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Merck

47561

Sigma-Aldrich

芴甲氧羰酰-色氨酸

≥97.0% (HPLC), for peptide synthesis

别名:

Nα-芴甲氧羰基-N(in)-叔丁氧羰基-L-色氨酸, N(in)-Boc-Nα-Fmoc-L-色氨酸

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About This Item

经验公式(希尔记法):
C31H30N2O6
分子量:
526.58
Beilstein:
7698009
MDL號碼:
分類程式碼代碼:
12352209
eCl@ss:
32160406
PubChem物質ID:
NACRES:
NA.26

产品名称

芴甲氧羰酰-色氨酸, ≥97.0% (HPLC)

化驗

≥97.0% (HPLC)

形狀

solid

光學活性

[α]20/D −21±2°, c = 1% in DMF

反應適用性

reaction type: Fmoc solid-phase peptide synthesis

應用

peptide synthesis

官能基

Boc
Fmoc

儲存溫度

2-8°C

SMILES 字串

CC(C)(C)OC(=O)n1cc(C[C@H](NC(=O)OCC2c3ccccc3-c4ccccc24)C(O)=O)c5ccccc15

InChI

1S/C31H30N2O6/c1-31(2,3)39-30(37)33-17-19(20-10-8-9-15-27(20)33)16-26(28(34)35)32-29(36)38-18-25-23-13-6-4-11-21(23)22-12-5-7-14-24(22)25/h4-15,17,25-26H,16,18H2,1-3H3,(H,32,36)(H,34,35)/t26-/m0/s1

InChI 密鑰

ADOHASQZJSJZBT-SANMLTNESA-N

應用

芴甲氧羰酰-色氨酸(叔丁氧羰酰)可用于合成治疗2型糖尿病的胰高血糖素样肽1(GLP-1)类似物和通过芴甲氧羰酰(Fmoc)固相多肽合成(SPPS)各种多肽。

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

Limiting racemization and aspartimide formation in microwave-enhanced Fmoc solid phase peptide synthesis.
Palasek SA, et al.
Journal of Peptide Science, 13(3), 143-148 (2007)
Potent derivatives of glucagon-like peptide-1 with pharmacokinetic properties suitable for once daily administration.
Knudsen LB, et al.
Journal of Medicinal Chemistry, 43(9), 1664-1669 (2000)
Taru Dube et al.
Amino acids, 49(5), 975-993 (2017-03-12)
Surging reports of peptide-based nanosystems and their growing potency in terms of biological utility demand for the search of newer and simpler peptide-based systems that could serve as smart templates for the development of self-assembled nanostructures. Use of simple amino
Severin J Sigg et al.
Biomacromolecules, 17(3), 935-945 (2016-02-13)
Ever more emerging combined treatments exploiting synergistic effects of drug combinations demand smart, responsive codelivery carriers to reveal their full potential. In this study, a multifunctional stimuli-responsive amphiphilic peptide was designed and synthesized to self-assemble into nanoparticles capable of co-bearing
Solid-phase peptide synthesis: from standard procedures to the synthesis of difficult sequences.
Coin I, et al.
Nature Protocols, 2(12), 3247-3247 (2007)

商品

With a growing peptide drug market the fast, reliable and uncomplicated synthesis of peptides is of paramount importance.

With a growing peptide drug market the fast, reliable and uncomplicated synthesis of peptides is of paramount importance.

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