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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-06 15:16:50 UTC
Update Date2022-03-07 02:51:46 UTC
HMDB IDHMDB0014864
Secondary Accession Numbers
  • HMDB14864
Metabolite Identification
Common NameTrimipramine
DescriptionTrimipramine, also known as RP-7162 or sapilent, belongs to the class of organic compounds known as dibenzazepines. Dibenzazepines are compounds with two benzene rings connected by an azepine ring. Azepine is an unsaturated seven-member heterocycle with one nitrogen atom replacing a carbon atom. Trimipramine is a drug which is used for the treatment of depression and depression accompanied by anxiety, agitation or sleep disturbance. Trimipramine is a very strong basic compound (based on its pKa). In humans, trimipramine is involved in imipramine action pathway. Trimipramine is a potentially toxic compound. If signs of toxicity occur at any time during this period, extended monitoring is required.
Structure
Data?1582753229
Synonyms
ValueSource
10,11-Dihydro-N,N,beta-trimethyl-5H-dibenz[b,F]azepine-5-propanamineChEBI
5-(gamma-Dimethylamino-beta-methylpropyl)-10,11-dihydro-5H-dibenzo[b,F]azepineChEBI
5-[3-(Dimethylamino)-2-methylpropyl]-10,11-dihydro-5H-dibenz[b,F]azepineChEBI
beta-MethylimipramineChEBI
RP-7162ChEBI
SapilentChEBI
TrimeprimineChEBI
TrimeproprimineChEBI
10,11-Dihydro-N,N,b-trimethyl-5H-dibenz[b,F]azepine-5-propanamineGenerator
10,11-Dihydro-N,N,β-trimethyl-5H-dibenz[b,F]azepine-5-propanamineGenerator
5-(g-Dimethylamino-b-methylpropyl)-10,11-dihydro-5H-dibenzo[b,F]azepineGenerator
5-(Γ-dimethylamino-β-methylpropyl)-10,11-dihydro-5H-dibenzo[b,F]azepineGenerator
b-MethylimipramineGenerator
Β-methylimipramineGenerator
ApoTrimipHMDB
Aventis brand OF trimipramineHMDB
EldoralHMDB
Nu pharm brand OF trimipramine maleateHMDB
Rhone-poulenc rorer brand OF trimipramine maleateHMDB
TrimiduraHMDB
Trimipramine aventis brandHMDB
Neurazpharm brand OF trimipramine maleateHMDB
Aventis brand OF trimipramine maleateHMDB
Azupharma brand OF trimipramine maleateHMDB
Nu-pharm brand OF trimipramine maleateHMDB
NuTrimipramineHMDB
Odyssey brand OF trimipramine maleateHMDB
Trimineurin maleateHMDB
Trimipramin stadaHMDB
Trimipramine hexal brandHMDB
Trimipramine maleateHMDB
Trimipramine maleate (1:1)HMDB
10,11 Dihydro-N,N,beta-trimethyl-5H-dibenz(b,F)azepine-5-propanamineHMDB
AWD.pharma brand OF trimipramine maleateHMDB
Apo trimipHMDB
Merck dura brand OF trimipramine maleateHMDB
Novo tripramineHMDB
Novo-tripramineHMDB
Novopharm brand OF trimipramine maleateHMDB
Nu-trimipramineHMDB
Rhodiapharm brand OF trimipramine maleateHMDB
RhotrimineHMDB
Surmontil maleateHMDB
TrimineurinHMDB
Trimipramine maleate (1:1), (+)-isomerHMDB
Trimipramine maleate (1:1), (+-)-isomerHMDB
Trimipramine mesylateHMDB
TrimipraminneurazpharmHMDB
Betapharm brand OF trimipramine maleateHMDB
Apo-trimipHMDB
Apotex brand OF trimipramine maleateHMDB
HerphonalHMDB
Hexal brand OF trimipramineHMDB
Neuro hexal brand OF trimipramine maleateHMDB
NovoTripramineHMDB
Nu trimipramineHMDB
Rhone poulenc rorer brand OF trimipramine maleateHMDB
Stadapharm brand OF trimipramine maleateHMDB
StangylHMDB
SurmontilHMDB
Temmler brand OF trimipramine maleateHMDB
Trimipramin azuHMDB
Trimipramin betaHMDB
Trimipramin neurazpharmHMDB
Trimipramin-neurazpharmHMDB
Trimipramine maleate (1:1), (-)-isomerHMDB
Trimipramine monohydrochlorideHMDB
Trimipramine, (+-)-isomerHMDB
Trimipramine, (-)-isomerHMDB
beta, TrimipraminMeSH
Chemical FormulaC20H26N2
Average Molecular Weight294.4338
Monoisotopic Molecular Weight294.209598842
IUPAC Name(3-{2-azatricyclo[9.4.0.0³,⁸]pentadeca-1(15),3,5,7,11,13-hexaen-2-yl}-2-methylpropyl)dimethylamine
Traditional Nametrimipramine
CAS Registry Number739-71-9
SMILES
CC(CN(C)C)CN1C2=CC=CC=C2CCC2=CC=CC=C12
InChI Identifier
InChI=1S/C20H26N2/c1-16(14-21(2)3)15-22-19-10-6-4-8-17(19)12-13-18-9-5-7-11-20(18)22/h4-11,16H,12-15H2,1-3H3
InChI KeyZSCDBOWYZJWBIY-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as dibenzazepines. Dibenzazepines are compounds with two benzene rings connected by an azepine ring. Azepine is an unsaturated seven-member heterocycle with one nitrogen atom replacing a carbon atom.
KingdomOrganic compounds
Super ClassOrganoheterocyclic compounds
ClassBenzazepines
Sub ClassDibenzazepines
Direct ParentDibenzazepines
Alternative Parents
Substituents
  • Dibenzazepine
  • Alkyldiarylamine
  • Tertiary aliphatic/aromatic amine
  • Azepine
  • Benzenoid
  • Tertiary aliphatic amine
  • Tertiary amine
  • Azacycle
  • Organic nitrogen compound
  • Organopnictogen compound
  • Hydrocarbon derivative
  • Organonitrogen compound
  • Amine
  • Aromatic heteropolycyclic compound
Molecular FrameworkAromatic heteropolycyclic compounds
External Descriptors
Ontology
Physiological effectNot Available
Disposition
ProcessNot Available
Role
Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting Point45 °CNot Available
Boiling PointNot AvailableNot Available
Water Solubility0.026 g/LNot Available
LogP4.2Not Available
Experimental Chromatographic Properties

Experimental Collision Cross Sections

Adduct TypeData SourceCCS Value (Å2)Reference
[M+H]+CBM171.230932474
[M+H]+Not Available169.949http://allccs.zhulab.cn/database/detail?ID=AllCCS00001053
Predicted Molecular Properties
PropertyValueSource
Water Solubility0.026 g/LALOGPS
logP4.67ALOGPS
logP4.76ChemAxon
logS-4ALOGPS
pKa (Strongest Basic)9.42ChemAxon
Physiological Charge1ChemAxon
Hydrogen Acceptor Count2ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area6.48 ŲChemAxon
Rotatable Bond Count4ChemAxon
Refractivity95.02 m³·mol⁻¹ChemAxon
Polarizability35.67 ųChemAxon
Number of Rings3ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DarkChem[M+H]+168.53431661259
DarkChem[M-H]-171.36631661259
DeepCCS[M-2H]-196.9330932474
DeepCCS[M+Na]+172.49530932474
AllCCS[M+H]+170.932859911
AllCCS[M+H-H2O]+167.532859911
AllCCS[M+NH4]+174.132859911
AllCCS[M+Na]+175.132859911
AllCCS[M-H]-182.332859911
AllCCS[M+Na-2H]-182.132859911
AllCCS[M+HCOO]-182.132859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
TrimipramineCC(CN(C)C)CN1C2=CC=CC=C2CCC2=CC=CC=C123388.0Standard polar33892256
TrimipramineCC(CN(C)C)CN1C2=CC=CC=C2CCC2=CC=CC=C122247.1Standard non polar33892256
TrimipramineCC(CN(C)C)CN1C2=CC=CC=C2CCC2=CC=CC=C122209.9Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Trimipramine GC-MS (Non-derivatized) - 70eV, Positivesplash10-0a4i-8190000000-adf34fd522dfa7cde9c92017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Trimipramine GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
MSMass Spectrum (Electron Ionization)splash10-0a4m-5790000000-53c724efbeeb45818f392014-09-20Not AvailableView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Experimental LC-MS/MSLC-MS/MS Spectrum - Trimipramine LC-ESI-ITFT , positive-QTOFsplash10-0udi-0900000000-68bace4e48742b76d7b42017-09-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Trimipramine LC-ESI-ITFT , positive-QTOFsplash10-0002-0090000000-683044c8af33df0709672017-09-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Trimipramine LC-ESI-ITFT , positive-QTOFsplash10-0udj-1960000000-2c69c2591b0ff915ccc22017-09-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Trimipramine LC-ESI-ITFT , positive-QTOFsplash10-0zfr-3920000000-7c68e89e7f53026fdb802017-09-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Trimipramine LC-ESI-ITFT , positive-QTOFsplash10-0zfr-4930000000-f1fe2a4f61bfbec6d7782017-09-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Trimipramine LC-ESI-ITFT , positive-QTOFsplash10-0pb9-7920000000-b085a14dd7e5d88d49222017-09-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Trimipramine LC-ESI-ITFT , positive-QTOFsplash10-0a4l-9810000000-b67a0e6866c4bcb274882017-09-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Trimipramine LC-ESI-ITFT , positive-QTOFsplash10-0002-0090000000-90da643ba602b4854ad42017-09-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Trimipramine LC-ESI-ITFT , positive-QTOFsplash10-0udj-1960000000-953dd8f5d50ce412ae552017-09-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Trimipramine LC-ESI-ITFT , positive-QTOFsplash10-0zfr-2920000000-493d39be6384cb3b09d42017-09-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Trimipramine LC-ESI-ITFT , positive-QTOFsplash10-0zfr-4920000000-02c877be6bc360fbe70e2017-09-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Trimipramine LC-ESI-ITFT , positive-QTOFsplash10-0pb9-6920000000-eb3878e47d12e47927442017-09-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Trimipramine LC-ESI-ITFT , positive-QTOFsplash10-0a4l-8910000000-5341bd1feea3e6a75bc82017-09-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Trimipramine LC-ESI-ITFT , positive-QTOFsplash10-0udi-0900000000-875e7a40df38e129227c2017-09-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Trimipramine 35V, Positive-QTOFsplash10-0udi-0900000000-875e7a40df38e129227c2021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Trimipramine 15V, Positive-QTOFsplash10-0002-0090000000-c7676d9efba94a25f2822021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Trimipramine 90V, Positive-QTOFsplash10-0a4l-8910000000-0f071349530cec77e23e2021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Trimipramine 90V, Positive-QTOFsplash10-0a4l-8910000000-2ed4e3c08247eb4c74a32021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Trimipramine 75V, Positive-QTOFsplash10-0pb9-6920000000-bee472ec2568402ac0c52021-09-20HMDB team, MONAView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Trimipramine 10V, Positive-QTOFsplash10-0f6t-0290000000-85938604c243b5e91c812016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Trimipramine 20V, Positive-QTOFsplash10-0udi-4890000000-37dae27bffa887e150d22016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Trimipramine 40V, Positive-QTOFsplash10-0k9x-9410000000-a5bca37be9f86be7016b2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Trimipramine 10V, Negative-QTOFsplash10-0006-0190000000-5907ba9e02f71d9f9d522016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Trimipramine 20V, Negative-QTOFsplash10-0006-1390000000-55eb72cacf51064923122016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Trimipramine 40V, Negative-QTOFsplash10-00kf-3910000000-883d550f0015aadef8b62016-08-03Wishart LabView Spectrum
Biological Properties
Cellular Locations
  • Membrane
Biospecimen Locations
  • Blood
  • Urine
Tissue LocationsNot Available
Pathways
Normal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
BloodExpected but not QuantifiedNot QuantifiedNot AvailableNot AvailableTaking drug identified by DrugBank entry DB00726 details
UrineExpected but not QuantifiedNot QuantifiedNot AvailableNot AvailableTaking drug identified by DrugBank entry DB00726 details
Abnormal Concentrations
Not Available
Predicted Concentrations
BiospecimenValueOriginal ageOriginal sexOriginal conditionComments
Blood0.000 uMAdult (>18 years old)BothNormalPredicted based on drug qualities
Blood0.000 umol/mmol creatinineAdult (>18 years old)BothNormalPredicted based on drug qualities
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDDB00726
Phenol Explorer Compound IDNot Available
FooDB IDNot Available
KNApSAcK IDNot Available
Chemspider ID5382
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkTrimipramine
METLIN IDNot Available
PubChem Compound5584
PDB IDNot Available
ChEBI ID9738
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available

Only showing the first 10 proteins. There are 16 proteins in total.

Enzymes

General function:
Involved in monooxygenase activity
Specific function:
Cytochromes P450 are a group of heme-thiolate monooxygenases. In liver microsomes, this enzyme is involved in an NADPH-dependent electron transport pathway. It performs a variety of oxidation reactions (e.g. caffeine 8-oxidation, omeprazole sulphoxidation, midazolam 1'-hydroxylation and midazolam 4-hydroxylation) of structurally unrelated compounds, including steroids, fatty acids, and xenobiotics. Acts as a 1,8-cineole 2-exo-monooxygenase. The enzyme also hydroxylates etoposide.
Gene Name:
CYP3A4
Uniprot ID:
P08684
Molecular weight:
57255.585
References
  1. Preissner S, Kroll K, Dunkel M, Senger C, Goldsobel G, Kuzman D, Guenther S, Winnenburg R, Schroeder M, Preissner R: SuperCYP: a comprehensive database on Cytochrome P450 enzymes including a tool for analysis of CYP-drug interactions. Nucleic Acids Res. 2010 Jan;38(Database issue):D237-43. doi: 10.1093/nar/gkp970. Epub 2009 Nov 24. [PubMed:19934256 ]
General function:
Involved in monooxygenase activity
Specific function:
Cytochromes P450 are a group of heme-thiolate monooxygenases. In liver microsomes, this enzyme is involved in an NADPH-dependent electron transport pathway. It oxidizes a variety of structurally unrelated compounds, including steroids, fatty acids, and xenobiotics. This enzyme contributes to the wide pharmacokinetics variability of the metabolism of drugs such as S-warfarin, diclofenac, phenytoin, tolbutamide and losartan.
Gene Name:
CYP2C9
Uniprot ID:
P11712
Molecular weight:
55627.365
References
  1. Preissner S, Kroll K, Dunkel M, Senger C, Goldsobel G, Kuzman D, Guenther S, Winnenburg R, Schroeder M, Preissner R: SuperCYP: a comprehensive database on Cytochrome P450 enzymes including a tool for analysis of CYP-drug interactions. Nucleic Acids Res. 2010 Jan;38(Database issue):D237-43. doi: 10.1093/nar/gkp970. Epub 2009 Nov 24. [PubMed:19934256 ]
General function:
Involved in monooxygenase activity
Specific function:
Responsible for the metabolism of a number of therapeutic agents such as the anticonvulsant drug S-mephenytoin, omeprazole, proguanil, certain barbiturates, diazepam, propranolol, citalopram and imipramine.
Gene Name:
CYP2C19
Uniprot ID:
P33261
Molecular weight:
55944.565
References
  1. Preissner S, Kroll K, Dunkel M, Senger C, Goldsobel G, Kuzman D, Guenther S, Winnenburg R, Schroeder M, Preissner R: SuperCYP: a comprehensive database on Cytochrome P450 enzymes including a tool for analysis of CYP-drug interactions. Nucleic Acids Res. 2010 Jan;38(Database issue):D237-43. doi: 10.1093/nar/gkp970. Epub 2009 Nov 24. [PubMed:19934256 ]
General function:
Involved in monooxygenase activity
Specific function:
Responsible for the metabolism of many drugs and environmental chemicals that it oxidizes. It is involved in the metabolism of drugs such as antiarrhythmics, adrenoceptor antagonists, and tricyclic antidepressants.
Gene Name:
CYP2D6
Uniprot ID:
P10635
Molecular weight:
55768.94
References
  1. Baumann P: Pharmacokinetic-pharmacodynamic relationship of the selective serotonin reuptake inhibitors. Clin Pharmacokinet. 1996 Dec;31(6):444-69. [PubMed:8968657 ]
  2. Preissner S, Kroll K, Dunkel M, Senger C, Goldsobel G, Kuzman D, Guenther S, Winnenburg R, Schroeder M, Preissner R: SuperCYP: a comprehensive database on Cytochrome P450 enzymes including a tool for analysis of CYP-drug interactions. Nucleic Acids Res. 2010 Jan;38(Database issue):D237-43. doi: 10.1093/nar/gkp970. Epub 2009 Nov 24. [PubMed:19934256 ]
General function:
Involved in G-protein coupled receptor protein signaling pathway
Specific function:
Alpha-2 adrenergic receptors mediate the catecholamine- induced inhibition of adenylate cyclase through the action of G proteins. The rank order of potency for agonists of this receptor is clonidine > norepinephrine > epinephrine = oxymetazoline > dopamine > p-tyramine = phenylephrine > serotonin > p-synephrine / p-octopamine. For antagonists, the rank order is yohimbine > chlorpromazine > phentolamine > mianserine > spiperone > prazosin > alprenolol > propanolol > pindolol
Gene Name:
ADRA2B
Uniprot ID:
P18089
Molecular weight:
49953.1
References
  1. Berger M, Gastpar M: Trimipramine: a challenge to current concepts on antidepressives. Eur Arch Psychiatry Clin Neurosci. 1996;246(5):235-9. [PubMed:8863001 ]
General function:
Involved in G-protein coupled receptor protein signaling pathway
Specific function:
This is one of the five types (D1 to D5) of receptors for dopamine. The activity of this receptor is mediated by G proteins which inhibit adenylyl cyclase
Gene Name:
DRD2
Uniprot ID:
P14416
Molecular weight:
50618.9
References
  1. Berger M, Gastpar M: Trimipramine: a challenge to current concepts on antidepressives. Eur Arch Psychiatry Clin Neurosci. 1996;246(5):235-9. [PubMed:8863001 ]
General function:
Involved in neurotransmitter:sodium symporter activity
Specific function:
Amine transporter. Terminates the action of dopamine by its high affinity sodium-dependent reuptake into presynaptic terminals.
Gene Name:
SLC6A3
Uniprot ID:
Q01959
Molecular weight:
68494.255
References
  1. Tatsumi M, Groshan K, Blakely RD, Richelson E: Pharmacological profile of antidepressants and related compounds at human monoamine transporters. Eur J Pharmacol. 1997 Dec 11;340(2-3):249-58. [PubMed:9537821 ]
General function:
Involved in G-protein coupled receptor protein signaling pathway
Specific function:
This is one of the several different receptors for 5- hydroxytryptamine (serotonin), a biogenic hormone that functions as a neurotransmitter, a hormone, and a mitogen. The activity of this receptor is mediated by G proteins that inhibit adenylate cyclase activity
Gene Name:
HTR1A
Uniprot ID:
P08908
Molecular weight:
46106.3
References
  1. Berger M, Gastpar M: Trimipramine: a challenge to current concepts on antidepressives. Eur Arch Psychiatry Clin Neurosci. 1996;246(5):235-9. [PubMed:8863001 ]
General function:
Involved in G-protein coupled receptor protein signaling pathway
Specific function:
This is one of the several different receptors for 5- hydroxytryptamine (serotonin), a biogenic hormone that functions as a neurotransmitter, a hormone, and a mitogen. This receptor mediates its action by association with G proteins that activate a phosphatidylinositol-calcium second messenger system. This receptor is involved in tracheal smooth muscle contraction, bronchoconstriction, and control of aldosterone production
Gene Name:
HTR2A
Uniprot ID:
P28223
Molecular weight:
52602.6
References
  1. Berger M, Gastpar M: Trimipramine: a challenge to current concepts on antidepressives. Eur Arch Psychiatry Clin Neurosci. 1996;246(5):235-9. [PubMed:8863001 ]
General function:
Involved in G-protein coupled receptor protein signaling pathway
Specific function:
In peripheral tissues, the H1 subclass of histamine receptors mediates the contraction of smooth muscles, increase in capillary permeability due to contraction of terminal venules, and catecholamine release from adrenal medulla, as well as mediating neurotransmission in the central nervous system
Gene Name:
HRH1
Uniprot ID:
P35367
Molecular weight:
55783.6
References
  1. Berger M, Gastpar M: Trimipramine: a challenge to current concepts on antidepressives. Eur Arch Psychiatry Clin Neurosci. 1996;246(5):235-9. [PubMed:8863001 ]

Transporters

General function:
Involved in ATP binding
Specific function:
Energy-dependent efflux pump responsible for decreased drug accumulation in multidrug-resistant cells
Gene Name:
ABCB1
Uniprot ID:
P08183
Molecular weight:
141477.3
References
  1. Nagy H, Goda K, Fenyvesi F, Bacso Z, Szilasi M, Kappelmayer J, Lustyik G, Cianfriglia M, Szabo G Jr: Distinct groups of multidrug resistance modulating agents are distinguished by competition of P-glycoprotein-specific antibodies. Biochem Biophys Res Commun. 2004 Mar 19;315(4):942-9. [PubMed:14985103 ]
General function:
Involved in neurotransmitter:sodium symporter activity
Specific function:
Amine transporter. Terminates the action of noradrenaline by its high affinity sodium-dependent reuptake into presynaptic terminals.
Gene Name:
SLC6A2
Uniprot ID:
P23975
Molecular weight:
69331.42
References
  1. Overington JP, Al-Lazikani B, Hopkins AL: How many drug targets are there? Nat Rev Drug Discov. 2006 Dec;5(12):993-6. [PubMed:17139284 ]
  2. Imming P, Sinning C, Meyer A: Drugs, their targets and the nature and number of drug targets. Nat Rev Drug Discov. 2006 Oct;5(10):821-34. [PubMed:17016423 ]
General function:
Involved in neurotransmitter:sodium symporter activity
Specific function:
Serotonin transporter whose primary function in the central nervous system involves the regulation of serotonergic signaling via transport of serotonin molecules from the synaptic cleft back into the pre-synaptic terminal for re-utilization. Plays a key role in mediating regulation of the availability of serotonin to other receptors of serotonergic systems. Terminates the action of serotonin and recycles it in a sodium-dependent manner.
Gene Name:
SLC6A4
Uniprot ID:
P31645
Molecular weight:
70324.165
References
  1. Diamond M, Kelly JP, Connor TJ: Antidepressants suppress production of the Th1 cytokine interferon-gamma, independent of monoamine transporter blockade. Eur Neuropsychopharmacol. 2006 Oct;16(7):481-90. Epub 2006 Jan 4. [PubMed:16388933 ]
  2. Tatsumi M, Groshan K, Blakely RD, Richelson E: Pharmacological profile of antidepressants and related compounds at human monoamine transporters. Eur J Pharmacol. 1997 Dec 11;340(2-3):249-58. [PubMed:9537821 ]

Only showing the first 10 proteins. There are 16 proteins in total.