288617-73-2
288617-73-2
Chemical Structure
Fmoc-(S)-2-(4-pentenyl)Ala-OH
- CAS No.: 288617-73-2
- Formula:C23H25NO4
- Molecular Weight:379.45
IUPAC Name: (S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-2-methylhept-6-enoic acid
InChIKey: MRJFPZWLOJOINV-QHCPKHFHSA-N
SMILES: C=CCCC[C@](C)(NC(OCC1C2=C(C3=C1C=CC=C3)C=CC=C2)=O)C(O)=O
Biological Activity: Fmoc-(S)-2-(4-pentenyl) Ala-OH is an Fmoc-protected unnatural amino acid. Fmoc-(S)-2-(4-pentenyl) Ala-OH can be used for polypeptide synthesis, such as NYAD-13 (HY-P10834)[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
Fmoc-(S)-2-(4-pentenyl)Ala-OH | 98.75% | Fmoc-(S)-2-(4-pentenyl) Ala-OH is an Fmoc-protected unnatural amino acid. Fmoc-(S)-2-(4-pentenyl) Ala-OH can be used for polypeptide synthesis, such as NYAD-13 (HY-P10834). | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
Structural Analogs
-
Similarity Score 1.00
HY-W018847Fmoc-(R)-2-(pentenyl)Ala-OH -
Similarity Score 0.93
HY-W048199(S)-N-FMoc-2-(6'-heptenyl)alanine -
Similarity Score 0.91
HY-W006886Fmoc-(R)-2-(7-octenyl)Ala-OH -
Similarity Score 0.86
HY-W005913(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-methylpent-4-enoic acid -
Similarity Score 0.86
HY-W007052Fmoc-alpha-allyl-L-alanine -
Similarity Score 0.83
HY-W048739Fmoc-α-Me-Leu-OH -
Similarity Score 0.79
HY-79648Fmoc-Aib-OH -
Similarity Score 0.78
HY-W018849(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2,3-dimethylbutanoic acid -
Similarity Score 0.78
HY-W008273Fmoc-D-Nle-OH -
Explore the MedChemAI to find more analogs
References
- [1]. Zero J, et al. Universal peptide synthesis via solid-phase methods fused with chemputation. Nat Commun. 2025;16(1):7322. Published 2025 Aug 8. [Content Brief]
- [2]. Adak A, et al. Evolution of Potential Antimitotic Stapled Peptides from Multiple Helical Peptide Stretches of the Tubulin Heterodimer Interface: Helix-Mimicking Stapled Peptide Tubulin Inhibitors. J Med Chem. 2022;65(20):13866-13878. [Content Brief]
