Page last updated: 2024-12-10

18-crown-6 2,3,11,12-tetracarboxylic acid

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

Description

## 18-Crown-6 2,3,11,12-tetracarboxylic acid: A Versatile Platform for Research

**What it is:**

18-Crown-6 2,3,11,12-tetracarboxylic acid is a macrocyclic molecule. It is comprised of:

* **18-crown-6:** A cyclic polyether containing six ethylene glycol units (CH₂CH₂O) linked together in a ring. This part gives the molecule its crown-like shape and ability to bind cations.
* **2,3,11,12-tetracarboxylic acid:** Four carboxyl groups (COOH) are attached to the 18-crown-6 ring at specific positions (2, 3, 11, and 12). These acidic groups contribute to the molecule's reactivity and ability to form salts.

**Importance for Research:**

This compound is a valuable tool in various research areas due to its unique properties:

* **Cation Binding:** The 18-crown-6 moiety acts as a host molecule, capable of encapsulating cations (like potassium, sodium, or ammonium ions) within its ring. This makes it useful for:
* **Separating cations:** It can differentiate between cations based on their size and charge.
* **Cation transport:** It can facilitate the movement of cations across membranes.
* **Studying cation-mediated processes:** It can be used to investigate how cations influence biological or chemical reactions.
* **Functionalization:** The carboxylic acid groups provide sites for further modification. This allows for the attachment of different functional groups, leading to the development of:
* **Sensors:** By attaching specific groups that respond to changes in the environment, it can be used to detect ions, pH, or other analytes.
* **Catalysis:** The presence of acidic groups allows for the molecule to act as a catalyst in various reactions.
* **Materials:** By controlling the functional groups attached, it can be incorporated into polymers or other materials with specific properties.

**Specific Applications:**

* **Separation Science:** 18-Crown-6 2,3,11,12-tetracarboxylic acid is used in chromatography for separating and purifying different cations.
* **Biomedical Research:** It can be employed as a drug delivery vehicle, targeting specific cells or organs due to its cation binding ability.
* **Analytical Chemistry:** It finds applications in developing sensors for detecting various chemical species.
* **Material Science:** It can be incorporated into materials with specific properties, such as ion conductivity or catalysis.

**In summary, 18-Crown-6 2,3,11,12-tetracarboxylic acid is a versatile platform for researchers across various disciplines. Its ability to bind cations, facilitate functionalization, and act as a catalyst makes it a valuable tool for advancing scientific knowledge and developing new technologies.**

18-crown-6 2,3,11,12-tetracarboxylic acid: structure in first source; RN given for (2R*,3R*,11*,12*)-isomer [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID3082976
CHEMBL ID2375078
SCHEMBL ID9516478
MeSH IDM0239714

Synonyms (14)

Synonym
18-crown-6 2,3,11,12-tetracarboxylic acid
18-crown-6 4cooh
(2r*,3r*,11r*,12r*)-1,4,7,10,13,16-hexaoxacyclooctadecane-2,3,11,12-tetracarboxylic acid
1,4,7,10,13,16-hexaoxacyclooctadecane-2,3,11,12-tetracarboxylic acid, (2r*,3r*,11r*,12r*)-
119719-58-3
(+)-(18-crown-6)-2,3,11,12-tetracarboxylic acid, 97%
(+)-(18-crown-6)-2,3,11,12-tetracarboxylic acid
(2r,3r,11r,12r)-1,4,7,10,13,16-hexaoxacyclooctadecane-2,3,11,12-tetracarboxylic acid
AKOS015893908
SCHEMBL9516478
CHEMBL2375078
DTXSID60152559
(+)-(18-crown-6)-2
rel-(2r,3r,11r,12r)-1,4,7,10,13,16-hexaoxacyclooctadecane-2,3,11,12-tetracarboxylic acid
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (1)

Assay IDTitleYearJournalArticle
AID1669222Inhibition of human recombinant-Sialin expressed in HEK293 cells assessed as reduction in [3H]Neu5Ac uptake at 30 to 300 uM incubated for 15 mins by liquid scintillation counting method2020Journal of medicinal chemistry, 08-13, Volume: 63, Issue:15
Amino Acids Bearing Aromatic or Heteroaromatic Substituents as a New Class of Ligands for the Lysosomal Sialic Acid Transporter Sialin.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (56)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's3 (5.36)18.2507
2000's29 (51.79)29.6817
2010's23 (41.07)24.3611
2020's1 (1.79)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 11.20

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be weak demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index11.20 (24.57)
Research Supply Index4.04 (2.92)
Research Growth Index5.25 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (11.20)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews3 (5.36%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other53 (94.64%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]