Exact Mass: 287.2464402

Exact Mass Matches: 287.2464402

Found 107 metabolites which its exact mass value is equals to given mass value 287.2464402, within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error 0.01 dalton.

Procyclidine

1-cyclohexyl-1-phenyl-3-(pyrrolidin-1-yl)propan-1-ol

C19H29NO (287.2249024)


Procyclidine is only found in individuals that have used or taken this drug. It is a muscarinic antagonist that crosses the blood-brain barrier and is used in the treatment of drug-induced extrapyramidal disorders and in parkinsonism. [PubChem]The mechanism of action is unknown. It is thought that Procyclidine acts by blocking central cholinergic receptors, and thus balancing cholinergic and dopaminergic activity in the basal ganglia. Many of its effects are due to its pharmacologic similarities with atropine. Procyclidine exerts an antispasmodic effect on smooth muscle, and may produce mydriasis and reduction in salivation. D002491 - Central Nervous System Agents > D018726 - Anti-Dyskinesia Agents > D000978 - Antiparkinson Agents N - Nervous system > N04 - Anti-parkinson drugs > N04A - Anticholinergic agents > N04AA - Tertiary amines C78272 - Agent Affecting Nervous System > C66880 - Anticholinergic Agent > C29704 - Antimuscarinic Agent D018377 - Neurotransmitter Agents > D018678 - Cholinergic Agents > D018680 - Cholinergic Antagonists

   

Octanoylcarnitine

O-octanoyl-R-carnitine

C15H29NO4 (287.2096474)


CONFIDENCE standard compound; INTERNAL_ID 253 L-Octanoylcarnitine is a plasma metabolite and a physiologically active form of octanoylcarnitine. L-Octanoylcarnitine can be used for the research of breast cancer[1][2][3].

   
   

Lauroyl diethanolamide

N,N-Bis(2-hydroxyethyl)dodecanamide, 9ci. N,N-bis(2-hydroxyethyl)lauramide

C16H33NO3 (287.24603079999997)


Lauroyl diethanolamide is used as a food additive [EAFUS] ("EAFUS: Everything Added to Food in the United States. [http://www.eafus.com/]") It is used as a food additive .

   

Cycrimine

1-cyclopentyl-1-phenyl-3-(piperidin-1-yl)propan-1-ol

C19H29NO (287.2249024)


Cycrimine is only found in individuals that have used or taken this drug. It is a drug used to reduce levels of acetylcholine to return a balance with dopamine in the treatment and management of Parkinsons disease. Cycrimine binds the muscarinic acetylcholine receptor M1, effectively inhibiting acetylcholine. This decrease in acetylcholine restores the normal dopamine-acetylcholine balance and relieves the symptoms of Parkinsons disease. C78272 - Agent Affecting Nervous System > C66880 - Anticholinergic Agent > C29704 - Antimuscarinic Agent C78272 - Agent Affecting Nervous System > C38149 - Antiparkinsonian Agent Cycrimine is an orally active muscarinic cholinergic receptor (mAChR) M1 antagonist, reduces the acetylcholine levels in parkinson model. Cycrimine shows antispasmodic activity, can be used in studies of behavioral and mental disorder[1][2][3][4].

   

3-Methylheptanoylcarnitine

3-[(3-methylheptanoyl)oxy]-4-(trimethylazaniumyl)butanoate

C15H29NO4 (287.2096474)


3-Methylheptanoylcarnitine is an acylcarnitine. More specifically, it is an 3-methylheptanoic 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. 3-Methylheptanoylcarnitine is therefore classified as a medium chain AC. As a medium-chain acylcarnitine 3-Methylheptanoylcarnitine is somewhat less abundant than short-chain acylcarnitines. These are formed either through esterification with L-carnitine or through the peroxisomal metabolism of longer chain acylcarnitines (PMID: 30540494). Many medium-chain acylcarnitines can serve as useful markers for inherited disorders of fatty acid metabolism. Carnitine octanoyltransferase (CrOT, EC:2.3.1.137) is responsible for the synthesis of all medium-chain (MCAC, C5-C12) and medium-length branched-chain acylcarnitines in peroxisomes (PMID: 10486279). 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].

   

4-Methylheptanoylcarnitine

3-[(4-methylheptanoyl)oxy]-4-(trimethylazaniumyl)butanoate

C15H29NO4 (287.2096474)


4-Methylheptanoylcarnitine is an acylcarnitine. More specifically, it is an 4-methylheptanoic 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. 4-Methylheptanoylcarnitine is therefore classified as a medium chain AC. As a medium-chain acylcarnitine 4-Methylheptanoylcarnitine is somewhat less abundant than short-chain acylcarnitines. These are formed either through esterification with L-carnitine or through the peroxisomal metabolism of longer chain acylcarnitines (PMID: 30540494). Many medium-chain acylcarnitines can serve as useful markers for inherited disorders of fatty acid metabolism. Carnitine octanoyltransferase (CrOT, EC:2.3.1.137) is responsible for the synthesis of all medium-chain (MCAC, C5-C12) and medium-length branched-chain acylcarnitines in peroxisomes (PMID: 10486279). 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].

   

6-Methylheptanoylcarnitine

3-[(6-methylheptanoyl)oxy]-4-(trimethylazaniumyl)butanoate

C15H29NO4 (287.2096474)


6-Methylheptanoylcarnitine is an acylcarnitine. More specifically, it is an 6-methylheptanoic 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. 6-Methylheptanoylcarnitine is therefore classified as a medium chain AC. As a medium-chain acylcarnitine 6-Methylheptanoylcarnitine is somewhat less abundant than short-chain acylcarnitines. These are formed either through esterification with L-carnitine or through the peroxisomal metabolism of longer chain acylcarnitines (PMID: 30540494). Many medium-chain acylcarnitines can serve as useful markers for inherited disorders of fatty acid metabolism. Carnitine octanoyltransferase (CrOT, EC:2.3.1.137) is responsible for the synthesis of all medium-chain (MCAC, C5-C12) and medium-length branched-chain acylcarnitines in peroxisomes (PMID: 10486279). 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].

   

5-Methylheptanoylcarnitine

3-[(5-methylheptanoyl)oxy]-4-(trimethylazaniumyl)butanoate

C15H29NO4 (287.2096474)


5-Methylheptanoylcarnitine is an acylcarnitine. More specifically, it is an 5-methylheptanoic 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. 5-Methylheptanoylcarnitine is therefore classified as a medium chain AC. As a medium-chain acylcarnitine 5-Methylheptanoylcarnitine is somewhat less abundant than short-chain acylcarnitines. These are formed either through esterification with L-carnitine or through the peroxisomal metabolism of longer chain acylcarnitines (PMID: 30540494). Many medium-chain acylcarnitines can serve as useful markers for inherited disorders of fatty acid metabolism. Carnitine octanoyltransferase (CrOT, EC:2.3.1.137) is responsible for the synthesis of all medium-chain (MCAC, C5-C12) and medium-length branched-chain acylcarnitines in peroxisomes (PMID: 10486279). 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-Lauroyl Serine

2-dodecanamido-3-hydroxypropanoic acid

C15H29NO4 (287.2096474)


N-lauroyl serine, also known as N-dodecanoyl-ser belongs to the class of compounds known as N-acylamides. These are molecules characterized by a fatty acyl group linked to a primary amine by an amide bond. More specifically, it is a Lauric acid amide of Serine. It is believed that there are more than 800 types of N-acylamides in the human body. N-acylamides fall into several categories: amino acid conjugates (e.g., those acyl amides conjugated with amino acids), neurotransmitter conjugates (e.g., those acylamides conjugated with neurotransmitters), ethanolamine conjugates (e.g., those acylamides conjugated to ethanolamine), and taurine conjugates (e.g., those acyamides conjugated to taurine). N-Lauroyl Serine is an amino acid conjugate. N-acylamides can be classified into 9 different categories depending on the size of their acyl-group: 1) short-chain N-acylamides; 2) medium-chain N-acylamides; 3) long-chain N-acylamides; and 4) very long-chain N-acylamides; 5) hydroxy N-acylamides; 6) branched chain N-acylamides; 7) unsaturated N-acylamides; 8) dicarboxylic N-acylamides and 9) miscellaneous N-acylamides. N-Lauroyl Serine is therefore classified as a long chain N-acylamide. N-acyl amides have a variety of signaling functions in physiology, including in cardiovascular activity, metabolic homeostasis, memory, cognition, pain, motor control and others (PMID: 15655504). N-acyl amides have also been shown to play a role in cell migration, inflammation and certain pathological conditions such as diabetes, cancer, neurodegenerative disease, and obesity (PMID: 23144998; PMID: 25136293; PMID: 28854168).N-acyl amides can be synthesized both endogenously and by gut microbiota (PMID: 28854168). N-acylamides can be biosynthesized via different routes, depending on the parent amine group. N-acyl ethanolamines (NAEs) are formed via the hydrolysis of an unusual phospholipid precursor, N-acyl-phosphatidylethanolamine (NAPE), by a specific phospholipase D. N-acyl amino acids are synthesized via a circulating peptidase M20 domain containing 1 (PM20D1), which can catalyze the bidirectional the condensation and hydrolysis of a variety of N-acyl amino acids. The degradation of N-acylamides is largely mediated by an enzyme called fatty acid amide hydrolase (FAAH), which catalyzes the hydrolysis of N-acylamides into fatty acids and the biogenic amines. Many N-acylamides are involved in lipid signaling system through interactions with transient receptor potential channels (TRP). TRP channel proteins interact with N-acyl amides such as N-arachidonoyl ethanolamide (Anandamide), N-arachidonoyl dopamine and others in an opportunistic fashion (PMID: 23178153). This signaling system has been shown to play a role in the physiological processes involved in inflammation (PMID: 25136293). Other N-acyl amides, including N-oleoyl-glutamine, have also been characterized as TRP channel antagonists (PMID: 29967167). N-acylamides have also been shown to have G-protein-coupled receptors (GPCRs) binding activity (PMID: 28854168). The study of N-acylamides is an active area of research and it is likely that many novel N-acylamides will be discovered in the coming years. It is also likely that many novel roles in health and disease will be uncovered for these molecules.

   

(2S)-1-[2-(2-Adamantylamino)acetyl]pyrrolidine-2-carbonitrile

1-{2-[(adamantan-2-yl)amino]acetyl}pyrrolidine-2-carbonitrile

C17H25N3O (287.199752)


   

Dipropyl-5-CT

3-[2-(Dipropylamino)ethyl]-1H-indole-5-carboximidate

C17H25N3O (287.199752)


   

Valproylcarnitine

3-[(2-Propylpentanoyl)oxy]-4-(trimethylazaniumyl)butanoic acid

C15H29NO4 (287.2096474)


   

1-methyl-2-(9-phenylnonyl)pyrrolidine

1-methyl-2-(9-phenylnonyl)pyrrolidine

C20H33N (287.26128580000005)


   
   

Solaurethin|Solaurethine

Solaurethin|Solaurethine

C15H33N3O2 (287.2572638)


   
   
   

Lauryl diethanolamide

N,N-Bis(2-hydroxyethyl)dodecanamide

C16H33NO3 (287.24603079999997)


CONFIDENCE standard compound; INTERNAL_ID 2846 CONFIDENCE standard compound; INTERNAL_ID 8767

   

L-Octanoylcarnitine

(3R)-3-(octanoyloxy)-4-(trimethylazaniumyl)butanoate

C15H29NO4 (287.2096474)


L-Octanoylcarnitine is a plasma metabolite and a physiologically active form of octanoylcarnitine. L-Octanoylcarnitine can be used for the research of breast cancer[1][2][3].

   

Lauric Acid Diethanolamide

N,N-Bis(2-hydroxyethyl)dodecanamide

C16H33NO3 (287.24603079999997)


Literature spectrum; CONFIDENCE Tentative identification: isomers possible (Level 3); May be an alkyl homologue; Digitised from figure: approximate intensities

   

Sphinganine (C17 base)

Sphinganine (C17 base)

C17H37NO2 (287.2824142)


   

Octanoyl-carnitine; AIF; CE10; CorrDec

Octanoyl-carnitine; AIF; CE10; CorrDec

C15H29NO4 (287.2096474)


   

Octanoyl-carnitine; AIF; CE30; CorrDec

Octanoyl-carnitine; AIF; CE30; CorrDec

C15H29NO4 (287.2096474)


   

Octanoyl-carnitine; AIF; CE0; MS2Dec

Octanoyl-carnitine; AIF; CE0; MS2Dec

C15H29NO4 (287.2096474)


   

Octanoyl-carnitine; AIF; CE10; MS2Dec

Octanoyl-carnitine; AIF; CE10; MS2Dec

C15H29NO4 (287.2096474)


   

Octanoyl-carnitine; AIF; CE30; MS2Dec

Octanoyl-carnitine; AIF; CE30; MS2Dec

C15H29NO4 (287.2096474)


   
   

(2S,6R,7S,8S)-7-((E)-buta-1,3-dien-1-yl)-2-(penta-3,4-dien-1-yl)-1-azaspiro[5.5]undecan-8-ol

(2S,6R,7S,8S)-7-((E)-buta-1,3-dien-1-yl)-2-(penta-3,4-dien-1-yl)-1-azaspiro[5.5]undecan-8-ol

C19H29NO (287.2249024)


   

(2S,6R,7S,8S)-7-((E)-buta-1,3-dien-1-yl)-2-((E)-penta-2,4-dien-1-yl)-1-azaspiro[5.5]undecan-8-ol

(2S,6R,7S,8S)-7-((E)-buta-1,3-dien-1-yl)-2-((E)-penta-2,4-dien-1-yl)-1-azaspiro[5.5]undecan-8-ol

C19H29NO (287.2249024)


   

(2R,6R,7S,8S)-7-((E)-buta-1,3-dien-1-yl)-2-(pent-4-yn-1-yl)-1-azaspiro[5.5]undecan-8-ol

(2R,6R,7S,8S)-7-((E)-buta-1,3-dien-1-yl)-2-(pent-4-yn-1-yl)-1-azaspiro[5.5]undecan-8-ol

C19H29NO (287.2249024)


   

2-((1S,3aS,6S)-6-((E)-pent-2-en-4-yn-1-yl)dodecahydropyrrolo[1,2-a]quinolin-1-yl)ethan-1-ol

2-((1S,3aS,6S)-6-((E)-pent-2-en-4-yn-1-yl)dodecahydropyrrolo[1,2-a]quinolin-1-yl)ethan-1-ol

C19H29NO (287.2249024)


   

C17 Sphinganine

heptadecasphinganine

C17H37NO2 (287.2824142)


   

CAY10434

6-[4-(1H-imidazol-1-yl)phenoxy]-N,N-dimethyl-1-hexanamine

C17H25N3O (287.199752)


   

CAY10462

6-[4-(1H-imidazol-1-yl)phenoxy]-N,N-dimethyl-1-hexanamine, dihydrochloride

C17H25N3O (287.199752)


   

Prosopinine

6R-(8-hydroxydecyl)-2R-(hydroxymethyl)-piperidin-3R-ol

C16H33NO3 (287.24603079999997)


A piperidine alkaloid that is a hydroxypiperidine with a hydroxy group at position C-3, a hydroxymethyl group at C-2, and an 8-hydroxydecyl group at C-6.

   

(±)-Octanoylcarnitine

(±)-Octanoylcarnitine

C15H29NO4 (287.2096474)


   

cycrimine

1-cyclopentyl-1-phenyl-3-(piperidin-1-yl)propan-1-ol

C19H29NO (287.2249024)


C78272 - Agent Affecting Nervous System > C66880 - Anticholinergic Agent > C29704 - Antimuscarinic Agent C78272 - Agent Affecting Nervous System > C38149 - Antiparkinsonian Agent Cycrimine is an orally active muscarinic cholinergic receptor (mAChR) M1 antagonist, reduces the acetylcholine levels in parkinson model. Cycrimine shows antispasmodic activity, can be used in studies of behavioral and mental disorder[1][2][3][4].

   

Clindrol

N,N-Bis(2-hydroxyethyl)dodecanamide, 9ci. N,N-bis(2-hydroxyethyl)lauramide

C16H33NO3 (287.24603079999997)


   

Stearic acid(d3)

Octadecanoic acid(d3)

C18H33D3O2 (287.290347134)


   

Oleic acid (d5)

9Z-octadecenoic acid (d5)

C18H29D5O2 (287.28725229)


   

CAR 8:0

3-(octanoyloxy)-4-(trimethylammonio)butanoate;octanoylcarnitine

C15H29NO4 (287.2096474)


   

Lauroyl diethanolamide

N,N-Bis(2-hydroxyethyl)dodecanamide

C16H33NO3 (287.24603079999997)


   

SPB 17:0;O2

15-Methylhexadecasphinganine

C17H37NO2 (287.2824142)


   

Octanoylcarnitine (C8)

(3R)-3-(octanoyloxy)-4-(trimethylazaniumyl)butanoate

C15H29NO4 (287.2096474)


L-Octanoylcarnitine is the physiologically active form of octanoylcarnitine (PMID: 11274033). Octanoylcarnitine is detected in medium-chain acyl-CoA dehydrogenase (MCAD) deficiency. MCAD is characterized by an intolerance to prolonged fasting, recurrent episodes of hypoglycemic coma with medium-chain dicarboxylic aciduria, impaired ketogenesis, and low plasma and tissue carnitine levels (OMIM: 201450). L-Octanoylcarnitine is also found to be associated with celiac disease and glutaric aciduria II, which are inborn errors of metabolism. L-Octanoylcarnitine is the physiologically active form of octanoylcarnitine. (PMID 11274033) L-Octanoylcarnitine is a plasma metabolite and a physiologically active form of octanoylcarnitine. L-Octanoylcarnitine can be used for the research of breast cancer[1][2][3].

   

2-dodecoxybenzonitrile

2-dodecoxybenzonitrile

C19H29NO (287.2249024)


   

4-(pyrrolidin-1-ylmethyl)benzeneboronic acid, pinacol ester

4-(pyrrolidin-1-ylmethyl)benzeneboronic acid, pinacol ester

C17H26BNO2 (287.2056486)


   

lauric acid, compound with morpholine (1:1)

lauric acid, compound with morpholine (1:1)

C16H33NO3 (287.24603079999997)


   

octadecanoic-18,18,18-d3 acid

octadecanoic-18,18,18-d3 acid

C18H33D3O2 (287.290347134)


   

1,3-Dioxolane-4-methanol,2-methyl-2-nonyl-, 4-carbamate

1,3-Dioxolane-4-methanol,2-methyl-2-nonyl-, 4-carbamate

C15H29NO4 (287.2096474)


   
   

N-BOC-2-OCTYL-L-GLYCINE

N-BOC-2-OCTYL-L-GLYCINE

C15H29NO4 (287.2096474)


   

1-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]piperidine

1-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]piperidine

C17H26BNO2 (287.2056486)


   

n,o-bis(tert-butyldimethylsilyl)acetamide

n,o-bis(tert-butyldimethylsilyl)acetamide

C14H33NOSi2 (287.21005679999996)


   

tetrabutylazanium,formate

tetrabutylazanium,formate

C17H37NO2 (287.2824142)


   

1-(3-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PHENYL)PIPERIDINE

1-(3-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PHENYL)PIPERIDINE

C17H26BNO2 (287.2056486)


   

N-Cyclohexyl-4-[(piperidin-1-yl)methyl]benzene-1,2-diamine

N-Cyclohexyl-4-[(piperidin-1-yl)methyl]benzene-1,2-diamine

C18H29N3 (287.2361354)


   

1-(2-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)BENZYL)PYRROLIDINE

1-(2-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)BENZYL)PYRROLIDINE

C17H26BNO2 (287.2056486)


   
   

1-(3-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)BENZYL)PYRROLIDINE

1-(3-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)BENZYL)PYRROLIDINE

C17H26BNO2 (287.2056486)


   
   

Lithium triisopropyl 2-(6-methylpyridyl)borate

Lithium triisopropyl 2-(6-methylpyridyl)borate

C15H27BLiNO3 (287.2243932)


   

Lithium triisopropyl 2-(5-methylpyridyl)borate

Lithium triisopropyl 2-(5-methylpyridyl)borate

C15H27BLiNO3 (287.2243932)


   

N-tert-butyl-1-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methanimine

N-tert-butyl-1-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methanimine

C17H26BNO2 (287.2056486)


   

N-[2-(2-Hydroxyethoxy)ethyl]dodecanamide

N-[2-(2-Hydroxyethoxy)ethyl]dodecanamide

C16H33NO3 (287.24603079999997)


   

proxazole

proxazole

C17H25N3O (287.199752)


A - Alimentary tract and metabolism > A03 - Drugs for functional gastrointestinal disorders > A03A - Drugs for functional gastrointestinal disorders C78272 - Agent Affecting Nervous System > C29698 - Antispasmodic Agent

   

alpha-Pyrrolidinononanophenone

alpha-Pyrrolidinononanophenone

C19H29NO (287.2249024)


   
   

(2S,3R)-2-aminoheptadecane-1,3-diol

(2S,3R)-2-aminoheptadecane-1,3-diol

C17H37NO2 (287.2824142)


   

Plasmocid

Plasmocid

C17H25N3O (287.199752)


D000890 - Anti-Infective Agents > D000977 - Antiparasitic Agents > D000981 - Antiprotozoal Agents

   

O-octanoyl-D-carnitine

O-octanoyl-D-carnitine

C15H29NO4 (287.2096474)


An O-acyl-D-carnitine in which the acyl group specified as octanoyl.

   
   

(1s,2s,3r,6r)-4-(Hydroxymethyl)-6-(Octylamino)cyclohex-4-Ene-1,2,3-Triol

(1s,2s,3r,6r)-4-(Hydroxymethyl)-6-(Octylamino)cyclohex-4-Ene-1,2,3-Triol

C15H29NO4 (287.2096474)


   

10,16-Dihydroxyhexadecanoate

10,16-Dihydroxyhexadecanoate

C16H31O4- (287.2222226)


   

9,16-Dihydroxyhexadecanoate

9,16-Dihydroxyhexadecanoate

C16H31O4- (287.2222226)


   

3-Methylheptanoylcarnitine

3-Methylheptanoylcarnitine

C15H29NO4 (287.2096474)


   

4-Methylheptanoylcarnitine

4-Methylheptanoylcarnitine

C15H29NO4 (287.2096474)


   

6-Methylheptanoylcarnitine

6-Methylheptanoylcarnitine

C15H29NO4 (287.2096474)


   

5-Methylheptanoylcarnitine

5-Methylheptanoylcarnitine

C15H29NO4 (287.2096474)


   
   

3,16-Dihydroxypalmitate

3,16-Dihydroxypalmitate

C16H31O4- (287.2222226)


A hydroxy fatty acid anion that is the conjugate base of 3,16-dihydroxypalmitic acid, arising from deprotonation of the carboxy group; major species at pH 7.3.

   

(2R)-2-hydroperoxyhexadecanoate

(2R)-2-hydroperoxyhexadecanoate

C16H31O4- (287.2222226)


   

1-Piperidinyl-[1-(3-pyridinylmethyl)-3-piperidinyl]methanone

1-Piperidinyl-[1-(3-pyridinylmethyl)-3-piperidinyl]methanone

C17H25N3O (287.199752)


   

9,14-Dihydroxyhexadecanoate

9,14-Dihydroxyhexadecanoate

C16H31O4- (287.2222226)


   

9,15-Dihydroxyhexadecanoate

9,15-Dihydroxyhexadecanoate

C16H31O4- (287.2222226)


   

9,13-Dihydroxyhexadecanoate

9,13-Dihydroxyhexadecanoate

C16H31O4- (287.2222226)


   

Octanoyl-L-carnitine-(N-methyl-d3), analytical standard

Octanoyl-L-carnitine-(N-methyl-d3), analytical standard

C15H29NO4 (287.2096474)


   

N-(1,3-dihydroxytetradecan-2-yl)acetamide

N-(1,3-dihydroxytetradecan-2-yl)acetamide

C16H33NO3 (287.24603079999997)


   

1-(N,N-Dimethylamino)-3,7,11-trimethyl-2,3-dodecanediol

1-(N,N-Dimethylamino)-3,7,11-trimethyl-2,3-dodecanediol

C17H37NO2 (287.2824142)


   

N-(1,3-dihydroxynonan-2-yl)heptanamide

N-(1,3-dihydroxynonan-2-yl)heptanamide

C16H33NO3 (287.24603079999997)


   

N-(1,3-dihydroxyoctan-2-yl)octanamide

N-(1,3-dihydroxyoctan-2-yl)octanamide

C16H33NO3 (287.24603079999997)


   

N-(1,3-dihydroxydecan-2-yl)hexanamide

N-(1,3-dihydroxydecan-2-yl)hexanamide

C16H33NO3 (287.24603079999997)


   

N-(1,3-dihydroxyundecan-2-yl)pentanamide

N-(1,3-dihydroxyundecan-2-yl)pentanamide

C16H33NO3 (287.24603079999997)


   

N-(1,3-dihydroxytridecan-2-yl)propanamide

N-(1,3-dihydroxytridecan-2-yl)propanamide

C16H33NO3 (287.24603079999997)


   

N-(1,3-dihydroxydodecan-2-yl)butanamide

N-(1,3-dihydroxydodecan-2-yl)butanamide

C16H33NO3 (287.24603079999997)


   

1,1,3,3-Tetra-isopropyl-1,2,3-trimethyldisilazane

1,1,3,3-Tetra-isopropyl-1,2,3-trimethyldisilazane

C15H37NSi2 (287.2464402)


   

procyclidine

1-Pyrrolidinepropanol, a-cyclohexyl-a-phenyl-

C19H29NO (287.2249024)


D002491 - Central Nervous System Agents > D018726 - Anti-Dyskinesia Agents > D000978 - Antiparkinson Agents N - Nervous system > N04 - Anti-parkinson drugs > N04A - Anticholinergic agents > N04AA - Tertiary amines C78272 - Agent Affecting Nervous System > C66880 - Anticholinergic Agent > C29704 - Antimuscarinic Agent D018377 - Neurotransmitter Agents > D018678 - Cholinergic Agents > D018680 - Cholinergic Antagonists

   

Lauric Acid Diethanolamide

N,N-Bis(2-hydroxyethyl)dodecanamide

C16H33NO3 (287.24603079999997)


   
   

O-octanoylcarnitine

O-octanoylcarnitine

C15H29NO4 (287.2096474)


An O-acylcarnitine having octanoyl as the acyl substituent.

   

15-Methylhexadecasphinganine

15-Methylhexadecasphinganine

C17H37NO2 (287.2824142)


   

O-octanoyl-L-carnitine

O-octanoyl-L-carnitine

C15H29NO4 (287.2096474)


The L-enantiomer of an O-octanoylcarnitine.

   

Sphingosine (d17:0)

SPH(d17:0)

C17H37NO2 (287.2824142)


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