Exact Mass: 265.14853100000005
Exact Mass Matches: 265.14853100000005
Found 103 metabolites which its exact mass value is equals to given mass value 265.14853100000005,
within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error
0.001 dalton.
Acridine orange
D019995 - Laboratory Chemicals > D007202 - Indicators and Reagents > D049408 - Luminescent Agents D004396 - Coloring Agents > D005456 - Fluorescent Dyes D009676 - Noxae > D009153 - Mutagens
Mirtazapine
Mirtazapine is an antidepressant introduced by Organon International in 1996 used for the treatment of moderate to severe depression. Mirtazapine has a tetracyclic chemical structure and is classified as a noradrenergic and specific serotonergic antidepressant (NaSSA). It is the only tetracyclic antidepressant that has been approved by the Food and Drug Administration to treat depression. [Wikipedia] D002492 - Central Nervous System Depressants > D014149 - Tranquilizing Agents > D014151 - Anti-Anxiety Agents D002491 - Central Nervous System Agents > D011619 - Psychotropic Drugs > D000928 - Antidepressive Agents D002491 - Central Nervous System Agents > D011619 - Psychotropic Drugs > D014149 - Tranquilizing Agents D018377 - Neurotransmitter Agents > D018663 - Adrenergic Agents > D018674 - Adrenergic Antagonists D018377 - Neurotransmitter Agents > D018490 - Serotonin Agents > D012702 - Serotonin Antagonists D018377 - Neurotransmitter Agents > D018494 - Histamine Agents > D006633 - Histamine Antagonists D002491 - Central Nervous System Agents > D002492 - Central Nervous System Depressants C78272 - Agent Affecting Nervous System > C265 - Antidepressant Agent N - Nervous system > N06 - Psychoanaleptics > N06A - Antidepressants CONFIDENCE standard compound; EAWAG_UCHEM_ID 3622 CONFIDENCE standard compound; INTERNAL_ID 1551 (R)-Mirtazapine ((R)-Org3770) is a R(?)-enantiomer of Mirtazapine with antinociceptive properties in an animal model of acute thermal nociception. (R)-Mirtazapine is a 5-HT3 receptor antagonist. (R)-Mirtazapine is mainly metabolized by CYP3A4[1]. Mirtazapine (Org3770) is a potent and orally active noradrenergic and specific serotonergic antidepressant (NaSSA) agent. Mirtazapine is also a 5-HT2, 5-HT3, histamine H1 receptor and α2-adrenoceptor antagonist with pKi values of 8.05, 8.1, 9.3 and 6.95, respectively[1][2].
N-Desmethyldoxepin
N-Desmethyldoxepin is a metabolite of doxepin. Doxepin is a psychotropic agent with tricyclic antidepressant and anxiolytic properties, known under many brand-names such as Aponal, the original preparation by Boehringer-Mannheim, now part of the Roche group; Adapine, Doxal, Deptran, Sinquan and Sinequan. As doxepin hydrochloride, it is the active ingredient in cream-based preparations (Zonalon and Xepin) for the treatment of dermatological itch. (Wikipedia) D002491 - Central Nervous System Agents > D011619 - Psychotropic Drugs > D000928 - Antidepressive Agents
Lansiumamide C
Lansiumamide C is found in fruits. Lansiumamide C is an alkaloid from seeds of Clausena lansium (wampee). Alkaloid from seeds of Clausena lansium (wampee). Lansiumamide C is found in fruits.
Mukoenine A
Mukoenine A is found in herbs and spices. Mukoenine A is an alkaloid from stem bark and roots of Murraya koenigii (curryleaf tree). Alkaloid from stem bark and roots of Murraya koenigii (curryleaf tree). Mukoenine A is found in herbs and spices.
Antazoline
Antazoline is only found in individuals that have used or taken this drug. It is a 1st generation antihistamine that also anticholinergic properties used to relieve nasal congestion and in eye drops, usually in combination with naphazoline, to relieve the symptoms of allergic conjunctivitis.Antazoline binds to the histamine H1 receptor. This blocks the action of endogenous histamine, which subsequently leads to temporary relief of the negative symptoms brought on by histamine. R - Respiratory system > R01 - Nasal preparations > R01A - Decongestants and other nasal preparations for topical use > R01AC - Antiallergic agents, excl. corticosteroids R - Respiratory system > R06 - Antihistamines for systemic use > R06A - Antihistamines for systemic use D018377 - Neurotransmitter Agents > D018494 - Histamine Agents > D006633 - Histamine Antagonists C308 - Immunotherapeutic Agent > C29578 - Histamine-1 Receptor Antagonist D018926 - Anti-Allergic Agents Antazoline (Phenazoline) is an H1 receptor antagonist that affects the activity of the central nervous system, has a potent antiarrhythmic effect[1][2][3].
E-10-Hydroxydesmethylnortriptyline
E-10-Hydroxydesmethylnortriptyline is only found in individuals that have used or taken Amitriptyline. E-10-Hydroxydesmethylnortriptyline is a metabolite of Amitriptyline. E-10-hydroxydesmethylnortriptyline belongs to the family of Dibenzocycloheptenes. These are compounds containing a dibenzocycloheptene moiety, which consists of two benzene connected by a cycloheptene ring.
(E)-Desmethyldoxepin
10-Methyl-11-hydroxyaporphine
2-Decene-6,8-diynoic acid, 9CI-2-Phenylethylamide|dec-1c-en-6,8-diinsaeure-2-phenylethylamid
1-methoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline
Siamenol
A carbazole alkaloid that is 9H-carbazole substituted by a hydroxy group at position 2, a methyl group at position 6 and a prenyl group at position 3. Isolated from Murraya siamensis, it exhibits anti-HIV activity.
mirtazapine
D002492 - Central Nervous System Depressants > D014149 - Tranquilizing Agents > D014151 - Anti-Anxiety Agents D002491 - Central Nervous System Agents > D011619 - Psychotropic Drugs > D000928 - Antidepressive Agents D002491 - Central Nervous System Agents > D011619 - Psychotropic Drugs > D014149 - Tranquilizing Agents D018377 - Neurotransmitter Agents > D018663 - Adrenergic Agents > D018674 - Adrenergic Antagonists D018377 - Neurotransmitter Agents > D018490 - Serotonin Agents > D012702 - Serotonin Antagonists D018377 - Neurotransmitter Agents > D018494 - Histamine Agents > D006633 - Histamine Antagonists D002491 - Central Nervous System Agents > D002492 - Central Nervous System Depressants C78272 - Agent Affecting Nervous System > C265 - Antidepressant Agent N - Nervous system > N06 - Psychoanaleptics > N06A - Antidepressants Mirtazapine (Org3770) is a potent and orally active noradrenergic and specific serotonergic antidepressant (NaSSA) agent. Mirtazapine is also a 5-HT2, 5-HT3, histamine H1 receptor and α2-adrenoceptor antagonist with pKi values of 8.05, 8.1, 9.3 and 6.95, respectively[1][2].
antazoline
R - Respiratory system > R01 - Nasal preparations > R01A - Decongestants and other nasal preparations for topical use > R01AC - Antiallergic agents, excl. corticosteroids R - Respiratory system > R06 - Antihistamines for systemic use > R06A - Antihistamines for systemic use D018377 - Neurotransmitter Agents > D018494 - Histamine Agents > D006633 - Histamine Antagonists C308 - Immunotherapeutic Agent > C29578 - Histamine-1 Receptor Antagonist D018926 - Anti-Allergic Agents Antazoline (Phenazoline) is an H1 receptor antagonist that affects the activity of the central nervous system, has a potent antiarrhythmic effect[1][2][3].
3-(methoxymethoxy)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
C13H20BNO4 (265.14853100000005)
2-(6-methyl-2-p-tolyl-imidazo[1,2-a]pyridin-3-yl)-ethylamine
2-(4-aminophenyl)-3-[4-(dimethylamino)phenyl]propanenitrile
4-Cyano-4-pentyloxybiphenyl
D018377 - Neurotransmitter Agents > D015320 - Tachykinins
TERT-BUTYL 2-METHOXY-7,8-DIHYDROPYRIDO[4,3-D]PYRIMIDINE-6(5H)-CARBOXYLATE
2,6-Dimethoxypyridine-4-boronic acid,pinacol ester
C13H20BNO4 (265.14853100000005)
2,3-Dimethoxy-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
C13H20BNO4 (265.14853100000005)
1-[8-(4-Fluorophenyl)-1,4-dioxaspiro[4.5]dec-8-yl]Methanamine
4,4-dimethyl-2-[2-(4-methylphenyl)phenyl]-5H-1,3-oxazole
ETHYL (1S,2R)-2-(4-FLUOROBENZYLAMINO)CYCLOPENTANECARBOXYLATE
2,6-Dimethoxypyridine-3-boronic acid pinacol ester
C13H20BNO4 (265.14853100000005)
4-(tert-Butoxycarbonylamino)-2,6-dimethylphenylboronic acid
C13H20BNO4 (265.14853100000005)
Pyroxamide
C471 - Enzyme Inhibitor > C1946 - Histone Deacetylase Inhibitor C274 - Antineoplastic Agent > C163758 - Targeted Therapy Agent
TERT-BUTYL 4-(N-HYDROXYCARBAMIMIDOYL)-BENZYLCARBAMATE
2-(2-(tert-butoxycarbonylamino)ethyl)phenylboronicacid
C13H20BNO4 (265.14853100000005)
2,3-DIMETHOXYPYRIDINE-5-BORONIC ACID PINACOL ESTER
C13H20BNO4 (265.14853100000005)
{3-[3-(4-Morpholinyl)propoxy]phenyl}boronic acid
C13H20BNO4 (265.14853100000005)
(3R,5S)-5-([1,1-biphenyl]-4-ylmethyl)-3-methylpyrrolidin-2-one
1-(Ethoxycarbonyl)pyrrole-3-boronic acid, pinacol ester
C13H20BNO4 (265.14853100000005)
TERT-BUTYL (1-(4-FLUOROPHENYL)BUT-3-EN-1-YL)CARBAMATE
trans-(2-Cyclohexylvinyl)boronic acid MIDA ester
C13H20BNO4 (265.14853100000005)
N,N,N-Trimethyl-1-nonanaminium bromide
C12H28BrN (265.14049880000005)
ETHYL (1R,2S)-2-(4-FLUOROBENZYLAMINO)CYCLOPENTANECARBOXYLATE
Esmirtazapine
D002492 - Central Nervous System Depressants > D014149 - Tranquilizing Agents > D014151 - Anti-Anxiety Agents D002491 - Central Nervous System Agents > D011619 - Psychotropic Drugs > D000928 - Antidepressive Agents D002491 - Central Nervous System Agents > D011619 - Psychotropic Drugs > D014149 - Tranquilizing Agents D018377 - Neurotransmitter Agents > D018663 - Adrenergic Agents > D018674 - Adrenergic Antagonists D018377 - Neurotransmitter Agents > D018490 - Serotonin Agents > D012702 - Serotonin Antagonists D018377 - Neurotransmitter Agents > D018494 - Histamine Agents > D006633 - Histamine Antagonists D002491 - Central Nervous System Agents > D002492 - Central Nervous System Depressants C78272 - Agent Affecting Nervous System > C29756 - Sedative and Hypnotic C78272 - Agent Affecting Nervous System > C66885 - Serotonin Antagonist (S)-Mirtazapine ((S)-Org3770) is a S(+)-enantiomer of Mirtazapine with pronociceptive properties in an animal model of acute thermal nociception. (S)-Mirtazapine is a stereoselective 5-HT2 receptor antagonist. (S)-Mirtazapine is metabolized by CYP2D6 and CYP1A2[1].
(E)-Desmethyldoxepin
D002491 - Central Nervous System Agents > D011619 - Psychotropic Drugs > D000928 - Antidepressive Agents The (E)-isomer of desmethyldoxepin.
6alpha,8beta-Hydroxygermacra-1(10),4,11(13)-trien-12-oate
C15H21O4- (265.14397660000003)
1,4-Dihydroxy-gamma-ionylideneacetate
C15H21O4- (265.14397660000003)
(R)-Mirtazapine
(R)-Mirtazapine ((R)-Org3770) is a R(?)-enantiomer of Mirtazapine with antinociceptive properties in an animal model of acute thermal nociception. (R)-Mirtazapine is a 5-HT3 receptor antagonist. (R)-Mirtazapine is mainly metabolized by CYP3A4[1].
Methyl 2-[4-(diethylamino)-2-hydroxybenzylidene]hydrazinecarboxylate
2-Methyl-2,6-diphenyl-7-oxa-1-azabicyclo[2.2.1]heptane
N-(2-naphthalenyl)-3-bicyclo[2.2.1]heptanecarboxamide
(2E)-3-[(3,4-dimethylphenyl)amino]-1-(4-methylphenyl)prop-2-en-1-one
1,3-Benzodioxole-4-ethanamine, N-ethyl-, TMS derivative
Acridine orange
D019995 - Laboratory Chemicals > D007202 - Indicators and Reagents > D049408 - Luminescent Agents D004396 - Coloring Agents > D005456 - Fluorescent Dyes D009676 - Noxae > D009153 - Mutagens
Desmethyldoxepin
A dibenzooxepine resulting from the demethylation of the antidepressant doxepin. It is the active metabolite of doxepin. D002491 - Central Nervous System Agents > D011619 - Psychotropic Drugs > D000928 - Antidepressive Agents
asperaculane G(1-)
A monocarboxylic acid anion that is the conjugate base of asperaculane G, arising from the deprotonation of the carboxy group. Major species at pH 7.3.