Cyclo(L-Phe-L-Pro-) - Names and Identifiers
Name | CYCLO(-PHE-PRO)
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Synonyms | Cyclo(Pro-Phe-) CYCLO(-PHE-PRO) Cyclo(D-Pro-L-Phe-) Cyclo(L-Phe-L-Pro-) (3S,8aα)-3β-Benzyloctahydropyrrolo[1,2-a]pyrazine-1,4-dione (3S-trans)-3-benzylhexahydropyrrolo[1,2-a]pyrazine-1,4-dione (3S,8aS)-3β-Benzyl-6,7,8,8a-tetrahydropyrrolo[1,2-a]pyrazine-1,4(2H,3H)-dione (3S,8aS)-3-Benzyl-6,7,8,8aα-tetrahydropyrrolo[1,2-a]pyrazine-1,4(2H,3H)-dione (3S)-2,3,6,7,8,8aβ-Hexahydro-3β-(phenylmethyl)pyrrolo[1,2-a]pyrazine-1,4-dione
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CAS | 3705-26-8
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EINECS | 223-047-0 |
Cyclo(L-Phe-L-Pro-) - Physico-chemical Properties
Molecular Formula | C14H16N2O2
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Molar Mass | 244.29 |
Density | 1.26±0.1 g/cm3(Predicted) |
Melting Point | 146-148 °C |
Boling Point | 509.5±39.0 °C(Predicted) |
Solubility | Chloroform (Slightly), Ethanol (Slightly, Sonicated) |
Appearance | Solid |
Color | White to Off-White |
pKa | 13.21±0.40(Predicted) |
Storage Condition | -15°C |
Cyclo(L-Phe-L-Pro-) - Introduction
CYCLO(-PHE-PRO) (CYCLO(-PHE-PRO)) is a dipeptide compound formed by linking phenylalanine and proline molecules through a peptide bond to form a cyclic structure. It is mainly used to study and analyze the structure and function of peptides.
The properties of CYCLO(-PHE-PRO) (CYCLO(-PHE-PRO)) include certain solubility and stability, which can exist stably under appropriate conditions.
Its uses include:
1. Biomedical research: CYCLO(-PHE-PRO) (CYCLO(-PHE-PRO)) is widely used in biomedical research to study the biological activity of peptides, interactions and drug design.
2. Drug development: Because the cyclic structure of CYCLO(-PHE-PRO) (CYCLO(-PHE-PRO)) has certain biological activity and stability, it can be used as a precursor molecule for drug development.
3. Organic Synthesis: CYCLO(-PHE-PRO) (CYCLO(-PHE-PRO)) is an important intermediate in organic synthesis and can be used to synthesize other organic molecules.
There are two main methods for preparing CYCLO(-PHE-PRO) (CYCLO(-PHE-PRO)):
1. Chemical synthesis: CYCLO(-PHE-PRO) (CYCLO(-PHE-PRO)) is formed by mixing phenylalanine and proline in an appropriate ratio and carrying out a condensation reaction under appropriate reaction conditions.
2. Biosynthesis: Synthesis of phenylalanine and proline into CYCLO(-PHE-PRO) (CYCLO(-PHE-PRO)) by utilizing a biological reaction, for example, by the action of an enzyme or fermentation by a microorganism.
Safety information about CYCLO(-PHE-PRO) (CYCLO(-PHE-PRO)), which is a common compound in the laboratory, it is relatively safe when used and handled correctly. However, for all chemicals, appropriate safety handling and protective measures must be taken, such as wearing appropriate personal protective equipment (laboratory clothing, goggles and gloves), avoid contact with skin and inhalation of dust or vapours. When using and handling the compound, the relevant safety operation guidelines and laboratory rules and regulations should be strictly followed to ensure the safety and health of the laboratory environment.
Last Update:2024-04-09 21:54:55