Exact Mass: 145.110273

Exact Mass Matches: 145.110273

Found 500 metabolites which its exact mass value is equals to given mass value 145.110273, within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error 0.01 dalton.

4-Acetamidobutanoate

N-Acetyl-gamma-amino-N-butyric acid

C6H11NO3 (145.0738896)


4-Acetamidobutanoic acid, also known as 4-acetamidobutanoate or N-acetyl-4-aminobutyric acid, is a member of the class of compounds known as gamma amino acids and derivatives. These compounds are amino acids having an -NH2 group attached to the gamma carbon atom. 4-Acetamidobutanoic acid is soluble in water. 4-Acetamidobutanoic acid can be found in a number of food items such as Rubus species (blackberry, raspberry), cassava, pepper (Capsicum frutescens), and napa cabbage, which makes 4-acetamidobutanoic acid a potential biomarker for the consumption of these food products. 4-Acetamidobutanoic acid can be found in blood, feces, and urine, as well as in human prostate tissue. 4-Acetamidobutanoic acid exists in all eukaryotes, ranging from yeast to humans. 4-Acetamidobutanoic acid is a GABA derivative, a product of the urea cycle and the metabolism of amino groups, and the product of NAD-linked aldehyde dehydrogenase (EC 1.2.1.3) (KEGG). 4-Acetamidobutanoic acid is a GABA derivative, product of the Urea cycle and metabolism of amino groups, the product of NAD-linked aldehyde dehydrogenase (EC 1.2.1.3) (KEGG) [HMDB]. 4-Acetamidobutanoic acid is found in many foods, some of which are custard apple, japanese walnut, shiitake, and oxheart cabbage. 4-Acetamidobutanoic acid (N-acetyl GABA), the main metabolite of GABA, exhibits antioxidant and antibacterial activities[1]. 4-Acetamidobutanoic acid (N-acetyl GABA), the main metabolite of GABA, exhibits antioxidant and antibacterial activities[1]. 4-Acetamidobutanoic acid (N-acetyl GABA), the main metabolite of GABA, exhibits antioxidant and antibacterial activities[1].

   

4-Guanidinobutanoic acid

4-[(diaminomethylidene)amino]butanoic acid

C5H11N3O2 (145.0851226)


4-Guanidinobutanoic acid, also known as gamma-guanidinobutyrate or 4-(carbamimidamido)butanoate, belongs to the class of organic compounds known as gamma amino acids and derivatives. These are amino acids having a (-NH2) group attached to the gamma carbon atom. 4-Guanidinobutanoic acid is a normal metabolite present in low concentrations. 4-Guanidinobutanoic acid exists in all eukaryotes, ranging from yeast to humans. Outside of the human body, 4-Guanidinobutanoic acid has been detected, but not quantified in a few different foods, such as apples, french plantains, and loquats. This could make 4-guanidinobutanoic acid a potential biomarker for the consumption of these foods. Patients with hyperargininemia have an arginase deficiency which leads to blockade of the urea cycle in the last step with several clinical symptoms. Owing to the arginase deficiency this patients accumulate arginine which leads eventually to epileptogenic guanidino compounds (PMID 7752905). 4-guanidinobutanoic acid, also known as gamma-guanidinobutyrate or 4-(carbamimidamido)butanoate, belongs to gamma amino acids and derivatives class of compounds. Those are amino acids having a (-NH2) group attached to the gamma carbon atom. 4-guanidinobutanoic acid is slightly soluble (in water) and a weakly acidic compound (based on its pKa). 4-guanidinobutanoic acid can be found in apple, french plantain, and loquat, which makes 4-guanidinobutanoic acid a potential biomarker for the consumption of these food products. 4-guanidinobutanoic acid can be found primarily in blood, cerebrospinal fluid (CSF), and urine, as well as in human prostate tissue. 4-guanidinobutanoic acid exists in all eukaryotes, ranging from yeast to humans. Moreover, 4-guanidinobutanoic acid is found to be associated with cirrhosis. CONFIDENCE standard compound; ML_ID 15 KEIO_ID G032 4-Guanidinobutanoic acid is a normal metabolite present in low concentrations. 4-Guanidinobutanoic acid is a normal metabolite present in low concentrations.

   

Lysinamide

2,6-diaminohexanamide

C6H15N3O (145.12150599999998)


KEIO_ID L027

   

Allysine

alpha-Aminoadipic acid delta-semialdehyde

C6H11NO3 (145.0738896)


Allysine (CAS: 1962-83-0), also known as 2-amino-6-oxohexanoic acid or 6-oxonorleucine, belongs to the class of organic compounds known as alpha-amino acids. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon). Outside of the human body, allysine has been detected, but not quantified in, several different foods, such as winged beans, wasabi, common verbena, arrowhead, and oats. This could make allysine a potential biomarker for the consumption of these foods. Allysine is a derivative of lysine used in the production of elastin and collagen. It is produced by the actions of the enzyme lysyl oxidase in the extracellular matrix and is essential in the crosslink formation that stabilizes collagen and elastin.

   

2-Keto-6-aminocaproate

alpha-keto-epsilon-Aminohexanoic acid

C6H11NO3 (145.0738896)


2-Keto-6-aminocaproate is an intermediate in lysine degradation and can be formed from L-lysine. L-Lysine is an essential amino-acid that is a necessary building block for all protein in the body. L-Lysine plays a major role in calcium absorption; building muscle protein; recovering from surgery or sports injuries; and the bodys production of hormones, enzymes, and antibodies. L-Lysine can be converted to 2-keto-6-aminocaproate via the enzyme L-lysine alpha-oxidase. 2-Keto-6-aminocaproate can spontaneously decarboxylate to 5-aminovalerate in the presence of the reaction product, hydrogen peroxide. It can also be spontaneously converted in solution to its cyclic form delta-piperideine-2-carboxylate. This has been demonstrated in vitro in the presence of catalase, which splits hydrogen peroxide. [HMDB] 2-Keto-6-aminocaproate is an intermediate in lysine degradation and can be formed from L-lysine. L-Lysine is an essential amino-acid that is a necessary building block for all protein in the body. L-Lysine plays a major role in calcium absorption; building muscle protein; recovering from surgery or sports injuries; and the bodys production of hormones, enzymes, and antibodies. L-Lysine can be converted to 2-keto-6-aminocaproate via the enzyme L-lysine alpha-oxidase. 2-Keto-6-aminocaproate can spontaneously decarboxylate to 5-aminovalerate in the presence of the reaction product, hydrogen peroxide. It can also be spontaneously converted in solution to its cyclic form delta-piperideine-2-carboxylate. This has been demonstrated in vitro in the presence of catalase, which splits hydrogen peroxide.

   

(S)-5-Amino-3-oxohexanoate

(5S)-5-Amino-3-oxohexanoic acid

C6H11NO3 (145.0738896)


S)-5-Amino-3-oxohexanoate is an intermediate in lysine degradation. L-Lysine is an essential amino acid that is a necessary building block for all protein in the body and It plays a major role in calcium absorption; building muscle protein; recovering from surgery or sports injuries; and the bodys production of hormones, enzymes, and antibodies. In lysine degradation pathway, (S)-5-Amino-3-oxohexanoate is a substrate for the enzyme L-erythro-3,5-diaminohexanoate dehydrogenase (EC 1.4.1.11) and can be generated from L-erythro-3,5-Diaminohexanoate. [HMDB] (S)-5-Amino-3-oxohexanoate is an intermediate in lysine degradation. L-Lysine is an essential amino acid that is a necessary building block for all protein in the body and It plays a major role in calcium absorption; building muscle protein; recovering from surgery or sports injuries; and the bodys production of hormones, enzymes, and antibodies. In lysine degradation pathway, (S)-5-Amino-3-oxohexanoate is a substrate for the enzyme L-erythro-3,5-diaminohexanoate dehydrogenase (EC 1.4.1.11) and can be generated from L-erythro-3,5-Diaminohexanoate.

   

2-Amino-5-oxohexanoate

2-amino-5-oxohexanoic acid

C6H11NO3 (145.0738896)


   

Fibrin

2-amino-N-[(methylcarbamoyl)methyl]acetamide

C5H11N3O2 (145.0851226)


   

2,4-dimethyl-1H-indole

2,4-dimethyl-1H-indole

C10H11N (145.0891446)


   

2-Aminoheptanoic acid

2-Aminoheptanoic acid

C7H15NO2 (145.110273)


An alpha-amino acid that is heptanoic acid in which one of the hydrogens at position 2 is replaced by an amino group.

   

(R)-2-AMINOHEPTANOIC ACID

(R)-2-AMINOHEPTANOIC ACID

C7H15NO2 (145.110273)


   

Isobutyrylglycine

2-(2-methylpropanamido)acetic acid

C6H11NO3 (145.0738896)


Isobutyrylglycine is an acyl glycine. Acyl glycines are normally minor metabolites of fatty acids. However, the excretion of certain acyl glycines is increased in several inborn errors of metabolism. In certain cases the measurement of these metabolites in body fluids can be used to diagnose disorders associated with mitochondrial fatty acid beta-oxidation. Acyl glycines are produced through the action of glycine N-acyltransferase (EC 2.3.1.13) which is an enzyme that catalyzes the chemical reaction: acyl-CoA + glycine < -- > CoA + N-acylglycine. Isobutyrylglycine is identified in large amount in urine of patients with isobutyryl-CoA dehydrogenase deficiency. Isobutyryl-CoA dehydrogenase deficiency is a disorder caused by the deficiency of isobutyryl-CoA dehydrogenase that is involved in the catabolism of the branched-chain amino acid valine (PMID 15505379). Moreover, Isobutyrylglycine is found to be associated with ethylmalonic encephalopathy and propionic acidemia, which are also inborn errors of metabolism. Isobutyrylglycine is a biomarker for the consumption of cheese. Isobutyrylglycine is an acyl glycine. Acyl glycines are normally minor metabolites of fatty acids. However, the excretion of certain acyl glycines is increased in several inborn errors of metabolism. In certain cases the measurement of these metabolites in body fluids can be used to diagnose disorders associated with mitochondrial fatty acid beta-oxidation. Acyl glycines are produced through the action of glycine N-acyltransferase (EC 2.3.1.13) which is an enzyme that catalyzes the chemical reaction:

   

Deoxycarnitine

4-(N-Trimethylamino)butyric acid

C7H15NO2 (145.110273)


4-Trimethylammoniobutanoic acid, also known as gamma-butyrobetaine (GBB) or 3-dehydroxycarnitine, is a highly water-soluble derivative of gamma-aminobutyric acid (GABA). It is also a precursor of L-carnitine. It is a substrate of gamma butyrobetaine hydroxylase/dioxygenase (also known as BBOX) which catalyzes the formation of L-carnitine from gamma-butyrobetaine, the last step in the L-carnitine biosynthesis pathway. Carnitine is essential for the transport of activated fatty acids across the mitochondrial membrane during mitochondrial beta-oxidation. Numerous disorders have been described that lead to disturbances in energy production and in intermediary metabolism which are characterized by the production and excretion of unusual acylcarnitines. A mutation in the gene coding for carnitine-acylcarnitine translocase, or the OCTN2 transporter aetiologically, causes a carnitine deficiency that results in poor intestinal absorption of dietary L-carnitine, impaired reabsorption by the kidney, and increased urinary loss. Determination of the qualitative pattern of acylcarnitines can be of diagnostic and therapeutic importance. The betaine structure of carnitine requires special analytical procedures for recording. The ionic nature of L-carnitine causes a high water solubility which decreases with increasing chain length of the ester group in the acylcarnitines. Therefore, the distribution of L-carnitine and acylcarnitines in various organs is defined by their function and their physicochemical properties as well. High-performance liquid chromatography (HPLC) permits screening for free and total carnitine, as well as complete quantitative acylcarnitine determination, including the long-chain acylcarnitine profile (PMID: 17508264, Monatshefte fuer Chemie (2005), 136(8), 1279-1291., Int J Mass Spectrom. 1999;188:39-52.). 3-Dehydroxycarnitine is an acylcarnitine. Numerous disorders have been described that lead to disturbances in energy production and in intermediary metabolism in the organism which are characterized by the production and excretion of unusual acylcarnitines. A mutation in the gene coding for carnitine-acylcarnitine translocase or the OCTN2 transporter aetiologically causes a carnitine deficiency that results in poor intestinal absorption of dietary L-carnitine, its impaired reabsorption by the kidney and, consequently, in increased urinary loss of L-carnitine. Determination of the qualitative pattern of acylcarnitines can be of diagnostic and therapeutic importance. The betaine structure of carnitine requires special analytical procedures for recording. The ionic nature of L-carnitine causes a high water solubility which decreases with increasing chain length of the ester group in the acylcarnitines. Therefore, the distribution of L-carnitine and acylcarnitines in various organs is defined by their function and their physico-chemical properties as well. High performance liquid chromatography (HPLC) permits screening for free and total carnitine, as well as complete quantitative acylcarnitine determination, including the long-chain acylcarnitine profile. (PMID: 17508264, Monatshefte fuer Chemie (2005), 136(8), 1279-1291., Int J Mass Spectrom. 1999;188:39-52.) [HMDB] COVID info from COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS

   

Butyrylglycine

2-Butyramidoacetic acid

C6H11NO3 (145.0738896)


N-Butyrylglycine is an acyl glycine. Acyl glycines are normally minor metabolites of fatty acids. However, the excretion of certain acyl glycines is increased in several inborn errors of metabolism, such as ethylmalonic encephalopathy. In certain cases the measurement of these metabolites in body fluids can be used to diagnose disorders associated with mitochondrial fatty acid beta-oxidation. Acyl glycines are produced through the action of glycine N-acyltransferase (EC 2.3.1.13), which is an enzyme that catalyzes the chemical reaction: acyl-CoA + glycine < -- > CoA + N-acylglycine amino acids composed of glycine substituted at the nitrogen rather than the usual carbon position, resulting in the loss of hydrogen bonding donors. Polymers of these compounds are called Peptoids. N-Butyrylglycine is an acyl glycine. Acyl glycines are normally minor metabolites of fatty acids. However, the excretion of certain acyl glycines is increased in several inborn errors of metabolism. In certain cases the measurement of these metabolites in body fluids can be used to diagnose disorders associated with mitochondrial fatty acid beta-oxidation. Acyl glycines are produced through the action of glycine N-acyltransferase (EC 2.3.1.13) which is an enzyme that catalyzes the chemical reaction:

   

2-Aminoheptanoate

alpha-DL-Aminoheptanoic acid

C7H15NO2 (145.110273)


2-Aminoheptanoate (CAS: 1115-90-8), also known as homonorleucine, is classified as a member of the alpha-amino acids. alpha-Amino acids are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon). 2-Aminoheptanoate is considered to be a soluble (in water) and a moderately acidic compound. 2-Aminoheptanoate can be found in feces.

   

L-cis-4-(Hydroxymethyl)-2-pyrrolidinecarboxylic acid

(2R,4S)-4-(Hydroxymethyl)-2-pyrrolidinecarboxylic acid

C6H11NO3 (145.0738896)


(2R,4S)-4-(Hydroxymethyl)-2-pyrrolidinecarboxylic acid is found in fruits. (2R,4S)-4-(Hydroxymethyl)-2-pyrrolidinecarboxylic acid is a constituent of the seeds of Eriobotrya japonica (loquat). Constituent of the seeds of Eriobotrya japonica (loquat). (2R,4S)-4-(Hydroxymethyl)-2-pyrrolidinecarboxylic acid is found in fruits.

   

L-trans-5-Hydroxy-2-piperidinecarboxylic acid

(2S,5R)-trans-5-Hydroxypiperidine-2-carboxylic acid

C6H11NO3 (145.0738896)


L-cis-5-Hydroxy-2-piperidinecarboxylic acid is found in fruits. L-cis-5-Hydroxy-2-piperidinecarboxylic acid is present in the leaves of Morus alba (white mulberry

   

2,4-Dimethyl-1H-indole

2,4-dimethyl-1H-indole

C10H11N (145.0891446)


2,4-Dimethyl-1H-indole is found in mushrooms. 2,4-Dimethyl-1H-indole is an alkaloid from fruit bodies of the unpalatable mushrooms Tricholoma sciodes and Tricholoma virgatum. Alkaloid from fruit bodies of the unpalatable mushrooms Tricholoma sciodes and Tricholoma virgatum. 2,4-Dimethyl-1H-indole is found in mushrooms.

   

Methyl aminolevulinate

delta-Aminolevulinic acid methyl ester

C6H11NO3 (145.0738896)


Methyl aminolevulinate is only found in individuals that have used or taken this drug. It is a prodrug that is metabolised to Protoporphyrin IX (a photosensitizer) used in photodynamic therapy.Photosensitization following application of methyl aminolevulinate cream occurs through the metabolic conversion of methyl aminolevulinate (prodrug) to photoactive porphyrins (PAP), which accumulates in the skin lesions to which the cream has been applied. When exposed to light of appropriate wavelength and energy, the accumulated photoactive porphyrins produce a photodynamic reaction, resulting in a cytotoxic process dependent upon the simultaneous presence of oxygen. The absorption of light results in an excited state of porphyrin molecules, and subsequent spin transfer from photoactive porphyrins to molecular oxygen generates singlet oxygen, which can further react to form superoxide and hydroxyl radicals. L - Antineoplastic and immunomodulating agents > L01 - Antineoplastic agents > L01X - Other antineoplastic agents > L01XD - Sensitizers used in photodynamic/radiation therapy D011838 - Radiation-Sensitizing Agents > D017319 - Photosensitizing Agents C1420 - Photosensitizing Agent D003879 - Dermatologic Agents

   

(±)-2-Butylthiazolidine

2-butyl-1,3-thiazolidine

C7H15NS (145.092515)


(±)-2-Butylthiazolidine is a flavouring ingredient. Flavouring ingredient

   

(±)-2-(2-Methylpropyl)thiazolidine

2-(2-methylpropyl)-1,3-thiazolidine

C7H15NS (145.092515)


(±)-2-(2-Methylpropyl)thiazolidine is a flavouring ingredient. Flavouring ingredient

   

N-(2-Carboxymethyl)-morpholine

N-(2-Carboxymethyl)-morpholine

C6H11NO3 (145.0738896)


N-(2-Carboxymethyl)-morpholine is a metabolite of mycophenolate mofetil. Mycophenolate mofetil (MMF) (brand names CellCept, Myfortic) is an immunosuppressant and prodrug of mycophenolic acid, used extensively in transplant medicine. It is a reversible inhibitor of inosine monophosphate dehydrogenase (IMPDH) in purine biosynthesis which is necessary for the growth of T cells and B cells. Other cells are able to recover purines via a separate, scavenger, pathway and are, thus, able to escape the effect. MMF is a less toxic alternative to azathioprine. (Wikipedia)

   

N-Propionylalanine

(2S)-2-[(1-hydroxypropylidene)amino]propanoic acid

C6H11NO3 (145.0738896)


N-propionylalanine is classified as a member of the n-acyl-l-alpha-amino acids. N-acyl-L-alpha-amino acids are n-acylated alpha amino acids which have the L-configuration of the alpha-carbon atom. N-propionylalanine is considered to be a slightly soluble (in water) and a weak acidic compound. N-propionylalanine can be found in humans.

   

2-Aminoheptanoic acid

alpha-Aminoenanthic acid

C7H15NO2 (145.110273)


   

1-Butyl-1-nitrosourea

Urea,N-butyl-N-nitroso-

C5H11N3O2 (145.0851226)


D009676 - Noxae > D002273 - Carcinogens

   

1-Methyl-3,4-dihydroisoquinoline

1-Methyl-3,4-dihydroisoquinoline

C10H11N (145.0891446)


   

1,3-Dimethylindole

1H-indole, 1,3-dimethyl-

C10H11N (145.0891446)


   

N-Benzylprop-2-yn-1-amine

N-Propargylbenzylamine hydrochloride

C10H11N (145.0891446)


   

2-Guanidinobutanoic acid

2-[(diaminomethylidene)amino]butanoic acid

C5H11N3O2 (145.0851226)


   

[(3-Methylbutyl)amino]acetic acid

2-[(3-methylbutyl)amino]acetic acid

C7H15NO2 (145.110273)


   

4-(3-Hydroxypropyl)morpholine

3-(morpholin-4-yl)propan-1-ol

C7H15NO2 (145.110273)


   

1H-Pyrido[3,2-c][1,2]diazepine

1H-Pyrido[3,2-c][1,2]diazepine

C8H7N3 (145.0639942)


   

7-Aminoheptanoic acid

Omega-aminoheptanoic acid

C7H15NO2 (145.110273)


   

Glutamamide

2-aminopentanediamide

C5H11N3O2 (145.0851226)


   

Heptaminol

Novartis brand OF heptaminol hydrochloride

C8H19NO (145.14665639999998)


C - Cardiovascular system > C01 - Cardiac therapy > C01D - Vasodilators used in cardiac diseases C78274 - Agent Affecting Cardiovascular System > C78322 - Cardiotonic Agent

   

L-Lysinamide

2,6-Diaminohexanimidate

C6H15N3O (145.12150599999998)


   

methyl 2-amino-4-oxopentanoate

Methyl 2-amino-4-oxopentanoic acid

C6H11NO3 (145.0738896)


   

Methyl L-leucinate

methyl 2-amino-4-methylpentanoate

C7H15NO2 (145.110273)


   

quinazolin-4-ylamine

3,4-dihydroquinazolin-4-imine

C8H7N3 (145.0639942)


   

But-2-en-2-yl 2-aminoethaneperoxoate

But-2-en-2-yl 2-aminoethaneperoxoic acid

C6H11NO3 (145.0738896)


   

Amino 6-oxohexanoate

Amino 6-oxohexanoic acid

C6H11NO3 (145.0738896)


   

L-2-Amino-6-oxohexanoic acid

alpha-Aminoadipic acid delta-semialdehyde

C6H11NO3 (145.0738896)


Found in collagen, elastin and heart muscle

   

trans-4-Hydroxy-N-methyl-L-proline

(-)-trans-4-Hydroxy-N-methyl-L-proline

C6H11NO3 (145.0738896)


4-Hydroxyhygric acid is a compound isolated from leaves of five species of the leguminous tropical tree Copuiferq. 4-Hydroxyhygric acid is the inhibitor of larval development of the seed-feeding bruchid beetle Callosobruchus maculatus and to have significant feeding deterrence of the leaf-feeding lepidopteran Spodoprera littoralis[1].

   

cis-5-Hydroxypipecolic acid

cis-5-Hydroxypipecolic acid

C6H11NO3 (145.0738896)


   

epsilon-Amino-alpha-ketocarproic acid

epsilon-Amino-alpha-ketocarproic acid

C6H11NO3 (145.0738896)


   

4-Hydroxypipecolic acid

4-HYDROXYPIPERIDINE-2-CARBOXYLIC ACID

C6H11NO3 (145.0738896)


   

4-Guanidinobutanoic acid

4-[(Aminoiminomethyl)amino]butanoic acid

C5H11N3O2 (145.0851226)


The 4-guanidino derivative of butanoic acid. MS2 deconvoluted using MS2Dec from all ion fragmentation data, MetaboLights identifier MTBLS1040; TUHVEAJXIMEOSA-UHFFFAOYSA-N_STSL_0214_4-Guanidinobutanoic acid_0031fmol_190326_S2_LC02MS02_086; 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. 4-Guanidinobutanoic acid is a normal metabolite present in low concentrations. 4-Guanidinobutanoic acid is a normal metabolite present in low concentrations.

   

N-acetyl-GABA

4-Acetamidobutanoic acid

C6H11NO3 (145.0738896)


4-Acetamidobutanoic acid (N-acetyl GABA), the main metabolite of GABA, exhibits antioxidant and antibacterial activities[1]. 4-Acetamidobutanoic acid (N-acetyl GABA), the main metabolite of GABA, exhibits antioxidant and antibacterial activities[1]. 4-Acetamidobutanoic acid (N-acetyl GABA), the main metabolite of GABA, exhibits antioxidant and antibacterial activities[1].

   

1,3-Diiminoisoindoline

1,3-Diiminoisoindoline

C8H7N3 (145.0639942)


   

heptaminol

heptaminol

C8H19NO (145.14665639999998)


C - Cardiovascular system > C01 - Cardiac therapy > C01D - Vasodilators used in cardiac diseases C78274 - Agent Affecting Cardiovascular System > C78322 - Cardiotonic Agent

   

tert-butyl 2-aminopropanoate

tert-butyl 2-aminopropanoate

C7H15NO2 (145.110273)


   

N-Methylisoleucine

N-Methylisoleucine

C7H15NO2 (145.110273)


   

N-Methyl-dl-leucine

N-Methyl-dl-leucine

C7H15NO2 (145.110273)


   

3-Amino-5-methylhexanoic acid

(S)-3-Amino-5-methyl-hexanoic acid

C7H15NO2 (145.110273)


   

3-amino-4-methylhexanoic acid

3-amino-4-methylhexanoic acid

C7H15NO2 (145.110273)


   

PAR_146.0966_8.3

Benzenemethanamine,N-2-propyn-1-yl-

C10H11N (145.0891446)


CONFIDENCE Probable structure via diagnostic evidence, tentative identification (Level 2b); INTERNAL_ID 1403

   

2-amino-4-oxohexanoic acid

2-amino-4-oxohexanoic acid

C6H11NO3 (145.0738896)


   

2-(2-amino-1-hydroxycyclobutyl)acetic acid

2-(2-amino-1-hydroxycyclobutyl)acetic acid

C6H11NO3 (145.0738896)


   
   

1,4-Lactone-(2S,3S,4R)-2,3,5-Triamino-4-hydroxypentanoic acid

1,4-Lactone-(2S,3S,4R)-2,3,5-Triamino-4-hydroxypentanoic acid

C5H11N3O2 (145.0851226)


   

1-amino-3-(hydroxymethyl)cyclobutane-1-carboxylic acid

1-amino-3-(hydroxymethyl)cyclobutane-1-carboxylic acid

C6H11NO3 (145.0738896)


   

2-Acetylamino-3-pentanol

2-Acetylamino-3-pentanol

C7H15NO2 (145.110273)


   

ethyl 4-amino-4-oxobutanoate

ethyl 4-amino-4-oxobutanoate

C6H11NO3 (145.0738896)


   
   

3-hydroxypiperidine-2-carboxylic acid

3-hydroxypiperidine-2-carboxylic acid

C6H11NO3 (145.0738896)


   
   

methyl 2-amino-3,3-dimethylbutanoate

methyl 2-amino-3,3-dimethylbutanoate

C7H15NO2 (145.110273)


   

2-amino-3-(hydroxymethyl)pent-3-enoic acid

2-amino-3-(hydroxymethyl)pent-3-enoic acid

C6H11NO3 (145.0738896)


   

2-hydroxyiminohexanoic acid

2-hydroxyiminohexanoic acid

C6H11NO3 (145.0738896)


   

2-amino-5-methylhexanoic acid

2-amino-5-methylhexanoic acid

C7H15NO2 (145.110273)


   

methyl 4-(dimethylamino)butanoate

methyl 4-(dimethylamino)butanoate

C7H15NO2 (145.110273)


   
   

2-amino-3-methyl-4-oxopentanoic acid

2-amino-3-methyl-4-oxopentanoic acid

C6H11NO3 (145.0738896)


   

3-Hydroxy-4-methylproline #

3-Hydroxy-4-methylproline #

C6H11NO3 (145.0738896)


   

2-Amino-3-methylhexanoic acid

2-Amino-3-methylhexanoic acid

C7H15NO2 (145.110273)


   
   

N,N-dimethylvaline

N,N-dimethylvaline

C7H15NO2 (145.110273)


   

hydroxypipecolic acid

2-Piperidinecarboxylicacid,1-hydroxy-(9CI)

C6H11NO3 (145.0738896)


N-hydroxypipecolic acid is an N-hydroxy-alpha-amino-acid resulting from the formal N-hydroxylation of the amino group of piperidine-carboxylic acid (pipecolic acid). It is a N-hydroxy-alpha-amino-acid and a piperidinemonocarboxylic acid. It is functionally related to a pipecolic acid. N-Hydroxypipecolic acid (1-Hydroxy-2-piperidinecarboxylic acid), a plant metabolite and a systemic acquired resistance (SAR) regulator, orchestrates SAR establishment in concert with the immune signal salicylic acid. N-Hydroxypipecolic acid accumulates systemically in the plant foliage in response to pathogen attack. N-Hydroxypipecolic acid induces SAR to bacterial and oomycete infection[1][2][3].

   

NMH-Pro

(2S, 4R)-4-hydroxy-1-methyl-2-pyrrolidinecarboxylic acid

C6H11NO3 (145.0738896)


(R)-4-hydroxy-1-methyl-L-proline is an L-proline derivative that is trans-4-hydroxy-L-proline in which the amino hydrogen has been replaced by a methyl group. It has a role as a plant metabolite and an anti-HIV-1 agent. It is a L-proline derivative and a pyrrolidine alkaloid. It is functionally related to a trans-4-hydroxy-L-proline. An L-proline derivative that is trans-4-hydroxy-L-proline in which the amino hydrogen has been replaced by a methyl group. 4-Hydroxyhygric acid is a compound isolated from leaves of five species of the leguminous tropical tree Copuiferq. 4-Hydroxyhygric acid is the inhibitor of larval development of the seed-feeding bruchid beetle Callosobruchus maculatus and to have significant feeding deterrence of the leaf-feeding lepidopteran Spodoprera littoralis[1].

   

g-Butyrobetaine

g-Butyrobetaine

C7H15NO2 (145.110273)


KEIO_ID C220

   

L-beta-Homoleucine

L-beta-Homoleucine

C7H15NO2 (145.110273)


Acquisition and generation of the data is financially supported in part by CREST/JST.

   

L-beta-Homoisoleucine

3-amino-4-methylhexanoic acid

C7H15NO2 (145.110273)


Acquisition and generation of the data is financially supported in part by CREST/JST.

   

4-Acetamidobutanoate

4-Acetamidobutanoic acid

C6H11NO3 (145.0738896)


4-Acetamidobutanoic acid (N-acetyl GABA), the main metabolite of GABA, exhibits antioxidant and antibacterial activities[1]. 4-Acetamidobutanoic acid (N-acetyl GABA), the main metabolite of GABA, exhibits antioxidant and antibacterial activities[1]. 4-Acetamidobutanoic acid (N-acetyl GABA), the main metabolite of GABA, exhibits antioxidant and antibacterial activities[1].

   
   

4-Guanidinobutanoate

4-Guanidinobutanoic acid

C5H11N3O2 (145.0851226)


4-Guanidinobutanoic acid is a normal metabolite present in low concentrations. 4-Guanidinobutanoic acid is a normal metabolite present in low concentrations.

   

L-beta-homoleucine-HCl

L-beta-homoleucine-HCl

C7H15NO2 (145.110273)


   

L-beta-Homoisoleucine hydrochloride

L-beta-Homoisoleucine hydrochloride

C7H15NO2 (145.110273)


   

Isobutyrylglycine

Isobutyrylglycine

C6H11NO3 (145.0738896)


   
   

4-Acetamidobutyric acid

4-Acetamidobutanoic acid

C6H11NO3 (145.0738896)


4-Acetamidobutanoic acid (N-acetyl GABA), the main metabolite of GABA, exhibits antioxidant and antibacterial activities[1]. 4-Acetamidobutanoic acid (N-acetyl GABA), the main metabolite of GABA, exhibits antioxidant and antibacterial activities[1]. 4-Acetamidobutanoic acid (N-acetyl GABA), the main metabolite of GABA, exhibits antioxidant and antibacterial activities[1].

   

4-Guanidinobutyric acid

4-Guanidinobutanoic acid

C5H11N3O2 (145.0851226)


4-Guanidinobutanoic acid is a normal metabolite present in low concentrations. 4-Guanidinobutanoic acid is a normal metabolite present in low concentrations.

   

N-Isobutyrylglycine

N-Isobutyrylglycine

C6H11NO3 (145.0738896)


An N-acylglycine in which the acyl group is specified as isobutryl.

   

N-Methylleucine

N-Methylleucine

C7H15NO2 (145.110273)


   

Butyrylglycine

Butyrylglycine

C6H11NO3 (145.0738896)


A N-acylglycine obtained by formal condensation of the carboxy group of butyric acid with the amino group of glycine.

   

4-GUANIDINO-BUTANOATE

4-GUANIDINO-BUTANOATE

C5H11N3O2 (145.0851226)


   

4-aminobutyric acid betaine

4-aminobutyric acid betaine

C7H15NO2 (145.110273)


MS2 deconvoluted using MS2Dec from all ion fragmentation data, MetaboLights identifier MTBLS1040; JHPNVNIEXXLNTR-UHFFFAOYSA-N_STSL_0045_4-aminobutyric acid betaine_0500fmol_180407_S2_LC02_MS02_49; 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.

   

Allysine (not validated)

Allysine (not validated)

C6H11NO3 (145.0738896)


Annotation level-3

   

g-Guanidinobutyrate

g-Guanidinobutyrate

C5H11N3O2 (145.0851226)


   
   

Leucine methyl ester

Leucine methyl ester

C7H15NO2 (145.110273)


   

Leucine ethyl ester

Leucine ethyl ester

C7H15NO2 (145.110273)


   

4-Guanidinobutanoic acid; LC-tDDA; CE10

4-Guanidinobutanoic acid; LC-tDDA; CE10

C5H11N3O2 (145.0851226)


   

4-Guanidinobutanoic acid; LC-tDDA; CE20

4-Guanidinobutanoic acid; LC-tDDA; CE20

C5H11N3O2 (145.0851226)


   

4-Guanidinobutanoic acid; LC-tDDA; CE30

4-Guanidinobutanoic acid; LC-tDDA; CE30

C5H11N3O2 (145.0851226)


   

4-Acetamidobutanoic acid; LC-tDDA; CE10

4-Acetamidobutanoic acid; LC-tDDA; CE10

C6H11NO3 (145.0738896)


   

4-Acetamidobutanoic acid; LC-tDDA; CE20

4-Acetamidobutanoic acid; LC-tDDA; CE20

C6H11NO3 (145.0738896)


   

4-Acetamidobutanoic acid; LC-tDDA; CE30

4-Acetamidobutanoic acid; LC-tDDA; CE30

C6H11NO3 (145.0738896)


   

4-Acetamidobutanoic acid; LC-tDDA; CE40

4-Acetamidobutanoic acid; LC-tDDA; CE40

C6H11NO3 (145.0738896)


   

N-Butyrylglycine; LC-tDDA; CE10

N-Butyrylglycine; LC-tDDA; CE10

C6H11NO3 (145.0738896)


   

N-Butyrylglycine; LC-tDDA; CE20

N-Butyrylglycine; LC-tDDA; CE20

C6H11NO3 (145.0738896)


   

N-Butyrylglycine; LC-tDDA; CE30

N-Butyrylglycine; LC-tDDA; CE30

C6H11NO3 (145.0738896)


   

N-Butyrylglycine; LC-tDDA; CE40

N-Butyrylglycine; LC-tDDA; CE40

C6H11NO3 (145.0738896)


   

N-Butyrylglycine; AIF; CE0; CorrDec

N-Butyrylglycine; AIF; CE0; CorrDec

C6H11NO3 (145.0738896)


   

N-Butyrylglycine; AIF; CE10; CorrDec

N-Butyrylglycine; AIF; CE10; CorrDec

C6H11NO3 (145.0738896)


   

N-Butyrylglycine; AIF; CE30; CorrDec

N-Butyrylglycine; AIF; CE30; CorrDec

C6H11NO3 (145.0738896)


   

4-Acetamidobutyric acid; AIF; CE0; CorrDec

4-Acetamidobutyric acid; AIF; CE0; CorrDec

C6H11NO3 (145.0738896)


   

4-Acetamidobutyric acid; AIF; CE10; CorrDec

4-Acetamidobutyric acid; AIF; CE10; CorrDec

C6H11NO3 (145.0738896)


   

4-Acetamidobutyric acid; AIF; CE30; CorrDec

4-Acetamidobutyric acid; AIF; CE30; CorrDec

C6H11NO3 (145.0738896)


   

4-Acetamidobutyric acid; AIF; CE0; MS2Dec

4-Acetamidobutyric acid; AIF; CE0; MS2Dec

C6H11NO3 (145.0738896)


   

4-Acetamidobutyric acid; AIF; CE10; MS2Dec

4-Acetamidobutyric acid; AIF; CE10; MS2Dec

C6H11NO3 (145.0738896)


   

4-Acetamidobutyric acid; AIF; CE30; MS2Dec

4-Acetamidobutyric acid; AIF; CE30; MS2Dec

C6H11NO3 (145.0738896)


   

4-Acetamidobutanoic acid

4-Acetamidobutanoic acid

C6H11NO3 (145.0738896)


An N-acyl-gamma-aminobutyric acid resulting from the monoacetylation of the nitrogen of GABA.

   
   

3-Carboxypropyl trimethylammonium

3-Carboxypropyl trimethylammonium

C7H15NO2 (145.110273)


   

L-Alanine n-butyl ester

(S)-BUTYL 2-AMINOPROPANOATE

C7H15NO2 (145.110273)


   

2R-aminoheptanoic acid

Heptanoic acid, 2-amino-, (R)-

C7H15NO2 (145.110273)


   

2S-aminoheptanoic acid

2S-aminoheptanoic acid

C7H15NO2 (145.110273)


   

2-amino-heptanoic acid

2-amino-heptanoic acid

C7H15NO2 (145.110273)


   

4-Aminomethylindole

1H-indole-4-methanamine

C9H9N2 (145.0765694)


   

N,N-Dimethyl-L-valine

N,N-Dimethyl-L-valine

C7H15NO2 (145.110273)


   

Propionylglycine methyl ester

Propionylglycine methyl ester

C6H11NO3 (145.0738896)


   

allysine

allysine

C6H11NO3 (145.0738896)


An alpha-amino acid consisting of lysine having an oxo group in place of the side-chain amino group.

   

L-Homonorleucine

Heptanoic acid, 2-amino-, (S)-

C7H15NO2 (145.110273)


   

DL-Homonorleucine

Heptanoic acid, 2-amino-, (1)-

C7H15NO2 (145.110273)


   

1-Nitroheptane

1-Nitroheptane

C7H15NO2 (145.110273)


A primary nitroalkane that is heptane substituted by a nitro group at position 1.

   

Methyl aminolevulinate

5-Aminolevulinic acid methyl ester;Aminolevulinic acid methyl ester

C6H11NO3 (145.0738896)


L - Antineoplastic and immunomodulating agents > L01 - Antineoplastic agents > L01X - Other antineoplastic agents > L01XD - Sensitizers used in photodynamic/radiation therapy D011838 - Radiation-Sensitizing Agents > D017319 - Photosensitizing Agents C1420 - Photosensitizing Agent D003879 - Dermatologic Agents

   

4-(hydroxymethyl)pyrrolidine-2-carboxylic acid

L-cis-4-(Hydroxymethyl)-2-pyrrolidinecarboxylic acid

C6H11NO3 (145.0738896)


   

5-hydroxypipecolic acid

(2S,5R)-trans-5-Hydroxypiperidine-2-carboxylic acid

C6H11NO3 (145.0738896)


A piperidinemonocarboxylic acid that is pipecolic acid with a hydroxy substituent at position 5.

   

2,4-Dimethylindole

2,4-dimethyl-1H-indole

C10H11N (145.0891446)


   

2-butyl-1,3-thiazolidine

(±)-2-Butylthiazolidine

C7H15NS (145.092515)


   

2-(2-methylpropyl)-1,3-thiazolidine

(±)-2-(2-Methylpropyl)thiazolidine

C7H15NS (145.092515)


   

Actinine

(3-carboxypropyl)trimethylazanium

C7H15NO2 (145.110273)


   

3-oxo-5S-amino-hexanoic acid

(5S)-5-Amino-3-oxohexanoic acid

C6H11NO3 (145.0738896)


   

trans-5-Hydroxypipecolic acid

trans-5-Hydroxypipecolic acid

C6H11NO3 (145.0738896)


   

Quinoline, 1,2-dihydro-1-methyl- (6CI,8CI,9CI)

Quinoline, 1,2-dihydro-1-methyl- (6CI,8CI,9CI)

C10H11N (145.0891446)


   

4-(1H-PYRAZOL-3-YL)PYRIDINE

4-(1H-PYRAZOL-3-YL)PYRIDINE

C8H7N3 (145.0639942)


   

Ethyl 3-dimethylaminopropionate

Ethyl 3-dimethylaminopropionate

C7H15NO2 (145.110273)


   

3-Aminotetrahydro-2H-pyran-3-carboxylic acid

3-Aminotetrahydro-2H-pyran-3-carboxylic acid

C6H11NO3 (145.0738896)


   
   

N-methyl-D-alloisoleucine

N-methyl-D-alloisoleucine

C7H15NO2 (145.110273)


   

N-ACETYL-N-METHYL-BETAALANIN

N-ACETYL-N-METHYL-BETAALANIN

C6H11NO3 (145.0738896)


   

Adipamic acid

6-Amino-6-oxohexanoic acid

C6H11NO3 (145.0738896)


   

2-(2,3-Dimethylphenyl)acetonitrile

2-(2,3-Dimethylphenyl)acetonitrile

C10H11N (145.0891446)


   
   

Morpholin-3-yl-acetic acid

Morpholin-3-yl-acetic acid

C6H11NO3 (145.0738896)


   

2(1H)-Pyrimidinone,4-amino-5-fluoro-1-methyl-

2(1H)-Pyrimidinone,4-amino-5-fluoro-1-methyl-

C5H8FN3O (145.065137)


   
   

2,5-Dimethylphenylacetonitrile

2,5-Dimethylphenylacetonitrile

C10H11N (145.0891446)


   

Alanine,N-acetyl-2-methyl-

Alanine,N-acetyl-2-methyl-

C6H11NO3 (145.0738896)


   

D-β,β-Diethylalanine

D-β,β-Diethylalanine

C7H15NO2 (145.110273)


   

4-(2-HYDRAZINYLETHYL)MORPHOLINE

4-(2-HYDRAZINYLETHYL)MORPHOLINE

C6H15N3O (145.12150599999998)


   

(S)-2-Isopropylamino-3-methyl-1-butanol

(S)-2-Isopropylamino-3-methyl-1-butanol

C8H19NO (145.14665639999998)


   

5-Methyl-L-norleucine

5-Methyl-L-norleucine

C7H15NO2 (145.110273)


   

L-2-Amino-3-ethylpentanoic acid

L-2-Amino-3-ethylpentanoic acid

C7H15NO2 (145.110273)


   

2-AMINO-3-ETHYL-PENTANOIC ACID

2-AMINO-3-ETHYL-PENTANOIC ACID

C7H15NO2 (145.110273)


   

Pyrido[3,4-d]pyrimidine, 4-methyl- (9CI)

Pyrido[3,4-d]pyrimidine, 4-methyl- (9CI)

C8H7N3 (145.0639942)


   

3-hydroxypipecolic acid

3-hydroxypipecolic acid

C6H11NO3 (145.0738896)


   

4,4-DIFLUOROCYCLOHEXANECARBONITRILE

4,4-DIFLUOROCYCLOHEXANECARBONITRILE

C7H9F2N (145.0703018)


   

2-MORPHOLINEACETIC ACID

2-MORPHOLINEACETIC ACID

C6H11NO3 (145.0738896)


   

Phridine Acetate

Phridine Acetate

C7H15NO2 (145.110273)


   

Quinazolin-4-amine

Quinazolin-4-ylamine

C8H7N3 (145.0639942)


COVID info from PDB, Protein Data Bank Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS

   

1H,3H,5H-Oxazolo[3,4-c]oxazole-7a(7H)-methanol

1H,3H,5H-Oxazolo[3,4-c]oxazole-7a(7H)-methanol

C6H11NO3 (145.0738896)


   

2,2,4-Trimethyl-1,4,2-oxazasilinan

2,2,4-Trimethyl-1,4,2-oxazasilinan

C6H15NOSi (145.092286)


   

(2,6-Dimethylphenyl)acetonitrile

(2,6-Dimethylphenyl)acetonitrile

C10H11N (145.0891446)


   
   

6-ETHYL-4-METHYL-2-MORPHOLINOL

6-ETHYL-4-METHYL-2-MORPHOLINOL

C7H15NO2 (145.110273)


   

ETHYL5-AMINOVALERATE

ETHYL5-AMINOVALERATE

C7H15NO2 (145.110273)


   
   

ethyl 2-ethoxy-2-iminoacetate

ethyl 2-ethoxy-2-iminoacetate

C6H11NO3 (145.0738896)


   

gamma-methyl-l-leucine

gamma-methyl-l-leucine

C7H15NO2 (145.110273)


   

4-Methylleucine

4-Methylleucine

C7H15NO2 (145.110273)


   

Urea, N-[(methoxyimino)methyl]-N,N-dimethyl- (9CI)

Urea, N-[(methoxyimino)methyl]-N,N-dimethyl- (9CI)

C5H11N3O2 (145.0851226)


   

Urea, N-[(E)-(methoxyimino)methyl]-N,N-dimethyl- (9CI)

Urea, N-[(E)-(methoxyimino)methyl]-N,N-dimethyl- (9CI)

C5H11N3O2 (145.0851226)


   

2-Piperidinecarboxylicacid,5-hydroxy-,(2R,5S)-(9CI)

2-Piperidinecarboxylicacid,5-hydroxy-,(2R,5S)-(9CI)

C6H11NO3 (145.0738896)


   

1,5-Naphthyridin-4-amine

1,5-Naphthyridin-4-amine

C8H7N3 (145.0639942)


   

Benzeneacetonitrile,3,4-dimethyl-

Benzeneacetonitrile,3,4-dimethyl-

C10H11N (145.0891446)


   

1-Ethyl-1H-indole

1-Ethyl-1H-indole

C10H11N (145.0891446)


   

(sec-butylamino)(oxo)acetic acid

(sec-butylamino)(oxo)acetic acid

C6H11NO3 (145.0738896)


   

3-AMINO-3-(2-PYRIDINYL)ACRYLONITRILE

3-AMINO-3-(2-PYRIDINYL)ACRYLONITRILE

C8H7N3 (145.0639942)


   

3-PHENYLPROPYL ISOCYANIDE

3-PHENYLPROPYL ISOCYANIDE

C10H11N (145.0891446)


   

4-Hydroxy-4-piperidinecarboxylic acid

4-Hydroxy-4-piperidinecarboxylic acid

C6H11NO3 (145.0738896)


   

N-Methoxy-N-methylpentanamide

N-Methoxy-N-methylpentanamide

C7H15NO2 (145.110273)


   

7-Quinazolinamine

7-Quinazolinamine

C8H7N3 (145.0639942)


   

Urea, N-(2-aminoethyl)-N-(1-methylethyl)- (9CI)

Urea, N-(2-aminoethyl)-N-(1-methylethyl)- (9CI)

C6H15N3O (145.12150599999998)


   

Pyrido[2,3-b]pyrazine, 7-methyl- (9CI)

Pyrido[2,3-b]pyrazine, 7-methyl- (9CI)

C8H7N3 (145.0639942)


   

5,8-dimethylindolizine

5,8-dimethylindolizine

C10H11N (145.0891446)


   

1,8-Naphthyridin-2-amine

1,8-Naphthyridin-2-amine

C8H7N3 (145.0639942)


   

1,6-naphthyridin-2-amine

1,6-naphthyridin-2-amine

C8H7N3 (145.0639942)


   
   

2,3-dihydro-1h-pyrrolo[2,3-b]pyridine-5-carbonitrile

2,3-dihydro-1h-pyrrolo[2,3-b]pyridine-5-carbonitrile

C8H7N3 (145.0639942)


   

2 4 5-TRIMETHYLBENZONITRILE

2 4 5-TRIMETHYLBENZONITRILE

C10H11N (145.0891446)


   

7-Aminoheptanoic acid

7-Aminoheptanoic acid

C7H15NO2 (145.110273)


   

cis-3-hydroxy-L-proline methyl ester

cis-3-hydroxy-L-proline methyl ester

C6H11NO3 (145.0738896)


   

2-(2-methylpropylamino)-2-oxoacetic acid

2-(2-methylpropylamino)-2-oxoacetic acid

C6H11NO3 (145.0738896)


   

(tert-butylamino)(oxo)acetic acid

(tert-butylamino)(oxo)acetic acid

C6H11NO3 (145.0738896)


   
   
   

3,3,3-Trimethoxypropionitrile

3,3,3-Trimethoxypropionitrile

C6H11NO3 (145.0738896)


   

(Diethyl-phosphinoyl)-acetonitrile

(Diethyl-phosphinoyl)-acetonitrile

C6H12NOP (145.0656472)


   

4,4-piperidinediyldimethanol()

4,4-piperidinediyldimethanol()

C7H15NO2 (145.110273)


   

2-(propanoylamino)propanoic acid

2-(propanoylamino)propanoic acid

C6H11NO3 (145.0738896)


   

Hexyl carbamate

Hexyl carbamate

C7H15NO2 (145.110273)


   

cis-4-hydroxy-d-proline methyl ester

cis-4-hydroxy-d-proline methyl ester

C6H11NO3 (145.0738896)


   
   

(3R)-3-Ammonio-4,4-dimethylpentanoate

(3R)-3-Ammonio-4,4-dimethylpentanoate

C7H15NO2 (145.110273)


   

3-Amino-4,4-dimethylpentanoic acid

3-Amino-4,4-dimethylpentanoic acid

C7H15NO2 (145.110273)


   

Ethyl 3-amino-3-methylbutanoate

Ethyl 3-amino-3-methylbutanoate

C7H15NO2 (145.110273)


   

1-(Nitromethyl)cyclopentanol

1-(Nitromethyl)cyclopentanol

C6H11NO3 (145.0738896)


   

N-Methyl-L-leucine

N-Methyl-L-leucine

C7H15NO2 (145.110273)


   

(4-Methoxytetrahydro-2h-pyran-4-yl)Methanamine

(4-Methoxytetrahydro-2h-pyran-4-yl)Methanamine

C7H15NO2 (145.110273)


   

4-(hydroxymethyl)-1-methylpiperidin-4-ol

4-(hydroxymethyl)-1-methylpiperidin-4-ol

C7H15NO2 (145.110273)


   

ethyl N-ethoxycarbonylmethanimidate

ethyl N-ethoxycarbonylmethanimidate

C6H11NO3 (145.0738896)


   

(R)-2-(MORPHOLIN-3-YL)ACETIC ACID

(R)-2-(MORPHOLIN-3-YL)ACETIC ACID

C6H11NO3 (145.0738896)


   

3-HYDRAZINO-3-IMINO-PROPANOIC ACID, ETHYL ESTER

3-HYDRAZINO-3-IMINO-PROPANOIC ACID, ETHYL ESTER

C5H11N3O2 (145.0851226)


   

(R)-2-(MORPHOLIN-2-YL)ACETIC ACID

(R)-2-(MORPHOLIN-2-YL)ACETIC ACID

C6H11NO3 (145.0738896)


   

(S)-2-MORPHOLINEACETIC ACID

(S)-2-MORPHOLINEACETIC ACID

C6H11NO3 (145.0738896)


   

(S)-2-(MORPHOLIN-3-YL)ACETIC ACID

(S)-2-(MORPHOLIN-3-YL)ACETIC ACID

C6H11NO3 (145.0738896)


   

1,2-Dimethylindole

1,2-Dimethylindole

C10H11N (145.0891446)


   

N-(2-hydroxyethyl)acetoacetamide

N-(2-hydroxyethyl)acetoacetamide

C6H11NO3 (145.0738896)


   

1-(dimethoxymethyl)pyrrolidine

1-(dimethoxymethyl)pyrrolidine

C7H15NO2 (145.110273)


   

morpholine-4-carbohydrazide

morpholine-4-carbohydrazide

C5H11N3O2 (145.0851226)


   

3-PYRROLIDINO-1,2-PROPANEDIOL

3-PYRROLIDINO-1,2-PROPANEDIOL

C7H15NO2 (145.110273)


   
   

4-(1H-imidazol-2-yl)pyridine

4-(1H-imidazol-2-yl)pyridine

C8H7N3 (145.0639942)


   

6,7-Dimethyl-1H-indole

6,7-Dimethyl-1H-indole

C10H11N (145.0891446)


   

5-Methylnorleucine

5-Methylnorleucine

C7H15NO2 (145.110273)


   

Pentanenitrile,5-chloro-2,2-dimethyl-

Pentanenitrile,5-chloro-2,2-dimethyl-

C7H12ClN (145.06582219999999)


   

1H-1,2,3-Triazole,1-phenyl-

1H-1,2,3-Triazole,1-phenyl-

C8H7N3 (145.0639942)


   

N-ACETYL-DL-2-AMINO-N-BUTYRIC ACID

N-ACETYL-DL-2-AMINO-N-BUTYRIC ACID

C6H11NO3 (145.0738896)


   

2-MORPHOLIN-4-YL-2-OXOETHANOL

2-MORPHOLIN-4-YL-2-OXOETHANOL

C6H11NO3 (145.0738896)


   

1,7-Naphthyridin-4-amine(9CI)

1,7-Naphthyridin-4-amine(9CI)

C8H7N3 (145.0639942)


   

Pyrimidine, 2-(1H-pyrrol-1-yl)- (9CI)

Pyrimidine, 2-(1H-pyrrol-1-yl)- (9CI)

C8H7N3 (145.0639942)


   

4-hydroxynipecotic acid

4-hydroxynipecotic acid

C6H11NO3 (145.0738896)


   

4-Piperidinecarboxylic acid, 3-hydroxy-, trans- (9CI)

4-Piperidinecarboxylic acid, 3-hydroxy-, trans- (9CI)

C6H11NO3 (145.0738896)


   

Quinazoline, 5-amino- (6CI)

Quinazoline, 5-amino- (6CI)

C8H7N3 (145.0639942)


   

2-AMINO-2-(TETRAHYDROFURAN-3-YL)ACETIC ACID

2-AMINO-2-(TETRAHYDROFURAN-3-YL)ACETIC ACID

C6H11NO3 (145.0738896)


   

CINNOLIN-4-AMINE

CINNOLIN-4-AMINE

C8H7N3 (145.0639942)


   

3-Methoxymorpholine-4-carbaldehyde

3-Methoxymorpholine-4-carbaldehyde

C6H11NO3 (145.0738896)


   

3-(2-pyridyl)pyrazole

3-(2-pyridyl)pyrazole

C8H7N3 (145.0639942)


   

2,3-Dimethylindole

2,3-Dimethyl-1H-indole

C10H11N (145.0891446)


   

1-phenyl-1H-1,2,4-triazole

1-phenyl-1H-1,2,4-triazole

C8H7N3 (145.0639942)


   

5,7-DIMETHYLINDOLE

5,7-Dimethyl-1H-indole

C10H11N (145.0891446)


   

N,N-Diethyl-1,1,1-trimethylsilanamine

N,N-Diethyl-1,1,1-trimethylsilanamine

C7H19NSi (145.12866939999998)


   

2-IMIDAZOL-1-YL-PYRIDINE

2-IMIDAZOL-1-YL-PYRIDINE

C8H7N3 (145.0639942)


   

4,6-Dimethylindole

4,6-Dimethylindole

C10H11N (145.0891446)


   

2-ACETAMIDOPROPIONIC ACID METHYL ESTER

2-ACETAMIDOPROPIONIC ACID METHYL ESTER

C6H11NO3 (145.0738896)


   

Ethyl 3-amino-2,2-dimethylpropanoate

Ethyl 3-amino-2,2-dimethylpropanoate

C7H15NO2 (145.110273)


   

5-(Dimethylamino)pentanoic acid

5-(Dimethylamino)pentanoic acid

C7H15NO2 (145.110273)


   

2-Methyl-1,3-dioxolane-2-acetamide

2-Methyl-1,3-dioxolane-2-acetamide

C6H11NO3 (145.0738896)


   

5-Amino-1,6-naphthyridine

5-Amino-1,6-naphthyridine

C8H7N3 (145.0639942)


   

6-Cinnolinamine

6-Cinnolinamine

C8H7N3 (145.0639942)


   

4-methylmorpholine-3-carboxylic acid

4-methylmorpholine-3-carboxylic acid

C6H11NO3 (145.0738896)


   

1-pyrazin-2-ylcyclopropane-1-carbonitrile

1-pyrazin-2-ylcyclopropane-1-carbonitrile

C8H7N3 (145.0639942)


   

2,5-Dimethylindole

2,5-Dimethyl-1H-indole

C10H11N (145.0891446)


   

4-Aminotetrahydro-2H-pyran-4-carboxylic acid

4-Aminotetrahydro-2H-pyran-4-carboxylic acid

C6H11NO3 (145.0738896)


   

2-Methylleucine

2-Methylleucine

C7H15NO2 (145.110273)


   

1,6-Naphthyridin-4-amine

1,6-Naphthyridin-4-amine

C8H7N3 (145.0639942)


   

8-Amino-1,7-naphthyridine

8-Amino-1,7-naphthyridine

C8H7N3 (145.0639942)


   

oxamic acid n-butyl ester

oxamic acid n-butyl ester

C6H11NO3 (145.0738896)


   

N-methyl-1-(thian-4-yl)methanamine

N-methyl-1-(thian-4-yl)methanamine

C7H15NS (145.092515)


   

1-ETHYL-4-(PIPERIDIN-4-YLMETHYL)PIPERAZINE

1-ETHYL-4-(PIPERIDIN-4-YLMETHYL)PIPERAZINE

C6H11NO3 (145.0738896)


   

(2S,4R)-METHYL 4-HYDROXYPYRROLIDINE-2-CARBOXYLATE

(2S,4R)-METHYL 4-HYDROXYPYRROLIDINE-2-CARBOXYLATE

C6H11NO3 (145.0738896)


   

(3-Hydroxy-1-pyrrolidinyl)acetic acid

(3-Hydroxy-1-pyrrolidinyl)acetic acid

C6H11NO3 (145.0738896)


   

2,6-Dimethyl-1H-indole

2,6-Dimethyl-1H-indole

C10H11N (145.0891446)


   

5-Hydroxy-3-piperidinecarboxylic acid

5-Hydroxy-3-piperidinecarboxylic acid

C6H11NO3 (145.0738896)


   

(2S,5S)-5-Hydroxy-2-piperidinecarboxylic acid

(2S,5S)-5-Hydroxy-2-piperidinecarboxylic acid

C6H11NO3 (145.0738896)


   

((2S,5R)-5-ETHYLMORPHOLIN-2-YL)METHANOL

((2S,5R)-5-ETHYLMORPHOLIN-2-YL)METHANOL

C7H15NO2 (145.110273)


   

Pyrido[3,4-b]pyrazine, 3-methyl- (7CI,8CI,9CI)

Pyrido[3,4-b]pyrazine, 3-methyl- (7CI,8CI,9CI)

C8H7N3 (145.0639942)


   

4-(2-hydroxyethyl)morpholin-3-one

4-(2-hydroxyethyl)morpholin-3-one

C6H11NO3 (145.0738896)


   

2-phenylbutyronitrile

2-phenylbutyronitrile

C10H11N (145.0891446)


   

1,4-Dimethyl-1H-indole

1,4-Dimethyl-1H-indole

C10H11N (145.0891446)


   

1,5-dimethylindole

1,5-dimethylindole

C10H11N (145.0891446)


   

ETHYL (S)-2-AMINO-2-METHYLBUTYRATE

ETHYL (S)-2-AMINO-2-METHYLBUTYRATE

C7H15NO2 (145.110273)


   

4-Phenylbutanenitrile

4-Phenylbutanenitrile

C10H11N (145.0891446)


   

4-(2-Methoxyethyl)Morpholine

4-(2-Methoxyethyl)Morpholine

C7H15NO2 (145.110273)


   

1-Propanol,2-(diethylamino)-2-methyl-

1-Propanol,2-(diethylamino)-2-methyl-

C8H19NO (145.14665639999998)


   

2-(TETRAHYDRO-2-FURANYLMETHOXY)-1-ETHANAMINE

2-(TETRAHYDRO-2-FURANYLMETHOXY)-1-ETHANAMINE

C7H15NO2 (145.110273)


   

2-(1H-Pyrazol-4-yl)pyridine

2-(1H-Pyrazol-4-yl)pyridine

C8H7N3 (145.0639942)


   

4-(1H-Pyrazol-4-yl)pyridine

4-(1H-Pyrazol-4-yl)pyridine

C8H7N3 (145.0639942)


   

4-Morpholineacetic Acid

Morpholin-4-yl-acetic acid

C6H11NO3 (145.0738896)


   

4-Methyl-L-leucine

4-Methyl-L-leucine

C7H15NO2 (145.110273)


   

(R)-3-Amino-5-methylhexanoic acid

(R)-3-Amino-5-methylhexanoic acid

C7H15NO2 (145.110273)


   
   
   

6-methylpyrido[2,3-b]pyrazine

6-methylpyrido[2,3-b]pyrazine

C8H7N3 (145.0639942)


   

4-ethenyl-2,3-dihydro-1H-isoindole

4-ethenyl-2,3-dihydro-1H-isoindole

C10H11N (145.0891446)


   

methyl morpholine-4-carboxylate

methyl morpholine-4-carboxylate

C6H11NO3 (145.0738896)


   

Ethyl-N-methyl malonamide

Ethyl-N-methyl malonamide

C6H11NO3 (145.0738896)


   

4-Morpholineethanol, a-methyl-

4-Morpholineethanol, a-methyl-

C7H15NO2 (145.110273)


   

METHYL BETA-(DIMETHYLAMINO)ISOBUTYRATE

METHYL BETA-(DIMETHYLAMINO)ISOBUTYRATE

C7H15NO2 (145.110273)


   

1,5-Naphthyridin-3-amine

1,5-Naphthyridin-3-amine

C8H7N3 (145.0639942)


   
   

(3R)-3-(2-Methoxyethoxy)pyrrolidine

(3R)-3-(2-Methoxyethoxy)pyrrolidine

C7H15NO2 (145.110273)


   

1-Phenyl-2,5-dihydro-1H-pyrrole

1-Phenyl-2,5-dihydro-1H-pyrrole

C10H11N (145.0891446)


   

Methyl (3S)-3-hydroxy-D-prolinate

Methyl (3S)-3-hydroxy-D-prolinate

C6H11NO3 (145.0738896)


   

2,6-Naphthyridin-1-amine(9CI)

2,6-Naphthyridin-1-amine(9CI)

C8H7N3 (145.0639942)


   

2-AMINO-2-(TETRAHYDRO-PYRAN-4-YL)-ETHANOL

2-AMINO-2-(TETRAHYDRO-PYRAN-4-YL)-ETHANOL

C7H15NO2 (145.110273)


   

2-AMINO-3-METHYL-HEXANOIC ACID

2-AMINO-3-METHYL-HEXANOIC ACID

C7H15NO2 (145.110273)


   

4-HYDROXY-1-PIPERIDINEETHANOL

4-HYDROXY-1-PIPERIDINEETHANOL

C7H15NO2 (145.110273)


   

2-Propenal, 3-(diethylamino)-2-fluoro-, (2Z)-

2-Propenal, 3-(diethylamino)-2-fluoro-, (2Z)-

C7H12FNO (145.0902874)


   

O-(2-ethylhexyl)hydroxylamine

O-(2-ethylhexyl)hydroxylamine

C8H19NO (145.14665639999998)


   

ethyl N-tert-butylcarbamate

ethyl N-tert-butylcarbamate

C7H15NO2 (145.110273)


   

D-Proline, 4-hydroxy-, methyl ester, (4S)

D-Proline, 4-hydroxy-, methyl ester, (4S)

C6H11NO3 (145.0738896)


   

2-Isoxazolidinecarboxylicacid,ethylester(9CI)

2-Isoxazolidinecarboxylicacid,ethylester(9CI)

C6H11NO3 (145.0738896)


   
   

Methyl 2-morpholinecarboxylate

Methyl 2-morpholinecarboxylate

C6H11NO3 (145.0738896)


   

5-Hydroxypiperidine-3-carboxylic Acid

5-Hydroxypiperidine-3-carboxylic Acid

C6H11NO3 (145.0738896)


   

6-Aminoquinazoline

6-Aminoquinazoline

C8H7N3 (145.0639942)


   

Methyl 3-methyl-L-valinate

Methyl 3-methyl-L-valinate

C7H15NO2 (145.110273)


   

N-(1-ISOPROPOXYETHYL)ACETAMIDE

N-(1-ISOPROPOXYETHYL)ACETAMIDE

C7H15NO2 (145.110273)


   

Carbamic acid,N-butyl-, ethyl ester

Carbamic acid,N-butyl-, ethyl ester

C7H15NO2 (145.110273)


   

emylcamate

emylcamate

C7H15NO2 (145.110273)


N - Nervous system > N05 - Psycholeptics > N05B - Anxiolytics > N05BC - Carbamates C78272 - Agent Affecting Nervous System > C28197 - Antianxiety Agent

   

Phthalimide diimide

Phthalimide diimide

C8H7N3 (145.0639942)


   

3-PHENYL-1H-1,2,4-TRIAZOLE

3-PHENYL-1H-1,2,4-TRIAZOLE

C8H7N3 (145.0639942)


   

Methyl 3-morpholinecarboxylate

Methyl 3-morpholinecarboxylate

C6H11NO3 (145.0738896)


   

2-((1-Methylpyrrolidin-3-yl)oxy)ethanol

2-((1-Methylpyrrolidin-3-yl)oxy)ethanol

C7H15NO2 (145.110273)


   

1,7-Naphthyridin-2-amine

1,7-Naphthyridin-2-amine

C8H7N3 (145.0639942)


   

Tricyclo[4.2.2.01,6]deca-2,4,9-trien-7-amine (9CI)

Tricyclo[4.2.2.01,6]deca-2,4,9-trien-7-amine (9CI)

C10H11N (145.0891446)


   
   

ethyl n,n-dimethyloxamate

ethyl n,n-dimethyloxamate

C6H11NO3 (145.0738896)


   

1,5-Naphthyridin-2-amine

1,5-Naphthyridin-2-amine

C8H7N3 (145.0639942)


   

N-Methyl-N-(trimethylsilyl)acetamide

N-Methyl-N-(trimethylsilyl)acetamide

C6H15NOSi (145.092286)


   

6-Quinoxalinamine

Quinoxalin-6-amine

C8H7N3 (145.0639942)


   

ALLYL N-(2-HYDROXYETHYL)CARBAMATE

ALLYL N-(2-HYDROXYETHYL)CARBAMATE

C6H11NO3 (145.0738896)


   

SUCCINAMICACIDETHYLESTER

SUCCINAMICACIDETHYLESTER

C6H11NO3 (145.0738896)


   

4-Methyl-4-nitrovaleraldehyde

4-Methyl-4-nitrovaleraldehyde

C6H11NO3 (145.0738896)


   

methyl 2-(diethylamino)acetate

methyl 2-(diethylamino)acetate

C7H15NO2 (145.110273)


   
   

indole, 2,7-dimethyl-

indole, 2,7-dimethyl-

C10H11N (145.0891446)


   

Acetyl-D-2-aminobutyric acid

Acetyl-D-2-aminobutyric acid

C6H11NO3 (145.0738896)


   

(4-(AMINOMETHYL)TETRAHYDRO-2H-PYRAN-4-YL)METHANOL

(4-(AMINOMETHYL)TETRAHYDRO-2H-PYRAN-4-YL)METHANOL

C7H15NO2 (145.110273)


   

L-Proline, 4-hydroxy-, methyl ester, (4S)- (9CI)

L-Proline, 4-hydroxy-, methyl ester, (4S)- (9CI)

C6H11NO3 (145.0738896)


   

4-Ethynyl-N,N-dimethylaniline

4-Ethynyl-N,N-dimethylaniline

C10H11N (145.0891446)


   

7-methyl-3,4-dihydroisoquinoline

7-methyl-3,4-dihydroisoquinoline

C10H11N (145.0891446)


   

(R)-Methyl morpholine-3-carboxylate

(R)-Methyl morpholine-3-carboxylate

C6H11NO3 (145.0738896)


   

butyl 2-aminopropanoate

butyl 2-aminopropanoate

C7H15NO2 (145.110273)


   

n,n-dimethylsuccinamic acid

n,n-dimethylsuccinamic acid

C6H11NO3 (145.0738896)


   

6-methyl-3,4-dihydroisoquinoline

6-methyl-3,4-dihydroisoquinoline

C10H11N (145.0891446)


   

4-methoxypyrrolidine-3-carboxylic acid

4-methoxypyrrolidine-3-carboxylic acid

C6H11NO3 (145.0738896)


   

3-Amino-2,2,4,4-tetramethylthietane

3-Amino-2,2,4,4-tetramethylthietane

C7H15NS (145.092515)


   

5-Dimethylamino-3-methyl-pentanol

5-Dimethylamino-3-methyl-pentanol

C8H19NO (145.14665639999998)


   

2-DIETHYLAMINO-N-HYDROXY-ACETAMIDINE

2-DIETHYLAMINO-N-HYDROXY-ACETAMIDINE

C6H15N3O (145.12150599999998)


   

2-ethyl-6-methylbenzonitrile

2-ethyl-6-methylbenzonitrile

C10H11N (145.0891446)


   

3-Aminoheptanoic acid

3-Aminoheptanoic acid

C7H15NO2 (145.110273)


   

(2S)-2-(methylamino)hexanoic acid

(2S)-2-(methylamino)hexanoic acid

C7H15NO2 (145.110273)


   

2,4-Dimethylphenylacetonitrile

2,4-Dimethylphenylacetonitrile

C10H11N (145.0891446)


   

3,5-Dimethylphenylacetonitrile

3,5-Dimethylphenylacetonitrile

C10H11N (145.0891446)


   

2-ethyl-2-(methylaminomethyl)butan-1-ol

2-ethyl-2-(methylaminomethyl)butan-1-ol

C8H19NO (145.14665639999998)


   

N-tert-Butyltrimethylsilylamine

2-methyl-N-trimethylsilylpropan-2-amine

C7H19NSi (145.12866939999998)


   

(3-amino-oxetan-3-yl)-acetic acid methyl ester

(3-amino-oxetan-3-yl)-acetic acid methyl ester

C6H11NO3 (145.0738896)


   

BUTANOIC ACID, 2-AMINO-3-OXO-, ETHYL ESTER

BUTANOIC ACID, 2-AMINO-3-OXO-, ETHYL ESTER

C6H11NO3 (145.0738896)


   
   

b-Alanine, N,N-diethyl-

b-Alanine, N,N-diethyl-

C7H15NO2 (145.110273)


   
   

2-[bis(trideuteriomethyl)amino]acetic acid,hydrochloride

2-[bis(trideuteriomethyl)amino]acetic acid,hydrochloride

C4H4ClD6NO2 (145.07766606799998)


   

(R)-(-)-2-CHLOROPHENYLGLYCINEMETHYLESTER

(R)-(-)-2-CHLOROPHENYLGLYCINEMETHYLESTER

C10H11N (145.0891446)


   

β-TBU-DL-ALANINE

β-TBU-DL-ALANINE

C7H15NO2 (145.110273)


   

N-Methyl-L-isoleucine

N-Methyl-L-isoleucine

C7H15NO2 (145.110273)


An N-methyl-L-amino acid that is L-isoleucine in which one of the hydrogens attached to the alpha-nitrogen is substituted by a methyl group.

   

N-Acetyl-D-alanine methylester

(R)-Methyl 2-acetamidopropanoate

C6H11NO3 (145.0738896)


   

5-Phenyl-3,4-dihydro-2H-pyrrole

2H-Pyrrole,3,4-dihydro-5-phenyl-

C10H11N (145.0891446)


   

4-ETHYLPHENYLACETONITRILE

4-ETHYLPHENYLACETONITRILE

C10H11N (145.0891446)


   

(3S)-3-(2-Methoxyethoxy)pyrrolidine

(3S)-3-(2-Methoxyethoxy)pyrrolidine

C7H15NO2 (145.110273)


   

4-Morpholinylacetic acid

4-Morpholinylacetic acid

C6H11NO3 (145.0738896)


   

2-Methyl-2-phenylpropanenitrile

2-Methyl-2-phenylpropanenitrile

C10H11N (145.0891446)


   

N-methyl-L-alloisoleucine

N-methyl-L-alloisoleucine

C7H15NO2 (145.110273)


   

N-Methyl-D-isoleucine

N-Methyl-D-isoleucine

C7H15NO2 (145.110273)


   

2-(tetrahydro-2H-thiopyran-4-yl)ethanamine

2-(tetrahydro-2H-thiopyran-4-yl)ethanamine

C7H15NS (145.092515)


   

(S)-(+)-N-Acetyl-L-Alanine Methyl Ester

(S)-(+)-N-Acetyl-L-Alanine Methyl Ester

C6H11NO3 (145.0738896)


   

(-)-3-oxetanylglycine methyl ester

(-)-3-oxetanylglycine methyl ester

C6H11NO3 (145.0738896)


   

N-methyl(2,2-dimethyl-1,3-dioxolan-4-yl)methanamine

N-methyl(2,2-dimethyl-1,3-dioxolan-4-yl)methanamine

C7H15NO2 (145.110273)


   

3,3-diMethoxyPiperidine

3,3-diMethoxyPiperidine

C7H15NO2 (145.110273)


   

4,7-Dimethyl-1H-indole

4,7-Dimethyl-1H-indole

C10H11N (145.0891446)


   

2-(Methoxycarbonylamino)-2-(oxetan-3-yl)acetic acid

2-(Methoxycarbonylamino)-2-(oxetan-3-yl)acetic acid

C6H11NO3 (145.0738896)


   
   

2,3-Dimethyl-3H-indole

2,3-Dimethyl-3H-indole

C10H11N (145.0891446)


   

2,4-Dimethyl-3H-indole

2,4-Dimethyl-3H-indole

C10H11N (145.0891446)


   

5,8-Dihydro-1-naphthalenamine

5,8-Dihydro-1-naphthalenamine

C10H11N (145.0891446)


   
   

DL-ALPHA-METHYLLEUCINE

DL-ALPHA-METHYLLEUCINE

C7H15NO2 (145.110273)


   

n,n-diethyl-2-methoxyacetamide

n,n-diethyl-2-methoxyacetamide

C7H15NO2 (145.110273)


   

5-21-04-00366 (Beilstein Handbook Reference)

5-21-04-00366 (Beilstein Handbook Reference)

C7H15NO2 (145.110273)


   

Methyl L-isoleucinate

Methyl L-isoleucinate

C7H15NO2 (145.110273)


   

(2R,5R)-5-Hydroxy-2-piperidinecarboxylic acid

(2R,5R)-5-Hydroxy-2-piperidinecarboxylic acid

C6H11NO3 (145.0738896)


   

(R)-(3-HYDROXYPYRROLIDIN-1-YL)-ACETIC ACID

(R)-(3-HYDROXYPYRROLIDIN-1-YL)-ACETIC ACID

C6H11NO3 (145.0738896)


   

4-ETHYNYL-2,6-DIMETHYL-PHENYLAMINE

4-ETHYNYL-2,6-DIMETHYL-PHENYLAMINE

C10H11N (145.0891446)


   

N-Boc ethylamine

N-Boc ethylamine

C7H15NO2 (145.110273)


   
   
   

((S)-3-Hydroxy-pyrrolidin-1-yl)-acetic acid

((S)-3-Hydroxy-pyrrolidin-1-yl)-acetic acid

C6H11NO3 (145.0738896)


   

CIS-3-AMINO-TETRAHYDROPYRAN-4-CARBOXYLIC ACID

CIS-3-AMINO-TETRAHYDROPYRAN-4-CARBOXYLIC ACID

C6H11NO3 (145.0738896)


   

Quinoline, 5,6-dihydro-4-methyl- (9CI)

Quinoline, 5,6-dihydro-4-methyl- (9CI)

C10H11N (145.0891446)


   

Quinoline, 5,6-dihydro-3-methyl- (9CI)

Quinoline, 5,6-dihydro-3-methyl- (9CI)

C10H11N (145.0891446)


   

(2S,4R)-1-BOC-4-AMINO-PYRROLIDINE-2-CARBOXYLICACID

(2S,4R)-1-BOC-4-AMINO-PYRROLIDINE-2-CARBOXYLICACID

C6H11NO3 (145.0738896)


   

3-(butylamino)propanoic acid

3-(butylamino)propanoic acid

C7H15NO2 (145.110273)


   

1,2,3,4-tetrahydro-naphthalen-1,4-imine

1,2,3,4-tetrahydro-naphthalen-1,4-imine

C10H11N (145.0891446)


   

7-Ethyl-1H-indole

7-Ethyl-1H-indole

C10H11N (145.0891446)


   

2-Ethyl-1H-indole

2-Ethyl-1H-indole

C10H11N (145.0891446)


   
   

2-[(Isopropylideneamino)oxy]propanoic acid

2-[(Isopropylideneamino)oxy]propanoic acid

C6H11NO3 (145.0738896)


   

Ethanol,2,2-(2-propenylimino)bis-

Ethanol,2,2-(2-propenylimino)bis-

C7H15NO2 (145.110273)


   

(S)-2-(TERT-BUTOXYCARBONYLAMINO)-3-(TERT-BUTYLDIPHENYLSILYLOXY)PROPANOICACID

(S)-2-(TERT-BUTOXYCARBONYLAMINO)-3-(TERT-BUTYLDIPHENYLSILYLOXY)PROPANOICACID

C7H15NO2 (145.110273)


   

2-(2-Methoxyethyl)Morpholine

2-(2-Methoxyethyl)Morpholine

C7H15NO2 (145.110273)


   

2-(4-MethylMorpholin-2-yl)ethanol

2-(4-MethylMorpholin-2-yl)ethanol

C7H15NO2 (145.110273)


   

2-Piperidinecarboxylicacid, 4-hydroxy-, (2R,4R)-rel-

2-Piperidinecarboxylicacid, 4-hydroxy-, (2R,4R)-rel-

C6H11NO3 (145.0738896)


   

cuminyl nitrile

cuminyl nitrile

C10H11N (145.0891446)


   

3-carbamoyl-2,2-dimethyl-propanoic acid

3-carbamoyl-2,2-dimethyl-propanoic acid

C6H11NO3 (145.0738896)


   

2-Morpholin-4-ylpropan-1-ol

2-Morpholin-4-ylpropan-1-ol

C7H15NO2 (145.110273)


   

3-Amino-4,4-dimethyl-pentanoic acid

3-Amino-4,4-dimethyl-pentanoic acid

C7H15NO2 (145.110273)


   

3-ETHYNYLPIPERIDINE HYDROCHLORIDE

3-ETHYNYLPIPERIDINE HYDROCHLORIDE

C7H12ClN (145.06582219999999)


   
   

N-Methyl-3-phenyl-2-propyn-1-amine

N-Methyl-3-phenyl-2-propyn-1-amine

C10H11N (145.0891446)


   

(2R)-4-methyl-2-(methylamino)pentanoic acid

(2R)-4-methyl-2-(methylamino)pentanoic acid

C7H15NO2 (145.110273)


   

5-Oxo-L-norleucine

5-Oxo-L-norleucine

C6H11NO3 (145.0738896)


   

(5S)-5-ammonio-3-oxohexanoate

(5S)-5-ammonio-3-oxohexanoate

C6H11NO3 (145.0738896)


   
   

(2s,3r)-2-Amino-3-methyl-4-oxopentanoic acid

(2s,3r)-2-Amino-3-methyl-4-oxopentanoic acid

C6H11NO3 (145.0738896)


   

(R)-2-Amino-6-oxohexanoic acid

(R)-2-Amino-6-oxohexanoic acid

C6H11NO3 (145.0738896)


   

2-Butylthiazolidine

2-Butylthiazolidine

C7H15NS (145.092515)


   

2-Isobutylthiazolidine

2-Isobutylthiazolidine

C7H15NS (145.092515)


   

2-amino-6-oxohexanoic acid

L-2-Amino-6-oxohexanoic acid

C6H11NO3 (145.0738896)


Found in collagen, elastin and heart muscle

   

[(3-Methylbutyl)amino]acetic acid

[(3-Methylbutyl)amino]acetic acid

C7H15NO2 (145.110273)


   

Methyl L-leucinate

Methyl L-leucinate

C7H15NO2 (145.110273)


   

Methyl 2-aminohexanoate

Methyl 2-aminohexanoate

C7H15NO2 (145.110273)


   
   

(2S)-2-amino-4-methylhexanoic acid

(2S)-2-amino-4-methylhexanoic acid

C7H15NO2 (145.110273)


   

L-lysinate

L-lysinate

C6H13N2O2- (145.0976978)


An optically active form of lysinate having L-configuration.

   

1,7-Dimethyl-1H-indole

1,7-Dimethyl-1H-indole

C10H11N (145.0891446)


   

(3R,4S)-3-amino-4-methylhexanoic acid

(3R,4S)-3-amino-4-methylhexanoic acid

C7H15NO2 (145.110273)


   

4-Guanidinobutyrate

4-Guanidinobutyrate

C5H11N3O2 (145.0851226)


   

(S)-2-Amino-6-oxohexanoate

(S)-2-Amino-6-oxohexanoate

C6H11NO3 (145.0738896)


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6-Amino-2-oxohexanoate

6-Amino-2-oxohexanoate

C6H11NO3 (145.0738896)


   

5-Hydroxypipecolate

5-Hydroxypipecolate

C6H11NO3 (145.0738896)


   

4-Guanidiniumylbutanamide(1+)

4-Guanidiniumylbutanamide(1+)

C5H13N4O+ (145.1089308)


A guanidinium ion arising from protonation of the imino NH of 4-guanidinobutanamide; major species at pH 7.3.

   

N-hydroxy-L-pipecolic acid

N-hydroxy-L-pipecolic acid

C6H11NO3 (145.0738896)


   

3-Hydroxy-3-methylhexanoate

3-Hydroxy-3-methylhexanoate

C7H13O3- (145.0864648)


A hydroxy monocarboxylic acid anion that is the conjugate base of 3-hydroxy-3-methylhexanoic acid, arising from deprotonation of the carboxy group.

   

2-Azaniumyl-5-oxohexanoate

2-Azaniumyl-5-oxohexanoate

C6H11NO3 (145.0738896)


   

l-Proline, 3-hydroxy-4-methyl-, (3S,4S)-

l-Proline, 3-hydroxy-4-methyl-, (3S,4S)-

C6H11NO3 (145.0738896)


   

N-acetylcadaverine(1+)

N-acetylcadaverine(1+)

C7H17N2O+ (145.1340812)


An ammonium ion resulting from the protonation of the primary amino group of N-acetylcadaverine. The major microspecies at pH 7.3.

   

3-hydroxy-4-methyl-L-proline

3-hydroxy-4-methyl-L-proline

C6H11NO3 (145.0738896)


   
   

beta-Homoleucine

beta-Homoleucine

C7H15NO2 (145.110273)


   

3-Hydroxy-4-methylhexanoate

3-Hydroxy-4-methylhexanoate

C7H13O3- (145.0864648)


   

(2S,3R)-2-amino-3-methyl-4-ketopentanoate

(2S,3R)-2-amino-3-methyl-4-ketopentanoate

C6H11NO3 (145.0738896)


   
   

But-2-en-2-yl 2-aminoethaneperoxoate

But-2-en-2-yl 2-aminoethaneperoxoate

C6H11NO3 (145.0738896)


   

2-Azaniumylheptanoate

2-Azaniumylheptanoate

C7H15NO2 (145.110273)


   

N-Hexylcarbamic acid

N-Hexylcarbamic acid

C7H15NO2 (145.110273)


COVID info from PDB, Protein Data Bank Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS

   

Lysinate

Lysinate

C6H13N2O2- (145.0976978)


An alpha-amino-acid anion that is the conjugate base of lysine, arising from deprotonation of the carboxy group.

   
   

(2E)-2-(hydroxyimino)isocaproic acid

(2E)-2-(hydroxyimino)isocaproic acid

C6H11NO3 (145.0738896)


   

(E)-2-(methoxyimino)-3-methylbutanoic acid

(E)-2-(methoxyimino)-3-methylbutanoic acid

C6H11NO3 (145.0738896)


   

(4R)-5-oxo-L-leucine

(4R)-5-oxo-L-leucine

C6H11NO3 (145.0738896)


A L-leucine derivative that is L-leucine substituted by an oxo group at position 5.

   

2-Azaniumyl-6-oxohexanoate

2-Azaniumyl-6-oxohexanoate

C6H11NO3 (145.0738896)


   

D-lysinate

D-lysinate

C6H13N2O2- (145.0976978)


An optically active form of lysinate having D-configuration.

   

(3S,5S)-3,5-Diaminocaproate

(3S,5S)-3,5-Diaminocaproate

C6H13N2O2- (145.0976978)


   
   

N-Ethylidenethreonine

N-Ethylidenethreonine

C6H11NO3 (145.0738896)


   

5-(1-Butynyl)-2-methylpyridine

5-(1-Butynyl)-2-methylpyridine

C10H11N (145.0891446)


   

5-Hydroxy-3,N-dimethylpentanamide

5-Hydroxy-3,N-dimethylpentanamide

C7H15NO2 (145.110273)


   
   

6-amino-2-oxohexanoic acid

6-amino-2-oxohexanoic acid

C6H11NO3 (145.0738896)


   

(S)-5-Amino-3-oxohexanoate

(S)-5-Amino-3-oxohexanoate

C6H11NO3 (145.0738896)


   

2-amino-5-oxohexanoic acid

2-amino-5-oxohexanoic acid

C6H11NO3 (145.0738896)


   

4-(Trimethylammonio)butanoate

4-(Trimethylammonio)butanoate

C7H15NO2 (145.110273)


An amino-acid betaine gamma-aminobutyric acid zwitterion in which all of the hydrogens attached to the nitrogen are replaced by methyl groups. COVID info from COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS

   

4-guanidinobutanoic acid zwitterion

4-guanidinobutanoic acid zwitterion

C5H11N3O2 (145.0851226)


Zwitterionic form of 4-guanidinobutanoic acid.

   

L-2-Aminoheptanoic acid

L-2-Aminoheptanoic acid

C7H15NO2 (145.110273)


An optically active form of 2-aminoheptanoic acid having L-configuration.

   
   

N-Propionylalanine

N-Propionylalanine

C6H11NO3 (145.0738896)


   

allysine zwitterion

allysine zwitterion

C6H11NO3 (145.0738896)


Zwitterionic form of allysine arising from transfer of a proton from the carboxy to the amino group; major species at pH 7.3.

   

(2R)-aminoheptanoic acid

(2R)-aminoheptanoic acid

C7H15NO2 (145.110273)


An alpha-amino fatty acid that is heptanoic acid substituted by an amino group at position 2 (the 2R stereoisomer).

   

6-amino-2-oxohexanoic acid zwitterion

6-amino-2-oxohexanoic acid zwitterion

C6H11NO3 (145.0738896)


Zwitterionic form of 6-amino-2-oxohexanoic acid arising from transfer of a proton from the carboxy to the amino group; major species at pH 7.3.

   

L-allysine

L-allysine

C6H11NO3 (145.0738896)


An optically active form of allysine having L-configuration.

   

L-allysine zwitterion

L-allysine zwitterion

C6H11NO3 (145.0738896)


An amino acid zwitterion arising from transfer of a proton from the carboxy to the amino group of L-allysine; major species at pH 7.3.

   

Aminoheptanoic acid

Aminoheptanoic acid

C7H15NO2 (145.110273)


   

N,N-Dimethyl-5-aminovaleric acid

N,N-Dimethyl-5-aminovaleric acid

C7H15NO2 (145.110273)


   
   

Dehydroxycarnitine

Dehydroxycarnitine

C7H15NO2 (145.110273)


   

Acetamidobutanoic acid

Acetamidobutanoic acid

C6H11NO3 (145.0738896)


   

beta-Homoisoleucine

beta-Homoisoleucine

C7H15NO2 (145.110273)


   

Guanidinobutanoic acid

Guanidinobutanoic acid

C5H11N3O2 (145.0851226)


   

N-Methyl-4-hydroxyproline

N-Methyl-4-hydroxyproline

C6H11NO3 (145.0738896)


   

Ketoaminocaproate

Ketoaminocaproate

C6H11NO3 (145.0738896)


   

(2r,4s)-4-hydroxypiperidine-2-carboxylic acid

(2r,4s)-4-hydroxypiperidine-2-carboxylic acid

C6H11NO3 (145.0738896)


   

(2s,4r)-4-(hydroxymethyl)pyrrolidine-2-carboxylic acid

(2s,4r)-4-(hydroxymethyl)pyrrolidine-2-carboxylic acid

C6H11NO3 (145.0738896)


   

(2s)-4-hydroxy-1-methylpyrrolidine-2-carboxylic acid

(2s)-4-hydroxy-1-methylpyrrolidine-2-carboxylic acid

C6H11NO3 (145.0738896)


   

(2r,3s)-1-amino-3-hydroxy-2-methylcyclobutane-1-carboxylic acid

(2r,3s)-1-amino-3-hydroxy-2-methylcyclobutane-1-carboxylic acid

C6H11NO3 (145.0738896)


   

(3r,6r)-3,6-dihydroxy-1-methylpiperidin-2-one

(3r,6r)-3,6-dihydroxy-1-methylpiperidin-2-one

C6H11NO3 (145.0738896)


   

(2r,5s)-5-hydroxypiperidine-2-carboxylic acid

(2r,5s)-5-hydroxypiperidine-2-carboxylic acid

C6H11NO3 (145.0738896)


   

3-ethyl-1h-indole

3-ethyl-1h-indole

C10H11N (145.0891446)