- ￥218 - 4706
- MedChemExpress(MCE)
- 美国
- HY-W007108
- 2025年12月05日
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- 详细信息
- 文献和实验
- 技术资料
- 保存条件：
Powder: -20°C, 3 years; 4°C, 2 years.In solvent: -80°C, 6 months; -20°C, 1 month.
- 库存：
货期：1-2天
- 供应商：
MedChemExpress LLC
- CAS号：
269066-08-2
- 规格：
100 mg/250 mg/1 g/5 g
| 规格： | 100 mg | 产品价格： | ￥218.0 |
|---|---|---|---|
| 规格： | 250 mg | 产品价格： | ￥383.0 |
| 规格： | 1 g | 产品价格： | ￥1016.0 |
| 规格： | 5 g | 产品价格： | ￥4706.0 |
产品活性：Fmoc-Asp(ODMAB)-OH 是一种天冬氨酸衍生物。
产品来源： www.medchemexpress.cn/fmoc-asp-odmab-oh.html
研究领域：Others
作用靶点：Amino Acid Derivatives
In Vitro: Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances.
相关产品：N6-Diazo-L-Fmoc-lysine | Fmoc-Arg(Pbf)-OH | (S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-5-(tert-butoxy)-5-oxopentanoic acid | Fmoc-L-Lys(Dde)-OH | (S)-2-Amino-6-((tert-butoxycarbonyl)amino)hexanoic acid | Fmoc-Hyp(tBu)-OH | L-tert-Leucine Methyl Ester Hydrochloride | DL-Propargylglycine | Fmoc-Ala-OH | Fmoc-Gly-OH | Fmoc-Ile-OH | N-Boc-O-tosyl hydroxylamine | N-ε-propargyloxycarbonyl-L-lysine hydrochloride | tert-Butyl 2-aminoacetate | Fmoc-Lys(Alloc)-OH | Fmoc-Pra-OH | Methyl (R)-2-((tert-butoxycarbonyl)amino)-3-iodopropanoate | N-(9-Fluorenylmethoxycarbonyl)glutamic acid α-tert-butyl ester | Fmoc-L-Lys (Boc)-OH | Fmoc-Glu(OAll)-OH | Fmoc-Gly(allyl)-OH | Fmoc-Bip(4,4')-OH | (S)-2-amino-3-(4-benzoylphenyl)propanoic acid | Fmoc-1-Nal-OH | Fmoc-D-Gln(Trt)-OH | Fmoc-Lys(Mtt)-OH | N-Boc-L-tert-Leucine | (S)-2-Amino-3-(4-bromophenyl)propanoic acid | Fmoc-Asp(OtBu)-OH | Fmoc-Phe-OH
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文献和实验Solid-Phase Synthesis of Neuropeptides by Fmoc Strategies
an automated peptide synthesizer that performs solid-phase peptide synthesis using the Fmoc strategy (1 ). This is based on the sequential addition of amino acid residues to an insoluble polymeric support. The base-labile Fmoc group
Identification of Asp Isomerization in Proteins by 18O Labeling and Tandem Mass Spectrometry
Isomerization of aspartic acid (Asp) to isoaspartic acid (isoAsp) via succinimide intermediate is a common route of degradation for proteins that can affect their structural integrity. As Asp/isoAsp is isobaric in mass, it is difficult
-ASP1), which is a potential vaccine candidate against hookworm infections, has been expressed in Pichia pastoris . Na- ASP1 protein was expressed extracellulary by employing the leader sequence of the α-mating factor of Saccharomyces cerevisiae
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