Do I need a prescription for Pyridoxal phosphate 25mg tablets?

Pyridoxal phosphate 25mg tablets is classified as a Valid as a prescribable product in the UK. However, always consult a pharmacist or doctor before use. (Source: NHS dm+d)

What are the brand names for Pyridoxal phosphate 25mg tablets?

Pyridoxal phosphate 25mg tablets is the generic name. It is available under brand names including: Adoxal 25mg tablets, Vitamin B6 25mg tablets. (Source: NHS dm+d — Actual Medicinal Products)

Pyridoxal phosphate 25mg tablets

Tablet

25mg

Oral

This is the active form of vitamin B6 serving as a coenzyme for synthesis of amino acids, neurotransmitters (serotonin, norepinephrine), sphingolipids, aminolevulinic acid.

Active ingredients:

Pyridoxal phosphate

ATC classificationBrowse ATC index

International classification by the WHO, grouping medicines by the organ system they act on

ATC A11HA06

Chemical classBrowse classes

Classification based on the molecule's chemical structure and properties

Check interactions for Pyridoxal phosphate

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Safety monitoring data

Yellow Card reports

MHRA

The MHRA Yellow Card scheme collects reports of suspected side effects from healthcare professionals and patients. View the Drug Analysis Profile (iDAP) for real-world adverse reaction data.

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Data from the MHRA Yellow Card scheme. A reported reaction does not necessarily mean the medicine caused it. Contains public sector information licensed under the Open Government Licence v3.0.

EudraVigilance

EMA

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EudraVigilance data is published by the European Medicines Agency (EMA). A suspected adverse reaction is not necessarily caused by the medicine.

2 branded products available

2 products

Possibly available on the UK marketDiscontinuedAvailability per NHS dm+d

MHRA licensed products

View all licensed products for Pyridoxal phosphate on the MHRA register

Adoxal 25mg tablets

Essential-Healthcare Ltd

None

Vitamin B6 25mg tablets

Nutri Advanced Ltd

None

Source: NHS dm+dOGL 3.0

Updated 4 months ago(1 Mar 2026)

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Nicotinamide 50mg capsules

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Biotin 900microgram capsules

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Similarity is based on WHO Anatomical Therapeutic Chemical (ATC) classification and on a factual NHS dm+d therapeutic-grouping code prefix. Source data: NHS dm+d via TRUD (OGL v3.0), WHO ATC/DDD Index.

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Guidelines from the National Institute for Health and Care Excellence

NICE clinical guidance(1)

Eladocagene exuparvovec for treating aromatic L-amino acid decarboxylase deficiency (HST26)

HST26

Highly specialised technology

Updated Apr 2023

Source: National Institute for Health and Care Excellence (NICE). Contains public sector information licensed under the Open Government Licence v3.0.

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Pharmacy links redirect to the retailer's own search and do not represent real-time stock levels. Shortage and safety information sourced from MHRA drug safety updates (gov.uk, Crown Copyright under OGL v3.0).

Codes for healthcare professionals and prescribing systems

These codes are used by healthcare IT systems and prescribers to identify this medicine.

NHS UK identifiers

SNOMED CT

43170611000001104

dm+d ID

43170611000001104

VTM (Virtual Therapeutic Moiety)

13295901000001106

VMP (Virtual Medicinal Product)

43170611000001104

BNF code (NHS dm+d)

09060208

International identifiers

ATC code — Anatomical Therapeutic Chemical (WHO)

A11HA06

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NHSBSA medicines dictionary lookup

SNOMED CT and dm+d codes from NHS TRUD (Technology Reference data Update Distribution), licensed under the Open Government Licence v3.0. BNF code shown is the factual mapping value distributed by NHS Business Services Authority (NHSBSA) in the dm+d supplementary file under OGL v3.0; it is not affiliated with, nor licensed from, the publishers of the British National Formulary. ATC codes from the WHO Collaborating Centre for Drug Statistics Methodology (whocc.no).

Active and completed clinical studies from ClinicalTrials.gov

Searching UK clinical trials...

Source: ClinicalTrials.gov, a database of the U.S. National Library of Medicine (NLM), National Institutes of Health (NIH). Data accessed via ClinicalTrials.gov API v2. Trial information is provided for research purposes and does not constitute medical advice.

Academic studies and reviews for this medicine's active substance

Showing the 50 most relevant studies.

Reviews & meta-analyses: 20 · 1945–2025

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Pyridoxal Phosphate Enzymes: Mechanistic, Structural, and Evolutionary Considerations

Andrew C. Eliot, Jack F. Kirsch

Annual Review of Biochemistry, 2004

Review

Highly cited for its field

Cited by 940

Enzyme Inhibitors
Enzymes
Models, Molecular

A genomic overview of pyridoxal‐phosphate‐dependent enzymes

Riccardo Percudani, Alessio Peracchi

EMBO Reports, 2003

Review

Cited by 556

Enzymes
Pyridoxal Phosphate
Substrate Specificity

Reaction specificity in pyridoxal phosphate enzymes

Michael D. Toney

Archives of Biochemistry and Biophysics, 2004

Review

Highly cited for its field

Cited by 274

Alanine Racemase
Binding Sites
Carboxy-Lyases

Current Advances on Structure-Function Relationships of Pyridoxal 5′-Phosphate-Dependent Enzymes

Jing Liang, Q. Han, Yang Tan, et al.

Frontiers in Molecular Biosciences, 2019

Review

Cited by 155

Controlling reaction specificity in pyridoxal phosphate enzymes

Michael D. Toney

Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics, 2011

Review

Highly cited for its field

Cited by 184

Enzymes
Glycine
Models, Molecular

Pyridoxal phosphate-dependent reactions in the biosynthesis of natural products

Yi‐Ling Du, Katherine S. Ryan

Natural Product Reports, 2018

Review

Highly cited for its field

Cited by 143

Biological Products
Imidazoles
Lactams

Phylogenetic analyses and comparative genomics of vitamin B6 (pyridoxine) and pyridoxal phosphate biosynthesis pathways.

G. Mittenhuber

Journal of molecular microbiology and biotechnology, 2001

Review

Highly cited for its field

Cited by 183

Ligases
Oxidoreductases
Escherichia coli Proteins

Stereoselective amino acid synthesis by synergistic photoredox-pyridoxal radical biocatalysis

Lei Cheng, Dian Li, Binh Khanh Mai, et al.

Science, 2023

Cited by 164

Hyperhomocysteinemia and low pyridoxal phosphate. Common and independent reversible risk factors for coronary artery disease.

K. Robinson, E. Mayer, David P Miller, et al.

Circulation, 1995

Highly cited for its field

Cited by 412

Age Factors
Coronary Artery Disease
Folic Acid Deficiency

Evolutionary relationships among pyridoxal‐5′‐phosphate‐dependent enzymes

Frederick W. ALEXANDER, Erika Sandmeier, Perdeep K. Mehta, et al.

European Journal of Biochemistry, 1994

Highly cited for its field

Cited by 373

Biological Evolution
Amino Acid Sequence
Enzymes

Sources: aggregated from Europe PMC (EMBL-EBI), OpenAlex, Crossref, PubMed and other open scholarly databases. Retracted articles are excluded. Study information is provided for research purposes and does not constitute medical advice.

Pharmacology and chemical data from DrugBank

go.drugbank.com

Key facts

Drug status

Approved

Major interactions

None known

Half-life

Not available

Mechanism

Pyridoxal Phosphate is a coenzyme of many enzymatic reactions.

Food interactions

None known

Human targets

55 targets

Data: DrugBank · CC BY-NC 4.0

Pharmacokinetics at a glance

Status:

Approved

Investigational

Nutraceutical

Small molecule

About this compound

This is the active form of vitamin B6 serving as a coenzyme for synthesis of amino acids, neurotransmitters (serotonin, norepinephrine), sphingolipids, aminolevulinic acid. During transamination of amino acids, pyridoxal phosphate is transiently converted into pyridoxamine phosphate (pyridoxamine).

Properties:

solid

Avg. mass: 247.14 Da

DrugBank indication

For nutritional supplementation and for treating dietary shortage or imbalance.

Also known as(345)

3-hydroxy-2-methyl-5-((phosphonooxy)methyl)-4-pyridinecarboxaldehyde

3-hydroxy-5-(hydroxymethyl)-2-methylisonicotinaldehyde 5-phosphate

Codecarboxylase

PLP

Pyridoxal 5-monophosphoric acid ester

Pyridoxal 5-phosphate

Pyridoxal 5'-phosphate

Pyridoxal P

Molecular properties(19)

How it works

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.

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.

Drug targets(55)

Proteins and enzymes this drug interacts with in the body

4-aminobutyrate aminotransferase, mitochondrial

BE0000253

ABAT

inhibitor

Specific function(S)-3-amino-2-methylpropionate transaminase activity

Cellular location

Mitochondrion matrix

General function & pharmacology

Catalyzes the conversion of gamma-aminobutyrate and L-beta-aminoisobutyrate to succinate semialdehyde and methylmalonate semialdehyde, respectively .
PMID:10407778 PMID:15528998
Can also convert delta-aminovalerate and beta-alanine (By similarity)

Prothrombin

BE0000048

inhibitor

Specific functioncalcium ion binding

Cellular location

Secreted, extracellular space

General function & pharmacology

Thrombin, which cleaves bonds after Arg and Lys, converts fibrinogen to fibrin and activates factors V, VII, VIII, XIII, and, in complex with thrombomodulin, protein C. Functions in blood homeostasis, inflammation and wound healing. Activates coagulation factor XI (F11); activation is promoted by the contact with negatively charged surfaces .
PMID:2019570 PMID:21976677
Triggers the production of pro-inflammatory cytokines, such as MCP-1/CCL2 and IL8/CXCL8, in endothelial cells PMID:30568593 PMID:9780208

Alanine--glyoxylate aminotransferase 2, mitochondrial

BE0000102

AGXT2

cofactor

Specific function(R)-3-amino-2-methylpropionate-pyruvate transaminase activity

Cellular location

Mitochondrion

General function & pharmacology

Multifunctional aminotransferase with a broad substrate specificity .
PMID:20018850 PMID:23023372 PMID:24586340

Catalyzes the conversion of glyoxylate to glycine using alanine as the amino donor (By similarity). Catalyzes metabolism of not L- but the D-isomer of D-beta-aminoisobutyric acid to generate 2-methyl-3-oxopropanoate and alanine .
PMID:24586340
Catalyzes the transfer of the amino group from beta-alanine to pyruvate to yield L-alanine and 3-oxopropanoate (By similarity). Can metabolize NG-monomethyl-L-arginine (NMMA), asymmetric NG,NG-dimethyl-L-arginine (ADMA) and symmetric NG,N'G-dimethyl-L-arginine (SDMA) .
PMID:20018850 PMID:23023372
ADMA is a potent inhibitor of nitric-oxide (NO) synthase, and this activity provides mechanism through which the kidney regulates blood pressure PMID:20018850 PMID:23023372

Glutamate decarboxylase 1

BE0000378

GAD1

cofactor

Specific functionglutamate decarboxylase activity

General function & pharmacology

Catalyzes the synthesis of the inhibitory neurotransmitter gamma-aminobutyric acid (GABA) with pyridoxal 5'-phosphate as cofactor

Cystathionine beta-synthase

BE0000323

CBS

cofactor

Specific functioncarbon monoxide binding

Cellular location

Cytoplasm

General function & pharmacology

Hydro-lyase catalyzing the first step of the transsulfuration pathway, where the hydroxyl group of L-serine is displaced by L-homocysteine in a beta-replacement reaction to form L-cystathionine, the precursor of L-cysteine. This catabolic route allows the elimination of L-methionine and the toxic metabolite L-homocysteine .
PMID:20506325 PMID:23974653 PMID:23981774

Also involved in the production of hydrogen sulfide, a gasotransmitter with signaling and cytoprotective effects on neurons (By similarity)

Biological pathways(137)

Citrullinemia Type I

disease

Involved compounds

Oxogluric acid,Adenosine phosphate,ATP,Calcium,Pyrophosphoric acid,Alanine,Arginine,Aspartic acid,Citrulline,Glutamic acid,L-Glutamine,Ornithine,Maleic acid,NADH,Pyridoxal phosphate,Pyruvic acid,Urea

Carbamoyl Phosphate Synthetase Deficiency

disease

Involved compounds

Oxogluric acid,Adenosine phosphate,ATP,Calcium,Pyrophosphoric acid,Alanine,Arginine,Aspartic acid,Citrulline,Glutamic acid,L-Glutamine,Ornithine,Maleic acid,NADH,Pyridoxal phosphate,Pyruvic acid,Urea

Argininosuccinic Aciduria

disease

Involved compounds

Oxogluric acid,Adenosine phosphate,ATP,Calcium,Pyrophosphoric acid,Alanine,Arginine,Aspartic acid,Citrulline,Glutamic acid,L-Glutamine,Ornithine,Maleic acid,NADH,Pyridoxal phosphate,Pyruvic acid,Urea

beta-Alanine Metabolism

metabolic

Involved compounds

Oxogluric acid,Dihydrouracil,beta-Alanine,Calcium,Flavin adenine dinucleotide,Aspartic acid,Glutamic acid,Histidine,NADH,Pantothenic acid,Pyridoxal phosphate,Flavin mononucleotide,Uracil,Zinc

Phenylalanine and Tyrosine Metabolism

metabolic

Involved compounds

Oxogluric acid,Homogentisic acid,4-Hydroxyphenylpyruvic acid,Phenylpyruvic acid,Acetoacetic acid,Adenosine phosphate,ATP,Calcium,Pyrophosphoric acid,Flavin adenine dinucleotide,Iron,Glutamic acid,Phenylalanine,Tyrosine,Magnesium cation,Maleic acid,Pyridoxal phosphate

Catecholamine Biosynthesis

metabolic

Involved compounds

Dopamine,Epinephrine,Iron,Tyrosine,Levodopa,Norepinephrine,Pyridoxal phosphate,Pyrroloquinoline Quinone,Ademetionine,Ascorbic acid

Cysteine Metabolism

metabolic

Involved compounds

Oxogluric acid,Adenosine phosphate,ATP,Pyrophosphoric acid,gamma-Glutamylcysteine,Iron,Cysteine,Glutamic acid,NADH,Pyridoxal phosphate,Pyruvic acid,Zinc

Propanoate Metabolism

metabolic

Involved compounds

Oxogluric acid,2-Oxobutanoic Acid,Hydracrylic acid,Adenosine phosphate,ATP,beta-Alanine,Biotin,Pyrophosphoric acid,Flavin adenine dinucleotide,Glutamic acid,Valine,Malonyl-CoA,Methylmalonic Acid,NADH,Propanoic acid,Pyridoxal phosphate

Vitamin B6 Metabolism

metabolic

Involved compounds

Flavin adenine dinucleotide,Magnesium cation,Pyridoxal,Pyridoxal phosphate,Pyridoxamine-5'-Phosphate,Pyridoxine,Pyridoxine phosphate,Flavin mononucleotide,Zinc

Taurine and Hypotaurine Metabolism

metabolic

Involved compounds

Taurine,Cysteamine,Iron,Cysteine,Pyridoxal phosphate

Porphyrin Metabolism

metabolic

Involved compounds

Aminolevulinic acid,Coproporphyrinogen III,Farnesyl diphosphate,Flavin adenine dinucleotide,Glycine,Iron,Mesoheme,NADH,Protoporphyrin,Pyridoxal phosphate,Uridine-5'-Diphosphate,Zinc

Selenoamino Acid Metabolism

metabolic

Involved compounds

2-Oxobutanoic Acid,Adenosine,Adenosine phosphate,ATP,Pyrophosphoric acid,Alanine,Serine,Pyridoxal phosphate,Selenocysteine

Valine, Leucine, and Isoleucine Degradation

metabolic

Involved compounds

Oxogluric acid,alpha-Ketoisocaproic acid,Acetoacetic acid,ATP,alpha-Ketoisovalerate,Biotin,Flavin adenine dinucleotide,Glutamic acid,Isoleucine,Leucine,Valine,Methylmalonic Acid,NADH,Pyridoxal,Pyridoxal phosphate,Succinic acid

Sphingolipid Metabolism

metabolic

Involved compounds

ATP,Calcium,Uridine diphosphate glucose,Hexadecanal,Serine,Magnesium cation,N,N,N-Trimethyl-2-(phosphonooxy)ethanaminium,Pyridoxal phosphate,Uridine-5'-Diphosphate,Zinc

Lysine Degradation

metabolic

Involved compounds

Oxogluric acid,Flavin adenine dinucleotide,Glutamic acid,Lysine,L-Saccharopine,NADH,Pyridoxal phosphate

Histidine Metabolism

metabolic

Involved compounds

1-Methylhistidine,Adenosine phosphate,ATP,beta-Alanine,Calcium,Pyrophosphoric acid,Flavin adenine dinucleotide,Glutamic acid,Histidine,NADH,Pyridoxal phosphate,Ademetionine,Tetrahydrofolic acid,trans-urocanic acid,Zinc

Folate Metabolism

metabolic

Involved compounds

ATP,Calcium,Flavin adenine dinucleotide,Folic acid,Formic acid,Glutamic acid,Leucovorin,Magnesium cation,NADH,Pyridoxal phosphate,Tetrahydrofolic acid

Alanine Metabolism

metabolic

Involved compounds

Oxogluric acid,Adenosine phosphate,ATP,Biotin,Pyrophosphoric acid,Glycine,Glyoxylic acid,Alanine,Glutamic acid,Pyridoxal phosphate,Pyruvic acid,Zinc

Starch and Sucrose Metabolism

metabolic

Involved compounds

ATP,Calcium,Pyrophosphoric acid,Uridine diphosphate glucose,Magnesium cation,Maltose,NADH,Pyridoxal phosphate,Uridine-5'-Diphosphate

Urea Cycle

metabolic

Involved compounds

Oxogluric acid,Adenosine phosphate,ATP,Calcium,Pyrophosphoric acid,Alanine,Arginine,Aspartic acid,Citrulline,Glutamic acid,L-Glutamine,Ornithine,Maleic acid,NADH,Pyridoxal phosphate,Pyruvic acid,Urea

Glucose-Alanine Cycle

metabolic

Involved compounds

Oxogluric acid,Alanine,Glutamic acid,NADH,Pyridoxal phosphate,Pyruvic acid

Malate-Aspartate Shuttle

metabolic

Involved compounds

Oxogluric acid,Calcium,Aspartic acid,Glutamic acid,NADH,Pyridoxal phosphate

2-Methyl-3-hydroxybutryl-CoA Dehydrogenase Deficiency

disease

Involved compounds

3-Hydroxy-3-methylglutaryl-CoA Lyase Deficiency

disease

Involved compounds

3-Methylglutaconic Aciduria Type I

disease

Involved compounds

3-Methylglutaconic Aciduria Type III

disease

Involved compounds

3-Methylglutaconic Aciduria Type IV

disease

Involved compounds

Aromatic L-Aminoacid Decarboxylase Deficiency

disease

Involved compounds

Dopamine,Epinephrine,Iron,Tyrosine,Levodopa,Norepinephrine,Pyridoxal phosphate,Pyrroloquinoline Quinone,Ademetionine,Ascorbic acid

beta-Ketothiolase Deficiency

disease

Involved compounds

Glutaric Aciduria Type I

disease

Involved compounds

Oxogluric acid,Flavin adenine dinucleotide,Glutamic acid,Lysine,L-Saccharopine,NADH,Pyridoxal phosphate

Histidinemia

disease

Involved compounds

Malonic Aciduria

disease

Involved compounds

Maple Syrup Urine Disease

disease

Involved compounds

Methylmalonic Aciduria

disease

Involved compounds

Methylmalonic Aciduria Due to Cobalamin-Related Disorders

disease

Involved compounds

Ornithine Transcarbamylase Deficiency (OTC Deficiency)

disease

Involved compounds

Oxogluric acid,Adenosine phosphate,ATP,Calcium,Pyrophosphoric acid,Alanine,Arginine,Aspartic acid,Citrulline,Glutamic acid,L-Glutamine,Ornithine,Maleic acid,NADH,Pyridoxal phosphate,Pyruvic acid,Urea

Phenylketonuria

disease

Involved compounds

Propionic Acidemia

disease

Involved compounds

3-Methylcrotonyl-CoA Carboxylase Deficiency Type I

disease

Involved compounds

Isovaleric Aciduria

disease

Involved compounds

Saccharopinuria/Hyperlysinemia II

disease

Involved compounds

Oxogluric acid,Flavin adenine dinucleotide,Glutamic acid,Lysine,L-Saccharopine,NADH,Pyridoxal phosphate

Lactic Acidemia

disease

Involved compounds

Oxogluric acid,Adenosine phosphate,ATP,Biotin,Pyrophosphoric acid,Glycine,Glyoxylic acid,Alanine,Glutamic acid,Pyridoxal phosphate,Pyruvic acid,Zinc

Hereditary Coproporphyria (HCP)

disease

Involved compounds

Aminolevulinic acid,Coproporphyrinogen III,Farnesyl diphosphate,Flavin adenine dinucleotide,Glycine,Iron,Mesoheme,NADH,Protoporphyrin,Pyridoxal phosphate,Uridine-5'-Diphosphate,Zinc

Acute Intermittent Porphyria

disease

Involved compounds

Aminolevulinic acid,Coproporphyrinogen III,Farnesyl diphosphate,Flavin adenine dinucleotide,Glycine,Iron,Mesoheme,NADH,Protoporphyrin,Pyridoxal phosphate,Uridine-5'-Diphosphate,Zinc

Congenital Erythropoietic Porphyria (CEP) or Gunther Disease

disease

Involved compounds

Aminolevulinic acid,Coproporphyrinogen III,Farnesyl diphosphate,Flavin adenine dinucleotide,Glycine,Iron,Mesoheme,NADH,Protoporphyrin,Pyridoxal phosphate,Uridine-5'-Diphosphate,Zinc

Porphyria Variegata (PV)

disease

Involved compounds

Aminolevulinic acid,Coproporphyrinogen III,Farnesyl diphosphate,Flavin adenine dinucleotide,Glycine,Iron,Mesoheme,NADH,Protoporphyrin,Pyridoxal phosphate,Uridine-5'-Diphosphate,Zinc

Metachromatic Leukodystrophy (MLD)

disease

Involved compounds

ATP,Calcium,Uridine diphosphate glucose,Hexadecanal,Serine,Magnesium cation,N,N,N-Trimethyl-2-(phosphonooxy)ethanaminium,Pyridoxal phosphate,Uridine-5'-Diphosphate,Zinc

Globoid Cell Leukodystrophy

disease

Involved compounds

ATP,Calcium,Uridine diphosphate glucose,Hexadecanal,Serine,Magnesium cation,N,N,N-Trimethyl-2-(phosphonooxy)ethanaminium,Pyridoxal phosphate,Uridine-5'-Diphosphate,Zinc

Gaucher Disease

disease

Involved compounds

ATP,Calcium,Uridine diphosphate glucose,Hexadecanal,Serine,Magnesium cation,N,N,N-Trimethyl-2-(phosphonooxy)ethanaminium,Pyridoxal phosphate,Uridine-5'-Diphosphate,Zinc

Pyruvate Carboxylase Deficiency

disease

Involved compounds

Oxogluric acid,Adenosine phosphate,ATP,Biotin,Pyrophosphoric acid,Glycine,Glyoxylic acid,Alanine,Glutamic acid,Pyridoxal phosphate,Pyruvic acid,Zinc

GABA-Transaminase Deficiency

disease

Involved compounds

Oxogluric acid,Dihydrouracil,beta-Alanine,Calcium,Flavin adenine dinucleotide,Aspartic acid,Glutamic acid,Histidine,NADH,Pantothenic acid,Pyridoxal phosphate,Flavin mononucleotide,Uracil,Zinc

Primary Hyperoxaluria Type I

disease

Involved compounds

Oxogluric acid,Adenosine phosphate,ATP,Biotin,Pyrophosphoric acid,Glycine,Glyoxylic acid,Alanine,Glutamic acid,Pyridoxal phosphate,Pyruvic acid,Zinc

Argininemia

disease

Involved compounds

Oxogluric acid,Adenosine phosphate,ATP,Calcium,Pyrophosphoric acid,Alanine,Arginine,Aspartic acid,Citrulline,Glutamic acid,L-Glutamine,Ornithine,Maleic acid,NADH,Pyridoxal phosphate,Pyruvic acid,Urea

Tyrosinemia Type 2 (or Richner-Hanhart Syndrome)

disease

Involved compounds

Tyrosinemia Type 3 (TYRO3)

disease

Involved compounds

Methylmalonate Semialdehyde Dehydrogenase Deficiency

disease

Involved compounds

Methotrexate Action Pathway

Involved compounds

ATP,Calcium,Flavin adenine dinucleotide,Folic acid,Formic acid,Glutamic acid,Leucovorin,Magnesium cation,Methotrexate,NADH,Pyridoxal phosphate,Tetrahydrofolic acid

Spermidine and Spermine Biosynthesis

metabolic

Involved compounds

ATP,Pyrophosphoric acid,Methionine,Ornithine,Magnesium cation,Potassium cation,Putrescine,Pyridoxal phosphate,Pyruvaldehyde,Ademetionine,Spermidine,Spermine

Threonine and 2-Oxobutanoate Degradation

metabolic

Involved compounds

2-Oxobutanoic Acid,ATP,Biotin,Flavin adenine dinucleotide,Threonine,NADH,Pyridoxal phosphate

Homocysteine Degradation

metabolic

Involved compounds

2-Oxobutanoic Acid,Cysteine,Serine,Pyridoxal phosphate

Carnitine Synthesis

metabolic

Involved compounds

Oxogluric acid,Glycine,Iron,Levocarnitine,Lysine,NADH,Pyridoxal phosphate,Ademetionine,Succinic acid,Ascorbic acid

Ureidopropionase Deficiency

disease

Involved compounds

Oxogluric acid,Dihydrouracil,beta-Alanine,Calcium,Flavin adenine dinucleotide,Aspartic acid,Glutamic acid,Histidine,NADH,Pantothenic acid,Pyridoxal phosphate,Flavin mononucleotide,Uracil,Zinc

Carnosinuria, Carnosinemia

disease

Involved compounds

Oxogluric acid,Dihydrouracil,beta-Alanine,Calcium,Flavin adenine dinucleotide,Aspartic acid,Glutamic acid,Histidine,NADH,Pantothenic acid,Pyridoxal phosphate,Flavin mononucleotide,Uracil,Zinc

Tyrosine Hydroxylase Deficiency

disease

Involved compounds

Dopamine,Epinephrine,Iron,Tyrosine,Levodopa,Norepinephrine,Pyridoxal phosphate,Pyrroloquinoline Quinone,Ademetionine,Ascorbic acid

beta-Mercaptolactate-Cysteine Disulfiduria

disease

Involved compounds

Oxogluric acid,Adenosine phosphate,ATP,Pyrophosphoric acid,gamma-Glutamylcysteine,Iron,Cysteine,Glutamic acid,NADH,Pyridoxal phosphate,Pyruvic acid,Zinc

Malonyl-CoA Decarboxylase Deficiency

disease

Involved compounds

Hypophosphatasia

disease

Involved compounds

Flavin adenine dinucleotide,Magnesium cation,Pyridoxal,Pyridoxal phosphate,Pyridoxamine-5'-Phosphate,Pyridoxine,Pyridoxine phosphate,Flavin mononucleotide,Zinc

gamma-Cystathionase Deficiency (CTH)

disease

Involved compounds

2-Oxobutanoic Acid,Cysteine,Serine,Pyridoxal phosphate

Homocystinuria, Cystathionine beta-Synthase Deficiency

disease

Involved compounds

2-Oxobutanoic Acid,Cysteine,Serine,Pyridoxal phosphate

3-Hydroxyisobutyric Acid Dehydrogenase Deficiency

disease

Involved compounds

3-Hydroxyisobutyric Aciduria

disease

Involved compounds

Isobutyryl-CoA Dehydrogenase Deficiency

disease

Involved compounds

Isovaleric Acidemia

disease

Involved compounds

Fabry Disease

disease

Involved compounds

ATP,Calcium,Uridine diphosphate glucose,Hexadecanal,Serine,Magnesium cation,N,N,N-Trimethyl-2-(phosphonooxy)ethanaminium,Pyridoxal phosphate,Uridine-5'-Diphosphate,Zinc

Krabbe Disease

disease

Involved compounds

ATP,Calcium,Uridine diphosphate glucose,Hexadecanal,Serine,Magnesium cation,N,N,N-Trimethyl-2-(phosphonooxy)ethanaminium,Pyridoxal phosphate,Uridine-5'-Diphosphate,Zinc

Hyperlysinemia I, Familial

disease

Involved compounds

Oxogluric acid,Flavin adenine dinucleotide,Glutamic acid,Lysine,L-Saccharopine,NADH,Pyridoxal phosphate

Hyperlysinemia II or Saccharopinuria

disease

Involved compounds

Oxogluric acid,Flavin adenine dinucleotide,Glutamic acid,Lysine,L-Saccharopine,NADH,Pyridoxal phosphate

Methylenetetrahydrofolate Reductase Deficiency (MTHFRD)

disease

Involved compounds

ATP,Calcium,Flavin adenine dinucleotide,Folic acid,Formic acid,Glutamic acid,Leucovorin,Magnesium cation,NADH,Pyridoxal phosphate,Tetrahydrofolic acid

Glycogen Synthetase Deficiency

disease

Involved compounds

ATP,Calcium,Pyrophosphoric acid,Uridine diphosphate glucose,Magnesium cation,Maltose,NADH,Pyridoxal phosphate,Uridine-5'-Diphosphate

Glycogenosis, Type III. Cori Disease, Debrancher Glycogenosis

disease

Involved compounds

ATP,Calcium,Pyrophosphoric acid,Uridine diphosphate glucose,Magnesium cation,Maltose,NADH,Pyridoxal phosphate,Uridine-5'-Diphosphate

Glycogenosis, Type IV. Amylopectinosis, Anderson Disease

disease

Involved compounds

ATP,Calcium,Pyrophosphoric acid,Uridine diphosphate glucose,Magnesium cation,Maltose,NADH,Pyridoxal phosphate,Uridine-5'-Diphosphate

Glycogenosis, Type VI. Hers Disease

disease

Involved compounds

ATP,Calcium,Pyrophosphoric acid,Uridine diphosphate glucose,Magnesium cation,Maltose,NADH,Pyridoxal phosphate,Uridine-5'-Diphosphate

Mucopolysaccharidosis VI. Sly Syndrome

disease

Involved compounds

ATP,Calcium,Pyrophosphoric acid,Uridine diphosphate glucose,Magnesium cation,Maltose,NADH,Pyridoxal phosphate,Uridine-5'-Diphosphate

Sucrase-Isomaltase Deficiency

disease

Involved compounds

ATP,Calcium,Pyrophosphoric acid,Uridine diphosphate glucose,Magnesium cation,Maltose,NADH,Pyridoxal phosphate,Uridine-5'-Diphosphate

Pyridoxine Dependency with Seizures

disease

Involved compounds

Oxogluric acid,Flavin adenine dinucleotide,Glutamic acid,Lysine,L-Saccharopine,NADH,Pyridoxal phosphate

2-Aminoadipic 2-Oxoadipic Aciduria

disease

Involved compounds

Oxogluric acid,Flavin adenine dinucleotide,Glutamic acid,Lysine,L-Saccharopine,NADH,Pyridoxal phosphate

Cystinosis, Ocular Nonnephropathic

disease

Involved compounds

Oxogluric acid,Adenosine phosphate,ATP,Pyrophosphoric acid,gamma-Glutamylcysteine,Iron,Cysteine,Glutamic acid,NADH,Pyridoxal phosphate,Pyruvic acid,Zinc

Folate Malabsorption, Hereditary

disease

Involved compounds

ATP,Calcium,Flavin adenine dinucleotide,Folic acid,Formic acid,Glutamic acid,Leucovorin,Magnesium cation,NADH,Pyridoxal phosphate,Tetrahydrofolic acid

Glutaminolysis and Cancer

disease

Involved compounds

Oxogluric acid,ATP,Biotin,Citric acid,Flavin adenine dinucleotide,Alanine,Aspartic acid,Glutamic acid,L-Glutamine,Leucine,Magnesium cation,Maleic acid,NADH,Pyridoxal phosphate,Pyruvic acid,Succinic acid

Sarcosine Oncometabolite Pathway

disease

Involved compounds

Betaine aldehyde,ATP,Choline,N,N-dimethylglycine,Pyrophosphoric acid,Flavin adenine dinucleotide,Glycine,Methionine,Serine,Magnesium cation,NADH,Potassium cation,Pyridoxal phosphate,Ademetionine,Tetrahydrofolic acid,Zinc

ATC classification(1 code)

ATC A11HA06

Affected organisms(1)

Humans and other mammals

Salt forms(1)

Pyridoxal phosphate hydrate(DBSALT001801)

Experimental properties(3)

External resources(1)

PDRhealth

Protein Data Bank entries(1358)

Chemical identifiers

CAS, UNII, InChI Key and database cross-references

Show

Linked compound data from DrugBank Open Data (CC BY-NC 4.0)

Pyridoxal phosphate

DB00114

CAS number

54-47-7

UNII (FDA)

0ABW0CG2BM

InChI Key (molecular fingerprint)

NGVDGCNFYWLIFO-UHFFFAOYSA-N

Additional database identifiers

ChEBI

18405

PubChem Compound

1051

PubChem Substance

46506428

KEGG Compound

C00018

KEGG Drug

D00006

ChemSpider

1022

BindingDB

50118216

PharmGKB

PA164749650

PDB

PLP

Therapeutic Targets Database

DNC001499

Wikipedia

Pyridoxal_phosphate

ChEMBL

CHEMBL82202

ZINC

ZINC000001532514

RxCUI

9004

HUGO Gene Nomenclature Committee (HGNC)

HGNC:23

GenAtlas

ABAT

GeneCards

ABAT

GenBank Gene Database

L32961

GenBank Protein Database

602705

Guide to Pharmacology

2464

UniProtKB

P80404

UniProt Accession

GABT_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:3535

GenAtlas

GeneCards

GenBank Gene Database

M17262

GenBank Protein Database

339641

Guide to Pharmacology

2362

UniProtKB

P00734

UniProt Accession

THRB_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:14412

GenAtlas

AGXT2

GeneCards

AGXT2

GenBank Gene Database

AJ292204

GenBank Protein Database

12406973

UniProtKB

Q9BYV1

UniProt Accession

AGT2_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:4092

GenAtlas

GAD1

GeneCards

GAD1

GenBank Gene Database

M81883

GenBank Protein Database

182936

UniProtKB

Q99259

UniProt Accession

DCE1_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:1550

GenAtlas

CBS

GeneCards

CBS

GenBank Gene Database

L19501

GenBank Protein Database

388716

Guide to Pharmacology

1443

UniProtKB

P35520

UniProt Accession

CBS_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:6469

GenAtlas

KYNU

GeneCards

KYNU

GenBank Gene Database

U57721

GenBank Protein Database

1323715

UniProtKB

Q16719

UniProt Accession

KYNU_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:10850

GenAtlas

SHMT1

GeneCards

SHMT1

GenBank Gene Database

L11931

GenBank Protein Database

307422

UniProtKB

P34896

UniProt Accession

GLYC_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:15910

GenAtlas

NFS1

GeneCards

NFS1

GenBank Gene Database

AF097025

GenBank Protein Database

24042327

UniProtKB

Q9Y697

UniProt Accession

NFS1_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:4432

GenAtlas

GOT1

GeneCards

GOT1

GenBank Gene Database

M37400

GenBank Protein Database

179067

UniProtKB

P17174

UniProt Accession

AATC_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:8091

GenAtlas

OAT

GeneCards

OAT

GenBank Gene Database

M12267

GenBank Protein Database

189329

UniProtKB

P04181

UniProt Accession

OAT_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:8109

GenAtlas

ODC1

GeneCards

ODC1

GenBank Gene Database

M16650

GenBank Protein Database

29893806

Guide to Pharmacology

1276

UniProtKB

P11926

UniProt Accession

DCOR_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:17929

GenAtlas

AADAT

GeneCards

AADAT

GenBank Gene Database

AF097994

GenBank Protein Database

6165634

UniProtKB

Q8N5Z0

UniProt Accession

AADAT_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:30260

GenAtlas

PNPO

GeneCards

PNPO

GenBank Gene Database

AF468030

GenBank Protein Database

21728336

UniProtKB

Q9NVS9

UniProt Accession

PNPO_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:10817

GenAtlas

SGPL1

GeneCards

SGPL1

GenBank Gene Database

AJ011304

GenBank Protein Database

10129683

Guide to Pharmacology

2522

UniProtKB

O95470

UniProt Accession

SGPL1_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:11573

GenAtlas

TAT

GeneCards

TAT

GenBank Gene Database

X52520

GenBank Protein Database

36713

UniProtKB

P17735

UniProt Accession

ATTY_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:1564

GenAtlas

CCBL1

GeneCards

KYAT1

GenBank Gene Database

X82224

GenBank Protein Database

758591

UniProtKB

Q16773

UniProt Accession

KAT1_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:9725

GenAtlas

PYGL

GeneCards

PYGL

GenBank Gene Database

M14636

GenBank Protein Database

183353

UniProtKB

P06737

UniProt Accession

PYGL_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:11278

GenAtlas

SPTLC2

GeneCards

SPTLC2

GenBank Gene Database

Y08686

GenBank Protein Database

2564249

UniProtKB

O15270

UniProt Accession

SPTC2_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:18966

GenAtlas

CSAD

GeneCards

CSAD

GenBank Gene Database

AF116546

GenBank Protein Database

4894558

UniProtKB

Q9Y600

UniProt Accession

CSAD_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:4855

GenAtlas

HDC

GeneCards

HDC

GenBank Gene Database

X54297

GenBank Protein Database

32109

UniProtKB

P19113

UniProt Accession

DCHS_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:29957

GenAtlas

ADC

GeneCards

AZIN2

GenBank Gene Database

AY050634

GenBank Protein Database

15858863

UniProtKB

Q96A70

UniProt Accession

AZIN2_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:10691

GenAtlas

SDS

GeneCards

SDS

GenBank Gene Database

J05037

GenBank Protein Database

338030

UniProtKB

P20132

UniProt Accession

SDHL_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:4188

GenAtlas

GCAT

GeneCards

GCAT

GenBank Gene Database

AF077740

GenBank Protein Database

3342906

UniProtKB

O75600

UniProt Accession

KBL_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:4313

GenAtlas

GLDC

GeneCards

GLDC

GenBank Gene Database

M63635

GenBank Protein Database

190287

UniProtKB

P23378

UniProt Accession

GCSP_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:4552

GenAtlas

GPT

GeneCards

GPT

GenBank Gene Database

U70732

GenBank Protein Database

1763096

UniProtKB

P24298

UniProt Accession

ALAT1_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:19129

GenAtlas

PSAT1

GeneCards

PSAT1

GenBank Gene Database

AF113132

GenBank Protein Database

5326802

UniProtKB

Q9Y617

UniProt Accession

SERC_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:396

GenAtlas

ALAS1

GeneCards

ALAS1

GenBank Gene Database

X56351

GenBank Protein Database

28583

UniProtKB

P13196

UniProt Accession

HEM1_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:341

GenAtlas

AGXT

GeneCards

AGXT

GenBank Gene Database

X56092

GenBank Protein Database

36582

UniProtKB

P21549

UniProt Accession

AGT1_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:30259

GenAtlas

PDXP

GeneCards

PDXP

GenBank Gene Database

AY125047

GenBank Protein Database

37545684

UniProtKB

Q96GD0

UniProt Accession

PLPP_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:11277

GenAtlas

SPTLC1

GeneCards

SPTLC1

GenBank Gene Database

Y08685

GenBank Protein Database

2564247

UniProtKB

O15269

UniProt Accession

SPTC1_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:2501

GenAtlas

CTH

GeneCards

CTH

GenBank Gene Database

S52784

GenBank Protein Database

262476

Guide to Pharmacology

1444

UniProtKB

P32929

UniProt Accession

CGL_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:976

GenAtlas

BCAT1

GeneCards

BCAT1

GenBank Gene Database

U21551

GenBank Protein Database

1036780

Guide to Pharmacology

3210

UniProtKB

P54687

UniProt Accession

BCAT1_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:977

GenAtlas

BCAT2

GeneCards

BCAT2

GenBank Gene Database

U68418

GenBank Protein Database

2342862

Guide to Pharmacology

2893

UniProtKB

O15382

UniProt Accession

BCAT2_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:9457

GenAtlas

PROSC

GeneCards

PLPBP

GenBank Gene Database

AB018566

GenBank Protein Database

4126978

UniProtKB

O94903

UniProt Accession

PLPHP_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:4433

GenAtlas

GOT2

GeneCards

GOT2

GenBank Gene Database

M22632

GenBank Protein Database

179104

UniProtKB

P00505

UniProt Accession

AATM_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:9723

GenAtlas

PYGB

GeneCards

PYGB

GenBank Gene Database

J03544

GenBank Protein Database

307200

UniProtKB

P11216

UniProt Accession

PYGB_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:9726

GenAtlas

PYGM

GeneCards

PYGM

GenBank Gene Database

M32598

GenBank Protein Database

190784

UniProtKB

P11217

UniProt Accession

PYGM_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:2719

GenAtlas

DDC

GeneCards

DDC

GenBank Gene Database

M76180

GenBank Protein Database

181521

UniProtKB

P20711

UniProt Accession

DDC_HUMAN

GenBank Gene Database

AK223555

GenBank Protein Database

62898842

UniProtKB

Q53ET4

UniProt Accession

Q53ET4_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:4093

GenAtlas

GAD2

GeneCards

GAD2

GenBank Gene Database

M81882

GenBank Protein Database

182934

UniProtKB

Q05329

UniProt Accession

DCE2_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:33238

GenAtlas

CCBL2

GeneCards

KYAT3

GenBank Gene Database

AY028624

GenBank Protein Database

37542047

UniProtKB

Q6YP21

UniProt Accession

KAT3_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:27949

GenAtlas

GADL1

GeneCards

GADL1

GenBank Gene Database

AK128643

GenBank Protein Database

34536121

UniProtKB

Q6ZQY3

UniProt Accession

GADL1_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:18161

GeneCards

SCLY

UniProtKB

Q96I15

UniProt Accession

SCLY_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:26384

GeneCards

IGSF10

UniProtKB

Q6WRI0

UniProt Accession

IGS10_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:28249

GenAtlas

AGXT2L2

GeneCards

PHYKPL

GenBank Gene Database

AF318375

GenBank Protein Database

18027842

UniProtKB

Q8IUZ5

UniProt Accession

AT2L2_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:10852

GenAtlas

SHMT2

GeneCards

SHMT2

GenBank Gene Database

U23143

GenBank Protein Database

746436

UniProtKB

P34897

UniProt Accession

GLYM_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:397

GenAtlas

ALAS2

GeneCards

ALAS2

GenBank Gene Database

X56352

GenBank Protein Database

28586

UniProtKB

P22557

UniProt Accession

HEM0_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:18062

GenAtlas

GPT2

GeneCards

GPT2

GenBank Gene Database

AY029173

GenBank Protein Database

19046894

UniProtKB

Q8TD30

UniProt Accession

ALAT2_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:18234

GenAtlas

MOCOS

GeneCards

MOCOS

GenBank Gene Database

AK000740

GenBank Protein Database

7021017

UniProtKB

Q96EN8

UniProt Accession

MOCOS_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:30404

GenAtlas

SDSL

GeneCards

SDSL

GenBank Gene Database

AF134473

GenBank Protein Database

33150744

UniProtKB

Q96GA7

UniProt Accession

SDSL_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:14398

GenAtlas

SRR

GeneCards

SRR

GenBank Gene Database

AF169974

GenBank Protein Database

11034785

UniProtKB

Q9GZT4

UniProt Accession

SRR_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:30605

GenAtlas

SEPSECS

GeneCards

SEPSECS

GenBank Gene Database

AF146396

GenBank Protein Database

7652498

UniProtKB

Q9HD40

UniProt Accession

SPCS_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:16253

GenAtlas

SPTLC3

GeneCards

SPTLC3

GenBank Gene Database

AK001974

GenBank Protein Database

7023574

UniProtKB

Q9NUV7

UniProt Accession

SPTC3_HUMAN

GenAtlas

GAD65

GenBank Gene Database

AJ251501

GenBank Protein Database

6562440

UniProtKB

Q9UGI5

UniProt Accession

Q9UGI5_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:4432

GenAtlas

GOT1

GeneCards

GOT1

GenBank Gene Database

M37400

GenBank Protein Database

179067

UniProtKB

P17174

UniProt Accession

AATC_HUMAN

HUGO Gene Nomenclature Committee (HGNC)

HGNC:4433

GenAtlas

GOT2

GeneCards

GOT2

GenBank Gene Database

M22632

GenBank Protein Database

179104

UniProtKB

P00505

UniProt Accession

AATM_HUMAN

DrugBank citations

If you use DrugBank data in your research, please cite the following publications:

Knox C., Wilson M., Klinger C.M., et al

DrugBank 6.

0: the DrugBank Knowledgebase for 2024

Nucleic Acids Res. 2024 Jan 552(D1):D1265-D1275

PMID: 37953279

Wishart D.S., Feunang Y.D., Guo A.C., et al

DrugBank 5.

0: a major update to the DrugBank database for 2018

Nucleic Acids Res. 2017 Nov 846(D1):D1074-D1082

PMID: 29126136

Show earlier publications

Law V., Knox C., Djoumbou Y., et al

DrugBank 4.

0: shedding new light on drug metabolism

Nucleic Acids Res. 2014 Jan 142(1):D1091-7

PMID: 24203711

Knox C., Law V., Jewison T., et al

DrugBank 3.

0: a comprehensive resource for 'omics' research on drugs

Nucleic Acids Res. 2011 Jan39(Database issue):D1035-41

PMID: 21059682

Wishart D.S., Knox C., Guo A.C., et al

DrugBank: a knowledgebase for drugs, drug actions and drug targets.

Nucleic Acids Research

2008 Jan36(Database issue):D901-6

PMID: 18048412

Wishart D.S., Knox C., Guo A.C., et al

DrugBank: a comprehensive resource for in silico drug discovery and exploration.

Nucleic Acids Research

2006 Jan 134(Database issue):D668-72

PMID: 16381955

Source: go.drugbank.comCC BY-NC 4.0

Updated 4 months ago(4 Mar 2026)

Structured knowledge from the free knowledge base

Q418957

Wikipedia article

chemical compound

Read on Wikipedia

Research database identifiers

ChEBI

CHEBI:18405

ATC classifications (Wikidata)

A11HA06

Linked open data from Wikidata (Q418957), a free and open knowledge base operated by the Wikimedia Foundation. Data is available under the Creative Commons CC0 1.0 Public Domain Dedication.

Source: Q418957CC0 1.0

Updated about 6 hours ago(5 Jul 2026)

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Pyridoxal phosphate 25mg tablets

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