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5'-ester with 3-(aminocarbonyl)-1-b-D-ribofuranosylpyridinium hydroxide, inner salt beta-Diphosphopyridine nucleotide Adenine-nicotinamide dinucleotide
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Product introduction:
Density | 1.2±0.1 g/cm3 |
---|---|
Boiling Point | 758.6±60.0 °C at 760 mmHg |
Melting Point | -83ºC |
Molecular Formula | C40H62O19 |
Molecular Weight | 846.909 |
Flash Point | 296.6±32.9 °C |
Exact Mass | 846.388550 |
PSA | 238.09000 |
LogP | 8.46 |
Vapour Pressure | 0.0±2.6 mmHg at 25°C |
Index of Refraction | 1.500 |
Physical and Chemical Properties | Chemical properties white powder, easy to absorb moisture, the aqueous solution is acidic. The solid is stable under dry conditions. The neutral or weakly acidic aqueous solution of this product can be stored for 7 days at room temperature, and it will accelerate deterioration and decomposition in case of alkali and heat. The specific rotation [α]23D-34.8 °(1%, water); its aqueous solution has the maximum absorption at 260nm and 340nm wavelengths. Easily soluble in water, insoluble in organic solvents such as acetone. |
Use | Purpose 1. It is an essential coenzyme in vivo for biochemical research, clinical diagnosis, clinical drug and drug research. 2. Coenzyme drugs. Clinically, it is mainly used for adjuvant treatment of coronary heart disease, which can improve chest tightness, angina pectoris and other symptoms. Adverse reactions occasionally include dry mouth, dizziness, nausea, etc. |
Introduction
Nicotinamide adenine dinucleotide (abbreviated as NAD), also known as pyridine diphosphate nucleotide (abbreviated as DPN), or co-dehydrogenase I or coenzyme I. There are two states of oxidized (NAD) and reduced (NADH) in mammals. The oxidized (NAD) has the maximum ultraviolet absorption spectrum at 260nm. Through various deaminases, it accepts a hydrogen atom and an electron from the substrate., Becomes a reduced type (NADH), has the maximum absorption at 340nm.
β-nicotinamide adenine dinucleotide is used as a coenzyme in redox reactions, as a donor of ADP ribose moiety in ADP ribosylation reactions, and also as a second messenger molecule ring ADP ribose Precursor. β-nicotinamide adenine dinucleotide also acts as a substrate for bacterial DNA ligases and a group of enzymes called sirtuins that use NAD to remove acetyl groups from proteins.
Physiological functions and effects
Nicotinamide adenine dinucleotide participates in various physiological activities such as cell substance metabolism, energy synthesis, cell DNA repair, and plays an important role in the body's immune ability. In a healthy state, the concentration of nicotinamide adenine dinucleotide in the human body is stable, maintaining the normal function of various cells. The concentration of nicotinamide adenine dinucleotide in the body determines the process and degree of cell senescence, and the decrease of concentration will accelerate the process of cell senescence. Studies have shown that NAD has a protective effect on renal infarction caused by ischemic surgery, and can significantly reduce the levels of urea nitrogen and creatinine in serum. NAD has a protective effect on renal tubular injury caused by ischemic surgery. NAD (nicotinamide adenine dinucleotide, Nicotinamideadeninedinucleotide, referred to as NAD) can effectively protect kidney injury caused by renal ischemia. NAD has important application value in the preparation of drugs for the prevention and treatment of renal ischemic injury. In addition, nicotinamide adenine dinucleotide has certain applications in the preparation of drugs for the treatment of inflammatory pain. NAD participates in the regulation of formalin and complete Freund's adjuvant (CFA) through NAD-dependent deacetylase SIRT1 and SIRT2 participate in the inhibition of inflammatory pain by NAD through different mechanisms, thus achieving an analgesic effect on inflammatory pain.
Preparation
The preparation method of nicotinamide adenine dinucleotide proposed by CN201511022464.3 includes the following steps:
S1, broken cells: yeast cells are added into hydrochloric acid aqueous solution and soaked for 0.5-2.5h. after temperature difference wall breaking treatment, ceramic membrane is used for filtration, and the filtrate is taken to obtain clear liquid a;
S2, concentration: ultrafiltration of clear liquid a obtained from S1, nanofiltration of ultrafiltration to obtain concentrated liquid B, and adjusting the pH = 2-2.5 of concentrated liquid B with hydrochloric acid aqueous solution to obtain concentrated liquid c;
S3, elution: the concentrated solution c obtained in S2 is passed through D152 resin column, eluted with ammonia water, eluent d is collected, pH = 7-8 of eluent d is adjusted with hydrochloric acid aqueous solution, then the concentrated solution c is passed through 717 resin column, eluted with potassium chloride aqueous solution, and comprehensive solution e is collected;
S4, separation: nanofiltration of composite liquid e obtained in S3 to obtain concentrated solution f; Adjust the pH = 1-3 of concentrated solution f with nitric acid aqueous solution, add acetone to precipitate, and centrifuge to obtain solid g;
S5, purification: the solid G obtained in S4 is dissolved in water, subjected to preparative chromatography, desalination, separation, collection of separation liquid, concentration, freeze-drying to obtain nicotinamide adenine dinucleotide.
Production method
yeast is extracted in boiling water, lead acetate is acidified and precipitated to obtain crude product, which is treated with formic acid cation exchange resin column and refined.
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