MiMeDB: Browsing Metabolites

Metabolite Type:	Structure Class:	Host:
Site:	Microbial Metabolism:	Health Outcome:
Biospecimen:	Status in Biospecimen:	Bioactivity:
Exposure Source:

Displaying metabolites 24401 - 24425 of 24443 in total

Metabolite ID	Name	Molecular Formula Average Mass Monoisotopic Mass	Structure Class	Host and Biospecimen	# Microbes	Metabolite Type	Exposure Sources	Health Effects	Detection Status
MMDBc0000188	Hydrogen	H₂ 2.0159 2.015650064	Other non-metal organides	Human Feces	1835	Co-metabolite	Not Available	Not Available	Detected and Quantified
MMDBc0029589	Acetyl-CoA	C₂₃H₃₈N₇O₁₇P₃S 809.571 809.125773051	Fatty Acyls	Human Feces Human Adipose Tissue Human Brain Human Platelet Human Prostate Human Skeletal Muscle Human Spleen	1842	Co-metabolite		Not Available	Detected and Quantified
MMDBc0000054	L-Asparagine	C₄H₈N₂O₃ 132.1179 132.053492132	Carboxylic acids and derivatives	Human Feces Human Saliva Human Cerebrospinal Fluid (CSF) Human Blood Human Urine Human Breast Milk Human All Tissues Human Placenta Human Prostate	1844	Co-metabolite		Alzheimer's disease; Alzheimer's disease; Epilepsy; Frontotemporal dementia; Fumarase deficiency; Fumarase deficiency; Leukemia; Schizophrenia; Uremia; Eosinophilic esophagitis; Eosinophilic esophagitis	Detected and Quantified
MMDBc0000016	Ammonia	H₃N 17.0305 17.026549101	Homogeneous other non-metal compounds	Human Feces Human Blood Human Urine Human Cellular Cytoplasm Human Cerebrospinal Fluid (CSF) Human All Tissues	1850	Co-metabolite		3-Hydroxy-3-methylglutaryl-CoA lyase deficiency; 3-Hydroxy-3-methylglutaryl-CoA lyase deficiency; 3-Hydroxy-3-methylglutaryl-CoA lyase deficiency; 3-Hydroxy-3-methylglutaryl-CoA lyase deficiency; Argininosuccinic aciduria; Carnitine palmitoyltransferase I deficiency; Citrullinemia type I; Fumarase deficiency; Hyperdibasic aminoaciduria I; Mitochondrial trifunctional protein deficiency; N-acetylglutamate synthetase deficiency; Pyruvate carboxylase deficiency; Short bowel syndrome; 3-Methyl-crotonyl-glycinuria; 3-Methyl-crotonyl-glycinuria; Argininosuccinic aciduria	Detected and Quantified
MMDBc0000497	Hypoxanthine	C₅H₄N₄O 136.1115 136.03851077	Imidazopyrimidines	Human Feces Human Cerebrospinal Fluid (CSF) Human Saliva Human Urine Human Blood Human Cellular Cytoplasm Human Amniotic Fluid Human Breast Milk Human Adipose Tissue Human Epidermis Human Erythrocyte Human Fibroblasts Human Intestine Human Kidney Human Liver Human Placenta Human Platelet Human Prostate Human Skeletal Muscle Human Spleen Human Testis	1854	Co-metabolite		3-Methyl-crotonyl-glycinuria; Alzheimer's disease; Canavan disease; Canavan disease; Degenerative disc disease; Frontotemporal dementia; Hydrocephalus; Lesch-Nyhan syndrome; Lesch-Nyhan syndrome; Lesch-Nyhan syndrome; Lung Cancer; Uremia; Uremia; Eosinophilic esophagitis	Detected and Quantified
MMDBc0000335	Glycerol 3-phosphate	C₃H₉O₆P 172.0737 172.013674532	Glycerophospholipids	Human Feces Human Saliva Human Blood Human Placenta Human Prostate Human Urine	1893	Co-metabolite		Alzheimer's disease; Frontotemporal dementia	Detected and Quantified
MMDBc0032835	Guanosine triphosphate	C₁₀H₁₆N₅O₁₄P₃ 523.1804 522.990659781	Purine nucleotides	Human Feces Human Cerebrospinal Fluid (CSF) Human Blood Human Neuron Human Placenta Human Platelet Human Testis	1893	Co-metabolite		Epilepsy; Neuroinfection; Rachialgia; Stroke; Subarachnoid hemorrhage	Detected and Quantified
MMDBc0000062	L-Lactic acid	C₃H₆O₃ 90.0779 90.031694058		Human Feces Human Blood Human Cerebrospinal Fluid (CSF) Human Urine Human Saliva Human Cellular Cytoplasm Human Bile Human Sweat Human Breast Milk Human All Tissues Human Placenta	1895	Co-metabolite		2-Ketoglutarate dehydrogenase complex deficiency; 2-Ketoglutarate dehydrogenase complex deficiency; 2-Ketoglutarate dehydrogenase complex deficiency; 2-Ketoglutarate dehydrogenase complex deficiency; 3-Hydroxy-3-methylglutaryl-CoA lyase deficiency; 3-Hydroxy-3-methylglutaryl-CoA lyase deficiency; 3-Methylglutaconic Aciduria type V; Alzheimer's disease; Anoxia; Dementia; Diabetes mellitus type 1; Ethanol intoxication; Frontotemporal dementia; Fructose-1,6-diphosphatase deficiency; Mitochondrial trifunctional protein deficiency; Paraquat poisoning; Propionic acidemia; Pyruvate carboxylase deficiency; Pyruvate carboxylase deficiency; Sepsis; Eosinophilic esophagitis; Eosinophilic esophagitis; Diabetes mellitus type 1; Cytochrome C oxidase deficiency; Cytochrome C oxidase deficiency; Cytochrome C oxidase deficiency; Cytochrome C oxidase deficiency; Temporomandibular joint disorder	Detected and Quantified
MMDBc0000072	Ornithine	C₅H₁₂N₂O₂ 132.161 132.089877638	Carboxylic acids and derivatives	Human Feces Human Urine Human Saliva Human Blood Human Cerebrospinal Fluid (CSF) Human Sweat Human Epidermis Human Intestine Human Liver Human Prostate	1907	Co-metabolite		Alzheimer's disease; Alzheimer's disease; Alzheimer's disease; Cystinuria; Frontotemporal dementia; Fumarase deficiency; Fumarase deficiency; Hyperdibasic aminoaciduria I; Leukemia; Lysinuric protein intolerance; Lysinuric protein intolerance; Lysinuric protein intolerance; N-acetylglutamate synthetase deficiency; N-acetylglutamate synthetase deficiency; Ornithine transcarbamylase deficiency; Uremia; Eosinophilic esophagitis; Eosinophilic esophagitis; Lysinuric protein intolerance; Obesity; Obesity; Cystinuria; Cystinuria	Detected and Quantified
MMDBc0000117	L-Cysteine	C₃H₇NO₂S 121.158 121.019749163		Human Feces Human Blood Human Urine Human Cerebrospinal Fluid (CSF) Human Sweat Human Saliva Human Adrenal Cortex Human Epidermis Human Fibroblasts Human Intestine Human Kidney Human Liver Human Neuron Human Placenta Human Platelet Human Prostate Human Skeletal Muscle Human Spleen Human Testis Human Thyroid Gland	1923	Co-metabolite		AIDS; Alzheimer's disease; Dementia; Dementia; Multiple sclerosis; Multiple sclerosis; Peripheral neuropathy; Peripheral neuropathy; Stroke; Stroke; Uremia; Eosinophilic esophagitis	Detected and Quantified
MMDBc0000058	L-Histidine	C₆H₉N₃O₂ 155.1546 155.069476547		Human Feces Human Blood Human Cerebrospinal Fluid (CSF) Human Saliva Human Urine Human Sweat Human Breast Milk Human All Tissues Human Placenta Human Prostate	1930	Co-metabolite	Not Available	Alzheimer's disease; Alzheimer's disease; Alzheimer's disease; Alzheimer's disease; Argininosuccinic aciduria; Dengue fever; Epilepsy; Frontotemporal dementia; Fumarase deficiency; Fumarase deficiency; Histidinemia; Histidinemia; Histidinemia; Histidinemia; Histidinemia; Histidinemia; Histidinemia; Leukemia; Maple syrup urine disease; Phenylketonuria; Propionic acidemia; Schizophrenia; Tyrosinemia I; Eosinophilic esophagitis; Eosinophilic esophagitis; Obesity; Obesity	Detected and Quantified
MMDBc0000083	Pyruvic acid	C₃H₄O₃ 88.0621 88.016043994	Keto acids and derivatives	Human Blood Human Urine Human Cerebrospinal Fluid (CSF) Human Cellular Cytoplasm Human Saliva Human Feces Human Breast Milk Human Sweat Human Adipose Tissue Human Brain Human Fibroblasts Human Heart Human Kidney Human Liver Human Neuron Human Pancreas Human Placenta Human Skeletal Muscle Human Spleen Human Testis Human Thyroid Gland	1945	Co-metabolite		2-Ketoglutarate dehydrogenase complex deficiency; 2-Ketoglutarate dehydrogenase complex deficiency; 2-Ketoglutarate dehydrogenase complex deficiency; 2-Ketoglutarate dehydrogenase complex deficiency; 3-Hydroxy-3-methylglutaryl-CoA lyase deficiency; 3-Methyl-crotonyl-glycinuria; Alzheimer's disease; Anoxia; Frontotemporal dementia; Fructose-1,6-diphosphatase deficiency; Fumarase deficiency; Glucagon deficiency; Meningitis; Eosinophilic esophagitis; Eosinophilic esophagitis; Diabetes mellitus type 1; 3-methylglutaconic aciduria type II, X-linked; 3-methylglutaconic aciduria type II, X-linked	Detected and Quantified
MMDBc0000053	L-Threonine	C₄H₉NO₃ 119.1192 119.058243159		Human Feces Human Urine Human Saliva Human Blood Human Cerebrospinal Fluid (CSF) Human Sweat Human Breast Milk Human All Tissues Human Placenta Human Prostate	1956	Co-metabolite	Meat	Alzheimer's disease; Alzheimer's disease; Epilepsy; Frontotemporal dementia; Fumarase deficiency; Fumarase deficiency; Heart failure; Leukemia; Schizophrenia; Schizophrenia; Eosinophilic esophagitis; Eosinophilic esophagitis; Obesity; Obesity	Detected and Quantified
MMDBc0000119	Sodium	Na 22.9898 22.989769675	Homogeneous alkali metal compounds	Human Feces Human Blood Human Urine Human Cerebrospinal Fluid (CSF) Human Saliva Human Kidney	1975	Co-metabolite		21-Hydroxylase deficiency; Corticosterone methyl oxidase I deficiency; Corticosterone methyl oxidase I deficiency; Primary hypomagnesemia; Primary hypomagnesemia	Detected and Quantified
MMDBc0000036	Glycerol	C₃H₈O₃ 92.0938 92.047344122	Organooxygen compounds	Human Feces Human Blood Human Urine Human Cerebrospinal Fluid (CSF) Human Sweat Human Saliva Human Adipose Tissue Human Bladder Human Brain Human Epidermis Human Kidney Human Liver Human Neuron Human Pancreas Human Placenta Human Prostate Human Skeletal Muscle Human Spleen Human Testis Human Thyroid Gland	1978	Co-metabolite		Diabetes mellitus type 2; Glycerol kinase deficiency; Glycerol kinase deficiency; Glycerol kinase deficiency; Glycerol kinase deficiency; Glycerol kinase deficiency; Eosinophilic esophagitis	Detected and Quantified
MMDBc0000292	Iron(3+)	Fe 55.845 55.934942133	Homogeneous transition metal compounds	Human Feces	1993	Co-metabolite		Not Available	Detected and Quantified
MMDBc0000069	Pantothenic acid	C₉H₁₇NO₅ 219.235 219.110672659	Organooxygen compounds	Human Feces Human Cerebrospinal Fluid (CSF) Human Urine Human Breast Milk Human Blood Human Saliva Human Liver Human Placenta Human Prostate	1997	Co-metabolite		Alcoholism; Eosinophilic esophagitis	Detected and Quantified
MMDBc0000033	D-Glucose	C₆H₁₂O₆ 180.1559 180.063388116	Organooxygen compounds	Human Feces Human Blood Human Cerebrospinal Fluid (CSF) Human Urine Human Sweat Human Saliva Human Breast Milk Human Adipose Tissue Human Adrenal Cortex Human Adrenal Gland Human Adrenal Medulla Human Bladder Human Brain Human Epidermis Human Eye Lens Human Fibroblasts Human Intestine Human Kidney Human Liver Human Lung Human Neuron Human Ovary Human Pancreas Human Placenta Human Prostate Human Skeletal Muscle Human Testis	2001	Co-metabolite		21-Hydroxylase deficiency; 3-Hydroxy-3-methylglutaryl-CoA lyase deficiency; 3-Hydroxy-3-methylglutaryl-CoA lyase deficiency; 3-Hydroxy-3-methylglutaryl-CoA lyase deficiency; Acute myelogenous leukemia; Alzheimer's disease; Carnitine palmitoyltransferase I deficiency; Diabetes mellitus type 2; Diabetes mellitus type 2; Fructose-1,6-diphosphatase deficiency; Fructose-1,6-diphosphatase deficiency; Glucagon deficiency; Glucose transporter type 1 deficiency syndrome; Glucose transporter type 1 deficiency syndrome; Growth hormone deficiency; Hyperlipoproteinemia; Mitochondrial trifunctional protein deficiency; Primary hypomagnesemia; Sepsis; Eosinophilic esophagitis; Diabetes mellitus type 1; 3-Methyl-crotonyl-glycinuria; 3-Methyl-crotonyl-glycinuria; Addison's Disease; Diabetes mellitus type 2; Diabetes mellitus type 2	Detected and Quantified
MMDBc0000196	Sulfate	H₂O₄S 98.078 97.967379242	Non-metal oxoanionic compounds	Human Feces Human Urine Human Saliva Human Blood Human Placenta Human Sweat	2041	Co-metabolite	Not Available	Not Available	Detected and Quantified
MMDBc0000170	L-Tryptophan	C₁₁H₁₂N₂O₂ 204.2252 204.089877638	Indoles and derivatives	Human Feces Human Saliva Human Urine Human Cerebrospinal Fluid (CSF) Human Blood Human Sweat Human Breast Milk Human Fibroblasts Human Neuron Human Placenta Human Prostate	2046	Co-metabolite	Meat	Alzheimer's disease; Alzheimer's disease; Alzheimer's disease; Alzheimer's disease; Cachexia; Celiac disease; Epilepsy; Epilepsy; Friedreich's ataxia; Frontotemporal dementia; Hartnup disease; Hereditary spastic paraplegia; Hypothyroidism; Leukemia; Olivopontocerebral atrophy; Schizophrenia; Schizophrenia; Schizophrenia; Schizophrenia; Sepsis; Eosinophilic esophagitis; Obesity; Obesity; Alzheimer's Disease	Detected and Quantified
MMDBc0029795	NADPH	C₂₁H₃₀N₇O₁₇P₃ 745.4209 745.091102105		Human Feces Human Blood Human All Tissues	2049	Co-metabolite		Not Available	Detected and Quantified
MMDBc0029463	Adenosine monophosphate	C₁₀H₁₄N₅O₇P 347.2212 347.063084339	Purine nucleotides	Human Feces Human Saliva Human Cellular Cytoplasm Human Cerebrospinal Fluid (CSF) Human Blood Human All Tissues Human Placenta Human Urine	2073	Co-metabolite		Alzheimer's disease; Frontotemporal dementia	Detected and Quantified
MMDBc0029659	NADH	C₂₁H₂₉N₇O₁₄P₂ 665.441 665.124771695		Human Feces Human Blood Human Bladder Human Brain Human Fibroblasts Human Platelet Human Skeletal Muscle	2077	Co-metabolite	Not Available	Not Available	Detected and Quantified
MMDBc0029513	NAD	C₂₁H₂₈N₇O₁₄P₂ 664.433 664.116946663	(5'->5')-dinucleotides	Human Feces Human Blood Human Cellular Cytoplasm Human Adrenal Gland Human Brain Human Epidermis Human Fibroblasts Human Liver Human Placenta Human Platelet Human Prostate Human Skeletal Muscle	2085	Co-metabolite	Not Available	Pellagra	Detected and Quantified
MMDBc0000095	Uracil	C₄H₄N₂O₂ 112.0868 112.027277382	Diazines	Human Feces Human Urine Human Blood Human Cerebrospinal Fluid (CSF) Human Amniotic Fluid Human Saliva Human All Tissues Human Placenta Human Prostate	2156	Co-metabolite		Argininemia; Argininemia; Canavan disease; Canavan disease; Cerebral infarction; Dihydropyrimidine dehydrogenase deficiency; Hypertension; Liver disease; Uremia; Eosinophilic esophagitis; Argininemia; Argininemia; Carbamoyl Phosphate Synthetase Deficiency	Detected and Quantified

Displaying metabolites 24401 - 24425 of 24443 in total

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