A0262
Lithium potassium acetyl phosphate
≥85% (elemental analysis), powder
동의어(들):
Acetyl phosphate lithium potassium salt
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모든 사진(1)
About This Item
Linear Formula:
CH3COOP(O)(OK)(OLi)
CAS Number:
Molecular Weight:
184.06
Beilstein:
5689718
EC Number:
MDL number:
UNSPSC 코드:
12352204
PubChem Substance ID:
NACRES:
NA.32
추천 제품
제품명
Lithium potassium acetyl phosphate, high-energy phosphate donor
Quality Level
분석
≥85% (elemental analysis)
양식
powder
mp
>300 °C (lit.)
solubility
water: 25 mg/mL, clear, colorless
저장 온도
−20°C
SMILES string
[Li+].[K+].CC(=O)OP([O-])([O-])=O
InChI
1S/C2H5O5P.K.Li/c1-2(3)7-8(4,5)6;;/h1H3,(H2,4,5,6);;/q;2*+1/p-2
InChI key
RLQMPLKXFIXRCV-UHFFFAOYSA-L
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관련 카테고리
애플리케이션
Lithium potassium acetyl phosphate:
- has been used as a substrate for CpxR (transcription factor) in x-ray crystallography to soak CpxR receiver domain (CpxRRD) crystals to obtain the phosphorylated form
- may be used as a phosphate (P) donor in a study to screen a wide range of natural and synthetic organic phosphate donors with several enzymes on various hydroxyl?compounds for the improved enzymatic synthesis of phosphate monoesters
- has been used to set up premixA for in vitro translation reaction
생화학적/생리학적 작용
Lithium potassium acetyl phosphate is commonly used as the source for acetyl phosphate. So acetyl phosphate can be used as a suitable alternative to replace inorganic oligophosphates in phosphatase-catalyzed transphosphorylation to reduce inorganic monophosphate by-product formation.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Eye Dam. 1 - Repr. 2 - Skin Corr. 1B
Storage Class Code
8B - Non-combustible corrosive hazardous materials
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Gloves, type N95 (US)
이미 열람한 고객
Gábor Tasnádi et al.
Advanced synthesis & catalysis, 360(12), 2394-2401 (2018-10-20)
Undesired product hydrolysis along with large amounts of waste in form of inorganic monophosphate by-product are the main obstacles associated with the use of pyrophosphate in the phosphatase-catalyzed synthesis of phosphate monoesters on large scale. In order to overcome both
Soma Mukhopadhyay et al.
Bioorganic chemistry, 36(2), 65-69 (2008-02-26)
Acetate kinase, a member of the ASKHA (Acetate and Sugar Kinases, Hsp70, Actin) phosphotransferase superfamily is a central enzyme in prokaryotic carbon and energy metabolism. Recently extensive structural and biochemical studies of acetate kinase and related carboxylate kinases have been
Ariel E Mechaly et al.
Structure (London, England : 1993), 25(6), 939-944 (2017-05-30)
Bacterial two-component systems consist of a sensor histidine kinase (HK) and a response regulator (RR). HKs are homodimers that catalyze the autophosphorylation of a histidine residue and the subsequent phosphoryl transfer to its RR partner, triggering an adaptive response. How
Sebastian R Schmidl et al.
Nature chemical biology, 15(7), 690-698 (2019-05-22)
Two-component systems (TCSs) are the largest family of multi-step signal transduction pathways and valuable sensors for synthetic biology. However, most TCSs remain uncharacterized or difficult to harness for applications. Major challenges are that many TCS output promoters are unknown, subject
Birgit Dreier et al.
Methods in molecular biology (Clifton, N.J.), 687, 283-306 (2010-10-23)
The selection and concomitant affinity maturation of proteins to bind to user-defined target molecules have become a key technology in biochemical research, diagnostics, and therapy. One of the most potent selection technologies for such applications is ribosome display. It works
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