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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-06 15:16:51 UTC
Update Date2022-03-07 02:51:54 UTC
HMDB IDHMDB0015234
Secondary Accession Numbers
  • HMDB15234
Metabolite Identification
Common NameArbutamine
DescriptionArbutamine, also known as genesa, belongs to the class of organic compounds known as phenylbutylamines. Phenylbutylamines are compounds containing a phenylbutylamine moiety, which consists of a phenyl group substituted at the fourth carbon by an butan-1-amine. Arbutamine is a drug which is used to elicit acute cardiovascular responses (cardiac stumulant), similar to those produced by exercise, in order to aid in diagnosing the presence or absence of coronary artery disease (cad) in patients who cannot exercise adequately. Arbutamine is a very strong basic compound (based on its pKa). In humans, arbutamine is involved in arbutamine action pathway.
Structure
Data?1582753273
Synonyms
ValueSource
ArbutaminaChEBI
ArbutaminumChEBI
Arbutamine hydrochlorideHMDB
Arbutamine hydrochloride, (R)-isomerHMDB
GenESAHMDB
Chemical FormulaC18H23NO4
Average Molecular Weight317.3795
Monoisotopic Molecular Weight317.162708229
IUPAC Name4-[(1R)-1-hydroxy-2-{[4-(4-hydroxyphenyl)butyl]amino}ethyl]benzene-1,2-diol
Traditional Namearbutamine
CAS Registry Number128470-16-6
SMILES
O[C@@H](CNCCCCC1=CC=C(O)C=C1)C1=CC(O)=C(O)C=C1
InChI Identifier
InChI=1S/C18H23NO4/c20-15-7-4-13(5-8-15)3-1-2-10-19-12-18(23)14-6-9-16(21)17(22)11-14/h4-9,11,18-23H,1-3,10,12H2/t18-/m0/s1
InChI KeyIIRWWTKISYTTBL-SFHVURJKSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as phenylbutylamines. Phenylbutylamines are compounds containing a phenylbutylamine moiety, which consists of a phenyl group substituted at the fourth carbon by an butan-1-amine.
KingdomOrganic compounds
Super ClassBenzenoids
ClassBenzene and substituted derivatives
Sub ClassPhenylbutylamines
Direct ParentPhenylbutylamines
Alternative Parents
Substituents
  • Phenylbutylamine
  • Catechol
  • 1-hydroxy-4-unsubstituted benzenoid
  • 1-hydroxy-2-unsubstituted benzenoid
  • Phenol
  • Aralkylamine
  • 1,2-aminoalcohol
  • Secondary alcohol
  • Secondary aliphatic amine
  • Secondary amine
  • Hydrocarbon derivative
  • Organopnictogen compound
  • Organooxygen compound
  • Organonitrogen compound
  • Organic nitrogen compound
  • Organic oxygen compound
  • Amine
  • Aromatic alcohol
  • Alcohol
  • Aromatic homomonocyclic compound
Molecular FrameworkAromatic homomonocyclic compounds
External Descriptors
Ontology
Disposition

Biological location

Process

Naturally occurring process

Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water Solubility0.084 g/LNot Available
LogP2.9Not Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility0.084 g/LALOGPS
logP2.08ALOGPS
logP2ChemAxon
logS-3.6ALOGPS
pKa (Strongest Acidic)8.97ChemAxon
pKa (Strongest Basic)9.76ChemAxon
Physiological Charge1ChemAxon
Hydrogen Acceptor Count5ChemAxon
Hydrogen Donor Count5ChemAxon
Polar Surface Area92.95 ŲChemAxon
Rotatable Bond Count8ChemAxon
Refractivity89.78 m³·mol⁻¹ChemAxon
Polarizability35.54 ųChemAxon
Number of Rings2ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DarkChem[M+H]+177.14831661259
DarkChem[M-H]-177.20931661259
DeepCCS[M+H]+180.88330932474
DeepCCS[M-H]-178.33330932474
DeepCCS[M-2H]-212.55730932474
DeepCCS[M+Na]+188.80330932474

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
ArbutamineO[C@@H](CNCCCCC1=CC=C(O)C=C1)C1=CC(O)=C(O)C=C14464.5Standard polar33892256
ArbutamineO[C@@H](CNCCCCC1=CC=C(O)C=C1)C1=CC(O)=C(O)C=C13129.7Standard non polar33892256
ArbutamineO[C@@H](CNCCCCC1=CC=C(O)C=C1)C1=CC(O)=C(O)C=C13206.2Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
Arbutamine,1TMS,isomer #1C[Si](C)(C)O[C@@H](CNCCCCC1=CC=C(O)C=C1)C1=CC=C(O)C(O)=C13208.3Semi standard non polar33892256
Arbutamine,1TMS,isomer #2C[Si](C)(C)OC1=CC=C(CCCCNC[C@H](O)C2=CC=C(O)C(O)=C2)C=C13122.8Semi standard non polar33892256
Arbutamine,1TMS,isomer #3C[Si](C)(C)OC1=CC([C@@H](O)CNCCCCC2=CC=C(O)C=C2)=CC=C1O3084.7Semi standard non polar33892256
Arbutamine,1TMS,isomer #4C[Si](C)(C)OC1=CC=C([C@@H](O)CNCCCCC2=CC=C(O)C=C2)C=C1O3113.6Semi standard non polar33892256
Arbutamine,1TMS,isomer #5C[Si](C)(C)N(CCCCC1=CC=C(O)C=C1)C[C@H](O)C1=CC=C(O)C(O)=C13228.6Semi standard non polar33892256
Arbutamine,2TMS,isomer #1C[Si](C)(C)OC1=CC=C(CCCCNC[C@H](O[Si](C)(C)C)C2=CC=C(O)C(O)=C2)C=C13056.0Semi standard non polar33892256
Arbutamine,2TMS,isomer #10C[Si](C)(C)OC1=CC=C([C@@H](O)CN(CCCCC2=CC=C(O)C=C2)[Si](C)(C)C)C=C1O3147.4Semi standard non polar33892256
Arbutamine,2TMS,isomer #2C[Si](C)(C)OC1=CC=C([C@H](CNCCCCC2=CC=C(O)C=C2)O[Si](C)(C)C)C=C1O3077.5Semi standard non polar33892256
Arbutamine,2TMS,isomer #3C[Si](C)(C)OC1=CC([C@H](CNCCCCC2=CC=C(O)C=C2)O[Si](C)(C)C)=CC=C1O3058.4Semi standard non polar33892256
Arbutamine,2TMS,isomer #4C[Si](C)(C)O[C@@H](CN(CCCCC1=CC=C(O)C=C1)[Si](C)(C)C)C1=CC=C(O)C(O)=C13213.3Semi standard non polar33892256
Arbutamine,2TMS,isomer #5C[Si](C)(C)OC1=CC=C(CCCCNC[C@H](O)C2=CC=C(O[Si](C)(C)C)C(O)=C2)C=C13065.1Semi standard non polar33892256
Arbutamine,2TMS,isomer #6C[Si](C)(C)OC1=CC=C(CCCCNC[C@H](O)C2=CC=C(O)C(O[Si](C)(C)C)=C2)C=C13044.4Semi standard non polar33892256
Arbutamine,2TMS,isomer #7C[Si](C)(C)OC1=CC=C(CCCCN(C[C@H](O)C2=CC=C(O)C(O)=C2)[Si](C)(C)C)C=C13146.3Semi standard non polar33892256
Arbutamine,2TMS,isomer #8C[Si](C)(C)OC1=CC=C([C@@H](O)CNCCCCC2=CC=C(O)C=C2)C=C1O[Si](C)(C)C3078.3Semi standard non polar33892256
Arbutamine,2TMS,isomer #9C[Si](C)(C)OC1=CC([C@@H](O)CN(CCCCC2=CC=C(O)C=C2)[Si](C)(C)C)=CC=C1O3129.7Semi standard non polar33892256
Arbutamine,3TMS,isomer #1C[Si](C)(C)OC1=CC=C(CCCCNC[C@H](O[Si](C)(C)C)C2=CC=C(O[Si](C)(C)C)C(O)=C2)C=C13003.7Semi standard non polar33892256
Arbutamine,3TMS,isomer #10C[Si](C)(C)OC1=CC=C([C@@H](O)CN(CCCCC2=CC=C(O)C=C2)[Si](C)(C)C)C=C1O[Si](C)(C)C3131.5Semi standard non polar33892256
Arbutamine,3TMS,isomer #2C[Si](C)(C)OC1=CC=C(CCCCNC[C@H](O[Si](C)(C)C)C2=CC=C(O)C(O[Si](C)(C)C)=C2)C=C12987.7Semi standard non polar33892256
Arbutamine,3TMS,isomer #3C[Si](C)(C)OC1=CC=C(CCCCN(C[C@H](O[Si](C)(C)C)C2=CC=C(O)C(O)=C2)[Si](C)(C)C)C=C13097.0Semi standard non polar33892256
Arbutamine,3TMS,isomer #4C[Si](C)(C)OC1=CC=C([C@H](CNCCCCC2=CC=C(O)C=C2)O[Si](C)(C)C)C=C1O[Si](C)(C)C3036.0Semi standard non polar33892256
Arbutamine,3TMS,isomer #5C[Si](C)(C)OC1=CC=C([C@H](CN(CCCCC2=CC=C(O)C=C2)[Si](C)(C)C)O[Si](C)(C)C)C=C1O3107.1Semi standard non polar33892256
Arbutamine,3TMS,isomer #6C[Si](C)(C)OC1=CC([C@H](CN(CCCCC2=CC=C(O)C=C2)[Si](C)(C)C)O[Si](C)(C)C)=CC=C1O3095.3Semi standard non polar33892256
Arbutamine,3TMS,isomer #7C[Si](C)(C)OC1=CC=C(CCCCNC[C@H](O)C2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)C=C13082.4Semi standard non polar33892256
Arbutamine,3TMS,isomer #8C[Si](C)(C)OC1=CC=C(CCCCN(C[C@H](O)C2=CC=C(O[Si](C)(C)C)C(O)=C2)[Si](C)(C)C)C=C13091.7Semi standard non polar33892256
Arbutamine,3TMS,isomer #9C[Si](C)(C)OC1=CC=C(CCCCN(C[C@H](O)C2=CC=C(O)C(O[Si](C)(C)C)=C2)[Si](C)(C)C)C=C13071.4Semi standard non polar33892256
Arbutamine,4TMS,isomer #1C[Si](C)(C)OC1=CC=C(CCCCNC[C@H](O[Si](C)(C)C)C2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)C=C13045.9Semi standard non polar33892256
Arbutamine,4TMS,isomer #2C[Si](C)(C)OC1=CC=C(CCCCN(C[C@H](O[Si](C)(C)C)C2=CC=C(O[Si](C)(C)C)C(O)=C2)[Si](C)(C)C)C=C13090.1Semi standard non polar33892256
Arbutamine,4TMS,isomer #3C[Si](C)(C)OC1=CC=C(CCCCN(C[C@H](O[Si](C)(C)C)C2=CC=C(O)C(O[Si](C)(C)C)=C2)[Si](C)(C)C)C=C13073.7Semi standard non polar33892256
Arbutamine,4TMS,isomer #4C[Si](C)(C)OC1=CC=C([C@H](CN(CCCCC2=CC=C(O)C=C2)[Si](C)(C)C)O[Si](C)(C)C)C=C1O[Si](C)(C)C3085.7Semi standard non polar33892256
Arbutamine,4TMS,isomer #5C[Si](C)(C)OC1=CC=C(CCCCN(C[C@H](O)C2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)[Si](C)(C)C)C=C13115.2Semi standard non polar33892256
Arbutamine,5TMS,isomer #1C[Si](C)(C)OC1=CC=C(CCCCN(C[C@H](O[Si](C)(C)C)C2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)[Si](C)(C)C)C=C13135.2Semi standard non polar33892256
Arbutamine,5TMS,isomer #1C[Si](C)(C)OC1=CC=C(CCCCN(C[C@H](O[Si](C)(C)C)C2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)[Si](C)(C)C)C=C12826.9Standard non polar33892256
Arbutamine,5TMS,isomer #1C[Si](C)(C)OC1=CC=C(CCCCN(C[C@H](O[Si](C)(C)C)C2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)[Si](C)(C)C)C=C13038.3Standard polar33892256
Arbutamine,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)O[C@@H](CNCCCCC1=CC=C(O)C=C1)C1=CC=C(O)C(O)=C13441.7Semi standard non polar33892256
Arbutamine,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC1=CC=C(CCCCNC[C@H](O)C2=CC=C(O)C(O)=C2)C=C13399.3Semi standard non polar33892256
Arbutamine,1TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC1=CC([C@@H](O)CNCCCCC2=CC=C(O)C=C2)=CC=C1O3387.9Semi standard non polar33892256
Arbutamine,1TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC1=CC=C([C@@H](O)CNCCCCC2=CC=C(O)C=C2)C=C1O3413.5Semi standard non polar33892256
Arbutamine,1TBDMS,isomer #5CC(C)(C)[Si](C)(C)N(CCCCC1=CC=C(O)C=C1)C[C@H](O)C1=CC=C(O)C(O)=C13498.2Semi standard non polar33892256
Arbutamine,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC1=CC=C(CCCCNC[C@H](O[Si](C)(C)C(C)(C)C)C2=CC=C(O)C(O)=C2)C=C13606.7Semi standard non polar33892256
Arbutamine,2TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC1=CC=C([C@@H](O)CN(CCCCC2=CC=C(O)C=C2)[Si](C)(C)C(C)(C)C)C=C1O3681.3Semi standard non polar33892256
Arbutamine,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC1=CC=C([C@H](CNCCCCC2=CC=C(O)C=C2)O[Si](C)(C)C(C)(C)C)C=C1O3604.6Semi standard non polar33892256
Arbutamine,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC1=CC([C@H](CNCCCCC2=CC=C(O)C=C2)O[Si](C)(C)C(C)(C)C)=CC=C1O3582.8Semi standard non polar33892256
Arbutamine,2TBDMS,isomer #4CC(C)(C)[Si](C)(C)O[C@@H](CN(CCCCC1=CC=C(O)C=C1)[Si](C)(C)C(C)(C)C)C1=CC=C(O)C(O)=C13717.8Semi standard non polar33892256
Arbutamine,2TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC1=CC=C(CCCCNC[C@H](O)C2=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C2)C=C13647.9Semi standard non polar33892256
Arbutamine,2TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC1=CC=C(CCCCNC[C@H](O)C2=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C2)C=C13615.6Semi standard non polar33892256
Arbutamine,2TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC1=CC=C(CCCCN(C[C@H](O)C2=CC=C(O)C(O)=C2)[Si](C)(C)C(C)(C)C)C=C13662.9Semi standard non polar33892256
Arbutamine,2TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC1=CC=C([C@@H](O)CNCCCCC2=CC=C(O)C=C2)C=C1O[Si](C)(C)C(C)(C)C3640.3Semi standard non polar33892256
Arbutamine,2TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC1=CC([C@@H](O)CN(CCCCC2=CC=C(O)C=C2)[Si](C)(C)C(C)(C)C)=CC=C1O3652.8Semi standard non polar33892256
Arbutamine,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC1=CC=C(CCCCNC[C@H](O[Si](C)(C)C(C)(C)C)C2=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C2)C=C13765.3Semi standard non polar33892256
Arbutamine,3TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC1=CC=C([C@@H](O)CN(CCCCC2=CC=C(O)C=C2)[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C3851.9Semi standard non polar33892256
Arbutamine,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC1=CC=C(CCCCNC[C@H](O[Si](C)(C)C(C)(C)C)C2=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C2)C=C13746.4Semi standard non polar33892256
Arbutamine,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC1=CC=C(CCCCN(C[C@H](O[Si](C)(C)C(C)(C)C)C2=CC=C(O)C(O)=C2)[Si](C)(C)C(C)(C)C)C=C13864.6Semi standard non polar33892256
Arbutamine,3TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC1=CC=C([C@H](CNCCCCC2=CC=C(O)C=C2)O[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C3754.0Semi standard non polar33892256
Arbutamine,3TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC1=CC=C([C@H](CN(CCCCC2=CC=C(O)C=C2)[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C=C1O3854.1Semi standard non polar33892256
Arbutamine,3TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC1=CC([C@H](CN(CCCCC2=CC=C(O)C=C2)[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)=CC=C1O3839.7Semi standard non polar33892256
Arbutamine,3TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC1=CC=C(CCCCNC[C@H](O)C2=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C2)C=C13848.7Semi standard non polar33892256
Arbutamine,3TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC1=CC=C(CCCCN(C[C@H](O)C2=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C2)[Si](C)(C)C(C)(C)C)C=C13872.1Semi standard non polar33892256
Arbutamine,3TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC1=CC=C(CCCCN(C[C@H](O)C2=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C2)[Si](C)(C)C(C)(C)C)C=C13838.7Semi standard non polar33892256
Arbutamine,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC1=CC=C(CCCCNC[C@H](O[Si](C)(C)C(C)(C)C)C2=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C2)C=C13957.8Semi standard non polar33892256
Arbutamine,4TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC1=CC=C(CCCCN(C[C@H](O[Si](C)(C)C(C)(C)C)C2=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C2)[Si](C)(C)C(C)(C)C)C=C14051.9Semi standard non polar33892256
Arbutamine,4TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC1=CC=C(CCCCN(C[C@H](O[Si](C)(C)C(C)(C)C)C2=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C2)[Si](C)(C)C(C)(C)C)C=C14034.9Semi standard non polar33892256
Arbutamine,4TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC1=CC=C([C@H](CN(CCCCC2=CC=C(O)C=C2)[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C4040.4Semi standard non polar33892256
Arbutamine,4TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC1=CC=C(CCCCN(C[C@H](O)C2=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C2)[Si](C)(C)C(C)(C)C)C=C14090.6Semi standard non polar33892256
Arbutamine,5TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC1=CC=C(CCCCN(C[C@H](O[Si](C)(C)C(C)(C)C)C2=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C2)[Si](C)(C)C(C)(C)C)C=C14267.6Semi standard non polar33892256
Arbutamine,5TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC1=CC=C(CCCCN(C[C@H](O[Si](C)(C)C(C)(C)C)C2=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C2)[Si](C)(C)C(C)(C)C)C=C13678.6Standard non polar33892256
Arbutamine,5TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC1=CC=C(CCCCN(C[C@H](O[Si](C)(C)C(C)(C)C)C2=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C2)[Si](C)(C)C(C)(C)C)C=C13433.4Standard polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Arbutamine GC-MS (Non-derivatized) - 70eV, Positivesplash10-0a4r-0900000000-beab4528e7ae0c5e38b52017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Arbutamine GC-MS (4 TMS) - 70eV, Positivesplash10-001l-1191070000-bc9a7cc5fdaffaee18152017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Arbutamine GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Arbutamine 10V, Positive-QTOFsplash10-0uxr-0209000000-cb09be2863ef695c2d292016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Arbutamine 20V, Positive-QTOFsplash10-0udj-0913000000-0491c75318d1f3342f092016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Arbutamine 40V, Positive-QTOFsplash10-0a4j-5900000000-053a6953711858f147902016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Arbutamine 10V, Negative-QTOFsplash10-014i-0229000000-c34a09d0f43937c799542016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Arbutamine 20V, Negative-QTOFsplash10-03xs-0933000000-11bf8026af6aaad0368d2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Arbutamine 40V, Negative-QTOFsplash10-0bt9-1900000000-1c392070d0270adc6ce82016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Arbutamine 10V, Positive-QTOFsplash10-0uxr-0109000000-38c3340b26375b90d1bb2021-10-11Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Arbutamine 20V, Positive-QTOFsplash10-0udi-0947000000-265ff6fc9fb91b44eb442021-10-11Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Arbutamine 40V, Positive-QTOFsplash10-0a4j-3910000000-475756670ba2db15f4f42021-10-11Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Arbutamine 10V, Negative-QTOFsplash10-014i-0009000000-3fe3b20def364ac29f1a2021-10-11Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Arbutamine 20V, Negative-QTOFsplash10-00ri-0944000000-82eb66b772a067f48e572021-10-11Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Arbutamine 40V, Negative-QTOFsplash10-0acc-3980000000-a6c3b823ca6dc07e05fb2021-10-11Wishart 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 DB01102 details
UrineExpected but not QuantifiedNot QuantifiedNot AvailableNot AvailableTaking drug identified by DrugBank entry DB01102 details
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDDB01102
Phenol Explorer Compound IDNot Available
FooDB IDNot Available
KNApSAcK IDNot Available
Chemspider ID54785
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkArbutamine
METLIN IDNot Available
PubChem Compound60789
PDB IDNot Available
ChEBI ID50580
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

Enzymes

General function:
Involved in G-protein coupled receptor protein signaling pathway
Specific function:
Beta-adrenergic receptors mediate the catecholamine- induced activation of adenylate cyclase through the action of G proteins. This receptor binds epinephrine and norepinephrine with approximately equal affinity
Gene Name:
ADRB1
Uniprot ID:
P08588
Molecular weight:
51322.1
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 ]
  3. Abou-Mohamed G, Nagarajan R, Ibrahim TM, Caldwell RW: Characterization of the adrenergic activity of arbutamine, a novel agent for pharmacological stress testing. Cardiovasc Drugs Ther. 1996 Mar;10(1):39-47. [PubMed:8723169 ]
General function:
Involved in G-protein coupled receptor protein signaling pathway
Specific function:
Beta-adrenergic receptors mediate the catecholamine- induced activation of adenylate cyclase through the action of G proteins. The beta-2-adrenergic receptor binds epinephrine with an approximately 30-fold greater affinity than it does norepinephrine
Gene Name:
ADRB2
Uniprot ID:
P07550
Molecular weight:
46458.3
References
  1. Abou-Mohamed G, Nagarajan R, Ibrahim TM, Caldwell RW: Characterization of the adrenergic activity of arbutamine, a novel agent for pharmacological stress testing. Cardiovasc Drugs Ther. 1996 Mar;10(1):39-47. [PubMed:8723169 ]
General function:
Involved in G-protein coupled receptor protein signaling pathway
Specific function:
Beta-adrenergic receptors mediate the catecholamine- induced activation of adenylate cyclase through the action of G proteins. Beta-3 is involved in the regulation of lipolysis and thermogenesis
Gene Name:
ADRB3
Uniprot ID:
P13945
Molecular weight:
43518.6
References
  1. Abou-Mohamed G, Nagarajan R, Ibrahim TM, Caldwell RW: Characterization of the adrenergic activity of arbutamine, a novel agent for pharmacological stress testing. Cardiovasc Drugs Ther. 1996 Mar;10(1):39-47. [PubMed:8723169 ]