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Merck
모든 사진(1)

문서

10108294001

Roche

Phosphoenol-pyruvate

97% (PEP-K), pkg of 1 g

동의어(들):

Phospho(enol)pyruvic acid monopotassium salt, 2-(Phosphonooxy)-2-propenoic acid monopotassium salt, mono-Potassium phosphoenolpyruvate, PEP-K

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About This Item

실험식(Hill 표기법):
C3H4KO6P
CAS Number:
Molecular Weight:
206.13
Beilstein:
4603446
MDL number:
UNSPSC 코드:
12352204
PubChem Substance ID:

설명

C3H4O6PK (Formula)
PEP, monopotassium salt

Quality Level

분석

97% (PEP-K)

형태

solid

분자량

Mr 168.0 (PEP)
Mr 206.1 (PEP-K)

포장

pkg of 1 g

제조업체/상표

Roche

저장 온도

2-8°C

SMILES string

[K+].OC(=O)C(=C)OP(O)([O-])=O

InChI

1S/C3H5O6P.K/c1-2(3(4)5)9-10(6,7)8;/h1H2,(H,4,5)(H2,6,7,8);/q;+1/p-1

InChI key

SOSDSEAIODNVPX-UHFFFAOYSA-M

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관련 카테고리

일반 설명

Contents: 80% PEP (enzymatic)

애플리케이션

Phosphoenolpyruvate (PEP) has been used in:
  • glutamate-cysteine ligase activity
  • v-ATPase enzyme activity assay
  • meso kinase assay

Substrate for pyruvate kinase.

생화학적/생리학적 작용

Phosphoenolpyruvate (PEP) plays a vital role in metabolism. It has a high phosphate group-transfer potential and it serves a versatile C3-synthon in C–C, C–P and C–O bond-formation reactions. PEP acts as a substrate for pyruvate kinase (PK) in the last step of glycolysis.

기타 정보

For life science research only. Not for use in diagnostic procedures.

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable


시험 성적서(COA)

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문서 라이브러리 방문

Synthesis of phosphoenol pyruvate (PEP) analogues and evaluation as inhibitors of PEP-utilizing enzymes.
Garcia A, et al.
FEBS Journal, 269(13), 3226-3236 (2002)
Glutathione participates in the modulation of starvation-induced autophagy in carcinoma cells.
Desideri E
Autophagy, 8(12), 1769-1781 (2012)
Jasmine M Hershewe et al.
Nature communications, 12(1), 2363-2363 (2021-04-24)
Cell-free gene expression (CFE) systems from crude cellular extracts have attracted much attention for biomanufacturing and synthetic biology. However, activating membrane-dependent functionality of cell-derived vesicles in bacterial CFE systems has been limited. Here, we address this limitation by characterizing native
Maria B Bagh et al.
Nature communications, 8, 14612-14612 (2017-03-08)
Defective lysosomal acidification contributes to virtually all lysosomal storage disorders (LSDs) and to common neurodegenerative diseases like Alzheimer's and Parkinson's. Despite its fundamental importance, the mechanism(s) underlying this defect remains unclear. The v-ATPase, a multisubunit protein complex composed of cytosolic
Brian S Muntean et al.
Cell reports, 34(5), 108718-108718 (2021-02-04)
The G protein alpha subunit o (Gαo) is one of the most abundant proteins in the nervous system, and pathogenic mutations in its gene (GNAO1) cause movement disorder. However, the function of Gαo is ill defined mechanistically. Here, we show

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