205528-32-1
205528-32-1
Chemical Structure
Fmoc-L-(4-thiazolyl)-Alanine
- CAS No.: 205528-32-1
- Formula:C21H18N2O4S
- Molecular Weight:394.44
IUPAC Name: (S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(thiazol-4-yl)propanoic acid
InChIKey: LSBAZFASKHLHKB-IBGZPJMESA-N
SMILES: O=C(N[C@H](C(O)=O)CC1=CSC=N1)OCC2C3=C(C4=C2C=CC=C4)C=CC=C3
Biological Activity: Fmoc-L-(4-thiazolyl)-Alanine is an alanine derivative[1].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
Fmoc-L-(4-thiazolyl)-Alanine | 99.53% | Fmoc-L-(4-thiazolyl)-Alanine is an alanine derivative. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
(αS)-α-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-2-pyridinepropanoic acid | 99.51% | (αS)-α-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-2-pyridinepropanoic acid is an alanine derivative. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Fmoc-3-Ala(2-thienyl)-OH | 99.42% | Fmoc-3-Ala(2-thienyl)-OH is an alanine derivative. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(thiophen-3-yl)propanoic acid | 99.35% | (R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(thiophen-3-yl)propanoic acid is an alanine derivative. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Fmoc-2-D-Pal-OH | Fmoc-2-D-Pal-OH is an alanine derivative. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Fmoc-3-Ala(3-thienyl)-OH | 99.82% | Fmoc-3-Ala(3-thienyl)-OH is an alanine derivative. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Fmoc-1-methyl-L-histidine | 99.66% | Fmoc-1-methyl-L-histidine is an Fmoc-protected amino acid as well as an amino acid-containing building block. Fmoc-1-methyl-L-histidine is applicable to the generation of the ε-nitrogen-coordinated copper center in nitrite copper reductase. It also serves as an intermediate in peptide synthesis. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
(((9H-Fluoren-9-yl)methoxy)carbonyl)-D-histidine | (((9H-Fluoren-9-yl)methoxy)carbonyl)-D-histidine is a histidine derivative. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Fmoc-D-Thi-OH | 99.69% | Fmoc-D-Thi-OH (Fmoc-D-2-Thienylalanine) is an amino acid derivative with an Fmoc protecting group, which can be used to synthesize AS-Z-P with thrombin inhibitory activity. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
(((9H-Fluoren-9-yl)methoxy)carbonyl)-L-histidine | 99.73% | (((9H-Fluoren-9-yl)methoxy)carbonyl)-L-histidine is a histidine derivative. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Fmoc-His(3-Me)-OH | 99.67% | Fmoc-His (3-Me)-OH is a histidine derivative with a methylated imidazole group. Fmoc-His (3-Me)-OH can be used for the synthesis of the chemically modified tripeptide His (3-methyl)-Arg-Trp (H (3-Me)-RW). Fmoc-His (3-Me)-OH serves as a resin in Fmoc solid-phase synthesis for the generation of the His-(3-Me)-Gly-Lys peptide. Fmoc-His (3-Me)-OH is a building block for the synthesis of NAHIS02-(p-Met). Fmoc-His (3-Me)-OH can be applied in research related to Alzheimer's disease. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
