(S)-2-((S)-2-Amino-3-methylbutanamido)pentanedioic acid
97%
- Product Code: 38076
CAS:
3062-07-5
| Molecular Weight: | 246.2600 g./mol | Molecular Formula: | C₁₀H₁₈N₂O₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00037298 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of biochemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of peptides and peptidomimetics, which are essential for developing therapeutic agents targeting various diseases. Its structure, containing both amino and carboxylic acid functional groups, makes it valuable for constructing complex molecules with specific biological activities. Additionally, it is employed in studies related to enzyme inhibition and receptor binding, aiding in the discovery of new drugs. Its chiral nature also allows for the exploration of stereospecific interactions in biological systems, contributing to the design of more effective and selective medications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿5,454.00 |
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(S)-2-((S)-2-Amino-3-methylbutanamido)pentanedioic acid
This compound is primarily utilized in the field of biochemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of peptides and peptidomimetics, which are essential for developing therapeutic agents targeting various diseases. Its structure, containing both amino and carboxylic acid functional groups, makes it valuable for constructing complex molecules with specific biological activities. Additionally, it is employed in studies related to enzyme inhibition and receptor binding, aiding in the discovery of new drugs. Its chiral nature also allows for the exploration of stereospecific interactions in biological systems, contributing to the design of more effective and selective medications.
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