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Merck
모든 사진(3)

Key Documents

452483

Sigma-Aldrich

1-Methyl-D-tryptophan

95%

동의어(들):

(2R)-2-Amino-3-(1-methyl-1H-indol-3-yl)propanoic acid, D-(+)-1-Methyltryptophan

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About This Item

실험식(Hill 표기법):
C12H14N2O2
CAS Number:
Molecular Weight:
218.25
MDL number:
UNSPSC 코드:
12352209
PubChem Substance ID:
NACRES:
NA.22

Quality Level

분석

95%

형태

lumps and powder

광학 활성

[α]22/D +12.4°, c = 2 in acetic acid

반응 적합성

reaction type: solution phase peptide synthesis

mp

242-245 °C (lit.)

응용 분야

peptide synthesis

SMILES string

Cn1cc(C[C@@H](N)C(O)=O)c2ccccc12

InChI

1S/C12H14N2O2/c1-14-7-8(6-10(13)12(15)16)9-4-2-3-5-11(9)14/h2-5,7,10H,6,13H2,1H3,(H,15,16)/t10-/m1/s1

InChI key

ZADWXFSZEAPBJS-SNVBAGLBSA-N

애플리케이션

Used to prepare a number of natural products including macroline alkaloids using the Pictet-Spengler reaction of tryptophan esters with aldehydes also used in the synthesis of 1-substituted indolactam precursors.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable


시험 성적서(COA)

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문서 라이브러리 방문

Irie, K. et al.
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Cook, J.M. et al.
Heterocycles, 27, 2795-2795 (1988)
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Dendritic cells (DC) have the potential to control the outcome of autoimmunity by modulating the immune response. In this study, we tested the ability of Fasciola hepatica total extract (TE) to induce tolerogenic properties in CpG-ODN (CpG) maturated DC, to
Luciana Cavalheiro Marti et al.
Memorias do Instituto Oswaldo Cruz, 109(1), 70-79 (2013-10-22)
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