52498-32-5
52498-32-5
Chemical Structure
Boc-N-methyl-L-isoleucine
Synonym(s): Boc-N-Me-Ile-OH
- CAS No.: 52498-32-5
- Formula:C12H23NO4
- Molecular Weight:245.32
IUPAC Name: N-(tert-butoxycarbonyl)-N-methyl-L-isoleucine
InChIKey: HTBIAUMDQYXOFG-IUCAKERBSA-N
SMILES: CC[C@H](C)[C@H](N(C)C(=O)OC(C)(C)C)C(=O)O
Biological Activity: Boc-N-methyl-L-isoleucine (Boc-N-Me-Ile-OH) is a Boc-protected N-methylated derivative of L-isoleucine (HY-N0771), as well as a protected amino acid building block[1][2].
| Cat. No. | Nom du produit | Pureté | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
Boc-N-methyl-L-isoleucine | 99.17% | Boc-N-methyl-L-isoleucine (Boc-N-Me-Ile-OH) is a Boc-protected N-methylated derivative of L-isoleucine (HY-N0771), as well as a protected amino acid building block. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
References
- [1]. Zhang W, et al. From Target-Oriented to Motif-Oriented: A Case Study on Nannocystin Total Synthesis. Molecules (Basel, Switzerland). 2020 Nov 15;25(22):5327.
- [2]. Pham THD, et al. Biosynthesis, Chemical Synthesis, and Pharmacological Evaluation of Lyngbyapeptin A as a GPCR Antagonist of Motilin, Cannabinoid, and Amylin Receptors. Journal of natural products. 2025 Nov 28;88(11):2610-2624.
