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Merck
모든 사진(2)

문서

A8292

Sigma-Aldrich

Acetobromo-α-D-glucuronic acid methyl ester

≥93% (GC)

동의어(들):

(2,3,4-Tri-O-acetyl-α-D-glucopyranosyl bromide)uronic acid methyl ester, Bromo-2,3,4-tri-O-acetyl-α-D-glucopyranuronic acid methyl ester, Methyl acetobromo-α-D-glucuronate

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About This Item

실험식(Hill 표기법):
C13H17BrO9
CAS Number:
Molecular Weight:
397.17
Beilstein:
96281
EC Number:
MDL number:
UNSPSC 코드:
12352201
PubChem Substance ID:
NACRES:
NA.25

분석

≥93% (GC)

형태

powder

광학 활성

[α]/D 188 to 198 °, c = 1% (w/v) in ethyl acetate

색상

white

mp

80-110 °C (lit.)

solubility

ethyl acetate: 50 mg/mL, clear, colorless to faintly yellow

배송 상태

dry ice

저장 온도

−20°C

SMILES string

COC(=O)[C@H]1O[C@H](Br)[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O

InChI

1S/C13H17BrO9/c1-5(15)20-8-9(21-6(2)16)11(13(18)19-4)23-12(14)10(8)22-7(3)17/h8-12H,1-4H3/t8-,9-,10+,11-,12-/m0/s1

InChI key

GWTNLHGTLIBHHZ-SVNGYHJRSA-N

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애플리케이션

Acetobromo-α-D-glucuronic acid methyl ester is used for the synthesis of HMR1098-S-Glucuronide Methyl Ester, a new K-ATP-blocking agent being developed as a drug for prevention of sudden cardiac death.

기타 정보

To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Gloves, type N95 (US)


시험 성적서(COA)

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문서 라이브러리 방문

Katarzyna Choma et al.
Journal of bioenergetics and biomembranes, 41(4), 323-334 (2009-10-13)
Mitochondrial potassium channels in the brain have been suggested to have an important role in neuroprotection. The single channel activity of mitochondrial potassium channels was measured after reconstitution of the purified inner membrane from rat brain mitochondria into a planar
Brian T Ethell et al.
Drug metabolism and disposition: the biological fate of chemicals, 31(8), 1027-1034 (2003-07-18)
HMR1098, a novel KATP-blocking agent, is metabolized to form an S-glucuronide in rat and dog bile. Synthesis of the S-glucuronide metabolite was studied in human liver and kidney microsomes. Recombinant UPD-glucuronosyltransferases (UGTs) were screened for activity, and kinetic analysis was
John C Quindry et al.
American journal of physiology. Heart and circulatory physiology, 299(1), H175-H183 (2010-05-04)
The mechanisms responsible for anti-arrhythmic protection during ischemia-reperfusion (IR) in exercised hearts are not fully understood. The purpose of this investigation was to examine whether the ATP-sensitive potassium channels in the mitochondria (mito K(ATP)) and sarcolemma (sarc K(ATP)) provide anti-arrhythmic

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