Exact Mass: 415.2359
Exact Mass Matches: 415.2359
Found 500 metabolites which its exact mass value is equals to given mass value 415.2359,
within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error
0.01 dalton.
(4Z)-3-Hydroxytetradec-4-enedioylcarnitine
(4Z)-3-Hydroxytetradec-4-enedioylcarnitine is an acylcarnitine. More specifically, it is an (4Z)-3-hydroxytetradec-4-enedioic 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. (4Z)-3-Hydroxytetradec-4-enedioylcarnitine is therefore classified as a long chain AC. As a long-chain acylcarnitine (4Z)-3-Hydroxytetradec-4-enedioylcarnitine is generally formed through esterification with long-chain fatty acids obtained from the diet. The main function of most long-chain acylcarnitines is to ensure long chain fatty acid transport into the mitochondria (PMID: 22804748). Altered levels of long-chain acylcarnitines can serve as useful markers for inherited disorders of long-chain fatty acid metabolism. Carnitine palmitoyltransferase I (CPT I, EC:2.3.1.21) is involved in the synthesis of long-chain acylcarnitines (more than C12) on the mitochondrial outer membrane. Elevated serum/plasma levels of long-chain acylcarnitines are not only markers for incomplete FA oxidation but also are indicators of altered carbohydrate and lipid metabolism. High serum concentrations of long-chain acylcarnitines in the postprandial or fed state are markers of insulin resistance and arise from insulins inability to inhibit CPT-1-dependent fatty acid metabolism in muscles and the heart (PMID: 19073774). Increased intracellular content of long-chain acylcarnitines is thought to serve as a feedback inhibition mechanism of insulin action (PMID: 23258903). In healthy subjects, increased concentrations of insulin effectively inhibits long-chain acylcarnitine production. Several studies have also found increased levels of circulating long-chain acylcarnitines in chronic heart failure patients (PMID: 26796394). 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].
(9E)-3-Hydroxytetradec-5-enedioylcarnitine
(9E)-3-Hydroxytetradec-5-enedioylcarnitine is an acylcarnitine. More specifically, it is an (9E)-3-hydroxytetradec-5-enedioic 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. (9E)-3-Hydroxytetradec-5-enedioylcarnitine is therefore classified as a long chain AC. As a long-chain acylcarnitine (9E)-3-Hydroxytetradec-5-enedioylcarnitine is generally formed through esterification with long-chain fatty acids obtained from the diet. The main function of most long-chain acylcarnitines is to ensure long chain fatty acid transport into the mitochondria (PMID: 22804748). Altered levels of long-chain acylcarnitines can serve as useful markers for inherited disorders of long-chain fatty acid metabolism. Carnitine palmitoyltransferase I (CPT I, EC:2.3.1.21) is involved in the synthesis of long-chain acylcarnitines (more than C12) on the mitochondrial outer membrane. Elevated serum/plasma levels of long-chain acylcarnitines are not only markers for incomplete FA oxidation but also are indicators of altered carbohydrate and lipid metabolism. High serum concentrations of long-chain acylcarnitines in the postprandial or fed state are markers of insulin resistance and arise from insulins inability to inhibit CPT-1-dependent fatty acid metabolism in muscles and the heart (PMID: 19073774). Increased intracellular content of long-chain acylcarnitines is thought to serve as a feedback inhibition mechanism of insulin action (PMID: 23258903). In healthy subjects, increased concentrations of insulin effectively inhibits long-chain acylcarnitine production. Several studies have also found increased levels of circulating long-chain acylcarnitines in chronic heart failure patients (PMID: 26796394). 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].
(2E)-5-Hydroxytetradec-2-enedioylcarnitine
(2E)-5-Hydroxytetradec-2-enedioylcarnitine is an acylcarnitine. More specifically, it is an (2E)-5-hydroxytetradec-2-enedioic 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. (2E)-5-Hydroxytetradec-2-enedioylcarnitine is therefore classified as a long chain AC. As a long-chain acylcarnitine (2E)-5-Hydroxytetradec-2-enedioylcarnitine is generally formed through esterification with long-chain fatty acids obtained from the diet. The main function of most long-chain acylcarnitines is to ensure long chain fatty acid transport into the mitochondria (PMID: 22804748). Altered levels of long-chain acylcarnitines can serve as useful markers for inherited disorders of long-chain fatty acid metabolism. Carnitine palmitoyltransferase I (CPT I, EC:2.3.1.21) is involved in the synthesis of long-chain acylcarnitines (more than C12) on the mitochondrial outer membrane. Elevated serum/plasma levels of long-chain acylcarnitines are not only markers for incomplete FA oxidation but also are indicators of altered carbohydrate and lipid metabolism. High serum concentrations of long-chain acylcarnitines in the postprandial or fed state are markers of insulin resistance and arise from insulins inability to inhibit CPT-1-dependent fatty acid metabolism in muscles and the heart (PMID: 19073774). Increased intracellular content of long-chain acylcarnitines is thought to serve as a feedback inhibition mechanism of insulin action (PMID: 23258903). In healthy subjects, increased concentrations of insulin effectively inhibits long-chain acylcarnitine production. Several studies have also found increased levels of circulating long-chain acylcarnitines in chronic heart failure patients (PMID: 26796394). 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].
(5Z)-3-Hydroxytetradec-5-enedioylcarnitine
(5Z)-3-Hydroxytetradec-5-enedioylcarnitine is an acylcarnitine. More specifically, it is an (5Z)-3-hydroxytetradec-5-enedioic 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. (5Z)-3-Hydroxytetradec-5-enedioylcarnitine is therefore classified as a long chain AC. As a long-chain acylcarnitine (5Z)-3-Hydroxytetradec-5-enedioylcarnitine is generally formed through esterification with long-chain fatty acids obtained from the diet. The main function of most long-chain acylcarnitines is to ensure long chain fatty acid transport into the mitochondria (PMID: 22804748). Altered levels of long-chain acylcarnitines can serve as useful markers for inherited disorders of long-chain fatty acid metabolism. Carnitine palmitoyltransferase I (CPT I, EC:2.3.1.21) is involved in the synthesis of long-chain acylcarnitines (more than C12) on the mitochondrial outer membrane. Elevated serum/plasma levels of long-chain acylcarnitines are not only markers for incomplete FA oxidation but also are indicators of altered carbohydrate and lipid metabolism. High serum concentrations of long-chain acylcarnitines in the postprandial or fed state are markers of insulin resistance and arise from insulins inability to inhibit CPT-1-dependent fatty acid metabolism in muscles and the heart (PMID: 19073774). Increased intracellular content of long-chain acylcarnitines is thought to serve as a feedback inhibition mechanism of insulin action (PMID: 23258903). In healthy subjects, increased concentrations of insulin effectively inhibits long-chain acylcarnitine production. Several studies have also found increased levels of circulating long-chain acylcarnitines in chronic heart failure patients (PMID: 26796394). 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].
(7Z)-3-Hydroxytetradec-7-enedioylcarnitine
(7Z)-3-Hydroxytetradec-7-enedioylcarnitine is an acylcarnitine. More specifically, it is an (7Z)-3-hydroxytetradec-7-enedioic 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. (7Z)-3-Hydroxytetradec-7-enedioylcarnitine is therefore classified as a long chain AC. As a long-chain acylcarnitine (7Z)-3-Hydroxytetradec-7-enedioylcarnitine is generally formed through esterification with long-chain fatty acids obtained from the diet. The main function of most long-chain acylcarnitines is to ensure long chain fatty acid transport into the mitochondria (PMID: 22804748). Altered levels of long-chain acylcarnitines can serve as useful markers for inherited disorders of long-chain fatty acid metabolism. Carnitine palmitoyltransferase I (CPT I, EC:2.3.1.21) is involved in the synthesis of long-chain acylcarnitines (more than C12) on the mitochondrial outer membrane. Elevated serum/plasma levels of long-chain acylcarnitines are not only markers for incomplete FA oxidation but also are indicators of altered carbohydrate and lipid metabolism. High serum concentrations of long-chain acylcarnitines in the postprandial or fed state are markers of insulin resistance and arise from insulins inability to inhibit CPT-1-dependent fatty acid metabolism in muscles and the heart (PMID: 19073774). Increased intracellular content of long-chain acylcarnitines is thought to serve as a feedback inhibition mechanism of insulin action (PMID: 23258903). In healthy subjects, increased concentrations of insulin effectively inhibits long-chain acylcarnitine production. Several studies have also found increased levels of circulating long-chain acylcarnitines in chronic heart failure patients (PMID: 26796394). 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].
N-Demethyl Mifepristone
(2S)-2-[[(2S)-2-Amino-3-(1H-imidazol-5-yl)propanoyl]-(2-benzamidoethyl)amino]-4-methylpentanoic acid
3-benzhydryloxy-1-[2-(1,3-benzodioxol-5-yl)ethyl]piperidine
AM toxin-II|Am-II-Toxin|AM-toxin II|N-(L-2-hydroxy-3-methyl-butyryl)-5-phenyl-L-norvalyl->2,3-didehydro-alanyl->L-alanine lactone|toxin II (Alternaria mali)
zamifenacin
C78272 - Agent Affecting Nervous System > C66880 - Anticholinergic Agent > C29704 - Antimuscarinic Agent CONFIDENCE standard compound; INTERNAL_ID 734; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8319; ORIGINAL_PRECURSOR_SCAN_NO 8318 CONFIDENCE standard compound; INTERNAL_ID 734; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8358; ORIGINAL_PRECURSOR_SCAN_NO 8357 CONFIDENCE standard compound; INTERNAL_ID 734; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8363; ORIGINAL_PRECURSOR_SCAN_NO 8361 CONFIDENCE standard compound; INTERNAL_ID 734; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8403; ORIGINAL_PRECURSOR_SCAN_NO 8402 CONFIDENCE standard compound; INTERNAL_ID 734; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8404; ORIGINAL_PRECURSOR_SCAN_NO 8402 CONFIDENCE standard compound; INTERNAL_ID 734; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8409; ORIGINAL_PRECURSOR_SCAN_NO 8407 Zamifenacin (UK-76654) is a potent gut-selective muscarinic M3 receptor antagonist. Zamifenacin significantly reduces colonic motility in irritable bowel syndrome[1].
Ala Ala Arg Val
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Ala Lys Pro Thr
Ala Lys Thr Pro
Ala Leu Gly Arg
Ala Leu Asn Val
Ala Leu Arg Gly
Ala Leu Val Asn
Ala Asn Ile Val
Ala Asn Leu Val
Ala Asn Val Ile
Ala Asn Val Leu
Ala Pro Lys Thr
Ala Pro Gln Thr
Ala Pro Thr Lys
Ala Pro Thr Gln
Ala Gln Pro Thr
Ala Gln Thr Pro
Ala Gln Val Val
Ala Arg Ala Val
Ala Arg Gly Ile
Ala Arg Gly Leu
Ala Arg Ile Gly
Ala Arg Leu Gly
Ala Arg Val Ala
Ala Thr Lys Pro
Ala Thr Pro Lys
Ala Thr Pro Gln
Ala Thr Gln Pro
Ala Val Ala Arg
Ala Val Ile Asn
Ala Val Leu Asn
Ala Val Asn Ile
Ala Val Asn Leu
Ala Val Gln Val
Ala Val Arg Ala
Ala Val Val Gln
Asp Gly Lys Pro
Asp Gly Pro Lys
Asp Lys Gly Pro
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Gly Ala Ile Arg
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Gly Ala Arg Ile
Gly Ala Arg Leu
Gly Ile Ala Arg
Gly Ile Ile Asn
Gly Ile Leu Asn
Gly Ile Asn Ile
Gly Ile Asn Leu
Gly Ile Gln Val
Gly Ile Arg Ala
Gly Ile Val Gln
Gly Leu Ala Arg
Gly Leu Ile Asn
Gly Leu Leu Asn
Gly Leu Asn Ile
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Gly Leu Gln Val
Gly Leu Arg Ala
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Gly Asn Ile Ile
Gly Asn Ile Leu
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Gly Asn Leu Leu
Gly Pro Arg Ser
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Gly Gln Ile Val
Gly Gln Leu Val
Gly Gln Val Ile
Gly Gln Val Leu
Gly Arg Ala Ile
Gly Arg Ala Leu
Gly Arg Ile Ala
Gly Arg Leu Ala
Gly Arg Pro Ser
Gly Arg Ser Pro
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Gly Ser Arg Pro
Gly Val Ile Gln
Gly Val Leu Gln
Gly Val Gln Ile
Gly Val Gln Leu
Ile Ala Gly Arg
Ile Ala Asn Val
Ile Ala Arg Gly
Ile Ala Val Asn
Ile Gly Ala Arg
Ile Gly Ile Asn
Ile Gly Leu Asn
Ile Gly Asn Ile
Ile Gly Asn Leu
Ile Gly Gln Val
Ile Gly Arg Ala
Ile Gly Val Gln
Ile Ile Gly Asn
Ile Ile Asn Gly
Ile Leu Gly Asn
Ile Leu Asn Gly
Ile Asn Ala Val
Ile Asn Gly Ile
Ile Asn Gly Leu
Ile Asn Ile Gly
Ile Asn Leu Gly
Ile Asn Val Ala
Ile Gln Gly Val
Ile Gln Val Gly
Ile Arg Ala Gly
Ile Arg Gly Ala
Ile Val Ala Asn
Ile Val Gly Gln
Ile Val Asn Ala
Ile Val Gln Gly
Lys Ala Pro Thr
Lys Ala Thr Pro
Lys Pro Ala Thr
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Lys Thr Ala Pro
Lys Thr Pro Ala
Leu Ala Gly Arg
Leu Ala Asn Val
Leu Ala Arg Gly
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Leu Gly Ala Arg
Leu Gly Ile Asn
Leu Gly Leu Asn
Leu Gly Asn Ile
Leu Gly Asn Leu
Leu Gly Gln Val
Leu Gly Arg Ala
Leu Gly Val Gln
Leu Ile Gly Asn
Leu Ile Asn Gly
Leu Leu Gly Asn
Leu Leu Asn Gly
Leu Asn Ala Val
Leu Asn Gly Ile
Leu Asn Gly Leu
Leu Asn Ile Gly
Leu Asn Leu Gly
Leu Asn Val Ala
Leu Gln Gly Val
Leu Gln Val Gly
Leu Arg Ala Gly
Leu Arg Gly Ala
Leu Val Ala Asn
Leu Val Gly Gln
Leu Val Asn Ala
Leu Val Gln Gly
Asn Ala Ile Val
Asn Ala Leu Val
Asn Ala Val Ile
Asn Ala Val Leu
Asn Gly Ile Ile
Asn Gly Ile Leu
Asn Gly Leu Ile
Asn Gly Leu Leu
Asn Ile Ala Val
Asn Ile Gly Ile
Asn Ile Gly Leu
Asn Ile Ile Gly
Asn Ile Leu Gly
Asn Ile Val Ala
Asn Leu Ala Val
Asn Leu Gly Ile
Asn Leu Gly Leu
Asn Leu Ile Gly
Asn Leu Leu Gly
Asn Leu Val Ala
Asn Val Ala Ile
Asn Val Ala Leu
Asn Val Ile Ala
Asn Val Leu Ala
Pro Ala Lys Thr
Pro Ala Thr Lys
Pro Gly Arg Ser
Pro Gly Ser Arg
Pro Lys Ala Thr
Pro Lys Thr Ala
Pro Arg Gly Ser
Pro Arg Ser Gly
Pro Ser Gly Arg
Pro Ser Arg Gly
Pro Thr Ala Lys
Pro Thr Lys Ala
Gln Ala Val Val
Gln Gly Ile Val
Gln Gly Leu Val
Gln Gly Val Ile
Gln Gly Val Leu
Gln Ile Gly Val
Gln Ile Val Gly
Gln Leu Gly Val
Gln Leu Val Gly
Gln Val Ala Val
Gln Val Gly Ile
Gln Val Gly Leu
Gln Val Ile Gly
Gln Val Leu Gly
Gln Val Val Ala
Arg Ala Ala Val
Arg Ala Gly Ile
Arg Ala Gly Leu
Arg Ala Ile Gly
Arg Ala Leu Gly
Arg Ala Val Ala
Arg Gly Ala Ile
Arg Gly Ala Leu
Arg Gly Ile Ala
Arg Gly Leu Ala
Arg Gly Pro Ser
Arg Gly Ser Pro
Arg Ile Ala Gly
Arg Ile Gly Ala
Arg Leu Ala Gly
Arg Leu Gly Ala
Arg Pro Gly Ser
Arg Pro Ser Gly
Arg Ser Gly Pro
Arg Ser Pro Gly
Arg Val Ala Ala
Ser Gly Pro Arg
Ser Gly Arg Pro
Ser Pro Gly Arg
Ser Pro Arg Gly
Ser Arg Gly Pro
Ser Arg Pro Gly
Thr Ala Lys Pro
Thr Ala Pro Lys
Thr Lys Ala Pro
Thr Lys Pro Ala
Thr Pro Ala Lys
Thr Pro Lys Ala
Val Ala Ala Arg
Val Ala Ile Asn
Val Ala Leu Asn
Val Ala Asn Ile
Val Ala Asn Leu
Val Ala Gln Val
Val Ala Arg Ala
Val Ala Val Gln
Val Gly Ile Gln
Val Gly Leu Gln
Val Gly Gln Ile
Val Gly Gln Leu
Val Ile Ala Asn
Val Ile Gly Gln
Val Ile Asn Ala
Val Ile Gln Gly
Val Leu Ala Asn
Val Leu Gly Gln
Val Leu Asn Ala
Val Leu Gln Gly
Val Asn Ala Ile
Val Asn Ala Leu
Val Asn Ile Ala
Val Asn Leu Ala
Val Gln Ala Val
Val Gln Gly Ile
Val Gln Gly Leu
Val Gln Ile Gly
Val Gln Leu Gly
Val Gln Val Ala
Val Arg Ala Ala
Val Val Ala Gln
Val Val Gln Ala
3-phenylacrylic acid (2r,3s)-3-dibenzylamino-2-hydroxybutyl ester
Celiprolol HCl
C78272 - Agent Affecting Nervous System > C29747 - Adrenergic Agent > C72900 - Adrenergic Antagonist D018373 - Peripheral Nervous System Agents > D001337 - Autonomic Agents > D013566 - Sympathomimetics D018377 - Neurotransmitter Agents > D018663 - Adrenergic Agents > D018674 - Adrenergic Antagonists D002317 - Cardiovascular Agents > D000959 - Antihypertensive Agents D002317 - Cardiovascular Agents > D000889 - Anti-Arrhythmia Agents D002317 - Cardiovascular Agents > D014665 - Vasodilator Agents
(S)-2-(3-BENZOYLPHENYL)-N-(4-HYDROXYPHENETHYL)-N-ISOPROPYLPROPANAMIDE
(2R)-2-[4-[(4-chlorophenyl)methyl]-5-methyl-1,2,4-triazol-3-yl]-N-cycloheptylpyrrolidine-1-carboxamide
N-(3,4-Diethyloxy)phenylethyl-3,4-diethyloxyphenyl acetamide
N-[(1S)-2-[(1S,3S,5S)-3-Cyano-2-azabicyclo[3.1.0]hex-2-yl]-1-(3-hydroxytricyclo[3.3.1.13,7]dec-1-yl)-2-oxoethyl]carbamic acid 1,1-dimethylethyl ester
[1-acetyl-4-tert-butyl-3,6-bis(tert-butylsulfanyl)-3,6-dihydro-2H-pyridin-2-yl] acetate
N-[[4-(2-propan-2-yl-5-pyridin-4-ylpyrimidin-4-yl)cyclohexyl]methyl]pyridine-3-carboxamide
17-O-deacetylvindolinium
A vinca alkaloid cation that is the conjugate acid of 17-O-deacetylvindoline.
(2S)-2-[[(2S)-2-Amino-3-(1H-imidazol-5-yl)propanoyl]-(2-benzamidoethyl)amino]-4-methylpentanoic acid
smenospongines C
A sesquiterpenoid isolated from the marine sponge Dactylospongia elegans.
(12R,15S,16R,8R)-15-methoxy-7,8,10-trimethyl-6,9-dioxo-13,14,15,16-tetrahydro-12H-4-oxa-7,10-diaza-1(2,6)-pyrana-5(1,2)-benzenacycloundecaphane-56-carbonitrile
(1R,4R,5R,5S,8S)-1-methyl-5-(2-methylpropyl)-4-[(2S)-3-oxobutan-2-yl]spiro[2-oxatricyclo[6.4.1.04,13]tridec-4(13)-ene-5,3-pyrrolidine]-2,3,6-trione
[1-[3-(4-Methylphenoxy)propyl]-4-piperidinyl]-diphenylmethanol
(1S,12R,17S,20S)-20-methoxy-11,12,14-trimethyl-10,13-dioxo-3,21-dioxa-11,14-diazatricyclo[15.3.1.04,9]henicosa-4,6,8-triene-5-carbonitrile
4-[(3aR,4R,9bR)-1-[cyclohexyl(oxo)methyl]-4-(hydroxymethyl)-2,3,3a,4,5,9b-hexahydropyrrolo[3,2-c]quinolin-8-yl]benzonitrile
4-[(3aS,4R,9bS)-1-[cyclohexyl(oxo)methyl]-4-(hydroxymethyl)-2,3,3a,4,5,9b-hexahydropyrrolo[3,2-c]quinolin-8-yl]benzonitrile
4-[(3aR,4S,9bR)-1-[cyclohexyl(oxo)methyl]-4-(hydroxymethyl)-2,3,3a,4,5,9b-hexahydropyrrolo[3,2-c]quinolin-8-yl]benzonitrile
(1S,9R,10R,11R)-5-(cyclohexen-1-yl)-12-ethyl-10-(hydroxymethyl)-N-(2-methoxyethyl)-6-oxo-7,12-diazatricyclo[7.2.1.02,7]dodeca-2,4-diene-11-carboxamide
(1R,9S,10S,11S)-5-(cyclohexen-1-yl)-12-ethyl-10-(hydroxymethyl)-N-(2-methoxyethyl)-6-oxo-7,12-diazatricyclo[7.2.1.02,7]dodeca-2,4-diene-11-carboxamide
N-[[(2S,3R)-5-[(2S)-1-hydroxypropan-2-yl]-3-methyl-8-(3-methylbut-1-ynyl)-6-oxo-3,4-dihydro-2H-pyrido[2,3-b][1,5]oxazocin-2-yl]methyl]-N-methylpropanamide
N-[[(2R,3R)-5-[(2R)-1-hydroxypropan-2-yl]-3-methyl-8-(3-methylbut-1-ynyl)-6-oxo-3,4-dihydro-2H-pyrido[2,3-b][1,5]oxazocin-2-yl]methyl]-N-methylpropanamide
(1S,13S,17R,18R)-18-methoxy-12,13,15-trimethyl-11,14-dioxo-4,21-dioxa-12,15-diazatricyclo[15.3.1.05,10]henicosa-5,7,9-triene-6-carbonitrile
(1S,13R,17R,18S)-18-methoxy-12,13,15-trimethyl-11,14-dioxo-4,21-dioxa-12,15-diazatricyclo[15.3.1.05,10]henicosa-5,7,9-triene-6-carbonitrile
(1S,13R,17S,18S)-18-methoxy-12,13,15-trimethyl-11,14-dioxo-4,21-dioxa-12,15-diazatricyclo[15.3.1.05,10]henicosa-5,7,9-triene-6-carbonitrile
(1R,13R,17R,18R)-18-methoxy-12,13,15-trimethyl-11,14-dioxo-4,21-dioxa-12,15-diazatricyclo[15.3.1.05,10]henicosa-5,7,9-triene-6-carbonitrile
(1R,13R,17S,18S)-18-methoxy-12,13,15-trimethyl-11,14-dioxo-4,21-dioxa-12,15-diazatricyclo[15.3.1.05,10]henicosa-5,7,9-triene-6-carbonitrile
(1S,13R,17S,18R)-18-methoxy-12,13,15-trimethyl-11,14-dioxo-4,21-dioxa-12,15-diazatricyclo[15.3.1.05,10]henicosa-5,7,9-triene-6-carbonitrile
(1R,13R,17R,18R)-18-methoxy-12,13,15-trimethyl-11,14-dioxo-4,21-dioxa-12,15-diazatricyclo[15.3.1.05,10]henicosa-5(10),6,8-triene-8-carbonitrile
(1S,13S,17R,18R)-18-methoxy-12,13,15-trimethyl-11,14-dioxo-4,21-dioxa-12,15-diazatricyclo[15.3.1.05,10]henicosa-5(10),6,8-triene-8-carbonitrile
(1S,13R,17S,18R)-18-methoxy-12,13,15-trimethyl-11,14-dioxo-4,21-dioxa-12,15-diazatricyclo[15.3.1.05,10]henicosa-5(10),6,8-triene-8-carbonitrile
(1R,13S,17R,18S)-18-methoxy-12,13,15-trimethyl-11,14-dioxo-4,21-dioxa-12,15-diazatricyclo[15.3.1.05,10]henicosa-5(10),6,8-triene-8-carbonitrile
(1S,13R,17R,18R)-18-methoxy-12,13,15-trimethyl-11,14-dioxo-4,21-dioxa-12,15-diazatricyclo[15.3.1.05,10]henicosa-5(10),6,8-triene-8-carbonitrile
(1R,12S,17S,20S)-20-methoxy-11,12,14-trimethyl-10,13-dioxo-3,21-dioxa-11,14-diazatricyclo[15.3.1.04,9]henicosa-4(9),5,7-triene-7-carbonitrile
(1S,12S,17R,20R)-20-methoxy-11,12,14-trimethyl-10,13-dioxo-3,21-dioxa-11,14-diazatricyclo[15.3.1.04,9]henicosa-4(9),5,7-triene-7-carbonitrile
(1R,12S,17R,20S)-20-methoxy-11,12,14-trimethyl-10,13-dioxo-3,21-dioxa-11,14-diazatricyclo[15.3.1.04,9]henicosa-4(9),5,7-triene-7-carbonitrile
(1R,12S,17R,20R)-20-methoxy-11,12,14-trimethyl-10,13-dioxo-3,21-dioxa-11,14-diazatricyclo[15.3.1.04,9]henicosa-4(9),5,7-triene-7-carbonitrile
(1S,12S,17S,20S)-20-methoxy-11,12,14-trimethyl-10,13-dioxo-3,21-dioxa-11,14-diazatricyclo[15.3.1.04,9]henicosa-4(9),5,7-triene-7-carbonitrile
(1R,12R,17S,20R)-20-methoxy-11,12,14-trimethyl-10,13-dioxo-3,21-dioxa-11,14-diazatricyclo[15.3.1.04,9]henicosa-4,6,8-triene-5-carbonitrile
(1S,12S,17S,20R)-20-methoxy-11,12,14-trimethyl-10,13-dioxo-3,21-dioxa-11,14-diazatricyclo[15.3.1.04,9]henicosa-4,6,8-triene-5-carbonitrile
(1R,12R,17R,20S)-20-methoxy-11,12,14-trimethyl-10,13-dioxo-3,21-dioxa-11,14-diazatricyclo[15.3.1.04,9]henicosa-4,6,8-triene-5-carbonitrile
(1S,12R,17S,20R)-20-methoxy-11,12,14-trimethyl-10,13-dioxo-3,21-dioxa-11,14-diazatricyclo[15.3.1.04,9]henicosa-4,6,8-triene-5-carbonitrile
(1S,12R,17R,20S)-20-methoxy-11,12,14-trimethyl-10,13-dioxo-3,21-dioxa-11,14-diazatricyclo[15.3.1.04,9]henicosa-4,6,8-triene-5-carbonitrile
1-[(2R,3R)-6-[(2,5-difluorophenyl)methyl]-2-(hydroxymethyl)-3-phenyl-1,6-diazaspiro[3.3]heptan-1-yl]-2-(dimethylamino)ethanone
N-[[(2S,3S)-5-[(2R)-1-hydroxypropan-2-yl]-3-methyl-8-(3-methylbut-1-ynyl)-6-oxo-3,4-dihydro-2H-pyrido[2,3-b][1,5]oxazocin-2-yl]methyl]-N-methylpropanamide
N-[[(2R,3R)-5-[(2S)-1-hydroxypropan-2-yl]-3-methyl-8-(3-methylbut-1-ynyl)-6-oxo-3,4-dihydro-2H-pyrido[2,3-b][1,5]oxazocin-2-yl]methyl]-N-methylpropanamide
N-[[(2S,3S)-5-[(2S)-1-hydroxypropan-2-yl]-3-methyl-8-(3-methylbut-1-ynyl)-6-oxo-3,4-dihydro-2H-pyrido[2,3-b][1,5]oxazocin-2-yl]methyl]-N-methylpropanamide
N-[[(2R,3S)-5-[(2R)-1-hydroxypropan-2-yl]-3-methyl-8-(3-methylbut-1-ynyl)-6-oxo-3,4-dihydro-2H-pyrido[2,3-b][1,5]oxazocin-2-yl]methyl]-N-methylpropanamide
(1S,13S,17R,18S)-18-methoxy-12,13,15-trimethyl-11,14-dioxo-4,21-dioxa-12,15-diazatricyclo[15.3.1.05,10]henicosa-5,7,9-triene-6-carbonitrile
(1R,13S,17R,18S)-18-methoxy-12,13,15-trimethyl-11,14-dioxo-4,21-dioxa-12,15-diazatricyclo[15.3.1.05,10]henicosa-5,7,9-triene-6-carbonitrile
(1R,13S,17R,18R)-18-methoxy-12,13,15-trimethyl-11,14-dioxo-4,21-dioxa-12,15-diazatricyclo[15.3.1.05,10]henicosa-5,7,9-triene-6-carbonitrile
(1R,13R,17S,18R)-18-methoxy-12,13,15-trimethyl-11,14-dioxo-4,21-dioxa-12,15-diazatricyclo[15.3.1.05,10]henicosa-5,7,9-triene-6-carbonitrile
(1S,13S,17S,18R)-18-methoxy-12,13,15-trimethyl-11,14-dioxo-4,21-dioxa-12,15-diazatricyclo[15.3.1.05,10]henicosa-5,7,9-triene-6-carbonitrile
(1S,13S,17S,18S)-18-methoxy-12,13,15-trimethyl-11,14-dioxo-4,21-dioxa-12,15-diazatricyclo[15.3.1.05,10]henicosa-5,7,9-triene-6-carbonitrile
(1R,13S,17S,18R)-18-methoxy-12,13,15-trimethyl-11,14-dioxo-4,21-dioxa-12,15-diazatricyclo[15.3.1.05,10]henicosa-5,7,9-triene-6-carbonitrile
(1R,13R,17S,18S)-18-methoxy-12,13,15-trimethyl-11,14-dioxo-4,21-dioxa-12,15-diazatricyclo[15.3.1.05,10]henicosa-5(10),6,8-triene-8-carbonitrile
(1S,13S,17S,18S)-18-methoxy-12,13,15-trimethyl-11,14-dioxo-4,21-dioxa-12,15-diazatricyclo[15.3.1.05,10]henicosa-5(10),6,8-triene-8-carbonitrile
(1S,13S,17S,18R)-18-methoxy-12,13,15-trimethyl-11,14-dioxo-4,21-dioxa-12,15-diazatricyclo[15.3.1.05,10]henicosa-5(10),6,8-triene-8-carbonitrile
(1R,13R,17S,18R)-18-methoxy-12,13,15-trimethyl-11,14-dioxo-4,21-dioxa-12,15-diazatricyclo[15.3.1.05,10]henicosa-5(10),6,8-triene-8-carbonitrile
(1S,13S,17R,18S)-18-methoxy-12,13,15-trimethyl-11,14-dioxo-4,21-dioxa-12,15-diazatricyclo[15.3.1.05,10]henicosa-5(10),6,8-triene-8-carbonitrile
(1R,13S,17R,18R)-18-methoxy-12,13,15-trimethyl-11,14-dioxo-4,21-dioxa-12,15-diazatricyclo[15.3.1.05,10]henicosa-5(10),6,8-triene-8-carbonitrile
(1R,12S,17S,20R)-20-methoxy-11,12,14-trimethyl-10,13-dioxo-3,21-dioxa-11,14-diazatricyclo[15.3.1.04,9]henicosa-4(9),5,7-triene-7-carbonitrile
(1S,12R,17R,20S)-20-methoxy-11,12,14-trimethyl-10,13-dioxo-3,21-dioxa-11,14-diazatricyclo[15.3.1.04,9]henicosa-4(9),5,7-triene-7-carbonitrile
(1S,12R,17R,20R)-20-methoxy-11,12,14-trimethyl-10,13-dioxo-3,21-dioxa-11,14-diazatricyclo[15.3.1.04,9]henicosa-4(9),5,7-triene-7-carbonitrile
(1S,12S,17R,20S)-20-methoxy-11,12,14-trimethyl-10,13-dioxo-3,21-dioxa-11,14-diazatricyclo[15.3.1.04,9]henicosa-4(9),5,7-triene-7-carbonitrile
(1S,12R,17S,20R)-20-methoxy-11,12,14-trimethyl-10,13-dioxo-3,21-dioxa-11,14-diazatricyclo[15.3.1.04,9]henicosa-4(9),5,7-triene-7-carbonitrile
(1S,12S,17S,20R)-20-methoxy-11,12,14-trimethyl-10,13-dioxo-3,21-dioxa-11,14-diazatricyclo[15.3.1.04,9]henicosa-4(9),5,7-triene-7-carbonitrile
(1R,12R,17R,20S)-20-methoxy-11,12,14-trimethyl-10,13-dioxo-3,21-dioxa-11,14-diazatricyclo[15.3.1.04,9]henicosa-4(9),5,7-triene-7-carbonitrile
(1R,12R,17R,20R)-20-methoxy-11,12,14-trimethyl-10,13-dioxo-3,21-dioxa-11,14-diazatricyclo[15.3.1.04,9]henicosa-4(9),5,7-triene-7-carbonitrile
(1S,12R,17S,20S)-20-methoxy-11,12,14-trimethyl-10,13-dioxo-3,21-dioxa-11,14-diazatricyclo[15.3.1.04,9]henicosa-4(9),5,7-triene-7-carbonitrile
(1R,12R,17S,20S)-20-methoxy-11,12,14-trimethyl-10,13-dioxo-3,21-dioxa-11,14-diazatricyclo[15.3.1.04,9]henicosa-4(9),5,7-triene-7-carbonitrile
(1R,12R,17R,20R)-20-methoxy-11,12,14-trimethyl-10,13-dioxo-3,21-dioxa-11,14-diazatricyclo[15.3.1.04,9]henicosa-4,6,8-triene-5-carbonitrile
(1R,12R,17S,20S)-20-methoxy-11,12,14-trimethyl-10,13-dioxo-3,21-dioxa-11,14-diazatricyclo[15.3.1.04,9]henicosa-4,6,8-triene-5-carbonitrile
(1S,12S,17R,20R)-20-methoxy-11,12,14-trimethyl-10,13-dioxo-3,21-dioxa-11,14-diazatricyclo[15.3.1.04,9]henicosa-4,6,8-triene-5-carbonitrile
(1S,12S,17R,20S)-20-methoxy-11,12,14-trimethyl-10,13-dioxo-3,21-dioxa-11,14-diazatricyclo[15.3.1.04,9]henicosa-4,6,8-triene-5-carbonitrile
(1R,12S,17S,20S)-20-methoxy-11,12,14-trimethyl-10,13-dioxo-3,21-dioxa-11,14-diazatricyclo[15.3.1.04,9]henicosa-4,6,8-triene-5-carbonitrile
(1R,12S,17R,20R)-20-methoxy-11,12,14-trimethyl-10,13-dioxo-3,21-dioxa-11,14-diazatricyclo[15.3.1.04,9]henicosa-4,6,8-triene-5-carbonitrile
(1R,12S,17S,20R)-20-methoxy-11,12,14-trimethyl-10,13-dioxo-3,21-dioxa-11,14-diazatricyclo[15.3.1.04,9]henicosa-4,6,8-triene-5-carbonitrile
(1R,12S,17R,20S)-20-methoxy-11,12,14-trimethyl-10,13-dioxo-3,21-dioxa-11,14-diazatricyclo[15.3.1.04,9]henicosa-4,6,8-triene-5-carbonitrile
(1S,12R,17R,20R)-20-methoxy-11,12,14-trimethyl-10,13-dioxo-3,21-dioxa-11,14-diazatricyclo[15.3.1.04,9]henicosa-4,6,8-triene-5-carbonitrile
4-[(3aS,4S,9bS)-1-[cyclohexyl(oxo)methyl]-4-(hydroxymethyl)-2,3,3a,4,5,9b-hexahydropyrrolo[3,2-c]quinolin-8-yl]benzonitrile
1-[(2S,3R)-6-[(2,5-difluorophenyl)methyl]-2-(hydroxymethyl)-3-phenyl-1,6-diazaspiro[3.3]heptan-1-yl]-2-(dimethylamino)ethanone
(2R,3R)-6-[(3,5-difluorophenyl)methyl]-2-(hydroxymethyl)-3-phenyl-N-propan-2-yl-1,6-diazaspiro[3.3]heptane-1-carboxamide
GSK163090
GSK163090 is a potent, selective and orally active 5-HT1A/1B/1D receptor antagonist with pKi values of 9.4/8.5/9.7, respectively. GSK163090 inhibits the functional activity of serotonin reuptake transporter (SerT) with a pKi value of 6.1. GSK163090 has antidepressant and anxiolytic activities[1].
Ninerafaxstat
Ninerafaxstat (IMB-1018972) is a novel mitotropic agent. Ninerafaxstat increases myocardial metabolic efficiency by shifting substrate utilization towards glucose through reducing fatty acid oxidation (inhibiting 3-ketoacyl CoA thiolase). Ninerafaxstat can be used for the research of cardiovascular diseases[1].
