N-α-(t-Butoxycarbonyl)-β-[benzo[b]acridin-12(5H)-on-2-yl]-L-alanine
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N-α-(t-Butoxycarbonyl)-β-[benzo[b]acridin-12(5H)-on-2-yl]-L-alanine

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Category
BOC-Amino Acids
Catalog number
BAT-003191
CAS number
916834-72-5
Molecular Formula
C25H24N2O5
Molecular Weight
432.47
N-α-(t-Butoxycarbonyl)-β-[benzo[b]acridin-12(5H)-on-2-yl]-L-alanine
IUPAC Name
(2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-(12-oxo-5H-benzo[b]acridin-2-yl)propanoic acid
Synonyms
Boc-Ala(2-Bacd)-OH; Boc-badAla-OH; N-α-(t-Butoxycarbonyl)-β-[5-azanaphthacen-12(5H)-on-2-yl]-L-alanine
Density
1.302±0.060 g/cm3 (20 °C,760 mmHg)
Boiling Point
679.8±55.0 °C at 760 mmHg
InChI
InChI=1S/C25H24N2O5/c1-25(2,3)32-24(31)27-21(23(29)30)11-14-8-9-19-17(10-14)22(28)18-12-15-6-4-5-7-16(15)13-20(18)26-19/h4-10,12-13,21H,11H2,1-3H3,(H,26,28)(H,27,31)(H,29,30)/t21-/m0/s1
InChI Key
YNBIJRCHSMEHTG-NRFANRHFSA-N
Canonical SMILES
CC(C)(C)OC(=O)NC(CC1=CC2=C(C=C1)NC3=CC4=CC=CC=C4C=C3C2=O)C(=O)O

N-α-(t-Butoxycarbonyl)-β-[benzo[b]acridin-12(5H)-on-2-yl]-L-alanine, a chemical compound with promising applications in pharmaceutical research and development, is multifaceted in its potential. Here are the key applications presented with a high degree of perplexity and burstiness:

Anticancer Drug Development: Delving into the realm of cancer research, scientists explore the potential anticancer properties of this compound. By integrating it into diverse assays and in vivo models, researchers assess its effectiveness in halting tumor growth. Understanding its mechanism of action is pivotal in crafting novel chemotherapeutic agents with enhanced efficacy and mitigated side effects.

Fluorescent Probes: As a fluorescent probe in biochemical research, N-α-(t-Butoxycarbonyl)-β-[benzo[b]acridin-12(5H)-on-2-yl]-L-alanine shines brightly. With its unique chromophoric properties, it serves as a valuable tool for labeling and tracking biomolecules within live cells. This application offers a dynamic perspective on visualizing real-time cellular processes and intricate molecular interactions.

Peptide Synthesis: Acting as a fundamental building block in peptide synthesis, this compound plays a pivotal role in crafting peptides and peptide-based medications. Leveraging its distinctive structural attributes, researchers can forge peptides with tailored biological activities setting the stage for the development of innovative peptide therapeutics and exploration of protein interactions.

Enzyme Inhibitors: Unveiling its potential as an enzyme inhibitor, this compound targets specific enzymes implicated in disease pathways. By scrutinizing its inhibitory effects on enzyme function, researchers unveil new avenues for drug development. This application is paramount in forging novel treatments for an array of diseases spanning metabolic disorders to infectious ailments.

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