产品名称
L-2-磷酸甘油酸 二钠盐, ≥80% (CE)
SMILES string
O.[Na+].[Na+].OC[C@H](OP(O)([O-])=O)C([O-])=O
InChI
1S/C3H7O7P.2Na.H2O/c4-1-2(3(5)6)10-11(7,8)9;;;/h2,4H,1H2,(H,5,6)(H2,7,8,9);;;1H2/q;2*+1;/p-2/t2-;;;/m0.../s1
InChI key
VQNAIZNPWBGZNQ-SQGDDOFFSA-L
assay
≥80% (CE)
form
solid
impurities
≤0.2% P(i)
≤35% water
color
white to faintly brown
storage temp.
−20°C
Quality Level
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Xiangan Han et al.
Molecular biology reports, 39(3), 2705-2711 (2011-06-16)
Brucella abortus is the etiological agent of brucellosis, a disease causing human public health problems as well as major economic losses in domestic animal industries. In this study, the enolase gene of B. abortus A19 was cloned, sequenced and expressed
Sampathkumar Parthasarathy et al.
The Journal of biological chemistry, 278(52), 52461-52470 (2003-10-18)
Triose-phosphate isomerase, a key enzyme of the glycolytic pathway, catalyzes the isomerization of dihydroxy acetone phosphate and glyceraldehyde 3-phosphate. In this communication we report the crystal structure of Plasmodium falciparum triose-phosphate isomerase complexed to the inhibitor 2-phosphoglycerate at 1.1-A resolution.
R Götz et al.
Yeast (Chichester, England), 15(15), 1619-1629 (1999-11-26)
Numerous individual enzymes participate in a given synthetic or degradative pathway in which the product of one reaction becomes the substrate for the subsequent enzyme. This raises the question of whether the product of one 'soluble' enzyme diffuses freely through
C K Brown et al.
Journal of protein chemistry, 17(8), 855-866 (1999-02-13)
Purified enolase from Bacillus subtilis has a native mass of approximately 370 kDa. Since B. subtilis enolase was found to have a subunit mass of 46.58 kDa, the quaternary structure of B. subtilis is octameric. The pl for B. subtilis
Xingjue Xu et al.
Drug design and discovery, 18(2-3), 91-99 (2003-12-17)
3-Deoxy-D-manno-octulosonate 8-phosphate (KDO8P) is the phosphorylated precursor of KDO, an essential sugar of the lipopolysaccharide of Gram negative bacteria. KDO8P is produced by a specific synthase (KDO8PS) by condensing arabinose 5-phosphate (A5P) and phosphoenolpyruvate (PEP), with release of inorganic phosphate.
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