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Merck

47625

Sigma-Aldrich

芴甲氧羰酰-色氨酸

≥98.0% (HPLC), for peptide synthesis

别名:

芴甲氧羰基-L-谷氨酸 5-叔丁酯

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About This Item

经验公式(希尔记法):
C24H27NO6
CAS号:
分子量:
425.47
Beilstein:
3636375
EC號碼:
MDL號碼:
分類程式碼代碼:
12352209
eCl@ss:
32160406
PubChem物質ID:
NACRES:
NA.26

product name

芴甲氧羰酰-色氨酸, ≥98.0% (HPLC)

化驗

≥98.0% (HPLC)

形狀

powder

光學活性

[α]20/D −5.0±2.0°, c = 1% in acetic acid: water (4:1)

反應適用性

reaction type: Fmoc solid-phase peptide synthesis

雜質

~4% water

應用

peptide synthesis

官能基

Fmoc

儲存溫度

2-8°C

SMILES 字串

CC(C)(C)OC(=O)CC[C@H](NC(=O)OCC1c2ccccc2-c3ccccc13)C(O)=O

InChI

1S/C24H27NO6/c1-24(2,3)31-21(26)13-12-20(22(27)28)25-23(29)30-14-19-17-10-6-4-8-15(17)16-9-5-7-11-18(16)19/h4-11,19-20H,12-14H2,1-3H3,(H,25,29)(H,27,28)/t20-/m0/s1

InChI 密鑰

OTKXCALUHMPIGM-FQEVSTJZSA-N

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一般說明

Fmoc-Glu(OtBu)-OH 被广泛用于肽合成中保护胺基的合成嵌段。

應用

Fmoc-Glu(OtBu)-OH(氧羰基-L-谷氨酸 5--丁酯)可用于:
  • 配体,以使用Pd催化剂通过环丙烷酰胺C-H活化反应合成顺式取代环丙烷羧酸。
  • 多小分子共轭PTX(紫杉醇)衍生物制备中的连接剂。

还可用作基本构成要素制备钉状α-螺旋肽和肽C-端硫代酸酯

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)


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分析证书(COA)

Lot/Batch Number

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访问文档库

Solid phase synthesis of peptide C-terminal thioesters by Fmoc/t-Bu chemistry
Ingenito R, et al.
Journal of the American Chemical Society, 121(49), 11369-11374 (1999)
Multi-small molecule conjugations as new targeted delivery carriers for tumor therapy
Shan L, et al.
International journal of nanomedicine, 10(49), 5571-5571 (2015)
Stapled α-helical peptide drug development: A potent dual inhibitor of MDM2 and MDMX for p53-dependent cancer therapy
Chang YS, et al.
Proceedings of the National Academy of Sciences of the USA, 110(36), E3445-E3454 (2013)
Linda C Weiss et al.
Nature chemical biology, 14(12), 1133-1139 (2018-11-16)
Infochemicals play important roles in aquatic ecosystems. They even modify food web interactions, such as by inducing defenses in prey. In one classic but still not fully understood example, the planktonic freshwater crustacean Daphnia pulex forms specific morphological defenses (neckteeth)
Pd (II)-catalyzed enantioselective C-H activation of cyclopropanes
Wasa M, et al.
Journal of the American Chemical Society, 133(49), 19598-19601 (2011)

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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