Exact Mass: 146.1127

Exact Mass Matches: 146.1127

Found 132 metabolites which its exact mass value is equals to given mass value 146.1127, within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error 0.001 dalton.

L-Lysine

(2S)-2,6-diaminohexanoic acid

C6H14N2O2 (146.1055)


Lysine (Lys), also known as L-lysine is an alpha-amino acid. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon). Amino acids are organic compounds that contain amino (–NH2) and carboxyl (–COOH) functional groups, along with a side chain (R group) specific to each amino acid. Lysine is one of 20 proteinogenic amino acids, i.e., the amino acids used in the biosynthesis of proteins. Lysine is found in all organisms ranging from bacteria to plants to animals. It is classified as an aliphatic, positively charged or basic amino acid. In humans, lysine is an essential amino acid, meaning the body cannot synthesize it, and it must be obtained from the diet. Lysine is high in foods such as wheat germ, cottage cheese and chicken. Of meat products, wild game and pork have the highest concentration of lysine. Fruits and vegetables contain little lysine, except avocados. Normal requirements for lysine have been found to be about 8 g per day or 12 mg/kg in adults. Children and infants need more, 44 mg/kg per day for an eleven to-twelve-year old, and 97 mg/kg per day for three-to six-month old. In organisms that synthesise lysine, it has two main biosynthetic pathways, the diaminopimelate and α-aminoadipate pathways, which employ distinct enzymes and substrates and are found in diverse organisms. Lysine catabolism occurs through one of several pathways, the most common of which is the saccharopine pathway. Lysine plays several roles in humans, most importantly proteinogenesis, but also in the crosslinking of collagen polypeptides, uptake of essential mineral nutrients, and in the production of carnitine, which is key in fatty acid metabolism. Lysine is also often involved in histone modifications, and thus, impacts the epigenome. Lysine is highly concentrated in muscle compared to most other amino acids. Normal lysine metabolism is dependent upon many nutrients including niacin, vitamin B6, riboflavin, vitamin C, glutamic acid and iron. Excess arginine antagonizes lysine. Several inborn errors of lysine metabolism are known, such as cystinuria, hyperdibasic aminoaciduria I, lysinuric protein intolerance, propionic acidemia, and tyrosinemia I. Most are marked by mental retardation with occasional diverse symptoms such as absence of secondary sex characteristics, undescended testes, abnormal facial structure, anemia, obesity, enlarged liver and spleen, and eye muscle imbalance. Lysine also may be a useful adjunct in the treatment of osteoporosis. Although high protein diets result in loss of large amounts of calcium in urine, so does lysine deficiency. Lysine may be an adjunct therapy because it reduces calcium losses in urine. Lysine deficiency also may result in immunodeficiency. Requirements for lysine are probably increased by stress. Lysine toxicity has not occurred with oral doses in humans. Lysine dosages are presently too small and may fail to reach the concentrations necessary to prove potential therapeutic applications. Lysine metabolites, amino caproic acid and carnitine have already shown their therapeutic potential. Thirty grams daily of amino caproic acid has been used as an initial daily dose in treating blood clotting disorders, indicating that the proper doses of lysine, its precursor, have yet to be used in medicine. Low lysine levels have been found in patients with Parkinsons, hypothyroidism, kidney disease, asthma and depression. The exact significance of these levels is unclear, yet lysine therapy can normalize the level and has been associated with improvement of some patients with these conditions. Abnormally elevated hydroxylysines have been found in virtually all chronic degenerative diseases and those treated with coumadin therapy. The levels of this stress marker may be improved by high doses of vitamin C. Lysine is particularly useful in therapy for marasmus (wasting) (http://www.dcnutrition.com). Lysine has also been sh... [Spectral] L-Lysine (exact mass = 146.10553) and Carnosine (exact mass = 226.10659) were not completely separated on HPLC under the present analytical conditions as described in AC$XXX. Additionally some of the peaks in this data contains dimers and other unidentified ions. Dietary supplement, nutrient. Found widely in protein hydrolysates, e.g. casein, egg albumen, fibrin, gelatin, beet molasses. Flavouring agent for a variety of foods L-Lysine. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=56-87-1 (retrieved 2024-07-01) (CAS RN: 56-87-1). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). L-lysine is an essential amino acid[1][2] with important roles in connective tissues and carnitine synthesis, energy production, growth in children, and maintenance of immune functions[2]. L-lysine is an essential amino acid[1][2] with important roles in connective tissues and carnitine synthesis, energy production, growth in children, and maintenance of immune functions[2].

   

Acetylcholine

Bournonville brand OF acetylcholine chloride

[C7H16NO2]+ (146.1181)


Acetylcholine (ACh) is a neurotransmitter. Acetylcholine in vertebrates is the major transmitter at neuromuscular junctions, autonomic ganglia, parasympathetic effector junctions, a subset of sympathetic effector junctions, and at many sites in the central nervous system. Its physiological and pharmacological effects, metabolism, release, and receptors have been well documented in several species. ACh has been considered an important excitatory neurotransmitter in the carotid body (CB). Various nicotinic and muscarinic ACh receptors are present in both afferent nerve endings and glomus cells. Therefore, ACh can depolarize or hyperpolarize the cell membrane depending on the available receptor type in the vicinity. Binding of ACh to its receptor can create a wide variety of cellular responses including opening cation channels (nicotinic ACh receptor activation), releasing Ca2+ from intracellular storage sites (via muscarinic ACh receptors), and modulating activities of K+ and Ca2+ channels. Interactions between ACh and other neurotransmitters (dopamine, adenosine, nitric oxide) have been known, and they may induce complicated responses. Cholinergic biology in the CB differs among species and even within the same species due to different genetic composition. Development and environment influence cholinergic biology. Pharmacological data clearly indicate that both muscarinic and nicotinic acetylcholine receptors have a role in the encoding of new memories. Localized lesions and antagonist infusions demonstrate the anatomical locus of these cholinergic effects, and computational modeling links the function of cholinergic modulation to specific cellular effects within these regions. Acetylcholine has been shown to increase the strength of afferent input relative to feedback, to contribute to theta rhythm oscillations, activate intrinsic mechanisms for persistent spiking, and increase the modification of synapses. These effects might enhance different types of encoding in different cortical structures. In particular, the effects in entorhinal and perirhinal cortex and hippocampus might be important for encoding new episodic memories. The role of ACh in attention has been repeatedly demonstrated in several tasks. Acetylcholine is linked to response accuracy in voluntary and reflexive attention and also to response speed in reflexive attention. It is well known that those with Attention-deficit/hyperactivity disorders tend to be inaccurate and slow to respond. (PMID:17284361, 17011181, 15556286). Acetylcholine has been found to be a microbial product, urinary acetylcholine is produced by Lactobacillus (PMID:24621061). S - Sensory organs > S01 - Ophthalmologicals > S01E - Antiglaucoma preparations and miotics > S01EB - Parasympathomimetics D018377 - Neurotransmitter Agents > D018678 - Cholinergic Agents > D018679 - Cholinergic Agonists Acquisition and generation of the data is financially supported in part by CREST/JST. C78272 - Agent Affecting Nervous System > C47796 - Cholinergic Agonist D002317 - Cardiovascular Agents > D014665 - Vasodilator Agents IPB_RECORD: 232; CONFIDENCE confident structure COVID info from COVID-19 Disease Map Corona-virus KEIO_ID A060 Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS

   

4-Trimethylammoniobutanoate

4-Trimethylammoniobutanoate

C7H16NO2+ (146.1181)


   

(3S)-3,6-Diaminohexanoate

(3S)-3,6-Diaminohexanoic acid

C6H14N2O2 (146.1055)


(3S)-3,6-Diaminohexanoate is found in the lysine degradation pathway. (3S)-3,6-Diaminohexanoate is created from L-lysine through the action of lysine 2,3-aminomutase [EC:5.4.3.2]. (3S)-3,6-Diaminohexanoate is then reversibly converted to (3S,5S)-3,5-Diaminohexanoate by beta-lysine 5,6-aminomutase [EC:5.4.3.3]. (3S)-3,6-Diaminohexanoate is found in the lysine degradation pathway.

   

(3S,5S)-3,5-Diaminohexanoate

3,5-Diaminohexanoate dihydrochloride

C6H14N2O2 (146.1055)


3,5-diaminohexanoic acid,which requires a cobamide coenzyme for formation. , is readily fermented to volatile acids by extracts of Clostridium SB4. (3S,5S)-3,5-Diaminohexanoate is involved in the lysine degradation pathway. (3S,5S)-3,5-Diaminohexanoate is produced from (3S)-3,6-Diaminohexanoate through the action of beta-lysine 5,6-aminomutase [EC:5.4.3.3]. (3S,5S)-3,5-Diaminohexanoate is then converted into(S)-5-Amino-3-oxohexanoic acid. 3,5-diaminohexanoic acid,which requires a cobamide coenzyme for formation

   

2,5-Diaminohexanoate

(2R,5S)-2,5-diaminohexanoic acid

C6H14N2O2 (146.1055)


   

beta-Methyl-DL-ornithine

(3R)-3-methyl-D-ornithine

C6H14N2O2 (146.1055)


   

D-Lysine

(2R)-2,6-diaminohexanoic acid

C6H14N2O2 (146.1055)


D-Lysine, also known as D-lysin or DLY, belongs to the class of organic compounds known as d-alpha-amino acids. These are alpha amino acids which have the D-configuration of the alpha-carbon atom. D-Lysine exists in all living organisms, ranging from bacteria to humans. D-Lysine is a potentially toxic compound. The D-enantiomer of the alpha-amino acid lysine. An essential amino acid. It is often added to animal feed. [HMDB]

   

Lysine

L-Lysine

C6H14N2O2 (146.1055)


A diamino acid that is caproic (hexanoic) acid bearing two amino substituents at positions 2 and 6. B - Blood and blood forming organs > B05 - Blood substitutes and perfusion solutions > B05X - I.v. solution additives > B05XB - Amino acids L-lysine is an essential amino acid[1][2] with important roles in connective tissues and carnitine synthesis, energy production, growth in children, and maintenance of immune functions[2]. L-lysine is an essential amino acid[1][2] with important roles in connective tissues and carnitine synthesis, energy production, growth in children, and maintenance of immune functions[2].

   

1-Nitroheptane

heptyl(hydroxy)oxoazanium

C7H16NO2 (146.1181)


1-nitroheptane is used for the synthesis of dihydrojasmone (PMID 17340535). 1-nitroheptane has been studied for its ability to induce DNA repair in rat hepatocytes (PMID 776204).

   

Dibutyl sulfide

1-(Butylsulphanyl)butane

C8H18S (146.1129)


Dibutyl sulfide is found in animal foods. Dibutyl sulfide is present in raw cabbage, boiled and cooked beef, and some varieties of mushroom. Dibutyl sulfide is a flavouring ingredien Present in raw cabbage, boiled and cooked beef, and some varieties of mushroom. Flavouring ingredient. Dibutyl sulfide is found in mushrooms, brassicas, and animal foods.

   

2-Ethyl-1-hexanethiol

2-(Mercaptomethyl)heptane

C8H18S (146.1129)


(±)-2-Ethyl-1-hexanethiol is a food flavouring. It is used as a food additive

   

(3-Methyl-2-butenyl)-benzene

(3-methylbut-2-en-1-yl)benzene

C11H14 (146.1095)


(3-Methyl-2-butenyl)-benzene belongs to the class of organic compounds known as benzene and substituted derivatives. These are aromatic compounds containing one monocyclic ring system consisting of benzene.

   

1-Octanethiol

1-Mercaptooctane

C8H18S (146.1129)


   

Pentacyclo(5.4.0.02,6.03,10.05,9)undecane

pentacyclo[5.4.0.0^{2,6}.0^{3,10}.0^{5,9}]undecane

C11H14 (146.1095)


   

2,5-Diamino-2-methylpentanoic acid

alpha-Methylornithine monohydrochloride, (DL)-isomer, (14)C-labeled

C6H14N2O2 (146.1055)


D000970 - Antineoplastic Agents

   

Amino leucine

2-hydrazinyl-4-methylpentanoic acid

C6H14N2O2 (146.1055)


   

Meldonium

3-(2,2,2-trimethylhydrazin-2-ium-1-yl)propanoate

C6H14N2O2 (146.1055)


COVID info from clinicaltrial, clinicaltrials, clinical trial, clinical trials C26170 - Protective Agent > C2079 - Cardioprotective Agent C - Cardiovascular system > C01 - Cardiac therapy C78274 - Agent Affecting Cardiovascular System D002317 - Cardiovascular Agents D007155 - Immunologic Factors C471 - Enzyme Inhibitor Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS Meldonium (MET-88) functions as a cardioprotective agent by cpmpetetively inhibiting γ-butyrobetaine hydroxylase (BBOX) and carnitine/organic cation transporter type 2 (OCTN2). Mildronate (Meldonium) exhibits IC50 values of 34-62 μM for human recombinant BBOX and an EC50 of 21 μM for human OCTN2. Meldonium is a fatty acid oxidation inhibitor[1][2].

   

Amino (2S)-2-amino-4-methylpentanoate

Amino (2S)-2-amino-4-methylpentanoic acid

C6H14N2O2 (146.1055)


   

Pentenylbenzene

(1E)-pent-1-en-1-ylbenzene

C11H14 (146.1095)


Pentenylbenzene is a member of the class of compounds known as styrenes. Styrenes are organic compounds containing an ethenylbenzene moiety. Pentenylbenzene can be found in wild celery, which makes pentenylbenzene a potential biomarker for the consumption of this food product.

   

Lysine

L-Lysine

C6H14N2O2 (146.1055)


B - Blood and blood forming organs > B05 - Blood substitutes and perfusion solutions > B05X - I.v. solution additives > B05XB - Amino acids L-lysine is an essential amino acid[1][2] with important roles in connective tissues and carnitine synthesis, energy production, growth in children, and maintenance of immune functions[2]. L-lysine is an essential amino acid[1][2] with important roles in connective tissues and carnitine synthesis, energy production, growth in children, and maintenance of immune functions[2].

   

Viridiene

(3R,4S)-cis-3-(1Z,3-Butadienry)-4-vinylcyclopentene

C11H14 (146.1095)


   

Desmarestene

Desmarestene

C11H14 (146.1095)


   
   

6-methyl-1,2,3,4-tetrahydronaphthalene

6-methyl-1,2,3,4-tetrahydronaphthalene

C11H14 (146.1095)


   

5-METHYLTETRALINE

5-METHYLTETRALINE

C11H14 (146.1095)


   

undec-1-ene-5,7-diyne

undec-1-ene-5,7-diyne

C11H14 (146.1095)


   

trinoranastreptene

trinoranastreptene

C11H14 (146.1095)


   

2,4-Diamino-2,3,4,6-tetradeoxy-arabino-hexose,9CI,8CI-D-form

2,4-Diamino-2,3,4,6-tetradeoxy-arabino-hexose,9CI,8CI-D-form

C6H14N2O2 (146.1055)


   

2,6-Diamino-2,3,4,6-tetradeoxy-erythro-hexose,9CI,8CI-D-form

2,6-Diamino-2,3,4,6-tetradeoxy-erythro-hexose,9CI,8CI-D-form

C6H14N2O2 (146.1055)


   

4,6-DIMETHYLINDAN

4,6-DIMETHYLINDAN

C11H14 (146.1095)


   

L-Lysine

L-Lysine monohydrochloride

C6H14N2O2 (146.1055)


An L-alpha-amino acid; the L-isomer of lysine. L-lysine is an essential amino acid[1][2] with important roles in connective tissues and carnitine synthesis, energy production, growth in children, and maintenance of immune functions[2]. L-lysine is an essential amino acid[1][2] with important roles in connective tissues and carnitine synthesis, energy production, growth in children, and maintenance of immune functions[2].

   

Acetylcholine

(2-acetoxyethyl)trimethylammonium

[C7H16NO2]+ (146.1181)


MS2 deconvoluted using MS2Dec from all ion fragmentation data, MetaboLights identifier MTBLS1040; OIPILFWXSMYKGL_STSL_0140_Acetylcholine_0125fmol_180506_S2_LC02_MS02_248; 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.

   

Acetylcholine chloride

(2-acetoxyethyl)trimethylammonium

[C7H16NO2]+ (146.1181)


   

D-Lysine

D-Lysine

C6H14N2O2 (146.1055)


The D-enantiomer of the alpha-amino acid lysine.

   

4-Trimethylammoniobutanoic acid

4-Trimethylammoniobutanoic acid

C7H16NO2+ (146.1181)


   

Acetylcholine

Acetylcholine

C7H16NO2 (146.1181)


   

Lysine; AIF; CE0; CorrDec

Lysine; AIF; CE0; CorrDec

C6H14N2O2 (146.1055)


   

Lysine; AIF; CE10; CorrDec

Lysine; AIF; CE10; CorrDec

C6H14N2O2 (146.1055)


   

Lysine; AIF; CE30; CorrDec

Lysine; AIF; CE30; CorrDec

C6H14N2O2 (146.1055)


   

Lysine; AIF; CE0; MS2Dec

Lysine; AIF; CE0; MS2Dec

C6H14N2O2 (146.1055)


   

Lysine; AIF; CE10; MS2Dec

Lysine; AIF; CE10; MS2Dec

C6H14N2O2 (146.1055)


   

Lysine; AIF; CE30; MS2Dec

Lysine; AIF; CE30; MS2Dec

C6H14N2O2 (146.1055)


   

Lysine; LC-tDDA; CE10

Lysine; LC-tDDA; CE10

C6H14N2O2 (146.1055)


   

Lysine; LC-tDDA; CE20

Lysine; LC-tDDA; CE20

C6H14N2O2 (146.1055)


   

Lysine; LC-tDDA; CE30

Lysine; LC-tDDA; CE30

C6H14N2O2 (146.1055)


   

Lysine; LC-tDDA; CE40

Lysine; LC-tDDA; CE40

C6H14N2O2 (146.1055)


   

Acetylcholine

(2-acetoxyethyl)trimethylammonium

C7H16NO2+ (146.1181)


S - Sensory organs > S01 - Ophthalmologicals > S01E - Antiglaucoma preparations and miotics > S01EB - Parasympathomimetics D018377 - Neurotransmitter Agents > D018678 - Cholinergic Agents > D018679 - Cholinergic Agonists Actylcholine is an ester of acetic acid and choline, which acts as a neurotransmitter. C78272 - Agent Affecting Nervous System > C47796 - Cholinergic Agonist D002317 - Cardiovascular Agents > D014665 - Vasodilator Agents COVID info from COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS

   
   
   

Butyl sulfide

1,1'-Thiobisbutane, 9CI

C8H18S (146.1129)


   

UNII:9M9TA4S7BL

2-(Mercaptomethyl)heptane

C8H18S (146.1129)


   

2,4,6-trimethylstyrene

2,4,6-trimethylstyrene

C11H14 (146.1095)


   

6-METHYLTETRALIN

6-METHYLTETRALIN

C11H14 (146.1095)


   

L-LEUCINE HYDROXAMATE

L-Leucyl-Hydroxylamine

C6H14N2O2 (146.1055)


   

(2,2-dimethylcyclopropyl)benzene

(2,2-dimethylcyclopropyl)benzene

C11H14 (146.1095)


   

2-Octanethiol

2-Octanethiol

C8H18S (146.1129)


   

di-sec-butyl sulfide

di-sec-butyl sulfide

C8H18S (146.1129)


   

N-(2-methoxyethyl)-2-(methylamino)acetamide

N-(2-methoxyethyl)-2-(methylamino)acetamide

C6H14N2O2 (146.1055)


   

ethyl 2-(2-aminoethylamino)acetate

ethyl 2-(2-aminoethylamino)acetate

C6H14N2O2 (146.1055)


   

5-PHENYL-1-PENTENE

5-PHENYL-1-PENTENE

C11H14 (146.1095)


   

Phosphine, di-tert-butyl-

Phosphine, di-tert-butyl-

C8H19P (146.1224)


   

DL-Lysine

Lysine, DL-

C6H14N2O2 (146.1055)


DL-Lysine is a racemic mixture of the D-Lysine and L-Lysine. Lysine is an α-amino acid that is used in the biosynthesis of proteins[1].

   

Butanoic acid,3-Methyl-2-(1-Methyl hydrazinyl)

Butanoic acid,3-Methyl-2-(1-Methyl hydrazinyl)

C6H14N2O2 (146.1055)


   

tert-Butyl 2-methylcarbazate

tert-Butyl 2-methylcarbazate

C6H14N2O2 (146.1055)


   

1,2-dimethyl-3-prop-2-enylbenzene

1,2-dimethyl-3-prop-2-enylbenzene

C11H14 (146.1095)


   

4-(4-Methylphenyl)-1-butene

4-(4-Methylphenyl)-1-butene

C11H14 (146.1095)


   

5-Chloro-3-fluoropyridine-2-carboxylic acid

5-Chloro-3-fluoropyridine-2-carboxylic acid

C11H14 (146.1095)


   

triethylsilylmethanol

triethylsilylmethanol

C7H18OSi (146.1127)


   

2-PHENYL-1-PENTENE

2-PHENYL-1-PENTENE

C11H14 (146.1095)


   

5-METHYLTETRALIN

5-METHYLTETRALIN

C11H14 (146.1095)


   

2-methyl-1-phenyl-1-butene

2-methyl-1-phenyl-1-butene

C11H14 (146.1095)


   

2-Cyclopropyl-1,3-dimethylbenzene

2-Cyclopropyl-1,3-dimethylbenzene

C11H14 (146.1095)


   

4-ISO-PROPYL STYRENE

4-ISO-PROPYL STYRENE

C11H14 (146.1095)


   

2,2-DIETHOXY-ACETAMIDINE

2,2-DIETHOXY-ACETAMIDINE

C6H14N2O2 (146.1055)


   

heptyl methyl sulfide

heptyl methyl sulfide

C8H18S (146.1129)


   

3-PHENYL-1-PENTENE

3-PHENYL-1-PENTENE

C11H14 (146.1095)


   

5-phenyl-2-pentene

5-phenyl-2-pentene

C11H14 (146.1095)


   

2-Methyl-2-propanyl 2-methylhydrazinecarboxylate

2-Methyl-2-propanyl 2-methylhydrazinecarboxylate

C6H14N2O2 (146.1055)


   

STARBURST(R) (PAMAM) DENDRIMER, GENERATION 4.5

STARBURST(R) (PAMAM) DENDRIMER, GENERATION 4.5

C6H14N2O2 (146.1055)


   

2,4,4-trimethylpentane-2-thiol

2,4,4-trimethylpentane-2-thiol

C8H18S (146.1129)


   

1-Piperidine ethanamine,4-fluoro-(9CI)

1-Piperidine ethanamine,4-fluoro-(9CI)

C7H15FN2 (146.1219)


   

1-Piperidine ethanamine,3-fluoro-(9CI)

1-Piperidine ethanamine,3-fluoro-(9CI)

C7H15FN2 (146.1219)


   

O-(2-morpholin-4-ylethyl)hydroxylamine

O-(2-morpholin-4-ylethyl)hydroxylamine

C6H14N2O2 (146.1055)


   

1-Ethylindane

1-Ethylindane

C11H14 (146.1095)


   

Propane,1,1-thiobis[2-methyl-

Propane,1,1-thiobis[2-methyl-

C8H18S (146.1129)


   

N-ETHYL-N-BUTAN-4-OL-NITROSAMINE

N-ETHYL-N-BUTAN-4-OL-NITROSAMINE

C6H14N2O2 (146.1055)


   

1,4-dimethyl-1,4-dioxidopiperazine-1,4-diium

1,4-dimethyl-1,4-dioxidopiperazine-1,4-diium

C6H14N2O2 (146.1055)


   

3-(3,5-DIMETHYLPHENYL)-1-PROPENE

3-(3,5-DIMETHYLPHENYL)-1-PROPENE

C11H14 (146.1095)


   

tert-Butyl sulfide

tert-Butyl sulfide

C8H18S (146.1129)


   

DL-NORLEUCINE HYDROXAMATE

DL-NORLEUCINE HYDROXAMATE

C6H14N2O2 (146.1055)


   

2,4,4-trimethylpentylphosphane

2,4,4-trimethylpentylphosphane

C8H19P (146.1224)


   

1-Methyl-3-(1-methyl-2-propenyl)benzene

1-Methyl-3-(1-methyl-2-propenyl)benzene

C11H14 (146.1095)


   

1-Methyl-4-(1-Methyl-2-propenyl)benzene

1-Methyl-4-(1-Methyl-2-propenyl)benzene

C11H14 (146.1095)


   

Triethyl borate

Triethyl borate

C6H15BO3 (146.1114)


   

2-PHENYL-2-PENTENE

2-PHENYL-2-PENTENE

C11H14 (146.1095)


   

1-Methyldicyclopentadiene

1-Methyldicyclopentadiene

C11H14 (146.1095)


   

4-(Trimethylsilyl)Butan-1-Ol

4-(Trimethylsilyl)Butan-1-Ol

C7H18OSi (146.1127)


   

1-(2-fluoroethyl)-4-Piperidinamine

1-(2-fluoroethyl)-4-Piperidinamine

C7H15FN2 (146.1219)


   

di-i-butylphosphine

di-i-butylphosphine

C8H19P (146.1224)


   

DIBUTYLPHOSPHINE

DIBUTYLPHOSPHINE

C8H19P (146.1224)


   

1,4-dihydroxy-2,2-dimethylpiperazine

1,4-dihydroxy-2,2-dimethylpiperazine

C6H14N2O2 (146.1055)


   

tert-Butoxytrimethylsilane

tert-butoxy(trimethyl)silane

C7H18OSi (146.1127)


   

TRANS-1-PHENYL-1-PENTENE

TRANS-1-PHENYL-1-PENTENE

C11H14 (146.1095)


   

(3R)-3,6-diaminohexanoic acid

(3R)-3,6-diaminohexanoic acid

C6H14N2O2 (146.1055)


   

(3-Methyl-2-butenyl)benzene

(3-Methyl-2-butenyl)benzene

C11H14 (146.1095)


   
   

2-Methyl-2-heptanethiol

2-Methyl-2-heptanethiol

C8H18S (146.1129)


   

Butoxytrimethylsilane

Butoxytrimethylsilane

C7H18OSi (146.1127)


   

Silane, isobutoxytrimethyl-

Silane, isobutoxytrimethyl-

C7H18OSi (146.1127)


   

Trimethyl(1-methylpropoxy)silane

Trimethyl(1-methylpropoxy)silane

C7H18OSi (146.1127)


   

Meldonium

Mildronate

C6H14N2O2 (146.1055)


COVID info from clinicaltrial, clinicaltrials, clinical trial, clinical trials C26170 - Protective Agent > C2079 - Cardioprotective Agent C - Cardiovascular system > C01 - Cardiac therapy C78274 - Agent Affecting Cardiovascular System D002317 - Cardiovascular Agents D007155 - Immunologic Factors C471 - Enzyme Inhibitor Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS Meldonium (MET-88) functions as a cardioprotective agent by cpmpetetively inhibiting γ-butyrobetaine hydroxylase (BBOX) and carnitine/organic cation transporter type 2 (OCTN2). Mildronate (Meldonium) exhibits IC50 values of 34-62 μM for human recombinant BBOX and an EC50 of 21 μM for human OCTN2. Meldonium is a fatty acid oxidation inhibitor[1][2].

   

Acetylcholine

Bournonville brand OF acetylcholine chloride

C7H16NO2+ (146.1181)


Acetylcholine (ACh) is a neurotransmitter. Acetylcholine in vertebrates is the major transmitter at neuromuscular junctions, autonomic ganglia, parasympathetic effector junctions, a subset of sympathetic effector junctions, and at many sites in the central nervous system. Its physiological and pharmacological effects, metabolism, release, and receptors have been well documented in several species. ACh has been considered an important excitatory neurotransmitter in the carotid body (CB). Various nicotinic and muscarinic ACh receptors are present in both afferent nerve endings and glomus cells. Therefore, ACh can depolarize or hyperpolarize the cell membrane depending on the available receptor type in the vicinity. Binding of ACh to its receptor can create a wide variety of cellular responses including opening cation channels (nicotinic ACh receptor activation), releasing Ca2+ from intracellular storage sites (via muscarinic ACh receptors), and modulating activities of K+ and Ca2+ channels. Interactions between ACh and other neurotransmitters (dopamine, adenosine, nitric oxide) have been known, and they may induce complicated responses. Cholinergic biology in the CB differs among species and even within the same species due to different genetic composition. Development and environment influence cholinergic biology. Pharmacological data clearly indicate that both muscarinic and nicotinic acetylcholine receptors have a role in the encoding of new memories. Localized lesions and antagonist infusions demonstrate the anatomical locus of these cholinergic effects, and computational modeling links the function of cholinergic modulation to specific cellular effects within these regions. Acetylcholine has been shown to increase the strength of afferent input relative to feedback, to contribute to theta rhythm oscillations, activate intrinsic mechanisms for persistent spiking, and increase the modification of synapses. These effects might enhance different types of encoding in different cortical structures. In particular, the effects in entorhinal and perirhinal cortex and hippocampus might be important for encoding new episodic memories. The role of ACh in attention has been repeatedly demonstrated in several tasks. Acetylcholine is linked to response accuracy in voluntary and reflexive attention and also to response speed in reflexive attention. It is well known that those with Attention-deficit/hyperactivity disorders tend to be inaccurate and slow to respond. (PMID:17284361, 17011181, 15556286). Acetylcholine has been found to be a microbial product, urinary acetylcholine is produced by Lactobacillus (PMID:24621061). S - Sensory organs > S01 - Ophthalmologicals > S01E - Antiglaucoma preparations and miotics > S01EB - Parasympathomimetics D018377 - Neurotransmitter Agents > D018678 - Cholinergic Agents > D018679 - Cholinergic Agonists C78272 - Agent Affecting Nervous System > C47796 - Cholinergic Agonist D002317 - Cardiovascular Agents > D014665 - Vasodilator Agents Occurs in Capsella bursa-pastoris (shepherds purse) COVID info from COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS

   

Amino (2S)-2-amino-4-methylpentanoate

Amino (2S)-2-amino-4-methylpentanoic acid

C6H14N2O2 (146.1055)


   

(3R,5R)-3,5-diaminohexanoic acid

(3R,5R)-3,5-diaminohexanoic acid

C6H14N2O2 (146.1055)


   

(1S,2S,3R,5S)-3,5-diaminocyclohexane-1,2-diol

(1S,2S,3R,5S)-3,5-diaminocyclohexane-1,2-diol

C6H14N2O2 (146.1055)


   

purpurosamine C

purpurosamine C

C6H14N2O2 (146.1055)


   

(2S)-6-amino-2-azaniumylhexanoate

(2S)-6-amino-2-azaniumylhexanoate

C6H14N2O2 (146.1055)


   

(2S)-2-amino-6-azaniumylhexanoate

(2S)-2-amino-6-azaniumylhexanoate

C6H14N2O2 (146.1055)


   

(3S)-3,6-Diaminohexanoic acid

(3S)-3,6-Diaminohexanoic acid

C6H14N2O2 (146.1055)


   

(3R)-3-methyl-D-ornithine

(3R)-3-methyl-D-ornithine

C6H14N2O2 (146.1055)


   

(3S,5S)-3,5-Diaminohexanoic acid

(3S,5S)-3,5-Diaminohexanoic acid

C6H14N2O2 (146.1055)


   

(2R,5S)-2,5-diaminohexanoic acid

(2R,5S)-2,5-diaminohexanoic acid

C6H14N2O2 (146.1055)


   

2,5-diaminohexanoic acid

2,5-diaminohexanoic acid

C6H14N2O2 (146.1055)


   

1-Octanethiol

1-Mercaptooctane

C8H18S (146.1129)


   

Dibutyl sulfide

n-Dibutyl sulfide

C8H18S (146.1129)


   

L-lysine zwitterion

L-lysine zwitterion

C6H14N2O2 (146.1055)


An L-alpha-amino acid zwitterion obtained by transfer of a proton from the carboxy to the amino group of L-lysine; major species at pH 7.3.

   

4-(trimethylammonio)butanoic acid

4-(trimethylammonio)butanoic acid

C7H16NO2 (146.1181)


A quaternary ammonium ion that is the conjugate acid of 4-(trimethylammonio)butanoate.

   

N1-Acetyl-N1-hydroxyputrescine

N1-Acetyl-N1-hydroxyputrescine

C6H14N2O2 (146.1055)


   

(3r,4s)-3-[(1e)-buta-1,3-dien-1-yl]-4-ethenylcyclopent-1-ene

(3r,4s)-3-[(1e)-buta-1,3-dien-1-yl]-4-ethenylcyclopent-1-ene

C11H14 (146.1095)


   

undec-1-en-5,7-diyne

undec-1-en-5,7-diyne

C11H14 (146.1095)


   

(3r,4r)-3-[(1z)-buta-1,3-dien-1-yl]-4-ethenylcyclopent-1-ene

(3r,4r)-3-[(1z)-buta-1,3-dien-1-yl]-4-ethenylcyclopent-1-ene

C11H14 (146.1095)