Exact Mass: 236.1082

Exact Mass Matches: 236.1082

Found 21 metabolites which its exact mass value is equals to given mass value 236.1082, within given mass tolerance error 0.001 dalton. Try search metabolite list with more accurate mass tolerance error 0.0002 dalton.

OCTAMETHYLTRISILOXANE

OCTAMETHYLTRISILOXANE

C8H24O2Si3 (236.1084)


P - Antiparasitic products, insecticides and repellents > P03 - Ectoparasiticides, incl. scabicides, insecticides and repellents > P03A - Ectoparasiticides, incl. scabicides D001697 - Biomedical and Dental Materials

   

3-glycidoxypropyltrimethoxysilane

3-glycidoxypropyltrimethoxysilane

C9H20O5Si (236.108)


   

(5Z)-dec-5-en-1-yl sulfate

(5Z)-dec-5-en-1-yl sulfate

C10H20O4S (236.1082)


   

(3E)-dec-3-en-1-yl sulfate|ammonium dec-3-enyl sulfate

(3E)-dec-3-en-1-yl sulfate|ammonium dec-3-enyl sulfate

C10H20O4S (236.1082)


   

Dexmedetomidine hydrochloride

Dexmedetomidine HCl (Precedex)

C13H17ClN2 (236.108)


D002491 - Central Nervous System Agents > D002492 - Central Nervous System Depressants > D006993 - Hypnotics and Sedatives C78272 - Agent Affecting Nervous System > C29747 - Adrenergic Agent > C87053 - Adrenergic Agonist D018377 - Neurotransmitter Agents > D018663 - Adrenergic Agents > D000322 - Adrenergic Agonists D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents D002491 - Central Nervous System Agents > D000700 - Analgesics Dexmedetomidine hydrochloride ((+)-Medetomidine hydrochloride) is a potent, selective and orally active agonist of α2-adrenoceptor, with a Ki of 1.08 nM. Dexmedetomidine hydrochloride shows 1620-fold selectivity against α1-adrenoceptor. Dexmedetomidine hydrochloride exhibits anxiolysis, sedation, and modest analgesia effects[1][2][3].

   

Medetomidine HCl

Medetomidine hydrochloride,4-[1-(2,3-Dimethylphenyl)ethyl]-1H-imidazolehydrochloride

C13H17ClN2 (236.108)


D002491 - Central Nervous System Agents > D002492 - Central Nervous System Depressants > D006993 - Hypnotics and Sedatives C78272 - Agent Affecting Nervous System > C29747 - Adrenergic Agent > C87053 - Adrenergic Agonist D018377 - Neurotransmitter Agents > D018663 - Adrenergic Agents > D000322 - Adrenergic Agonists D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents D002491 - Central Nervous System Agents > D000700 - Analgesics Medetomidine hydrochloride is an orally active α2-adrenoceptor agonist (Ki: 1.08 nM). Medetomidine hydrochloride has sedative and analgesic effects. Medetomidine hydrochloride can cause peripheral vasoconstriction through the activation of α2 adrenoceptors on blood vessels[1][2][3][4].

   

Tetrahydrozoline HCl

Tetrahydrozoline HCl

C13H17ClN2 (236.108)


   

Tetrahydrozoline hydrochloride

Tetrahydrozoline hydrochloride

C13H17ClN2 (236.108)


D018373 - Peripheral Nervous System Agents > D001337 - Autonomic Agents > D013566 - Sympathomimetics C78272 - Agent Affecting Nervous System > C29747 - Adrenergic Agent > C87053 - Adrenergic Agonist D019999 - Pharmaceutical Solutions > D009883 - Ophthalmic Solutions D019141 - Respiratory System Agents > D014663 - Nasal Decongestants D002317 - Cardiovascular Agents > D014662 - Vasoconstrictor Agents Tetrahydrozoline hydrochloride (Tetryzoline hydrochloride), a derivative of imidazoline, is an α-adrenergic agonist that causes vasoconstriction. Tetrahydrozoline hydrochloride is widely used for the research of nasal congestion and conjunctival congestion[1][2].

   

4-(Piperidin-4-ylmethyl)benzonitrile hydrochloride

4-(Piperidin-4-ylmethyl)benzonitrile hydrochloride

C13H17ClN2 (236.108)


   

2-chloro-4-(dipropylamino)benzonitrile

2-chloro-4-(dipropylamino)benzonitrile

C13H17ClN2 (236.108)


   

4-[butyl(ethyl)amino]-2-chlorobenzonitrile

4-[butyl(ethyl)amino]-2-chlorobenzonitrile

C13H17ClN2 (236.108)


   

Acetoxymethyltriethoxysilane

Acetoxymethyltriethoxysilane

C9H20O5Si (236.108)


   

1-METHYL-4-PHENYLPIPERIDINE-4-CARBONITRILE HYDROCHLORIDE

1-METHYL-4-PHENYLPIPERIDINE-4-CARBONITRILE HYDROCHLORIDE

C13H17ClN2 (236.108)


   

PNU 22394 hydrochloride

PNU 22394 hydrochloride

C13H17ClN2 (236.108)


   

Levomedetomidine hydrochloride

4-[(1R)-1-(2,3-Dimethylphenyl)ethyl]-1H-imidazole monohydrochloride

C13H17ClN2 (236.108)


   

N-((6-CHLORO-1H-INDOL-3-YL)METHYL)-N-ETHYLETHANAMINE

N-((6-CHLORO-1H-INDOL-3-YL)METHYL)-N-ETHYLETHANAMINE

C13H17ClN2 (236.108)


   

3-Ethyl-1,1,1,5,5,5-hexamethyltrisiloxane

3-Ethyl-1,1,1,5,5,5-hexamethyltrisiloxane

C8H24O2Si3 (236.1084)


   

3-(PIPERIDIN-4-YL)-1H-INDOLE HYDROCHLORIDE

3-(PIPERIDIN-4-YL)-1H-INDOLE HYDROCHLORIDE

C13H17ClN2 (236.108)


   

(3E)-dec-3-en-1-yl hydrogen sulfate

(3E)-dec-3-en-1-yl hydrogen sulfate

C10H20O4S (236.1082)


A sulfuric ester obtained by the formal condensation of (3E)-dec-3-en-1-ol with sulfuric acid.

   

(3Z)-dec-3-en-1-yl hydrogen sulfate

(3Z)-dec-3-en-1-yl hydrogen sulfate

C10H20O4S (236.1082)


A sulfuric ester of (3Z)-dec-3-en-1-ol.

   

ST1936

ST1936

C13H17ClN2 (236.108)


ST1936 is a selective, nanomolar affinity 5-HT6 receptor agonist with Ki values of 13 nM, 168 nM and 245 nM for human 5-HT6, 5-HT7 and 5-HT2B receptors, respectively. ST1936 also shows moderate affinity (Ki of 300 nM) for human and rat α2 adrenergic receptor[1].