WO2021192683A1 - β－ニコチンアミドモノヌクレオチド又はその薬理学的に許容される塩からなる化合物、並びにその品質評価方法および酵素反応性の判定方法 - Google Patents

β－ニコチンアミドモノヌクレオチド又はその薬理学的に許容される塩からなる化合物、並びにその品質評価方法および酵素反応性の判定方法 Download PDF

Info

Publication number
WO2021192683A1
WO2021192683A1 PCT/JP2021/004912 JP2021004912W WO2021192683A1 WO 2021192683 A1 WO2021192683 A1 WO 2021192683A1 JP 2021004912 W JP2021004912 W JP 2021004912W WO 2021192683 A1 WO2021192683 A1 WO 2021192683A1
Authority
WO
WIPO (PCT)
Prior art keywords
nmn
compound
reactivity
measured
lactate dehydrogenase
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/JP2021/004912
Other languages
English (en)
French (fr)
Japanese (ja)
Inventor
由葵子 竹谷
寛和 松川
美子 砂原
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Oriental Yeast Co Ltd
Original Assignee
Oriental Yeast Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Oriental Yeast Co Ltd filed Critical Oriental Yeast Co Ltd
Priority to CN202180024394.2A priority Critical patent/CN115427422A/zh
Priority to US17/907,346 priority patent/US20230348520A1/en
Priority to JP2022509376A priority patent/JP7648026B2/ja
Publication of WO2021192683A1 publication Critical patent/WO2021192683A1/ja
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Images

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
    • C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
    • C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
    • C07H19/048—Pyridine radicals
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D15/00—Separating processes involving the treatment of liquids with solid sorbents; Apparatus therefor
    • B01D15/08—Selective adsorption, e.g. chromatography
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/46—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
    • C07K14/47—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/26—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving oxidoreductase
    • C12Q1/32—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving oxidoreductase involving dehydrogenase
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Y—ENZYMES
    • C12Y101/00—Oxidoreductases acting on the CH-OH group of donors (1.1)
    • C12Y101/01—Oxidoreductases acting on the CH-OH group of donors (1.1) with NAD+ or NADP+ as acceptor (1.1.1)
    • C12Y101/01027—L-Lactate dehydrogenase (1.1.1.27)

Definitions

  • the present invention relates to a compound consisting of ⁇ -nicotinamide mononucleotide or a pharmacologically acceptable salt thereof, and a method for evaluating the quality thereof and a method for determining enzyme reactivity.
  • ⁇ -NMN The ⁇ -nicotinamide mononucleotide
  • ⁇ -NMN has an effect of improving insulin secretory capacity in aged mice and a dramatic improvement in insulin sensitivity and secretion in a mouse model of type 2 diabetes caused by a high-fat diet and aging (for example,). It has been reported that it is involved in the control of circadianism (see, for example, Patent Document 2), and has an effect of significantly enhancing the mitochondrial function of aged muscles (see Patent Document 1).
  • ⁇ -NMN is useful for improving or preventing symptoms of various age-related diseases such as obesity, increased blood lipid concentration, decreased insulin sensitivity, decreased memory, and deterioration of eye function such as macular degeneration. It has also been reported (see, for example, Patent Document 3). Furthermore, administration of ⁇ -NMN is expected to have an anti-aging effect by increasing the amount of NAD + in the living body and activating the sirtuin gene, thereby suppressing / delaying the decline in physical function associated with aging of the living body. (See, for example, Patent Document 4).
  • the present inventors also refer to ⁇ -nicotinamide mononucleotides produced by themselves and ⁇ -NMN products available on the market as high performance liquid chromatography (hereinafter referred to as “HPLC”). ), Despite the high purity measured in (), and even if crystallized to increase the purity, it was found that the same effect could not be obtained even at the same dose when administered to a living body. That is, since there are ⁇ -NMNs having the same purity as measured by HPLC but different physiological activities, it is necessary to provide ⁇ -NMNs having higher physiological activities.
  • HPLC high performance liquid chromatography
  • the present invention is a compound consisting of ⁇ -nicotinamide mononucleotide or a pharmacologically acceptable salt thereof, which has high purity and high enzymatic reactivity as measured by HPLC, and thus has high physiological activity.
  • a method for evaluating the quality of a compound consisting of ⁇ -nicotinamide mononucleotide or a pharmacologically acceptable salt thereof, and a method for determining enzyme reactivity is a compound consisting of ⁇ -nicotinamide mononucleotide or a pharmacologically acceptable salt thereof, which has high purity and high enzymatic reactivity as measured by HPLC, and thus has high physiological activity.
  • the present inventors have different physiological activities even if the purity measured by HPLC is the same, that is, the enzymatic reactivity of ⁇ -NMN in these products.
  • the present invention has been completed by finding that the above is due to the difference.
  • the present invention is based on the above-mentioned findings of the present inventors, and the means for solving the above-mentioned problems are as follows. That is, ⁇ 1> A compound consisting of ⁇ -nicotinamide mononucleotide or a pharmacologically acceptable salt thereof, having a purity of 95% or more as measured by HPLC and having a reactivity with lactate dehydrogenase of 30. It is a compound characterized by being a unit or more. ⁇ 2> The compound according to ⁇ 1>, which has a purity of 98% or more as measured by HPLC and a reactivity with lactate dehydrogenase of 33 units or more.
  • ⁇ 3> The compound according to ⁇ 1> or ⁇ 2>, which is in crystalline form.
  • ⁇ 4> The compound according to any one of ⁇ 1> to ⁇ 3> above, wherein the lactate dehydrogenase is a lactate dehydrogenase derived from skeletal muscle of mammals.
  • the lactate dehydrogenase is the compound according to ⁇ 4>, which has the amino acid sequence of SEQ ID NO: 1.
  • ⁇ 6> The compound according to any one of ⁇ 1> to ⁇ 5>, which does not substantially contain nicotinamide dinucleotide.
  • ⁇ 7> A method for evaluating the quality of a compound consisting of ⁇ -nicotinamide mononucleotide or a pharmacologically acceptable salt thereof.
  • a method comprising assessing the quality of a compound consisting of.
  • ⁇ 8> A method for determining the enzymatic reactivity of a compound consisting of ⁇ -nicotinamide mononucleotide or a pharmacologically acceptable salt thereof.
  • the ⁇ -nicotinamide mononucleotide or a pharmacologically acceptable salt thereof with the purity as measured by HPLC being 95% or more and the reactivity to lactate dehydrogenase being 30 units or more as an index. It is a method characterized by comprising determining the reactivity of lactate dehydrogenase to lactate dehydrogenase.
  • ⁇ - that can solve the above-mentioned problems in the past, achieve the above-mentioned object, have high purity when measured by HPLC, and show high enzymatic reactivity, thereby having high physiological activity.
  • a method for evaluating the quality of a compound consisting of a nicotinamide mononucleotide or a pharmacologically acceptable salt thereof, and a method for evaluating the quality of a compound consisting of a ⁇ -nicotinamide mononucleotide or a pharmacologically acceptable salt thereof, and a method for determining enzyme reactivity. can be provided.
  • FIG. 1 is a diagram showing the reaction between ⁇ -NMN and lactate dehydrogenase.
  • FIG. 2 is a graph showing the enzyme reactivity of the ⁇ -NMN compound of one example of the present invention measured in Test Example 1 with the lactate dehydrogenase (SEQ ID NO: 1) of a commercially available ⁇ -NMN product.
  • FIG. 3A is a graph showing the enzymatic reactivity of the ⁇ -NMN compound of one example of the present invention measured in Test Example 3 and the commercially available ⁇ -NMN product with lactate dehydrogenase (LDH) 1 (SEQ ID NO: 4) derived from pigs. Is.
  • FIG. 1 is a diagram showing the reaction between ⁇ -NMN and lactate dehydrogenase.
  • FIG. 2 is a graph showing the enzyme reactivity of the ⁇ -NMN compound of one example of the present invention measured in Test Example 1 with the lactate dehydrogenase (SEQ ID NO: 1) of
  • FIG. 3B is a graph showing the enzymatic reactivity of the ⁇ -NMN compound of one example of the present invention measured in Test Example 3 with human-derived lactate dehydrogenase (LDH) 1 (SEQ ID NO: 2) of a commercially available ⁇ -NMN product.
  • FIG. 3C is a graph showing the enzymatic reactivity of the ⁇ -NMN compound of one example of the present invention measured in Test Example 3 with human-derived lactate dehydrogenase (LDH) 5 (SEQ ID NO: 3) of a commercially available ⁇ -NMN product. Is.
  • FIG. 3B is a graph showing the enzymatic reactivity of the ⁇ -NMN compound of one example of the present invention measured in Test Example 3 with human-derived lactate dehydrogenase (LDH) 1 (SEQ ID NO: 2) of a commercially available ⁇ -NMN product.
  • LDH human-derived lactate dehydrogenase
  • FIG. 4A is a graph showing the relative activity values of lactate dehydrogenase (SEQ ID NO: 1) with respect to various concentrations of the ⁇ -NMN compound of the present invention and the commercially available ⁇ -NMN product 1 measured in Test Example 4. be.
  • FIG. 4B is a graph showing the relative activity values of lactate dehydrogenase (SEQ ID NO: 1) with respect to various concentrations of the ⁇ -NMN compound of the present invention and the commercially available ⁇ -NMN product 2 measured in Test Example 4. be.
  • FIG. 4A is a graph showing the relative activity values of lactate dehydrogenase (SEQ ID NO: 1) with respect to various concentrations of the ⁇ -NMN compound of the present invention and the commercially available ⁇ -NMN product 1 measured in Test Example 4. be.
  • FIG. 4C is a graph showing the relative activity values of lactate dehydrogenase (SEQ ID NO: 1) with respect to various concentrations of the ⁇ -NMN compound of the present invention and the commercially available ⁇ -NMN product 3 measured in Test Example 4. be.
  • FIG. 4D shows the relative activity of human-derived lactate dehydrogenase (LDH) 1 (SEQ ID NO: 2) with respect to various concentrations of the ⁇ -NMN compound of the present invention and the commercially available ⁇ -NMN product 1 measured in Test Example 4. It is a graph which showed the value.
  • LDH human-derived lactate dehydrogenase
  • FIG. 4E shows the relative activity of human-derived lactate dehydrogenase (LDH) 1 (SEQ ID NO: 2) with respect to various concentrations of the ⁇ -NMN compound of the present invention and the commercially available ⁇ -NMN product 2 measured in Test Example 4. It is a graph which showed the value.
  • FIG. 4F shows the relative activity of human-derived lactate dehydrogenase (LDH) 1 (SEQ ID NO: 2) with respect to various concentrations of the ⁇ -NMN compound of the present invention and the commercially available ⁇ -NMN product 3 measured in Test Example 4. It is a graph which showed the value.
  • FIG. 5A is a graph showing the cell damage rate determined from the AST activity inside and outside the cell when the ⁇ -NMN compound of one example of the present invention was used, which was measured in Test Example 5.
  • FIG. 5B is a graph showing the cell damage rate determined from the AST activity inside and outside the cell when the ⁇ -NMN product 3 was used, which was measured in Test Example 5.
  • FIG. 6A is a graph showing the intracellular NAD content measured in Test Example 5 when the ⁇ -NMN compound of one example of the present invention was used.
  • FIG. 6B is a graph showing the intracellular NAD content when ⁇ -NMN product 3 was used, which was measured in Test Example 5.
  • the compound of the present invention is a compound consisting of ⁇ -nicotinamide mononucleotide or a pharmacologically acceptable salt thereof, which has a purity of 95% or more as measured by HPLC and a reaction to lactate dehydrogenase.
  • the sex is 30 units or more.
  • ⁇ -nicotinamide mononucleotide There are two types of ⁇ -nicotinamide mononucleotides, ⁇ and ⁇ , as optical isomers.
  • the structure of ⁇ -nicotinamide mononucleotide (CAS number: 1094-61-7) according to the present invention is as follows. Is.
  • ⁇ -NMN compound The compound composed of ⁇ -NMN or a pharmacologically acceptable salt thereof according to the present invention (hereinafter, may be referred to as “ ⁇ -NMN compound”) is prepared by any method. May be good.
  • ⁇ -NMN that has been artificially synthesized by a chemical synthesis method, an enzyme method, a fermentation method, or the like can be used as an active ingredient.
  • ⁇ -NMN is a component widely present in a living body
  • ⁇ -NMN obtained by extracting and purifying from natural raw materials such as animals, plants and microorganisms can also be used as an active ingredient.
  • commercially available purified ⁇ -NMN may be used.
  • ⁇ -NMN As a chemical synthesis method for synthesizing ⁇ -NMN, for example, ⁇ -NMN can be produced by reacting nicotinamide with L-ribose tetraacetate and phosphorylating the obtained nicotinamide mononucleoside. Further, as an enzymatic method, for example, from nicotinamide and 5'-phosphoribosyl-1'-pyrrolic acid (hereinafter, may be referred to as "PRPP”), nicotinamide phosphoribosyl transferase (hereinafter, referred to as "NAMPT").
  • PRPP 5'-phosphoribosyl-1'-pyrrolic acid
  • NAMPT nicotinamide phosphoribosyl transferase
  • ⁇ -NMN can be produced by nicotinamide riboside kinase, and ⁇ -NMN can be produced from nicotinamide riboside by nicotinamide riboside kinase. Further, as a fermentation method, for example, ⁇ -NMN can be produced from nicotinamide by utilizing the metabolic system of a microorganism expressing NAMPT.
  • the ⁇ -NMN may be a pharmacologically acceptable salt.
  • the pharmacologically acceptable salt of ⁇ -NMN may be an inorganic acid salt or an organic acid salt having a basic moiety such as amine.
  • Examples of the acids constituting such acid salts include acetic acid, benzenesulfonic acid, benzoic acid, camphorsulfonic acid, citric acid, ethenesulfonic acid, fumaric acid, gluconic acid, glutamic acid, hydrobromic acid, hydrochloric acid and ISEthione.
  • the pharmacologically acceptable salt of ⁇ -NMN may be an alkaline salt or an organic salt having an acidic moiety such as a carboxylic acid.
  • Examples of the base constituting such an acid salt are alkali metal salts or alkaline earth metal salts, such as sodium hydride, potassium hydroxide, calcium hydroxide, aluminum hydroxide, lithium hydroxide, and magnesium hydroxide.
  • Zinc hydroxide ammonia, trimethylamonia, triethylammonia, ethylenediamine, lysine, arginine, ornithine, choline, N, N'-dibenzylethylenediamine, chloroprocine, procaine, diethanolamine, N-benzylphenethylamine, diethylamine, piperazin, tris ( Those derived from bases such as hydroxymethyl) -aminomethane and tetramethylammonium hydroxide can be mentioned.
  • the ⁇ -NMN compound according to the present invention may be in a crystalline form or in an amorphous form, but in order to suppress the mixing of impurities to a lower level, the stability as a compound is further enhanced. In order to obtain it, it is preferable that it is crystallized by being subjected to a crystallization step using an alcohol-containing solution such as a methanol solution or ethanol.
  • the method for crystallization of the ⁇ -NMN compound is not particularly limited, and a known method can be appropriately selected. For example, the method described in JP-A-2018-534265 or WO 2018/047715 is used. be able to.
  • HPLC purity The purity of the ⁇ -NMN compound according to the present invention is not particularly limited as long as the purity measured by HPLC (hereinafter, may be referred to as “HPLC purity”) is 95% or more, and is appropriately selected. However, 98% or more is preferable.
  • the HPLC analysis method for measuring the HPLC purity is not particularly limited as long as it is a method and conditions capable of efficiently separating and measuring ⁇ -NMN, and can be appropriately selected, for example, as a column.
  • Hypercarb TM length: 15 cm, inner diameter: 4.6 mm, particle size: 3 ⁇ m, manufactured by Thermo Fisher Scientific
  • a TSK-GEL ODS column length: 15 cm, inner diameter: 4.6 mm, particle size: 5 ⁇ m, manufactured by Toso
  • ⁇ Enzyme reactivity> The reactivity of the ⁇ -NMN compound according to the present invention with respect to lactate dehydrogenase (hereinafter, may be referred to as “enzyme reactivity”) is not particularly limited as long as it is 30 units or more, and may be appropriately selected. However, 33 units or more are preferable.
  • the lactate dehydrogenase (hereinafter sometimes referred to as “LDH”) in the present invention is a dehydrogenase also referred to as L-lactate dehydrogenase (EC 1.1.1.27).
  • L-lactate dehydrogenase a lactate dehydrogenase derived from mammalian skeletal muscle is preferable, and a lactate dehydrogenase (LDH) 5 derived from skeletal muscle consisting of a tetramer of a subunit having the amino acid sequence of SEQ ID NO: 1.
  • R-LDH5 mammalian lactate dehydrogenases
  • LDH pig-derived lactate dehydrogenase
  • LH human-derived lactate dehydrogenase
  • LDH uses lactic acid as a substrate to catalyze the dehydrogenation reaction and convert it to pyruvic acid, at which time ⁇ -NMN is converted to reduced ⁇ -NMN (see FIG. 1).
  • enzyme reactivity refers to a value obtained by measuring with the following reagents and methods.
  • ⁇ R1 reagent 80 mM Tris-HCl (pH 8.5) ⁇ 19 mM ⁇ -NMN (It is assumed that the purity of ⁇ -NMN in the measurement sample is 100%.
  • ⁇ -NMN is dissolved in an 80 mM sodium carbonate solution.
  • ⁇ R2 reagent 100 mM Tris-HCl (pH 8.5) ⁇ 100 mM L-lactic acid ⁇ enzyme solution> -Adjust the enzyme solution so that LDH has a final concentration of 245 U / mL in the reaction solution.
  • the activity unit (U) of LDH is the activity unit when NAD is used as a coenzyme, and the activity unit when measured by the IFCC-compliant human LDH measurement method is used.
  • ⁇ Activity measurement> A 7180 Hitachi automatic analyzer (manufactured by Hitachi High-Tech) is used to measure the enzyme activity. The measurement parameters are shown below.
  • -Measurement parameters- ⁇ Analysis method ⁇ ⁇ ⁇ Rate A ⁇ Measurement wavelength (secondary / main) ⁇ ⁇ ⁇ 405nm / 340nm ⁇ Reaction time ⁇ ⁇ ⁇ 10 minutes ⁇ Measurement point ⁇ ⁇ ⁇ 20-24 ⁇ Sample solution (enzyme solution) ⁇ ⁇ ⁇ 18 ⁇ L ⁇ R1 reagent ⁇ ⁇ ⁇ 120 ⁇ L ⁇ R2 reagent ⁇ ⁇ 87 ⁇ L -Measurement procedure- After mixing 18 ⁇ L of the enzyme solution and 120 ⁇ L of the R1 reagent and incubating at 37 ° C.
  • the value of the change in absorbance per minute ( ⁇ mAbs / min) is calculated by subtracting the absorbance of water (blank) at the same photometric point from the absorbance value of the measurement sample 1-2 minutes after the start of the reaction (photometric point 20-24). do.
  • the active unit (unit of reactivity to lactate dehydrogenase R-LDH5) is 0.1 mAbs, which is the value of change in absorbance per minute.
  • the ⁇ -NMN compound according to the present invention does not substantially contain nicotinamide dinucleotide (hereinafter, may be referred to as “NAD”). This is because if NAD is contained, the reactivity to lactate dehydrogenase may not be accurately measured.
  • substantially free of nicotinamide dinucleotide means that NAD in the ⁇ -NMN compound is not detected by the above-mentioned HPLC analysis. It should be noted that the embodiment in which NAD is contained in the preparation or food or drink containing the ⁇ -NMN compound according to the present invention is not excluded.
  • the ⁇ -NMN compound of the present invention not only has high purity when measured by HPLC, but also has high enzymatic reactivity to lactate dehydrogenase. Therefore, it has higher bioavailability than conventional ⁇ -NMN products (drug substances), and is considered to be of high quality as ⁇ -nicotinamide mononucleotides or pharmacologically acceptable salts thereof and products containing them. At the same time, it has a high physiological effect. Therefore, it can be highly effective not only as a medicine containing ⁇ -NMN as an active ingredient, but also as a raw material for foods and drinks (including, but not limited to, supplements) and feeds, or by administering or ingesting the same. ..
  • the method for evaluating the quality of a compound of the present invention is a method for evaluating the quality of a compound consisting of ⁇ -nicotinamide mononucleotide or a pharmacologically acceptable salt thereof, and includes at least an evaluation step, and further a measurement step if necessary. Including other steps such as.
  • ⁇ -nicotinamide is used as an index that the purity as measured by HPLC is 95% or more and the reactivity to lactate dehydrogenase is 30 units or more.
  • This is a step of evaluating the quality of a compound consisting of a mononucleotide or a pharmacologically acceptable salt thereof.
  • the index of purity as measured by HPLC is not particularly limited as long as it is 95% or more, and can be appropriately selected, but 98% or more is preferable.
  • the index of reactivity with the lactate dehydrogenase is not particularly limited as long as it is 30 units or more, and can be appropriately selected, but 33 units or more is preferable.
  • the purity of the compound consisting of ⁇ -nicotinamide mononucleotide or a pharmacologically acceptable salt thereof to be evaluated is 95% or more as measured by HPLC.
  • the reactivity to lactate dehydrogenase is 30 units or more, the quality of the evaluation target is evaluated as good. More specifically, when the purity as measured by HPLC is 95% or more and the reactivity to lactate dehydrogenase is 30 units or more, the evaluation target is ⁇ -nicotinamide having high bioavailability. It is evaluated as a compound consisting of a mononucleotide or a pharmacologically acceptable salt thereof.
  • the purity and reactivity to lactate dehydrogenase as measured by the HPLC may be measured when the method for evaluating the quality of the compound of the present invention is carried out, or may be measured separately.
  • the other steps in the method for evaluating the quality of the compound of the present invention are not particularly limited as long as the effects of the present invention are not impaired, and can be appropriately selected. Examples thereof include a measurement step.
  • the measurement step in the method for evaluating the quality of the compound of the present invention includes the purity of the compound consisting of the ⁇ -nicotinamide mononucleotide to be evaluated or a pharmacologically acceptable salt thereof measured by HPLC and the reaction to lactate dehydrogenase. This is the process of measuring sex.
  • the purity and reactivity to lactate dehydrogenase as measured by the HPLC can be measured in the same manner as described in the items of ⁇ HPLC purity> and ⁇ enzyme reactivity> of the above-mentioned (compound). can.
  • the method for determining the enzyme reactivity of a compound of the present invention is a method for determining the enzyme reactivity of a compound consisting of ⁇ -nicotinamide mononucleotide or a pharmacologically acceptable salt thereof, which includes at least a determination step and is necessary. It further includes other steps depending on the situation.
  • ⁇ is used as an index that the purity as measured by HPLC is 95% or more and the reactivity to lactate dehydrogenase is 30 units or more.
  • the index of purity as measured by HPLC is not particularly limited as long as it is 95% or more, and can be appropriately selected, but 98% or more is preferable.
  • the index of reactivity with the lactate dehydrogenase is not particularly limited as long as it is 30 units or more, and can be appropriately selected, but 33 units or more is preferable.
  • the purity of the compound consisting of the ⁇ -nicotinamide mononucleotide to be determined or a pharmaceutically acceptable salt thereof is 95% when measured by HPLC.
  • the reactivity to lactate dehydrogenase is 30 units or more, it is determined that the enzyme reactivity of the determination target is high. More specifically, when the purity as measured by HPLC is 95% or more and the reactivity to lactate dehydrogenase is 30 units or more, the evaluation target has high reactivity to lactate dehydrogenase.
  • the compound consists of ⁇ -nicotinamide mononucleotide or a pharmacologically acceptable salt thereof.
  • the purity and reactivity to lactate dehydrogenase as measured by the HPLC may be those measured when determining the enzyme reactivity of the compound of the present invention, or those measured separately. May be good.
  • the measurement step in the method for determining the enzyme reactivity of the compound of the present invention is the purity and lactate dehydrogenase measured by HPLC of a compound consisting of ⁇ -nicotinamide mononucleotide to be evaluated or a pharmaceutically acceptable salt thereof.
  • This is a step of measuring the reactivity to an enzyme.
  • the purity and reactivity to lactate dehydrogenase as measured by the HPLC can be measured in the same manner as described in the items of ⁇ HPLC purity> and ⁇ enzyme reactivity> of the above-mentioned (compound). can.
  • bioavailability that cannot be evaluated only by the HPLC purity of ⁇ -nicotinamide mononucleotide or a pharmacologically acceptable salt thereof is evaluated and determined.
  • This can provide a compound consisting of high quality ⁇ -NMN or a pharmacologically acceptable salt thereof.
  • the present invention also includes a method for producing a compound consisting of high-quality ⁇ -NMN or a pharmacologically acceptable salt thereof, which includes a method for evaluating the compound or a method for determining the enzymatic reactivity of the compound. ..
  • ⁇ Crystallization treatment> A 5 mL aqueous solution prepared by mixing water and ethanol at a volume ratio of 1: 2 was weighed in a test tube, and a ⁇ -NMN sample was dissolved therein to prepare a saturated aqueous solution of NMN. Then, when the aqueous solution was allowed to stand at 25 ° C. for 3 days, crystals were precipitated. Subsequently, the solution containing crystals was centrifuged to remove the supernatant. The obtained crystals were suspended in an excess amount of ethanol and then centrifuged to remove the supernatant. Subsequently, crystals were obtained by heating and drying at 60 ° C. for 1 hour.
  • Test Example 1 In addition to the ⁇ -NMN compound produced in Production Example 1, the following ⁇ -NMN products that are commercially available and have been subjected to crystallization treatment were used in this test example.
  • ⁇ ⁇ -NMN product 1 Fermented product, manufactured by company A
  • ⁇ ⁇ -NMN product 2 chemically synthesized product, manufactured by company A
  • ⁇ ⁇ -NMN product 3 manufactured by company B
  • HPLC purity measurement The HPLC system Prominence (manufactured by Shimadzu Corporation) was used as the HPLC equipment.
  • ⁇ -NMN sample was dissolved in distilled water so as to have a concentration of 2 mM, and this was used as a sample solution.
  • -Applied 10 ⁇ L of the sample solution to a TSK-GEL ODS-80TS column (length: 15 cm, inner diameter: 4.6 mm, particle size: 5 ⁇ m, manufactured by Tosoh Corporation).
  • -Separation of the ⁇ -NMN fraction adsorbed on the column was carried out by the following method.
  • Test Example 2 For the ⁇ -NMN compounds produced in Production Examples 2 to 4, HPLC purity and enzyme reactivity were measured by the same method as in Test Example 1. As a result, it was confirmed that the ⁇ -NMN compound of the present invention has high HPLC purity and high enzyme reactivity even when raw materials having different production lots are used. The results are shown in Table 2 below together with the test results of Production Example 1. The measurement result is an average value obtained three times. In each of the ⁇ -NMN compounds of Production Examples 2 to 4, no peak of NAD was observed by HPLC, and the ⁇ -NMN compounds were substantially free of NAD.
  • Test Example 3 ⁇ Evaluation of enzyme reactivity with LDH derived from other animal species>
  • the ⁇ -NMN compound produced in Production Example 1 and the same ⁇ -NMN products 1 to 3 used in Test Example 1 are used.
  • the enzyme reactivity with LDH ((A) pig-derived LDH1, (B) human-derived LDH1, (C) human-derived LDH5) was evaluated.
  • the evaluation of the enzyme reactivity was carried out in the same manner as in Test Example 1 except that the following enzyme solution was used.
  • FIGS. 3A to 3C FIGS. 3A: pig-derived LDH1, FIG. 3B: human-derived LDH1, FIG.
  • 3C human-derived LDH5).
  • -Enzyme solution- (A) Pig-derived LDH1 The enzyme solution was adjusted so that the LDH had a final concentration of 45 U / mL in the reaction solution. (B) Human-derived LDH1 The enzyme solution was adjusted so that the LDH had a final concentration of 45 U / mL in the reaction solution. (C) Human-derived LDH5 The enzyme solution was adjusted so that the LDH had a final concentration of 245 U / mL in the reaction solution.
  • Test Example 4 ⁇ -NMN compound concentration dependence of LDH activity value>
  • the R1 reagent was used with the ⁇ -NMN compound produced in Production Example 1 and the same ⁇ -NMN products 1 to 3 used in Test Example 1.
  • the enzyme activity of LDH was measured by changing the ⁇ -NMN concentration in the mixture.
  • the enzyme activity of LDH was measured in the same manner as in [Enzyme reactivity evaluation] of Test Example 1 except that the following R1 reagent and enzyme solution were used, and the value of change in absorbance per minute ( ⁇ mAbs / min). was calculated.
  • FIGS. 4A to 4F the relative activity value (%) of each concentration in each NMN was shown in FIGS. 4A to 4F (FIGS. 4A to C: R-LDH5, FIGS. 4D to F: Human-derived LDH1).
  • the measurement result is an average value obtained three times.
  • ⁇ -NMN was dissolved in a 100 mM sodium carbonate solution.
  • -Enzyme solution- R-LDH5 The enzyme solution was adjusted so that the LDH had a final concentration of 245 U / mL in the reaction solution.
  • the ⁇ -NMN compounds of Production Example 1 and ⁇ -NMN product 3 were added so that the final concentrations were 0 and 0.1 mM, respectively, and 7 in a CO 2 incubator at 37 ° C. without changing the medium. It was shake-cultured for a day. After 7 days of shaking culture, cells and culture supernatant were collected for various analyses.
  • L-type Wako AST / J2 manufactured by Fujifilm Wako Pure Chemical Industries, Ltd. was used for intracellular and extracellular aspartate aminotransferase (AST) activity to detect deviation enzymes, and the reagent was specified.
  • the measurement was performed with a 7180 type Hitachi automatic analyzer (manufactured by Hitachi High-Tech).
  • NAD was detected using a NAD / NADH measurement kit (manufactured by Dojin Chemical Research Institute). Specifically, the weight of the collected cells was measured, and the NAD was measured for the cells extracted with the Extension buffer attached to the kit. The intracellular NAD content was calculated from the calibration curve obtained by measuring the NAD solution at each concentration.
  • FIG. 5A shows the cytotoxicity obtained from the AST activity inside and outside each cell when the ⁇ -NMN compound of Production Example 1 was used
  • FIG. 5B shows the cytotoxicity obtained from the AST activity inside and outside each cell when the ⁇ -NMN compound of ⁇ -NMN product 3 was used. The rate was shown.
  • FIG. 6A shows the intracellular NAD content when the ⁇ -NMN compound of Production Example 1 was used
  • FIG. 6B shows the intracellular NAD content when the ⁇ -NMN compound of ⁇ -NMN product 3 was used.
  • the rate of cell damage due to nutrient depletion associated with culturing for 7 days without changing the medium was higher when the ⁇ -NMN compound of Production Example 1 was added than in the ⁇ -NMN of ⁇ -NMN product 3.
  • the intracellular NAD content was lower when the compound was added, and the intracellular NAD content was higher when the ⁇ -NMN compound of Production Example 1 was added than when the ⁇ -NMN compound of ⁇ -NMN product 3 was added. ..

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Molecular Biology (AREA)
  • Zoology (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Biochemistry (AREA)
  • Biotechnology (AREA)
  • Wood Science & Technology (AREA)
  • Analytical Chemistry (AREA)
  • Biophysics (AREA)
  • General Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Physics & Mathematics (AREA)
  • Immunology (AREA)
  • Microbiology (AREA)
  • Medicinal Chemistry (AREA)
  • Toxicology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
PCT/JP2021/004912 2020-03-27 2021-02-10 β－ニコチンアミドモノヌクレオチド又はその薬理学的に許容される塩からなる化合物、並びにその品質評価方法および酵素反応性の判定方法 Ceased WO2021192683A1 (ja)

Priority Applications (3)

Application Number Priority Date Filing Date Title
CN202180024394.2A CN115427422A (zh) 2020-03-27 2021-02-10 包含β-烟酰胺单核苷酸或其药理学上所容许的盐的化合物、以及其品质评估方法及酶反应性的判定方法
US17/907,346 US20230348520A1 (en) 2020-03-27 2021-02-10 Compound comprising beta-nicotinamide mononucleotide or pharmacologically acceptable salt thereof, and method for evaluating quality and method for assessing enzymatic reactivity of said compound
JP2022509376A JP7648026B2 (ja) 2020-03-27 2021-02-10 β－ニコチンアミドモノヌクレオチド又はその薬理学的に許容される塩からなる化合物を含む組成物、並びにその品質評価方法および酵素反応性の判定方法

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2020-058429 2020-03-27
JP2020058429 2020-03-27

Publications (1)

Publication Number Publication Date
WO2021192683A1 true WO2021192683A1 (ja) 2021-09-30

Family

ID=77891415

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2021/004912 Ceased WO2021192683A1 (ja) 2020-03-27 2021-02-10 β－ニコチンアミドモノヌクレオチド又はその薬理学的に許容される塩からなる化合物、並びにその品質評価方法および酵素反応性の判定方法

Country Status (4)

Country Link
US (1) US20230348520A1 (https=)
JP (1) JP7648026B2 (https=)
CN (1) CN115427422A (https=)
WO (1) WO2021192683A1 (https=)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2023145872A1 (ja) * 2022-01-28 2023-08-03 オリエンタル酵母工業株式会社 ニコチンアミドアデニンジヌクレオチドの安定化方法及び安定化用組成物

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2017504616A (ja) * 2015-03-16 2017-02-09 邦泰生物工程（深▲セン▼）有限公司 β−ニコチンアミドモノヌクレオチドの精製方法
WO2018047715A1 (ja) * 2016-09-06 2018-03-15 協和発酵バイオ株式会社 β－ニコチンアミドモノヌクレオチドの結晶及びその製造方法
JP2018534265A (ja) * 2015-10-02 2018-11-22 メトロ インターナショナル バイオテック，エルエルシー β−ニコチンアミドモノヌクレオチドの結晶形態
JP2019525760A (ja) * 2016-07-30 2019-09-12 邦泰生物工程（深▲セン▼）有限公司 ニコチンアミドホスホリボシルトランスフェラーゼ突然変異体及びその応用

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101601679B (zh) * 2009-03-17 2011-08-10 中国人民解放军第二军医大学 一种烟酰胺单核苷酸的应用
CN106659729A (zh) * 2015-12-11 2017-05-10 邦泰生物工程(深圳)有限公司 烟酰胺单核苷酸在制备防治动脉硬化、心脑血管疾病的药物中的应用及其药物
WO2018023205A1 (zh) * 2016-07-30 2018-02-08 邦泰生物工程(深圳)有限公司 一种烟酰胺单核苷酸的纯化方法
CN106755209B (zh) * 2016-12-29 2021-07-23 苏州汉酶生物技术有限公司 一种酶法制备β-烟酰胺单核苷酸的方法
US11634690B2 (en) * 2017-01-31 2023-04-25 Oriental Yeast Co., Ltd. Agent for accelerating growth of pluripotent stem cells

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2017504616A (ja) * 2015-03-16 2017-02-09 邦泰生物工程（深▲セン▼）有限公司 β−ニコチンアミドモノヌクレオチドの精製方法
JP2018534265A (ja) * 2015-10-02 2018-11-22 メトロ インターナショナル バイオテック，エルエルシー β−ニコチンアミドモノヌクレオチドの結晶形態
JP2019525760A (ja) * 2016-07-30 2019-09-12 邦泰生物工程（深▲セン▼）有限公司 ニコチンアミドホスホリボシルトランスフェラーゼ突然変異体及びその応用
WO2018047715A1 (ja) * 2016-09-06 2018-03-15 協和発酵バイオ株式会社 β－ニコチンアミドモノヌクレオチドの結晶及びその製造方法

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
MCPHERSON ALEXANDER JR.: "Interaction of lactate dehydrogenase with its coenzyme, Nicotinamide-adenine dinucleotide", JOURNAL OF MOLECULAR BIOLOGY, vol. 51, no. 1, 1970, pages 39 - 46, XP024015008, DOI: 10.1016/0022-2836(70)90268-8 *

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2023145872A1 (ja) * 2022-01-28 2023-08-03 オリエンタル酵母工業株式会社 ニコチンアミドアデニンジヌクレオチドの安定化方法及び安定化用組成物
JPWO2023145872A1 (https=) * 2022-01-28 2023-08-03
JP7809729B2 (ja) 2022-01-28 2026-02-02 オリエンタル酵母工業株式会社 ニコチンアミドアデニンジヌクレオチドの安定化方法及び安定化用組成物

Also Published As

Publication number Publication date
CN115427422A (zh) 2022-12-02
JPWO2021192683A1 (https=) 2021-09-30
JP7648026B2 (ja) 2025-03-18
US20230348520A1 (en) 2023-11-02

Similar Documents

Publication Publication Date Title
JP7658528B2 (ja) 還元型β－ニコチンアミドモノヌクレオチド又はその薬理学的に許容される塩からなる還元型β－ニコチンアミドアデニンジヌクレオチド前駆体化合物を含む組成物、並びにその品質評価方法および酵素反応性の判定方法
CN102812119B (zh) 酵母培养方法
JP2005520515A (ja) セレン酵母製品、セレン酵母製品を調製する方法、および食品、栄養補助食品または薬剤を調製するための製品の使用
Krassner Proline metabolism in Leishmania tarentolae
JP7648026B2 (ja) β－ニコチンアミドモノヌクレオチド又はその薬理学的に許容される塩からなる化合物を含む組成物、並びにその品質評価方法および酵素反応性の判定方法
Mayeur et al. Effects of agmatine accumulation in human colon carcinoma cells on polyamine metabolism, DNA synthesis and the cell cycle
JP2005029571A (ja) ＤＮＡ合成酵素λ阻害作用を有する化合物とその利用
US9700629B2 (en) Composition containing S-adenosyl-L-methionine with excellent storage stability
DK2557151T3 (en) S-adenosyl-L-methionine-containing dry yeast composition with excellent storage stability and process for preparing the same
TWI627278B (zh) 生產l-組胺酸之麩胺酸棒狀桿菌變異株與使用其生產l-組胺酸之方法
CN109310725A (zh) 具有糖尿病预防效果的酵母提取物
Bonnen et al. Germination physiology ofNeurospora crassa conidia
JP6887663B2 (ja) アグマチンの製造方法及びその利用
Skinner et al. Mutants of Aspergillus nidulans lacking pyruvate carboxylase
EP4345103A1 (en) Thiazole-lactam-spiroheterocyclic compounds and applications thereof
CN101250563A (zh) 添加α-酮戊二酸脱氢酶抑制剂实现α-酮戊二酸过量积累的方法
Zeng et al. Transcriptome and metabolome integration analysis reveals the effect of citric acid on cell metabolism in Aureobasidium pullulans NG
Delaunay et al. Glutamate as an inhibitor of phosphoenolpyruvate carboxylase activity in Corynebacterium glutamicum
AU2023254626A1 (en) eNAMPT INCREASING AGENT, SIRTUIN ACTIVATION OR EXPRESSION ENHANCER, NAD+ INCREASING AGENT, AND SENESCENT CELL INHIBITOR
CN101781625B (zh) 一株乙硫氨酸抗性产朊假丝酵母及其应用
Nimmanwudipong et al. Determination of intramolecular 13C isotope distribution of pyruvate by headspace solid phase microextraction-gas chromatography-pyrolysis-gas chromatography-combustion-isotope ratio mass spectrometry (HS-SPMEGC-Py-GC-C-IRMS) method
WO2022050230A1 (ja) アデノシン受容体の活性化を抑制する組成物
JP2006042637A (ja) 酵母変異株、グルタチオン高含有酵母の製造方法、その培養物、その分画物、酵母エキスおよびグルタチオン含有飲食品
US20030144345A1 (en) Treatment of metabolic diseases with soraphen derivatives
YAMANOI et al. STUDIES ON INOSINE FERMENTATION-PRODUCTION OF INOSINE BY MUTANTS OF BACILLUS SUBTILIS V. SPECIFIC REQUIREMENT OF ADENINE FOR REGULATION OF INOSINE FORMATION AND ADENINE-SPARING ACTION OF AICA AND AMINO ACID MIXTURE

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 21777141

Country of ref document: EP

Kind code of ref document: A1

ENP Entry into the national phase

Ref document number: 2022509376

Country of ref document: JP

Kind code of ref document: A

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 21777141

Country of ref document: EP

Kind code of ref document: A1