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Merck
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Key Documents

추가 자료

367559

Sigma-Aldrich

(S)-(+)-1-Aminoethylphosphonic acid

99%

동의어(들):

D-(+)-1-Aminoethylphosphonic acid, D-Ala(P)

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모든 사진(1)

About This Item

Linear Formula:
CH3CH(NH2)P(O)(OH)2
CAS Number:
66068-76-6
Molecular Weight:
125.06
Beilstein:
4291033
MDL number:
MFCD00066503
UNSPSC 코드:
12352116
PubChem Substance ID:
24862769
NACRES:
NA.22

Quality Level

100

분석

99%

형태

solid

광학 활성

[α]20/D +4.8°, c = 5 in H2O

mp

290 °C (dec.) (lit.)

SMILES string

C[C@@H](N)P(O)(O)=O

InChI

1S/C2H8NO3P/c1-2(3)7(4,5)6/h2H,3H2,1H3,(H2,4,5,6)/t2-/m0/s1

InChI key

UIQSKEDQPSEGAU-REOHCLBHSA-N

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관련 카테고리

픽토그램

Exclamation mark
GHS07

신호어

Warning

유해 및 위험 성명서

H315 - H319 - H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

표적 기관

Respiratory system

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

시험 성적서(COA)

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문서 라이브러리 방문

V Copié et al.
Biochemistry, 27(14), 4966-4970 (1988-07-12)
Inhibition of alanine racemase from the Gram-positive bacterium Bacillus stearothermophilus by (1-aminoethyl) phosphonic acid (Ala-P) proceeds via a two-step reaction pathway in which reactivation occurs very slowly. In order to determine the mechanism of inhibition, we have recorded low-temperature, solid-state
O Ploux et al.
European journal of biochemistry, 259(1-2), 63-70 (1999-01-23)
8-Amino-7-oxopelargonate synthase catalyzes the first committed step of biotin biosynthesis in micro-organisms and plants. Because inhibitors of this pathway might lead to antibacterials or herbicides, we have undertaken an inhibition study on 8-amino-7-oxopelargonate synthase using six different compounds. d-Alanine, the
D A Mironenko et al.
Biokhimiia (Moscow, Russia), 55(6), 1124-1131 (1990-06-01)
Penicillin acylase from E. coli (EC 3.5.1.11) was found to hydrolyze N-phenylacetylated 1-aminoethylphosphonic acid and its esters. The enzyme preferentially converts the R-form of the substrates: the ratios of the bimolecular rate constants of penicillin acylasecatalyzed hydrolysis of R- and
F R Atherton et al.
Journal of medicinal chemistry, 29(1), 29-40 (1986-01-01)
Phosphonodipeptides and phosphonooligopeptides based on L- and D-(1-aminoethyl)phosphonic acids L-Ala(P) and D-Ala(P) and (aminomethyl)phosphonic acid Gly(P) at the acid terminus have been synthesized and investigated as antibacterial agents, which owe their activity to the inhibition of bacterial cell-wall biosynthesis. A

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