Exact Mass: 415.2470938000001
Exact Mass Matches: 415.2470938000001
Found 307 metabolites which its exact mass value is equals to given mass value 415.2470938000001
,
within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error
0.001 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
C28H33NO2 (415.25111580000004)
Ala Ala Arg Val
Ala Ala Val Arg
Ala Gly Ile Arg
Ala Gly Leu Arg
Ala Gly Arg Ile
Ala Gly Arg Leu
Ala Ile Gly Arg
Ala Ile Asn Val
Ala Ile Arg Gly
Ala Ile Val Asn
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 Thr Lys
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 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
Gly Ala Ile Arg
Gly Ala Leu Arg
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
Gly Leu Asn Leu
Gly Leu Gln Val
Gly Leu Arg Ala
Gly Leu Val Gln
Gly Asn Ile Ile
Gly Asn Ile Leu
Gly Asn Leu Ile
Gly Asn Leu Leu
Gly Gln Ile Val
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Gly Gln Val Ile
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Gly Arg Ala Ile
Gly Arg Ala Leu
Gly Arg Ile Ala
Gly Arg Leu Ala
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
Lys Pro Thr Ala
Lys Thr Ala Pro
Lys Thr Pro Ala
Leu Ala Gly Arg
Leu Ala Asn Val
Leu Ala Arg Gly
Leu Ala Val Asn
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
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Leu Asn Val Ala
Leu Gln Gly Val
Leu Gln Val Gly
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Leu Val Gly Gln
Leu Val Asn Ala
Leu Val Gln Gly
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Asn Ala Val Ile
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Asn Gly Ile Ile
Asn Gly Ile Leu
Asn Gly Leu Ile
Asn Gly Leu Leu
Asn Ile Ala Val
Asn Ile Gly Ile
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Asn Ile Ile Gly
Asn Ile Leu Gly
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Asn Leu Ala Val
Asn Leu Gly Ile
Asn Leu Gly Leu
Asn Leu Ile Gly
Asn Leu Leu Gly
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Asn Val Ala Ile
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Asn Val Ile Ala
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Pro Ala Lys Thr
Pro Ala Thr Lys
Pro Lys Ala Thr
Pro Lys Thr Ala
Pro Thr Ala Lys
Pro Thr Lys Ala
Gln Ala Val Val
Gln Gly Ile Val
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Gln Gly Val Ile
Gln Gly Val Leu
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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
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Arg Ala Gly Leu
Arg Ala Ile Gly
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Arg Ala Val Ala
Arg Gly Ala Ile
Arg Gly Ala Leu
Arg Gly Ile Ala
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Arg Ile Ala Gly
Arg Ile Gly Ala
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Arg Leu Gly Ala
Arg Val Ala Ala
Thr Ala Lys Pro
Thr Ala Pro Lys
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Thr Lys Pro Ala
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Val Ala Ile Asn
Val Ala Leu Asn
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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
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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
C23H33N3O4 (415.2470938000001)
N-[[4-(2-propan-2-yl-5-pyridin-4-ylpyrimidin-4-yl)cyclohexyl]methyl]pyridine-3-carboxamide
[1-[3-(4-Methylphenoxy)propyl]-4-piperidinyl]-diphenylmethanol
C28H33NO2 (415.25111580000004)
(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
C23H33N3O4 (415.2470938000001)
(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
C23H33N3O4 (415.2470938000001)
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
C23H33N3O4 (415.2470938000001)
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
C23H33N3O4 (415.2470938000001)
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
C23H33N3O4 (415.2470938000001)
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
C23H33N3O4 (415.2470938000001)
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
C23H33N3O4 (415.2470938000001)
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
C23H33N3O4 (415.2470938000001)
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].