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911-77-3 , N-Benzoyl-DL-arginine 4-nitroanilide hydrochloride ,BANI; N-Benzoyl-DL-arginine p-nitroanilide hydrochloride; BAPNA

911-77-3 , N-Benzoyl-DL-arginine 4-nitroanilide hydrochloride,
BANI;
N-Benzoyl-DL-arginine p-nitroanilide hydrochloride;
BAPNA
Cas:911-77-3
C19H22N6O4·HCl / 434.88
MFCD00012846

N-Benzoyl-DL-arginine 4-nitroanilide hydrochloride  ,BANI;

 N-Benzoyl-DL-arginine p-nitroanilide hydrochloride; BAPNA

N-Benzoyl-DL-arginine 4-nitroanilide hydrochloride (BAN) is a pharmacological agent that inhibits the enzyme activity of trypsin, which is involved in protein breakdown. It also has insecticidal properties and can be used for the control of insect pests. BAN is a proteolytic ester hydrochloride that can be used to produce polymers. It is an experimental model for studying the molecular mechanisms of proteolysis and polymerization, as well as for investigating the mechanism of enzyme inhibition in human serum. BAN has been shown to have histological effects on experimental animals and can be used in an experimental model for studying the effect of cyclic peptides on tissue cultures.

N-(5-Guanidino-1-((4-nitrophenyl)amino)-1-oxopentan-2-yl)benzamide hydrochloride, commonly known as SNAP-25, is a peptide that plays a crucial role in the regulation of neurotransmitter release. Its diverse properties have led to its use in various scientific fields, including neuroscience, biochemistry, and pharmacology. This paper will cover the definition and background of SNAP-25, its physical and chemical properties, synthesis and characterization techniques, analytical methods, biological properties, toxicity and safety in scientific experiments, applications in scientific experiments, current state of research, potential implications in various fields of research and industry, limitations, and future directions.

Definition and Background

SNAP-25 is a 25-kilodalton peptide that is widely expressed in neurons and serves as a crucial component of the SNARE complex. This complex is a key player in the process of neurotransmitter release. SNAP-25 plays a vital role in regulating vesicle docking, fusion, and exocytosis. Research has shown that defects in SNAP-25 are linked to several neurological disorders, including ADHD, autism, and schizophrenia.

Physical and Chemical Properties

SNAP-25 is a hydrophilic peptide with a molecular weight of 25 kiloDaltons. It is a white to off-white powder that is highly soluble in water. The peptide consists of 206 amino acid residues, and its structure comprises of two α-helices connected by a random coil.

Synthesis and Characterization

SNAP-25 can be synthesized through solid-phase peptide synthesis (SPPS), a common technique used to create peptides. Synthesized peptides can be characterized using different methods, including high-performance liquid chromatography (HPLC), mass spectrometry (MS), and nuclear magnetic resonance (NMR) spectroscopy.

Analytical Methods

Analytical methods play a vital role in the quantification and identification of SNAP-25 in biological samples. HPLC, MS, and NMR spectroscopy are common methods that can be used to analyze and quantify SNAP-25 in different biological samples.

Biological Properties

SNAP-25 plays a crucial role in regulating neurotransmitter release. Research has shown that defective SNARE complex function due to SNAP-25 mutations is linked to several neurological disorders. SNAP-25 knock-out mice exhibit behavioral abnormalities, and defects in SNAP-25 expression are evident in various neurological disorders, including ADHD, schizophrenia, and autism.

Toxicity and Safety in Scientific Experiments

Studies have shown that SNAP-25 is safe and non-toxic when used in scientific experiments. However, the toxicity of SNAP-25 can vary depending on the method of administration, dosage, and route of administration.

Applications in Scientific Experiments

SNAP-25 can be used in various scientific experiments, including the study of synaptic transmission, regulation of neuronal function, and mechanisms of neurotransmitter release. SNAP-25 can also be used in drug discovery studies aimed at discovering new drugs that can modulate SNAP-25's functions.

Current State of Research

The current research on SNAP-25 has focused on its role in regulating synaptic transmission, defects in its function, and potential therapeutic intervention. There is also ongoing research aimed at discovering new tools that can be used for drug discovery studies that target SNAP-25.

Potential Implications in Various Fields of Research and Industry

SNAP-25 has the potential to be applied in several industries, including the pharmaceutical industry, where it can be used in drug discovery studies aimed at developing new drugs for neurological disorders. Additionally, SNAP-25 can be applied in biotechnology and medical research, where it can be used in the development of new diagnostic tools and therapeutics.

Limitations and Future Directions

Despite the progress made in the research focused on SNAP-25, several limitations need to be addressed, including the need for more research to understand SNAP-25's complex structure and function. Additionally, more research is needed to uncover the role of SNAP-25 in pathologies associated with its defects. Future research should also focus on developing new methods that can be used to target SNAP-25's functions, as well as uncovering new roles of SNAP-25 in biological processes.

Future Directions

Future research directions should focus on discovering new tools that can be used to understand SNAP-25's structure and function. Additionally, more research is needed to uncover the role of SNAP-25 in various biological systems. Future research should also focus on developing new drugs that can modulate SNAP-25's functions, as well as uncovering new roles of SNAP-25 in pathologies associated with its defects. Finally, more research is needed to understand the potential implications of SNAP-25 in various fields of research and industry, including the biotechnology and pharmaceutical industry.

CAS Number911-77-3
Product NameN-(5-Guanidino-1-((4-nitrophenyl)amino)-1-oxopentan-2-yl)benzamide hydrochloride
IUPAC NameN-[1-benzamido-4-(diaminomethylideneamino)butyl]-4-nitrobenzamide;hydrochloride
Molecular FormulaC19H22ClN6O4-
Molecular Weight434.88 g/mol
InChIInChI=1S/C19H22N6O4.ClH/c20-19(21)22-12-4-7-16(23-17(26)13-5-2-1-3-6-13)24-18(27)14-8-10-15(11-9-14)25(28)29;/h1-3,5-6,8-11,16H,4,7,12H2,(H,23,26)(H,24,27)(H4,20,21,22);1H
InChI KeyDEOKFPFLXFNAON-UHFFFAOYSA-N
SMILESC1=CC=C(C=C1)C(=O)NC(CCCN=C(N)N)NC(=O)C2=CC=C(C=C2)[N+](=O)[O-].Cl
SynonymsBAPNA, Benzoylarginine Nitroanilide, Benzoylarginine Nitroanilide Monohydrochloride, Benzoylarginine Nitroanilide, (R)-Isomer, Benzoylarginine Nitroanilide, (S)-Isomer, Benzoylarginine Nitroanilide, Monosodium Salt, Monohydrochloride, Monohydrochloride, Benzoylarginine Nitroanilide, N alpha Benzoyl DL arginine 4 nitroanilide, N Benzoylarginine 4 nitroanilide, N Benzoylarginyl 4 nitroanilide, N-alpha-Benzoyl-DL-arginine-4-nitroanilide, N-Benzoylarginine-4-nitroanilide, N-Benzoylarginyl-4-nitroanilide, Nitroanilide, Benzoylarginine
Canonical SMILESC1=CC=C(C=C1)C(=O)NC(CCCN=C(N)N)C(=O)NC2=CC=C(C=C2)[N+](=O)[O-].[Cl-]


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