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Catalog Number:
29634
Ácido S -Fmoc-3-amino-5-[( N -Pbf-pirrolidin-1-carboximidoil)-amino]-pentanoico
Purity:
≥ 99 % (HPLC)
Documents
$93.14 /25 mg
Tamaño
Request Bulk Quote
Product Information

(S)-Fmoc-3-amino-5-[(N'-Pbf-pyrrolidine-1-carboximidoyl)-amino]-pentanoic acid is a versatile compound widely utilized in peptide synthesis and drug development. This amino acid derivative features a protective Fmoc group, which allows for selective deprotection during solid-phase peptide synthesis, making it an essential building block for researchers in the field of medicinal chemistry. The presence of the N'-Pbf-pyrrolidine moiety enhances its stability and reactivity, facilitating the formation of complex peptide structures that are crucial for developing therapeutic agents.

This compound is particularly valuable in the design of peptide-based drugs, where precise amino acid sequences can significantly influence biological activity. Its unique structure not only aids in the synthesis of bioactive peptides but also provides researchers with the flexibility to modify and optimize peptide properties for specific applications, such as targeted drug delivery and enzyme inhibition. By incorporating (S)-Fmoc-3-amino-5-[(N'-Pbf-pyrrolidine-1-carboximidoyl)-amino]-pentanoic acid into their research, professionals can enhance their peptide synthesis strategies and contribute to advancements in pharmaceutical development.

Purity
≥ 99 % (HPLC)
Molecular Formula
C38H46N4O7S
Molecular Weight
702.87
MDL Number
MFCD18782821
Appearance
Polvo blanco
Optical Rotation
[a] D 20 = -6 ± 2º (C=1 en DMF)
Conditions
Conservar entre 0 y 8 °C.
General Information
Purity
≥ 99 % (HPLC)
Molecular Formula
C38H46N4O7S
Molecular Weight
702.87
MDL Number
MFCD18782821
Appearance
Polvo blanco
Optical Rotation
[a] D 20 = -6 ± 2º (C=1 en DMF)
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(S)-Fmoc-3-amino-5-[(N'-Pbf-pyrrolidine-1-carboximidoyl)-amino]-pentanoic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing researchers to create complex molecules for drug development and biological studies.
  • Drug Development: Its unique structure aids in the design of novel therapeutic agents, particularly in the field of oncology and neurology, where targeted therapies are crucial.
  • Bioconjugation: The compound can be used to attach biologically active molecules to peptides, enhancing their stability and efficacy, which is vital in vaccine development and targeted delivery systems.
  • Research in Neuroscience: By modifying neurotransmitter pathways, it can help in studying neurological disorders, providing insights into potential treatments for conditions like Alzheimer’s and Parkinson’s disease.
  • Customizable Drug Formulations: Its versatility allows for the creation of tailored drug formulations that can improve bioavailability and reduce side effects, addressing specific patient needs in personalized medicine.

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