Exact Mass: 215.08786980000002
Exact Mass Matches: 215.08786980000002
Found 500 metabolites which its exact mass value is equals to given mass value 215.08786980000002,
within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error
0.01 dalton.
Kinetin
Kinetin is a member of the class of 6-aminopurines that is adenine carrying a (furan-2-ylmethyl) substituent at the exocyclic amino group. It has a role as a geroprotector and a cytokinin. It is a member of furans and a member of 6-aminopurines. Kinetin is a cytokinin which are plant hormones promotes cell division and plant growth. It was shown to naturally exist in DNA of organisms including humans and various plants. While kinetin is used in tissue cultures to produce new plants, it is also found in cosmetic products as an anti-aging agents. Kinetin is a natural product found in Cocos nucifera, Beta vulgaris, and other organisms with data available. A furanyl adenine found in PLANTS and FUNGI. It has plant growth regulation effects. Kinetin can react with UDP-D-glucose to produce kinetin-7-N-glucoside or kinetin-9-N-glucoside, with UDP as a byproduct. The reaction is catalyzed by UDP glycosyltransferase. Kinetin is a hormone derived from plants. Kinetin can react with UDP-D-glucose to produce kinetin-7-N-glucoside or kinetin-9-N-glucoside, with UDP as a byproduct. The reaction is catalyzed by UDP glycosyltransferase. D006133 - Growth Substances > D010937 - Plant Growth Regulators > D003583 - Cytokinins COVID info from PDB, Protein Data Bank Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS CONFIDENCE standard compound; INTERNAL_ID 781; DATASET 20200303_ENTACT_RP_MIX501; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 2712; ORIGINAL_PRECURSOR_SCAN_NO 2710 CONFIDENCE standard compound; INTERNAL_ID 781; DATASET 20200303_ENTACT_RP_MIX501; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 2714; ORIGINAL_PRECURSOR_SCAN_NO 2711 CONFIDENCE standard compound; INTERNAL_ID 781; DATASET 20200303_ENTACT_RP_MIX501; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 5910; ORIGINAL_PRECURSOR_SCAN_NO 5905 CONFIDENCE standard compound; INTERNAL_ID 781; DATASET 20200303_ENTACT_RP_MIX501; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 2699; ORIGINAL_PRECURSOR_SCAN_NO 2696 CONFIDENCE standard compound; INTERNAL_ID 781; DATASET 20200303_ENTACT_RP_MIX501; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 5865; ORIGINAL_PRECURSOR_SCAN_NO 5864 CONFIDENCE standard compound; INTERNAL_ID 781; DATASET 20200303_ENTACT_RP_MIX501; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 5900; ORIGINAL_PRECURSOR_SCAN_NO 5896 CONFIDENCE standard compound; INTERNAL_ID 781; DATASET 20200303_ENTACT_RP_MIX501; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 2691; ORIGINAL_PRECURSOR_SCAN_NO 2689 CONFIDENCE standard compound; INTERNAL_ID 781; DATASET 20200303_ENTACT_RP_MIX501; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 5890; ORIGINAL_PRECURSOR_SCAN_NO 5889 CONFIDENCE standard compound; INTERNAL_ID 781; DATASET 20200303_ENTACT_RP_MIX501; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 2693; ORIGINAL_PRECURSOR_SCAN_NO 2691 CONFIDENCE standard compound; INTERNAL_ID 781; DATASET 20200303_ENTACT_RP_MIX501; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 5911; ORIGINAL_PRECURSOR_SCAN_NO 5908 CONFIDENCE standard compound; INTERNAL_ID 781; DATASET 20200303_ENTACT_RP_MIX501; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 5893; ORIGINAL_PRECURSOR_SCAN_NO 5891 CONFIDENCE standard compound; INTERNAL_ID 781; DATASET 20200303_ENTACT_RP_MIX501; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 2689; ORIGINAL_PRECURSOR_SCAN_NO 2687 IPB_RECORD: 305; CONFIDENCE confident structure KEIO_ID F014; [MS2] KO008961 KEIO_ID F014 Kinetin (N6-furfuryladenine) belongs to the family of N6-substituted adenine derivatives known as cytokinins, which are plant hormones involved in cell division, differentiation and other physiological processes. Kinetin has anti-aging effects[1]. Kinetin (N6-furfuryladenine) belongs to the family of N6-substituted adenine derivatives known as cytokinins, which are plant hormones involved in cell division, differentiation and other physiological processes. Kinetin has anti-aging effects[1]. Kinetin (N6-furfuryladenine) belongs to the family of N6-substituted adenine derivatives known as cytokinins, which are plant hormones involved in cell division, differentiation and other physiological processes. Kinetin has anti-aging effects[1].
atrazine
A diamino-1,3,5-triazine that is 1,3,5-triazine-2,4-diamine substituted by a chloro group at position 6 while one of hydrogens of each amino group is replaced respectively by an ethyl and a propan-2-yl group. D010575 - Pesticides > D006540 - Herbicides D016573 - Agrochemicals CONFIDENCE standard compound; INTERNAL_ID 718; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8568; ORIGINAL_PRECURSOR_SCAN_NO 8565 CONFIDENCE standard compound; INTERNAL_ID 718; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8581; ORIGINAL_PRECURSOR_SCAN_NO 8579 CONFIDENCE standard compound; INTERNAL_ID 718; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8572; ORIGINAL_PRECURSOR_SCAN_NO 8570 CONFIDENCE standard compound; INTERNAL_ID 718; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8520; ORIGINAL_PRECURSOR_SCAN_NO 8518 CONFIDENCE standard compound; INTERNAL_ID 718; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8527; ORIGINAL_PRECURSOR_SCAN_NO 8525 CONFIDENCE standard compound; INTERNAL_ID 718; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8492; ORIGINAL_PRECURSOR_SCAN_NO 8489 CONFIDENCE standard compound; EAWAG_UCHEM_ID 288 CONFIDENCE standard compound; INTERNAL_ID 4033 CONFIDENCE standard compound; INTERNAL_ID 3109 CONFIDENCE standard compound; INTERNAL_ID 8414 CONFIDENCE standard compound; INTERNAL_ID 29
Atrazine
Atrazine is an organic compound consisting of an s-triazine-ring is a widely used herbicide. Its use is controversial due to widespread contamination in drinking water and its associations with birth defects and menstrual problems when consumed by humans at concentrations below government standards. Although it has been banned in the European Union,[2] it is still one of the most widely used herbicides in the world (Wikipedia). Atrazine is a suspected teratogen, causing demasculinization in male northern leopard frog even at low concentrations, and an estrogen disruptor. A 2010 study found that atrazine rendered 75 percent of male frogs sterile and turned one in 10 into females. A 2002 study found that exposure to atrazine caused male tadpoles to turn into hermaphrodites - frogs with both male and female sexual characteristics. But another study, requested by EPA and funded by Syngenta, was unable to reproduce these results. Atrazine was banned in the European Union (EU) in 2004 because of its persistent groundwater contamination. In the United States, however, atrazine is one of the most widely used herbicides, with 76 million pounds of it applied each year, in spite of the restriction that used to be imposed. Its endocrine disruptor effects, possible carcinogenic effect, and epidemiological connection to low sperm levels in men has led several researchers to call for banning it in the US.Rates of biodegradation are affected by atrazines low solubility, thus surfactants may increase the degradation rate. Though the two alkyl moieties readily support growth of certain microorganisms, the atrazine ring is a poor energy source due to the oxidized state of ring carbon. In fact, the most common pathway for atrazine degradation involves the intermediate, cyanuric acid, in which carbon is fully oxidized, thus the ring is primarily a nitrogen source for aerobic microorganisms. Atrazine may be catabolized as a carbon and nitrogen source in reducing environments, and some aerobic atrazine degraders have been shown to use the compound for growth under anoxia in the presence of nitrate as an electron acceptor, a process referred to as a denitrification. When atrazine is used as a nitrogen source for bacterial growth, degradation may be regulated by the presence of alternative sources of nitrogen. In pure cultures of atrazine-degrading bacteria, as well as active soil communitites, atrazine ring nitrogen, but not carbon are assimilated into microbial biomass. Low concentrations of glucose can decrease the bioavailability, whereas higher concentrations promote the catabolism of atrazine. Tyrone Hayes, Department of Integrative Biology, University of California, notes that all of the studies that failed to conclude that atrazine caused hermaphroditism were plagued by poor experimental controls and were funded by Syngenta, one of the companies that produce the chemical. The U.S. Environmental Protection Agency (EPA) and its independent Scientific Advisory Panel (SAP) examined all available studies on this topic including Hayes work and concluded that there are currently insufficient data to determine if atrazine affects amphibian development. Hayes, formerly part of the SAP panel, resigned in 2000 to continue studies independently. The EPA and its SAP made recommendations concerning proper study design needed for further investigation into this issue. As required by the EPA, Syngenta conducted two experiments under Good Laboratory Practices (GLP) and inspection by the EPA and German regulatory authorities. The paper concluded These studies demonstrate that long-term exposure of larval X. laevis to atrazine at concentrations ranging from 0.01 to 100 microg/l does not affect growth, larval development, or sexual differentiation. Another independent study in 2008 determined that the failure of recent studies to find that atrazine feminizes X. laevis calls into question the herbicides role in that decline. A report written in Environmental Scien... D010575 - Pesticides > D006540 - Herbicides D016573 - Agrochemicals
Macaridine
C13H13NO2 (215.09462380000002)
Macaridine is found in root vegetables. Macaridine is an alkaloid from the tubers of Lepidium meyenii (maca). Alkaloid from the tubers of Lepidium meyenii (maca). Macaridine is found in root vegetables.
Propenoylcarnitine
Propenoylcarnitine is an acylcarnitine. More specifically, it is an propenoic acid ester of carnitine. Acylcarnitines were first discovered more than 70 year ago (PMID: 13825279). It is believed that there are more than 1000 types of acylcarnitines in the human body. The general role of acylcarnitines is to transport acyl-groups (organic acids and fatty acids) from the cytoplasm into the mitochondria so that they can be broken down to produce energy. This process is known as beta-oxidation. According to a recent review [Dambrova et al. 2021, Physiological Reviews], acylcarnitines (ACs) can be classified into 9 different categories depending on the type and size of their acyl-group: 1) short-chain ACs; 2) medium-chain ACs; 3) long-chain ACs; 4) very long-chain ACs; 5) hydroxy ACs; 6) branched chain ACs; 7) unsaturated ACs; 8) dicarboxylic ACs and 9) miscellaneous ACs. Short-chain ACs have acyl-groups with two to five carbons (C2-C5), medium-chain ACs have acyl-groups with six to thirteen carbons (C6-C13), long-chain ACs have acyl-groups with fourteen to twenty once carbons (C14-C21) and very long-chain ACs have acyl groups with more than 22 carbons. Propenoylcarnitine is therefore classified as a short chain AC. As a short-chain acylcarnitine Propenoylcarnitine is a member of the most abundant group of carnitines in the body, comprising more than 50\\% of all acylcarnitines quantified in tissues and biofluids (PMID: 31920980). Some short-chain carnitines have been studied as supplements or treatments for a number of diseases, including neurological disorders and inborn errors of metabolism. Carnitine acetyltransferase (CrAT, EC:2.3.1.7) is responsible for the synthesis of all short-chain and short branched-chain acylcarnitines (PMID: 23485643). The study of acylcarnitines is an active area of research and it is likely that many novel acylcarnitines will be discovered in the coming years. It is also likely that many novel roles in health and disease will be uncovered. An excellent review of the current state of knowledge for acylcarnitines is available at [Dambrova et al. 2021, Physiological Reviews]. A human metabolite taken as a putative food compound of mammalian origin [HMDB]
Acetyl vitamin K5
C13H13NO2 (215.09462380000002)
Prothrombogenic vitamin. Prothrombogenic vitamin
1-hydroxyoct-2-enoylglycine
1-Hydroxyoct-2-enoylglycine is classified as a member of the Alpha amino acids. Alpha amino acids are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon). 1-Hydroxyoct-2-enoylglycine is considered to be practically insoluble (in water) and acidic.
1-hydroxyoct-3-enoylglycine
1-Hydroxyoct-3-enoylglycine is classified as a member of the Alpha amino acids. Alpha amino acids are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon). 1-Hydroxyoct-3-enoylglycine is considered to be slightly soluble (in water) and acidic.
1-hydroxyoct-4-enoylglycine
1-Hydroxyoct-4-enoylglycine is classified as a member of the Alpha amino acids. Alpha amino acids are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon). 1-Hydroxyoct-4-enoylglycine is considered to be slightly soluble (in water) and acidic.
1-hydroxyoct-5-enoylglycine
1-Hydroxyoct-5-enoylglycine is classified as a member of the Alpha amino acids. Alpha amino acids are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon). 1-Hydroxyoct-5-enoylglycine is considered to be slightly soluble (in water) and acidic.
1-hydroxyoct-6-enoylglycine
1-Hydroxyoct-6-enoylglycine is classified as a member of the Alpha amino acids. Alpha amino acids are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon). 1-Hydroxyoct-6-enoylglycine is considered to be slightly soluble (in water) and acidic.
1-hydroxyoct-7-enoylglycine
1-Hydroxyoct-7-enoylglycine is classified as a member of the Alpha amino acids. Alpha amino acids are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon). 1-Hydroxyoct-7-enoylglycine is considered to be slightly soluble (in water) and acidic.
2-hydroxyoct-1-enoylglycine
2-Hydroxyoct-1-enoylglycine is classified as a member of the Alpha amino acids. Alpha amino acids are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon). 2-Hydroxyoct-1-enoylglycine is considered to be slightly soluble (in water) and acidic.
2-hydroxyoct-2-enoylglycine
2-Hydroxyoct-2-enoylglycine is classified as a member of the N-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. 2-Hydroxyoct-2-enoylglycine is considered to be practically insoluble (in water) and acidic.
2-hydroxyoct-3-enoylglycine
2-Hydroxyoct-3-enoylglycine is classified as a member of the N-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. 2-Hydroxyoct-3-enoylglycine is considered to be practically insoluble (in water) and acidic.
2-hydroxyoct-4-enoylglycine
2-Hydroxyoct-4-enoylglycine is classified as a member of the N-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. 2-Hydroxyoct-4-enoylglycine is considered to be practically insoluble (in water) and acidic.
2-hydroxyoct-5-enoylglycine
2-Hydroxyoct-5-enoylglycine is classified as a member of the N-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. 2-Hydroxyoct-5-enoylglycine is considered to be practically insoluble (in water) and acidic.
2-hydroxyoct-6-enoylglycine
2-Hydroxyoct-6-enoylglycine is classified as a member of the N-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. 2-Hydroxyoct-6-enoylglycine is considered to be practically insoluble (in water) and acidic.
2-hydroxyoct-7-enoylglycine
2-Hydroxyoct-7-enoylglycine is classified as a member of the N-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. 2-Hydroxyoct-7-enoylglycine is considered to be slightly soluble (in water) and acidic.
3-hydroxyoct-1-enoylglycine
3-Hydroxyoct-1-enoylglycine is classified as a member of the Alpha amino acids. Alpha amino acids are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon). 3-Hydroxyoct-1-enoylglycine is considered to be slightly soluble (in water) and acidic.
3-hydroxyoct-2-enoylglycine
3-Hydroxyoct-2-enoylglycine is classified as a member of the N-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. 3-Hydroxyoct-2-enoylglycine is considered to be practically insoluble (in water) and acidic.
3-hydroxyoct-3-enoylglycine
3-Hydroxyoct-3-enoylglycine is classified as a member of the N-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. 3-Hydroxyoct-3-enoylglycine is considered to be practically insoluble (in water) and acidic.
3-hydroxyoct-4-enoylglycine
3-Hydroxyoct-4-enoylglycine is classified as a member of the N-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. 3-Hydroxyoct-4-enoylglycine is considered to be practically insoluble (in water) and acidic.
3-hydroxyoct-5-enoylglycine
3-Hydroxyoct-5-enoylglycine is classified as a member of the N-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. 3-Hydroxyoct-5-enoylglycine is considered to be practically insoluble (in water) and acidic.
3-hydroxyoct-6-enoylglycine
3-Hydroxyoct-6-enoylglycine is classified as a member of the N-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. 3-Hydroxyoct-6-enoylglycine is considered to be practically insoluble (in water) and acidic.
3-hydroxyoct-7-enoylglycine
3-Hydroxyoct-7-enoylglycine is classified as a member of the N-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. 3-Hydroxyoct-7-enoylglycine is considered to be slightly soluble (in water) and acidic.
4-hydroxyoct-1-enoylglycine
4-Hydroxyoct-1-enoylglycine is classified as a member of the Alpha amino acids. Alpha amino acids are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon). 4-Hydroxyoct-1-enoylglycine is considered to be slightly soluble (in water) and acidic.
4-hydroxyoct-2-enoylglycine
4-Hydroxyoct-2-enoylglycine is classified as a member of the N-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. 4-Hydroxyoct-2-enoylglycine is considered to be practically insoluble (in water) and acidic.
4-hydroxyoct-3-enoylglycine
4-Hydroxyoct-3-enoylglycine is classified as a member of the N-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. 4-Hydroxyoct-3-enoylglycine is considered to be practically insoluble (in water) and acidic.
4-hydroxyoct-4-enoylglycine
4-Hydroxyoct-4-enoylglycine is classified as a member of the N-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. 4-Hydroxyoct-4-enoylglycine is considered to be practically insoluble (in water) and acidic.
4-hydroxyoct-5-enoylglycine
4-Hydroxyoct-5-enoylglycine is classified as a member of the N-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. 4-Hydroxyoct-5-enoylglycine is considered to be practically insoluble (in water) and acidic.
4-hydroxyoct-6-enoylglycine
4-Hydroxyoct-6-enoylglycine is classified as a member of the N-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. 4-Hydroxyoct-6-enoylglycine is considered to be practically insoluble (in water) and acidic.
4-hydroxyoct-7-enoylglycine
4-Hydroxyoct-7-enoylglycine is classified as a member of the N-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. 4-Hydroxyoct-7-enoylglycine is considered to be slightly soluble (in water) and acidic.
5-hydroxyoct-1-enoylglycine
5-Hydroxyoct-1-enoylglycine is classified as a member of the Alpha amino acids. Alpha amino acids are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon). 5-Hydroxyoct-1-enoylglycine is considered to be slightly soluble (in water) and acidic.
5-hydroxyoct-2-enoylglycine
5-Hydroxyoct-2-enoylglycine is classified as a member of the N-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. 5-Hydroxyoct-2-enoylglycine is considered to be practically insoluble (in water) and acidic.
5-hydroxyoct-3-enoylglycine
5-Hydroxyoct-3-enoylglycine is classified as a member of the N-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. 5-Hydroxyoct-3-enoylglycine is considered to be practically insoluble (in water) and acidic.
5-hydroxyoct-4-enoylglycine
5-Hydroxyoct-4-enoylglycine is classified as a member of the N-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. 5-Hydroxyoct-4-enoylglycine is considered to be practically insoluble (in water) and acidic.
5-hydroxyoct-5-enoylglycine
5-Hydroxyoct-5-enoylglycine is classified as a member of the N-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. 5-Hydroxyoct-5-enoylglycine is considered to be practically insoluble (in water) and acidic.
5-hydroxyoct-6-enoylglycine
5-Hydroxyoct-6-enoylglycine is classified as a member of the N-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. 5-Hydroxyoct-6-enoylglycine is considered to be practically insoluble (in water) and acidic.
5-hydroxyoct-7-enoylglycine
5-Hydroxyoct-7-enoylglycine is classified as a member of the N-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. 5-Hydroxyoct-7-enoylglycine is considered to be slightly soluble (in water) and acidic.
6-hydroxyoct-1-enoylglycine
6-Hydroxyoct-1-enoylglycine is classified as a member of the Alpha amino acids. Alpha amino acids are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon). 6-Hydroxyoct-1-enoylglycine is considered to be slightly soluble (in water) and acidic.
6-hydroxyoct-2-enoylglycine
6-Hydroxyoct-2-enoylglycine is classified as a member of the N-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. 6-Hydroxyoct-2-enoylglycine is considered to be practically insoluble (in water) and acidic.
6-hydroxyoct-3-enoylglycine
6-Hydroxyoct-3-enoylglycine is classified as a member of the N-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. 6-Hydroxyoct-3-enoylglycine is considered to be practically insoluble (in water) and acidic.
6-hydroxyoct-4-enoylglycine
6-Hydroxyoct-4-enoylglycine is classified as a member of the N-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. 6-Hydroxyoct-4-enoylglycine is considered to be practically insoluble (in water) and acidic.
6-hydroxyoct-5-enoylglycine
6-Hydroxyoct-5-enoylglycine is classified as a member of the N-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. 6-Hydroxyoct-5-enoylglycine is considered to be practically insoluble (in water) and acidic.
6-hydroxyoct-6-enoylglycine
6-Hydroxyoct-6-enoylglycine is classified as a member of the N-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. 6-Hydroxyoct-6-enoylglycine is considered to be practically insoluble (in water) and acidic.
6-hydroxyoct-7-enoylglycine
6-Hydroxyoct-7-enoylglycine is classified as a member of the N-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. 6-Hydroxyoct-7-enoylglycine is considered to be slightly soluble (in water) and acidic.
7-hydroxyoct-1-enoylglycine
7-Hydroxyoct-1-enoylglycine is classified as a member of the Alpha amino acids. Alpha amino acids are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon). 7-Hydroxyoct-1-enoylglycine is considered to be slightly soluble (in water) and acidic.
7-hydroxyoct-2-enoylglycine
7-Hydroxyoct-2-enoylglycine is classified as a member of the N-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. 7-Hydroxyoct-2-enoylglycine is considered to be practically insoluble (in water) and acidic.
7-hydroxyoct-3-enoylglycine
7-Hydroxyoct-3-enoylglycine is classified as a member of the N-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. 7-Hydroxyoct-3-enoylglycine is considered to be practically insoluble (in water) and acidic.
7-hydroxyoct-4-enoylglycine
7-Hydroxyoct-4-enoylglycine is classified as a member of the N-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. 7-Hydroxyoct-4-enoylglycine is considered to be practically insoluble (in water) and acidic.
7-hydroxyoct-5-enoylglycine
7-Hydroxyoct-5-enoylglycine is classified as a member of the N-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. 7-Hydroxyoct-5-enoylglycine is considered to be practically insoluble (in water) and acidic.
7-hydroxyoct-6-enoylglycine
7-Hydroxyoct-6-enoylglycine is classified as a member of the N-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. 7-Hydroxyoct-6-enoylglycine is considered to be practically insoluble (in water) and acidic.
7-hydroxyoct-7-enoylglycine
7-Hydroxyoct-7-enoylglycine is classified as a member of the N-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. 7-Hydroxyoct-7-enoylglycine is considered to be slightly soluble (in water) and acidic.
(+/-)-(E)-Ethyl-2-[(E)-hydroxyimino]-5-nitro-3-hexeneamide
4-(2-Pyridylazo)resorcinol
D019995 - Laboratory Chemicals > D007202 - Indicators and Reagents > D002863 - Chromogenic Compounds D004396 - Coloring Agents
3-(1,2,5,6-Tetrahydropyrid-4-yl)pyrrolo(3,2-b)pyrid-5-one
Naftazone
C - Cardiovascular system > C05 - Vasoprotectives > C05C - Capillary stabilizing agents D006401 - Hematologic Agents > D003029 - Coagulants > D006490 - Hemostatics C78275 - Agent Affecting Blood or Body Fluid > C78311 - Hemostatic Agent
1-(3-phenylpropanoyl)-2H-pyrrol-5-one
C13H13NO2 (215.09462380000002)
4-(2-Pyridylazo)resorcinol
D019995 - Laboratory Chemicals > D007202 - Indicators and Reagents > D002863 - Chromogenic Compounds D004396 - Coloring Agents
2,3,4,9-tetrahydro-1H-carbazole-3-carboxylic acid
C13H13NO2 (215.09462380000002)
N-(3-(p-hydroxyphenyl)propanoyl)pyrrole|piperlotine-E
C13H13NO2 (215.09462380000002)
1-(4-amino-imidazol-1-yl)-xi-D-1-deoxy-ribofuranose|5-Amino-imidazolribosid
1-(3-phenylprop-2-enoyl)pyrrolidin-2-one
C13H13NO2 (215.09462380000002)
(E)-4-hydroxy-2,2-bipyridine-6-carbaldehyde oxime|caerulomycin H
3-(2-oxo-2-phenylethyl)-5, 6-dihydropyridin-2(1H)-one|callylactam A
C13H13NO2 (215.09462380000002)
(E)-2-cyano-3-phenyl-but-2-enoic acid ethyl ester|2-Cyan-3-phenyl-cis-crotonsaeure-aethylester|2-cyano-3-phenyl-cis-crotonic acid ethyl ester|ethyl (E)-2-cyano-3-methyl-3-phenyl-2-propenoate|ethyl(E)-2-cyano-3-methyl-3-phenyl-2-propenoate
C13H13NO2 (215.09462380000002)
3-(benzyloxy)-2-methyl-4(1H)-pyridinone
C13H13NO2 (215.09462380000002)
4-(1-methyl-5-hydroxy-2-pyrrolidinyl)-3-oxobutanoate methyl ester
Kinetin
D006133 - Growth Substances > D010937 - Plant Growth Regulators > D003583 - Cytokinins relative retention time with respect to 9-anthracene Carboxylic Acid is 0.604 COVID info from PDB, Protein Data Bank Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS relative retention time with respect to 9-anthracene Carboxylic Acid is 0.594 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.598 Acquisition and generation of the data is financially supported by the Max-Planck-Society IPB_RECORD: 2421; CONFIDENCE confident structure Kinetin (N6-furfuryladenine) belongs to the family of N6-substituted adenine derivatives known as cytokinins, which are plant hormones involved in cell division, differentiation and other physiological processes. Kinetin has anti-aging effects[1]. Kinetin (N6-furfuryladenine) belongs to the family of N6-substituted adenine derivatives known as cytokinins, which are plant hormones involved in cell division, differentiation and other physiological processes. Kinetin has anti-aging effects[1]. Kinetin (N6-furfuryladenine) belongs to the family of N6-substituted adenine derivatives known as cytokinins, which are plant hormones involved in cell division, differentiation and other physiological processes. Kinetin has anti-aging effects[1].
3-(2-Naphthyl)-D-alanine
C13H13NO2 (215.09462380000002)
relative retention time with respect to 9-anthracene Carboxylic Acid is 0.477 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.475 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.471
2-hydroxy-1-phenyl-5,6,7,8-tetrahydropyrrolizin-3-one
C13H13NO2 (215.09462380000002)
2-hydroxy-1-phenyl-5,6,7,8-tetrahydropyrrolizin-3-one
C13H13NO2 (215.09462380000002)
3-hydroxy-C6-homoserine lactone
CONFIDENCE standard compound; INTERNAL_ID 214
2,2-(3-Chlorophenylimino)diethanol
CONFIDENCE standard compound; INTERNAL_ID 763; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8088; ORIGINAL_PRECURSOR_SCAN_NO 8086 CONFIDENCE standard compound; INTERNAL_ID 763; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8109; ORIGINAL_PRECURSOR_SCAN_NO 8107 CONFIDENCE standard compound; INTERNAL_ID 763; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8113; ORIGINAL_PRECURSOR_SCAN_NO 8111 CONFIDENCE standard compound; INTERNAL_ID 763; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8104; ORIGINAL_PRECURSOR_SCAN_NO 8103 CONFIDENCE standard compound; INTERNAL_ID 763; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8092; ORIGINAL_PRECURSOR_SCAN_NO 8090 CONFIDENCE standard compound; INTERNAL_ID 763; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8111; ORIGINAL_PRECURSOR_SCAN_NO 8109
N-(furan-2-ylmethyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine
N4-Benzoylcytosine
N4-Benzoylcytosine is a biochemical reagent that can be used as a biological material or organic compound for life science related research[1].
tert-butyl 3-hydroxy-4-oxopiperidine-1-carboxylate
3-FORMYL-MORPHOLINE-4-CARBOXYLIC ACID TERT-BUTYL ESTER
methyl 6-cyano-1-methylpyrrolo[3,2-b]pyridine-2-carboxylate
5-(4-FLUORO-3-NITROPHENYL)-2H-TETRAZOLE
C13H13NO2 (215.09462380000002)
3-(2,5-Dimethyl-1H-pyrrol-1-yl)benzoic acid
C13H13NO2 (215.09462380000002)
2-ETHYL-3-METHYL-QUINOLINE-4-CARBOXYLIC ACID
C13H13NO2 (215.09462380000002)
3-[3-(Trifluoromethyl)phenyl]pyrrolidine
C11H12F3N (215.09217879999997)
6-methoxy-1,2,3,4-tetrahydroisoquinolin-7-ol hydrochloride (en)
2,3,4,9-Tetrahydro-1H-carbazole-2-carboxylic acid
C13H13NO2 (215.09462380000002)
3-Phenyl-2-(1H-pyrrol-1-yl)propanoic acid
C13H13NO2 (215.09462380000002)
4-((TRIMETHYLSILYL)ETHYNYL)-7H-PYRROLO[2,3-D]PYRIMIDINE
C11H13N3Si (215.08786980000002)
2-(3-(TRIFLUOROMETHYL)PHENYL)PYRROLIDINE
C11H12F3N (215.09217879999997)
2,5,7-trimethylquinoline-4-carboxylic acid
C13H13NO2 (215.09462380000002)
N-(2-Amino-2-oxoethyl)-4-hydroxy-2-oxo-1-pyrrolidineacetamide
4-propan-2-yloxypyridine-2-carboximidamide,hydrochloride
2-Pentenoic Acid, 4-[[)1,1-Dimethylethoxy)Carbonyl]amino]-, (2E,4s)-(9CI)
(2-TRIFLUOROMETHYL-PYRIDIN-4-YL)-METHANOL
C13H13NO2 (215.09462380000002)
1-(2-benzofuranylcarbonyl)-pyrrolidine
C13H13NO2 (215.09462380000002)
3-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)benzonitrile
C12H14BNO2 (215.11175340000003)
5,6-Dihydro-4H-pyrrolo[3,2,1-ij]quinoline-1-carboxylic acid methyl ester
C13H13NO2 (215.09462380000002)
4-Pyridinecarboxylicacid, 2-(2-furanylmethylene)hydrazide
1-tert-butyl 2-methyl (2S)-azetidine-1,2-dicarboxylate
6-Quinolineacetic acid ethyl ester
C13H13NO2 (215.09462380000002)
1-(tert-Butoxycarbonyl)-3-methylazetidine-3-carboxylic acid
3-AMINO-3-(2,5-DIMETHOXYFURAN-3-YL)-PROPIONIC ACID
cyclopropylmethyl-(4-trifluoromethyl-phenyl)-amine hydrochloride
C11H12F3N (215.09217879999997)
(3S,7aR)-7a-methyl-3-phenyl-2,3-dihydropyrrolo[2,1-b][1,3]oxazol-5-one
C13H13NO2 (215.09462380000002)
ethyl 5-phenyl-1h-pyrrole-3-carboxylate
C13H13NO2 (215.09462380000002)
3-Quinolineaceticacid,2,4-dimethyl-(9CI)
C13H13NO2 (215.09462380000002)
5-(4-METHOXYPHENYL)-1-METHYLPYRIDIN-2(1H)-ONE
C13H13NO2 (215.09462380000002)
METHYL 2-(QUINOLIN-3-YL)PROPANOATE
C13H13NO2 (215.09462380000002)
1-methyl-3-Isoquinolinecarboxylic acid Ethyl ester
C13H13NO2 (215.09462380000002)
1-tert-butyl 2-methyl (2R)-azetidine-1,2-dicarboxylate
2-TERT-BUTOXYCARBONYLAMINO-3-(4-TERT-BUTOXYCARBONYLAMINO-PHENYL)-PROPIONICACID
Methyl 1-(tert-butoxycarbonylaMino)cyclopropanecarboxylate
Methyl 2-(4-(aminomethyl)phenyl)acetate hydrochloride
2-(hydroxyamino)-2-methyl-1-phenylpropan-1-one,hydrochloride
(R)-3-Amino-3-(1-naphthyl)-propionic acid
C13H13NO2 (215.09462380000002)
Ethyl 2-cyano-3-phenyl-2-butenoate
C13H13NO2 (215.09462380000002)
3-Furancarboxamide,2,5-dimethyl-N-phenyl-
C13H13NO2 (215.09462380000002)
4-(4-METHYLPHENYL)-1H-PYRROLE-3-CARBOXYLICACIDMETHYLESTER
C13H13NO2 (215.09462380000002)
methyl 2,4-dimethylquinoline-3-carboxylate
C13H13NO2 (215.09462380000002)
(R)-1-(1-PHENYLETHYL)-1H-PYRROLE-2-CARBOXYLIC ACID
C13H13NO2 (215.09462380000002)
1-(1-BENZYL-5-METHYL-1H-1,2,3-TRIAZOL-4-YL)ETHANONE
4-(2,5-dimethyl-pyrrol-1-yl)-benzoic acid
C13H13NO2 (215.09462380000002)
CYCLOPROPYLMETHYL-(3-TRIFLUOROMETHYL-PHENYL)-AMINE
C11H12F3N (215.09217879999997)
METHYL 2-(3-(AMINOMETHYL)PHENYL)ACETATE HYDROCHLORIDE
Methoxyphenamine hydrochloride
C78272 - Agent Affecting Nervous System > C29747 - Adrenergic Agent > C87053 - Adrenergic Agonist D018377 - Neurotransmitter Agents > D018663 - Adrenergic Agents > D000322 - Adrenergic Agonists
1-[(4-methoxyphenyl)methyl]pyrrole-2-carbaldehyde
C13H13NO2 (215.09462380000002)
2-propan-2-ylquinoline-4-carboxylic acid
C13H13NO2 (215.09462380000002)
Benzoic acid, 3-(1-aminoethyl)-, Methyl ester, hydrochloride
4-[(DIMETHYLAMINO)METHYL]-2,6-DIMETHYLPHENOL HYDROCHLORIDE
L-Methylephedrine hydrochloride
C78272 - Agent Affecting Nervous System > C29747 - Adrenergic Agent > C87053 - Adrenergic Agonist
Benzoic acid,2-(2,5-dimethyl-1H-pyrrol-1-yl)-
C13H13NO2 (215.09462380000002)
Ethyl 2-methyl-3-quinolinecarboxylate
C13H13NO2 (215.09462380000002)
6-ethyl-2-methylquinoline-3-carboxylic acid
C13H13NO2 (215.09462380000002)
3-(methoxymethyl)azetidine; trifluoroacetic acid
C7H12F3NO3 (215.07692379999997)
2-PHENYL-4,5,6,7-TETRAHYDRO-1H-PYRAZOLO[3,4-C]PYRIDIN-3(2H)-ONE
(4-METHYLPIPERIDINO)(4-PIPERIDINYL)METHANONEHYDROCHLORIDE
C8H13N3O2S (215.07284380000002)
3-(3-Trifluoromethylphenyl)pyrrolidine
C11H12F3N (215.09217879999997)
methyl 1-benzylpyrrole-2-carboxylate
C13H13NO2 (215.09462380000002)
2-METHYL-1,2,3,4-TETRAHYDRO-6,7-TSOQUINOLINEDIOL HYDROCHLORIDE
5-amino-1-(6-methoxypyridin-2-yl)pyrazole-4-carbonitrile
2-methyl-1-oxido-5-phenylmethoxypyridin-1-ium
C13H13NO2 (215.09462380000002)
(5-phenylmethoxypyridin-2-yl)methanol
C13H13NO2 (215.09462380000002)
2-(4-TRIFLUOROMETHYLphenyl)pyrrolidine
C11H12F3N (215.09217879999997)
(S)-3-AMino-3-phenyl propionic acid Methylester HCl
Mexiletine hydrochloride
D002317 - Cardiovascular Agents > D026941 - Sodium Channel Blockers > D061567 - Voltage-Gated Sodium Channel Blockers C78274 - Agent Affecting Cardiovascular System > C47793 - Antiarrhythmic Agent D002317 - Cardiovascular Agents > D000889 - Anti-Arrhythmia Agents D049990 - Membrane Transport Modulators C93038 - Cation Channel Blocker
1-(3-HYDROXY-PHENYL)-2,5-DIMETHYL-1H-PYRROLE-3-CARBALDEHYDE
C13H13NO2 (215.09462380000002)
4-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)benzonitrile
C12H14BNO2 (215.11175340000003)
1,2,3,4-Tetrahydro-7-methoxy-6-isoquinolinol hydrochloride
5-ETHOXY-1-METHYL-3,4-DIHYDRO-2H-PYRROL-1-IUM TETRAFLUOROBORATE
C7H14BF4NO (215.11045119999997)
(3-(Benzyloxy)pyridin-2-yl)methanol
C13H13NO2 (215.09462380000002)
4-(1-HYDROXY-2-(PYRIDIN-3-YL)ETHYL)PHENOL
C13H13NO2 (215.09462380000002)
2-(PYRIDIN-2-YL)-5,6,7,8-TETRAHYDRO-4H-OXAZOLO[4,5-C]AZEPINE
2-AMINO-1-(2-FURYLMETHYL)-4,5-DIMETHYL-1H-PYRROLE-3-CARBONITRILE
4-Oxo-1,3-piperidinedicarboxylic acid 1,3-dimethyl ester
3,4-Diamino-N,N-dimethylbenzenesulfonamide
C8H13N3O2S (215.07284380000002)
1,3-DIHYDRO-1-(1,2,3,6-TETRAHYDRO-4-PYRIDINYL)-2H-BENZIMIDAZOLE-2-ONE
CYCLOPROPYL(1-METHYL-1H-IMIDAZOL-2-YL)METHYL]AMINE
C13H13NO2 (215.09462380000002)
3-(3-CYANO-PHENYL)-2-METHYL-ACRYLIC ACID ETHYL ESTER
C13H13NO2 (215.09462380000002)
1-(6-Methoxy-2-naphthyl)ethan-1-one oxime
C13H13NO2 (215.09462380000002)
2,6-dimethylquinoline-4-carbohydrazide(SALTDATA: FREE)
4-Quinolinecarboxylicacid,2,8-dimethyl-,hydrazide(9CI)
Ethyl 2-methyl-6-quinolinecarboxylate
C13H13NO2 (215.09462380000002)
4-ETHYL-6-FLUORO-1,2,3,4-TETRAHYDROISOQUINOLINEHYDROCHLORIDE
(S)-2-(METHYLAMINO)-3-PHENYLPROPANOIC ACID HYDROCHLORIDE
4-(DIMETHYLAMINO)-1-NAPHTHOIC ACID
C13H13NO2 (215.09462380000002)
(4-((Dimethylamino)methyl)phenyl)boronic acid hydrochloride
1-(2-hydroxyphenyl)-2,5-dimethylpyrrole-3-carbaldehyde
C13H13NO2 (215.09462380000002)
2,5,7-Trimethylquinoline-3-carboxylic acid
C13H13NO2 (215.09462380000002)
2,5,8-Trimethylquinoline-3-carboxylic acid
C13H13NO2 (215.09462380000002)
8-ethyl-2-methylquinoline-4-carboxylic acid(SALTDATA: FREE)
C13H13NO2 (215.09462380000002)
2-Propylquinoline-4-carboxylic acid
C13H13NO2 (215.09462380000002)
(S)-3-Amino-3-(2-naphthyl)propanoic acid
C13H13NO2 (215.09462380000002)
(R)-3-Amino-3-(2-naphthyl)-propionic acid
C13H13NO2 (215.09462380000002)
1H-Pyrrolo[2,3-b]pyridine-2-carboxylic acid, 3-(cyanomethyl)-, Methyl ester
5-AMINO-NAPHTHALENE-1-CARBOXYLIC ACID ETHYL ESTER
C13H13NO2 (215.09462380000002)
2-METHYL-5-(PROPYLSULFONYL)PYRIMIDIN-4-AMINE
C8H13N3O2S (215.07284380000002)
l-3-(1-naphthyl)alanine
C13H13NO2 (215.09462380000002)
6-chloro-4-N-ethyl-2-N-propyl-1,3,5-triazine-2,4-diamine
4-AMINO-2,3-DIFLUOROBENZENE ACETIC ACID ETHYL ESTER
Glycine,N-(phenylmethyl)-, methyl ester, hydrochloride (9CI)
5-(dimethylamino)naphthalene-1-carboxylic acid
C13H13NO2 (215.09462380000002)
Benzeneacetic acid, 4-amino-, ethyl ester, hydrochloride(1:1)
(S)-3-AMINO-3-(NAPHTHALEN-1-YL)PROPANOIC ACID
C13H13NO2 (215.09462380000002)
4-HYDRAZINO-N-METHYLBENZENEMETHANESULFONAMIDE
C8H13N3O2S (215.07284380000002)
N-(BENZO[D][1,3]DIOXOL-5-YLMETHYL)ETHANAMINE HYDROCHLORIDE
1-(2,3-DIHYDROBENZO[B][1,4]DIOXIN-6-YL)-N-METHYLMETHANAMINE HYDROCHLORIDE
3-[4-(Trifluoromethyl)phenyl]pyrrolidine
C11H12F3N (215.09217879999997)
DL-3-Amino-3-(2-naphthyl)propionic acid
C13H13NO2 (215.09462380000002)
8-CYANO-IMIDAZO[1,2-A]PYRIDINE-2-CARBOXYLIC ACID ETHYL ESTER
2,6,8-TRIMETHYL-QUINOLINE-3-CARBOXYLIC ACID
C13H13NO2 (215.09462380000002)
3,4-dihydro-2H-1,5-benzodioxepin-6-ylmethanamine hydrochloride
Methyl 2-amino-4,5-dimethyl-benzoate hydrochloride
(S)-2-(2-(TRIFLUOROMETHYL)PHENYL)PYRROLIDINE
C11H12F3N (215.09217879999997)
(2S)-2-[3-(TRIFLUOROMETHYL)PHENYL]PYRROLIDINE
C11H12F3N (215.09217879999997)
(S)-3-(1-Amino-ethyl)-benzoic acid methyl ester hydrochloride
ALPHA-ETHYL-3-HYDROXY-4-METHYLPHENETHYLAMINE HYDROCHLORIDE
1-methyl-3-(phenylmethoxy)-4(1H)-Pyridinone
C13H13NO2 (215.09462380000002)
3-amino-3-naphthalen-1-ylpropanoic acid
C13H13NO2 (215.09462380000002)
N-(3-(Aminomethyl)pyridin-2-yl)-N-methylmethanesulfonamide
C8H13N3O2S (215.07284380000002)
2-chloro-4-ethylamino-15n-6-isopropylamino-1,3,5-triazine
2-(5,5-DIMETHYL-1,3,2-DIOXABORINAN-2-YL)BENZONITRILE
C12H14BNO2 (215.11175340000003)
[6-(4-methoxyphenyl)pyridin-3-yl]methanol
C13H13NO2 (215.09462380000002)
PYRROLIDINE, 1-[4-(TRIFLUOROMETHYL)PHENYL]-
C11H12F3N (215.09217879999997)
1-({6-[(1-CYANOCYCLOHEXYL)AMINO]-HEXYL}AMINO)CYCLOHEXANECARBONITRILE
C8H13N3O2S (215.07284380000002)
D-Phenylglycine ethyl ester hydrochloride
D-(-)-α-Phenylglycine ethyl ester hydrochloride is a Glycine (HY-Y0966) derivative[1].
2-(2-(TRIFLUOROMETHYL)PHENYL)PYRROLIDINE
C11H12F3N (215.09217879999997)
2h-1-benzopyran, 4-amino-3,4-dihydro-7-methoxy-, hydrochloride
ETHYL 4-PHENYLPYRROLE-3-CARBOXYLATE
C13H13NO2 (215.09462380000002)
ethyl 2-methylquinoline-4-carboxylate
C13H13NO2 (215.09462380000002)
n-(7-methoxynaphthalen-1-yl)acetamide
C13H13NO2 (215.09462380000002)
2,3,4,9-TETRAHYDRO-1H-CARBAZOLE-6-CARBOXYLIC ACID
C13H13NO2 (215.09462380000002)
1H-Pyrrole-2-propanoicacid, 5-phenyl-
C13H13NO2 (215.09462380000002)
2,5-dimethyl-1-phenyl-pyrrole-3-carboxylic acid
C13H13NO2 (215.09462380000002)
2,3,4,9-tetrahydro-1H-carbazole-8-carboxylic acid(SALTDATA: FREE)
C13H13NO2 (215.09462380000002)
ac-his-oh h2o
N-Acetyl-L-histidine monohydrate, a histidine derivative, is a prominent biomolecule in brain, retina and lens of poikilothermic vertebrates. N-Acetyl-L-histidine monohydrate has a role as an animal metabolite[1].
Ethyl (6-methyl-2-pyridinyl)acetate hydrochloride (1:1)
6-Amino-2-Methyl-1,7-Dihydro-8h-Imidazo[4,5-G]quinazolin-8-One
(E,2Z)-4-Ethyl-2-hydroxyimino-5-nitro-hex-3-enamide
D006401 - Hematologic Agents > D010975 - Platelet Aggregation Inhibitors D002317 - Cardiovascular Agents > D000959 - Antihypertensive Agents D002317 - Cardiovascular Agents > D020030 - Nitric Oxide Donors D002317 - Cardiovascular Agents > D014665 - Vasodilator Agents D004791 - Enzyme Inhibitors
3-(1,2,5,6-Tetrahydropyrid-4-yl)pyrrolo(3,2-b)pyrid-5-one
D018377 - Neurotransmitter Agents > D018490 - Serotonin Agents > D017366 - Serotonin Receptor Agonists
2,4,6-Heptatrienamide, N-hydroxy-7-phenyl-, (2E,4E,6E)-
C13H13NO2 (215.09462380000002)
D004791 - Enzyme Inhibitors > D056572 - Histone Deacetylase Inhibitors
2-Methyl-4-phenyl-1H-pyrrole-3-carboxylic acid methyl ester
C13H13NO2 (215.09462380000002)
6-Benzyl-1-Hydroxy-4-Methylpyridin-2(1h)-One
C13H13NO2 (215.09462380000002)
Bruceolline J
C13H13NO2 (215.09462380000002)
An indole alkaloid that is 1,2,3,4-tetrahydrocyclopenta[b]indole substituted by a hydroxy group at position 2, geminal-methyl groups at position 3 and an oxo group at position 1. It has been isolated from the ethanol extract of the stems of Brucea mollis.
1,8(2H,5H)-Acridinedione, 3,4,6,7-tetrahydro-
C13H13NO2 (215.09462380000002)
3-Hydroxy-2-methyl-1-(phenylmethyl)-4-pyridinone
C13H13NO2 (215.09462380000002)
6-(Dimethylamino)-2-naphthoic acid
C13H13NO2 (215.09462380000002)
6-(3-methylbut-2-enyl)-1H-indole-2,3-dione
C13H13NO2 (215.09462380000002)
Ovothiol B
C8H13N3O2S (215.07284380000002)
A L-histidine derivative that is N-methyl-L-histidine substituted at positions N3 and C5 on the imidazole ring by methyl and mercapto groups respectively.
2,7-Dimethyl-5-(trifluoromethyl)pyrazolo[1,5-a]pyrimidine
N-Crotonylglycine, trimethylsilyl ester
C9H17NO3Si (215.09776520000003)
Trimethylsilyl (methacryloylamino)acetate
C9H17NO3Si (215.09776520000003)
naftazone
C - Cardiovascular system > C05 - Vasoprotectives > C05C - Capillary stabilizing agents D006401 - Hematologic Agents > D003029 - Coagulants > D006490 - Hemostatics C78275 - Agent Affecting Blood or Body Fluid > C78311 - Hemostatic Agent
3-Methoxy-5-methyl-1-naphthoate
A naphthoate that is the conjugate base of 3-methoxy-5-methyl-1-naphthoic acid, obtained by deprotonation of the carboxy group; major species at pH 7.3.
Mexitil
D002317 - Cardiovascular Agents > D026941 - Sodium Channel Blockers > D061567 - Voltage-Gated Sodium Channel Blockers D002317 - Cardiovascular Agents > D000889 - Anti-Arrhythmia Agents D049990 - Membrane Transport Modulators
N-(4-methyl-5-thiadiazolyl)carbamic acid 2-methylpropyl ester
C8H13N3O2S (215.07284380000002)
(2S)-2-(methylazaniumyl)-3-(1-methyl-4-sulfanyl-1H-imidazol-5-yl)propanoate
C8H13N3O2S (215.07284380000002)
N(alpha)-acetyl-L-argininate
An N-acyl-L-alpha-amino acid anion arising from deprotonation of the carboxy group of N(alpha)-acetyl-L-arginine; major species at pH 7.3.
ovothiol B zwitterion
C8H13N3O2S (215.07284380000002)
An L-alpha-amino acid zwitterion formed from ovothiol B by transfer of a proton from the carboxy to the amino group; major species at pH 7.3.
desmethylnaproxen(1-)
A monocarboxylic acid anion that is the conjugate base of desmethylnaproxen, obtained by deprotonation of the carboxy group; major species at pH 7.3.
caerulomycin H
A pyridine alkaloid that is 2,2-bipyridine substituted by a hydroxy group at position 4 and a (E)-(hydroxyimino)methyl group at position 6. Isolated from the marine-derived actinomycete Actinoalloteichus cyanogriseus, it exhibits antineoplastic activity.
3-{[(2s)-3-(hydroxymethyl)-2,5-dihydrofuran-2-yl]-c-hydroxycarbonimidoyl}propanoic acid
1-(3-phenylpropanoyl)-5h-pyrrol-2-one
C13H13NO2 (215.09462380000002)
n-[4-chloro-6-(ethylimino)-1,3-dihydro-1,3,5-triazin-2-ylidene]propan-2-amine
(2z)-2-(3-carbamimidamidopropylidene)butanedioic acid
n-[2-(3h-imidazol-4-yl)ethyl]benzenecarboximidic acid
2-(5-aminoimidazol-1-yl)-5-(hydroxymethyl)oxolane-3,4-diol
(2e,3e)-2-(ethoxyimino)-5-nitrohex-3-enimidic acid
6-(3-methylbut-2-en-1-yl)-1h-indole-2,3-dione
C13H13NO2 (215.09462380000002)
(3s)-2,3,4,9-tetrahydro-1h-carbazole-3-carboxylic acid
C13H13NO2 (215.09462380000002)
(3s)-3,7-dimethyl-2-oxa-6-azatricyclo[7.3.1.0⁵,¹³]trideca-1(13),5,7,9,11-pentaen-11-ol
C13H13NO2 (215.09462380000002)
(2r,3r,4r,5s)-2-(5-aminoimidazol-1-yl)-5-(hydroxymethyl)oxolane-3,4-diol
1-[(2e)-3-phenylprop-2-enoyl]pyrrolidin-2-one
C13H13NO2 (215.09462380000002)
2-(4-methyl-1,3-thiazol-5-yl)ethyl 2-hydroxypropanoate
2-hydroxy-1-phenyl-5,6,7,7a-tetrahydropyrrolizin-3-one
C13H13NO2 (215.09462380000002)
(3r,5r)-3,5-dihydroxy-1-[3-(hydroxymethyl)-2,5-dihydrofuran-2-yl]pyrrolidin-2-one
3-(4-hydroxyphenyl)-1-(pyrrol-1-yl)propan-1-one
C13H13NO2 (215.09462380000002)
(7ar)-2-hydroxy-1-phenyl-5,6,7,7a-tetrahydropyrrolizin-3-one
C13H13NO2 (215.09462380000002)
2,3-dihydroxypropyl 1-hydroxy-4-methylpyrrole-2-carboxylate
(2e)-4-methoxy-n-[(2s)-1-methoxy-1-oxopropan-2-yl]-4-oxobut-2-enimidic acid
3,5-dihydroxy-1-[3-(hydroxymethyl)-2,5-dihydrofuran-2-yl]pyrrolidin-2-one
2-(hydroxymethyl)-4-methyl-1h,6h,7h-cyclopenta[g]indol-8-one
C13H13NO2 (215.09462380000002)
(3r,5r)-3,5-dihydroxy-1-[(2r)-3-(hydroxymethyl)-2,5-dihydrofuran-2-yl]pyrrolidin-2-one
5-(3-methylbut-2-en-1-yl)-1h-indole-2,3-dione
C13H13NO2 (215.09462380000002)
(3e)-4-ethyl-2-(hydroxyimino)-5-nitrohex-3-enimidic acid
10-imino-2,7-dimethyl-2,7-diazatricyclo[6.3.1.0⁴,¹²]dodeca-1(12),3,8-trien-11-one
3-{[3-(hydroxymethyl)-2,5-dihydrofuran-2-yl]-c-hydroxycarbonimidoyl}propanoic acid
7-(3-methylbut-2-en-1-yl)-1h-indole-2,3-dione
C13H13NO2 (215.09462380000002)
(3r)-3,7-dimethyl-2-oxa-6-azatricyclo[7.3.1.0⁵,¹³]trideca-1(13),5,7,9,11-pentaen-11-ol
C13H13NO2 (215.09462380000002)
6-(3-methylbut-1-en-2-yl)-1h-indole-2,3-dione
C13H13NO2 (215.09462380000002)
3-methoxy-5-methylnaphthalene-1-carboximidic acid
C13H13NO2 (215.09462380000002)