429692-85-3

Usage

Uses

Used in Pharmaceutical Applications:
(S)-2-[7-(1-carboxyethyl)-1,3,6,8-tetraoxo-3,6,7,8-tetrahydro-1H-benzo[lmn][3,8]phenanthrolin-2-yl]-propionic acid is used as a pharmaceutical compound for its potential therapeutic properties. (S)-2-[7-(1-carboxyethyl)-1,3,6,8-tetraoxo-3,6,7,8-tetrahydro-1H-benzo[lmn][3,8]phenanthrolin-2-yl]-propionic acid's unique structure and optical activity may allow it to target specific biological pathways or interact with certain receptors, making it a candidate for the development of new drugs.
Used in Chemical Research:
In the field of chemical research, (S)-2-[7-(1-carboxyethyl)-1,3,6,8-tetraoxo-3,6,7,8-tetrahydro-1H-benzo[lmn][3,8]phenanthrolin-2-yl]-propionic acid serves as a valuable compound for studying its chemical properties, reactivity, and potential applications in various chemical reactions. Its unique structure and optical activity make it an interesting subject for research in organic chemistry.
Used in Materials Science:
(S)-2-[7-(1-carboxyethyl)-1,3,6,8-tetraoxo-3,6,7,8-tetrahydro-1H-benzo[lmn][3,8]phenanthrolin-2-yl]-propionic acid is used as a component in the development of new materials. Its specific structure and properties may contribute to the creation of novel materials with unique characteristics, such as improved stability, enhanced reactivity, or specialized applications in various industries.
Used in Drug Delivery Systems:
(S)-2-[7-(1-carboxyethyl)-1,3,6,8-tetraoxo-3,6,7,8-tetrahydro-1H-benzo[lmn][3,8]phenanthrolin-2-yl]-propionic acid is used as a component in drug delivery systems to improve the bioavailability and efficacy of therapeutic agents. Its carboxyethyl group can be utilized for conjugation with drugs or other molecules, potentially enhancing the delivery and targeting of pharmaceuticals to specific tissues or cells.
Used in Anticancer Applications:
In the field of oncology, (S)-2-[7-(1-carboxyethyl)-1,3,6,8-tetraoxo-3,6,7,8-tetrahydro-1H-benzo[lmn][3,8]phenanthrolin-2-yl]-propionic acid may be employed as an anticancer agent. Its unique structure and optical activity could potentially allow it to interact with specific cancer-related targets, modulating signaling pathways and exhibiting inhibitory effects on tumor growth and progression.
Used in the Chemical Industry:
(S)-2-[7-(1-carboxyethyl)-1,3,6,8-tetraoxo-3,6,7,8-tetrahydro-1H-benzo[lmn][3,8]phenanthrolin-2-yl]-propionic acid is used as a specialty chemical in various applications within the chemical industry. Its unique properties and reactivity may be harnessed for the synthesis of other complex molecules, the development of new chemical processes, or the creation of novel materials with specific characteristics.

Upstream product

• 338-69-2 D-Alanine 
• 81-30-1 1,4,5,8-naphthalenetetracarboxylic dianhydride 
• 56-41-7 L-alanin 

Relevant academic research and scientific papers

Cyclomaltooligosaccharide (cyclodextrin)-assisted enantiomeric recognition of benzo[lmn][3,8]phenanthroline-derived amino acids

Formation of self-assembly molecular aggregates and cyclomaltooligosaccharide (cyclodextrin) molecular aggregates with benzo[lmn][3,8]phenanthroline-derived amino acids is presented. The nature of the molecular aggregates was studied by negative-ion elect

Hydrophobic Shielding of Outer Surface: Enhancing the Chemical Stability of Metal–Organic Polyhedra

Metal–organic polyhedra (MOP) are a promising class of crystalline porous materials with multifarious potential applications. Although MOPs and metal–organic frameworks (MOFs) have similar potential in terms of their intrinsic porosities and physicochemical properties, the exploitation of carboxylate MOPs is still rudimentary because of the lack of systematic development addressing their chemical stability. Herein we describe the fabrication of chemically robust carboxylate MOPs via outer-surface functionalization as an a priori methodology, to stabilize those MOPs system where metal–ligand bond is not so strong. Fine-tuning of hydrophobic shielding is key to attaining chemical inertness with retention of the framework integrity over a wide range of pH values, in strong acidic conditions, and in oxidizing and reducing media. These results are further corroborated by molecular modelling studies. Owing to the unprecedented transition from instability to a chemically ultra-stable regime using a rapid ambient-temperature gram-scale synthesis (within seconds), a prototype strategy towards chemically stable MOPs is reported.

Efficient and mild microwave-assisted stepwise functionalization of naphthalenediimide with α-amino acids

Microwave dielectric heating proved to be an efficient method for the one-pot and stepwise syntheses of sym-metrical and unsymmetrical naphthalenediimide derivatives of a-amino acids. Acid-labile side chain protecting groups are stable under the reaction

L-Dopa and dopamine conjugated naphthalenediimides modulate amyloid β toxicity

The process of protein misfolding and aggregation to form neurotoxic species is strongly implicated in most of the neurodegenerative disorders. In particular, amyloid beta (Aβ) misfolding and aggregation is central to pathophysiological processes of Alzhe

Steric effect on the self-assembly behaviours of amino acid derivatives

To investigate the steric effect of amino acids, N,N′-dialanine-1,4,5,8-naphthalene tetracarboxylic acid diethylamide (ANTA) and N,N′-diphenylalanine-1,4,5,8-naphthalene tetracarboxylic acid diethylamide (PNTA) were synthesized based on naphthalene-1,4,5,

Crystallographic insight-guided nanoarchitectonics and conductivity modulation of an n-type organic semiconductor through peptide conjugation

Crystallographic insight-guided nanoarchitectonics of peptide-conjugated naphthalene diimide (NDI) is described. In a bio-inspired approach, non-proteinogenic α-amino isobutyric acid (Aib)- and alanine (Ala)-derived peptides orchestrated the 1D achiral and 2D chiral molecular ordering of NDI, respectively, which resulted in modulation of nanoscale morphology, chiroptical and conductivity properties.

Molecular assembly of amino acid interlinked, topologically symmetric, π-complementary donor-acceptor-donor triads

Amino acid interlinked pyrene and naphthalenediimide (NDI) based novel donor-acceptor-donor (D-A-D) triads are designed to exploit their topological symmetry and complementary π-character for facile charge-transfer complexation. Consequently, free-floatin