Skip to main content

Bleomycin A2

ADVERTISEMENT
Identification
Molecular formula
C55H84N17O21S2
CAS number
11056-06-7
IUPAC name
3,6-diamino-N-[3-(2-amino-4-hydroxy-1,4,5,6-tetrahydropyrimidin-6-yl)-9,12-bis(hydroxymethyl)-2,5,8,11,14-pentaoxo-6-(ureidomethylene)-1,4,7,10,13-pentazacyclohexadec-15-yl]hexanamide
State
State
Bleomycin A2 is generally found in the solid state at room temperature. It is prepared as a lyophilized powder for pharmaceutical formulations.
Melting point (Celsius)
184.00
Melting point (Kelvin)
457.15
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.15
General information
Molecular weight
1415.55g/mol
Molar mass
1 415.5000g/mol
Density
1.2800g/cm3
Appearence
Bleomycin A2 is typically a pale blue powder when isolated. It often appears as lyophilized powder prepared for medical applications. In the solid state, it is stable when protected from light.
Comment on solubility

Solubility of 3,6-diamino-N-[3-(2-amino-4-hydroxy-1,4,5,6-tetrahydropyrimidin-6-yl)-9,12-bis(hydroxymethyl)-2,5,8,11,14-pentaoxo-6-(ureidomethylene)-1,4,7,10,13-pentazacyclohexadec-15-yl]hexanamide

The solubility of this complex compound is influenced by various factors including its structural characteristics and functional groups. Generally, compounds containing multiple polar groups tend to have higher solubility in polar solvents like water. Here are some key points regarding its solubility:

  • Hydrophilic groups: The presence of amino and hydroxyl functional groups contributes to the compound's ability to interact with water molecules.
  • Hydrophobic regions: Conversely, larger hydrophobic segments can decrease solubility in polar solvents, potentially leading to limited aqueous solubility.
  • pH dependency: Solubility may also vary with pH, as the ionization of amino groups can enhance solubility in certain pH ranges.
  • Temperature effects: Increasing temperature often enhances solubility, particularly for complex organic molecules.

While this compound may exhibit some solubility in water due to its polar functional groups, it's important to characterize its solubility through experimental methods to understand its behavior in different solvents accurately. Thus, research and testing will be crucial in determining the full extent of solubility for practical applications.

Interesting facts

Interesting Facts about 3,6-Diamino-N-[3-(2-amino-4-hydroxy-1,4,5,6-tetrahydropyrimidin-6-yl)-9,12-bis(hydroxymethyl)-2,5,8,11,14-pentaoxo-6-(ureidomethylene)-1,4,7,10,13-pentazacyclohexadec-15-yl]hexanamide

This fascinating compound, while lengthy in name, embodies intricate biochemical relationships that are crucial to understanding biological processes. Here are some engaging facts to consider:

  • Bioactivity Potential: The compound features a complex structure that suggests a potential role in pharmaceutical applications. Compounds with similar structural motifs have been explored for their antiviral and anticancer properties.
  • Structural Diversity: The presence of both tetrahydropyrimidine and pentaaza moieties indicates significant structural diversity, which can influence how the compound interacts with biological targets.
  • Hydroxy and Amino Groups: Functional groups like hydroxyl and amino are known for enhancing solubility and biological activity, making this compound a candidate for further research in medicinal chemistry.
  • Complex Interactions: The multi-cyclic structure can facilitate unique interactions within biological systems, potentially leading to discoveries in drug development.
  • Research Applications: Compounds of similar design have been utilized in the development of drug delivery systems, due to their ability to traverse biological membranes effectively.

As we delve deeper into the study of such compounds, researchers emphasize the need for thorough analysis of their mechanism of action and overall impact on biological systems.

Understanding the sophisticated chemistry behind compounds like this one is essential for pushing the boundaries of modern medicinal practices and enhancing therapeutic strategies.

Synonyms
Tuberactinomycin B; Vinacetin A; Vioactane
Prestwick0_001113
Prestwick1_001113
SPBio_003113