Exact Mass: 205.0506
Exact Mass Matches: 205.0506
Found 500 metabolites which its exact mass value is equals to given mass value 205.0506,
within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error
0.01 dalton.
5-Methoxyindoleacetate
5-Methoxyindoleacetate, also known as 5-methoxy-IAA or 5-MIAA, belongs to the class of organic compounds known as indole-3-acetic acid derivatives. Indole-3-acetic acid derivatives are compounds containing an acetic acid (or a derivative) linked to the C3 carbon atom of an indole. 5-Methoxyindoleacetic acid is formed through oxidative deamination. It is identified in the urine, and the concentration is determined to be 1.3 µg/mL using GC-MS (PMID: 12908946). An increase in urinary 5-MIAA excretion was shown in patients with cancer of the stomach, rectum, and lung (PMID: 2446428). D006133 - Growth Substances > D010937 - Plant Growth Regulators > D007210 - Indoleacetic Acids 5-methoxyindoleacetic acid(5-MIAA) is formed through oxidative deamination. COVID info from PDB, Protein Data Bank KEIO_ID M078; [MS2] KO009067 KEIO_ID M078 Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS 5-Methoxyindole-3-acetic acid is a metabolite of Melatonin[1].
Indole-3-lactic acid
Indolelactic acid (CAS: 1821-52-9) is a tryptophan metabolite found in human plasma, serum, and urine. Tryptophan is metabolized by two major pathways in humans, either through kynurenine or via a series of indoles, and some of its metabolites are known to be biologically active. Indolelactic acid is present in various amounts, significantly higher in umbilical fetal plasma than in maternal plasma in the protein-bound form (PMID 2361979, 1400722, 3597614, 11060358, 1400722). Indolelactic acid is also a microbial metabolite; urinary indole-3-lactate is produced by Clostridium sporogenes (PMID: 29168502). Indolelactic acid is a tryptophan metabolite found in human plasma and serum and normal urine. Tryptophan is metabolized by two major pathways in humans, either through kynurenine or via a series of indoles, and some of its metabolites are known to be biologically active. Indolelactic acid is present in various amounts, significantly higher in umbilical foetal plasma than in maternal plasma in the protein-bound form. (PMID 2361979, 1400722, 3597614, 11060358, 1400722) [HMDB] Indolelactic acid (Indole-3-lactic acid) is a tryptophan (Trp) catabolite in Azotobacter vinelandii cultures. Indolelactic acid has anti-inflammation and potential anti-viral activity[1][3][4].
Xanthurenic acid
Xanthurenic acid, also known as xanthurenate or 8-hydroxykynurenic acid, is a member of the class of compounds known as quinoline carboxylic acids. Quinoline carboxylic acids are quinolines in which the quinoline ring system is substituted by a carboxyl group at one or more positions. Xanthurenic acid is slightly soluble (in water). Xanthurenic acid can be found primarily in blood, feces, and urine, as well as in human epidermis tissue. Within the cell, xanthurenic acid is primarily located in the membrane. Xanthurenic acid exists in all eukaryotes, ranging from yeast to humans. In humans, xanthurenic acid is involved in the tryptophan metabolism. Moreover, xanthurenic acid is found to be associated with citrullinemia type I, which is an inborn error of metabolism. Xanthurenic acid is a metabolite from tryptophan catabolism. It is a substrate of the enzyme methyltransferases (EC 2.1.1.-) in pathway tryptophan metabolism (KEGG). Xanthurenic acid is a metabolite from tryptophan catabolism. It is a substrate of the enzyme methyltransferases [EC 2.1.1.-] in pathway tryptophan metabolism (KEGG). [HMDB] D057847 - Lipid Regulating Agents > D000960 - Hypolipidemic Agents [Raw Data] CBA13_Xanthurenic-aci_neg_40eV_1-5_01_737.txt [Raw Data] CBA13_Xanthurenic-aci_neg_50eV_1-5_01_738.txt [Raw Data] CBA13_Xanthurenic-aci_neg_10eV_1-5_01_734.txt [Raw Data] CBA13_Xanthurenic-aci_neg_30eV_1-5_01_736.txt [Raw Data] CBA13_Xanthurenic-aci_pos_40eV_1-5_01_684.txt [Raw Data] CBA13_Xanthurenic-aci_pos_50eV_1-5_01_685.txt [Raw Data] CBA13_Xanthurenic-aci_pos_30eV_1-5_01_683.txt [Raw Data] CBA13_Xanthurenic-aci_pos_10eV_1-5_01_681.txt [Raw Data] CBA13_Xanthurenic-aci_pos_20eV_1-5_01_682.txt [Raw Data] CBA13_Xanthurenic-aci_neg_20eV_1-5_01_735.txt Xanthurenic acid. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=59-00-7 (retrieved 2024-07-01) (CAS RN: 59-00-7). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). Xanthurenic acid is a putative endogenous Group II metabotropic glutamate receptor agonist, on sensory transmission in the thalamus. Xanthurenic acid is a putative endogenous Group II metabotropic glutamate receptor agonist, on sensory transmission in the thalamus.
Lipoamide
Lipoamide is a trivial name for 6,8-dithiooctanoic amide. It is 6,8-dithiooctanoic acids functional form where the carboxyl group is attached to protein (or any other amine) by an amide linkage (containing -NH2) to an amino group. Lipoamide forms a thioester bond, oxidizing the disulfide bond, with acetaldehyde (pyruvate after it has been decarboxylated). It then transfers the acetaldehyde group to CoA which can then continue in the TCA cycle. Lipoamide is an intermediate in glycolysis/gluconeogenesis, citrate cycle (TCA cycle), alanine, aspartate and pyruvate metabolism, and valine, leucine and isoleucine degradation (KEGG:C00248). It is generated from dihydrolipoamide via the enzyme dihydrolipoamide dehydrogenase (EC:1.8.1.4) and then converted to S-glutaryl-dihydrolipoamide via the enzyme oxoglutarate dehydrogenase (EC:1.2.4.2). Lipoamide is the oxidized form of glutathione. (PMID:8957191) KEIO_ID L031; [MS2] KO009031 KEIO_ID L031
4,6-Dihydroxy-2-quinolinecarboxylic acid
4,6-Dihydroxy-2-quinolinecarboxylic acid is found in fats and oils. 4,6-Dihydroxy-2-quinolinecarboxylic acid is an alkaloid from Ginkgo biloba (ginkgo). Alkaloid from Ginkgo biloba (ginkgo). 4,6-Dihydroxy-2-quinolinecarboxylic acid is found in fats and oils.
Cinnamoylglycine
Cinnamoylglycine is known as a urinary metabolite in man (PMID 649712) although whether it is formed de novo from plant cinnamate or is a plant product excreted. unchanged has not been conclusively demonstrated. When cinnamoylglycine occurs naturally it is probably a food constituent excreted unchanged. It is not found when small quantities (0.5-6 g) of cinnamic acid are fed to man, but by analogy with animal experiments may be produced when much larger quantities are given. (PMID 6743769). Cinnamoylglycine is known as a urinary metabolite in man (PMID 649712) although whether it is formed de novo from plant cinnamate or is a plant product excreted Cinnamoylglycine is a glycine conjugate of cinnamic acid and a urinary metabolite in human. Cinnamoylglycine is used as a potential urinary biomarker indicating intact or disrupted colonization resistance during and after antibiotic treatment[1].
1-Isothiocyanato-6-(methylsulfinyl)hexane
1-Isothiocyanato-6-(methylsulfinyl)hexane is found in brassicas. Mustard oil from dames violet (Hesperis matronalis). 1-Isothiocyanato-6-(methylsulfinyl)hexane is a flavour component of Japanese horseradish (Wasabia japonica). Mustard oil from dames violet (Hesperis matronalis). Flavour component of Japanese horseradish (Wasabia japonica). 1-Isothiocyanato-6-(methylsulfinyl)hexane is found in brassicas.
Zeanic acid
Zeanic acid is found in cereals and cereal products. Zeanic acid is isolated from corn steep liquor. Isolated from corn steep liquor. Zeanic acid is found in cereals and cereal products.
Methyl 1-methoxy-1H-indole-3-carboxylate
Methyl 1-methoxy-1H-indole-3-carboxylate is found in herbs and spices. Methyl 1-methoxy-1H-indole-3-carboxylate is produced by Japanese horseradish (Wasabia japonica). Production by Japanese horseradish (Wasabia japonica). Methyl 1-methoxy-1H-indole-3-carboxylate is found in herbs and spices.
3-Indolehydracrylic acid
3-Indolehydracrylic acid belongs to the family of Indolyl Carboxylic Acids and Derivatives. These are compounds containing a carboxylic acid chain (of at least 2 carbon atoms) linked to an indole ring.
Pyridoxine hydrochloride
Pyridoxine is one of the compounds that can be called vitamin B6, along with pyridoxal and pyridoxamine. It differs from pyridoxamine by the substituent at the 4 position. It is often used as pyridoxine hydrochloride. D018977 - Micronutrients > D014815 - Vitamins Pyridoxine hydrochloride (Pyridoxol; Vitamin B6) is a pyridine derivative. Pyridoxine (Pyridoxol; Vitamin B6) exerts antioxidant effects in cell model of Alzheimer's disease via the Nrf-2/HO-1 pathway. Pyridoxine hydrochloride (Pyridoxol; Vitamin B6) is a pyridine derivative. Pyridoxine (Pyridoxol; Vitamin B6) exerts antioxidant effects in cell model of Alzheimer's disease via the Nrf-2/HO-1 pathway.
Methyl oxindole-3-acetate
Isolated from rice bran. Methyl oxindole-3-acetate is found in cereals and cereal products.
Lysozyme
Preservative. Prevents late blowing in semi-hard cheeses due to Clostridium tyrobutyricum. Lysozyme is part of the innate immune system. Children fed infant formula lack lysozyme in their diet and have three times the rate of diarrheal disease.[citation needed] Since lysozyme is a natural form of protection from pathogens like Salmonella, E.coli and Pseudomonas, when it is deficient due to infant formula feeding, can lead to increased incidence of disease.; Whereas the skin is a protective barrier due to its dryness and acidity, the conjunctiva (membrane covering the eye) is instead protected by secreted enzymes, mainly lysozyme and defensin. However, when these protective barriers fail, conjunctivitis results. Lysozyme is found in garden onion, papaya, and soft-necked garlic. Preservative. Prevents late blowing in semi-hard cheeses due to Clostridium tyrobutyricum
Indolelactic acid
Indolelactic acid (Indole-3-lactic acid) is a tryptophan (Trp) catabolite in Azotobacter vinelandii cultures. Indolelactic acid has anti-inflammation and potential anti-viral activity[1][3][4].
5,6,7,8-Tetrahydro[1]benzothieno[2,3-d]pyrimidin-4-amine
4-methoxy-7,8-dihydro-[1,3]dioxolo[4,5-g]isoquinoline
2-Isobenzazol, 1,3-dioxo-2-methyl-5,6-methylenedioxy-
1H-Indole-3-acetic acid, 2,3-dihydro-2-oxo-, methyl ester
methyl 2-oxo-1,2,3,4-tetrahydroquinoline-3-carboxylate
7-hydroxy-1-oxo-1,2-dihydroisoquinoline-5-carboxylic acid
6-Hydroxy-2-oxo-1,2-dihydroquinoline-4-carboxylic acid
Levonor
Precursor of epinephrine that is secreted by the ADRENAL MEDULLA and is a widespread central and autonomic neurotransmitter. Norepinephrine is the principal transmitter of most postganglionic sympathetic fibers, and of the diffuse projection system in the brain that arises from the LOCUS CERULEUS. It is also found in plants and is used pharmacologically as a sympathomimetic. DL-Norepinephrine hydrochloride is a synthetic phenylethylamine that mimics the sympathomimetic actions of the endogenous norepinephrine．DL-Norepinephrine hydrochloride is a neurotransmitter targets α1 and β1 adrenoceptors, has an increasing effect on subendocardial oxygen tension[1]. DL-Norepinephrine hydrochloride is a synthetic phenylethylamine that mimics the sympathomimetic actions of the endogenous norepinephrine．DL-Norepinephrine hydrochloride is a neurotransmitter targets α1 and β1 adrenoceptors, has an increasing effect on subendocardial oxygen tension[1]. Norepinephrine (Levarterenol; L-Noradrenaline) hydrochloride is a potent adrenergic receptor (AR) agonist. Norepinephrine activates α1, α2, β1 receptors[1][2][3][4]. Norepinephrine (Levarterenol; L-Noradrenaline) hydrochloride is a potent adrenergic receptor (AR) agonist. Norepinephrine activates α1, α2, β1 receptors[1][2][3][4]. Norepinephrine (Levarterenol; L-Noradrenaline) hydrochloride is a potent adrenergic receptor (AR) agonist. Norepinephrine activates α1, α2, β1 receptors[1][2][3][4].
AI3-08897
Diphenylamine hydrochloride, an organic compound isolated from coriander, is used mainly for its antioxidant properties. Diphenylamine is used as an industrial antioxidant, dye mordant and is also applied in agriculture as a fungicide and antihelmintic[1].
Methoxyindoleacetic acid
CONFIDENCE confident structure; IPB_RECORD: 277 IPB_RECORD: 277; CONFIDENCE confident structure
1-Isothiocyanato-6-(methylsulfinyl)-hexane
Acquisition and generation of the data is financially supported in part by CREST/JST.
Xanthurenic acid
A quinolinemonocarboxylic acid that is quinoline-2-carboxylic acid substituted by hydroxy groups at C-4 and C-8. D057847 - Lipid Regulating Agents > D000960 - Hypolipidemic Agents D009676 - Noxae > D000963 - Antimetabolites Xanthurenic acid is a putative endogenous Group II metabotropic glutamate receptor agonist, on sensory transmission in the thalamus. Xanthurenic acid is a putative endogenous Group II metabotropic glutamate receptor agonist, on sensory transmission in the thalamus.
N-Cinnamoylglycine
An N-acylglycine in which the acyl group is specified as (2E)-3-phenylprop-2-enoyl (cinnamoyl). MS2 deconvoluted using MS2Dec from all ion fragmentation data, MetaboLights identifier MTBLS1040; YAADMLWHGMUGQL-VOTSOKGWSA-N_STSL_0224_N-Cinnamoylglycine_0500fmol_190325_S2_LC02MS02_008; Spectrum acquired as described in Naz et al 2017 PMID 28641411. Preparation and submission to MassBank of North America by Chaleckis R. and Tada I. MS2 deconvoluted using CorrDec from all ion fragmentation data, MetaboLights identifier MTBLS1040; Spectrum acquired as described in Naz et al 2017 PMID 28641411. Preparation and submission to MassBank of North America by Chaleckis R. and Tada I.
Cinnamoylglycine
Cinnamoylglycine is a glycine conjugate of cinnamic acid and a urinary metabolite in human. Cinnamoylglycine is used as a potential urinary biomarker indicating intact or disrupted colonization resistance during and after antibiotic treatment[1].
Xanthurenate
Xanthurenic acid is a putative endogenous Group II metabotropic glutamate receptor agonist, on sensory transmission in the thalamus. Xanthurenic acid is a putative endogenous Group II metabotropic glutamate receptor agonist, on sensory transmission in the thalamus.
2,4-Dioxo-1,2,3,4-tetrahydroquinazoline-6-carboxamide
N-Phthaloylglycine
COVID info from PDB, Protein Data Bank Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS
7-amino-2-oxo-1H-1,8-naphthyridine-4-carboxylic acid
Carbamimidothioic acid,N-cyano-N-(3-methylphenyl)-, methyl ester
(4-methyl-2-pyridin-4-yl-1,3-thiazol-5-yl)methanamine
(4-Methyl-2-pyrid-3-yl-1,3-thiazol-5-yl)methylamine
3-(methylamino)-1-thiophen-2-ylpropan-1-one,hydrochloride
2-(5-Methyl-1,2,4-oxadiazol-3-yl)isonicotinic acid
5(4H)-OXAZOLONE, 4-[(3-FLUOROPHENYL)METHYLENE]-2-METHYL-
Methyl 2-oxo-1,2,3,4-tetrahydroquinoline-6-carboxylate
(R)-1-(2-Fluoro-4-methoxyphenyl)ethanamine hydrochloride
(S)-1-(3-Chloro-4-methylphenyl)ethanamine hydrochloride
1H-1-Benzazepine-6,7-dione, 2,5-dihydro-9-methoxy- (9CI)
4-METHYL-5-(3-METHYLPHENYL)-1,2,4-TRIAZOLE-3-THIOL
Telmesteine
C78273 - Agent Affecting Respiratory System > C74536 - Mucolytic Agent
(3-METHYL-ISOTHIAZOL-5-YL)-PYRIDIN-4-YLMETHYL-AMINE
(2-methyl-2,3-dihydro-1H-indol-1-yl)(oxo)acetic acid
(1R,2S)-2-(3,4-Difluorophenyl)cyclopropanamine hydrochloride (1:1 )
5-(Piperidin-4-yl)-1,3,4-oxadiazol-2(3H)-one hydrochloride
(R)-1-(3-Chloro-4-Methylphenyl)ethanamine hydrochloride
(R)-1-(4-Chloro-2-Methylphenyl)ethanamine hydrochloride
3-(1-OXO-1,3-DIHYDRO-2H-ISOINDOL-2-YL)PROPANOIC ACID
(s)-2-isocyanato-3-phenylpropionic acid methyl ester
Benzenemethanamine,N-(2-chloroethyl)-, hydrochloride (1:1)
4-hydroxy-2-oxo-1H-quinoline-3-carboxylic acid
2-[(1s)-2-hydroxy-1-methylethyl]-1h-isoindole-1,3(2h)-dione
(S)-1-(2-Fluoro-3-Methoxyphenyl)ethanamine hydrochloride
(S)-1-(2-Fluoro-4-Methoxyphenyl)ethanamine hydrochloride
(R)-1-(3-Fluoro-4-methoxyphenyl)ethanamine hydrochloride
3-(4-Fluorophenyl)-5-methylisoxazole-4-carboxaldehyde
(2-(AMINOMETHYL)-5-FLUOROPHENYL)BORONIC ACID HYDROCHLORIDE
(4-(Aminomethyl)-3-fluorophenyl)boronic acid hydrochloride
[5-(aminomethyl)-2-fluorophenyl]boronic acid,hydrochloride
(3-(Aminomethyl)-2-fluorophenyl)boronic acid hydrochloride
4-Piperidinecarboxylic acid, 1-(chlorocarbonyl)-, methyl ester (9CI)
(R)-1-(3-Chlorophenyl)propan-1-amine hydrochloride
1-nitro-6,7,8,9-tetrahydro-5h-benzo[7]annulen-5-one
(2-(AMINOMETHYL)-4-FLUOROPHENYL)BORONIC ACID HYDROCHLORIDE
2-Oxazoline-4-carboxylic acid,5-oxo-2-phenyl- (5CI)
(S)-3-(1H-IMIDAZOL-4-YL)-2-(METHYLAMINO)PROPANOIC ACID HYDROCHLORIDE
3-AMINO-3-(4-FLUORO-PHENYL)-PROPAN-1-OL HYDROCHLORIDE
(S)-1-(4-Chloro-2-Methylphenyl)ethanamine hydrochloride
2-benzofurancarboxylic acid, 6-amino-, ethyl ester
[1]Benzothieno[2,3-d]pyrimidine, 4-amino-5,6,7,8-tetrahydro-
5-(3-hydroxyphenyl)isoxazole-3-carboxylic acid(SALTDATA: FREE)
ethyl 4-amino-1-methylimidazole-2-carboxylate,hydrochloride
1-Piperidinecarboxylic acid, 4-(chlorocarbonyl)-, methyl ester (9CI)
1H-INDOLE-3-CARBOXYLIC ACID,4-METHOXY-,METHYL ESTER
(3-METHYL-ISOTHIAZOL-5-YL)-PYRIDIN-2-YLMETHYL-AMINE
6-METHYL-4-(TRIFLUOROMETHYL)-1,6-DIHYDROPYRAZOLO[3,4-C]PYRAZOL-3-YLAMINE
1-(3,4-DIFLUOROPHENYL)CYCLOPROPYLAMINE HYDROCHLORIDE
4-methyl-3-(4-methylphenyl)-1H-1,2,4-triazole-5-thione
(2R)-2-amino-2-(4-fluorophenyl)acetic acid,hydrochloride
5-Chloro-2-ethyl-1H-pyrrolo[2,3-b]pyridine-3-carbonitrile
Pyrrolidine, 3-ethenyl-4-methylene-1-(trifluoroacetyl)- (9CI)
(3-METHYL-ISOTHIAZOL-5-YL)-PYRIDIN-3-YLMETHYL-AMINE
5,8-Difluoro-1,2,3,4-Tetrahydroisoquinoline Hydrochloride
(r)-3-amino-4-(2-furyl)butanoic acid hydrochloride
5H-Indeno[5,6-d]-1,3-dioxole-5,6(7H)-dione 6-Oxime
(1R,2S)-rel-2-(3,4-Difluorophenyl)cyclopropanamine hydrochloride
5,7-Difluoro-2,3-dihydro-1H-inden-1-amine hydrochloride
(5-(1-CYANOCYCLOPROPYL)-2-FLUOROPHENYL)BORONIC ACID
(R)-1-(2-FLUORO-6-METHOXYPHENYL)ETHANAMINE HYDROCHLORIDE
(R)-1-(2-Fluoro-3-methoxyphenyl)ethanamine hydrochloride
(R)-1-(4-CHLORO-3-METHYLPHENYL)ETHANAMINE HYDROCHLORIDE
(R)-1-(2-Chlorophenyl)propan-1-amine hydrochloride
2,2,2-TRIFLUORO-1-(2-METHOXYPHENYL)ETHANAMINE HYDROCHLORIDE
2-(1-Methyl-1H-benzo[d]imidazol-2-yl)ethanethioamide
ETHYL 2-AMINO-1-METHYL-1H-IMIDAZOLE-5-CARBOXYLATE HYDROCHLORIDE
METHYL 7-OXO-7,8-DIHYDROPYRIDO[2,3-D]PYRIMIDINE-4-CARBOXYLATE
(S)-AMINO-(4-FLUORO-PHENYL)-ACETIC ACID HYDROCHLORIDE
(R)-lipoamide
A lipoamide obtained by condensation of the carboxy group of (R)-lipoic acid with ammonia. COVID info from COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS
2-Imino-5-(1-Pyridin-2-Yl-Meth-(E)-Ylidene)-1,3-Thiazolidin-4-One
Pyridoxine hydrochloride
D018977 - Micronutrients > D014815 - Vitamins Pyridoxine hydrochloride (Pyridoxol; Vitamin B6) is a pyridine derivative. Pyridoxine (Pyridoxol; Vitamin B6) exerts antioxidant effects in cell model of Alzheimer's disease via the Nrf-2/HO-1 pathway. Pyridoxine hydrochloride (Pyridoxol; Vitamin B6) is a pyridine derivative. Pyridoxine (Pyridoxol; Vitamin B6) exerts antioxidant effects in cell model of Alzheimer's disease via the Nrf-2/HO-1 pathway.
Norepinephrine hydrochloride
DL-Norepinephrine hydrochloride is a synthetic phenylethylamine that mimics the sympathomimetic actions of the endogenous norepinephrine．DL-Norepinephrine hydrochloride is a neurotransmitter targets α1 and β1 adrenoceptors, has an increasing effect on subendocardial oxygen tension[1]. DL-Norepinephrine hydrochloride is a synthetic phenylethylamine that mimics the sympathomimetic actions of the endogenous norepinephrine．DL-Norepinephrine hydrochloride is a neurotransmitter targets α1 and β1 adrenoceptors, has an increasing effect on subendocardial oxygen tension[1].
Noradrenaline hydrochloride
D018373 - Peripheral Nervous System Agents > D001337 - Autonomic Agents > D013566 - Sympathomimetics D018377 - Neurotransmitter Agents > D018663 - Adrenergic Agents > D000322 - Adrenergic Agonists D002317 - Cardiovascular Agents > D014662 - Vasoconstrictor Agents Norepinephrine (Levarterenol; L-Noradrenaline) hydrochloride is a potent adrenergic receptor (AR) agonist. Norepinephrine activates α1, α2, β1 receptors[1][2][3][4]. Norepinephrine (Levarterenol; L-Noradrenaline) hydrochloride is a potent adrenergic receptor (AR) agonist. Norepinephrine activates α1, α2, β1 receptors[1][2][3][4]. Norepinephrine (Levarterenol; L-Noradrenaline) hydrochloride is a potent adrenergic receptor (AR) agonist. Norepinephrine activates α1, α2, β1 receptors[1][2][3][4].
(R)-Lipoate
A lipoate that is the conjugate base of (R)-lipoic acid, obtained by deprotonation of the carboxy group; major species at pH 7.3.
lipoate
A thia fatty acid anion that is the conjugate base of lipoic acid; major species at pH 7.3. COVID info from COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS
