields of allylic alcohol 4 and guaianolides 1 and 10.

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