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Bruceolide is a quassinoid compound that can be isolated from the plants Brucea javanica and Brucea sumatrana. It has been demonstrated to possess significant antimalarial properties, making it a valuable substance in the search for effective treatments against malaria.

25514-28-7

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25514-28-7 Usage

Uses

Used in Pharmaceutical Industry:
Bruceolide is used as an antimalarial agent for its ability to effectively combat the Plasmodium parasite, which is responsible for causing malaria. Its potent activity against the parasite makes it a promising candidate for the development of new drugs to treat this life-threatening disease.
Used in Research and Development:
In the field of research and development, Bruceolide serves as a valuable compound for studying the mechanisms of action against the Plasmodium parasite. This can lead to a better understanding of malaria and the development of novel therapeutic strategies to combat the disease.
Used in Drug Discovery:
Bruceolide's antimalarial properties make it a potential candidate for drug discovery, as it can be further studied and modified to create more effective and targeted treatments for malaria. Its unique structure and activity can also inspire the design of new drugs with improved efficacy and reduced side effects.

Check Digit Verification of cas no

The CAS Registry Mumber 25514-28-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,5,1 and 4 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 25514-28:
(7*2)+(6*5)+(5*5)+(4*1)+(3*4)+(2*2)+(1*8)=97
97 % 10 = 7
So 25514-28-7 is a valid CAS Registry Number.
InChI:InChI=1/C21H26O10/c1-7-8-4-10-20-6-30-21(18(28)29-3,15(20)13(25)17(27)31-10)16(26)12(24)14(20)19(8,2)5-9(22)11(7)23/h8,10,12-16,23-26H,4-6H2,1-3H3/t8-,10+,12+,13+,14+,15+,16-,19-,20+,21-/m0/s1

25514-28-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name bruceolide

1.2 Other means of identification

Product number -
Other names BRUCEOLIDE

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:25514-28-7 SDS

25514-28-7Downstream Products

25514-28-7Relevant academic research and scientific papers

Anti-malarial activities of acylated bruceolide derivatives

Murakarni, Nobutoshi,Umezome, Takashi,Mahmud, Taifo,Sugimoto, Masanori,Kobayashi, Motomasa,Wataya, Yusuke,Kim, Hye-Sook

, p. 459 - 462 (1998)

Several O-acylated derivatives of bruceolide (2) were synthesized and their anti-malarial activities together with selective toxicities were examined. It was found that 3,15-di-O-acetyl- (3c), 3,15-di-O-propionyl- (3d) and 15-O-propionylbruceolide (3b), as well as bruceine B (3a), exhibited potent anti-malarial activities with high selective toxicities.

Synthesis of cytotoxic fluorinated quassinoids

Ohno, Nobuhiro,Fukamiya, Narihiko,Okano, Masayoshi,Tagahara, Kiyoshi,Lee, Kuo-Hsiung

, p. 1489 - 1495 (2007/10/03)

The C-15 senecioyl side chain of brusatol was interchanged with fluorinated acyl groups, and the C-3 hydroxy group of bruceolide was esterified with fluorinated acyl chlorides. These fluorinated quassinoids 11, 12, 13, and 17 showed significant cytotoxic activity against eight human cancer cell lines including small and non-small cell lung, colon, CNS, ovarian and renal cancers, leukemia, and melanoma with 17 being about 100 times more potent than 11, 12, and 13. The activity of 17 was similar to that of bruceantin (1) in this in vitro cell line panel.

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