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Merck
모든 사진(2)

주요 문서

287288

Sigma-Aldrich

3-(2-Thienyl)-DL-alanine

≥98%

동의어(들):

2-Amino-3-(2-thienyl)propionic acid

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About This Item

실험식(Hill 표기법):
C7H9NO2S
CAS Number:
Molecular Weight:
171.22
Beilstein:
82874
EC Number:
MDL number:
UNSPSC 코드:
12352209
PubChem Substance ID:
NACRES:
NA.22

Quality Level

분석

≥98%

양식

powder

반응 적합성

reaction type: solution phase peptide synthesis

mp

275-277 °C (dec.) (lit.)

응용 분야

peptide synthesis

SMILES string

NC(Cc1cccs1)C(O)=O

InChI

1S/C7H9NO2S/c8-6(7(9)10)4-5-2-1-3-11-5/h1-3,6H,4,8H2,(H,9,10)

InChI key

WTOFYLAWDLQMBZ-UHFFFAOYSA-N

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Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves


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문서 라이브러리 방문

K J Brown et al.
Medical microbiology and immunology, 168(1), 11-24 (1980-02-01)
Faecal samples were taken from three diet-managed phenylketonuric children to determine effects of beta-2-thienylalanine (beta-2-t) on indigenous bacteria. From sample swabs, 127 anaerobes were identified and tested for beta-2-t inhibition on a phenylalanine (Phe)-free medium, Anaerobe Inhibition Test (AIT) agar.
I W Hamley et al.
The journal of physical chemistry. B, 114(32), 10674-10683 (2010-07-29)
The self-assembly of a peptide based on a sequence from the amyloid beta peptide but incorporating the non-natural amino acid beta-2-thienylalanine (2-Thi) has been investigated in aqueous and methanol solutions. The peptide AAKLVFF was used as a design motif, replacing
D G Adams et al.
Critical reviews in microbiology, 9(1), 45-100 (1981-01-01)
We will be concerned with the two major differentiated cell types of filamentous cyanobacteria--the heterocyst and the akinete. The former is generally accepted to be the site of aerobic nitrogen fixation in heterocystous cyanobacteria. The latter is a spore-like cell
Uptake and incorporation of amino acids by suspension cultured mammalian cells: a comparative study involving eleven naturally-occurring and four analogue amino acids.
D N Wheatley et al.
Cytobios, 30(118), 101-126 (1981-01-01)
D P Bedard et al.
Journal of bacteriology, 141(1), 100-105 (1980-01-01)
When treated with the amino acid analog beta-2-DL-thienylalanine, cells of the yeast Saccharomyces cerevisiae accumulated in the G1 portion of the cell cycle at the "start" event. This G1 arrest was accompanied by a rapid decrease in the rate of

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