모든 사진(2)
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100 MG
₩146,465
1 G
₩576,723
About This Item
실험식(Hill 표기법):
C6H12O6
CAS Number:
Molecular Weight:
180.16
EC Number:
MDL number:
UNSPSC 코드:
12352201
PubChem Substance ID:
NACRES:
NA.22
추천 제품
Quality Level
분석
95%
양식
solid
광학 활성
[α]23/D +60°, c = 1.2 in H2O
광학 순도
ee: 99% (GLC)
mp
230 °C (lit.)
저장 온도
2-8°C
SMILES string
O[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)[C@@H]1O
InChI
1S/C6H12O6/c7-1-2(8)4(10)6(12)5(11)3(1)9/h1-12H/t1-,2-,3-,4-,5+,6+/m0/s1
InChI key
CDAISMWEOUEBRE-LKPKBOIGSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
애플리케이션
The inositols and their phosphates have been used in the development of metabolically stable insulin mediators, inhibitors, and modulators of important metabolic functions such as glycolysis. Inositols are stable to degradative enzymes in vivo because they lack a hydrolytically labile glycosidic linkage.[1][2][3][4][5][6]
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)
이미 열람한 고객
M J Berridge et al.
Nature, 341(6239), 197-205 (1989-09-21)
Inositol 1,4,5-trisphosphate is a second messenger which regulates intracellular calcium both by mobilizing calcium from internal stores and, perhaps indirectly, by stimulating calcium entry. In these actions it may function with its phosphorylated metabolite, inositol 1,3,4,5-tetrakisphosphate. The subtlety of calcium
Hudlicky, T. et al.
Synthesis, 897-897 (1996)
Modern Methods of Monosaccharide Synthesis from Non-Carbohydrate Sources.
Tomas Hudlicky et al.
Chemical reviews, 96(3), 1195-1220 (1996-05-09)
Recent advances in the chemistry and biochemistry of inositol phosphates of biological interest.
B V Potter
Natural product reports, 7(1), 1-24 (1990-02-01)
Bellington, D.C.
Chemical Society Reviews, 18, 83-83 (1989)
활성 필터
자사의 과학자팀은 생명 과학, 재료 과학, 화학 합성, 크로마토그래피, 분석 및 기타 많은 영역을 포함한 모든 과학 분야에 경험이 있습니다..
고객지원팀으로 연락바랍니다.
