(2S,5S,8S,11S,14S)-5,14-Bis(4-aminobutyl)-8,11-bis((R)-1-hydroxyethyl)-2-(hydroxymethyl)-4,7,10,13,16-pentaoxo-3,6,9,12,15-pentaazahentriacontan-1-oic acid
≥97%
- Product Code: 36595
CAS:
214047-00-4
| Molecular Weight: | 802.05 g./mol | Molecular Formula: | C₃₉H₇₅N₇O₁₀ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 1120.1°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed away from light |
Product Description:
This compound is primarily utilized in the field of biochemistry and pharmaceutical research due to its complex structure and functional groups. It is often employed as a key intermediate in the synthesis of peptide-based drugs, particularly those targeting specific enzymatic pathways or receptor interactions. Its multiple hydroxyl and amino groups make it suitable for conjugation with other molecules, enhancing drug delivery and bioavailability. Additionally, it is explored in the development of novel antibiotics and antimicrobial agents, leveraging its ability to disrupt bacterial cell wall synthesis. Researchers also investigate its potential in cancer therapy, where it may serve as a carrier for targeted drug delivery systems. Its unique stereochemistry allows for precise interactions with biological targets, making it valuable in the design of highly specific therapeutic agents.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿8,370.00 |
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| 0.250 | 10-20 days | ฿13,419.00 |
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| 1.000 | 10-20 days | ฿33,651.00 |
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(2S,5S,8S,11S,14S)-5,14-Bis(4-aminobutyl)-8,11-bis((R)-1-hydroxyethyl)-2-(hydroxymethyl)-4,7,10,13,16-pentaoxo-3,6,9,12,15-pentaazahentriacontan-1-oic acid
This compound is primarily utilized in the field of biochemistry and pharmaceutical research due to its complex structure and functional groups. It is often employed as a key intermediate in the synthesis of peptide-based drugs, particularly those targeting specific enzymatic pathways or receptor interactions. Its multiple hydroxyl and amino groups make it suitable for conjugation with other molecules, enhancing drug delivery and bioavailability. Additionally, it is explored in the development of novel antibiotics and antimicrobial agents, leveraging its ability to disrupt bacterial cell wall synthesis. Researchers also investigate its potential in cancer therapy, where it may serve as a carrier for targeted drug delivery systems. Its unique stereochemistry allows for precise interactions with biological targets, making it valuable in the design of highly specific therapeutic agents.
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