Page last updated: 2024-12-07

1,5-aedans

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth

Description

It seems you are referring to **1,5-anhydro-D-fructose** (also known as **1,5-anhydro-D-fructose**). This molecule is not typically called 1,5-aedans.

**1,5-anhydro-D-fructose** is a sugar derivative with a unique structure. It's important in research for several reasons:

* **Chemical synthesis:** 1,5-anhydro-D-fructose is a valuable intermediate in the synthesis of other important molecules, including various carbohydrates, pharmaceuticals, and biomaterials.
* **Biochemistry and Biology:** It is involved in several biochemical processes, such as the formation of glycosidic bonds and the synthesis of complex carbohydrates.
* **Food Science:** This molecule is found in various fruits and vegetables, contributing to their sweetness and texture. Understanding its properties can help improve food processing and preservation.
* **Materials Science:** Its unique structure and properties make it a promising candidate for the development of new materials, particularly those with biocompatible and biodegradable properties.

**In research, scientists study 1,5-anhydro-D-fructose to:**

* **Understand its structure and properties:** This allows researchers to develop more efficient methods for its synthesis and utilization.
* **Develop new synthetic methods:** Scientists are constantly searching for new ways to synthesize this molecule and its derivatives, leading to the discovery of new compounds with valuable properties.
* **Investigate its role in biological processes:** Research aims to understand its involvement in various biochemical pathways and its potential use as a therapeutic agent.
* **Explore its applications in materials science:** Scientists are exploring its potential as a building block for new biomaterials and drug delivery systems.

Overall, 1,5-anhydro-D-fructose is an important molecule with diverse applications in various fields. Ongoing research continues to reveal new aspects of this molecule and its potential benefits.

5-[(2-acetamidoethyl)amino]naphthalene-1-sulfonic acid : An aminonaphthalenesulfonic acid fluorophore with a structure consisting of ethylenediamine substituted on the nitrogens with acetyl and 5-sulfonyl-1-naphthyl groups. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Cross-References

ID SourceID
PubMed CID121834
CHEBI ID40594
SCHEMBL ID6128009
MeSH IDM0140379

Synonyms (20)

Synonym
5-(1-sulfonaphthyl)-acetylamino-ethylamine
AEN ,
aed ,
5-[(2-acetamidoethyl)amino]naphthalene-1-sulfonic acid
1,5-aedans
n-acetyl-n'-(5-sulfo-1-naphthyl)ethylenediamine
CHEBI:40594 ,
n-(aminoethyl)-5-naphthylamine-l-sulfonic acid
n-acetyl-n'-(5-sulfonic-1-naphthyl) ethylene diamine
5-((2-(acetylamino)ethyl)amino)-1-naphthalenesulfonic acid
50402-62-5
1-naphthalenesulfonic acid, 5-((2-(acetylamino)ethyl)amino)-
4v4222f82y ,
unii-4v4222f82y
5-{[2-(acetylamino)ethyl]amino}naphthalene-1-sulfonic acid
EPITOPE ID:120373
SCHEMBL6128009
DTXSID00198456
5-(((acetylamino)ethyl)amino)naphthalene-1-sulphonic acid
Q27120401
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (1)

RoleDescription
fluorescent probeA role played by a fluorescent molecular entity used to study the microscopic environment by fluorescence spectroscopy.
[role information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Drug Classes (1)

ClassDescription
aminonaphthalenesulfonic acidA naphthalenesulfonic acid having at least one amino substituent.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Research

Studies (32)

TimeframeStudies, This Drug (%)All Drugs %
pre-19905 (15.63)18.7374
1990's14 (43.75)18.2507
2000's13 (40.63)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other33 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]