推荐产品
形式
powder
质量水平
SMILES字符串
O.O.O.O.O.O.[Na+].[Na+].[Na+].[O-]C(=O)P([O-])([O-])=O
InChI
1S/CH3O5P.3Na.6H2O/c2-1(3)7(4,5)6;;;;;;;;;/h(H,2,3)(H2,4,5,6);;;;6*1H2/q;3*+1;;;;;;/p-3
InChI key
ILRVASBWNRYBFD-UHFFFAOYSA-K
基因信息
human ... POLA1(5422) , POLD1(5424) , POLG(5428)
rat ... Slc17a1(171080)
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危险声明
危险分类
Muta. 2 - STOT RE 2
靶器官
Kidney,Bone
WGK
WGK 3
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
Tadashi Kato et al.
Calcified tissue international, 104(2), 201-206 (2018-10-21)
Nephronectin (Npnt), an extracellular matrix protein, is known to be a ligand of integrin α8β1, and it has also been known to play critical roles as various organs. In the present study, elevated extracellular inorganic phosphate (Pi) strongly inhibited the
Emily Rose et al.
Scientific reports, 9(1), 8798-8798 (2019-06-21)
How inorganic phosphate (Pi) homeostasis is regulated in Drosophila is currently unknown. We here identify MFS2 as a key Pi transporter in fly renal (Malpighian) tubules. Consistent with its role in Pi excretion, we found that dietary Pi induces MFS2
Liudi Tang et al.
PLoS pathogens, 15(4), e1007742-e1007742 (2019-04-27)
Persistent hepatitis B virus (HBV) infection relies on the establishment and maintenance of covalently closed circular (ccc) DNA, a 3.2 kb episome that serves as a viral transcription template, in the nucleus of an infected hepatocyte. Although evidence suggests that
Sampada Chande et al.
Scientific reports, 10(1), 3069-3069 (2020-02-23)
Low blood phosphate (Pi) reduces muscle function in hypophosphatemic disorders. Which Pi transporters are required and whether hormonal changes due to hypophosphatemia contribute to muscle function is unknown. To address these questions we generated a series of conditional knockout mice
Jocelyne Piret et al.
Journal of virology, 89(8), 4636-4644 (2015-02-13)
DNA polymerases of the Herpesviridae and bacteriophage RB69 belong to the α-like DNA polymerase family. In spite of similarities in structure and function, the RB69 enzyme is relatively resistant to foscarnet, requiring the mutation V478W in helix N to promote
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