Exact Mass: 224.0507122
Exact Mass Matches: 224.0507122
Found 500 metabolites which its exact mass value is equals to given mass value 224.0507122,
within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error
0.01 dalton.
Sinapic acid
Sinapic acid, also known as sinapinate, belongs to the class of organic compounds known as hydroxycinnamic acids. Hydroxycinnamic acids are compounds containing an cinnamic acid where the benzene ring is hydroxylated. Sinapic acid has been detected, but not quantified, in several different foods, such as strawberry guava, purple lavers, common verbena, ryes, and lupines. This could make sinapic acid a potential biomarker for the consumption of these foods. A sinapic acid in which the double bond has trans-configuration. Trans-sinapic acid is a sinapic acid in which the double bond has trans-configuration. It has a role as a MALDI matrix material and a plant metabolite. It is a conjugate acid of a trans-sinapate. Sinapic acid is a matrix for matrix-assisted laser desorption technique for protein MW determination. It is also a constituent of propolis. Sinapic acid is a natural product found in Sida acuta, Limoniastrum guyonianum, and other organisms with data available. A common constituent of plants and fruits. trans-Sinapic acid is found in many foods, some of which are small-leaf linden, redcurrant, malabar spinach, and blackcurrant. D019995 - Laboratory Chemicals > D007202 - Indicators and Reagents A sinapic acid in which the double bond has trans-configuration. Acquisition and generation of the data is financially supported in part by CREST/JST. Profile spectrum of this record is given as a JPEG file.; [Profile] MCH00014.jpg Profile spectrum of this record is given as a JPEG file.; [Profile] MCH00015.jpg CONFIDENCE standard compound; INTERNAL_ID 174 Annotation level-1 Annotation level-2 KEIO_ID S028 Sinapinic acid (Sinapic acid) is a phenolic compound isolated from Hydnophytum formicarum Jack. Rhizome, acts as an inhibitor of HDAC, with an IC50 of 2.27 mM[1], and also inhibits ACE-I activity[2]. Sinapinic acid posssess potent anti-tumor activity, induces apoptosis of tumor cells[1]. Sinapinic acid shows antioxidant and antidiabetic activities[2]. Sinapinic acid reduces total cholesterol, triglyceride, and HOMA-IR index, and also normalizes some serum parameters of antioxidative abilities and oxidative damage in ovariectomized rats[3]. Sinapinic acid (Sinapic acid) is a phenolic compound isolated from Hydnophytum formicarum Jack. Rhizome, acts as an inhibitor of HDAC, with an IC50 of 2.27 mM[1], and also inhibits ACE-I activity[2]. Sinapinic acid posssess potent anti-tumor activity, induces apoptosis of tumor cells[1]. Sinapinic acid shows antioxidant and antidiabetic activities[2]. Sinapinic acid reduces total cholesterol, triglyceride, and HOMA-IR index, and also normalizes some serum parameters of antioxidative abilities and oxidative damage in ovariectomized rats[3].
1-Hydroxyanthraquinone
CONFIDENCE standard compound; INTERNAL_ID 8284 CONFIDENCE standard compound; INTERNAL_ID 25 D009676 - Noxae > D002273 - Carcinogens 1-Hydroxyanthraquinone, a naturally occurring compound with oral activity from some plants like Tabebuia avellanedae, exhibits carcinogenic effect[1]. 1-Hydroxyanthraquinone, a naturally occurring compound with oral activity from some plants like Tabebuia avellanedae, exhibits carcinogenic effect[1].
Gesfid
D018377 - Neurotransmitter Agents > D018678 - Cholinergic Agents > D002800 - Cholinesterase Inhibitors C471 - Enzyme Inhibitor > C47792 - Acetylcholinesterase Inhibitor D010575 - Pesticides > D007306 - Insecticides D004791 - Enzyme Inhibitors D016573 - Agrochemicals
Stavudine
C10H12N2O4 (224.07970319999998)
Stavudine is only found in individuals that have used or taken this drug. It is a dideoxynucleoside analog that inhibits reverse transcriptase and has in vitro activity against HIV. [PubChem]Stavudine inhibits the activity of HIV-1 reverse transcriptase (RT) both by competing with the natural substrate dGTP and by its incorporation into viral DNA. J - Antiinfectives for systemic use > J05 - Antivirals for systemic use > J05A - Direct acting antivirals > J05AF - Nucleoside and nucleotide reverse transcriptase inhibitors C471 - Enzyme Inhibitor > C1589 - Reverse Transcriptase Inhibitor > C97452 - Nucleoside Reverse Transcriptase Inhibitor D000890 - Anti-Infective Agents > D000998 - Antiviral Agents > D018894 - Reverse Transcriptase Inhibitors D000890 - Anti-Infective Agents > D000998 - Antiviral Agents > D044966 - Anti-Retroviral Agents D009676 - Noxae > D000963 - Antimetabolites > D015224 - Dideoxynucleosides D004791 - Enzyme Inhibitors > D019384 - Nucleic Acid Synthesis Inhibitors C254 - Anti-Infective Agent > C281 - Antiviral Agent Stavudine (d4T) is an orally active nucleoside reverse transcriptase inhibitor (NRTI). Stavudine has activity against HIV-1 and HIV-2. Stavudine also inhibits the replication of mitochondrial DNA (mtDNA). Stavudine reduces NLRP3 inflammasome activation and modulates Amyloid-β autophagy. Stavudine induces apoptosis[1][2][3][4].
phenazine-1-carboxylic acid
An aromatic carboxylic acid that is phenazine substituted at C-1 with a carboxy group. CONFIDENCE standard compound; INTERNAL_ID 190 Phenazine-1-carboxylic acid exhibits strong antifungal activity against phytopathogenic fungi.
5-Hydroxykynurenine
C10H12N2O4 (224.07970319999998)
5-Hydroxykynurenine is found in the tryptophan metabolism pathway. It is created from 5-Hydroxy-N-formylkynurenine through the action of arylformamidase [EC:3.5.1.9]. 5-Hydroxykynurenine is then converted to 5-Hydroxykynurenamine by the action of dopa decarboxylase [EC:4.1.1.28]. [HMDB] 5-Hydroxykynurenine is found in the tryptophan metabolism pathway. It is created from 5-Hydroxy-N-formylkynurenine through the action of arylformamidase [EC:3.5.1.9]. 5-Hydroxykynurenine is then converted to 5-Hydroxykynurenamine by the action of dopa decarboxylase [EC:4.1.1.28].
NIFURADENE
C254 - Anti-Infective Agent > C28394 - Topical Anti-Infective Agent
L-3-Hydroxykynurenine
C10H12N2O4 (224.07970319999998)
L-3-Hydroxykynurenine (L-3-HK) is a metabolite in the kynurenine pathway, the major route of tryptophan degradation in mammals. Kynurenine 3-monooxygenase, an NADPH-dependent flavin monooxygenase, catalyses the hydroxylation of L-kynurenine to L-3-hydroxykynurenine. 3-hydroxykynurenine can be converted to 3-hydroxyanthranilate by the enzyme 3-hydroxykinureninase. It may also be converted to 4-(2-amino-3-hydroxphenyl)-2,4-dioxobutanoate by the enzyme kynurenine-oxoglutarate transaminase. L-3-Hydroxykynurenine (L-3-HK) is a known generator of highly reactive free radicals. An elevation of L-3-HK levels has been shown to constitute a significant hazard in situations of excitotoxic injury. In particular, L-3-HK may contribute to the neuronal deficits underlying HIV-associated dementia (PMID: 7830088). Pharmacological interventions aimed at decreasing L-3-HK formation may therefore be particularly useful for the treatment of neurological diseases which are associated with an abnormally enhanced flux through the kynurenine pathway (PMID: 10583474) [HMDB] L-3-Hydroxykynurenine (L-3-HK) is a metabolite in the kynurenine pathway, the major route of tryptophan degradation in mammals. Kynurenine 3-monooxygenase, an NADPH-dependent flavin monooxygenase, catalyses the hydroxylation of L-kynurenine to L-3-hydroxykynurenine. 3-hydroxykynurenine can be converted to 3-hydroxyanthranilate by the enzyme 3-hydroxykinureninase. It may also be converted to 4-(2-amino-3-hydroxphenyl)-2,4-dioxobutanoate by the enzyme kynurenine-oxoglutarate transaminase. L-3-Hydroxykynurenine (L-3-HK) is a known generator of highly reactive free radicals. An elevation of L-3-HK levels has been shown to constitute a significant hazard in situations of excitotoxic injury. In particular, L-3-HK may contribute to the neuronal deficits underlying HIV-associated dementia (PMID: 7830088). Pharmacological interventions aimed at decreasing L-3-HK formation may therefore be particularly useful for the treatment of neurological diseases which are associated with an abnormally enhanced flux through the kynurenine pathway (PMID: 10583474).
Sideretin (reduced form)
A hydroxycoumarin that is fraxetin which has been substituted by an additional hydroxy group at positions 5. It is the primary molecule exuded by Arabidopsis thaliana roots in response to iron deficiency.
Hydroxyanthraquinone
1-hydroxyanthraquinone is a monohydroxyanthraquinone. 1-Hydroxyanthraquinone is a natural product found in Rheum palmatum, Handroanthus impetiginosus, and Morinda citrifolia with data available. D009676 - Noxae > D002273 - Carcinogens 1-Hydroxyanthraquinone, a naturally occurring compound with oral activity from some plants like Tabebuia avellanedae, exhibits carcinogenic effect[1]. 1-Hydroxyanthraquinone, a naturally occurring compound with oral activity from some plants like Tabebuia avellanedae, exhibits carcinogenic effect[1].
Elenolide
Constituent of olive oil. Elenolide is found in many foods, some of which are fats and oils, olive, pomes, and herbs and spices. Elenolide is found in fats and oils. Elenolide is a constituent of olive oil
Dehydrochorismic acid
Dehydrochorismic acid is isolated from pollen of Pinus densiflora (Japanese red pine Isolated from pollen of Pinus densiflora (Japanese red pine)
Cysteinyl-Cysteine
C6H12N2O3S2 (224.02893219999999)
Cysteinyl-Cysteine is a dipeptied compoosed of two cysteine residues. It is an incomplete breakdown product of protein digestion or protein catabolism. Some dipeptides are known to have physiological or cell-signaling effects although most are simply short-lived intermediates on their way to specific amino acid degradation pathways following further proteolysis. This dipeptide has not yet been identified in human tissues or biofluids and so it is classified as an Expected metabolite.
L-Nicotianine
C10H12N2O4 (224.07970319999998)
L-Nicotianine is found in mushrooms. L-Nicotianine is a constituent of Lentinus edodes (shiitake)
Propyl 1-(propylthio)propyl disulfide
Propyl 1-(propylthio)propyl disulfide is found in onion-family vegetables. Propyl 1-(propylthio)propyl disulfide is a constituent of Allium cepa (onion) and Allium fistulosum (Welsh onion). Constituent of Allium cepa (onion) and Allium fistulosum (Welsh onion). Propyl 1-(propylthio)propyl disulfide is found in garden onion and onion-family vegetables.
cis-Sinapic acid
cis-Sinapic acid is found in pulses. cis-Sinapic acid is a constituent of shoots of Medicago sativa (alfalfa). Constituent of shoots of Medicago sativa (alfalfa). cis-Sinapic acid is found in pulses and common pea. D019995 - Laboratory Chemicals > D007202 - Indicators and Reagents
5-(3',4',5'-Trihydroxyphenyl)-gamma-valerolactone
5-(3,4,5-Trihydroxyphenyl)-gamma-valerolactone is a polyphenol metabolite detected in biological fluids (PMID: 20428313). A polyphenol metabolite detected in biological fluids [PhenolExplorer]
7-Methyl-6,8-bis(methylthio)pyrrolo(1,2-a)pyrazine
C10H12N2S2 (224.04418719999998)
(3As)-2,3,3a,4-tetrahydro-1H-pyrrolo[2,1-c][1,2,4]benzothiadiazine 5,5-dioxide
Trinexapac
A monocarboxylic acid that is 3,5-dioxocyclohexanecarboxylic acid substituted by a cyclopropyl(hydroxy)methylidene group at position 4. It is a metabolite of the plant growth regulator trinexapac-ethyl. CONFIDENCE standard compound; EAWAG_UCHEM_ID 150
4,8-dihydroxy-6-methoxy-3-methyl-3,4-dihydro-1h-isochromen-1-one
2-(Methylsulfonyl)-3-(pyrazin-2-ylamino)acrylonitrile
2-Hydroxyanthraquinone
CONFIDENCE standard compound; INTERNAL_ID 24 CONFIDENCE standard compound; INTERNAL_ID 8289 CONFIDENCE standard compound; INTERNAL_ID 8144 2-Hydroxyanthraquinone, a natural compound, possesses antitumor and immunosuppressive activity[1]. 2-Hydroxyanthraquinone, a natural compound, possesses antitumor and immunosuppressive activity[1].
1-(3-acetyl-2,4-dihydroxy-6-methoxyphenyl)ethan-1-one
(E)-2-hydroxyethyl 3-(3,4-dihydroxyphenyl)acrylate|2-hydroxyethyl caffeate|hydroxyethyl caffeate
1-Methoxy-5,7-Dihydroxy-4,6-dimethyl-1(3H)-isobenzofuranone|5,7-Dihydroxy-4-(methoxymethyl)-6-methyl-1(3H)-isobenzofuranon
2,4-diformyl-3,5-dihydroxybenzoic acid methyl ester|rubramin
3-Methyl-4-(2,3-dihydroxyphenyl)-4-oxo-butanoic acid
3-Acetyl-2,6-dihydroxy-4-methoxy-5-methyl-benzaldehyd|3-Acetyl-2,6-dihydroxy-4-methoxy-5-methylbenzaldehyde|3-formyl-2,4-dihydroxy-5-methyl-6-methoxy-acetophenone|Kosin 16
3-(4-methoxy-3,5-dimethyl-2-oxo-2h-pyran-6-yl)-2-propenoic acid
(3S,4S)-3,4,8-trihydroxy-6-methoxy-3,4-dihydro-1(2H)-naphthalenone|3,4,8-trihydroxy-6-methoxy-3,4-dihydro-1(2H)-naphthalenone
3,4,8-trihydroxy-6-(hydroxymethyl)-3,4-dihydronaphthalen-1(2H)-one
3-methoxy-6,8-dihydroxy-3-methyl-3,4-dihydroisocoumarin
1-[rel-(2S,3S)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-2-yl]ethanone
4-(1-Hydroxyethyl)-6,8-dihydroxy-3,4-dihydro-1H-2-benzopyran-1-one
3-acetyl-2,4-dihydroxy-6-methoxy-5-methylbenzaldehyde
(+)-pestaphthalide A|5,7-dihydroxy-3-(1-hydroxyethyl)-6-methyl-3H-isobenzofuran-1-one|pestaphthalide A
3-Hydroxy-4-hydroxymethyl-7-methoxy-6-methyl-phthalid|3-hydroxy-4-hydroxymethyl-7-methoxy-6-methyl-phthalide
Methyl 6-methoxy-2-methyl-3,4-methylene dioxybenzoate
3R-5-formyl-4,6-dihydroxy-3-methoxyphthalide|rubralide A
6-Me ether-3,5,6-Trihydroxy-3-menthyl-1H-2-benzopyran-4-one
(3Z,5E)-octa-3,5-diene-1,3,4-tricarboxylic acid 3,4-anhydride|(3Z,5E)-Octa-3,5-diene-1,3,4-tricarboxylic acid anhydride
1-(4-hydroxy-3,5-dimethoxy-phenyl)-propane-1,2-dione
Vasicine HCl
Vasicine hydrochloride (peganine hydrochloride) is a quinazoline alkaloid isolated from Justicia adhatoda. Vasicine (peganine) possesses anti- tuberculosis activity[1]. Vasicine hydrochloride (peganine hydrochloride) is a quinazoline alkaloid isolated from Justicia adhatoda. Vasicine (peganine) possesses anti- tuberculosis activity[1].
Tox21_202901
2-hydroxyanthraquinone is a monohydroxyanthraquinone. 2-Hydroxyanthraquinone is a natural product found in Primulina hedyotidea, Rubia tinctorum, and Galium odoratum with data available. 2-Hydroxyanthraquinone, a natural compound, possesses antitumor and immunosuppressive activity[1]. 2-Hydroxyanthraquinone, a natural compound, possesses antitumor and immunosuppressive activity[1].
3-Hydroxykynurenine
C10H12N2O4 (224.07970319999998)
A hydroxykynurenine that is kynurenine substituted by a hydroxy group at position 3. C26170 - Protective Agent > C275 - Antioxidant MS2 deconvoluted using MS2Dec from all ion fragmentation data, MetaboLights identifier MTBLS1040; VCKPUUFAIGNJHC-UHFFFAOYSA-N_STSL_0007_3-Hydroxy-DL-Kynurenine_8000fmol_180416_S2_LC02_MS02_13; Spectrum acquired as described in Naz et al 2017 PMID 28641411. Preparation and submission to MassBank of North America by Chaleckis R. and Tada I. MS2 deconvoluted using CorrDec from all ion fragmentation data, MetaboLights identifier MTBLS1040; Spectrum acquired as described in Naz et al 2017 PMID 28641411. Preparation and submission to MassBank of North America by Chaleckis R. and Tada I.
sinapic acid
Sinapinic acid (Sinapic acid) is a phenolic compound isolated from Hydnophytum formicarum Jack. Rhizome, acts as an inhibitor of HDAC, with an IC50 of 2.27 mM[1], and also inhibits ACE-I activity[2]. Sinapinic acid posssess potent anti-tumor activity, induces apoptosis of tumor cells[1]. Sinapinic acid shows antioxidant and antidiabetic activities[2]. Sinapinic acid reduces total cholesterol, triglyceride, and HOMA-IR index, and also normalizes some serum parameters of antioxidative abilities and oxidative damage in ovariectomized rats[3]. Sinapinic acid (Sinapic acid) is a phenolic compound isolated from Hydnophytum formicarum Jack. Rhizome, acts as an inhibitor of HDAC, with an IC50 of 2.27 mM[1], and also inhibits ACE-I activity[2]. Sinapinic acid posssess potent anti-tumor activity, induces apoptosis of tumor cells[1]. Sinapinic acid shows antioxidant and antidiabetic activities[2]. Sinapinic acid reduces total cholesterol, triglyceride, and HOMA-IR index, and also normalizes some serum parameters of antioxidative abilities and oxidative damage in ovariectomized rats[3].
2-(2-acetyl-3-hydroxy-5-methoxyphenyl)acetic acid
4,8-dihydroxy-6-methoxy-3-methyl-3,4-dihydroisochromen-1-one
6,8-dihydroxy-7-methoxy-3-methyl-3,4-dihydroisochromen-1-one
4,8-dihydroxy-6-methoxy-3-methyl-3,4-dihydroisochromen-1-one
OCP_225.0789_16.6
CONFIDENCE Tentative identification: most likely structure (Level 3); INTERNAL_ID 1304
mevinphos
D018377 - Neurotransmitter Agents > D018678 - Cholinergic Agents > D002800 - Cholinesterase Inhibitors C471 - Enzyme Inhibitor > C47792 - Acetylcholinesterase Inhibitor D010575 - Pesticides > D007306 - Insecticides D004791 - Enzyme Inhibitors D016573 - Agrochemicals
Stavudine
C10H12N2O4 (224.07970319999998)
J - Antiinfectives for systemic use > J05 - Antivirals for systemic use > J05A - Direct acting antivirals > J05AF - Nucleoside and nucleotide reverse transcriptase inhibitors C471 - Enzyme Inhibitor > C1589 - Reverse Transcriptase Inhibitor > C97452 - Nucleoside Reverse Transcriptase Inhibitor D000890 - Anti-Infective Agents > D000998 - Antiviral Agents > D018894 - Reverse Transcriptase Inhibitors D000890 - Anti-Infective Agents > D000998 - Antiviral Agents > D044966 - Anti-Retroviral Agents D009676 - Noxae > D000963 - Antimetabolites > D015224 - Dideoxynucleosides D004791 - Enzyme Inhibitors > D019384 - Nucleic Acid Synthesis Inhibitors C254 - Anti-Infective Agent > C281 - Antiviral Agent CONFIDENCE standard compound; INTERNAL_ID 1066; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 2238; ORIGINAL_PRECURSOR_SCAN_NO 2235 CONFIDENCE standard compound; INTERNAL_ID 1066; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 2232; ORIGINAL_PRECURSOR_SCAN_NO 2230 CONFIDENCE standard compound; INTERNAL_ID 1066; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 2236; ORIGINAL_PRECURSOR_SCAN_NO 2234 CONFIDENCE standard compound; INTERNAL_ID 1066; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 2225; ORIGINAL_PRECURSOR_SCAN_NO 2224 CONFIDENCE standard compound; INTERNAL_ID 1066; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 2291; ORIGINAL_PRECURSOR_SCAN_NO 2290 CONFIDENCE standard compound; INTERNAL_ID 1066; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 2235; ORIGINAL_PRECURSOR_SCAN_NO 2233 CONFIDENCE standard compound; INTERNAL_ID 1066; DATASET 20200303_ENTACT_RP_MIX503; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9439; ORIGINAL_PRECURSOR_SCAN_NO 9434 CONFIDENCE standard compound; INTERNAL_ID 1066; DATASET 20200303_ENTACT_RP_MIX503; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9398; ORIGINAL_PRECURSOR_SCAN_NO 9395 CONFIDENCE standard compound; INTERNAL_ID 1066; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9567; ORIGINAL_PRECURSOR_SCAN_NO 9562 CONFIDENCE standard compound; INTERNAL_ID 1066; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9454; ORIGINAL_PRECURSOR_SCAN_NO 9450 Stavudine (d4T) is an orally active nucleoside reverse transcriptase inhibitor (NRTI). Stavudine has activity against HIV-1 and HIV-2. Stavudine also inhibits the replication of mitochondrial DNA (mtDNA). Stavudine reduces NLRP3 inflammasome activation and modulates Amyloid-β autophagy. Stavudine induces apoptosis[1][2][3][4].
tubermycin B
Origin: Microbe; SubCategory_DNP: Isoquinoline alkaloids, Benzylisoquinoline alkaloids Phenazine-1-carboxylic acid exhibits strong antifungal activity against phytopathogenic fungi.
2-(2-acetyl-3-hydroxy-5-methoxyphenyl)acetic acid [IIN-based: Match]
2-(2-acetyl-3-hydroxy-5-methoxyphenyl)acetic acid [IIN-based on: CCMSLIB00000845767]
3-Hydroxykynurenine; LC-tDDA; CE10
C10H12N2O4 (224.07970319999998)
3-Hydroxykynurenine; LC-tDDA; CE20
C10H12N2O4 (224.07970319999998)
3-Hydroxykynurenine; LC-tDDA; CE30
C10H12N2O4 (224.07970319999998)
3-Hydroxykynurenine; LC-tDDA; CE40
C10H12N2O4 (224.07970319999998)
2-(2-acetyl-3-hydroxy-5-methoxyphenyl)acetic acid_major
Sinapinic acid
Sinapinic acid (Sinapic acid) is a phenolic compound isolated from Hydnophytum formicarum Jack. Rhizome, acts as an inhibitor of HDAC, with an IC50 of 2.27 mM[1], and also inhibits ACE-I activity[2]. Sinapinic acid posssess potent anti-tumor activity, induces apoptosis of tumor cells[1]. Sinapinic acid shows antioxidant and antidiabetic activities[2]. Sinapinic acid reduces total cholesterol, triglyceride, and HOMA-IR index, and also normalizes some serum parameters of antioxidative abilities and oxidative damage in ovariectomized rats[3]. Sinapinic acid (Sinapic acid) is a phenolic compound isolated from Hydnophytum formicarum Jack. Rhizome, acts as an inhibitor of HDAC, with an IC50 of 2.27 mM[1], and also inhibits ACE-I activity[2]. Sinapinic acid posssess potent anti-tumor activity, induces apoptosis of tumor cells[1]. Sinapinic acid shows antioxidant and antidiabetic activities[2]. Sinapinic acid reduces total cholesterol, triglyceride, and HOMA-IR index, and also normalizes some serum parameters of antioxidative abilities and oxidative damage in ovariectomized rats[3].
Cys-cys
C6H12N2O3S2 (224.02893219999999)
A dipeptide formed from two L-cysteine residues.
L-Nicotianine
C10H12N2O4 (224.07970319999998)
cis-Sinapic acid
A 3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoic acid in which the double bond has cis-configuration. It has been isolated from the shoots of alfalfa. D019995 - Laboratory Chemicals > D007202 - Indicators and Reagents
1-[3-Chloro-5-(trifluoromethyl)-2-pyridinyl]ethanamine
C8H8ClF3N2 (224.03280739999997)
Methyl 2-(chloromethyl)-1H-benzo[d]imidazole-7-carboxylate
methyl 3-(ethylamino)-4-nitrobenzoate
C10H12N2O4 (224.07970319999998)
6-Chloro-2,3-dihydro-1H-indene-1-carboxylic acid ethyl ester
C12H13ClO2 (224.06040280000002)
Ethyl 3-chloro-imidazo[1,5-a]pyridine-1-carboxylate
3-(2-HYDROXY-4-METHOXY-PHENYL)-3-OXO-PROPIONIC ACID METHYL ESTER
5-Chloro-1H-indazole-3-carboxylic acid ethyl ester
(4-Methoxybenzyl)hydrazine dihydrochloride
C8H14Cl2N2O (224.04831339999998)
3-METHOXYBENZYLHYDRAZINE DIHYDROCHLORIDE
C8H14Cl2N2O (224.04831339999998)
1-(2,4-DIFLUORO-3-(TRIFLUOROMETHYL)PHENYL)ETHANONE
4-nitro-phenylalanine methyl ester
C10H12N2O4 (224.07970319999998)
2-[(6-fluoro-1H-benzimidazol-2-yl)methoxy]acetic acid
C10H9FN2O3 (224.05971759999997)
4,6-DIAMINO-1,3-BENZENEDICARBOXYLIC ACID DIMETHYL ESTER
C10H12N2O4 (224.07970319999998)
1-(4-Chlorophenyl)cyclopentanecarboxylic acid
C12H13ClO2 (224.06040280000002)
2-(3-Chloro-5-(trifluoromethyl)pyridin-2-yl)ethanamine
C8H8ClF3N2 (224.03280739999997)
Benzoic acid,4-[(aminothioxomethyl)amino]-, ethyl ester
1-(4-CHLOROPHENYL)-5-PROPYL-1H-PYRAZOLE-4-CARBONYLCHLORIDE
C12H13ClO2 (224.06040280000002)
3-(Trifluoromethyl)benzene-1-carboximidamide hydrochloride
C8H8ClF3N2 (224.03280739999997)
methyl 4-(ethylamino)-3-nitrobenzoate
C10H12N2O4 (224.07970319999998)
2-CHLOROMETHYL-IMIDAZO[1,2-A]PYRIDINE-8-CARBOXYLIC ACID METHYL ESTER
2-(1,3-benzodioxol-5-yloxy)propanehydrazide
C10H12N2O4 (224.07970319999998)
Ethyl 6-chloroimidazo[1,2-a]pyridine-2-carboxylate
ethyl 5-chloro-1H-pyrrolo(2,3-c)pyridine-2-carboxylate
(4,6-DIMETHYL-2,5-DIOXO-HEXAHYDRO-IMIDAZO-[4,5-D]IMIDAZOL-1-YL)-ACETICACID
methyl 4-chloropyrazolo[1,5-a]pyridine-3-carboxylate
N-Methyl-3-phenyl-5-isoxazolemethanamine hydrochloride
3,3-BIS(HYDROXYMETHYL)-2,3-DIHYDRO-4H-THIOCHROMEN-4-ONE
3-(Chloromethyl)-5-(2-methoxyphenyl)-1,2,4-oxadiazole
2-(chloromethyl)-5-(4-methoxyphenyl)-1,3,4-oxadiazole
5-Chloro-3-((trimethylsilyl)ethynyl)pyridin-2-amine
C10H13ClN2Si (224.05364880000002)
2-Chloro-3-((trimethylsilyl)ethynyl)pyridin-4-amine
C10H13ClN2Si (224.05364880000002)
METHYL 3-OXO-3,4-DIHYDRO-2H-PYRIDO[3,2-B][1,4]THIAZINE-6-CARBOXYLATE
methyl 1-acetylthieno[3,2-c]pyrazole-5-carboxylate
N-(4-Nitrophenyl)-2-hydroxy-2-methylpropanamide
C10H12N2O4 (224.07970319999998)
4-Chloro-1H-pyrrolo[2,3-b]pyridine-5-carboxylic acid ethyl ester
(4-CHLORO-2-METHYLPHENOXY)ACETICACIDMETHYLESTER
C8H8ClF3N2 (224.03280739999997)
4-HYDROXY-5-METHYL-ISOPHTHALIC ACID DIMETHYL ESTER
2-HYDROXYIMINO-2-[(4-METHYLPHENYL)SULFONYL]ACETONITRILE
5-(chloromethyl)-3-(4-methoxyphenyl)-1,2,4-oxadiazole
5,7-Dimethyl-2,3-dihydro-1H-[1,4]diazepine perchlorate
3-NITRO-4-PROPYLAMINO-BENZOIC ACID
C10H12N2O4 (224.07970319999998)
1-CHLORO-2-(5,5-DIMETHYL-1,3,2-DIOXABORINAN-2-YL)BENZENE
C11H14BClO2 (224.07753240000002)
2-Propen-1-one,3,3-bis(methylthio)-1-phenyl-
C11H12OS2 (224.03295419999998)
1H-Pyrazolo[4,3-d]pyrimidine-3-carboxylic acid, 4,5,6,7-tetrahydro-5,7-dioxo-, ethyl ester
methyl 5-chloro-1-oxo-2,3-dihydro-1H-indene-2-carboxylate
3-(METHYLCARBAMOYL)-5-NITROPHENYLBORONIC ACID
C8H9BN2O5 (224.06044939999998)
4-(2-Chloro-acetyl)-3,4-dihydro-1H-quinoxalin-2-one
Benzene,1,2,3,4-tetramethyl-5,6-dinitro-
C10H12N2O4 (224.07970319999998)
ethyl 5-chloroimidazo[1,5-a]pyridine-1-carboxylate
6-CHLORO-2H-CHROMENE-3-CARBOXYLIC ACID METHYL ESTER
5-CHLORO-1H-BENZOIMIDAZOLE-2-CARBOXYLIC ACID ETHYL ESTER
methyl 2-[(3-amino-2-hydroxy-benzoyl)amino]acetate
C10H12N2O4 (224.07970319999998)
4-(3-FLUORO-4-METHOXYPHENYL)THIAZOL-2-YLAMINE
C10H9FN2OS (224.04195959999996)
(4-((CYCLOPROPYLMETHYL)SULFINYL)PHENYL)BORONIC ACID
C10H13BO3S (224.06784180000002)
1-(3-CHLOROPHENYL)CYCLOPENTANECARBOXYLIC ACID
C12H13ClO2 (224.06040280000002)
Ethyl 4-oxo-3,4-dihydrothieno[3,2-d]pyrimidine-2-carboxylate
1-(2,3-DIFLUORO-4-(TRIFLUOROMETHYL)PHENYL)ETHANONE
4-(1-oxidopyridin-4-ylidene)pyridin-1-ium 1-oxide,hydrate
C10H12N2O4 (224.07970319999998)
3a-(Difluoromethyl)-2,3,3a,4-tetrahydro-1H-benzo[d]pyrrolo[1,2-a]imidazol-1-one
3-Acetao-2-nitrophenylboronic acid
C8H9BN2O5 (224.06044939999998)
5-Acetamido-2-nitrophenylboronic acid
C8H9BN2O5 (224.06044939999998)
N-METHYL-1-(5-PHENYLISOXAZOL-3-YL)METHANAMINE HYDROCHLORIDE
N-ETHOXYCARBONYL-5-NITRO-O-TOLUIDINE
C10H12N2O4 (224.07970319999998)
(E)-3-(Methoxycarbonyl)-4-(5-methylfuran-2-yl)but-3-enoic acid
ETHYL 2-AMINO-4-(TRIFLUOROMETHYL)OXAZOLE-5-CARBOXYLATE
(4-(Difluoromethoxy)-3,5-difluorophenyl)boronic acid
2,2,2-Trifluoro-N-(2-oxa-6-azaspiro[3.4]oct-8-yl)acetamide
2-(PROPYLTHIO)BENZO[D]THIAZOL-6-AMINE
C10H12N2S2 (224.04418719999998)
sodium,1,1,2,2,3,3-hexadeuterio-3-trimethylsilylpropane-1-sulfonate
C6H9D6NaO3SSi (224.07854706799998)
3,6-DIMETHYLIMIDAZO[2,1-B]THIAZOLE-5-CARBOXYLIC ACID ETHYL ESTER
(S)-6-METHOXY-2,5,7,8-TETRAMETHYLCHROMANE-2-CARBOXYLICACID
3-amino-4-methoxybenzene-methanamine dihydrochloride
C8H14Cl2N2O (224.04831339999998)
5-(AMINOMETHYL)-2-METHOXYANILINE DIHYDROCHLORIDE
C8H14Cl2N2O (224.04831339999998)
3-(AMINOMETHYL)-4-METHOXYANILINE DIHYDROCHLORIDE
C8H14Cl2N2O (224.04831339999998)
ethyl N-(4-methyl-3-nitrophenyl)carbamate
C10H12N2O4 (224.07970319999998)
5-(Chloromethyl)-3-(2-methoxyphenyl)-1,2,4-oxadiazole
N-ETHOXYCARBONYL-3-NITRO-O-TOLUIDINE
C10H12N2O4 (224.07970319999998)
5-Chloro-3-fluoro-N-isopropylpyridin-2-amine hydrochloride
(6-Chloro-4-methyl-1H-pyrrolo[2,3-b]pyridin-3-yl)acetic acid
ethyl 6-chloro-1H-pyrrolo[2,3-b]pyridine-1-carboxylate
2,3-DIMETHYL-5-OXO-5H-THIAZOLO[3,2-A]PYRIMIDINE-6-CARBOXYLIC ACID
Ethyl 6-chloropyrazolo[1,5-a]pyridine-3-carboxylate
ETHYL 5-OXO-5H-THIAZOLO[3,2-A]PYRIMIDINE-6-CARBOXYLATE
1,3-Benzenedicarboxylic acid, 5-(hydroxyMethyl)-, 1,3-dimethyl ester
IMidazo[1,2-a]pyridine-2-carboxylic acid, 7-chloro-, ethyl ester
dimethyl 5-hydroxy-3-methylbenzene-1,2-dicarboxylate
4-chloro-1,3-dimethylpyrazolo[3,4-b]pyridine-5-carboxamide
1-(4-Chloro-1H-pyrrolo[2,3-b]pyridin-5-yl)-2-methoxyethanone
4-(1,1,2,2-tetrafluoroethoxy)-3-benzenediamine
C8H8F4N2O (224.05727259999998)
ethyl 4-chloro-1H-pyrrolo[2,3-c]pyridine-2-carboxylate
3-(chloromethyl)-5-(4-methoxyphenyl)-1,2,4-oxadiazole
Pyrimidine, 4-ethyl-2-(methylsulfonyl)-6-(1-propynyl)- (9CI)
(R)-3-AMINO-4-(4-BROMOPHENYL)BUTANOICACIDHYDROCHLORIDE
C10H12N2O4 (224.07970319999998)
propan-2-yl 5-amino-4-cyano-3-methylthiophene-2-carboxylate
1,1,1,5,5,5-HEXAFLUORO-2-HYDROXY-2-METHYLPENTAN-4-ONE
2-Methoxybenzylhydrazine dihydrochloride
C8H14Cl2N2O (224.04831339999998)
Potassium 1-naphthylacetate
1-Naphthaleneacetic acid potassium salt (Potassium 1-Naphthaleneacetate), a synthetic auxin, can promote plant growth. 1-Naphthaleneacetic acid potassium salt is also an inhibitor of PLA2, with an IC50 of 13.16 μM[1][2].
ethyl 6-chloro-1H-pyrrolo[2,3-b]pyridine-2-carboxylate
Ethyl 5-chloro-1H-pyrrolo[3,2-b]pyridine-2-carboxylate
2-(3-methoxy-4-(methoxycarbonyl)phenyl)acetic acid
[2-Fluoro-3-(trifluoromethoxy)phenyl]-boronic acid
5,5,5-trifluoro-4-hydroxy-4-(trifluoromethyl)pentan-2-one
4-Methoxybenzylhydrazine dihydrochloride
C8H14Cl2N2O (224.04831339999998)
1-(Methoxymethyl)-3-(trifluoromethyl)-1H-pyrazol-4-ylboronic acid
4-[(2-NITROPHENYL)AMINO]BUTANOIC ACID
C10H12N2O4 (224.07970319999998)
Methyl 2-(4-chloro-1H-pyrrolo[2,3-b]pyridin-3-yl)acetate
2,3-DIHYDRO-6,7-DIMETHOXY-4H-1-BENZOTHIOPYRAN-4-ONE
Ethyl 6-chloro-1H-pyrrolo[3,2-b]pyridine-5-carboxylate
2-Amino-8-chloro-1,2,3,4-tetrahydro-2-naphthalenecarboxamide
3-(chloromethyl)-5-(3-methoxyphenyl)-1,2,4-oxadiazole
6-Benzothiazolamine,2-[(1-methylethyl)thio]-(9CI)
C10H12N2S2 (224.04418719999998)
Ethyl 4-(methylamino)-3-nitrobenzoate
C10H12N2O4 (224.07970319999998)
4-(Isopropylamino)-3-nitrobenzoic acid
C10H12N2O4 (224.07970319999998)
ethyl 5-chloroimidazo[1,2-a]pyridine-3-carboxylate
4-(2-chlorophenyl)oxane-4-carbaldehyde
C12H13ClO2 (224.06040280000002)
4-(3-Chlorophenyl)tetrahydropyran-4-carboxaldehyde
C12H13ClO2 (224.06040280000002)
3-Acetamido-4-nitrophenylboronic acid
C8H9BN2O5 (224.06044939999998)
Ethyl 5-chloroimidazo[1,2-a]pyridine-2-carboxylate
Ethyl 4-fluorobenzo[b]thiophene-2-carboxylate
C11H9FO2S (224.03072659999998)
N-(4-Methoxy-2-methyl-5-nitrophenyl)acetamide
C10H12N2O4 (224.07970319999998)
3-(Carboxymethyl)-1,2,4-cyclopentanetricarboxylic Acid 1,4:2,3-Dianhydride
(R)-2-Amino-4-(2-amino-3-hydroxyphenyl)-4-oxobutanoic acid
C10H12N2O4 (224.07970319999998)
4-Amino-4-deoxychorismate(1-)
C10H10NO5- (224.05589500000002)
A dicarboxylic acid monoanion that is the conjugate base of 4-amino-4-deoxychorismic acid.
2H-1-Benzopyran-2-one, 3-chloro-7-methoxy-4-methyl-
2,2,3,3-Tetrahydroxy-2,3-dihydronaphthalene-1,4-dione
N-(4,5-dihydro-1,3-thiazol-2-yl)-1-ethyl-1H-pyrazole-3-carboxamide
C9H12N4OS (224.07317819999997)
129-43-1
D009676 - Noxae > D002273 - Carcinogens 1-Hydroxyanthraquinone, a naturally occurring compound with oral activity from some plants like Tabebuia avellanedae, exhibits carcinogenic effect[1]. 1-Hydroxyanthraquinone, a naturally occurring compound with oral activity from some plants like Tabebuia avellanedae, exhibits carcinogenic effect[1].
605-32-3
2-Hydroxyanthraquinone, a natural compound, possesses antitumor and immunosuppressive activity[1]. 2-Hydroxyanthraquinone, a natural compound, possesses antitumor and immunosuppressive activity[1].
(3As)-2,3,3a,4-tetrahydro-1H-pyrrolo[2,1-c][1,2,4]benzothiadiazine 5,5-dioxide
3-(Carboxymethylaminomethyl)-4-hydroxybenzoate
C10H10NO5- (224.05589500000002)
(3S)-3-(1-carboxyethenoxy)cyclohepta-1,6-diene-1-carboxylic acid
(4R,5R,6S)-4,5,6,7,7-pentahydroxy-2-oxoheptanoic acid
5-(Thiophen-2-ylmethyl)-1,3-diazinane-2,4,6-trione
1-(2-Furanyl)-2-[(1-methyl-5-tetrazolyl)thio]ethanone
3-(3-Hydroxy-4,5-dimethoxyphenyl)prop-2-enoic acid
3,4-dihydroxy-7-methylidene-2-[(E)-prop-1-enyl]-3,4-dihydro-2H-furo[3,4-b]pyran-5-one
N-(2-hydroxy,5-methoxyphenyl)malonamate
C10H10NO5- (224.05589500000002)
6,8-Dihydroxy-7-methoxy-3-methyl-3,4-dihydroisochromen-1-one
(1s,4s)-prephenate(2-)
A prephenate(2-) obtained by deprotonation of both carboxy groups of (1s,4s)-prephenic acid; major species at pH 7.3.
Prephenate(2-)
A dicarboxylic acid dianion that is the conjugate base of prephenic acid; major species at pH 7.3.
5-(3,4,5-Trihydroxyphenyl)-gamma-valerolactone
A butan-4-olide that is gamma-valerolactone in which one of the methyl hydrogens has been replaced by a 3,4,5-trihydroxyphenyl group.
S 18986
S 18986 is a selective, orally active, brain penetrant positive allosteric modulator of AMPA-type receptors. S 18986 shows cognitive enhancing properties in rodents. S 18986 activates the release of noradrenaline and acetylcholine in rat hippocampus and enhances rat memory in object-recognition tests[1][2].