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(2'R,10R,13S)-10,13-DIMETHYL-1,7,8,9,10,11,12,13,15,16-DECAHYDRO-3'H-SPIRO[CYCLOPENTA[A]PHENANTHRENE-17,2'-FURAN]-3,5',6(2H,4'H,14H)-TRIONE, also known as Discodermolide, is a natural polyketide compound isolated from the deep-sea sponge Discodermia dissoluta. It is characterized by its unique and complex chemical structure, featuring a spirocyclic framework with a 17-membered ring fused to a furan ring and a trione moiety. This potent microtubule-stabilizing agent has demonstrated potential as an anti-cancer drug candidate and is of interest for chemical synthesis and pharmaceutical research.

38753-78-5

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38753-78-5 Usage

Uses

Used in Pharmaceutical Industry:
Discodermolide is used as a microtubule-stabilizing agent for its potential as an anti-cancer drug candidate. Its ability to stabilize microtubules contributes to the inhibition of cell division and the prevention of cancer cell proliferation, making it a promising compound for the development of cancer treatments.
Used in Chemical Synthesis:
Discodermolide's unique and complex chemical structure makes it an interesting target for chemical synthesis. Researchers aim to develop efficient and scalable synthetic routes to produce (2'R,10R,13S)-10,13-DIMETHYL-1,7,8,9,10,11,12,13,15,16-DECAHYDRO-3'H-SPIRO[CYCLOPENTA[A]PHENANTHRENE-17,2'-FURAN]-3,5',6(2H,4'H,14H)-TRIONE, facilitating its use in pharmaceutical applications and further exploration of its potential therapeutic properties.
Used in Pharmaceutical Research:
The biological activity and structural complexity of Discodermolide make it a valuable subject for pharmaceutical research. Scientists are investigating its mechanism of action, potential side effects, and ways to improve its efficacy and safety as a potential anti-cancer agent.

Check Digit Verification of cas no

The CAS Registry Mumber 38753-78-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,7,5 and 3 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 38753-78:
(7*3)+(6*8)+(5*7)+(4*5)+(3*3)+(2*7)+(1*8)=155
155 % 10 = 5
So 38753-78-5 is a valid CAS Registry Number.

38753-78-5SDS

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 (10R,13S,17R)-10,13-dimethylspiro[1,2,7,8,9,11,12,14,15,16-decahydrocyclopenta[a]phenanthrene-17,5'-oxolane]-2',3,6-trione

1.2 Other means of identification

Product number -
Other names Pregn-4-ene-21-carboxylicacid,17-hydroxy-3,6-dioxo-,g-lactone,(17a)

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:38753-78-5 SDS

38753-78-5Upstream product

38753-78-5Downstream Products

38753-78-5Relevant academic research and scientific papers

Isolation and identification of novel sulfur-containing metabolites of spironolactone (Aldactone)

Karim, Aziz,Brown, Edward A.

, p. 41 - 62 (2007/10/10)

In the urine of subjects given an oral dose of spironolactone [3-(3-oxo-7α-acetylthio-17β-hydroxy-4-androsten-17α-y1)propionic acid γ-lactone], six metabolites have been detected. One of the major metabolites was found to be the previously characterized de-thioacetylated compound, 3-(3-oxo-17β-hydroxy-4,6-androstadien-17α-y1)propionic acid γ-lactone (canrenone). Besides this a new major sulfur-containing metabolite has been isolated and identified as 3-(3-oxo-7α-methylsulfinyl-6β,17β-dihydroxy-4-androsten-17α-y1)propionic acid γ-lactone. This structural assignment was based on detailed analysis of its IR, NMR and UV spectra as well as comparison of its physical constants and chromatographic (TLC and GLC) characteristics with a synthetic sample. The three minor metabolites were found to be very labile and were readily converted to canrenone.

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