基本情報
- 標準SMILES
Cc1ncc(COP(=O)(O)O)c(C=O)c1O- InChIKey
NGVDGCNFYWLIFO-UHFFFAOYSA-N- 分子式
- C8H10NO6P
- 平均分子量
- 247.14 g/mol
- 単同位体質量
- 247.02457367
概要
Pyridoxal 5'-phosphate is the monophosphate ester obtained by condensation of phosphoric acid with the primary hydroxy group of pyridoxal. It has a role as an EC 2.7.7.7 (DNA-directed DNA polymerase) inhibitor, a coenzyme, a cofactor, a mouse metabolite, a Saccharomyces cerevisiae metabolite, an Escherichia coli metabolite and a human metabolite. It is a member of methylpyridines, a vitamin B6 phosphate, a monohydroxypyridine and a pyridinecarbaldehyde. It is functionally related to a pyridoxal. It is a conjugate acid of a pyridoxal 5'-phosphate(2-).
名称と識別子
- 優先名称
- Pyridoxal 5'-phosphate
- IUPAC
- (4-formyl-5-hydroxy-6-methyl-3-pyridinyl)methyl dihydrogen phosphate
- 現地名
- りん酸(4-ホルミル-5-ヒドロキシ-6-メチル-3-ピリジニル)メチル
- 英語名
- Pyridoxal phosphate
- 分子式
- C8H10NO6P
- 分子量
- 247.14
名称と別名
名称をさらに表示
データベース識別子
- CAS
54-47-7- PubChem CID
- 1051
- DTXSID
DTXSID4048351- ChEMBL
CHEMBL3181870、CHEMBL82202- ChEBI
CHEBI:18405- UNII
- F06SGE49M6
- EC Number
- 200-208-3
- Nikkaji
- J10.690I
物性
構造計算による物性
- XLogP
- -1.1
- 極性表面積
- 117 Ų
- 水素結合供与体数
- 3
- 水素結合受容体数
- 7
- 回転可能結合数
- 4
- 重原子数
- 16
- 形式電荷
- 0
- 複雑度
- 292
実験および物理化学的性質
Drugs
Pharmaceuticals -> Listed in ZINC15
Pharmaceuticals
Solubility
Appreciable
28 mg/mL
Physical Description
Light yellow powder; [Acros Organics MSDS]
Solid
Collision Cross Section
153.2 Ų [M+Na-2H]- [CCS Type: DT; Method: single field calibrated with ESI Low Concentration Tuning Mix (Agilent)]
150.8 Ų [M-H]- [CCS Type: DT; Method: stepped-field]
151.4 Ų [M+H]+ [CCS Type: DT; Method: single field calibrated with Agilent tune mix (Agilent)]
165.05 Ų [M+Na]+ [CCS Type: DT; Method: stepped-field]
152.4 Ų [M+H]+
物理化学的性質
- 融点
- 140 · 140-143 °C
- 沸点
- 565.7 · 565.7±60.0 °C(Predicted)
- 比重(密度)
- 1.638 · 1.638±0.06 g/cm3(Predicted)
- 貯蔵温度
- -20 °C · Inert atmosphere,Store in freezer, under -20°C
- 溶解性
- DMSO (Slightly, Heated), Methanol (Slightly), Water (Slightly)
- 酸解離定数(Pka)
- 1.56 · 1.56±0.10(Predicted)
- 外見
- 粉
- 色
- Off-white to yellow
- 安定性
- Hygroscopic
- 主な用途
- 臨床検査
- 化粧品成分の機能
- スキンコンディショニング
- InChI
- InChI=1S/C8H10NO6P/c1-5-8(11)7(3-10)6(2-9-5)4-15-16(12,13)14/h2-3,11H,4H2,1H3,(H2,12,13,14)
- InChIKey
- NGVDGCNFYWLIFO-UHFFFAOYSA-N
- SMILES
- C1(C)=NC=C(COP(O)(O)=O)C(C=O)=C1O
- LogP
- -1.921 · -1.921 (est)
- CAS データベース
- 54 · 54-47-7(CAS DataBase Reference)
- EPAの化学物質情報
- 4 · 4-Pyridinecarboxaldehyde, 3-hydroxy-2-methyl-5-[(phosphonooxy)methyl]- (54-47-7)
化学的性質
化学的特性Pyridoxal phosphate is a white, odourless crystalline powder that turns bright yellow in alkaline solutions. Its aqueous solution remains stable at low temperatures and in the absence of light but decomposes gradually when exposed to light. It is soluble in formic acid, aqueous pyridine, and dilute alkaline solutions, with limited solubility in organic solvents such as water, ethanol, acetone, chloroform, and ether. The oral LD50 in rats is 5900 mg/kg.
安全と法規制
GHS分類
GHS Classification
This chemical does not meet GHS hazard criteria for 66.7% (4 of 6) of all reports.
Warning
H319 (33.3%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]
P264+P265, P280, P305+P351+P338, and P337+P317 (click each P-code to see the statement)
Aggregated GHS information provided per 6 reports by companies from 2 notifications to the ECHA C&L Inventory.
危険有害性情報
Regulatory Information
Chemical: 4-Pyridinecarboxaldehyde, 3-hydroxy-2-methyl-5-[(phosphonooxy)methyl]-
Regulation (EC) No 178/2002 (amended)
毒性情報
Drug Induced Liver Injury
Drug-Induced Liver Injury Severity and Toxicity (DILIst)
pyridoxal phosphate
DILI Negative
Oral
DOI:10.1016/j.drudis.2019.09.022
安全データ
- F
- 8-10-23
- wgk
- 3
- tsca
- TSCA listed
- hs_code
- 29362500
- safety_code
- 22-24/25
- Hazard Classifications
- Eye Irrit. 2Flam. Liq. 2
- ストレージクラス
- 3 - Flammable liquids
化学と産業
薬理情報
ATC Code
A - Alimentary tract and metabolism
QA - Alimentary tract and metabolism
Pharmacodynamics
The two major forms of vitamin B6 are pyridoxine and pyridoxamine. In the liver they are converted to pyridoxal phosphate (PLP) which is a cofactor in many reactions of amino acid metabolism. PLP also is necessary for the enzymatic reaction governing the release of glucose from glycogen. Pyroluria is one potential cause of vitamin B6 deficiency.
Mechanism of Action
Pyridoxal Phosphate is a coenzyme of many enzymatic reactions. It is the active form of vitamin B6 which comprises three natural organic compounds, pyridoxal, pyridoxamine and pyridoxine. Pyridoxal phosphate acts as a coenzyme in all transamination reactions, and in some oxylation and deamination reactions of amino acids. The aldehyde group of pyridoxal phosphate forms a Schiff-base linkage with the epsilon-amino group of a specific lysine group of the aminotransferase enzyme. The alpha-amino group of the amino acid substrate displaces the epsilon-amino group of the active-site lysine residue. The resulting aldimine becomes deprotonated to become a quinoid intermediate, which in turn accepts a proton at a different position to become a ketimine. Ketimine becomes hydrolyzed so that the amino group remains on the protein complex.
MC-1 is a biologically active natural product which can be regarded as a chemical entity that has been evolutionarily selected and validated for binding to particular protein domains. Thus, its underlying structural architecture, or scaffold, has already been biologically established as safe and active, providing a powerful guiding principle for novel drug and library development.
用途と製造
応用分野
解説アミノ酸代謝の酵素の補酵素.基質であるアミノ酸はピリドキサールリン酸のオキソ基との間でシッフ塩基を形成し,酵素の活性中心に結合する.ビタミンB6から体内で合成される.
使用Vitamin (enzyme co-factor).
調製方法
製造方法Synthesis of Pyridoxal Phosphate: Pyridoxal phosphate is synthesized from pyridoxine. Initially, pyridoxamine dihydrochloride is reacted with anhydrous phosphoric acid to produce pyridoxamine phosphate. This intermediate is then oxidized with manganese dioxide to yield pyridoxal phosphate.
純化方法PLP has been purified by dissolving 2g in H2O (10-15mL, in a dialysis bag a third full) and dialysing with gentle stirring against 1L of H2O (+ two drops of toluene) for 15hours in a cold room. The dialysate is evaporated to 80-100mL, then lyophilised. Lemon yellow microscopic needles of the monohydrate remain when all the ice crystals have been removed. The purity is checked by paper chromatography (in EtOH or n-PrOH/NH3) and the spot(s) visualised under UV light after reaction with a spray of p-phenylene diamine, NH3 and molybdate. Solutions stored in a freezer are 2-3% hydrolysed in 3weeks. At 25o, only 4-6% hydrolysis occurs even in N NaOH or HCl, and 2% is hydrolysed at 37o in 1day-but is complete at 100o in 4hours. It is best stored as a dry solid at -20o. In aqueous acid the solution is colourless but is yellow in alkaline solutions. It has UV max at 305nm ( 1100) and 380nm ( 6550) in 0.1 N NaOH; 330nm ( 2450) and 388nm ( 4,900) in 0.05M phosphate buffer pH 7.0 and 295nm ( 6700) in 0.1N HCl. [Peterson et al. Biochemical Preparations 3 34, 119 1953.] The oxime decomposes at 229-230o and is practically insoluble in H2O, EtOH and Et2O. The O-methyloxime decomposes at 212-213o. [Heyl et al. J Am Chem Soc 73 3430 1951.] It has also been purified by column chromatography through Amberlite IRC-50 (H+) [Peterson & Sober J Am Chem Soc 76 169 1954]. [Beilstein 21/13 V 46.]
上流・下流製品情報
上流原料
下流製品
サプライヤー50 社
補足説明
定義本品は、次の化学式で表される複素環式化合物である。
定義Pyridoxal Phosphate also known as PLP, pyridoxal 5'-phosphate or P5P, is the active form of vitamin B6 and a coenzyme for many pyridoxal phosphate (PLP)-dependent enzymes. PLP is involved in numerous enzymatic transamination, decarboxylation and deamination reactions; it is necessary for the synthesis of amino acids and amino acid metabolites, and for the synthesis and/or catabolism of certain neurotransmitters, including the conversion of glutamate into gamma-aminobutyric acid (GABA) and levodopa into dopamine. PLP can be used as a dietary supplement in cases of vitamin B6 deficiency. Reduced levels of PLP in the brain can cause neurological dysfunction.
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