Exact Mass: 176.0320868

Exact Mass Matches: 176.0320868

Found 162 metabolites which its exact mass value is equals to given mass value 176.0320868, within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error 0.001 dalton.

L-Ascorbic acid

(5R)-5-[(1S)-1,2-dihydroxyethyl]-3,4-dihydroxy-2,5-dihydrofuran-2-one

C6H8O6 (176.0320868)


L-ascorbic acid is a white to very pale yellow crystalline powder with a pleasant sharp acidic taste. Almost odorless. (NTP, 1992) L-ascorbic acid is the L-enantiomer of ascorbic acid and conjugate acid of L-ascorbate. It has a role as a coenzyme, a flour treatment agent, a food antioxidant, a plant metabolite, a cofactor, a skin lightening agent and a geroprotector. It is an ascorbic acid and a vitamin C. It is a conjugate acid of a L-ascorbate. It is an enantiomer of a D-ascorbic acid. A six carbon compound related to glucose. It is found naturally in citrus fruits and many vegetables. Ascorbic acid is an essential nutrient in human diets, and necessary to maintain connective tissue and bone. Its biologically active form, vitamin C, functions as a reducing agent and coenzyme in several metabolic pathways. Vitamin C is considered an antioxidant. Ascorbic acid is a metabolite found in or produced by Escherichia coli (strain K12, MG1655). Ascorbic acid is a Vitamin C. Ascorbic Acid is a natural product found in Populus tremula, Rosa platyacantha, and other organisms with data available. Ascorbic Acid is a natural water-soluble vitamin (Vitamin C). Ascorbic acid is a potent reducing and antioxidant agent that functions in fighting bacterial infections, in detoxifying reactions, and in the formation of collagen in fibrous tissue, teeth, bones, connective tissue, skin, and capillaries. Found in citrus and other fruits, and in vegetables, vitamin C cannot be produced or stored by humans and must be obtained in the diet. (NCI04) A six carbon compound related to glucose. It is found naturally in citrus fruits and many vegetables. Ascorbic acid is an essential nutrient in human diets, and necessary to maintain connective tissue and bone. Its biologically active form, vitamin C, functions as a reducing agent and coenzyme in several metabolic pathways. Vitamin C is considered an antioxidant. See also: Sodium Ascorbate (active moiety of); D-ascorbic acid (related); Magnesium Ascorbyl Phosphate (active moiety of) ... View More ... G - Genito urinary system and sex hormones > G01 - Gynecological antiinfectives and antiseptics > G01A - Antiinfectives and antiseptics, excl. combinations with corticosteroids > G01AD - Organic acids A - Alimentary tract and metabolism > A11 - Vitamins > A11G - Ascorbic acid (vitamin c), incl. combinations > A11GA - Ascorbic acid (vitamin c), plain B - Blood and blood forming organs > B03 - Antianemic preparations > B03A - Iron preparations > B03AA - Iron bivalent, oral preparations COVID info from clinicaltrial, clinicaltrials, clinical trial, clinical trials D020011 - Protective Agents > D000975 - Antioxidants C26170 - Protective Agent > C275 - Antioxidant D018977 - Micronutrients > D014815 - Vitamins S - Sensory organs > S01 - Ophthalmologicals L-Ascorbic acid (L-Ascorbate), an electron donor, is an endogenous antioxidant agent. L-Ascorbic acid inhibits selectively Cav3.2 channels with an IC50 of 6.5 μM. L-Ascorbic acid is also a collagen deposition enhancer and an elastogenesis inhibitor[1][2][3]. L-Ascorbic acid exhibits anti-cancer effects through the generation of reactive oxygen species (ROS) and selective damage to cancer cells[4]. L-Ascorbic acid. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=50-81-7 (retrieved 2024-10-29) (CAS RN: 50-81-7). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

   

D-Glucurono-6,3-lactone

(2R,3R,3aR,6R,6aR)-2,3,6-trihydroxy-3,3a,6,6a-tetrahydro-2H-furo[3,2-b]furan-5-one

C6H8O6 (176.0320868)


D-Glucurono-6,3-lactone belongs to the class of organic compounds known as isosorbides. These are organic polycyclic compounds containing an isosorbide(1,4-Dianhydrosorbitol) moiety, which consists of two -oxolan-3-ol rings. D-Glucurono-6,3-lactone is a very mild and mentholic tasting compound. Glucuronolactone is a naturally occurring substance that is an important structural component of nearly all connective tissues. It is frequently used in energy drinks to increase energy levels and improve alertness, and can also be used to reduce "brain fog" caused by various medical conditions. Glucuronolactone is also found in many plant gums. Glucuronolactone is a white solid odorless compound, soluble in hot and cold water. Its melting point ranges from 176 to 178 °C. The compound can exist in a monocyclic aldehyde form or in a bicyclic hemiacetal (lactol) form. Glucuronolactone is a popular ingredient in energy drinks because it has been shown to be effective at increasing energy levels and improving alertness. Glucuronolactone supplementation also significantly reduces "brain fog" cause by various medical conditions. Although levels of glucuronolactone in energy drinks can far exceed those found in the rest of the diet, glucuronolactone is extremely safe and well tolerated. The European Food Safety Authority (EFSA) has concluded that exposure to glucuronolactone from regular consumption of energy drinks is not a safety concern.[2] The no-observed-adverse-effect level of glucuronolactone is 1000 mg/kg/day. Additionally, according to The Merck Index, glucuronolactone is used as a detoxicant. The liver uses glucose to create glucuronolactone, which inhibits the enzyme B-glucuronidase (metabolizes glucuronides), which should cause blood-glucuronide levels to rise. Glucuronides combines with toxic substances, such as morphine and depot medroxyprogesterone acetate, by converting them to water-soluble glucuronide-conjugates which are excreted in the urine. Higher blood-glucuronides help remove toxins from the body, leading to the claim that energy drinks are detoxifying. Free glucuronic acid (or its self-ester glucuronolactone) has less effect on detoxification than glucose, because the body synthesizes UDP-glucuronic acid from glucose. Therefore, sufficient carbohydrate intake provides enough UDP-glucuronic acid for detoxication, and foods rich in glucose are usually abundant in developed nations. Glucuronolactone is also metabolized to glucaric acid, xylitol, and L-xylulose, and humans may also be able to use glucuronolactone as a precursor for ascorbic acid synthesis. D-glucurono-6,3-lactone participates in ascorbate and aldarate metabolism. D-glucurono-6,3-lactone is produced by the reaction between D-glucaric acid and the enzyme, aldehyde dehydrogenase (NAD+) [EC: 1.2.1.3]. [HMDB] D-Glucuronic acid lactone is an endogenous metabolite.

   

2-Hydroxy-3-oxoadipate

2-hydroxy-3-oxoadipic acid

C6H8O6 (176.0320868)


   

2-Ketogulonolactone

5-(1,2-dihydroxyethyl)-4-hydroxyoxolane-2,3-dione

C6H8O6 (176.0320868)


   

Glucuronolactone

D(+)-Glucurono-3,6-lactone

C6H8O6 (176.0320868)


D-Glucuronic acid lactone is an endogenous metabolite.

   

5-Dehydro-4-deoxy-D-glucuronate

4,5-dihydroxy-2,6-dioxohexanoic acid

C6H8O6 (176.0320868)


   

SCHEMBL1332210

3-deoxy-D-glycero-hexo-2,5-diulosonic acid

C6H8O6 (176.0320868)


   

Parapyruvate

4-Hydroxy-4-methyl-2-oxoglutaric acid

C6H8O6 (176.0320868)


   

2-Dehydro-D-glucono-1,5-lactone

4,5-dihydroxy-6-(hydroxymethyl)oxane-2,3-dione

C6H8O6 (176.0320868)


   

1,2,3-Propanetricarboxylic acid

Tricarballylic acid, trisodium salt

C6H8O6 (176.0320868)


1,2,3-Propanetricarboxylic acid is found in corn. 1,2,3-Propanetricarboxylic acid is isolated from plants e.g. sugarbeet sap, sap of Acer saccharinum (maple syrup). Propane-1,2,3-tricarboxylic acid, also known as tricarballylic acid, carballylic acid, and beta-carboxyglutaric acid, is a tricarboxylic acid that has three carboxylic acid functional groups. The compound is an inhibitor of the enzyme aconitase and interferes with the Krebs cycle. 1,2,3-Propanetricarboxylic acid can be produced by Bacteroides, Butyrivibrio, Megasphaera, Wolinella and fungi Nectriaceae (PMID:22815244; PMID:16346691). It is also associated with Fumonisins. Fumonisins are fungal toxins produced by Fusarium verticilloides. Detection of this compound indicates presence of fumonisins in gastrointestinal tract. Corn intake or corn contaminated with fumonisins can lead to increased levels of tricarballylic acid (PMID:22815244). Isolated from plants e.g. sugarbeet sap, sap of Acer saccharinum (maple syrup) Tricarballylic acid, a conjugate acid of a?tricarballylate, is a competitive inhibitor of the enzyme aconitate hydratase (aconitase; EC 4.2.1.3) with a Ki value of 0.52 mM[1]. Tricarballylic acid, a conjugate acid of a?tricarballylate, is a competitive inhibitor of the enzyme aconitate hydratase (aconitase; EC 4.2.1.3) with a Ki value of 0.52 mM[1]. Tricarballylic acid, a conjugate acid of a?tricarballylate, is a competitive inhibitor of the enzyme aconitate hydratase (aconitase; EC 4.2.1.3) with a Ki value of 0.52 mM[1].

   

3-Dehydro-scyllo-inosose

3-Dehydro-scyllo-inosose; 2,4-Didehydroinositol

C6H8O6 (176.0320868)


A beta-diketone obtained by formal oxidation of the 2 and 4 hydroxy groups of scyllo-inositol to the corresponding ketones.

   

Erythorbic acid

Erythorbic acid

C6H8O6 (176.0320868)


D020011 - Protective Agents > D000975 - Antioxidants C26170 - Protective Agent > C275 - Antioxidant

   

(4S,5S)-4,5-Dihydroxy-2,6-dioxohexanoate

(4S,5S)-4,5-dihydroxy-2,6-dioxohexanoic acid

C6H8O6 (176.0320868)


   

D-Galacturonolactone

(R)-2-((2S,3S,4S)-3,4-Dihydroxy-5-oxotetrahydrofuran-2-yl)-2-hydroxyacetaldehyde

C6H8O6 (176.0320868)


   

(2R)-2-[(3R,4S)-3,4-Dihydroxy-5-oxooxolan-2-yl]-2-hydroxyacetaldehyde

(2R)-2-[(3R,4S)-3,4-Dihydroxy-5-oxooxolan-2-yl]-2-hydroxyacetaldehyde

C6H8O6 (176.0320868)


   

5-(1,2-Dihydroxyethyl)-4-hydroxyoxolane-2,3-dione

5-(1,2-dihydroxyethyl)-4-hydroxyoxolane-2,3-dione

C6H8O6 (176.0320868)


   

3,4-Dihydroxy-5-[(S)-1,2-dihydroxyethyl]furan-2(5H)-one

5-(1,2-dihydroxyethyl)-3,4-dihydroxy-2,5-dihydrofuran-2-one

C6H8O6 (176.0320868)


The L-form Occurs widely in animals and plants. Good sources are citrus fruits and hip berries. Isolated from ox adrenal cortex, lemons and paprika. [CCD]. Ascorbic acid is found in nanking cherry. L-Ascorbic acid (L-Ascorbate), an electron donor, is an endogenous antioxidant agent. L-Ascorbic acid inhibits selectively Cav3.2 channels with an IC50 of 6.5 μM. L-Ascorbic acid is also a collagen deposition enhancer and an elastogenesis inhibitor[1][2][3]. L-Ascorbic acid exhibits anti-cancer effects through the generation of reactive oxygen species (ROS) and selective damage to cancer cells[4]. L-Ascorbic acid (L-Ascorbate), an electron donor, is an endogenous antioxidant agent. L-Ascorbic acid inhibits selectively Cav3.2 channels with an IC50 of 6.5 μM. L-Ascorbic acid is also a collagen deposition enhancer and an elastogenesis inhibitor[1][2][3]. L-Ascorbic acid exhibits anti-cancer effects through the generation of reactive oxygen species (ROS) and selective damage to cancer cells[4].

   

(R)-2-((S)-1,2-Dihydroxyethyl)-4,5-dihydroxyfuran-3(2H)-one

(R)-2-((S)-1,2-Dihydroxyethyl)-4,5-dihydroxyfuran-3(2H)-one

C6H8O6 (176.0320868)


   

Diglyceride

3,6-bis(hydroxymethyl)-1,4-dioxane-2,5-dione

C6H8O6 (176.0320868)


   

(3S,4R,5S)-3,4-Dihydroxy-5-(2-hydroxyacetyl)oxolan-2-one

(3S,4R,5S)-3,4-Dihydroxy-5-(2-hydroxyacetyl)oxolan-2-one

C6H8O6 (176.0320868)


   

2-Hydroxy-5-oxohexanedioic acid

2-Hydroxy-5-oxohexanedioic acid

C6H8O6 (176.0320868)


   

(5R)-5-(1,2-Dihydroxyethyl)-3-hydroxyoxolane-2,4-dione

(5R)-5-(1,2-Dihydroxyethyl)-3-hydroxyoxolane-2,4-dione

C6H8O6 (176.0320868)


   
   

Ascorbic acid

(5R)-5-[(1S)-1,2-dihydroxyethyl]-3,4-dihydroxy-2,5-dihydrofuran-2-one

C6H8O6 (176.0320868)


Ascorbic acid is found naturally in citrus fruits and many vegetables and is an essential nutrient in human diets. It is necessary to maintain connective tissue and bone. The biologically active form of ascorbic acid is vitamin C. Vitamin C is a water soluble vitamin. Primates (including humans) and a few other species in all divisions of the animal kingdom, notably the guinea pig, have lost the ability to synthesize ascorbic acid and must obtain it in their food. Vitamin C functions as a reducing agent and coenzyme in several metabolic pathways. Vitamin C is considered an antioxidant (PubChem). Ascorbic acid is an electron donor for enzymes involved in collagen hydroxylation, biosynthesis of carnitine and norepinephrine, tyrosine metabolism, and amidation of peptide hormones. Ascrobic acid (vitamin C) deficiency causes scurvy. The amount of vitamin C necessary to prevent scurvy may not be adequate to maintain optimal health. The ability of vitamin C to donate electrons also makes it a potent water-soluble antioxidant that readily scavenges free radicals such as molecular oxygen, superoxide, hydroxyl radical, and hypochlorous acid. In this setting, several mechanisms could account for a link between vitamin C and heart disease. One is the relation between LDL oxidation and vitamins C and E. Vitamin C in vitro can recycle vitamin E, which can donate electrons to prevent LDL oxidation in vitro. As the lipid-phase vitamin E is oxidized, it can be regenerated by aqueous vitamin C. Other possibilities are that vitamin C could decrease cholesterol by mechanisms not well characterized, or could improve vasodilatation and vascular reactivity, perhaps by decreasing the interactions of nitric oxide with oxidants (PMID: 10799361). Moreover, ascorbic acid is found to be associated with hyperoxalemia, which is an inborn error of metabolism. Ascorbic acid is also a microbial metabolite produced by Ketogulonicigenium (PMID: 15785002). Occurs widely in animals and plants. Good sources are citrus fruits and hip berries. Isolated from ox adrenal cortex, lemons and paprika. Production industrially on a large scale from glucose. Vitamin (antiscorbutic), antioxidant, nutrient, preservative consistency enhancer. It is used to reduce discoloration, mainly browning caused by polyphenol oxidase, in fruit and vegetable products. It is used to enhance colour formn. and to reduced the formn. of nitrosamines in meat products. It is used synergistically with Sulfur dioxide HVF10-P in wine and beer as a perservative. Assists formn. of the gluten network in bread making, thus enhancing bread volume. L-Ascorbic acid is found in many foods, some of which are cabbage, hyssop, ginseng, and pancake. L-Ascorbic acid (L-Ascorbate), an electron donor, is an endogenous antioxidant agent. L-Ascorbic acid inhibits selectively Cav3.2 channels with an IC50 of 6.5 μM. L-Ascorbic acid is also a collagen deposition enhancer and an elastogenesis inhibitor[1][2][3]. L-Ascorbic acid exhibits anti-cancer effects through the generation of reactive oxygen species (ROS) and selective damage to cancer cells[4]. L-Ascorbic acid (L-Ascorbate), an electron donor, is an endogenous antioxidant agent. L-Ascorbic acid inhibits selectively Cav3.2 channels with an IC50 of 6.5 μM. L-Ascorbic acid is also a collagen deposition enhancer and an elastogenesis inhibitor[1][2][3]. L-Ascorbic acid exhibits anti-cancer effects through the generation of reactive oxygen species (ROS) and selective damage to cancer cells[4].

   

Ascorbic Acid

5-(1,2-dihydroxyethyl)-3,4-dihydroxy-2,5-dihydrofuran-2-one

C6H8O6 (176.0320868)


L-Ascorbic acid (L-Ascorbate), an electron donor, is an endogenous antioxidant agent. L-Ascorbic acid inhibits selectively Cav3.2 channels with an IC50 of 6.5 μM. L-Ascorbic acid is also a collagen deposition enhancer and an elastogenesis inhibitor[1][2][3]. L-Ascorbic acid exhibits anti-cancer effects through the generation of reactive oxygen species (ROS) and selective damage to cancer cells[4]. L-Ascorbic acid (L-Ascorbate), an electron donor, is an endogenous antioxidant agent. L-Ascorbic acid inhibits selectively Cav3.2 channels with an IC50 of 6.5 μM. L-Ascorbic acid is also a collagen deposition enhancer and an elastogenesis inhibitor[1][2][3]. L-Ascorbic acid exhibits anti-cancer effects through the generation of reactive oxygen species (ROS) and selective damage to cancer cells[4].

   
   

3-(DIFLUOROMETHYL)-1-METHYL-1H-PYRAZOLE-4-CARBOXYLIC ACID

3-(DIFLUOROMETHYL)-1-METHYL-1H-PYRAZOLE-4-CARBOXYLIC ACID

C6H6F2N2O2 (176.03973200000001)


   

2-Hydroxy-2-methyl-4-oxopentanedioic acid

2-Hydroxy-2-methyl-4-oxopentanedioic acid

C6H8O6 (176.0320868)


   
   

D-Mannurono-6,3-lactone

D-Mannurono-6,3-lactone

C6H8O6 (176.0320868)


   

Dimethyl dihydroxyfumarate

Dimethyl dihydroxyfumarate

C6H8O6 (176.0320868)


   

5-methyl-4-phenyl-1,2,3-thiadiazole

5-methyl-4-phenyl-1,2,3-thiadiazole

C9H8N2S (176.0408168)


   

4-deoxy-L-threo-hex-4-enopyranuronate

4-deoxy-L-threo-hex-4-enopyranuronate

C6H8O6 (176.0320868)


   

ascorbate

L-Ascorbic acid

C6H8O6 (176.0320868)


L-Ascorbic acid (L-Ascorbate), an electron donor, is an endogenous antioxidant agent. L-Ascorbic acid inhibits selectively Cav3.2 channels with an IC50 of 6.5 μM. L-Ascorbic acid is also a collagen deposition enhancer and an elastogenesis inhibitor[1][2][3]. L-Ascorbic acid exhibits anti-cancer effects through the generation of reactive oxygen species (ROS) and selective damage to cancer cells[4]. L-Ascorbic acid (L-Ascorbate), an electron donor, is an endogenous antioxidant agent. L-Ascorbic acid inhibits selectively Cav3.2 channels with an IC50 of 6.5 μM. L-Ascorbic acid is also a collagen deposition enhancer and an elastogenesis inhibitor[1][2][3]. L-Ascorbic acid exhibits anti-cancer effects through the generation of reactive oxygen species (ROS) and selective damage to cancer cells[4].

   

L-Ascorbic acid

L-Ascorbic acid

C6H8O6 (176.0320868)


The L-enantiomer of ascorbic acid and conjugate acid of L-ascorbate.

   

Fluxapyroxad (BAS 700 F)-TP CSAA798670

3-(DIFLUOROMETHYL)-1-METHYL-1H-PYRAZOLE-4-CARBOXYLIC ACID

C6H6F2N2O2 (176.03973200000001)


CONFIDENCE standard compound; UCHEM_ID 4184 UCHEM_ID 4184; CONFIDENCE standard compound

   
   

D-Glucuronolactone

D(+)-Glucurono-3,6-lactone

C6H8O6 (176.0320868)


D-Glucuronic acid lactone is an endogenous metabolite.

   

Tricarballylic acid; LC-tDDA; CE10

Tricarballylic acid; LC-tDDA; CE10

C6H8O6 (176.0320868)


   

Tricarballylic acid; LC-tDDA; CE20

Tricarballylic acid; LC-tDDA; CE20

C6H8O6 (176.0320868)


   

Tricarballylic acid; LC-tDDA; CE30

Tricarballylic acid; LC-tDDA; CE30

C6H8O6 (176.0320868)


   

Tricarballylic acid; LC-tDDA; CE40

Tricarballylic acid; LC-tDDA; CE40

C6H8O6 (176.0320868)


   

Tricarballylic acid

Tricarballylic acid

C6H8O6 (176.0320868)


Tricarballylic acid, a conjugate acid of a?tricarballylate, is a competitive inhibitor of the enzyme aconitate hydratase (aconitase; EC 4.2.1.3) with a Ki value of 0.52 mM[1]. Tricarballylic acid, a conjugate acid of a?tricarballylate, is a competitive inhibitor of the enzyme aconitate hydratase (aconitase; EC 4.2.1.3) with a Ki value of 0.52 mM[1]. Tricarballylic acid, a conjugate acid of a?tricarballylate, is a competitive inhibitor of the enzyme aconitate hydratase (aconitase; EC 4.2.1.3) with a Ki value of 0.52 mM[1].

   

4-phenyl-5-methyl-1,2,3-Thiadiazole

4-phenyl-5-methyl-1,2,3-Thiadiazole

C9H8N2S (176.0408168)


   

FA 6:2;O4

(4S)-4,6-dihydroxy-2,5-dioxohexanoic acid;3-deoxy-D-glycero-hexo-2,5-diulosonic acid

C6H8O6 (176.0320868)


   
   
   
   

1H-indole-4-carbothioamide

1H-indole-4-carbothioamide

C9H8N2S (176.0408168)


   

1H-Indole-5-carbothioamide

1H-Indole-5-carbothioamide

C9H8N2S (176.0408168)


   

1H-Indole-6-carbothioamide

1H-Indole-6-carbothioamide

C9H8N2S (176.0408168)


   

(2,4,5-Trifluorophenyl)boronic acid

(2,4,5-Trifluorophenyl)boronic acid

C6H4BF3O2 (176.025643)


   

3-PHENYLISOTHIAZOL-5-AMINE

3-PHENYLISOTHIAZOL-5-AMINE

C9H8N2S (176.0408168)


   

Pyrrolo[1,2-a]thieno[3,2-e]pyrazine, 4,5-dihydro- (9CI)

Pyrrolo[1,2-a]thieno[3,2-e]pyrazine, 4,5-dihydro- (9CI)

C9H8N2S (176.0408168)


   

3,4,5-Trifluorophenylboronic acid

3,4,5-Trifluorophenylboronic acid

C6H4BF3O2 (176.025643)


   
   
   

2(1H)-Quinoxalinethione,3-methyl-(9CI)

2(1H)-Quinoxalinethione,3-methyl-(9CI)

C9H8N2S (176.0408168)


   

2,3,4-Trifluorophenylboronic acid

2,3,4-Trifluorophenylboronic acid

C6H4BF3O2 (176.025643)


   

2,4,6-Trifluorophenylboronic acid

2,4,6-Trifluorophenylboronic acid

C6H4BF3O2 (176.025643)


   

1H-Imidazole-4-sulfonamide,5-amino-1-methyl-

1H-Imidazole-4-sulfonamide,5-amino-1-methyl-

C4H8N4O2S (176.0367948)


   

Naphthalene,1-chloro-4-methyl-

Naphthalene,1-chloro-4-methyl-

C11H9Cl (176.03927439999998)


   

3-formyl-4-nitrobenzonitrile

3-formyl-4-nitrobenzonitrile

C8H4N2O3 (176.0221914)


   

4-Phenyl-1,3-thiazol-2-amine

4-Phenyl-1,3-thiazol-2-amine

C9H8N2S (176.0408168)


   

4-(Thiazol-2-yl)aniline

4-(Thiazol-2-yl)aniline

C9H8N2S (176.0408168)


   

1-Chloromethyl naphthalene

1-(Chloromethyl)naphthalene

C11H9Cl (176.03927439999998)


   

ALUMINUM SESQUICHLOROHYDREX PG

ALUMINUM SESQUICHLOROHYDREX PG

C3H14AlClO4 (176.0395984)


   

5-(3-Pyridinyl)-2-thiophenamine

5-(3-Pyridinyl)-2-thiophenamine

C9H8N2S (176.0408168)


   

1H,3H-Thiazolo[3,4-a]benzimidazole(9CI)

1H,3H-Thiazolo[3,4-a]benzimidazole(9CI)

C9H8N2S (176.0408168)


   

O-acetylmalic acid

O-acetylmalic acid

C6H8O6 (176.0320868)


   
   

3-methylbenzo[b]thiophene-2-carboxaldehyde

3-methylbenzo[b]thiophene-2-carboxaldehyde

C10H8OS (176.02958379999998)


   

5-(4-methylphenyl)-1,2,4-thiadiazole

5-(4-methylphenyl)-1,2,4-thiadiazole

C9H8N2S (176.0408168)


   

2,3,6-trifluorophenylboronic acid

2,3,6-trifluorophenylboronic acid

C6H4BF3O2 (176.025643)


   

Naphthalene,1-chloro-2-methyl-

Naphthalene,1-chloro-2-methyl-

C11H9Cl (176.03927439999998)


   

1-methyl-4-imidazoleacetic acid hydrochloride

1-methyl-4-imidazoleacetic acid hydrochloride

C6H9ClN2O2 (176.03525240000002)


   
   

Gaboxadol hydrochloride

Gaboxadol hydrochloride

C6H9ClN2O2 (176.03525240000002)


Gaboxadol hydrochloride (Lu 02-030 hydrochloride) is a potent agonist of the GABAA receptor and an antagonist of GABAC receptors (IC50=25 μM). Gaboxadol hydrochloride displays a partial agonist efficacy on subunit α1β2γ2 with an ED50 value of 143 μM, a full agonist efficacy at α5 subunit (ED50=28-129 μM) and a superagonist efficacy at α4β3δ (ED50=6 μM). Gaboxadol hydrochloride is a non-opioid agent[1][2].

   

1H-Indole-3-carbothioamide

1H-Indole-3-carbothioamide

C9H8N2S (176.0408168)


   

5-methyl-1-benzothiophene-2-carbaldehyde

5-methyl-1-benzothiophene-2-carbaldehyde

C10H8OS (176.02958379999998)


   

2-chloro-N-(prop-2-enylcarbamoyl)acetamide

2-chloro-N-(prop-2-enylcarbamoyl)acetamide

C6H9ClN2O2 (176.03525240000002)


   
   
   

CHEMBRDG-BB 4010333

CHEMBRDG-BB 4010333

C9H8N2S (176.0408168)


   

3-(1,3-thiazol-4-yl)aniline

3-(1,3-thiazol-4-yl)aniline

C9H8N2S (176.0408168)


   

6-THIEN-2-YLPYRID-3-YLAMINE

6-THIEN-2-YLPYRID-3-YLAMINE

C9H8N2S (176.0408168)


   

1H,4H-Thiazolo[3,4-a]benzimidazole(9CI)

1H,4H-Thiazolo[3,4-a]benzimidazole(9CI)

C9H8N2S (176.0408168)


   

1H-Iodole-2-carbothioamide

1H-Iodole-2-carbothioamide

C9H8N2S (176.0408168)


   
   

Potassium cyclopentyltrifluoroborate

Potassium cyclopentyltrifluoroborate

C5H9BF3K (176.03864399999998)


   

5-Phenylthiazol-2-amine

5-Phenylthiazol-2-amine

C9H8N2S (176.0408168)


   

4-(ISOTHIAZOL-5-YL)ANILINE

4-(ISOTHIAZOL-5-YL)ANILINE

C9H8N2S (176.0408168)


   

3-Methyl-5-phenyl-1,2,4-thiadiazole

1,2,4-THIADIAZOLE, 3-METHYL-5-PHENYL-

C9H8N2S (176.0408168)


   

5-(DIFLUOROMETHYL)-1-METHYL-1H-PYRAZOLE-4-CARBOXYLIC ACID

5-(DIFLUOROMETHYL)-1-METHYL-1H-PYRAZOLE-4-CARBOXYLIC ACID

C6H6F2N2O2 (176.03973200000001)


   

3-(ISOTHIAZOL-5-YL)ANILINE

3-(ISOTHIAZOL-5-YL)ANILINE

C9H8N2S (176.0408168)


   

di(1H-pyrrol-2-yl)methanethione

di(1H-pyrrol-2-yl)methanethione

C9H8N2S (176.0408168)


   

4(3H)-Quinazolinethione,2-methyl-

4(3H)-Quinazolinethione,2-methyl-

C9H8N2S (176.0408168)


   

4-Isoxazolesulfonamide,3,5-dimethyl-(9CI)

4-Isoxazolesulfonamide,3,5-dimethyl-(9CI)

C5H8N2O3S (176.0255618)


   

4-Phenylthiazol-5-amine

4-Phenylthiazol-5-amine

C9H8N2S (176.0408168)


   

7-HYDROXY-5-OXO-4,5-DIHYDROPYRAZOLO[1,5-A]PYRIMIDINE-3-CARBONITRILE

7-HYDROXY-5-OXO-4,5-DIHYDROPYRAZOLO[1,5-A]PYRIMIDINE-3-CARBONITRILE

C7H4N4O2 (176.0334244)


   

1-(1-Benzothien-3-yl)ethanone

1-(1-Benzothien-3-yl)ethanone

C10H8OS (176.02958379999998)


   

N-(2-Aminoethyl)maleimide hydrochloride salt

N-(2-Aminoethyl)maleimide hydrochloride salt

C6H9ClN2O2 (176.03525240000002)


   

1-phenylimidazoline-2-thione

1-phenylimidazoline-2-thione

C9H8N2S (176.0408168)


   

1H-Imidazole-5-sulfonamide,4-amino-1-methyl-

1H-Imidazole-5-sulfonamide,4-amino-1-methyl-

C4H8N4O2S (176.0367948)


   

4-Formyl-3-nitrobenzonitrile

4-Formyl-3-nitrobenzonitrile

C8H4N2O3 (176.0221914)


   

1H-Benzimidazole,2-(ethenylthio)-(9CI)

1H-Benzimidazole,2-(ethenylthio)-(9CI)

C9H8N2S (176.0408168)


   

4-(4-METHYLPHENYL)-1,2,3-THIADIAZOLE

4-(4-METHYLPHENYL)-1,2,3-THIADIAZOLE

C9H8N2S (176.0408168)


   

Cyclopropanecarboxylic acid, 2-(chlorocarbonyl)-, ethyl ester (9CI)

Cyclopropanecarboxylic acid, 2-(chlorocarbonyl)-, ethyl ester (9CI)

C7H9ClO3 (176.02401940000001)


   

(2,4,6-Trifluorophenyl)boronic acid

(2,4,6-Trifluorophenyl)boronic acid

C6H4BF3O2 (176.025643)


   

3-formyl-2-nitrobenzonitrile

3-formyl-2-nitrobenzonitrile

C8H4N2O3 (176.0221914)


   

PROPANE TRICARBOXYLIC ACID

PROPANE TRICARBOXYLIC ACID

C6H8O6 (176.0320868)


   

1H-Indole-7-carbothioamide

1H-Indole-7-carbothioamide

C9H8N2S (176.0408168)


   

METHYL 2-(1H-IMIDAZOL-4-YL)ACETATE HYDROCHLORIDE

METHYL 2-(1H-IMIDAZOL-4-YL)ACETATE HYDROCHLORIDE

C6H9ClN2O2 (176.03525240000002)


   

2-Phenyl-1,3-thiazol-4-amine

2-Phenyl-1,3-thiazol-4-amine

C9H8N2S (176.0408168)


   

4-Phenylimidazole-2-thiol

4-Phenylimidazole-2-thiol

C9H8N2S (176.0408168)


   

methyl (Z)-3,4-dihydroxy-4-methoxy-2-oxo-but-3-enoate

methyl (Z)-3,4-dihydroxy-4-methoxy-2-oxo-but-3-enoate

C6H8O6 (176.0320868)


   

(E)-5-(2-(thiophen-2-yl)vinyl)-1H-pyrazole

(E)-5-(2-(thiophen-2-yl)vinyl)-1H-pyrazole

C9H8N2S (176.0408168)


   

4-deoxy-alpha-L-threo-hex-4-enopyranuronic acid

4-deoxy-alpha-L-threo-hex-4-enopyranuronic acid

C6H8O6 (176.0320868)


   

D-ascorbic acid

D-ascorbic acid

C6H8O6 (176.0320868)


   

(2R)-2-Hydroxy-2-methyl-4-oxopentanedioic acid

(2R)-2-Hydroxy-2-methyl-4-oxopentanedioic acid

C6H8O6 (176.0320868)


   

L-isoascorbic acid

L-isoascorbic acid

C6H8O6 (176.0320868)


   

1,1,1-Propanetricarboxylic acid

1,1,1-Propanetricarboxylic acid

C6H8O6 (176.0320868)


   

2-Methyl-4H-1-benzothiopyran-4-one

2-Methyl-4H-1-benzothiopyran-4-one

C10H8OS (176.02958379999998)


   

4-Deoxy-Alpha-L-Erythro-Hex-4-Enopyranuronic Acid

4-Deoxy-Alpha-L-Erythro-Hex-4-Enopyranuronic Acid

C6H8O6 (176.0320868)


   

vitamin C

2-o-(beta-d-glucopyranosyl)-ascorbic acid_qt

C6H8O6 (176.0320868)


G - Genito urinary system and sex hormones > G01 - Gynecological antiinfectives and antiseptics > G01A - Antiinfectives and antiseptics, excl. combinations with corticosteroids > G01AD - Organic acids A - Alimentary tract and metabolism > A11 - Vitamins > A11G - Ascorbic acid (vitamin c), incl. combinations > A11GA - Ascorbic acid (vitamin c), plain B - Blood and blood forming organs > B03 - Antianemic preparations > B03A - Iron preparations > B03AA - Iron bivalent, oral preparations COVID info from clinicaltrial, clinicaltrials, clinical trial, clinical trials D020011 - Protective Agents > D000975 - Antioxidants C26170 - Protective Agent > C275 - Antioxidant D018977 - Micronutrients > D014815 - Vitamins S - Sensory organs > S01 - Ophthalmologicals Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS L-Ascorbic acid (L-Ascorbate), an electron donor, is an endogenous antioxidant agent. L-Ascorbic acid inhibits selectively Cav3.2 channels with an IC50 of 6.5 μM. L-Ascorbic acid is also a collagen deposition enhancer and an elastogenesis inhibitor[1][2][3]. L-Ascorbic acid exhibits anti-cancer effects through the generation of reactive oxygen species (ROS) and selective damage to cancer cells[4]. L-Ascorbic acid (L-Ascorbate), an electron donor, is an endogenous antioxidant agent. L-Ascorbic acid inhibits selectively Cav3.2 channels with an IC50 of 6.5 μM. L-Ascorbic acid is also a collagen deposition enhancer and an elastogenesis inhibitor[1][2][3]. L-Ascorbic acid exhibits anti-cancer effects through the generation of reactive oxygen species (ROS) and selective damage to cancer cells[4].

   

2,3,4-trihydroxy-3,4-dihydro-2H-pyran-6-carboxylic acid

2,3,4-trihydroxy-3,4-dihydro-2H-pyran-6-carboxylic acid

C6H8O6 (176.0320868)


   

N-formyl-L-methioninate

N-formyl-L-methioninate

C6H10NO3S- (176.038137)


The conjugate base of N-formyl-L-methionine; major species at pH 7.3.

   

D-Glucurono-6,2-lactone

D-Glucurono-6,2-lactone

C6H8O6 (176.0320868)


   

L-xylo-hex-3-ulono-1,4-lactone

L-xylo-hex-3-ulono-1,4-lactone

C6H8O6 (176.0320868)


   
   

4-Deoxy-l-erythro-hex-4-enopyranuronic acid

4-Deoxy-l-erythro-hex-4-enopyranuronic acid

C6H8O6 (176.0320868)


   

3,4-Dihydroxy-5-[(S)-1,2-dihydroxyethyl]furan-2(5H)-one

3,4-Dihydroxy-5-[(S)-1,2-dihydroxyethyl]furan-2(5H)-one

C6H8O6 (176.0320868)


   

L-xylo-hex-3-ulonolactone

L-xylo-hex-3-ulonolactone

C6H8O6 (176.0320868)


   

(5R)-5-[(1S)-1,2-dihydroxyethyl]-4-hydroxyoxolane-2,3-dione

(5R)-5-[(1S)-1,2-dihydroxyethyl]-4-hydroxyoxolane-2,3-dione

C6H8O6 (176.0320868)


   

4-deoxy-beta-L-threo-hex-4-enopyranuronic acid

4-deoxy-beta-L-threo-hex-4-enopyranuronic acid

C6H8O6 (176.0320868)


   

2,3-Didehydro-D-glucose

2,3-Didehydro-D-glucose

C6H8O6 (176.0320868)


   

3,4-didehydro-D-glucose

3,4-didehydro-D-glucose

C6H8O6 (176.0320868)


   

alpha-Mannofuranuronic acid gamma-lactone

alpha-Mannofuranuronic acid gamma-lactone

C6H8O6 (176.0320868)


A carbohydrate lactone obtained by intramolecular condensation of the 6-carboxy group with the 3-hydroxy group of alpha-mannofuranuronic acid.

   

S-methylmercapturate

S-methylmercapturate

C6H10NO3S- (176.038137)


   

Vitamin_C

L-Threoascorbic acid,Antiscorbutic factor,Vitamin C;(R)-5-((S)-1,2-Dihydroxyethyl)-3,4-dihydroxyfuran-2(5H)-one

C6H8O6 (176.0320868)


L-ascorbic acid is a white to very pale yellow crystalline powder with a pleasant sharp acidic taste. Almost odorless. (NTP, 1992) L-ascorbic acid is the L-enantiomer of ascorbic acid and conjugate acid of L-ascorbate. It has a role as a coenzyme, a flour treatment agent, a food antioxidant, a plant metabolite, a cofactor, a skin lightening agent and a geroprotector. It is an ascorbic acid and a vitamin C. It is a conjugate acid of a L-ascorbate. It is an enantiomer of a D-ascorbic acid. A six carbon compound related to glucose. It is found naturally in citrus fruits and many vegetables. Ascorbic acid is an essential nutrient in human diets, and necessary to maintain connective tissue and bone. Its biologically active form, vitamin C, functions as a reducing agent and coenzyme in several metabolic pathways. Vitamin C is considered an antioxidant. Ascorbic acid is a metabolite found in or produced by Escherichia coli (strain K12, MG1655). Ascorbic acid is a Vitamin C. Ascorbic Acid is a natural product found in Populus tremula, Rosa platyacantha, and other organisms with data available. Ascorbic Acid is a natural water-soluble vitamin (Vitamin C). Ascorbic acid is a potent reducing and antioxidant agent that functions in fighting bacterial infections, in detoxifying reactions, and in the formation of collagen in fibrous tissue, teeth, bones, connective tissue, skin, and capillaries. Found in citrus and other fruits, and in vegetables, vitamin C cannot be produced or stored by humans and must be obtained in the diet. (NCI04) A six carbon compound related to glucose. It is found naturally in citrus fruits and many vegetables. Ascorbic acid is an essential nutrient in human diets, and necessary to maintain connective tissue and bone. Its biologically active form, vitamin C, functions as a reducing agent and coenzyme in several metabolic pathways. Vitamin C is considered an antioxidant. See also: Sodium Ascorbate (active moiety of); D-ascorbic acid (related); Magnesium Ascorbyl Phosphate (active moiety of) ... View More ... G - Genito urinary system and sex hormones > G01 - Gynecological antiinfectives and antiseptics > G01A - Antiinfectives and antiseptics, excl. combinations with corticosteroids > G01AD - Organic acids A - Alimentary tract and metabolism > A11 - Vitamins > A11G - Ascorbic acid (vitamin c), incl. combinations > A11GA - Ascorbic acid (vitamin c), plain B - Blood and blood forming organs > B03 - Antianemic preparations > B03A - Iron preparations > B03AA - Iron bivalent, oral preparations COVID info from clinicaltrial, clinicaltrials, clinical trial, clinical trials D020011 - Protective Agents > D000975 - Antioxidants C26170 - Protective Agent > C275 - Antioxidant D018977 - Micronutrients > D014815 - Vitamins S - Sensory organs > S01 - Ophthalmologicals Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS L-Ascorbic acid (L-Ascorbate), an electron donor, is an endogenous antioxidant agent. L-Ascorbic acid inhibits selectively Cav3.2 channels with an IC50 of 6.5 μM. L-Ascorbic acid is also a collagen deposition enhancer and an elastogenesis inhibitor[1][2][3]. L-Ascorbic acid exhibits anti-cancer effects through the generation of reactive oxygen species (ROS) and selective damage to cancer cells[4]. L-Ascorbic acid (L-Ascorbate), an electron donor, is an endogenous antioxidant agent. L-Ascorbic acid inhibits selectively Cav3.2 channels with an IC50 of 6.5 μM. L-Ascorbic acid is also a collagen deposition enhancer and an elastogenesis inhibitor[1][2][3]. L-Ascorbic acid exhibits anti-cancer effects through the generation of reactive oxygen species (ROS) and selective damage to cancer cells[4].

   

Glucurolactone

D(+)-Glucurono-3,6-lactone

C6H8O6 (176.0320868)


D-Glucuronic acid lactone is an endogenous metabolite.

   

L-xylo-Hex-2-ulono-1,4-lactone

L-xylo-Hex-2-ulono-1,4-lactone

C6H8O6 (176.0320868)


   

(4S,5S)-4,5-dihydroxy-2,6-dioxohexanoic acid

(4S,5S)-4,5-dihydroxy-2,6-dioxohexanoic acid

C6H8O6 (176.0320868)


   

2-hydroxy-3-oxoadipic acid

2-hydroxy-3-oxoadipic acid

C6H8O6 (176.0320868)


   

4-Hydroxy-4-methyl-2-oxoglutaric acid

4-Hydroxy-4-methyl-2-oxoglutaric acid

C6H8O6 (176.0320868)


   

3-deoxy-D-glycero-hexo-2,5-diulosonic acid

3-deoxy-D-glycero-hexo-2,5-diulosonic acid

C6H8O6 (176.0320868)


   

5-dehydro-4-deoxy-D-glucuronic acid

5-dehydro-4-deoxy-D-glucuronic acid

C6H8O6 (176.0320868)


   

5-(1,2-dihydroxyethyl)-4-hydroxyoxolane-2,3-dione

5-(1,2-dihydroxyethyl)-4-hydroxyoxolane-2,3-dione

C6H8O6 (176.0320868)


   

N-acetyl-S-methyl-L-cysteine(1-)

N-acetyl-S-methyl-L-cysteine(1-)

C6H10NO3S (176.038137)


An S-substituted N-acetyl-L-cysteinate that is the conjugate base of N-acetyl-S-methyl-L-cysteine resulting from the deprotonation of the carboxy group; major species at pH 7.3.

   

Propanetricarboxylic acid

Propanetricarboxylic acid

C6H8O6 (176.0320868)


   

(4r)-2-chloro-4-hydroxy-4-[(1r)-1-hydroxyethyl]cyclopent-2-en-1-one

(4r)-2-chloro-4-hydroxy-4-[(1r)-1-hydroxyethyl]cyclopent-2-en-1-one

C7H9ClO3 (176.02401940000001)


   

3,4,8-trihydroxy-2,6-dioxabicyclo[3.2.1]octan-7-one

3,4,8-trihydroxy-2,6-dioxabicyclo[3.2.1]octan-7-one

C6H8O6 (176.0320868)


   

(1s,3r,4r,5s,8s)-3,4,8-trihydroxy-2,6-dioxabicyclo[3.2.1]octan-7-one

(1s,3r,4r,5s,8s)-3,4,8-trihydroxy-2,6-dioxabicyclo[3.2.1]octan-7-one

C6H8O6 (176.0320868)


   

(4s,5r,6s)-2-chloro-4,5-dihydroxy-6-methylcyclohex-2-en-1-one

(4s,5r,6s)-2-chloro-4,5-dihydroxy-6-methylcyclohex-2-en-1-one

C7H9ClO3 (176.02401940000001)


   

(4s,5s)-5-chloro-4-hydroxy-3-(1-hydroxyethyl)cyclopent-2-en-1-one

(4s,5s)-5-chloro-4-hydroxy-3-(1-hydroxyethyl)cyclopent-2-en-1-one

C7H9ClO3 (176.02401940000001)


   

(4s)-2-chloro-4-hydroxy-3-[(1r)-1-hydroxyethyl]cyclopent-2-en-1-one

(4s)-2-chloro-4-hydroxy-3-[(1r)-1-hydroxyethyl]cyclopent-2-en-1-one

C7H9ClO3 (176.02401940000001)


   
   

2-chloro-4-hydroxy-3-(1-hydroxyethyl)cyclopent-2-en-1-one

2-chloro-4-hydroxy-3-(1-hydroxyethyl)cyclopent-2-en-1-one

C7H9ClO3 (176.02401940000001)


   

(2r)-2-[(1r)-1,2-dihydroxyethyl]-4,5-dihydroxy-2h-furan-3-one

(2r)-2-[(1r)-1,2-dihydroxyethyl]-4,5-dihydroxy-2h-furan-3-one

C6H8O6 (176.0320868)


   

2-chloro-4,5-dihydroxy-6-methylcyclohex-2-en-1-one

2-chloro-4,5-dihydroxy-6-methylcyclohex-2-en-1-one

C7H9ClO3 (176.02401940000001)


   

(4s,5s,6r)-2-chloro-4,5-dihydroxy-6-methylcyclohex-2-en-1-one

(4s,5s,6r)-2-chloro-4,5-dihydroxy-6-methylcyclohex-2-en-1-one

C7H9ClO3 (176.02401940000001)