Exact Mass: 288.2273628

Exact Mass Matches: 288.2273628

Found 88 metabolites which its exact mass value is equals to given mass value 288.2273628, within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error 0.001 dalton.

Bupivacaine

1-butyl-N-(2,6-dimethylphenyl)piperidine-2-carboxamide

C18H28N2O (288.2201518)


Bupivacaine is only found in individuals that have used or taken this drug. It is a widely used local anesthetic agent. [PubChem]Bupivacaine blocks the generation and the conduction of nerve impulses, presumably by increasing the threshold for electrical excitation in the nerve, by slowing the propagation of the nerve impulse, and by reducing the rate of rise of the action potential. Bupivacaine binds to the intracellular portion of sodium channels and blocks sodium influx into nerve cells, which prevents depolarization. In general, the progression of anesthesia is related to the diameter, myelination and conduction velocity of affected nerve fibers. Clinically, the order of loss of nerve function is as follows: (1) pain, (2) temperature, (3) touch, (4) proprioception, and (5) skeletal muscle tone. The analgesic effects of Bupivicaine are thought to potentially be due to its binding to the prostaglandin E2 receptors, subtype EP1 (PGE2EP1), which inhibits the production of prostaglandins, thereby reducing fever, inflammation, and hyperalgesia. D002491 - Central Nervous System Agents > D002492 - Central Nervous System Depressants > D000777 - Anesthetics N - Nervous system > N01 - Anesthetics > N01B - Anesthetics, local > N01BB - Amides D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents C78272 - Agent Affecting Nervous System > C245 - Anesthetic Agent CONFIDENCE standard compound; EAWAG_UCHEM_ID 3305 Bupivacaine is a NMDA receptor inhibitor. Bupivacaine can block sodium, L-calcium, and potassium channels.Bupivacaine potently blocks SCN5A channels with the IC50 of 69.5 μM. Bupivacaine can be used for the research of chronic pain[1][2][3].

   

(S)-10,16-Dihydroxyhexadecanoic acid

(R)-10,16-Dihydroxyhexadecanoic acid

C16H32O4 (288.2300472)


10,16-dihydroxyhexadecanoic acid, also known as 10,16-dhha, is a member of the class of compounds known as long-chain fatty acids. Long-chain fatty acids are fatty acids with an aliphatic tail that contains between 13 and 21 carbon atoms. Thus, 10,16-dihydroxyhexadecanoic acid is considered to be a fatty acid lipid molecule. 10,16-dihydroxyhexadecanoic acid is practically insoluble (in water) and a weakly acidic compound (based on its pKa). 10,16-dihydroxyhexadecanoic acid can be found in garden tomato (variety) and gooseberry, which makes 10,16-dihydroxyhexadecanoic acid a potential biomarker for the consumption of these food products. (S)-10,16-Dihydroxyhexadecanoic acid is found in garden tomato. (S)-10,16-Dihydroxyhexadecanoic acid is a constituent of numerous plant cutins including apple and tomato.

   
   

Levobupivacaine

(2S)-1-butyl-N-(2,6-dimethylphenyl)piperidine-2-carboxamide

C18H28N2O (288.2201518)


Levobupivacaine is an amino-amide local anaesthetic drug belonging to the family of n-alkylsubstituted. pipecoloxylidide. It is the S-enantiomer of bupivacaine. Levobupivacaine hydrochloride is commonly marketed by AstraZeneca under the trade name Chirocaine. Compared to bupivacaine, levobupivacaine is associated with less vasodilation and has a longer duration of action. It is approximately 13 per cent less potent (by molarity) than racemic bupivacaine.Levobupivacaine is indicated for local anaesthesia including infiltration, nerve block, ophthalmic, epidural and intrathecal anaesthesia in adults; and infiltration analgesia in children. Adverse drug reactions (ADRs) are rare when it is administered correctly. Most ADRs relate to administration technique (resulting in systemic exposure) or pharmacological effects of anesthesia, however allergic reactions can rarely occur. [Wikipedia] D002491 - Central Nervous System Agents > D002492 - Central Nervous System Depressants > D000777 - Anesthetics N - Nervous system > N01 - Anesthetics > N01B - Anesthetics, local > N01BB - Amides D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents C78272 - Agent Affecting Nervous System > C245 - Anesthetic Agent

   

MG(a-13:0/0:0/0:0)[rac]

(2R)-2,3-dihydroxypropyl 10-methyldodecanoate

C16H32O4 (288.2300472)


MG(a-13:0/0:0/0:0) belongs to the family of monoradyglycerols, which are glycerolipids lipids containing a common glycerol backbone to which at one fatty acyl group is attached. Their general formula is [R1]OCC(CO[R2])O[R3]. MG(a-13:0/0:0/0:0) is made up of one 10-methyldodecanoyl(R1).

   

MG(0:0/a-13:0/0:0)[rac]

1,3-dihydroxypropan-2-yl 10-methyldodecanoate

C16H32O4 (288.2300472)


MG(0:0/a-13:0/0:0) belongs to the family of monoradyglycerols, which are glycerolipids lipids containing a common glycerol backbone to which at one fatty acyl group is attached. Their general formula is [R1]OCC(CO[R2])O[R3]. MG(0:0/a-13:0/0:0) is made up of one 10-methyldodecanoyl(R2).

   

MG(13:0/0:0/0:0)

(2R)-2,3-dihydroxypropyl tridecanoate

C16H32O4 (288.2300472)


MG(13:0/0:0/0:0) belongs to the family of monoradyglycerols, which are glycerolipids lipids containing a common glycerol backbone to which at one fatty acyl group is attached. Their general formula is [R1]OCC(CO[R2])O[R3]. MG(13:0/0:0/0:0) is made up of one tridecanoyl(R1).

   

MG(0:0/13:0/0:0)

Tridecanoic acid 2-hydroxy-1-(hydroxymethyl)ethyl ester

C16H32O4 (288.2300472)


MG(0:0/13:0/0:0) belongs to the family of monoradyglycerols, which are glycerolipids lipids containing a common glycerol backbone to which at one fatty acyl group is attached. Their general formula is [R1]OCC(CO[R2])O[R3]. MG(0:0/13:0/0:0) is made up of one tridecanoyl(R2).

   

MG(0:0/i-13:0/0:0)

1,3-dihydroxypropan-2-yl 11-methyldodecanoate

C16H32O4 (288.2300472)


MG(0:0/i-13:0/0:0) belongs to the family of monoradyglycerols, which are glycerolipids lipids containing a common glycerol backbone to which at one fatty acyl group is attached. Their general formula is [R1]OCC(CO[R2])O[R3]. MG(0:0/i-13:0/0:0) is made up of one 11-methyldodecanoyl(R2).

   
   

Epiethyl secoplakortide Z

epi-Ethyl seco-plakortide Z

C16H32O4 (288.2300472)


   

8-Deoxyserratinidine

8-Deoxyserratinidine

C18H28N2O (288.2201518)


   

Ethyl seco-plakortide Z

(-)-Ethyl secoplakortide Z

C16H32O4 (288.2300472)


   

3,12-Dihydroxyhexadecanoic acid

3,12-Dihydroxyhexadecanoic acid

C16H32O4 (288.2300472)


   

Ustilic acid A

15,16-dihydroxy-hexadecanoic acid

C16H32O4 (288.2300472)


   

malyngolide seco-acid

malyngolide seco-acid

C16H32O4 (288.2300472)


   

9,16-dihydroxyhexadecanoic acid

9,16-dihydroxyhexadecanoic acid

C16H32O4 (288.2300472)


   

Me ester-4,12-Dihydroxypentadecanoic acid

Me ester-4,12-Dihydroxypentadecanoic acid

C16H32O4 (288.2300472)


   

7,16-dihydroxyhexadecanoic acid

7,16-dihydroxyhexadecanoic acid

C16H32O4 (288.2300472)


   

9,10-dihydroxyhexadecanoic acid

9,10-dihydroxyhexadecanoic acid

C16H32O4 (288.2300472)


   

8,16-DIHYDROXYHEXADECANOIC ACID

8,16-DIHYDROXYHEXADECANOIC ACID

C16H32O4 (288.2300472)


   

Me ester-3,12-Dihydroxypentadecanoic acid

Me ester-3,12-Dihydroxypentadecanoic acid

C16H32O4 (288.2300472)


   

4,12-dihydroxyhexadecanoic acid

4,12-dihydroxyhexadecanoic acid

C16H32O4 (288.2300472)


   
   

3,15-dihydroxyhexadecanoic acid

NCGC00381202-01!3,15-dihydroxyhexadecanoic acid

C16H32O4 (288.2300472)


   

bupivacaine

bupivacaine

C18H28N2O (288.2201518)


D002491 - Central Nervous System Agents > D002492 - Central Nervous System Depressants > D000777 - Anesthetics N - Nervous system > N01 - Anesthetics > N01B - Anesthetics, local > N01BB - Amides D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents C78272 - Agent Affecting Nervous System > C245 - Anesthetic Agent Bupivacaine is a NMDA receptor inhibitor. Bupivacaine can block sodium, L-calcium, and potassium channels.Bupivacaine potently blocks SCN5A channels with the IC50 of 69.5 μM. Bupivacaine can be used for the research of chronic pain[1][2][3].

   

3,12-dihydroxy palmitic acid

3,12-dihydroxy-hexadecanoic acid

C16H32O4 (288.2300472)


   

9,16-dihydroxy-palmitic acid

9,16-dihydroxy-hexadecanoic acid

C16H32O4 (288.2300472)


   

4,12-dihydroxy-hexadecanoic acid

4,12-dihydroxy-hexadecanoic acid

C16H32O4 (288.2300472)


   

9,10-dihydroxy-hexadecanoic acid

9,10-dihydroxy-hexadecanoic acid

C16H32O4 (288.2300472)


   

FA 16:0;O2

10,16-dihydroxy-hexadecanoic acid

C16H32O4 (288.2300472)


   

diethylene glycol monolaurate

diethylene glycol monolaurate

C16H32O4 (288.2300472)


   
   

1-BENZYL-4-PIPERIDIN-1-YLMETHYL-PIPERIDIN-4-OL

1-BENZYL-4-PIPERIDIN-1-YLMETHYL-PIPERIDIN-4-OL

C18H28N2O (288.2201518)


   

2-[2-(4-tert-butylphenyl)ethyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

2-[2-(4-tert-butylphenyl)ethyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

C18H29BO2 (288.22604839999997)


   

1-[(trans,trans)-4-Ethyl[1,1-bicyclohexyl]-4-yl]-4-fluorobenzene

1-[(trans,trans)-4-Ethyl[1,1-bicyclohexyl]-4-yl]-4-fluorobenzene

C20H29F (288.2253166)


   

SODIUM LAURETH-6 CARBOXYLATE

SODIUM LAURETH-6 CARBOXYLATE

C16H32O4 (288.2300472)


   

2,4,7,9-Tetramethyl-5-decyne-4,7-diol ethoxylate

2,4,7,9-Tetramethyl-5-decyne-4,7-diol ethoxylate

C16H32O4 (288.2300472)


   
   

D-(+)-Bupivacaine

(2r)-1-Butyl-n-(2,6-dimethylphenyl)piperidine-2-carboxamide

C18H28N2O (288.2201518)


   

1,1-bis(2-methylbutan-2-ylperoxy)cyclohexane

1,1-bis(2-methylbutan-2-ylperoxy)cyclohexane

C16H32O4 (288.2300472)


   

1,6-Hexamethylene bis(N,N-dimethylsemicarbazide)

1,6-Hexamethylene bis(N,N-dimethylsemicarbazide)

C12H28N6O2 (288.2273628)


   

9,10-Dihydroxypalmitic acid

9,10-Dihydroxypalmitic acid

C16H32O4 (288.2300472)


   

2,3-Dihydroxypropyl tridecanoate

2,3-Dihydroxypropyl tridecanoate

C16H32O4 (288.2300472)


   

3-Carboxy-N,N,N-trimethyl-2-(octanoyloxy)propan-1-aminium

3-Carboxy-N,N,N-trimethyl-2-(octanoyloxy)propan-1-aminium

C15H30NO4+ (288.217472)


   

[(2R)-2,3-dihydroxypropyl] tridecanoate

[(2R)-2,3-dihydroxypropyl] tridecanoate

C16H32O4 (288.2300472)


   

(3-Carboxy-2-octanoyloxypropyl)-trimethylazanium

(3-Carboxy-2-octanoyloxypropyl)-trimethylazanium

C15H30NO4+ (288.217472)


   

3-Carboxylato-2-(2-propylvaleryloxy)-N,N,N-trimethyl-1-propaneaminium

3-Carboxylato-2-(2-propylvaleryloxy)-N,N,N-trimethyl-1-propaneaminium

C15H30NO4+ (288.217472)


   

[3-Carboxy-2-(3-methylheptanoyloxy)propyl]-trimethylazanium

[3-Carboxy-2-(3-methylheptanoyloxy)propyl]-trimethylazanium

C15H30NO4+ (288.217472)


   

[3-Carboxy-2-(4-methylheptanoyloxy)propyl]-trimethylazanium

[3-Carboxy-2-(4-methylheptanoyloxy)propyl]-trimethylazanium

C15H30NO4+ (288.217472)


   

[3-Carboxy-2-(6-methylheptanoyloxy)propyl]-trimethylazanium

[3-Carboxy-2-(6-methylheptanoyloxy)propyl]-trimethylazanium

C15H30NO4+ (288.217472)


   

[3-Carboxy-2-(5-methylheptanoyloxy)propyl]-trimethylazanium

[3-Carboxy-2-(5-methylheptanoyloxy)propyl]-trimethylazanium

C15H30NO4+ (288.217472)


   

(S)-10,16-Dihydroxyhexadecanoic acid

(S)-10,16-Dihydroxyhexadecanoic acid

C16H32O4 (288.2300472)


   

(3R)-3,16-dihydroxypalmitic acid

(3R)-3,16-dihydroxypalmitic acid

C16H32O4 (288.2300472)


A dihydroxy monocarboxylic acid that is juniperic acid (16-hydroxypalmitic acid, 16-hydroxyhexadecanoic acid) in which the pro-R hydrogen beta to the carboxy group is replaced by a hydroxy group.

   

(3R,15R)-3,15-dihydroxypalmitic acid

(3R,15R)-3,15-dihydroxypalmitic acid

C16H32O4 (288.2300472)


An (omega-1)-hydroxy fatty acid that is (15R)-15-hydroxypalmitic acid in which the 3-pro-R hydrogen is replaced by a hydroxy group.

   

(R)-2-Hydroperoxypalmitic acid

(R)-2-Hydroperoxypalmitic acid

C16H32O4 (288.2300472)


   

[(2S)-3-carboxy-2-octanoyloxypropyl]-trimethylazanium

[(2S)-3-carboxy-2-octanoyloxypropyl]-trimethylazanium

C15H30NO4+ (288.217472)


   

[(2R)-3-carboxy-2-octanoyloxypropyl]-dimethyl-(trideuteriomethyl)azanium

[(2R)-3-carboxy-2-octanoyloxypropyl]-dimethyl-(trideuteriomethyl)azanium

C15H30NO4+ (288.217472)


   

9,13-Dihydroxyhexadecanoic acid

9,13-Dihydroxyhexadecanoic acid

C16H32O4 (288.2300472)


   

9,14-Dihydroxyhexadecanoic acid

9,14-Dihydroxyhexadecanoic acid

C16H32O4 (288.2300472)


   

9,15-Dihydroxyhexadecanoic acid

9,15-Dihydroxyhexadecanoic acid

C16H32O4 (288.2300472)


   

(1-Hydroxy-3-nonoxypropan-2-yl) butanoate

(1-Hydroxy-3-nonoxypropan-2-yl) butanoate

C16H32O4 (288.2300472)


   

(1-Hydroxy-3-octoxypropan-2-yl) pentanoate

(1-Hydroxy-3-octoxypropan-2-yl) pentanoate

C16H32O4 (288.2300472)


   

(1-Decoxy-3-hydroxypropan-2-yl) propanoate

(1-Decoxy-3-hydroxypropan-2-yl) propanoate

C16H32O4 (288.2300472)


   

(1-Hydroxy-3-undecoxypropan-2-yl) acetate

(1-Hydroxy-3-undecoxypropan-2-yl) acetate

C16H32O4 (288.2300472)


   

[(2S)-2,3-dihydroxypropyl] tridecanoate

[(2S)-2,3-dihydroxypropyl] tridecanoate

C16H32O4 (288.2300472)


   

3,15-Dihydroxyhexadecanoic acid

3,15-Dihydroxyhexadecanoic acid

C16H32O4 (288.2300472)


   

Levobupivacaine

Levobupivacaine

C18H28N2O (288.2201518)


D002491 - Central Nervous System Agents > D002492 - Central Nervous System Depressants > D000777 - Anesthetics N - Nervous system > N01 - Anesthetics > N01B - Anesthetics, local > N01BB - Amides D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents C78272 - Agent Affecting Nervous System > C245 - Anesthetic Agent

   

10,16-Dihydroxyhexadecanoic acid

10,16-Dihydroxyhexadecanoic acid

C16H32O4 (288.2300472)


   

MG(a-13:0/0:0/0:0)[rac]

MG(a-13:0/0:0/0:0)[rac]

C16H32O4 (288.2300472)


   

3,16-dihydroxypalmitic acid

3,16-dihydroxypalmitic acid

C16H32O4 (288.2300472)


A dihydroxy monocarboxylic acid that consists of palmitic acid bearing two hydroxy substituents at positions 3 and 16.

   

MG(13:0)

MG(13:0)

C16H32O4 (288.2300472)


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

   

Dihydroxyhexadecanoic acid

Dihydroxyhexadecanoic acid

C16H32O4 (288.2300472)


   
   

1-[(1r,9s,10s,16r)-16-methyl-6,14-diazatetracyclo[7.5.3.0¹,¹⁰.0²,⁷]heptadec-2(7)-en-6-yl]ethanone

1-[(1r,9s,10s,16r)-16-methyl-6,14-diazatetracyclo[7.5.3.0¹,¹⁰.0²,⁷]heptadec-2(7)-en-6-yl]ethanone

C18H28N2O (288.2201518)


   

n-[(1r,4s,6r,8r,9r)-4-methyl-13-azatetracyclo[7.7.0.0¹,⁶.0²,¹³]hexadec-2-en-8-yl]ethanimidic acid

n-[(1r,4s,6r,8r,9r)-4-methyl-13-azatetracyclo[7.7.0.0¹,⁶.0²,¹³]hexadec-2-en-8-yl]ethanimidic acid

C18H28N2O (288.2201518)


   

1-{16-methyl-6,14-diazatetracyclo[7.5.3.0¹,¹⁰.0²,⁷]heptadec-2(7)-en-6-yl}ethanone

1-{16-methyl-6,14-diazatetracyclo[7.5.3.0¹,¹⁰.0²,⁷]heptadec-2(7)-en-6-yl}ethanone

C18H28N2O (288.2201518)


   

(9r)-9,16-dihydroxyhexadecanoic acid

(9r)-9,16-dihydroxyhexadecanoic acid

C16H32O4 (288.2300472)


   

ethyl (3s,4s,6s)-4,6-diethyl-3,6-dihydroxydecanoate

ethyl (3s,4s,6s)-4,6-diethyl-3,6-dihydroxydecanoate

C16H32O4 (288.2300472)


   

(10r)-10,16-dihydroxyhexadecanoic acid

(10r)-10,16-dihydroxyhexadecanoic acid

C16H32O4 (288.2300472)


   
   

2,2-dihydroxyhexadecanoic acid

2,2-dihydroxyhexadecanoic acid

C16H32O4 (288.2300472)


   

(10s)-10,16-dihydroxyhexadecanoic acid

(10s)-10,16-dihydroxyhexadecanoic acid

C16H32O4 (288.2300472)


   

5-hydroxy-5-(hydroxymethyl)-2-methyltetradecanoic acid

5-hydroxy-5-(hydroxymethyl)-2-methyltetradecanoic acid

C16H32O4 (288.2300472)


   

ethyl (3s,4r,6r)-4,6-diethyl-3,6-dihydroxydecanoate

ethyl (3s,4r,6r)-4,6-diethyl-3,6-dihydroxydecanoate

C16H32O4 (288.2300472)


   

(9r,10r)-9,10-dihydroxyhexadecanoic acid

(9r,10r)-9,10-dihydroxyhexadecanoic acid

C16H32O4 (288.2300472)


   

n-[(1r,2r,13s,15r)-15-methyl-6-azatetracyclo[8.6.0.0¹,⁶.0²,¹³]hexadec-10-en-11-yl]ethanimidic acid

n-[(1r,2r,13s,15r)-15-methyl-6-azatetracyclo[8.6.0.0¹,⁶.0²,¹³]hexadec-10-en-11-yl]ethanimidic acid

C18H28N2O (288.2201518)


   

(2r,5s)-5-hydroxy-5-(hydroxymethyl)-2-methyltetradecanoic acid

(2r,5s)-5-hydroxy-5-(hydroxymethyl)-2-methyltetradecanoic acid

C16H32O4 (288.2300472)