Exact Mass: 166.063

Exact Mass Matches: 166.063

Found 332 metabolites which its exact mass value is equals to given mass value 166.063, within given mass tolerance error 0.0002 dalton. Try search metabolite list with more accurate mass tolerance error 4.0E-5 dalton.

3,4-Dimethoxybenzaldehyde

InChI=1/C9H10O3/c1-11-8-4-3-7(6-10)5-9(8)12-2/h3-6H,1-2H

C9H10O3 (166.063)


Veratraldehyde appears as needles or chunky light peach powder. Has an odor of vanilla beans. (NTP, 1992) Veratraldehyde is a dimethoxybenzene that is benzaldehyde substituted by methoxy groups at positions 3 and 4. It is found in peppermint, ginger, raspberry, and other fruits. It has a role as an antifungal agent. It is a member of benzaldehydes and a dimethoxybenzene. 3,4-Dimethoxybenzaldehyde is a natural product found in Polygala senega, Pluchea sagittalis, and other organisms with data available. 3,4-Dimethoxybenzaldehyde is found in fruits. 3,4-Dimethoxybenzaldehyde is isolated from peppermint, raspberry, ginger and Bourbon vanilla. 3,4-Dimethoxybenzaldehyde is used in vanilla flavour Isolated from peppermint, raspberry, ginger and Bourbon vanilla. It is used in vanilla flavours. 3,4-Dimethoxybenzaldehyde is found in peppermint, herbs and spices, and fruits. CONFIDENCE standard compound; INTERNAL_ID 1016; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3940; ORIGINAL_PRECURSOR_SCAN_NO 3939 CONFIDENCE standard compound; INTERNAL_ID 1016; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3955; ORIGINAL_PRECURSOR_SCAN_NO 3954 CONFIDENCE standard compound; INTERNAL_ID 1016; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3930; ORIGINAL_PRECURSOR_SCAN_NO 3929 CONFIDENCE standard compound; INTERNAL_ID 1016; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3941; ORIGINAL_PRECURSOR_SCAN_NO 3940 CONFIDENCE standard compound; INTERNAL_ID 1016; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3963; ORIGINAL_PRECURSOR_SCAN_NO 3961 CONFIDENCE standard compound; INTERNAL_ID 1016; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3961; ORIGINAL_PRECURSOR_SCAN_NO 3960 Veratraldehyde is an important chemical used in perfumery, agrochemical, and pharmaceutical industries. Veratraldehyde is an important chemical used in perfumery, agrochemical, and pharmaceutical industries.

   

Tropate

Tropicamide impurity C, European Pharmacopoeia (EP) Reference Standard

C9H10O3 (166.063)


Tropic acid is a 3-hydroxy monocarboxylic acid that is propionic acid in which one of the hydrogens at position 2 is substituted by a phenyl group, and one of the methyl hydrogens is substituted by a hydroxy group. It has a role as a human xenobiotic metabolite. It is functionally related to a propionic acid and a hydratropic acid. It is a conjugate acid of a tropate. Tropic acid is a natural product found in Hyoscyamus muticus, Datura stramonium, and other organisms with data available. Tropic acid is a metabolite found in or produced by Saccharomyces cerevisiae. Tropate, also known as Tropic acid or alpha-(Hydroxymethyl)phenylacetic acid, is classified as a beta hydroxy acid or a Beta hydroxy acid derivative. Beta hydroxy acids are compounds containing a carboxylic acid substituted with a hydroxyl group on the C3 carbon atom. Tropate is considered to be soluble in water and acidic. Tropate can be synthesized from hydratropic acid and propionic acid. Tropate can be synthesized into tropan-3alpha-yl 3-hydroxy-2-phenylpropanoate A 3-hydroxy monocarboxylic acid that is propionic acid in which one of the hydrogens at position 2 is substituted by a phenyl group, and one of the methyl hydrogens is substituted by a hydroxy group. KEIO_ID T059 Tropic acid (DL-Tropic acid) is a laboratory reagent used in the chemical synthesis of Atropine and Hyoscyamine[1]. Tropic acid (DL-Tropic acid) is a laboratory reagent used in the chemical synthesis of Atropine and Hyoscyamine[1].

   

Desaminotyrosine

3-(4-hydroxyphenyl)propanoic acid

C9H10O3 (166.063)


Desaminotyrosine, also known as 4-hydroxyphenylpropionic acid, is a normal constituent of human urine. It is a product of tyrosine metabolism; its concentration in urine increases in patients with gastrointestinal diseases. Desaminotyrosine is a major phenolic acid breakdown product of proanthocyanidin metabolism (PMID:15315398). Urinary desaminotyrosine is produced by Clostridium sporogenes and C. botulinum (PMID:29168502). Desaminotyrosine is also found in Acinetobacter, Bacteroides, Bifidobacteria, Bifidobacterium, Clostridium, Enterococcus, Escherichia, Eubacterium, Klebsiella, Lactobacillus, Pseudomonas, and Staphylococcus (PMID:29168502, 28393285, 19961416). Desaminotyrosine is a phenolic acid metabolite formed by the gut microflora detected after the consumption of whole grain. A normal constituent of human urine. A product of tyrosine metabolism; concentration in urine increases in patients with gastrointestinal diseases. (Dictionary of Organic Compounds) May also result from phenolic acid metabolism by colonic bacteria. (PMID 15315398) [HMDB]. Phloretic acid is found in many foods, some of which are arrowroot, olive, avocado, and peanut. Desaminotyrosine is a microbially associated metabolite protecting from influenza through augmentation of type I interferon signaling. Desaminotyrosine is a microbially associated metabolite protecting from influenza through augmentation of type I interferon signaling.

   

L-3-Phenyllactic acid

(2R)-2-hydroxy-3-phenylpropanoic acid

C9H10O3 (166.063)


L-3-Phenyllactic acid (or PLA) is a chiral aromatic compound involved in phenylalanine metabolism. It is likely produced from phenylpyruvate via the action of lactate dehydrogenase. The D-form of this organic acid is typically derived from bacterial sources while the L-form is almost certainly endogenous. Levels of phenyllactate are normally very low in blood or urine. High levels of PLA in the urine or blood are often indicative of phenylketonuria (PKU) and hyperphenylalaninemia (HPA). PKU is due to lack of the enzyme phenylalanine hydroxylase (PAH), so that phenylalanine is converted not to tyrosine but to phenylpyruvic acid (a precursor of phenylactate). In particular, excessive phenylalanine is typically metabolized into phenylketones through, a transaminase pathway route involving glutamate. Metabolites of this transamination reaction include phenylacetate, phenylpyruvate and phenethylamine. In persons with PKU, dietary phenylalanine either accumulates in the body or some of it is converted to phenylpyruvic acid and then to phenyllactate through the action of lactate dehydrogenase. Individuals with PKU tend to excrete large quantities of phenylpyruvate, phenylacetate and phenyllactate, along with phenylalanine, in their urine. If untreated, mental retardation effects and microcephaly are evident by the first year along with other symptoms which include: unusual irritability, epileptic seizures and skin lesions. Hyperactivity, EEG abnormalities and seizures, and severe learning disabilities are major clinical problems later in life. A "musty or mousy" odor of skin, hair, sweat and urine (due to phenylacetate accumulation); and a tendency to hypopigmentation and eczema are also observed. The neural-development effects of PKU are primarily due to the disruption of neurotransmitter synthesis. In particular, phenylalanine is a large, neutral amino acid which moves across the blood-brain barrier (BBB) via the large neutral amino acid transporter (LNAAT). Excessive phenylalanine in the blood saturates the transporter. Thus, excessive levels of phenylalanine significantly decrease the levels of other LNAAs in the brain. But since these amino acids are required for protein and neurotransmitter synthesis, phenylalanine accumulation disrupts brain development, leading to mental retardation. [HMDB] L-3-Phenyllactic acid (or PLA) is a chiral aromatic compound involved in phenylalanine metabolism. It is likely produced from phenylpyruvate via the action of lactate dehydrogenase. The D-form of this organic acid is typically derived from bacterial sources while the L-form is almost certainly endogenous. Levels of phenyllactate are normally very low in blood or urine. High levels of PLA in the urine or blood are often indicative of phenylketonuria (PKU) and hyperphenylalaninemia (HPA). PKU is due to lack of the enzyme phenylalanine hydroxylase (PAH), so that phenylalanine is converted not to tyrosine but to phenylpyruvic acid (a precursor of phenylactate). In particular, excessive phenylalanine is typically metabolized into phenylketones through, a transaminase pathway route involving glutamate. Metabolites of this transamination reaction include phenylacetate, phenylpyruvate and phenethylamine. In persons with PKU, dietary phenylalanine either accumulates in the body or some of it is converted to phenylpyruvic acid and then to phenyllactate through the action of lactate dehydrogenase. Individuals with PKU tend to excrete large quantities of phenylpyruvate, phenylacetate and phenyllactate, along with phenylalanine, in their urine. If untreated, mental retardation effects and microcephaly are evident by the first year along with other symptoms which include: unusual irritability, epileptic seizures and skin lesions. Hyperactivity, EEG abnormalities and seizures, and severe learning disabilities are major clinical problems later in life. A "musty or mousy" odor of skin, hair, sweat and urine (due to phenylacetate accumulation); and a tendency to hypopigmentation and eczema are also observed. The neural-development effects of PKU are primarily due to the disruption of neurotransmitter synthesis. In particular, phenylalanine is a large, neutral amino acid which moves across the blood-brain barrier (BBB) via the large neutral amino acid transporter (LNAAT). Excessive phenylalanine in the blood saturates the transporter. Thus, excessive levels of phenylalanine significantly decrease the levels of other LNAAs in the brain. But since these amino acids are required for protein and neurotransmitter synthesis, phenylalanine accumulation disrupts brain development, leading to mental retardation. (±)-3-Phenyllactic acid. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=828-01-3 (retrieved 2024-07-04) (CAS RN: 828-01-3). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). (S)-2-Hydroxy-3-phenylpropanoic acid is a product of phenylalanine catabolism. An elevated level of phenyllactic acid is found in body fluids of patients with or phenylketonuria. D-?(+)?-?Phenyllactic acid is an anti-bacterial agent, excreted by Geotrichum candidum, inhibits a range of Gram-positive from humans and foodstuffs and Gram-negative bacteria found in humans[1]. DL-3-Phenyllactic acid is a broad-spectrum antimicrobial compound. DL-3-Phenyllactic acid is a broad-spectrum antimicrobial compound.

   

Acetovanillone

1-(4-hydroxy-3-methoxyphenyl)ethan-1-one

C9H10O3 (166.063)


Acetovanillone, also known as 4-hydroxy-3-methoxyacetophenone or acetoguaiacon, is a member of the class of compounds known as alkyl-phenylketones. Alkyl-phenylketones are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl group. Acetovanillone is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). Acetovanillone is a faint, sweet, and vanillin tasting compound found in corn and garden onion, which makes acetovanillone a potential biomarker for the consumption of these food products. Acetovanillone may be a unique S.cerevisiae (yeast) metabolite. D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents D002491 - Central Nervous System Agents > D000700 - Analgesics D020011 - Protective Agents > D000975 - Antioxidants D000893 - Anti-Inflammatory Agents D018501 - Antirheumatic Agents D004791 - Enzyme Inhibitors Apocynin is a selective NADPH-oxidase inhibitor with an IC50 of 10 μM[1][2]. Apocynin improves acute lung inflammation in Carrageenan (HY-125474)-induced pleurisy mice model[3]. Apocynin can also be used for cancer research[4]. Apocynin reverses the aging process in mesenchymal stem cells to promote osteogenesis and increases bone mass[5]. Apocynin is a selective NADPH-oxidase inhibitor with an IC50 of 10 μM[1][2]. Apocynin improves acute lung inflammation in Carrageenan (HY-125474)-induced pleurisy mice model[3]. Apocynin can also be used for cancer research[4]. Apocynin reverses the aging process in mesenchymal stem cells to promote osteogenesis and increases bone mass[5]. Apocynin is a selective NADPH-oxidase inhibitor with an IC50 of 10 μM[1][2]. Apocynin improves acute lung inflammation in Carrageenan (HY-125474)-induced pleurisy mice model[3]. Apocynin can also be used for cancer research[4]. Apocynin reverses the aging process in mesenchymal stem cells to promote osteogenesis and increases bone mass[5].

   

3-(3-hydroxyphenyl)propionate

dihydro-3-Coumaric acid, monosodium salt

C9H10O3 (166.063)


3-(3-Hydroxyphenyl)propanoic (hMPP) acid is one of the major metabolites of ingested caffeic acid (PMID: 15479001) and of the phenolic degradation products of proanthocyanidins (the most abundant polyphenol present in chocolate) by the microflora in the colon (PMID: 12663291). mHPP is suspected to have antioxidants properties and is actively absorbed by the monocarboxylic acid transporter (MCT) in intestinal Caco-2 cell monolayers (PMID: 15479001, 12663291). hMPP has been found to be a metabolite of Clostridium, Escherichia, and Eubacterium (PMID: 28393285, 19520845). 3-(3-Hydroxyphenyl)propanoic acid is a flavonoid metabolite. 3-(3-Hydroxyphenyl)propanoic acid is a phenolic acid metabolite formed by the gut microflora detected after the consumption of whole grain. 3-(3-Hydroxyphenyl)propanoic (hMPP) acid is one of the major metabolites of ingested caffeic acid (PMID 15479001) and of the phenolic degradation products of proanthocyanidins (the most abundant polyphenol present in chocolate) by the microflora in the colon (PMID 12663291). mHPP is suspected to have antioxidants properties and is actively absorbed by the monocarboxylic acid transporter (MCT) in intestinal Caco-2 cell monolayers (PMID 15479001, 12663291). [HMDB] 3-(3-Hydroxyphenyl)propionic acid is a flavonoid metabolite formed by human microflora. 3-(3-Hydroxyphenyl)propionic acid shows vasodilatory activity[1]. 3-(3-Hydroxyphenyl)propionic acid is a flavonoid metabolite formed by human microflora. 3-(3-Hydroxyphenyl)propionic acid shows vasodilatory activity[1].

   

3-(2-hydroxyphenyl)propionate

3-(O-Hydroxyphenyl)propionic acid, 8ci

C9H10O3 (166.063)


3-(2-Hydroxyphenyl)propanoic acid is found in bilberry. 3-(2-Hydroxyphenyl)propanoic acid is found in Melilotus alba (whilte melilot). Found in Melilotus alba (whilte melilot) KEIO_ID P072 Melilotic acid is an endogenous metabolite. Melilotic acid is an endogenous metabolite.

   

3-Ethoxybenzoate

3-ETHOXYBENZOIC ACID

C9H10O3 (166.063)


KEIO_ID E026

   

4-Hydroxyphenyl-2-propionic acid

4-Hydroxy-α-methylbenzeneacetic acid

C9H10O3 (166.063)


4-Hydroxyphenyl-2-propionic acid belongs to the class of organic compounds known as phenylpropanoic acids. Phenylpropanoic acids are compounds with a structure containing a benzene ring conjugated to a propanoic acid. 4-Hydroxyphenyl-2-propionic acid has been detected in multiple biofluids, such as urine and blood (PMID: 20428313). Within the cell, 4-hydroxyphenyl-2-propionic acid is primarily located in the cytoplasm. A polyphenol metabolite detected in biological fluids [PhenolExplorer] KEIO_ID H099

   

Paeonol

1-(2-hydroxy-4-methoxyphenyl)ethan-1-one

C9H10O3 (166.063)


A polyphenol metabolite detected in biological fluids [PhenolExplorer] Paeonol is an active extraction from the root of Paeonia suffruticosa, Paeonol inhibits MAO-A and MAO-B with IC50 of 54.6 μM and 42.5 μM, respectively. Paeonol is an active extraction from the root of Paeonia suffruticosa, Paeonol inhibits MAO-A and MAO-B with IC50 of 54.6 μM and 42.5 μM, respectively.

   

Caffeyl alcohol

Spectrum_001694

C9H10O3 (166.063)


   

Homovanillin

2-(4-HYDROXY-3-METHOXYPHENYL)ACETALDEHYDE

C9H10O3 (166.063)


3 -Methoxy-4-hydroxyphenylacetaldehyde is an intermediary aldehyde of dopamine metabolism, metabolized by the class I human liver alcohol dehydrogenases (ADHs) . ADH catalyzes both ethanol and acetaldehyde, and the dopamine intermediates compete for the same site of ADH, a basis for the ethanol-induced in vivo alterations of dopamine metabolism. (PMID 2432930) [HMDB] 3 -Methoxy-4-hydroxyphenylacetaldehyde is an intermediary aldehyde of dopamine metabolism, metabolized by the class I human liver alcohol dehydrogenases (ADHs). ADH catalyzes both ethanol and acetaldehyde, and the dopamine intermediates compete for the same site of ADH, a basis for the ethanol-induced in vivo alterations of dopamine metabolism. (PMID 2432930). COVID info from COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS

   

(R)-tropic acid

(R)-tropic acid

C9H10O3 (166.063)


   

(S)-tropic acid

(S)-tropic acid

C9H10O3 (166.063)


   

Ethylparaben

Ethylparaben, Pharmaceutical Secondary Standard; Certified Reference Material

C9H10O3 (166.063)


Ethylparaben is an ethyl ester resulting from the formal condensation of the carboxy group of 4-hydroxybenzoic acid with ethanol, It has a role as an antimicrobial food preservative, an antifungal agent, a plant metabolite and a phytoestrogen. It is a paraben and an ethyl ester. Ethylparaben is a Standardized Chemical Allergen. The physiologic effect of ethylparaben is by means of Increased Histamine Release, and Cell-mediated Immunity. Ethylparaben is a natural product found in Ulva australis, Andrographis paniculata, and other organisms with data available. Ethylparaben is found in alcoholic beverages. Ethylparaben is an antimicrobial agent, preservative. Ethylparaben is present in red wine, white wine and sake. Ethylparaben belongs to the family of Hydroxybenzoic Acid Derivatives. These are compounds containing an hydroxybenzoic acid (or a derivative), which is a benzene ring bearing a carboxylic acid. Ethyl-4-hydroxybenzoate is a metabolite found in or produced by Saccharomyces cerevisiae. Ethylparaben, also known as e-214 or aseptin a, belongs to the class of organic compounds known as p-hydroxybenzoic acid alkyl esters. These are aromatic compounds containing a benzoic acid, which is esterified with an alkyl group and para-substituted with a hydroxyl group. It is used as an antifungal preservative. Sodium ethyl para-hydroxybenzoate, the sodium salt of ethylparaben, has the same uses and is given the E number E215. Ethylparaben is a drug. Its formula is HO-C6H4-CO-O-CH2CH3. Ethylparaben is a mild and phenolic tasting compound. ethylparaben has been detected, but not quantified, in alcoholic beverages. This could make ethylparaben a potential biomarker for the consumption of these foods. Ethylparaben (ethyl para-hydroxybenzoate) is the ethyl ester of p-hydroxybenzoic acid. Ethylparaben is a potentially toxic compound. As a food additive, it has E number E214. An ethyl ester resulting from the formal condensation of the carboxy group of 4-hydroxybenzoic acid with ethanol, D010592 - Pharmaceutic Aids > D011310 - Preservatives, Pharmaceutical > D010226 - Parabens Ethylparaben is the ethyl ester of paraben and is used as an antifungal preservative and food additive.

   

4-Methoxyphenylacetic acid

InChI=1/C9H10O3/c1-12-8-4-2-7(3-5-8)6-9(10)11/h2-5H,6H2,1H3,(H,10,11

C9H10O3 (166.063)


4-methoxyphenylacetic acid is a monocarboxylic acid that is phenylacetic acid carrying a 4-methoxy substituent. It is used as an intermediate for pharmaceuticals and other organic synthesis. It has been found to inhibit the germination of cress and lettuce seeds. It has a role as a plant metabolite, a plant growth retardant and an Aspergillus metabolite. It is a monocarboxylic acid and a monomethoxybenzene. 4-Methoxyphenylacetic acid, also known as 4-methoxybenzeneacetate or 2-(p-anisyl)acetic acid, belongs to the class of organic compounds known as anisoles. These are organic compounds containing a methoxybenzene or a derivative thereof. 4-Methoxyphenylacetic acid is a 4-O-Methylated catecholamine metabolite found in normal human urine, cerebrospinal fluid and brain tissue. 4-methoxyphenylacetic acid appears as pale yellow or off white colored flakes. Severely irritates skin and eyes. May be toxic by ingestion. 4-methoxyphenylacetic acid is a monocarboxylic acid that is phenylacetic acid carrying a 4-methoxy substituent. It is used as an intermediate for pharmaceuticals and other organic synthesis. It has been found to inhibit the germination of cress and lettuce seeds. It has a role as a plant metabolite, a plant growth retardant and an Aspergillus metabolite. It is a monocarboxylic acid and a monomethoxybenzene. 4-Methoxyphenylacetic acid is a natural product found in Gloeophyllum odoratum, Berberis koreana, and other organisms with data available. A monocarboxylic acid that is phenylacetic acid carrying a 4-methoxy substituent. It is used as an intermediate for pharmaceuticals and other organic synthesis. It has been found to inhibit the germination of cress and lettuce seeds. 4-Methoxyphenylacetic acid is a 4-O-Methylated catecholamine metabolite found in normal human urine, cerebrospinal fluid and brain tissue. (PMIDs 6511847, 4645252, 12416886) [HMDB] 2-(4-Methoxyphenyl)acetic acid is a plasma metabolite, with high sensitivity and specificity value as a biomarker for discriminating between NSCLC and healthy controls. 2-(4-Methoxyphenyl)acetic acid is a plasma metabolite, with high sensitivity and specificity value as a biomarker for discriminating between NSCLC and healthy controls.

   

Paeonol

2 inverted exclamation mark -Hydroxy-4 inverted exclamation mark -methoxyacetophenone

C9H10O3 (166.063)


Paeonol is a member of phenols and a member of methoxybenzenes. It has a role as a metabolite. Paeonol is a natural product found in Vincetoxicum paniculatum, Vincetoxicum glaucescens, and other organisms with data available. See also: Paeonia lactiflora root (part of); Paeonia X suffruticosa root (part of). A natural product found in Paeonia rockii subspeciesrockii. Paeonol is an active extraction from the root of Paeonia suffruticosa, Paeonol inhibits MAO-A and MAO-B with IC50 of 54.6 μM and 42.5 μM, respectively. Paeonol is an active extraction from the root of Paeonia suffruticosa, Paeonol inhibits MAO-A and MAO-B with IC50 of 54.6 μM and 42.5 μM, respectively.

   

Apocynin

InChI=1/C9H10O3/c1-6(10)7-3-4-8(11)9(5-7)12-2/h3-5,11H,1-2H

C9H10O3 (166.063)


Apocynin is an aromatic ketone that is 1-phenylethanone substituted by a hydroxy group at position 4 and a methoxy group at position 3. It has a role as a non-narcotic analgesic, a non-steroidal anti-inflammatory drug, an antirheumatic drug, a peripheral nervous system drug, an EC 1.6.3.1. [NAD(P)H oxidase (H2O2-forming)] inhibitor and a plant metabolite. It is a member of acetophenones, a methyl ketone and an aromatic ketone. Acetovanillone has been used in trials studying the treatment of Bronchial Asthma and Chronic Obstructive Pulmonary Disease. Acetovanillone is a natural product found in Iris tectorum, Apocynum cannabinum, and other organisms with data available. Acetovanillone is a metabolite found in or produced by Saccharomyces cerevisiae. An aromatic ketone that is 1-phenylethanone substituted by a hydroxy group at position 4 and a methoxy group at position 3. D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents D002491 - Central Nervous System Agents > D000700 - Analgesics D020011 - Protective Agents > D000975 - Antioxidants D000893 - Anti-Inflammatory Agents D018501 - Antirheumatic Agents D004791 - Enzyme Inhibitors Apocynin is a selective NADPH-oxidase inhibitor with an IC50 of 10 μM[1][2]. Apocynin improves acute lung inflammation in Carrageenan (HY-125474)-induced pleurisy mice model[3]. Apocynin can also be used for cancer research[4]. Apocynin reverses the aging process in mesenchymal stem cells to promote osteogenesis and increases bone mass[5]. Apocynin is a selective NADPH-oxidase inhibitor with an IC50 of 10 μM[1][2]. Apocynin improves acute lung inflammation in Carrageenan (HY-125474)-induced pleurisy mice model[3]. Apocynin can also be used for cancer research[4]. Apocynin reverses the aging process in mesenchymal stem cells to promote osteogenesis and increases bone mass[5]. Apocynin is a selective NADPH-oxidase inhibitor with an IC50 of 10 μM[1][2]. Apocynin improves acute lung inflammation in Carrageenan (HY-125474)-induced pleurisy mice model[3]. Apocynin can also be used for cancer research[4]. Apocynin reverses the aging process in mesenchymal stem cells to promote osteogenesis and increases bone mass[5].

   

3-Methoxyphenylacetic acid

3-methoxyphenylacetic acid, potassium salt

C9H10O3 (166.063)


3-Methoxyphenylacetic acid, also known as m-Methoxyphenylacetic acid (m-OMePAA), a derivative of m-hydroxyphenylacetic acid (m-OHPAA) having the same chemical composition as that of the phytotoxic compound produced in culture by Rhizoctonia solani, a fungal pathogen of soybean. That phytotoxic compound reduced growth and symbiotic N2-fixation activity of Tracy soybeans in soil. The data indicate that phytotoxic compounds of R. solani are involved in nodule impairment and reduced N2-fixation in soybean (R. G. Orellana, and N. B. Mandava (1983) m-Hydroxyphenylacetic and m-Methoxyphenylacetic Acids of Rhizoctonia solani: Their Effect on Specific Root-Nodule Activity and Histopathology in Soybean. Journal of Phytopathology. Volume 107, Issue 2, pages 159167, June 1983). 3-Methoxyphenylacetic acid (m-Methoxyphenylacetic acid), a m-hydroxyphenylacetic acid (m-OHPAA) derivative, is a phytotoxin in Rhizoctonia solani. 3-Methoxyphenylacetic acid is used to develop a toxin-mediated bioassay for resistance to rhizoctonia root rot[1].

   

3-Phenoxypropionic acid

beta-Phenoxypropionic acid

C9H10O3 (166.063)


3-Phenoxypropionic acid is a histamine H3 (H3 receptors controls histaminergic neuron activity) receptor antagonist (PMID 16246552) [HMDB] 3-Phenoxypropionic acid is a histamine H3 (H3 receptors controls histaminergic neuron activity) receptor antagonist (PMID 16246552).

   

D-Phenyllactic acid

(R)-alpha-Hydroxy-3-phenylpropionic acid

C9H10O3 (166.063)


Phenyllactic acid is a product of phenylalanine catabolism. An elevated level of phenyllactic acid is found in body fluids of patients with or phenylketonuria. (+)-3-Phenyllactic acid. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=7326-19-4 (retrieved 2024-07-04) (CAS RN: 7326-19-4). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). (S)-2-Hydroxy-3-phenylpropanoic acid is a product of phenylalanine catabolism. An elevated level of phenyllactic acid is found in body fluids of patients with or phenylketonuria. D-?(+)?-?Phenyllactic acid is an anti-bacterial agent, excreted by Geotrichum candidum, inhibits a range of Gram-positive from humans and foodstuffs and Gram-negative bacteria found in humans[1]. DL-3-Phenyllactic acid is a broad-spectrum antimicrobial compound. DL-3-Phenyllactic acid is a broad-spectrum antimicrobial compound.

   

3,4-Dihydroxyphenylacetone

1-(3,4-dihydroxyphenyl)propan-2-one

C9H10O3 (166.063)


3,4-Dihydroxyphenylacetone is found in animal foods. 3,4-Dihydroxyphenylacetone is a component of wood smokes, present in smoked meats. Metabolite of 2-Amino-3-(3,4-dihydroxyphenyl)-2-methylpropanoic acid BDS26-B and N,a-Dimethyl-3,4-(methylenedioxy)phenethylamine NCZ31-DBDS26-B and N,a-Dimethyl-3,4-(methylenedioxy)phenethylamine NCZ31-D. 3,4-Dihydroxyphenylacetone is found in animal foods.

   

3-Hydroxy-1-(4-hydroxyphenyl)-1-propanone

3-Hydroxy-1-(4-hydroxyphenyl)-1-propanone

C9H10O3 (166.063)


3-Hydroxy-1-(4-hydroxyphenyl)-1-propanone is found in fruits. 3-Hydroxy-1-(4-hydroxyphenyl)-1-propanone is a constituent of Carissa edulis (agam). Constituent of Carissa edulis (agam). 3-Hydroxy-1-(4-hydroxyphenyl)-1-propanone is found in fruits.

   

Ethyl salicylate

Benzoic acid, 2-hydroxy-, ethyl ester

C9H10O3 (166.063)


Ethyl salicylate, also known as fema 2458 or mesotol, belongs to the class of organic compounds known as o-hydroxybenzoic acid esters. These are benzoic acid esters where the benzene ring is ortho-substituted with a hydroxy group. Ethyl salicylate is a sweet, balsam, and floral tasting compound. Ethyl salicylate has been detected, but not quantified, in several different foods, such as evergreen blackberries, alcoholic beverages, black elderberries, garden tomato, and fruits. Ethyl salicylate is the ester formed by the condensation of salicylic acid and ethanol. It is a clear liquid that is sparingly soluble in water, but soluble in alcohol and ether. It has a pleasant odor resembling wintergreen and is used in perfumery and artificial flavors. Present in feijoa fruit, raspberry, tomato, various spirits, red wine, mountain papaya and cape gooseberry. Flavouring agent. Ethyl salicylate is found in many foods, some of which are black elderberry, garden tomato, fruits, and alcoholic beverages. D000893 - Anti-Inflammatory Agents > D000894 - Anti-Inflammatory Agents, Non-Steroidal > D012459 - Salicylates

   

Guaicyl acetate

Phenol, O-methoxy-, acetate (8ci)

C9H10O3 (166.063)


Guaicyl acetate is a flavouring ingredien Flavouring ingredient

   

Ethyl vanillin

Ethyl proto-catechualdehyde-3-ethyl ether

C9H10O3 (166.063)


Ethyl vanillin is a flavouring agent with flavouring power 2-4 times greater than vanillin. Ethyl vanillin is used especially in cocoa product Flavouring agent with flavouring power 2-4 times greater than vanillin. It is used especies in cocoa products.

   

3-Hydroxy-3-phenylpropanoic acid

(betaR)-beta-Hydroxybenzenepropanoic acid

C9H10O3 (166.063)


3-Hydroxy-3-phenylpropanoic acid (CAS: 3480-87-3) belongs to the class of organic compounds known as phenylpropanoic acids. Phenylpropanoic acids are compounds with a structure containing a benzene ring conjugated to a propanoic acid. 3-Hydroxy-3-phenylpropanoic acid is an extremely weak basic (essentially neutral) compound (based on its pKa). BioTransformer predicts that 3-hydroxy-3-phenylpropanoic acid is a product of 3-hydroxy-3-(4-hydroxyphenyl)propanoic acid metabolism via a -4p-dehydroxylation-of-substituted-benzene reaction occurring in human gut microbiota and catalyzed by a dehydroxylase enzyme (PMID: 30612223).

   

4-[(E)-2-hydroxyethenyl]-2-methoxyphenol

4-[(E)-2-hydroxyethenyl]-2-methoxyphenol

C9H10O3 (166.063)


   

3,5-Dimethoxybenzaldehyde

3,5-dimethoxy-benzaldehyde

C9H10O3 (166.063)


3,5-Dimethoxybenzaldehyde is classified as a member of the dimethoxybenzenes. Dimethoxybenzenes are organic aromatic compounds containing a monocyclic benzene moiety carrying exactly two methoxy groups. 3,5-Dimethoxybenzaldehyde is considered to be slightly soluble (in water) and basic

   

Methyl 4-methoxybenzoate

Benzoic acid, 4-methoxy-, methyl ester

C9H10O3 (166.063)


Methyl 4-methoxybenzoate is found in star anise. Methyl 4-methoxybenzoate is a flavouring ingredien Flavouring ingredient. Methyl 4-methoxybenzoate is found in star anise. Methyl anisate is an endogenous metabolite.

   

Methyl 2-methoxybenzoate

Benzoic acid, 2-methoxy-, methyl ester

C9H10O3 (166.063)


Methyl 2-methoxybenzoate is found in mushrooms. Methyl 2-methoxybenzoate is present in the mushroom Tramates graveolens. Methyl 2-methoxybenzoate is a flavouring ingredien Present in the mushroom Tramates graveolens. Flavouring ingredient. Methyl 2-methoxybenzoate is found in mushrooms.

   

Ipomeanine

1,4-Pentanedione, 1-(3-furanyl)- (9ci)

C9H10O3 (166.063)


Ipomeanine is found in root vegetables. Ipomeanine is produced by Ceratostomella fimbriata; toxic substance in mouldy sweet potatoe Produced by Ceratostomella fimbriata; toxic substance in mouldy sweet potatoes. Ipomeanine is found in root vegetables.

   

2-Hydroxy-2-phenylpropanoic acid

2-Hydroxy-2-phenylpropanoic acid

C9H10O3 (166.063)


   

Phenyllactic acid

3-Phenyllactic acid, monosodium salt

C9H10O3 (166.063)


Phenyllactic acid a product of phenylalanine catabolism, appearing prominently in the urine in individuals with phenylketonuria. Levels of several phenylalanine metabolites, including phenylacetate (PAA), phenyllactate (PLA), and phenylpyruvate (PPA)) are elevated in Phenylketonuria (PKU) (OMIM 261600). Phenyllactic acid is likely produced from phenylpyruvate via the action of lactate dehydrogenase. The D-form of this organic acid is typically derived from bacterial sources while the L-form is almost certainly endogenous. Levels of phenyllactate are normally very low in blood or urine. High levels of PLA in the urine or blood are often indicative of phenylketonuria (PKU) and hyperphenylalaninemia (HPA). PKU is due to lack of the enzyme phenylalanine hydroxylase (PAH), so that phenylalanine is converted not to tyrosine but to phenylpyruvic acid (a precursor of phenylactate). In particular, excessive phenylalanine is typically metabolized into phenylketones through, a transaminase pathway route involving glutamate. Metabolites of this transamination reaction include phenylacetate, phenylpyruvate and phenethylamine. In persons with PKU, dietary phenylalanine either accumulates in the body or some of it is converted to phenylpyruvic acid and then to phenyllactate through the action of lactate dehydrogenase. Individuals with PKU tend to excrete large quantities of phenylpyruvate, phenylacetate and phenyllactate, along with phenylalanine, in their urine. If untreated, mental retardation effects and microcephaly are evident by the first year along with other symptoms which include: unusual irritability, epileptic seizures and skin lesions. Hyperactivity, EEG abnormalities and seizures, and severe learning disabilities are major clinical problems later in life. A "musty or mousy" odor of skin, hair, sweat and urine (due to phenylacetate accumulation); and a tendency to hypopigmentation and eczema are also observed. The neural-development effects of PKU are primarily due to the disruption of neurotransmitter synthesis. In particular, phenylalanine is a large, neutral amino acid which moves across the blood-brain barrier (BBB) via the large neutral amino acid transporter (LNAAT). Excessive phenylalanine in the blood saturates the transporter. Thus, excessive levels of phenylalanine significantly decrease the levels of other LNAAs in the brain. But since these amino acids are required for protein and neurotransmitter synthesis, phenylalanine accumulation disrupts brain development, leading to mental retardation. (PMID: 10790306; OMIM: 261600). Phenyllactic acid can be found in Acinetobacter, Bacteroides, Bifidobacterium, Clostridium, Enterococcus, Escherichia, Eubacterium, Klebsiella, Lactobacillus, Pseudomonas and Staphylococcus (PMID: 19961416). Phenyllactic acid a product of phenylalanine catabolism, appearing prominently in the urine in individuals with phenylketonuria. Levels of several phenylalanine metabolites, including phenylacetate (PAA), phenyllactate (PLA), and phenylpyruvate (PPA)) are elevated in Phenylketonuria (PKU) (OMIM 261600). Phenyllactic acid is likely produced from phenylpyruvate via the action of lactate dehydrogenase. The D-form of this organic acid is typically derived from bacterial sources while the L-form is almost certainly endogenous. Levels of phenyllactate are normally very low in blood or urine. High levels of PLA in the urine or blood are often indicative of phenylketonuria (PKU) and hyperphenylalaninemia (HPA). PKU is due to lack of the enzyme phenylalanine hydroxylase (PAH), so that phenylalanine is converted not to tyrosine but to phenylpyruvic acid (a precursor of phenylactate). In particular, excessive phenylalanine is typically metabolized into phenylketones through, a transaminase pathway route involving glutamate. Metabolites of this transamination reaction include phenylacetate, phenylpyruvate and phenethylamine. In persons with PKU, dietary phenylalanine either accumulates in the body or some of it is converted to phenylpyruvic acid and then to phenyllactate through the action of lactate dehydrogenase. Individuals with PKU tend to excrete large quantities of phenylpyruvate, phenylacetate and phenyllactate, along with phenylalanine, in their urine. If untreated, mental retardation effects and microcephaly are evident by the first year along with other symptoms which include: unusual irritability, epileptic seizures and skin lesions. Hyperactivity, EEG abnormalities and seizures, and severe learning disabilities are major clinical problems later in life. A "musty or mousy" odor of skin, hair, sweat and urine (due to phenylacetate accumulation); and a tendency to hypopigmentation and eczema are also observed. The neural-development effects of PKU are primarily due to the disruption of neurotransmitter synthesis. In particular, phenylalanine is a large, neutral amino acid which moves across the blood-brain barrier (BBB) via the large neutral amino acid transporter (LNAAT). Excessive phenylalanine in the blood saturates the transporter. Thus, excessive levels of phenylalanine significantly decrease the levels of other LNAAs in the brain. But since these amino acids are required for protein and neurotransmitter synthesis, phenylalanine accumulation disrupts brain development, leading to mental retardation. PMID: 10790306; OMIM: 261600 [HMDB] DL-3-Phenyllactic acid is a broad-spectrum antimicrobial compound. DL-3-Phenyllactic acid is a broad-spectrum antimicrobial compound.

   

4-Methoxybenzyl formate

Benzyl alcohol, P-methoxy-, formate (8ci)

C9H10O3 (166.063)


4-Methoxybenzyl formate is used extensively in food flavourin It is used extensively in food flavouring

   

Ethyl 2-furanacrylate

ethyl (2Z)-3-(furan-2-yl)prop-2-enoate

C9H10O3 (166.063)


Ethyl 2-furanacrylate is a flavouring ingredient [CCD]. Flavouring ingredient [CCD]

   

3-Methyltetrahydrophthalic anhydride

4-methyl-1,3,3a,4,5,7a-hexahydro-2-benzofuran-1,3-dione

C9H10O3 (166.063)


   

1,2,3,6-Tetrahydromethylphthalic anhydride

2-Methyl-3-(2,4,5-trihydroxyphenyl)alanine hydrochloride, (DL-tyr)-isomer

C9H10O3 (166.063)


   

3a,4,5,6,7,7a-Hexahydroindene-1,2,3-trione

3a,4,5,6,7,7a-Hexahydroindene-1,2,3-trione

C9H10O3 (166.063)


   

Methoxyphenylacetic acid

alpha-Methoxy-alpha-phenylacetic acid

C9H10O3 (166.063)


Methoxyphenylacetic acid is a member of the class of compounds known as benzylethers. Benzylethers are aromatic ethers with the general formula ROCR (R = alkyl, aryl; R=benzene). Methoxyphenylacetic acid is soluble (in water) and a weakly acidic compound (based on its pKa). Methoxyphenylacetic acid can be found in olive, which makes methoxyphenylacetic acid a potential biomarker for the consumption of this food product. 2-(4-Methoxyphenyl)acetic acid is a plasma metabolite, with high sensitivity and specificity value as a biomarker for discriminating between NSCLC and healthy controls. 2-(4-Methoxyphenyl)acetic acid is a plasma metabolite, with high sensitivity and specificity value as a biomarker for discriminating between NSCLC and healthy controls.

   

D-3-phenyllactic acid

(2R)-2-hydroxy-3-phenylpropanoic acid

C9H10O3 (166.063)


D-?(+)?-?Phenyllactic acid is an anti-bacterial agent, excreted by Geotrichum candidum, inhibits a range of Gram-positive from humans and foodstuffs and Gram-negative bacteria found in humans[1]. DL-3-Phenyllactic acid is a broad-spectrum antimicrobial compound. DL-3-Phenyllactic acid is a broad-spectrum antimicrobial compound.

   

isoacetovanillone

4-Methoxy-3-hydroxyacetophenone;1-(3-hydroxy-4-methoxy-phenyl)ethanone;Acetoisovanillone;3-Hydroxy-4-methoxyacetophenone

C9H10O3 (166.063)


Isoacetovanillone is a member of phenols and a member of methoxybenzenes. It has a role as a metabolite. 1-(3-Hydroxy-4-methoxyphenyl)ethanone is a natural product found in Lamprothamnus zanguebaricus, Saussurea superba, and Rhododendron ferrugineum with data available. A natural product found in Rhododendron ferrugineum. 3-Hydroxy-4-methoxyacetophenone(Acetoisovanillone; Isoacetovanillone) is an active compound isolated from P. spinosa. Isoacetovanillone possesses anti-inflammatory activity and prevented injuries due to administration of acetic acid in the colon[1]. 3-Hydroxy-4-methoxyacetophenone(Acetoisovanillone; Isoacetovanillone) is an active compound isolated from P. spinosa. Isoacetovanillone possesses anti-inflammatory activity and prevented injuries due to administration of acetic acid in the colon[1].

   

2,3-Dimethoxybenzaldehyde

InChI=1/C9H10O3/c1-11-8-5-3-4-7(6-10)9(8)12-2/h3-6H,1-2H

C9H10O3 (166.063)


2,3-Dimethoxybenzaldehyde (o-Veratraldehyde) is a benzaldehyde analog, with high antifungal activity (MIC=2.5 mM) 2,3-Dimethoxybenzaldehyde (o-Veratraldehyde) could be used for the synthesis of berberine[1].

   

2,5-Dihydroxy-4-methylacetophenone

2,5-Dihydroxy-4-methylacetophenone

C9H10O3 (166.063)


   

Methyl 4-hydroxyphenylacetate

p-Hydroxyphenyl acetic acid methyl ester

C9H10O3 (166.063)


Methyl 4-hydroxyphenylacetate, a natural compound, is a methyl ester resulting from the formal condensation of the carboxy group of 4-Hydroxyphenylacetic acid with methanol[1]. Methyl 4-hydroxyphenylacetate, a natural compound, is a methyl ester resulting from the formal condensation of the carboxy group of 4-Hydroxyphenylacetic acid with methanol[1].

   

Phenyllactic acid

L-(-)-3-Phenyllactic acid

C9H10O3 (166.063)


(S)-2-Hydroxy-3-phenylpropanoic acid is a product of phenylalanine catabolism. An elevated level of phenyllactic acid is found in body fluids of patients with or phenylketonuria. DL-3-Phenyllactic acid is a broad-spectrum antimicrobial compound. DL-3-Phenyllactic acid is a broad-spectrum antimicrobial compound.

   

Caffeoyl alcohol

Caffeoyl alcohol

C9H10O3 (166.063)


   

2-Phenoxypropionic acid

2-Phenoxypropionic acid

C9H10O3 (166.063)


   

2-methoxy-2-phenylacetic acid

2-methoxy-2-phenylacetic acid

C9H10O3 (166.063)


   

1-(4-hydroxy-2-methoxyphenyl)ethanone

1-(4-hydroxy-2-methoxyphenyl)ethanone

C9H10O3 (166.063)


   

Methyl mandelate

Benzeneacetic acid, a-hydroxy-, methyl ester

C9H10O3 (166.063)


D000890 - Anti-Infective Agents > D000892 - Anti-Infective Agents, Urinary > D008333 - Mandelic Acids

   

1-hydroxy-1-(4-hydroxyphenyl)propan-2-one

1-hydroxy-1-(4-hydroxyphenyl)propan-2-one

C9H10O3 (166.063)


   

2-Methoxy-6-methylbenzoic acid

2-Methoxy-6-methylbenzoic acid

C9H10O3 (166.063)


   

Methyl 2-hydroxy-6-methylbenzoate

Methyl 2-hydroxy-6-methylbenzoate

C9H10O3 (166.063)


   

1-(4-hydroxyphenyl)-2-methoxyethanone

1-(4-hydroxyphenyl)-2-methoxyethanone

C9H10O3 (166.063)


   

4-[5-(hydroxymethyl)furan-2-yl]but-3-en-2-one

4-[5-(hydroxymethyl)furan-2-yl]but-3-en-2-one

C9H10O3 (166.063)


   

(2S,3S)-non-4t-ene-6,8-diyne-1,2,3-triol|2D,3L-trans-Non-4-en-6,8-diin-1,2,3-triol

(2S,3S)-non-4t-ene-6,8-diyne-1,2,3-triol|2D,3L-trans-Non-4-en-6,8-diin-1,2,3-triol

C9H10O3 (166.063)


   

1-(2-hydroxy-6-methoxyphenyl)ethanone

1-(2-hydroxy-6-methoxyphenyl)ethanone

C9H10O3 (166.063)


   

SCHEMBL11238984

SCHEMBL11238984

C9H10O3 (166.063)


   

CHEBI:67435

CHEBI:67435

C9H10O3 (166.063)


   

1-(2,5-dihydroxy-4-methylphenyl)ethanone

1-(2,5-dihydroxy-4-methylphenyl)ethanone

C9H10O3 (166.063)


   

methyl 4-hydroxy-2-methylbenzoate

methyl 4-hydroxy-2-methylbenzoate

C9H10O3 (166.063)


   

3-hydroxy-4-methoxyacetophenone

1-(3-Hydroxy-4-methoxyphenyl)ethanone

C9H10O3 (166.063)


3-Hydroxy-4-methoxyacetophenone(Acetoisovanillone; Isoacetovanillone) is an active compound isolated from P. spinosa. Isoacetovanillone possesses anti-inflammatory activity and prevented injuries due to administration of acetic acid in the colon[1]. 3-Hydroxy-4-methoxyacetophenone(Acetoisovanillone; Isoacetovanillone) is an active compound isolated from P. spinosa. Isoacetovanillone possesses anti-inflammatory activity and prevented injuries due to administration of acetic acid in the colon[1].

   

2-Hydroxy-5-methoxyacetophenone

1-(2-Hydroxy-5-methoxyphenyl)ethanone

C9H10O3 (166.063)


   

Chromen-2-on; Verbindung mit Hydro-o-cumarsaeure|chromen-2-one; compound with hydro-o-coumaric acid

Chromen-2-on; Verbindung mit Hydro-o-cumarsaeure|chromen-2-one; compound with hydro-o-coumaric acid

C9H10O3 (166.063)


   

2-(1,3-benzodioxol-5-yl)ethanol

2-(1,3-benzodioxol-5-yl)ethanol

C9H10O3 (166.063)


   

1-(2,4-dihydroxy-6-methylphenyl)ethanone

1-(2,4-dihydroxy-6-methylphenyl)ethanone

C9H10O3 (166.063)


   

3-Methoxy-2,5-dimethylcyclohexa-2,5-diene-1,4-dione

3-Methoxy-2,5-dimethylcyclohexa-2,5-diene-1,4-dione

C9H10O3 (166.063)


   

34883-08-4

34883-08-4

C9H10O3 (166.063)


   

(E)-2-Butyliden-3-methylen-bernsteinsaeureanhydrid|waquafranone B

(E)-2-Butyliden-3-methylen-bernsteinsaeureanhydrid|waquafranone B

C9H10O3 (166.063)


   

1-(2,4-dihydroxy-5-methylphenyl)ethanone

1-(2,4-dihydroxy-5-methylphenyl)ethanone

C9H10O3 (166.063)


   

1-Me ether-(E)-2-(3,4-Dihydroxyphenyl)ethenol

1-Me ether-(E)-2-(3,4-Dihydroxyphenyl)ethenol

C9H10O3 (166.063)


   

4-acetonyl-3,5-dimethoxy-p-quinol

4-acetonyl-3,5-dimethoxy-p-quinol

C9H10O3 (166.063)


   

4,6-Dihydroxy-2,3-dimethylbenzaldehyde

4,6-Dihydroxy-2,3-dimethylbenzaldehyde

C9H10O3 (166.063)


   

(1R)-(3-formylphenyl)-1,2-ethanediol

(1R)-(3-formylphenyl)-1,2-ethanediol

C9H10O3 (166.063)


   

3-ethyl-4-hydroxybenzoic acid

3-ethyl-4-hydroxybenzoic acid

C9H10O3 (166.063)


   

4-Hydroxy-3,5-dimethylbenzoic acid

4-Hydroxy-3,5-dimethylbenzoic acid

C9H10O3 (166.063)


   

2-(4-Hydroxy-3-methylphenyl)acetic acid

2-(4-Hydroxy-3-methylphenyl)acetic acid

C9H10O3 (166.063)


   

Ethyl 3-hydroxybenzoate

Ethyl 3-hydroxybenzoate

C9H10O3 (166.063)


   

4-Hydroxy-2-methoxy-6-methylbenzaldehyde

4-Hydroxy-2-methoxy-6-methylbenzaldehyde

C9H10O3 (166.063)


   

2-(Hydroxymethyl)-3-methoxybenzaldehyde

2-(Hydroxymethyl)-3-methoxybenzaldehyde

C9H10O3 (166.063)


   

Methyl (2-hydroxyphenyl)acetate

Methyl 2-(2-hydroxyphenyl)acetate

C9H10O3 (166.063)


   

2,3-Dimethoxybenzaldehyde

2,3-Dimethoxybenzaldehyde

C9H10O3 (166.063)


2,3-Dimethoxybenzaldehyde (o-Veratraldehyde) is a benzaldehyde analog, with high antifungal activity (MIC=2.5 mM) 2,3-Dimethoxybenzaldehyde (o-Veratraldehyde) could be used for the synthesis of berberine[1].

   

4-acetoxy-2-methylphenol

4-acetoxy-2-methylphenol

C9H10O3 (166.063)


   

Orcinol, monoacetate

Orcinol, monoacetate

C9H10O3 (166.063)


   

3,4-Dihydroxypropiophenone

3,4-Dihydroxypropiophenone

C9H10O3 (166.063)


   

2,4-Dimethoxybenzaldehyde

2,4-Dimethoxybenzaldehyde

C9H10O3 (166.063)


   

4-ETHOXYBENZOIC ACID

4-ETHOXYBENZOIC ACID

C9H10O3 (166.063)


   

1-(3,5-Dihydroxyphenyl)propan-2-one

1-(3,5-Dihydroxyphenyl)propan-2-one

C9H10O3 (166.063)


   

2-ethoxy-5-methylcyclohexa-2,5-diene-1,4-dione

2-ethoxy-5-methylcyclohexa-2,5-diene-1,4-dione

C9H10O3 (166.063)


   

2-Hydroxy-1-(4-methoxyphenyl)ethanone

2-Hydroxy-1-(4-methoxyphenyl)ethanone

C9H10O3 (166.063)


   

2,4-Dihydroxy-3,6-dimethylbenzaldehyde

2,4-Dihydroxy-3,6-dimethylbenzaldehyde

C9H10O3 (166.063)


   

(R)-8,9-Dihydroxy-4,6-nonadiyn-3-one|(R)-8,9-dihydroxy-nona-4,6-diyn-3-one|8,9-dihydroxy-nona-4,6-diyn-3-one

(R)-8,9-Dihydroxy-4,6-nonadiyn-3-one|(R)-8,9-dihydroxy-nona-4,6-diyn-3-one|8,9-dihydroxy-nona-4,6-diyn-3-one

C9H10O3 (166.063)


   

AKOS006371996

AKOS006371996

C9H10O3 (166.063)


   

Methyl 3-hydroxy-5-methylbenzoate

Methyl 3-hydroxy-5-methylbenzoate

C9H10O3 (166.063)


   

Methyl 3-methoxybenzoate

Methyl 3-methoxybenzoate

C9H10O3 (166.063)


   

Ethylparaben

Ethylparaben

C9H10O3 (166.063)


CONFIDENCE standard compound; INTERNAL_ID 940; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3941; ORIGINAL_PRECURSOR_SCAN_NO 3940 D010592 - Pharmaceutic Aids > D011310 - Preservatives, Pharmaceutical > D010226 - Parabens CONFIDENCE standard compound; INTERNAL_ID 940; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3955; ORIGINAL_PRECURSOR_SCAN_NO 3954 ORIGINAL_ACQUISITION_NO 3955; ORIGINAL_PRECURSOR_SCAN_NO 3954; CONFIDENCE standard compound; INTERNAL_ID 940; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0 CONFIDENCE standard compound; INTERNAL_ID 940; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3930; ORIGINAL_PRECURSOR_SCAN_NO 3929 CONFIDENCE standard compound; INTERNAL_ID 940; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3940; ORIGINAL_PRECURSOR_SCAN_NO 3939 CONFIDENCE standard compound; INTERNAL_ID 940; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3961; ORIGINAL_PRECURSOR_SCAN_NO 3960 CONFIDENCE standard compound; INTERNAL_ID 940; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3963; ORIGINAL_PRECURSOR_SCAN_NO 3961 CONFIDENCE standard compound; INTERNAL_ID 2367 CONFIDENCE standard compound; INTERNAL_ID 4233 INTERNAL_ID 4233; CONFIDENCE standard compound CONFIDENCE standard compound; INTERNAL_ID 8635 CONFIDENCE standard compound; INTERNAL_ID 4156 Ethylparaben is the ethyl ester of paraben and is used as an antifungal preservative and food additive.

   

Paeonol

Paeonol

C9H10O3 (166.063)


Annotation level-1 Paeonol is an active extraction from the root of Paeonia suffruticosa, Paeonol inhibits MAO-A and MAO-B with IC50 of 54.6 μM and 42.5 μM, respectively. Paeonol is an active extraction from the root of Paeonia suffruticosa, Paeonol inhibits MAO-A and MAO-B with IC50 of 54.6 μM and 42.5 μM, respectively.

   

L-3-Phenyllactic acid

L-(-)-3-Phenyllactic acid

C9H10O3 (166.063)


(S)-2-Hydroxy-3-phenylpropanoic acid is a product of phenylalanine catabolism. An elevated level of phenyllactic acid is found in body fluids of patients with or phenylketonuria.

   

4-Methoxyphenylacetic acid

4-Methoxyphenylacetic acid

C9H10O3 (166.063)


2-(4-Methoxyphenyl)acetic acid is a plasma metabolite, with high sensitivity and specificity value as a biomarker for discriminating between NSCLC and healthy controls. 2-(4-Methoxyphenyl)acetic acid is a plasma metabolite, with high sensitivity and specificity value as a biomarker for discriminating between NSCLC and healthy controls.

   

Desaminotyrosine

3-(4-Hydroxyphenyl)propionic acid

C9H10O3 (166.063)


Desaminotyrosine is a microbially associated metabolite protecting from influenza through augmentation of type I interferon signaling. Desaminotyrosine is a microbially associated metabolite protecting from influenza through augmentation of type I interferon signaling.

   

3-Phenoxypropionic acid

3-Phenoxypropionic acid

C9H10O3 (166.063)


   

3,4-Dimethoxybenzaldehyde

3,4-Dimethoxybenzaldehyde

C9H10O3 (166.063)


   

3-(3-Hydroxyphenyl)propionic acid

3-(3-Hydroxyphenyl)propionic acid

C9H10O3 (166.063)


   

3-phenyllactic acid

DL-3-Phenyllactic acid

C9H10O3 (166.063)


A 2-hydroxy monocarboxylic acid that is lactic acid in which one of the methyl hydrogens is substituted by a phenyl group. DL-3-Phenyllactic acid is a broad-spectrum antimicrobial compound. DL-3-Phenyllactic acid is a broad-spectrum antimicrobial compound.

   

3-(2-hydroxyphenyl)propanoic acid

3-(2-hydroxyphenyl)propanoic acid

C9H10O3 (166.063)


   

Tropic acid

Tropic acid

C9H10O3 (166.063)


   

3-hydroxy-1-(4-hydroxyphenyl)propan-1-one

3-hydroxy-1-(4-hydroxyphenyl)propan-1-one

C9H10O3 (166.063)


   

Isopeonol

Isopeonol

C9H10O3 (166.063)


   

Mandelic Acid, Methyl Ester

Mandelic Acid, Methyl Ester

C9H10O3 (166.063)


   

3-(2-Hydroxyphenyl)propionic acid

3-(2-Hydroxyphenyl)propionic acid

C9H10O3 (166.063)


   

Caffeyl alcohol

Caffeyl alcohol

C9H10O3 (166.063)


A phenylpropanoid that is cinnamyl alcohol in which the hydrogens at positions 3 and 4 on the benzene ring are replaced by hydroxy groups. Annotation level-1

   

ETHYL VANILLIN

3-Ethoxy-4-hydroxybenzaldehyde

C9H10O3 (166.063)


CONFIDENCE standard compound; INTERNAL_ID 874; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3941; ORIGINAL_PRECURSOR_SCAN_NO 3940 CONFIDENCE standard compound; INTERNAL_ID 874; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3955; ORIGINAL_PRECURSOR_SCAN_NO 3954 CONFIDENCE standard compound; INTERNAL_ID 874; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3930; ORIGINAL_PRECURSOR_SCAN_NO 3929 CONFIDENCE standard compound; INTERNAL_ID 874; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3940; ORIGINAL_PRECURSOR_SCAN_NO 3939 CONFIDENCE standard compound; INTERNAL_ID 874; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3961; ORIGINAL_PRECURSOR_SCAN_NO 3960 CONFIDENCE standard compound; INTERNAL_ID 874; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3963; ORIGINAL_PRECURSOR_SCAN_NO 3961

   

Methyl 2-methoxybenzoate

Methyl 2-methoxybenzoate

C9H10O3 (166.063)


CONFIDENCE standard compound; INTERNAL_ID 1133; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3941; ORIGINAL_PRECURSOR_SCAN_NO 3940 CONFIDENCE standard compound; INTERNAL_ID 1133; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3955; ORIGINAL_PRECURSOR_SCAN_NO 3954 CONFIDENCE standard compound; INTERNAL_ID 1133; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3930; ORIGINAL_PRECURSOR_SCAN_NO 3929 CONFIDENCE standard compound; INTERNAL_ID 1133; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3940; ORIGINAL_PRECURSOR_SCAN_NO 3939 CONFIDENCE standard compound; INTERNAL_ID 1133; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3961; ORIGINAL_PRECURSOR_SCAN_NO 3960 CONFIDENCE standard compound; INTERNAL_ID 1133; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3963; ORIGINAL_PRECURSOR_SCAN_NO 3961

   

3-(2-Hydroxyphenyl)propanoate

3-(2-Hydroxyphenyl)propanoate

C9H10O3 (166.063)


   

2-(4-hydroxyphenyl)propionic acid

2-(4-hydroxyphenyl)propionic acid

C9H10O3 (166.063)


   

3-(4-Hydroxyphenyl)propionic acid

3-(4-Hydroxyphenyl)propionic acid

C9H10O3 (166.063)


   

3-hydroxy-1-(4-hydroxyphenyl)propan-1-one_major

3-hydroxy-1-(4-hydroxyphenyl)propan-1-one_major

C9H10O3 (166.063)


   

Isopeonol_major

Isopeonol_major

C9H10O3 (166.063)


   

Paeonol_major

Paeonol_major

C9H10O3 (166.063)


   

3(2-HYDROXYPHENYL)PROPANOATE

3-(2-Hydroxyphenyl)propionate

C9H10O3 (166.063)


Melilotic acid is an endogenous metabolite. Melilotic acid is an endogenous metabolite.

   

3-(2-Hydroxyphenyl)propionate

3-Hydroxy-3-phenylpropanoic acid

C9H10O3 (166.063)


Melilotic acid is an endogenous metabolite. Melilotic acid is an endogenous metabolite.

   

3,4-dihydroxyphenylacetone

1-(3,4-dihydroxyphenyl)propan-2-one

C9H10O3 (166.063)


   

L-Tropic acid

L-Tropic acid

C9H10O3 (166.063)


   

L-Phenyl lactate

Α-hydroxy-β-phenyl-propionic acid

C9H10O3 (166.063)


(S)-2-Hydroxy-3-phenylpropanoic acid is a product of phenylalanine catabolism. An elevated level of phenyllactic acid is found in body fluids of patients with or phenylketonuria.

   

Phenyllactate

DL-2-Hydroxy-3-phenylpropionic acid

C9H10O3 (166.063)


DL-3-Phenyllactic acid is a broad-spectrum antimicrobial compound. DL-3-Phenyllactic acid is a broad-spectrum antimicrobial compound.

   

o-Veratraldehyde

2,3-Dimethoxybenzaldehyde

C9H10O3 (166.063)


2,3-Dimethoxybenzaldehyde (o-Veratraldehyde) is a benzaldehyde analog, with high antifungal activity (MIC=2.5 mM) 2,3-Dimethoxybenzaldehyde (o-Veratraldehyde) could be used for the synthesis of berberine[1].

   

2-Hydroxyphenylacetic acid methyl ester

2-Hydroxyphenylacetic acid methyl ester

C9H10O3 (166.063)


   

Atrolactic acid

2-Hydroxy-2-phenylpropionic acid

C9H10O3 (166.063)


   

D-Phenyllactic acid

D-Phenyllactic acid

C9H10O3 (166.063)


   

Homoanisate

2-(4-methoxyphenyl)acetic acid

C9H10O3 (166.063)


2-(4-Methoxyphenyl)acetic acid is a plasma metabolite, with high sensitivity and specificity value as a biomarker for discriminating between NSCLC and healthy controls. 2-(4-Methoxyphenyl)acetic acid is a plasma metabolite, with high sensitivity and specificity value as a biomarker for discriminating between NSCLC and healthy controls.

   

Ethavan

InChI=1\C9H10O3\c1-2-12-9-5-7(6-10)3-4-8(9)11\h3-6,11H,2H2,1H

C9H10O3 (166.063)


   

Salstan

Benzoic acid, 2-hydroxy-, ethyl ester

C9H10O3 (166.063)


D000893 - Anti-Inflammatory Agents > D000894 - Anti-Inflammatory Agents, Non-Steroidal > D012459 - Salicylates

   

Eucol

Phenol, O-methoxy-, acetate (8ci)

C9H10O3 (166.063)


   

Sobrol A

InChI=1\C9H10O3\c1-2-12-9(11)7-3-5-8(10)6-4-7\h3-6,10H,2H2,1H

C9H10O3 (166.063)


D010592 - Pharmaceutic Aids > D011310 - Preservatives, Pharmaceutical > D010226 - Parabens Ethylparaben is the ethyl ester of paraben and is used as an antifungal preservative and food additive.

   

Dimethyl salicylate

Benzoic acid, 2-methoxy-, methyl ester

C9H10O3 (166.063)


   

Methyl anisate

Benzoic acid, 4-methoxy-, methyl ester

C9H10O3 (166.063)


Methyl anisate is an endogenous metabolite.

   

Ipomeanin

1,4-Pentanedione, 1-(3-furanyl)- (9ci)

C9H10O3 (166.063)


   

Anisyl formate

Benzyl alcohol, P-methoxy-, formate (8ci)

C9H10O3 (166.063)


   

3,4'-Dihydroxypropiophenone

3-Hydroxy-1-(4-hydroxyphenyl)-1-propanone

C9H10O3 (166.063)


   

Ethyl 2-furanacrylate

ethyl (2Z)-3-(furan-2-yl)prop-2-enoate

C9H10O3 (166.063)


   

2,5-Dimethyl-3-hydroxybenzoic acid

2,5-Dimethyl-3-hydroxybenzoic acid

C9H10O3 (166.063)


   

p-Hydroxyphenyl propanoate

p-Hydroxyphenyl propanoate

C9H10O3 (166.063)


   

5,6,7,8-Tetrahydro-1H-2-benzopyran-1,3(4H)-dione

5,6,7,8-Tetrahydro-1H-2-benzopyran-1,3(4H)-dione

C9H10O3 (166.063)


   

2,3-Dihydro-1,4-benzodioxin-6-ylmethanol

2,3-Dihydro-1,4-benzodioxin-6-ylmethanol

C9H10O3 (166.063)


   

(s)-Atrolactic acid

(S)-(+)-2-HYDROXY-2-PHENYLPROPIONIC ACID

C9H10O3 (166.063)


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

   

BENZENEACETALDEHYDE, 4-METHYL-.ALPHA.-OXO-

BENZENEACETALDEHYDE, 4-METHYL-.ALPHA.-OXO-

C9H10O3 (166.063)


   

2-(Methoxymethyl)benzoic acid

2-(Methoxymethyl)benzoic acid

C9H10O3 (166.063)


   

2-(BENZO[D][1,3]DIOXOL-5-YL)ETHANOL

2-(BENZO[D][1,3]DIOXOL-5-YL)ETHANOL

C9H10O3 (166.063)


   

4-Methoxy-3-methylbenzoic acid

4-Methoxy-3-methylbenzoic acid

C9H10O3 (166.063)


   

Methyl 4-hydroxy-3-methylbenzoate

Methyl 4-hydroxy-3-methylbenzoate

C9H10O3 (166.063)


   

2-METHOXY-5-METHYLBENZOIC ACID

2-METHOXY-5-METHYLBENZOIC ACID

C9H10O3 (166.063)


   

Methyl 5-Methylsalicylate

Methyl 5-Methylsalicylate

C9H10O3 (166.063)


   

Methyl 3-hydroxy-4-methylbenzoate

Methyl 3-hydroxy-4-methylbenzoate

C9H10O3 (166.063)


   

2-Methoxyphenylacetic acid

(2-Methoxyphenyl)acetic acid

C9H10O3 (166.063)


   

hexahydro-3,6-methanophthalic anhydride

hexahydro-3,6-methanophthalic anhydride

C9H10O3 (166.063)


   

(R)-(+)-2-DIPHENYLPHOSPHINO-2-HYDROXY-1,1-BINAPHTHYL

(R)-(+)-2-DIPHENYLPHOSPHINO-2-HYDROXY-1,1-BINAPHTHYL

C9H10O3 (166.063)


   

(4-Hydroxy-3-methylphenyl)acetic acid

(4-Hydroxy-3-methylphenyl)acetic acid

C9H10O3 (166.063)


   

Methyl 2-hydroxy-4-methylbenzoate

Methyl 2-hydroxy-4-methylbenzoate

C9H10O3 (166.063)


   

2-Methoxy-4-methylbenzoic acid

2-Methoxy-4-methylbenzoic acid

C9H10O3 (166.063)


   

(3-Methylphenoxy)acetic acid

(3-Methylphenoxy)acetic acid

C9H10O3 (166.063)


   

Benzeneacetic acid, a-hydroxy-4-methyl-

Benzeneacetic acid, a-hydroxy-4-methyl-

C9H10O3 (166.063)


   

Phenol, 3-methoxy-,1-acetate

Phenol, 3-methoxy-,1-acetate

C9H10O3 (166.063)


   

2,5-Dimethoxybenzaldehyde

2,5-Dimethoxybenzaldehyde

C9H10O3 (166.063)


   

3-Methoxy-2-methylbenzoic acid

3-Methoxy-2-methylbenzoic acid

C9H10O3 (166.063)


   

2-(4-methylphenyl)-2-oxo-acetaldehyde

2-(4-methylphenyl)-2-oxo-acetaldehyde

C9H10O3 (166.063)


   

3-Methoxy-5-methylbenzoic acid

3-Methoxy-5-methylbenzoic acid

C9H10O3 (166.063)


   

5-ethoxy-2-hydroxy-benzaldehyde

5-ethoxy-2-hydroxy-benzaldehyde

C9H10O3 (166.063)


   

2-Hydroxy-2-(4-methylphenyl)acetic acid

2-Hydroxy-2-(4-methylphenyl)acetic acid

C9H10O3 (166.063)


   

(S)-3-Hydroxy-3-phenylpropionic acid

(S)-3-CYANO-3-HYDROXY-PROPIONICACIDETHYLESTER

C9H10O3 (166.063)


   

Methyl (3-hydroxymethyl)benzoate

Methyl (3-hydroxymethyl)benzoate

C9H10O3 (166.063)


   

2-Oxo-2-(p-tolyl)acetaldehyde hydrate

2-Oxo-2-(p-tolyl)acetaldehyde hydrate

C9H10O3 (166.063)


   

4-methylphenoxyacetic acid

4-methylphenoxyacetic acid

C9H10O3 (166.063)


   

2,6-Dimetylphenol 1-carbonate

2,6-Dimetylphenol 1-carbonate

C9H10O3 (166.063)


   

Benzyloxyacetic acid

(Benzyloxy)acetic acid

C9H10O3 (166.063)


   

3-(3,4-DIHYDROXY-PHENYL)-PROPIONALDEHYDE

3-(3,4-DIHYDROXY-PHENYL)-PROPIONALDEHYDE

C9H10O3 (166.063)


   

5-HYDROXY-2-METHOXYACETOPHENONE

5-HYDROXY-2-METHOXYACETOPHENONE

C9H10O3 (166.063)


   

2,2-dimethylbenzo[1,3]dioxol-4-ol

2,2-dimethylbenzo[1,3]dioxol-4-ol

C9H10O3 (166.063)


   

3-(METHOXYMETHOXY)BENZALDEHYDE

3-(METHOXYMETHOXY)BENZALDEHYDE

C9H10O3 (166.063)


   

(1S,7S)-(-)-2-Oxotricyclo[2.2.1.03.5]heptan-7-carbonsaeure-methylester

(1S,7S)-(-)-2-Oxotricyclo[2.2.1.03.5]heptan-7-carbonsaeure-methylester

C9H10O3 (166.063)


   

2-Methylmandelic acid

2-Methylmandelic acid

C9H10O3 (166.063)


   

methyl 2-hydroxy-3-methylbenzoate

methyl 2-hydroxy-3-methylbenzoate

C9H10O3 (166.063)


   

3-(4,5-DIMETHYL-2-FURYL)PROPENOIC ACID

3-(4,5-DIMETHYL-2-FURYL)PROPENOIC ACID

C9H10O3 (166.063)


   

3-Ethoxysalicylaldehyde

3-Ethoxysalicylaldehyde

C9H10O3 (166.063)


   

Methyl (2S)-hydroxy(phenyl)acetate

Methyl (2S)-hydroxy(phenyl)acetate

C9H10O3 (166.063)


   

(3aR,4S,7R,7aS)-hexahydro-4,7-methanoisobenzofuran-1,3-dione

(3aR,4S,7R,7aS)-hexahydro-4,7-methanoisobenzofuran-1,3-dione

C9H10O3 (166.063)


   

2-Hydroxy-3-methoxy-5-methylbenzaldehyde

2-Hydroxy-3-methoxy-5-methylbenzaldehyde

C9H10O3 (166.063)


   

4-hydroxy-2,3-dimethyl-Benzoic acid

4-hydroxy-2,3-dimethyl-Benzoic acid

C9H10O3 (166.063)


   

anisyl acetate

anisyl acetate

C9H10O3 (166.063)


   

2,5-dihydroxypropiophenone

2,5-dihydroxypropiophenone

C9H10O3 (166.063)


   

4-hydroxy-5-methoxy-2-methylbenzaldehyde

4-hydroxy-5-methoxy-2-methylbenzaldehyde

C9H10O3 (166.063)


   

4-(2-Hydroxyethoxy)benzaldehyde

4-(2-Hydroxyethoxy)benzaldehyde

C9H10O3 (166.063)


   

(2-Methylphenoxy)acetic acid

(2-Methylphenoxy)acetic acid

C9H10O3 (166.063)


   

2-HYDROXY-2-METHOXYACETOPHENONE

2-HYDROXY-2-METHOXYACETOPHENONE

C9H10O3 (166.063)


   

Ethanone,2-hydroxy-1-(4-methoxyphenyl)-

Ethanone,2-hydroxy-1-(4-methoxyphenyl)-

C9H10O3 (166.063)


   

CHROMAN-3,8-DIOL

CHROMAN-3,8-DIOL

C9H10O3 (166.063)


   

3-Ethoxy-5-hydroxybenzaldehyde

3-Ethoxy-5-hydroxybenzaldehyde

C9H10O3 (166.063)


   

methyl 6-methylsalicylate

methyl 6-methylsalicylate

C9H10O3 (166.063)


   

4-(1-Hydroxyethyl)benzoic acid

4-(1-Hydroxyethyl)benzoic acid

C9H10O3 (166.063)


   

2-ethyl-5-hydroxybenzoic acid

2-ethyl-5-hydroxybenzoic acid

C9H10O3 (166.063)


   

Methyl 2-phenoxyacetate

Methyl 2-phenoxyacetate

C9H10O3 (166.063)


   

3-(2-Hydroxyethoxy)benzaldehyde

3-(2-Hydroxyethoxy)benzaldehyde

C9H10O3 (166.063)


   

4-ETHYL-3-HYDROXYBENZOIC ACID

4-ETHYL-3-HYDROXYBENZOIC ACID

C9H10O3 (166.063)


   

2-propenoic acid, 3-(3-furanyl)-, ethyl ester

2-propenoic acid, 3-(3-furanyl)-, ethyl ester

C9H10O3 (166.063)


   

Guaiacol acetate

2-Methoxyphenyl acetate

C9H10O3 (166.063)


   

2,3-Dihydro-1,4-benzodioxin-2-ylmethanol

2,3-Dihydro-1,4-benzodioxin-2-ylmethanol

C9H10O3 (166.063)


   

2,6-DIMETHOXYBENZALDEHYDE

2,6-DIMETHOXYBENZALDEHYDE

C9H10O3 (166.063)


   

3-(Methoxymethyl)benzoic acid

3-(Methoxymethyl)benzoic acid

C9H10O3 (166.063)


   

2-Ethyl-6-hydroxybenzoic acid

2-Ethyl-6-hydroxybenzoic acid

C9H10O3 (166.063)


   

4-Ethoxy-2-hydroxybenzaldehyde

4-Ethoxy-2-hydroxybenzaldehyde

C9H10O3 (166.063)


   

methyl 3-hydroxy-2-methylbenzoate

methyl 3-hydroxy-2-methylbenzoate

C9H10O3 (166.063)


   

4-ethoxy-3-hydroxybenzaldehyde

4-ethoxy-3-hydroxybenzaldehyde

C9H10O3 (166.063)


   

(2,3-Dihydrobenzo[b][1,4]dioxin-5-yl)methanol

(2,3-Dihydrobenzo[b][1,4]dioxin-5-yl)methanol

C9H10O3 (166.063)


   

3-Methoxy-4-methylbenzoic acid

3-Methoxy-4-methylbenzoic acid

C9H10O3 (166.063)


   

1-hydroxy-1-(3-hydroxyphenyl)-2-propanone

1-hydroxy-1-(3-hydroxyphenyl)-2-propanone

C9H10O3 (166.063)


   

3-(hydroxymethyl)-4-methoxybenzaldehyde

3-(hydroxymethyl)-4-methoxybenzaldehyde

C9H10O3 (166.063)


   

1-(2-Hydroxy-3-methoxyphenyl)ethanone

Ethanone,1-(2-hydroxy-3-methoxyphenyl)-

C9H10O3 (166.063)


   

Methyl 5-hydroxy-2-methylbenzoate

Methyl 5-hydroxy-2-methylbenzoate

C9H10O3 (166.063)


   

BENZYL GLYCOLATE

BENZYL GLYCOLATE

C9H10O3 (166.063)


   

5-methyl-4,5,6,7-tetrahydro-2-benzofuran-1,3-dione

5-methyl-4,5,6,7-tetrahydro-2-benzofuran-1,3-dione

C9H10O3 (166.063)


   

1-(2,6-Dihydroxy-4-methylphenyl)ethanone

1-(2,6-Dihydroxy-4-methylphenyl)ethanone

C9H10O3 (166.063)


   

1-(2,4-dihydroxy-3-methylphenyl)ethanone

1-(2,4-dihydroxy-3-methylphenyl)ethanone

C9H10O3 (166.063)


   

Methyl tetrahydrophthalic anhydride

Methyl tetrahydrophthalic anhydride

C9H10O3 (166.063)


   

2,4-Dihydroxypropiophenone

2,4-Dihydroxypropiophenone

C9H10O3 (166.063)


   

formaldehyde,phenyl acetate

formaldehyde,phenyl acetate

C9H10O3 (166.063)


   

p-Acetoxyanisole

p-Acetoxyanisole

C9H10O3 (166.063)


   

2-(2-hydroxyethyl)benzoic acid

2-(2-hydroxyethyl)benzoic acid

C9H10O3 (166.063)


   

2-Ethoxybenzoic acid

2-Ethoxybenzoic acid

C9H10O3 (166.063)


   

3-(2-Hydroxyphenyl)oxetan-3-ol

3-(2-Hydroxyphenyl)oxetan-3-ol

C9H10O3 (166.063)


   

Methyltetrahydrophthalic anhydride

Methyltetrahydrophthalic anhydride

C9H10O3 (166.063)


   

4-Methyltetrahydrophthalic anhydride

4-Methyltetrahydrophthalic anhydride

C9H10O3 (166.063)


   

4-Methyl-1,2,3,6-tetrahydrophthalic Anhydride

4-Methyl-1,2,3,6-tetrahydrophthalic Anhydride

C9H10O3 (166.063)


   

2-Methoxy-3-methyl-benzoic acid

2-Methoxy-3-methyl-benzoic acid

C9H10O3 (166.063)


   

4-Methoxy-2-methylbenzoic acid

4-Methoxy-2-methylbenzoic acid

C9H10O3 (166.063)


   

2-(2-hydroxyethoxy)benzaldehyde

2-(2-hydroxyethoxy)benzaldehyde

C9H10O3 (166.063)


   

METHYL 2-(HYDROXYMETHYL)BENZOATE

METHYL 2-(HYDROXYMETHYL)BENZOATE

C9H10O3 (166.063)


   

(r)-(-)-2-hydroxy-2-phenylpropionic acid

(r)-(-)-2-hydroxy-2-phenylpropionic acid

C9H10O3 (166.063)


   

(2S)-Methoxy(phenyl)acetic acid

(2S)-Methoxy(phenyl)acetic acid

C9H10O3 (166.063)


   

2-hydroxy-2-(3-methylphenyl)acetic acid

2-hydroxy-2-(3-methylphenyl)acetic acid

C9H10O3 (166.063)


   

METHYL 3-HYDROXYPHENYLACETATE

METHYL 3-HYDROXYPHENYLACETATE

C9H10O3 (166.063)


   

Benzoic acid, 4-(2-hydroxyethyl)-

Benzoic acid, 4-(2-hydroxyethyl)-

C9H10O3 (166.063)


   

ethylfurylacrylate

ethylfurylacrylate

C9H10O3 (166.063)


   

(R)-2-(3-CHLORO-4-METHANESULFONYLPHENYL)-3-(2-OXOCYCLOPENTYL)PROPIONICACID

(R)-2-(3-CHLORO-4-METHANESULFONYLPHENYL)-3-(2-OXOCYCLOPENTYL)PROPIONICACID

C9H10O3 (166.063)


   

4-Methoxy-6-methylsalicylaldehyde

4-Methoxy-6-methylsalicylaldehyde

C9H10O3 (166.063)


   

[4-(Hydroxymethyl)phenyl]acetic acid

[4-(Hydroxymethyl)phenyl]acetic acid

C9H10O3 (166.063)


   

1,3-Isobenzofurandione, tetrahydromethyl-

1,3-Isobenzofurandione, tetrahydromethyl-

C9H10O3 (166.063)


   

4-hydroxy-2,5-dimethylbenzoic acid

4-hydroxy-2,5-dimethylbenzoic acid

C9H10O3 (166.063)


   

4-Hydroxy-2,6-dimethylbenzoic acid

4-Hydroxy-2,6-dimethylbenzoic acid

C9H10O3 (166.063)


   

Methyl (4-hydroxymethyl)benzoate

Methyl (4-hydroxymethyl)benzoate

C9H10O3 (166.063)


   

Ethyl 3-(2-furyl)acrylate

2-Propenoic acid,3-(2-furanyl)-, ethyl ester

C9H10O3 (166.063)


   

2-Furylmethyl methacrylate

2-Furylmethyl methacrylate

C9H10O3 (166.063)


   

5-Methoxy-2-methylbenzoic acid

5-Methoxy-2-methylbenzoic acid

C9H10O3 (166.063)


   

4-(Methoxymethyl)benzoic acid

4-(Methoxymethyl)benzoic acid

C9H10O3 (166.063)


   

(R)-methyl mandelate

(R)-methyl mandelate

C9H10O3 (166.063)


   

2-hydroxy-3,4-dimethylbenzoic acid

2-hydroxy-3,4-dimethylbenzoic acid

C9H10O3 (166.063)


   

5-Ethyl-2-hydroxybenzoic acid

5-Ethyl-2-hydroxybenzoic acid

C9H10O3 (166.063)


   

4-(hydroxymethyl)phenylacetic acid

4-(hydroxymethyl)phenylacetic acid

C9H10O3 (166.063)


   

2-Hydroxy-2-methoxy-1-phenylethanone

2-Hydroxy-2-methoxy-1-phenylethanone

C9H10O3 (166.063)


   

2-Propenoic acid, 3-(2-furanyl)-, ethyl ester, (Z)-

2-Propenoic acid, 3-(2-furanyl)-, ethyl ester, (Z)-

C9H10O3 (166.063)


   

p-Acetoxybenzyl alcohol

p-Acetoxybenzyl alcohol

C9H10O3 (166.063)


   

Benzaldehyde, 4,6-dihydroxy-2,3-dimethyl-

Benzaldehyde, 4,6-dihydroxy-2,3-dimethyl-

C9H10O3 (166.063)


   

2-Hydroxy-3,6-dimethylbenzoic acid

2-Hydroxy-3,6-dimethylbenzoic acid

C9H10O3 (166.063)


   

1-[2-Hydroxy-4-(hydroxymethyl)phenyl]ethanone

1-[2-Hydroxy-4-(hydroxymethyl)phenyl]ethanone

C9H10O3 (166.063)


   

1-(Furan-2-yl)pentane-1,4-dione

1-(Furan-2-yl)pentane-1,4-dione

C9H10O3 (166.063)


   

3-Hydroxybenzyl acetate

3-Hydroxybenzyl acetate

C9H10O3 (166.063)


   

2-(3-Hydroxyphenyl)propanoic acid

2-(3-Hydroxyphenyl)propanoic acid

C9H10O3 (166.063)


   

3-Hydroxyphenyl propanoate

3-Hydroxyphenyl propanoate

C9H10O3 (166.063)


   

5-Ethenyl-3-methoxybenzene-1,2-diol

5-Ethenyl-3-methoxybenzene-1,2-diol

C9H10O3 (166.063)


   

2-Methoxy-4-(2-hydroxyethenyl)phenol

2-Methoxy-4-(2-hydroxyethenyl)phenol

C9H10O3 (166.063)


   

Paeonol-d3

Paeonol-d3

C9H10O3 (166.063)


   

apocynin

InChI=1\C9H10O3\c1-6(10)7-3-4-8(11)9(5-7)12-2\h3-5,11H,1-2H

C9H10O3 (166.063)


D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents D002491 - Central Nervous System Agents > D000700 - Analgesics D020011 - Protective Agents > D000975 - Antioxidants D000893 - Anti-Inflammatory Agents D018501 - Antirheumatic Agents D004791 - Enzyme Inhibitors Apocynin is a selective NADPH-oxidase inhibitor with an IC50 of 10 μM[1][2]. Apocynin improves acute lung inflammation in Carrageenan (HY-125474)-induced pleurisy mice model[3]. Apocynin can also be used for cancer research[4]. Apocynin reverses the aging process in mesenchymal stem cells to promote osteogenesis and increases bone mass[5]. Apocynin is a selective NADPH-oxidase inhibitor with an IC50 of 10 μM[1][2]. Apocynin improves acute lung inflammation in Carrageenan (HY-125474)-induced pleurisy mice model[3]. Apocynin can also be used for cancer research[4]. Apocynin reverses the aging process in mesenchymal stem cells to promote osteogenesis and increases bone mass[5]. Apocynin is a selective NADPH-oxidase inhibitor with an IC50 of 10 μM[1][2]. Apocynin improves acute lung inflammation in Carrageenan (HY-125474)-induced pleurisy mice model[3]. Apocynin can also be used for cancer research[4]. Apocynin reverses the aging process in mesenchymal stem cells to promote osteogenesis and increases bone mass[5].

   

peonol

InChI=1\C9H10O3\c1-6(10)8-4-3-7(12-2)5-9(8)11\h3-5,11H,1-2H

C9H10O3 (166.063)


Paeonol is an active extraction from the root of Paeonia suffruticosa, Paeonol inhibits MAO-A and MAO-B with IC50 of 54.6 μM and 42.5 μM, respectively. Paeonol is an active extraction from the root of Paeonia suffruticosa, Paeonol inhibits MAO-A and MAO-B with IC50 of 54.6 μM and 42.5 μM, respectively.

   

Veratral

InChI=1\C9H10O3\c1-11-8-4-3-7(6-10)5-9(8)12-2\h3-6H,1-2H

C9H10O3 (166.063)


Veratraldehyde is an important chemical used in perfumery, agrochemical, and pharmaceutical industries. Veratraldehyde is an important chemical used in perfumery, agrochemical, and pharmaceutical industries.

   

296244_SIAL

InChI=1\C9H10O3\c1-5-8(11)4-3-7(6(2)10)9(5)12\h3-4,11-12H,1-2H

C9H10O3 (166.063)


   

6100-74-9

Ethanone, 1-(3-hydroxy-4-methoxyphenyl)-

C9H10O3 (166.063)


3-Hydroxy-4-methoxyacetophenone(Acetoisovanillone; Isoacetovanillone) is an active compound isolated from P. spinosa. Isoacetovanillone possesses anti-inflammatory activity and prevented injuries due to administration of acetic acid in the colon[1]. 3-Hydroxy-4-methoxyacetophenone(Acetoisovanillone; Isoacetovanillone) is an active compound isolated from P. spinosa. Isoacetovanillone possesses anti-inflammatory activity and prevented injuries due to administration of acetic acid in the colon[1].

   

AI3-36062

Acetic acid, (p-hydroxyphenyl)-, methyl ester

C9H10O3 (166.063)


Methyl 4-hydroxyphenylacetate, a natural compound, is a methyl ester resulting from the formal condensation of the carboxy group of 4-Hydroxyphenylacetic acid with methanol[1]. Methyl 4-hydroxyphenylacetate, a natural compound, is a methyl ester resulting from the formal condensation of the carboxy group of 4-Hydroxyphenylacetic acid with methanol[1].

   

AI3-32395

InChI=1\C9H10O3\c10-8-3-1-2-7(6-8)4-5-9(11)12\h1-3,6,10H,4-5H2,(H,11,12

C9H10O3 (166.063)


3-(3-Hydroxyphenyl)propionic acid is a flavonoid metabolite formed by human microflora. 3-(3-Hydroxyphenyl)propionic acid shows vasodilatory activity[1]. 3-(3-Hydroxyphenyl)propionic acid is a flavonoid metabolite formed by human microflora. 3-(3-Hydroxyphenyl)propionic acid shows vasodilatory activity[1].

   

(2S)-3-hydroxy-2-phenyl-propanoic acid

(2S)-3-hydroxy-2-phenyl-propanoic acid

C9H10O3 (166.063)


   

Melilotate

InChI=1\C9H10O3\c10-8-4-2-1-3-7(8)5-6-9(11)12\h1-4,10H,5-6H2,(H,11,12

C9H10O3 (166.063)


Melilotic acid is an endogenous metabolite. Melilotic acid is an endogenous metabolite.

   

3-Cyclohexa-1,3-dien-1-yl-2-oxopropanoic acid

3-Cyclohexa-1,3-dien-1-yl-2-oxopropanoic acid

C9H10O3 (166.063)


   

2-Hydroxy-3-(2-hydroxyphenyl)propanal

2-Hydroxy-3-(2-hydroxyphenyl)propanal

C9H10O3 (166.063)


   

3-(2,5-Dihydroxyphenyl)propanal

3-(2,5-Dihydroxyphenyl)propanal

C9H10O3 (166.063)


   

3-(2,3-Dihydroxyphenyl)propanal

3-(2,3-Dihydroxyphenyl)propanal

C9H10O3 (166.063)


   

4-Ethenyl-6-methoxybenzene-1,3-diol

4-Ethenyl-6-methoxybenzene-1,3-diol

C9H10O3 (166.063)


   

4-Ethenyl-2-methoxybenzene-1,3-diol

4-Ethenyl-2-methoxybenzene-1,3-diol

C9H10O3 (166.063)


   

3-Hydroxy-3-(2-hydroxyphenyl)propanal

3-Hydroxy-3-(2-hydroxyphenyl)propanal

C9H10O3 (166.063)


   

2-[3-(Hydroxymethyl)oxiran-2-yl]phenol

2-[3-(Hydroxymethyl)oxiran-2-yl]phenol

C9H10O3 (166.063)


   

4-[3-(Hydroxymethyl)oxiran-2-yl]phenol

4-[3-(Hydroxymethyl)oxiran-2-yl]phenol

C9H10O3 (166.063)


   

Furfuryl crotonate

Furfuryl crotonate

C9H10O3 (166.063)


   

Phenoxy methyl acetate

Phenoxy methyl acetate

C9H10O3 (166.063)


   

2-Hydroxy-6-methoxyacetophenone (6,6,6-D3)

2-Hydroxy-6-methoxyacetophenone (6,6,6-D3)

C9H10O3 (166.063)


   

2-Hydroxy-5-methoxyacetophenone (5,5,5-D3)

2-Hydroxy-5-methoxyacetophenone (5,5,5-D3)

C9H10O3 (166.063)


   

2-Hydroxybenzenepropanoic acid

3-(2-hydroxyphenyl)propanoic acid

C9H10O3 (166.063)


A monocarboxylic acid that is propionic acid in which one of the hydrogens at position 3 is substituted by a 2-hydroxyphenyl group. Melilotic acid is an endogenous metabolite. Melilotic acid is an endogenous metabolite.

   

2-(4-hydroxyphenyl)propanoic acid

2-(4-hydroxyphenyl)propanoic acid

C9H10O3 (166.063)


   

3-ETHOXYBENZOIC ACID

3-ETHOXYBENZOIC ACID

C9H10O3 (166.063)


   

D-3-phenyllactic acid

(2R)-2-hydroxy-3-phenylpropanoic acid

C9H10O3 (166.063)


D-?(+)?-?Phenyllactic acid is an anti-bacterial agent, excreted by Geotrichum candidum, inhibits a range of Gram-positive from humans and foodstuffs and Gram-negative bacteria found in humans[1].

   

Homovanillin

2-(4-HYDROXY-3-METHOXYPHENYL)ACETALDEHYDE

C9H10O3 (166.063)


COVID info from COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS

   

Ethyl salicylate

Ethyl salicylate

C9H10O3 (166.063)


D000893 - Anti-Inflammatory Agents > D000894 - Anti-Inflammatory Agents, Non-Steroidal > D012459 - Salicylates

   

L-(-)-3-Phenyllactic acid

L-(-)-3-Phenyllactic acid

C9H10O3 (166.063)


(S)-2-Hydroxy-3-phenylpropanoic acid is a product of phenylalanine catabolism. An elevated level of phenyllactic acid is found in body fluids of patients with or phenylketonuria.

   

3-Hydroxyphenylpropanoate

3-(3-hydroxyphenyl)propanoic acid

C9H10O3 (166.063)


A monocarboxylic acid that is propionic acid carrying a 3-hydroxyphenyl substituent at C-3. 3-(3-Hydroxyphenyl)propionic acid is a flavonoid metabolite formed by human microflora. 3-(3-Hydroxyphenyl)propionic acid shows vasodilatory activity[1]. 3-(3-Hydroxyphenyl)propionic acid is a flavonoid metabolite formed by human microflora. 3-(3-Hydroxyphenyl)propionic acid shows vasodilatory activity[1].

   

3-methoxyphenylacetic acid

3-methoxyphenylacetic acid

C9H10O3 (166.063)


3-Methoxyphenylacetic acid (m-Methoxyphenylacetic acid), a m-hydroxyphenylacetic acid (m-OHPAA) derivative, is a phytotoxin in Rhizoctonia solani. 3-Methoxyphenylacetic acid is used to develop a toxin-mediated bioassay for resistance to rhizoctonia root rot[1].

   

4-Methoxybenzyl formate

Benzenemethanol,4-methoxy-, 1-formate

C9H10O3 (166.063)


   

3,5-Dimethoxybenzaldehyde

3,5-Dimethoxybenzaldehyde

C9H10O3 (166.063)


   

Methoxyphenylacetic acid

Methoxy(phenyl)acetic acid

C9H10O3 (166.063)


   

1,4-Pentanedione,1-(3-furanyl)-

1,4-Pentanedione,1-(3-furanyl)-

C9H10O3 (166.063)


   

(3R)-3-Hydroxy-3-phenylpropanoic acid

(R)-(+)-3-HYDROXY-3-PHENYLPROPIONIC ACID

C9H10O3 (166.063)


   

1,2,3,6-Tetrahydromethylphthalic anhydride

3A-METHYL-3A,4,7,7A-TETRAHYDROISOBENZOFURAN-1,3-DIONE

C9H10O3 (166.063)


   

methyl 2-(4-hydroxyphenyl)acetate

methyl 2-(4-hydroxyphenyl)acetate

C9H10O3 (166.063)


A methyl ester resulting from the formal condensation of the carboxy group of 4-hydroxyphenylacetic acid with methanol. It has been isolated from Penicillium chrysogenum.

   

(E)-caffeyl alcohol

(E)-caffeyl alcohol

C9H10O3 (166.063)


A caffeyl alcohol in which the double bond has E geochemistry.

   

1-[2-hydroxy-4-(hydroxymethyl)phenyl]ethan-1-one

1-[2-hydroxy-4-(hydroxymethyl)phenyl]ethan-1-one

C9H10O3 (166.063)


A natural product found in Eupatorium cannabinum subspecies asiaticum.

   

Phloretic acid

Phloretic acid

C9H10O3 (166.063)


A hydroxy monocarboxylic acid consisting of propionic acid having a 4-hydroxyphenyl group at the 3-position.

   

(4-Hydroxy-3-methoxyphenyl)acetaldehyde

(4-Hydroxy-3-methoxyphenyl)acetaldehyde

C9H10O3 (166.063)


   

(S)-3-Phenyllactic acid

(S)-3-Phenyllactic acid

C9H10O3 (166.063)


The (S)-enantiomer of 3-phenyllactic acid.

   

2,4-dihydroxy-5,6-dimethylbenzaldehyde

2,4-dihydroxy-5,6-dimethylbenzaldehyde

C9H10O3 (166.063)


A dihydroxybenzaldehyde that is 2,4-dihydroxybenzaldehyde in which the hydrogens at positions 5 and 6 have been replaced by methyl groups.

   

(R)-3-Phenyllactic acid

(R)-3-Phenyllactic acid

C9H10O3 (166.063)


A 3-phenyllactic acid that has (R)-configuration at the 2 position.

   

Hydroxyphenyl-propanoic acid

Hydroxyphenyl-propanoic acid

C9H10O3 (166.063)


   

Hydroxyphenylpropionic acid

Hydroxyphenylpropionic acid

C9H10O3 (166.063)


   

furan-2-ylmethyl (2e)-but-2-enoate

furan-2-ylmethyl (2e)-but-2-enoate

C9H10O3 (166.063)


   

(-)-tropic acid

(-)-tropic acid

C9H10O3 (166.063)


   

3-[(1r)-1,2-dihydroxyethyl]benzaldehyde

3-[(1r)-1,2-dihydroxyethyl]benzaldehyde

C9H10O3 (166.063)


   

2,4-dimethoxybenzyldehyde

NA

C9H10O3 (166.063)


{"Ingredient_id": "HBIN004340","Ingredient_name": "2,4-dimethoxybenzyldehyde","Alias": "NA","Ingredient_formula": "C9H10O3","Ingredient_Smile": "COC1=CC(=CC(=C1)C=O)OC","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "6208","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}

   

6-deoxyaucubigenin; 1-ketone (lactone)

NA

C9H10O3 (166.063)


{"Ingredient_id": "HBIN012315","Ingredient_name": "6-deoxyaucubigenin; 1-ketone (lactone)","Alias": "NA","Ingredient_formula": "C9H10O3","Ingredient_Smile": "NA","Ingredient_weight": "0","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "NA","TCMSP_id": "NA","TCM_ID_id": "7576","PubChem_id": "NA","DrugBank_id": "NA"}

   

2-ethyl-6-methoxycyclohexa-2,5-diene-1,4-dione

2-ethyl-6-methoxycyclohexa-2,5-diene-1,4-dione

C9H10O3 (166.063)


   

3-(1,2-dihydroxyethyl)benzaldehyde

3-(1,2-dihydroxyethyl)benzaldehyde

C9H10O3 (166.063)


   

4-hydroxy-4-(2-oxopropyl)cyclohexa-2,5-dien-1-one

4-hydroxy-4-(2-oxopropyl)cyclohexa-2,5-dien-1-one

C9H10O3 (166.063)


   

(1s)-2,3-dimethyl-5-methylidene-4-oxocyclopent-2-ene-1-carboxylic acid

(1s)-2,3-dimethyl-5-methylidene-4-oxocyclopent-2-ene-1-carboxylic acid

C9H10O3 (166.063)


   

6-acetyl-3-ethylpyran-2-one

6-acetyl-3-ethylpyran-2-one

C9H10O3 (166.063)


   

(3e)-4-[5-(hydroxymethyl)furan-2-yl]but-3-en-2-one

(3e)-4-[5-(hydroxymethyl)furan-2-yl]but-3-en-2-one

C9H10O3 (166.063)


   

methyl 2-hydroxy-2-phenylacetate

methyl 2-hydroxy-2-phenylacetate

C9H10O3 (166.063)


   

3-ethenyl-6-methoxybenzene-1,2-diol

3-ethenyl-6-methoxybenzene-1,2-diol

C9H10O3 (166.063)


   

(+)-tropic acid

(+)-tropic acid

C9H10O3 (166.063)


   

(2e)-3-(4-hydroxycyclohexa-2,4-dien-1-yl)prop-2-enoic acid

(2e)-3-(4-hydroxycyclohexa-2,4-dien-1-yl)prop-2-enoic acid

C9H10O3 (166.063)