Exact Mass: 325.2743

Exact Mass Matches: 325.2743

Found 189 metabolites which its exact mass value is equals to given mass value 325.2743, within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error 0.01 dalton.

Bisoprolol

1-[(propan-2-yl)amino]-3-(4-{[2-(propan-2-yloxy)ethoxy]methyl}phenoxy)propan-2-ol

C18H31NO4 (325.2253)


Bisoprolol is a cardioselective β1-adrenergic blocking agent used for secondary prevention of myocardial infarction (MI), heart failure, angina pectoris and mild to moderate hypertension. Bisoprolol is structurally similar to metoprolol, acebutolol and atenolol in that it has two substituents in the para position of the benzene ring. The β1-selectivity of these agents is thought to be due in part to the large substituents in the para position. At lower doses (less than 20 mg daily), bisoprolol selectively blocks cardiac β1-adrenergic receptors with little activity against β2-adrenergic receptors of the lungs and vascular smooth muscle. Receptor selectivity decreases with daily doses of 20 mg or greater. Unlike propranolol and pindolol, bisoprolol does not exhibit membrane-stabilizing or sympathomimetic activity. Bisoprolol possesses a single chiral centre and is administered as a racemic mixture. Only l-bisoprolol exhibits significant β-blocking activity. C - Cardiovascular system > C07 - Beta blocking agents > C07A - Beta blocking agents > C07AB - Beta blocking agents, selective C78272 - Agent Affecting Nervous System > C29747 - Adrenergic Agent > C72900 - Adrenergic Antagonist D018373 - Peripheral Nervous System Agents > D001337 - Autonomic Agents > D013565 - Sympatholytics D018377 - Neurotransmitter Agents > D018663 - Adrenergic Agents > D018674 - Adrenergic Antagonists D002317 - Cardiovascular Agents > D000959 - Antihypertensive Agents CONFIDENCE standard compound; EAWAG_UCHEM_ID 3013 CONFIDENCE standard compound; INTERNAL_ID 8595 CONFIDENCE standard compound; INTERNAL_ID 2677

   

10-Nitrolinoleic acid

(9E,12Z)-10-Nitrooctadeca-9,12-dienoic acid

C18H31NO4 (325.2253)


Nitrolinoleic acid is a nitrated fatty acid (or nitroalkene, a class of cell signaling mediators generated by Nitric Oxide (NO) and fatty acid-dependent redox reactions). Nitrated fatty acids such as 10- and 12-nitro-9,12-octadecadienoic acid exhibit pluripotent antiinflammatory cell signaling properties. (PMID 16537525) [HMDB] Nitrolinoleic acid is a nitrated fatty acid (or nitroalkene, a class of cell signaling mediators generated by Nitric Oxide (NO) and fatty acid-dependent redox reactions). Nitrated fatty acids such as 10- and 12-nitro-9,12-octadecadienoic acid exhibit pluripotent antiinflammatory cell signaling properties. (PMID 16537525).

   

Tolterodine

2-[(1R)-3-[bis(propan-2-yl)amino]-1-phenylpropyl]-4-methylphenol

C22H31NO (325.2406)


Tolterodine is only found in individuals that have used or taken this drug. It is an antimuscarinic drug that is used to treat urinary incontinence. Tolterodine acts on M2 and M3 subtypes of muscarinic receptors.Both tolterodine and its active metabolite, 5-hydroxymethyltolterodine, act as competitive antagonists at muscarinic receptors. This antagonism results in inhibition of bladder contraction, decrease in detrusor pressure, and an incomplete emptying of the bladder. G - Genito urinary system and sex hormones > G04 - Urologicals > G04B - Urologicals > G04BD - Drugs for urinary frequency and incontinence C78272 - Agent Affecting Nervous System > C66880 - Anticholinergic Agent > C29704 - Antimuscarinic Agent D018377 - Neurotransmitter Agents > D018678 - Cholinergic Agents > D018680 - Cholinergic Antagonists D000089162 - Genitourinary Agents > D064804 - Urological Agents Tolterodine(PNU-200583) is a potent muscarinic receptor antagonists that show selectivity for the urinary bladder over salivary glands in vivo. IC50 Value: Target: mAChR in vitro: Carbachol-induced contractions of isolated guinea pig bladder were effectively inhibited by tolterodine (IC50 14 nM) and 5-HM (IC50 5.7 nM). The IC50 values were in the microM range and the antimuscarinic potency of tolterodine was 27, 200 and 370-485 times higher, respectively, than its potency in blocking histamine receptors, alpha-adrenoceptors and calcium channels. The active metabolite, 5-HM, was >900 times less potent at these sites than at bladder muscarinic receptors [1]. in vivo: Tolterodine was extensively metabolized in vivo [2]. In the passive-avoidance test, tolterodine at 1 or 3 mg/kg had no effect on memory; the latency to cross and percentage of animals crossing were comparable to controls. In contrast, scopolamine induced a memory deficit; the latency to cross was decreased, and the number of animals crossing was increased [3].

   

Small bacteriocin

(7E)-3-Hydroxy-N-(2-oxooxolan-3-yl)tetradec-7-enimidate

C18H31NO4 (325.2253)


Bacteriocin. Small bacteriocin is produced by Rhizobium leguminosarum. Bacteriocin. Production by Rhizobium leguminosarum.

   

C12-LNO2

(9Z,12E)-12-nitrooctadeca-9,12-dienoic acid

C18H31NO4 (325.2253)


   

Oleoylethanolamide

N-Oleoylethanolamine

C20H39NO2 (325.2981)


D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones > D063385 - Cannabinoid Receptor Modulators D018377 - Neurotransmitter Agents > D063385 - Cannabinoid Receptor Modulators > D063386 - Cannabinoid Receptor Agonists COVID info from DrugBank Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS CONFIDENCE standard compound; INTERNAL_ID 31 Oleoylethanolamide is a high affinity endogenous PPAR-α agonist, which plays an important role in the treatment of obesity and arteriosclerosis. Oleoylethanolamide is a high affinity endogenous PPAR-α agonist, which plays an important role in the treatment of obesity and arteriosclerosis.

   

Oleoylethanolamide

N-Oleoyl ethanolamine, oleoyl monoethanolamide, oleoylethanolamide

C20H39NO2 (325.2981)


N-Oleoylethanolamine (NOE or OEA) is a N-acylethanolamine. N-acylethanolamines (NAEs) constitute a class of lipid compounds naturally present in both animal and plant membranes as constituents of the membrane-bound phospholipid, N-acylphosphatidylethanolamine (NAPE). NAPE is composed of a third fatty acid moiety linked to the amino head group of the commonly occurring membrane phospholipid, phosphatidylethanolamine. NAEs are released from NAPE by phospholipase D-type hydrolases in response to a variety of stimuli. Transient NAE release and accumulation has been attributed a variety of biological activities, including neurotransmission, membrane protection, and immunomodulation in animals. N-oleoylethanolamine is an inhibitor of the sphingolipid signaling pathway, via specific ceramidase inhibition (ceramidase converts ceramide to sphingosine). N-oleoylethanolamine blocks the effects of TNF- and arachidonic acid on intracellular Ca concentration. (PMID: 12692337, 12056855, 12560208, 11997249). N-oleoyl ethanolamine is related to the endocannabinoid anandamide. Endocannabinoids signal through cannabinoid receptors (also stimulated by the active ingredient of cannabis) but although related in structure, synthesis and degradation to anandamide, NOE cannot be considered an endocannabinoid as it does not activate the cannabinoid receptors. Most of the reported responses to NOE can be attributed to activation of peroxisome proliferator-activated receptor-alpha (PPAR-alpha). Administration of NOE inhibits body weight gain in rats. In adipocytes and hepatocytes, NOE inhibits mitogenic and metabolic signaling by the insulin receptor and produces glucose intolerance. It also inhibits gastric emptying, which might act together with the sensory neuronal signals to achieve satiety. NOE is permanently elevated in diabetic obese patients. NOE also reduces visceral and inflammatory responses through a PPAR-alpha-activation independent mechanism (PMID: 17449181). NOE has been shown to be an antagonist of TRVP1 (the transient receptor potential vanilloid type 1 receptor). Overall, NOE has beneficial effects on health by inducing food intake control, lipid beta-oxidation, body weight loss and analgesic effects (PMID: 18704536). [HMDB] Oleoylethanolamide (OEA or NOE) is an N-acylethanolamine. N-Acylethanolamines (NAEs) constitute a class of lipid compounds naturally present in both animal and plant membranes as constituents of the membrane-bound phospholipid, N-acylphosphatidylethanolamine (NAPE). NAPE is composed of a third fatty acid moiety linked to the amino head group of the commonly occurring membrane phospholipid, phosphatidylethanolamine. NAEs are released from NAPE by phospholipase D-type hydrolases in response to a variety of stimuli. Transient NAE release and accumulation have been attributed to a variety of biological activities, including neurotransmission, membrane protection, and immunomodulation in animals. Oleoylethanolamide is an inhibitor of the sphingolipid signalling pathway, via specific ceramidase inhibition (ceramidase converts ceramide to sphingosine). Oleoylethanolamide blocks the effects of TNF and arachidonic acid on intracellular Ca concentration (PMID: 12692337, 12056855, 12560208, 11997249). Oleoylethanolamide is related to the endocannabinoid anandamide. Endocannabinoids signal through cannabinoid receptors (also stimulated by the active ingredient of cannabis) but although related in structure, synthesis, and degradation to anandamide, OEA cannot be considered an endocannabinoid as it does not activate the cannabinoid receptors. Most of the reported responses to OEA can be attributed to the activation of peroxisome proliferator-activated receptor-alpha (PPAR-alpha). Administration of OEA inhibits body weight gain in rats. In adipocytes and hepatocytes, OEA inhibits mitogenic and metabolic signalling by the insulin receptor and produces glucose intolerance. It also inhibits gastric emptying, which might act together with the sensory neuronal signals to achieve satiety. OEA is permanently elevated in diabetic obese patients. OEA also reduces visceral and inflammatory responses through a PPAR-alpha-activation independent mechanism (PMID: 17449181). OEA is an antagonist of TRVP1 (the transient receptor potential vanilloid type 1 receptor). Overall, OEA has beneficial effects on health by inducing food intake control, lipid beta-oxidation, body weight loss and analgesic effects (PMID: 18704536). D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones > D063385 - Cannabinoid Receptor Modulators D018377 - Neurotransmitter Agents > D063385 - Cannabinoid Receptor Modulators > D063386 - Cannabinoid Receptor Agonists COVID info from DrugBank Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS Oleoylethanolamide is a high affinity endogenous PPAR-α agonist, which plays an important role in the treatment of obesity and arteriosclerosis. Oleoylethanolamide is a high affinity endogenous PPAR-α agonist, which plays an important role in the treatment of obesity and arteriosclerosis.

   

N-[[3-Hydroxy-2-(2-pentenyl)cyclopentyl]acetyl]isoleucine

2-[(1-Hydroxy-2-{3-hydroxy-2-[(2E)-pent-2-en-1-yl]cyclopentyl}ethylidene)amino]-3-methylpentanoate

C18H31NO4 (325.2253)


N-[[3-Hydroxy-2-(2-pentenyl)cyclopentyl]acetyl]isoleucine is a constituent of the pollen of Pinus mugo (dwarf mountain pine). Constituent of the pollen of Pinus mugo (dwarf mountain pine)

   

Dapiprazole

3-(2-(4-(2-Methylphenyl)-1-piperazinyl)ethyl)-5,6,7,8,-tetrahydro-1,2,4-triazolo(4,3-a)pyridine hydrochloride

C19H27N5 (325.2266)


Dapiprazole is only found in individuals that have used or taken this drug. It is an alpha blocker. It is used to reverse mydriasis after eye examination. [Wikipedia]Dapiprazole acts through blocking the alpha1-adrenergic receptors in smooth muscle. It produces miosis through an effect on the dilator muscle of the iris and does not have any significant activity on ciliary muscle contraction and, therefore does not induce a significant change in the anterior chamber depth or the thickness of the lens. D002492 - Central Nervous System Depressants > D014149 - Tranquilizing Agents > D014150 - Antipsychotic Agents D002491 - Central Nervous System Agents > D011619 - Psychotropic Drugs > D014149 - Tranquilizing Agents C78272 - Agent Affecting Nervous System > C29747 - Adrenergic Agent > C72900 - Adrenergic Antagonist D018377 - Neurotransmitter Agents > D018663 - Adrenergic Agents > D018674 - Adrenergic Antagonists S - Sensory organs > S01 - Ophthalmologicals > S01E - Antiglaucoma preparations and miotics D002491 - Central Nervous System Agents > D002492 - Central Nervous System Depressants

   

Undeca-3,8-dienoylcarnitine

4-(trimethylazaniumyl)-3-(undeca-3,8-dienoyloxy)butanoate

C18H31NO4 (325.2253)


Undeca-3,8-dienoylcarnitine is an acylcarnitine. More specifically, it is an undeca-3,8-dienoic 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. Undeca-3,8-dienoylcarnitine is therefore classified as a medium chain AC. As a medium-chain acylcarnitine Undeca-3,8-dienoylcarnitine 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].

   

Undeca-2,8-dienoylcarnitine

4-(trimethylazaniumyl)-3-(undeca-2,8-dienoyloxy)butanoate

C18H31NO4 (325.2253)


Undeca-2,8-dienoylcarnitine is an acylcarnitine. More specifically, it is an undeca-2,8-dienoic 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. Undeca-2,8-dienoylcarnitine is therefore classified as a medium chain AC. As a medium-chain acylcarnitine Undeca-2,8-dienoylcarnitine 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].

   

Undeca-5,8-dienoylcarnitine

4-(trimethylazaniumyl)-3-(undeca-5,8-dienoyloxy)butanoate

C18H31NO4 (325.2253)


Undeca-5,8-dienoylcarnitine is an acylcarnitine. More specifically, it is an undeca-5,8-dienoic 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. Undeca-5,8-dienoylcarnitine is therefore classified as a medium chain AC. As a medium-chain acylcarnitine Undeca-5,8-dienoylcarnitine 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].

   

Undeca-4,6-dienoylcarnitine

4-(trimethylazaniumyl)-3-(undeca-4,6-dienoyloxy)butanoate

C18H31NO4 (325.2253)


Undeca-4,6-dienoylcarnitine is an acylcarnitine. More specifically, it is an undeca-4,6-dienoic 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. Undeca-4,6-dienoylcarnitine is therefore classified as a medium chain AC. As a medium-chain acylcarnitine Undeca-4,6-dienoylcarnitine 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].

   

Undeca-2,6-dienoylcarnitine

4-(trimethylazaniumyl)-3-(undeca-2,6-dienoyloxy)butanoate

C18H31NO4 (325.2253)


Undeca-2,6-dienoylcarnitine is an acylcarnitine. More specifically, it is an undeca-2,6-dienoic 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. Undeca-2,6-dienoylcarnitine is therefore classified as a medium chain AC. As a medium-chain acylcarnitine Undeca-2,6-dienoylcarnitine 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].

   

Undeca-3,9-dienoylcarnitine

4-(trimethylazaniumyl)-3-(undeca-3,9-dienoyloxy)butanoate

C18H31NO4 (325.2253)


Undeca-3,9-dienoylcarnitine is an acylcarnitine. More specifically, it is an undeca-3,9-dienoic 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. Undeca-3,9-dienoylcarnitine is therefore classified as a medium chain AC. As a medium-chain acylcarnitine Undeca-3,9-dienoylcarnitine 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].

   

Undeca-3,5-dienoylcarnitine

4-(trimethylazaniumyl)-3-(undeca-3,5-dienoyloxy)butanoate

C18H31NO4 (325.2253)


Undeca-3,5-dienoylcarnitine is an acylcarnitine. More specifically, it is an undeca-3,5-dienoic 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. Undeca-3,5-dienoylcarnitine is therefore classified as a medium chain AC. As a medium-chain acylcarnitine Undeca-3,5-dienoylcarnitine 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].

   

Undeca-7,9-dienoylcarnitine

4-(trimethylazaniumyl)-3-(undeca-7,9-dienoyloxy)butanoate

C18H31NO4 (325.2253)


Undeca-7,9-dienoylcarnitine is an acylcarnitine. More specifically, it is an undeca-7,9-dienoic 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. Undeca-7,9-dienoylcarnitine is therefore classified as a medium chain AC. As a medium-chain acylcarnitine Undeca-7,9-dienoylcarnitine 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].

   

Undeca-5,7-dienoylcarnitine

4-(trimethylazaniumyl)-3-(undeca-5,7-dienoyloxy)butanoate

C18H31NO4 (325.2253)


Undeca-5,7-dienoylcarnitine is an acylcarnitine. More specifically, it is an undeca-5,7-dienoic 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. Undeca-5,7-dienoylcarnitine is therefore classified as a medium chain AC. As a medium-chain acylcarnitine Undeca-5,7-dienoylcarnitine 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].

   

Undeca-5,9-dienoylcarnitine

4-(trimethylazaniumyl)-3-(undeca-5,9-dienoyloxy)butanoate

C18H31NO4 (325.2253)


Undeca-5,9-dienoylcarnitine is an acylcarnitine. More specifically, it is an undeca-5,9-dienoic 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. Undeca-5,9-dienoylcarnitine is therefore classified as a medium chain AC. As a medium-chain acylcarnitine Undeca-5,9-dienoylcarnitine 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].

   

Undeca-2,9-dienoylcarnitine

4-(trimethylazaniumyl)-3-(undeca-2,9-dienoyloxy)butanoate

C18H31NO4 (325.2253)


Undeca-2,9-dienoylcarnitine is an acylcarnitine. More specifically, it is an undeca-2,9-dienoic 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. Undeca-2,9-dienoylcarnitine is therefore classified as a medium chain AC. As a medium-chain acylcarnitine Undeca-2,9-dienoylcarnitine 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].

   

Undeca-6,9-dienoylcarnitine

4-(trimethylazaniumyl)-3-(undeca-6,9-dienoyloxy)butanoate

C18H31NO4 (325.2253)


Undeca-6,9-dienoylcarnitine is an acylcarnitine. More specifically, it is an undeca-6,9-dienoic 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. Undeca-6,9-dienoylcarnitine is therefore classified as a medium chain AC. As a medium-chain acylcarnitine Undeca-6,9-dienoylcarnitine 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].

   

Undeca-6,8-dienoylcarnitine

4-(trimethylazaniumyl)-3-(undeca-6,8-dienoyloxy)butanoate

C18H31NO4 (325.2253)


Undeca-6,8-dienoylcarnitine is an acylcarnitine. More specifically, it is an undeca-6,8-dienoic 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. Undeca-6,8-dienoylcarnitine is therefore classified as a medium chain AC. As a medium-chain acylcarnitine Undeca-6,8-dienoylcarnitine 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].

   

Undeca-3,7-dienoylcarnitine

4-(trimethylazaniumyl)-3-(undeca-3,7-dienoyloxy)butanoate

C18H31NO4 (325.2253)


Undeca-3,7-dienoylcarnitine is an acylcarnitine. More specifically, it is an undeca-3,7-dienoic 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. Undeca-3,7-dienoylcarnitine is therefore classified as a medium chain AC. As a medium-chain acylcarnitine Undeca-3,7-dienoylcarnitine 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].

   

Undeca-2,4-dienoylcarnitine

4-(trimethylazaniumyl)-3-(undeca-2,4-dienoyloxy)butanoate

C18H31NO4 (325.2253)


Undeca-2,4-dienoylcarnitine is an acylcarnitine. More specifically, it is an undeca-2,4-dienoic 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. Undeca-2,4-dienoylcarnitine is therefore classified as a medium chain AC. As a medium-chain acylcarnitine Undeca-2,4-dienoylcarnitine 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].

   

Undeca-2,7-dienoylcarnitine

4-(trimethylazaniumyl)-3-(undeca-2,7-dienoyloxy)butanoate

C18H31NO4 (325.2253)


Undeca-2,7-dienoylcarnitine is an acylcarnitine. More specifically, it is an undeca-2,7-dienoic 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. Undeca-2,7-dienoylcarnitine is therefore classified as a medium chain AC. As a medium-chain acylcarnitine Undeca-2,7-dienoylcarnitine 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].

   

Undeca-4,8-dienoylcarnitine

4-(trimethylazaniumyl)-3-(undeca-4,8-dienoyloxy)butanoate

C18H31NO4 (325.2253)


Undeca-4,8-dienoylcarnitine is an acylcarnitine. More specifically, it is an undeca-4,8-dienoic 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. Undeca-4,8-dienoylcarnitine is therefore classified as a medium chain AC. As a medium-chain acylcarnitine Undeca-4,8-dienoylcarnitine 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].

   

Undeca-2,5-dienoylcarnitine

4-(trimethylazaniumyl)-3-(undeca-2,5-dienoyloxy)butanoate

C18H31NO4 (325.2253)


Undeca-2,5-dienoylcarnitine is an acylcarnitine. More specifically, it is an undeca-2,5-dienoic 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. Undeca-2,5-dienoylcarnitine is therefore classified as a medium chain AC. As a medium-chain acylcarnitine Undeca-2,5-dienoylcarnitine 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].

   

Undeca-4,9-dienoylcarnitine

4-(trimethylazaniumyl)-3-(undeca-4,9-dienoyloxy)butanoate

C18H31NO4 (325.2253)


Undeca-4,9-dienoylcarnitine is an acylcarnitine. More specifically, it is an undeca-4,9-dienoic 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. Undeca-4,9-dienoylcarnitine is therefore classified as a medium chain AC. As a medium-chain acylcarnitine Undeca-4,9-dienoylcarnitine 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].

   

Undeca-4,7-dienoylcarnitine

4-(trimethylazaniumyl)-3-(undeca-4,7-dienoyloxy)butanoate

C18H31NO4 (325.2253)


Undeca-4,7-dienoylcarnitine is an acylcarnitine. More specifically, it is an undeca-4,7-dienoic 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. Undeca-4,7-dienoylcarnitine is therefore classified as a medium chain AC. As a medium-chain acylcarnitine Undeca-4,7-dienoylcarnitine 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].

   

Undeca-3,6-dienoylcarnitine

4-(trimethylazaniumyl)-3-(undeca-3,6-dienoyloxy)butanoate

C18H31NO4 (325.2253)


Undeca-3,6-dienoylcarnitine is an acylcarnitine. More specifically, it is an undeca-3,6-dienoic 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. Undeca-3,6-dienoylcarnitine is therefore classified as a medium chain AC. As a medium-chain acylcarnitine Undeca-3,6-dienoylcarnitine 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-Myristoyl Proline

1-tetradecanoylpyrrolidine-2-carboxylic acid

C19H35NO3 (325.2617)


N-myristoyl proline 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 Myristic acid amide of Proline. 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-Myristoyl Proline 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-Myristoyl Proline 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.

   

2-(3-(Diisopropylamino)-1-phenylpropyl)-4-methylphenol

2-[3-[Bis(1-methylethyl)amino]-1-phenylpropyl]-4-methylphenol

C22H31NO (325.2406)


   

2-Aminoethyl oleate

2-Aminoethyl octadec-9-enoic acid

C20H39NO2 (325.2981)


   

9-Octadecenamide, N-(2-hydroxyethyl)-, (9Z)-

9-Octadecenamide, N-(2-hydroxyethyl)-, (9Z)-

C20H39NO2 (325.2981)


   

Nitrolinoleic acid

2-nitrooctadeca-9,12-dienoic acid

C18H31NO4 (325.2253)


   

18-Nitrooctadeca-9,12-dienoic acid

18-Nitrooctadeca-9,12-dienoic acid

C18H31NO4 (325.2253)


   

3-dehydrosphinganine (C20)

(1-hydroxy-3-oxoicosan-2-yl)azaniumyl

C20H39NO2 (325.2981)


3-dehydrosphinganine (c20) is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). 3-dehydrosphinganine (c20) can be found in a number of food items such as abiyuch, babassu palm, groundcherry, and gooseberry, which makes 3-dehydrosphinganine (c20) a potential biomarker for the consumption of these food products.

   

Broussonetine W

Broussonetine W

C18H31NO4 (325.2253)


   

Holadienine

Holadienine

C22H31NO (325.2406)


   

14-(5-hydroxy-6-methyl-2-piperidinyl)-2-tetradecanone

14-(5-hydroxy-6-methyl-2-piperidinyl)-2-tetradecanone

C20H39NO2 (325.2981)


   

Semiplenamide C

Semiplenamide C

C20H39NO2 (325.2981)


   

Tumonoic acid E

Tumonoic acid E

C18H31NO4 (325.2253)


A natural product found particularly in Oscillatoria margaritifera and Oscillatoria margaritifera.

   

N-3-oxo-tetradecanoyl-L-Homoserine lactone

N-3-oxo-tetradecanoyl-L-Homoserine lactone

C18H31NO4 (325.2253)


   

allopumiliotoxin 325A/325A

allopumiliotoxin 325A/325A

C19H35NO3 (325.2617)


   

kurchilidine

kurchilidine

C22H31NO (325.2406)


   

N-<9,10-dihydrojasmonoyl>-(S)-isoleucine

N-<9,10-dihydrojasmonoyl>-(S)-isoleucine

C18H31NO4 (325.2253)


   

1-methyl-2-[(Z)-5-dodecenyl]-4(1H)-quinolone|1-methyl-2-[(Z)-5?-dodecenyl]-4(1H)-quinolone

1-methyl-2-[(Z)-5-dodecenyl]-4(1H)-quinolone|1-methyl-2-[(Z)-5?-dodecenyl]-4(1H)-quinolone

C22H31NO (325.2406)


   

(2E,4E,8E,10E,14Z)-N-Isobutyl-2,4,8,10,14-octadecapentaen-12-insaeureamid

(2E,4E,8E,10E,14Z)-N-Isobutyl-2,4,8,10,14-octadecapentaen-12-insaeureamid

C22H31NO (325.2406)


   

Funtudienin, Cona-3,5-dienin-7-on

Funtudienin, Cona-3,5-dienin-7-on

C22H31NO (325.2406)


   

N-(2-oxooxolan-3-yl)pentadecanamide

N-(2-oxooxolan-3-yl)pentadecanamide

C19H35NO3 (325.2617)


   

BISOPROLOL

BISOPROLOL

C18H31NO4 (325.2253)


C - Cardiovascular system > C07 - Beta blocking agents > C07A - Beta blocking agents > C07AB - Beta blocking agents, selective C78272 - Agent Affecting Nervous System > C29747 - Adrenergic Agent > C72900 - Adrenergic Antagonist D018373 - Peripheral Nervous System Agents > D001337 - Autonomic Agents > D013565 - Sympatholytics D018377 - Neurotransmitter Agents > D018663 - Adrenergic Agents > D018674 - Adrenergic Antagonists D002317 - Cardiovascular Agents > D000959 - Antihypertensive Agents CONFIDENCE Reference Standard (Level 1)

   

MLS002153155-01!N-Oleoylethanolamine111-58-0

MLS002153155-01!N-Oleoylethanolamine111-58-0

C20H39NO2 (325.2981)


   

Denatonium

Denatonium

[C21H29N2O]+ (325.228)


D002491 - Central Nervous System Agents > D000075162 - Abuse-Deterrent Formulations D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents D010592 - Pharmaceutic Aids > D000075528 - Aversive Agents CONFIDENCE standard compound; INTERNAL_ID 2876 INTERNAL_ID 2876; CONFIDENCE standard compound CONFIDENCE Reference Standard (Level 1)

   

Tolterodine

Tolterodine-L-tartrate

C22H31NO (325.2406)


G - Genito urinary system and sex hormones > G04 - Urologicals > G04B - Urologicals > G04BD - Drugs for urinary frequency and incontinence C78272 - Agent Affecting Nervous System > C66880 - Anticholinergic Agent > C29704 - Antimuscarinic Agent D018377 - Neurotransmitter Agents > D018678 - Cholinergic Agents > D018680 - Cholinergic Antagonists D000089162 - Genitourinary Agents > D064804 - Urological Agents Tolterodine(PNU-200583) is a potent muscarinic receptor antagonists that show selectivity for the urinary bladder over salivary glands in vivo. IC50 Value: Target: mAChR in vitro: Carbachol-induced contractions of isolated guinea pig bladder were effectively inhibited by tolterodine (IC50 14 nM) and 5-HM (IC50 5.7 nM). The IC50 values were in the microM range and the antimuscarinic potency of tolterodine was 27, 200 and 370-485 times higher, respectively, than its potency in blocking histamine receptors, alpha-adrenoceptors and calcium channels. The active metabolite, 5-HM, was >900 times less potent at these sites than at bladder muscarinic receptors [1]. in vivo: Tolterodine was extensively metabolized in vivo [2]. In the passive-avoidance test, tolterodine at 1 or 3 mg/kg had no effect on memory; the latency to cross and percentage of animals crossing were comparable to controls. In contrast, scopolamine induced a memory deficit; the latency to cross was decreased, and the number of animals crossing was increased [3].

   

N-Oleoylethanolamine

N-Oleoylethanolamine

C20H39NO2 (325.2981)


   

3-oxo-C14 homoserine lactone

3-oxo-C14 homoserine lactone

C18H31NO4 (325.2253)


INTERNAL_ID 212; CONFIDENCE standard compound CONFIDENCE standard compound; INTERNAL_ID 212

   

10-Nitrolinoleic acid

10-Nitrolinoleic acid

C18H31NO4 (325.2253)


   

N-(3-Oxotetradecanoyl)-L-homoserine lactone

N-(3-Oxotetradecanoyl)-L-homoserine lactone

C18H31NO4 (325.2253)


   

Oleamide mea

(Z)-N-(2-hydroxyethyl)octadec-9-enamide

C20H39NO2 (325.2981)


D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones > D063385 - Cannabinoid Receptor Modulators D018377 - Neurotransmitter Agents > D063385 - Cannabinoid Receptor Modulators > D063386 - Cannabinoid Receptor Agonists COVID info from DrugBank Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS Oleoylethanolamide is a high affinity endogenous PPAR-α agonist, which plays an important role in the treatment of obesity and arteriosclerosis. Oleoylethanolamide is a high affinity endogenous PPAR-α agonist, which plays an important role in the treatment of obesity and arteriosclerosis.

   

(7R)-8-((8S,Z)-8-hydroxy-8-methylhexahydroindolizin-6(5H)-ylidene)-4,7-dimethyloctane-2,3-diol

(7R)-8-((8S,Z)-8-hydroxy-8-methylhexahydroindolizin-6(5H)-ylidene)-4,7-dimethyloctane-2,3-diol

C19H35NO3 (325.2617)


   

(7R,8R,E)-6-((2R)-6-hydroxy-2,5-dimethyloctylidene)-8-methyloctahydroindolizine-7,8-diol

(7R,8R,E)-6-((2R)-6-hydroxy-2,5-dimethyloctylidene)-8-methyloctahydroindolizine-7,8-diol

C19H35NO3 (325.2617)


   

5-Oxo-ETE-d7

5-oxo-6E,8Z,11Z,14Z-eicosatetraenoic acid-d7

C20H23D7O3 (325.2634)


   

Oleoyl-EA(d2)

N-(9Z-octadecenoyl)-ethanolamine(d2)

C20H39NO2 (325.2981)


   

N-3-oxo-myristoyl-L-Homoserine lactone

3-oxo-N-[(3S)-tetrahydro-2-oxo-3-furanyl]-tetradecanamide

C18H31NO4 (325.2253)


   

C15-HSL

N-[(3S)-tetrahydro-2-oxo-3-furanyl]-pentadecanamide

C19H35NO3 (325.2617)


   

10-nitro,9Z,12Z-octadecadienoic acid

10-nitro,9Z,12Z-octadecadienoic acid

C18H31NO4 (325.2253)


   

Dapiprazole

1-(2-methylphenyl)-4-(2-{5H,6H,7H,8H-[1,2,4]triazolo[4,3-a]pyridin-3-yl}ethyl)piperazine

C19H27N5 (325.2266)


D002492 - Central Nervous System Depressants > D014149 - Tranquilizing Agents > D014150 - Antipsychotic Agents D002491 - Central Nervous System Agents > D011619 - Psychotropic Drugs > D014149 - Tranquilizing Agents C78272 - Agent Affecting Nervous System > C29747 - Adrenergic Agent > C72900 - Adrenergic Antagonist D018377 - Neurotransmitter Agents > D018663 - Adrenergic Agents > D018674 - Adrenergic Antagonists S - Sensory organs > S01 - Ophthalmologicals > S01E - Antiglaucoma preparations and miotics D002491 - Central Nervous System Agents > D002492 - Central Nervous System Depressants

   

Small bacteriocin

(7E)-3-hydroxy-N-(2-oxooxolan-3-yl)tetradec-7-enamide

C18H31NO4 (325.2253)


   

N-(7-Isocucurbinoyl)isoleucine

2-(2-{3-hydroxy-2-[(2E)-pent-2-en-1-yl]cyclopentyl}acetamido)-3-methylpentanoic acid

C18H31NO4 (325.2253)


   

9-NO2-CLA

9-nitro-9Z,11E-octadecadienoic acid

C18H31NO4 (325.2253)


   

12-NO2-CLA

12-nitro-9E,11Z-octadecadienoic acid

C18H31NO4 (325.2253)


   

N-[9,10-Dihydrojasmonoyl]isoleucine

[(1R,2R)-3-oxo-2-pentylcyclopentyl]ethanoyl leucine

C18H31NO4 (325.2253)


   

NA 20:1;O

N-[(S)-1-Methyl-2-hydroxyethyl]-2-methyl-2-hexadeceneamide

C20H39NO2 (325.2981)


   

N-(3R-hydroxy-7Z-tetradecenoyl)-homoserine lactone

N-(3R-Hydroxy-7-cis-tetradecenoyl)homoserine lactone

C18H31NO4 (325.2253)


   

3O-C14-HSL

N-(3-oxo-tetradecanoyl)-homoserine lactone

C18H31NO4 (325.2253)


   

NAE 18:1

Trans-11-octadecenoic acid ethanolamide

C20H39NO2 (325.2981)


   

tPeEA

Trans-petroselinic acid ethanolamide

C20H39NO2 (325.2981)


   

4-(BENZYLAMINOMETHYL)-2,6-DI-TERT-BUTYLPHENOL

4-(BENZYLAMINOMETHYL)-2,6-DI-TERT-BUTYLPHENOL

C22H31NO (325.2406)


   

tert-butyl 9-(2-methoxy-2-oxoethyl)-3-azaspiro[5.5]undecane-3-carboxylate

tert-butyl 9-(2-methoxy-2-oxoethyl)-3-azaspiro[5.5]undecane-3-carboxylate

C18H31NO4 (325.2253)


   

dibutoxy(oxo)phosphanium,triethyl(methyl)azanium

dibutoxy(oxo)phosphanium,triethyl(methyl)azanium

C15H36NO4P (325.2382)


   

N-tert-butyl-2-methyl-1-phenyl-N-(1-phenylethoxy)propan-1-amine

N-tert-butyl-2-methyl-1-phenyl-N-(1-phenylethoxy)propan-1-amine

C22H31NO (325.2406)


   

4-CYCLOHEXYLCARBAMOYLMETHYL-PIPERAZINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER

4-CYCLOHEXYLCARBAMOYLMETHYL-PIPERAZINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER

C17H31N3O3 (325.2365)


   

(2s,3r,4e)-2-azido-4-octadecene-1,3-diol

(2s,3r,4e)-2-azido-4-octadecene-1,3-diol

C18H35N3O2 (325.2729)


   

N,N,N-Trimethyl-1-dodecanaminium hydrogen sulfate

N,N,N-Trimethyl-1-dodecanaminium hydrogen sulfate

C15H35NO4S (325.2287)


   

Miripirium chloride

Miripirium chloride

C20H36ClN (325.2536)


C254 - Anti-Infective Agent

   

N-Tetradecanoyl-L-proline

N-Tetradecanoyl-L-proline

C19H35NO3 (325.2617)


   

S-(-)-Tolterodine

S-(-)-Tolterodine

C22H31NO (325.2406)


   

2,5-Pyrrolidinedione, 1-2-2-2-(2-aminoethyl)aminoethylaminoethylaminoethyl-, monopolyisobutenyl derivs.

2,5-Pyrrolidinedione, 1-2-2-2-(2-aminoethyl)aminoethylaminoethylaminoethyl-, monopolyisobutenyl derivs.

C16H31N5O2 (325.2478)


   

1-(Isopropylamino)-3-{4-[(2-propoxyethoxy)methyl]phenoxy}-2-propanol

1-(Isopropylamino)-3-{4-[(2-propoxyethoxy)methyl]phenoxy}-2-propanol

C18H31NO4 (325.2253)


   

Bisoprolol EP Impurity F

Bisoprolol EP Impurity F

C18H31NO4 (325.2253)


   

(E)-N-(2-hydroxyethyl)octadec-9-enamide

(E)-N-(2-hydroxyethyl)octadec-9-enamide

C20H39NO2 (325.2981)


   

N-(3-Hydroxy-7-cis-tetradecenoyl)homoserine lactone

N-(3-Hydroxy-7-cis-tetradecenoyl)homoserine lactone

C18H31NO4 (325.2253)


   

N-(3-Oxotetradecanoyl)-DL-homoserine lactone

N-(3-Oxotetradecanoyl)-DL-homoserine lactone

C18H31NO4 (325.2253)


N-(3-Oxotetradecanoyl)-DL-homoserine lactone, a member of N-Acyl homoserine lactone (AHL) from gram-negative bacteria, is a quorum sensing (QS) signaling molecule[1][2].

   

3-(2,2,6-Trimethyl-3-piperiden-4-yl)-2(2-methyl-2-aminopropyl)-1-methylindole

3-(2,2,6-Trimethyl-3-piperiden-4-yl)-2(2-methyl-2-aminopropyl)-1-methylindole

C21H31N3 (325.2518)


   

3-oxo-N-[(3S)-2-oxotetrahydrofuran-3-yl]tetradecanamide

3-oxo-N-[(3S)-2-oxotetrahydrofuran-3-yl]tetradecanamide

C18H31NO4 (325.2253)


   

(Z)-N-(2-hydroxyethyl)octadec-11-enamide

(Z)-N-(2-hydroxyethyl)octadec-11-enamide

C20H39NO2 (325.2981)


   

(11Z,14R)-14-hydroxyicos-11-enoate

(11Z,14R)-14-hydroxyicos-11-enoate

C20H37O3- (325.2743)


   

(2R)-2-octyl-3-oxododecanoate

(2R)-2-octyl-3-oxododecanoate

C20H37O3- (325.2743)


   

(3S,7R,11R)-3,7,11,15-tetramethyl-2-oxohexadecanoate

(3S,7R,11R)-3,7,11,15-tetramethyl-2-oxohexadecanoate

C20H37O3- (325.2743)


   

(9E,12E)-2-nitrooctadeca-9,12-dienoic acid

(9E,12E)-2-nitrooctadeca-9,12-dienoic acid

C18H31NO4 (325.2253)


   

2-aminoethyl (E)-octadec-9-enoate

2-aminoethyl (E)-octadec-9-enoate

C20H39NO2 (325.2981)


   

Undeca-3,8-dienoylcarnitine

Undeca-3,8-dienoylcarnitine

C18H31NO4 (325.2253)


   

Undeca-2,8-dienoylcarnitine

Undeca-2,8-dienoylcarnitine

C18H31NO4 (325.2253)


   

Undeca-5,8-dienoylcarnitine

Undeca-5,8-dienoylcarnitine

C18H31NO4 (325.2253)


   

Undeca-4,6-dienoylcarnitine

Undeca-4,6-dienoylcarnitine

C18H31NO4 (325.2253)


   

Undeca-2,6-dienoylcarnitine

Undeca-2,6-dienoylcarnitine

C18H31NO4 (325.2253)


   

Undeca-3,9-dienoylcarnitine

Undeca-3,9-dienoylcarnitine

C18H31NO4 (325.2253)


   

Undeca-3,5-dienoylcarnitine

Undeca-3,5-dienoylcarnitine

C18H31NO4 (325.2253)


   

Undeca-7,9-dienoylcarnitine

Undeca-7,9-dienoylcarnitine

C18H31NO4 (325.2253)


   

Undeca-5,7-dienoylcarnitine

Undeca-5,7-dienoylcarnitine

C18H31NO4 (325.2253)


   

Undeca-5,9-dienoylcarnitine

Undeca-5,9-dienoylcarnitine

C18H31NO4 (325.2253)


   

Undeca-2,9-dienoylcarnitine

Undeca-2,9-dienoylcarnitine

C18H31NO4 (325.2253)


   

Undeca-6,9-dienoylcarnitine

Undeca-6,9-dienoylcarnitine

C18H31NO4 (325.2253)


   

Undeca-6,8-dienoylcarnitine

Undeca-6,8-dienoylcarnitine

C18H31NO4 (325.2253)


   

Undeca-3,7-dienoylcarnitine

Undeca-3,7-dienoylcarnitine

C18H31NO4 (325.2253)


   

Undeca-2,4-dienoylcarnitine

Undeca-2,4-dienoylcarnitine

C18H31NO4 (325.2253)


   

Undeca-2,7-dienoylcarnitine

Undeca-2,7-dienoylcarnitine

C18H31NO4 (325.2253)


   

Undeca-4,8-dienoylcarnitine

Undeca-4,8-dienoylcarnitine

C18H31NO4 (325.2253)


   

Undeca-2,5-dienoylcarnitine

Undeca-2,5-dienoylcarnitine

C18H31NO4 (325.2253)


   

Undeca-4,9-dienoylcarnitine

Undeca-4,9-dienoylcarnitine

C18H31NO4 (325.2253)


   

Undeca-4,7-dienoylcarnitine

Undeca-4,7-dienoylcarnitine

C18H31NO4 (325.2253)


   

Undeca-3,6-dienoylcarnitine

Undeca-3,6-dienoylcarnitine

C18H31NO4 (325.2253)


   

18-Nitrooctadeca-9,12-dienoic acid

18-Nitrooctadeca-9,12-dienoic acid

C18H31NO4 (325.2253)


   

N-pentadecanoyl-L-Homoserine lactone

N-pentadecanoyl-L-Homoserine lactone

C19H35NO3 (325.2617)


   

2-Oxophytanate

2-Oxophytanate

C20H37O3- (325.2743)


Conjugate base of 2-oxophytanic acid.

   

4-(1,4-Dioxaspiro[4.11]hexadecan-3-ylmethyl)morpholine

4-(1,4-Dioxaspiro[4.11]hexadecan-3-ylmethyl)morpholine

C19H35NO3 (325.2617)


   

Henicosanoate

Henicosanoate

C21H41O2- (325.3106)


A long-chain fatty acid anion resulting from the deprotonation of the carboxy group of henicosanoic acid. Major species at pH 7.3.

   

2-Hydroxygondoate

2-Hydroxygondoate

C20H37O3- (325.2743)


   

methoxymycolate type-3 (IX)

methoxymycolate type-3 (IX)

C19H33O4- (325.2379)


   

(3R,5R,7S,8E,10E,12E)-3-amino-5,7-dihydroxyoctadeca-8,10,12-trienoic acid

(3R,5R,7S,8E,10E,12E)-3-amino-5,7-dihydroxyoctadeca-8,10,12-trienoic acid

C18H31NO4 (325.2253)


   

(2S)-1-[(E)-3-hydroxy-2,4,6-trimethyldec-4-enoyl]pyrrolidine-2-carboxylic acid

(2S)-1-[(E)-3-hydroxy-2,4,6-trimethyldec-4-enoyl]pyrrolidine-2-carboxylic acid

C18H31NO4 (325.2253)


   

N-[(4E,8E)-1,3-dihydroxyhexadeca-4,8-dien-2-yl]propanamide

N-[(4E,8E)-1,3-dihydroxyhexadeca-4,8-dien-2-yl]propanamide

C19H35NO3 (325.2617)


   

N-[(4E,8E)-1,3-dihydroxydodeca-4,8-dien-2-yl]heptanamide

N-[(4E,8E)-1,3-dihydroxydodeca-4,8-dien-2-yl]heptanamide

C19H35NO3 (325.2617)


   

N-[(4E,8E)-1,3-dihydroxytetradeca-4,8-dien-2-yl]pentanamide

N-[(4E,8E)-1,3-dihydroxytetradeca-4,8-dien-2-yl]pentanamide

C19H35NO3 (325.2617)


   

N-[(4E,8E)-1,3-dihydroxyheptadeca-4,8-dien-2-yl]acetamide

N-[(4E,8E)-1,3-dihydroxyheptadeca-4,8-dien-2-yl]acetamide

C19H35NO3 (325.2617)


   

N-[(4E,8E)-1,3-dihydroxytrideca-4,8-dien-2-yl]hexanamide

N-[(4E,8E)-1,3-dihydroxytrideca-4,8-dien-2-yl]hexanamide

C19H35NO3 (325.2617)


   

N-[(4E,8E)-1,3-dihydroxypentadeca-4,8-dien-2-yl]butanamide

N-[(4E,8E)-1,3-dihydroxypentadeca-4,8-dien-2-yl]butanamide

C19H35NO3 (325.2617)


   

N-[3-(Acetyloxy)-2,2-dimethylpropionyl]-N-butyl-2,3-dimethyl-4-pentenamide

N-[3-(Acetyloxy)-2,2-dimethylpropionyl]-N-butyl-2,3-dimethyl-4-pentenamide

C18H31NO4 (325.2253)


   

C10-LNO2

(9E,12Z)-10-Nitrooctadeca-9,12-dienoic acid

C18H31NO4 (325.2253)


   

N-[[3-Hydroxy-2-(2-pentenyl)cyclopentyl]acetyl]isoleucine

N-[[3-Hydroxy-2-(2-pentenyl)cyclopentyl]acetyl]isoleucine

C18H31NO4 (325.2253)


   

Denatonium

Denatonium

C21H29N2O+ (325.228)


D002491 - Central Nervous System Agents > D000075162 - Abuse-Deterrent Formulations D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents D010592 - Pharmaceutic Aids > D000075528 - Aversive Agents

   

12-Nitrolinoleic acid

(9Z,12E)-12-nitrooctadeca-9,12-dienoic acid

C18H31NO4 (325.2253)


   

2-hydroxyicosenoate

2-hydroxyicosenoate

C20H37O3 (325.2743)


A 2-hydroxy fatty acid anion with a chain that is composed of 20 carbons and 1 double bond (position unspecified).

   

fatty acid anion 21:0

fatty acid anion 21:0

C21H41O2 (325.3106)


A saturated fatty acid anion containing 21 carbons (R(1) = C20H41). It is the major species at pH 7.3.

   

Oleoyl ethanolamide

Oleoyl ethanolamide

C20H39NO2 (325.2981)


An N-(long-chain-acyl)ethanolamine that is the ethanolamide of oleic acid. The monounsaturated analogue of the endocannabinoid anandamide.

   

AcCa(11:2)

AcCa(11:2)

C18H31NO4 (325.2253)


Provides by LipidSearch Vendor. © Copyright 2006-2024 Thermo Fisher Scientific Inc. All rights reserved

   

AEA(18:1)

AEA(18:1)

C20H39NO2 (325.2981)


Provides by LipidSearch Vendor. © Copyright 2006-2024 Thermo Fisher Scientific Inc. All rights reserved

   

Sphingosine (d20:2)

SPH(d20:2)

C20H39NO2 (325.2981)


Provides by LipidSearch Vendor. © Copyright 2006-2024 Thermo Fisher Scientific Inc. All rights reserved

   

NA-Ala 16:1(9Z)

NA-Ala 16:1(9Z)

C19H35NO3 (325.2617)


   

NA-Gly 17:1(9Z)

NA-Gly 17:1(9Z)

C19H35NO3 (325.2617)


   

NA-Val 14:1(9Z)

NA-Val 14:1(9Z)

C19H35NO3 (325.2617)


   
   
   

n-(1-hydroxy-3-methylpentan-2-yl)-3-[2-methyl-3-(4-oxohexan-2-yl)oxiran-2-yl]prop-2-enimidic acid

n-(1-hydroxy-3-methylpentan-2-yl)-3-[2-methyl-3-(4-oxohexan-2-yl)oxiran-2-yl]prop-2-enimidic acid

C18H31NO4 (325.2253)


   

(2s)-1-[(4e)-3-hydroxy-2,4,6-trimethyldec-4-enoyl]pyrrolidine-2-carboxylic acid

(2s)-1-[(4e)-3-hydroxy-2,4,6-trimethyldec-4-enoyl]pyrrolidine-2-carboxylic acid

C18H31NO4 (325.2253)


   

n-(1-hydroxypropan-2-yl)-2-methylhexadec-2-enimidic acid

n-(1-hydroxypropan-2-yl)-2-methylhexadec-2-enimidic acid

C20H39NO2 (325.2981)


   

n-[(2s,3s)-1-hydroxy-3-methylpentan-2-yl]-3-[(2r,3s)-2-methyl-3-[(2s)-4-oxohexan-2-yl]oxiran-2-yl]prop-2-enimidic acid

n-[(2s,3s)-1-hydroxy-3-methylpentan-2-yl]-3-[(2r,3s)-2-methyl-3-[(2s)-4-oxohexan-2-yl]oxiran-2-yl]prop-2-enimidic acid

C18H31NO4 (325.2253)


   

2-{7-[3,4-dihydroxy-5-(hydroxymethyl)pyrrolidin-2-yl]heptyl}cyclohex-2-en-1-one

2-{7-[3,4-dihydroxy-5-(hydroxymethyl)pyrrolidin-2-yl]heptyl}cyclohex-2-en-1-one

C18H31NO4 (325.2253)


   

(2e,7e,9e)-6-ethoxy-11-hydroxy-n-(2-hydroxy-2-methylpropyl)dodeca-2,7,9-trienimidic acid

(2e,7e,9e)-6-ethoxy-11-hydroxy-n-(2-hydroxy-2-methylpropyl)dodeca-2,7,9-trienimidic acid

C18H31NO4 (325.2253)


   

(2s,3r)-2-({1-hydroxy-2-[(1r,2s)-3-oxo-2-pentylcyclopentyl]ethylidene}amino)-3-methylpentanoic acid

(2s,3r)-2-({1-hydroxy-2-[(1r,2s)-3-oxo-2-pentylcyclopentyl]ethylidene}amino)-3-methylpentanoic acid

C18H31NO4 (325.2253)


   

12- acetoxy group-9-octadecadienoic acid

NA

C18H31NO4 (325.2253)


{"Ingredient_id": "HBIN000697","Ingredient_name": "12- acetoxy group-9-octadecadienoic acid","Alias": "NA","Ingredient_formula": "C18H31NO4","Ingredient_Smile": "CCCCCC=C(CC=CCCCCCCCC(=O)O)[N+](=O)[O-]","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "34800","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}

   

(2s,3r)-2-({1-hydroxy-2-[(1r,2r)-3-oxo-2-pentylcyclopentyl]ethylidene}amino)-3-methylpentanoic acid

(2s,3r)-2-({1-hydroxy-2-[(1r,2r)-3-oxo-2-pentylcyclopentyl]ethylidene}amino)-3-methylpentanoic acid

C18H31NO4 (325.2253)


   

(9z)-n-(2-hydroxyethyl)octadec-9-enimidic acid

(9z)-n-(2-hydroxyethyl)octadec-9-enimidic acid

C20H39NO2 (325.2981)


   

n-(2-methylpropyl)octadeca-2,4,8,10,14-pentaen-12-ynimidic acid

n-(2-methylpropyl)octadeca-2,4,8,10,14-pentaen-12-ynimidic acid

C22H31NO (325.2406)


   

(2e)-n-[(2s,3s)-1-hydroxy-3-methylpentan-2-yl]-3-[(2r,3s)-2-methyl-3-[(2s)-4-oxohexan-2-yl]oxiran-2-yl]prop-2-enimidic acid

(2e)-n-[(2s,3s)-1-hydroxy-3-methylpentan-2-yl]-3-[(2r,3s)-2-methyl-3-[(2s)-4-oxohexan-2-yl]oxiran-2-yl]prop-2-enimidic acid

C18H31NO4 (325.2253)


   

(2e,4e,8e,10z,14z)-n-(2-methylpropyl)octadeca-2,4,8,10,14-pentaen-12-ynimidic acid

(2e,4e,8e,10z,14z)-n-(2-methylpropyl)octadeca-2,4,8,10,14-pentaen-12-ynimidic acid

C22H31NO (325.2406)


   

(1r,2s,5s,6s,9r,12s,13r)-6-ethyl-13-methyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosa-14,17-dien-16-one

(1r,2s,5s,6s,9r,12s,13r)-6-ethyl-13-methyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosa-14,17-dien-16-one

C22H31NO (325.2406)


   

1-[(4e)-3-hydroxy-2,4,6-trimethyldec-4-enoyl]pyrrolidine-2-carboxylic acid

1-[(4e)-3-hydroxy-2,4,6-trimethyldec-4-enoyl]pyrrolidine-2-carboxylic acid

C18H31NO4 (325.2253)


   

(8e)-n-(2-methylpropyl)octadeca-2,4,8,10,14-pentaen-12-ynimidic acid

(8e)-n-(2-methylpropyl)octadeca-2,4,8,10,14-pentaen-12-ynimidic acid

C22H31NO (325.2406)


   

(1s,2s,5s,6s,9s,12s,13s)-6,7,13-trimethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosa-14,17-dien-16-one

(1s,2s,5s,6s,9s,12s,13s)-6,7,13-trimethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosa-14,17-dien-16-one

C22H31NO (325.2406)


   

(2e)-n-[(2s)-1-hydroxypropan-2-yl]-2-methylhexadec-2-enimidic acid

(2e)-n-[(2s)-1-hydroxypropan-2-yl]-2-methylhexadec-2-enimidic acid

C20H39NO2 (325.2981)


   

2-{7-[(2r,3r,4r,5r)-3,4-dihydroxy-5-(hydroxymethyl)pyrrolidin-2-yl]heptyl}cyclohex-2-en-1-one

2-{7-[(2r,3r,4r,5r)-3,4-dihydroxy-5-(hydroxymethyl)pyrrolidin-2-yl]heptyl}cyclohex-2-en-1-one

C18H31NO4 (325.2253)


   

2-({1-hydroxy-2-[(1r,2s)-3-oxo-2-pentylcyclopentyl]ethylidene}amino)-3-methylpentanoic acid

2-({1-hydroxy-2-[(1r,2s)-3-oxo-2-pentylcyclopentyl]ethylidene}amino)-3-methylpentanoic acid

C18H31NO4 (325.2253)


   

6,7,13-trimethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosa-14,17-dien-16-one

6,7,13-trimethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosa-14,17-dien-16-one

C22H31NO (325.2406)


   

2-{[1-hydroxy-2-(3-oxo-2-pentylcyclopentyl)ethylidene]amino}-3-methylpentanoic acid

2-{[1-hydroxy-2-(3-oxo-2-pentylcyclopentyl)ethylidene]amino}-3-methylpentanoic acid

C18H31NO4 (325.2253)


   

14-[(2r,5s,6s)-5-hydroxy-6-methylpiperidin-2-yl]tetradecan-2-one

14-[(2r,5s,6s)-5-hydroxy-6-methylpiperidin-2-yl]tetradecan-2-one

C20H39NO2 (325.2981)


   

(2e,7e,9e)-11-ethoxy-6-hydroxy-n-(2-hydroxy-2-methylpropyl)dodeca-2,7,9-trienimidic acid

(2e,7e,9e)-11-ethoxy-6-hydroxy-n-(2-hydroxy-2-methylpropyl)dodeca-2,7,9-trienimidic acid

C18H31NO4 (325.2253)


   

(1r,2s,5s,6s,9r,12s,13r)-6,7,13-trimethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosa-14,17-dien-16-one

(1r,2s,5s,6s,9r,12s,13r)-6,7,13-trimethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosa-14,17-dien-16-one

C22H31NO (325.2406)


   

14-(5-hydroxy-6-methylpiperidin-2-yl)tetradecan-2-one

14-(5-hydroxy-6-methylpiperidin-2-yl)tetradecan-2-one

C20H39NO2 (325.2981)


   

2-{7-[(2r,3r,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)pyrrolidin-2-yl]heptyl}cyclohex-2-en-1-one

2-{7-[(2r,3r,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)pyrrolidin-2-yl]heptyl}cyclohex-2-en-1-one

C18H31NO4 (325.2253)


   

(2e,4e,8e,10e,14z)-n-(2-methylpropyl)octadeca-2,4,8,10,14-pentaen-12-ynimidic acid

(2e,4e,8e,10e,14z)-n-(2-methylpropyl)octadeca-2,4,8,10,14-pentaen-12-ynimidic acid

C22H31NO (325.2406)


   

(2e)-n-[(2s,3s)-1-hydroxy-3-methylpentan-2-yl]-3-[(2r)-2-methyl-3-[(2s)-4-oxohexan-2-yl]oxiran-2-yl]prop-2-enimidic acid

(2e)-n-[(2s,3s)-1-hydroxy-3-methylpentan-2-yl]-3-[(2r)-2-methyl-3-[(2s)-4-oxohexan-2-yl]oxiran-2-yl]prop-2-enimidic acid

C18H31NO4 (325.2253)


   

(2e,4e)-n-(2-methylpropyl)octadeca-2,4,8,10,14-pentaen-12-ynimidic acid

(2e,4e)-n-(2-methylpropyl)octadeca-2,4,8,10,14-pentaen-12-ynimidic acid

C22H31NO (325.2406)


   

(2s)-1-[(2s,3r,4e,6r)-3-hydroxy-2,4,6-trimethyldec-4-enoyl]pyrrolidine-2-carboxylic acid

(2s)-1-[(2s,3r,4e,6r)-3-hydroxy-2,4,6-trimethyldec-4-enoyl]pyrrolidine-2-carboxylic acid

C18H31NO4 (325.2253)


   

14-[(2r,5r,6r)-5-hydroxy-6-methylpiperidin-2-yl]tetradecan-2-one

14-[(2r,5r,6r)-5-hydroxy-6-methylpiperidin-2-yl]tetradecan-2-one

C20H39NO2 (325.2981)


   

1-(3-hydroxy-2,4,6-trimethyldec-4-enoyl)pyrrolidine-2-carboxylic acid

1-(3-hydroxy-2,4,6-trimethyldec-4-enoyl)pyrrolidine-2-carboxylic acid

C18H31NO4 (325.2253)


   

6-ethyl-13-methyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosa-14,17-dien-16-one

6-ethyl-13-methyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosa-14,17-dien-16-one

C22H31NO (325.2406)


   

14-[(2s,5r,6r)-5-hydroxy-6-methylpiperidin-2-yl]tetradecan-2-one

14-[(2s,5r,6r)-5-hydroxy-6-methylpiperidin-2-yl]tetradecan-2-one

C20H39NO2 (325.2981)