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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-11 18:06:22 UTC
Update Date2022-03-07 02:53:41 UTC
HMDB IDHMDB0033390
Secondary Accession Numbers
  • HMDB33390
Metabolite Identification
Common NameC.I. Acid Green 50
DescriptionC.I. Acid Green 50 belongs to the class of organic compounds known as sulfonated stilbenes. These are stilbenes that carry a sulfone group at one or more positions of either benzene rings. Based on a literature review very few articles have been published on C.I. Acid Green 50.
Structure
Data?1563862398
Synonyms
ValueSource
Acid brilliant greenHMDB
C.I. 44090HMDB
C.I. FOOD green 4HMDB
e142HMDB
FOOD Green SHMDB
Green SHMDB
Lissamine green bHMDB
N-[4-[[4-(dimethylamino)Phenyl](2-hydroxy-3,6-disulfO-1-naphthalenyl)methylene]-2,5-cyclohexadien-1-ylidene]-1-methylmethanaminium hydroxide inner saltHMDB
(5-{[4-(dimethylamino)phenyl][4-(dimethyliminiumyl)cyclohexa-2,5-dien-1-ylidene]methyl}-6-oxo-7-sulfO-2,6-dihydronaphthalen-2-ylidene)(hydroxy)-λ⁶-sulfanoylolic acidGenerator
(5-{[4-(dimethylamino)phenyl][4-(dimethyliminiumyl)cyclohexa-2,5-dien-1-ylidene]methyl}-6-oxo-7-sulphO-2,6-dihydronaphthalen-2-ylidene)(hydroxy)-λ⁶-sulphanoylolateGenerator
(5-{[4-(dimethylamino)phenyl][4-(dimethyliminiumyl)cyclohexa-2,5-dien-1-ylidene]methyl}-6-oxo-7-sulphO-2,6-dihydronaphthalen-2-ylidene)(hydroxy)-λ⁶-sulphanoylolic acidGenerator
Chemical FormulaC27H26N2O7S2
Average Molecular Weight554.635
Monoisotopic Molecular Weight554.118142576
IUPAC Name4-{[4-(dimethylamino)phenyl][4-(dimethyliminiumyl)cyclohexa-2,5-dien-1-ylidene]methyl}-3-hydroxy-7-sulfonaphthalene-2-sulfonate
Traditional Name4-{[4-(dimethylamino)phenyl][4-(dimethyliminio)cyclohexa-2,5-dien-1-ylidene]methyl}-3-hydroxy-7-sulfonaphthalene-2-sulfonate
CAS Registry Number25317-10-6
SMILES
CN(C)C1=CC=C(C=C1)C(=C1C=CC(C=C1)=[N+](C)C)C1=C(O)C(=CC2=C1C=CC(=C2)S(O)(=O)=O)S([O-])(=O)=O
InChI Identifier
InChI=1S/C27H26N2O7S2/c1-28(2)20-9-5-17(6-10-20)25(18-7-11-21(12-8-18)29(3)4)26-23-14-13-22(37(31,32)33)15-19(23)16-24(27(26)30)38(34,35)36/h5-16H,1-4H3,(H2,31,32,33,34,35,36)
InChI KeyQEFJYMFUMVHTBR-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as sulfonated stilbenes. These are stilbenes that carry a sulfone group at one or more positions of either benzene rings.
KingdomOrganic compounds
Super ClassPhenylpropanoids and polyketides
ClassStilbenes
Sub ClassSulfonated stilbenes
Direct ParentSulfonated stilbenes
Alternative Parents
Substituents
  • Sulfonated stilbene
  • Naphthalene sulfonate
  • 2-naphthalene sulfonic acid or derivatives
  • Naphthalene sulfonic acid or derivatives
  • 2-naphthalene sulfonate
  • 2-naphthol
  • Naphthalene
  • Arylsulfonic acid or derivatives
  • 1-sulfo,2-unsubstituted aromatic compound
  • Aniline or substituted anilines
  • Dialkylarylamine
  • Tertiary aliphatic/aromatic amine
  • Benzenoid
  • Monocyclic benzene moiety
  • Secondary ketimine
  • Organic sulfonic acid or derivatives
  • Organosulfonic acid or derivatives
  • Azomethine
  • Sulfonyl
  • Organosulfonic acid
  • Tertiary amine
  • Organic 1,3-dipolar compound
  • Propargyl-type 1,3-dipolar organic compound
  • Amine
  • Organosulfur compound
  • Organooxygen compound
  • Organonitrogen compound
  • Hydrocarbon derivative
  • Organic oxide
  • Organopnictogen compound
  • Organic oxygen compound
  • Organic nitrogen compound
  • Organic zwitterion
  • Aromatic homopolycyclic compound
Molecular FrameworkAromatic homopolycyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
ProcessNot Available
Role
Physical Properties
StateNot Available
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility0.0016 g/LALOGPS
logP-0.94ALOGPS
logP1.96ChemAxon
logS-5.6ALOGPS
pKa (Strongest Acidic)-2.4ChemAxon
pKa (Strongest Basic)4.46ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count8ChemAxon
Hydrogen Donor Count2ChemAxon
Polar Surface Area138.05 ŲChemAxon
Rotatable Bond Count5ChemAxon
Refractivity170.13 m³·mol⁻¹ChemAxon
Polarizability57.1 ųChemAxon
Number of Rings4ChemAxon
BioavailabilityYesChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DeepCCS[M+H]+212.2230932474
DeepCCS[M-H]-210.06730932474
DeepCCS[M-2H]-243.30430932474
DeepCCS[M+Na]+217.96130932474
AllCCS[M+H]+226.832859911
AllCCS[M+H-H2O]+225.032859911
AllCCS[M+NH4]+228.432859911
AllCCS[M+Na]+228.832859911
AllCCS[M-H]-219.532859911
AllCCS[M+Na-2H]-220.932859911
AllCCS[M+HCOO]-222.732859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
C.I. Acid Green 50CN(C)C1=CC=C(C=C1)C(=C1C=CC(C=C1)=[N+](C)C)C1=C(O)C(=CC2=C1C=CC(=C2)S(O)(=O)=O)S([O-])(=O)=O7705.9Standard polar33892256
C.I. Acid Green 50CN(C)C1=CC=C(C=C1)C(=C1C=CC(C=C1)=[N+](C)C)C1=C(O)C(=CC2=C1C=CC(=C2)S(O)(=O)=O)S([O-])(=O)=O3318.5Standard non polar33892256
C.I. Acid Green 50CN(C)C1=CC=C(C=C1)C(=C1C=CC(C=C1)=[N+](C)C)C1=C(O)C(=CC2=C1C=CC(=C2)S(O)(=O)=O)S([O-])(=O)=O5054.4Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
C.I. Acid Green 50,1TMS,isomer #1CN(C)C1=CC=C(C(=C2C=CC(=[N+](C)C)C=C2)C2=C(O[Si](C)(C)C)C(S(=O)(=O)[O-])=CC3=CC(S(=O)(=O)O)=CC=C23)C=C14993.4Semi standard non polar33892256
C.I. Acid Green 50,1TMS,isomer #2CN(C)C1=CC=C(C(=C2C=CC(=[N+](C)C)C=C2)C2=C(O)C(S(=O)(=O)[O-])=CC3=CC(S(=O)(=O)O[Si](C)(C)C)=CC=C23)C=C15020.6Semi standard non polar33892256
C.I. Acid Green 50,2TMS,isomer #1CN(C)C1=CC=C(C(=C2C=CC(=[N+](C)C)C=C2)C2=C(O[Si](C)(C)C)C(S(=O)(=O)[O-])=CC3=CC(S(=O)(=O)O[Si](C)(C)C)=CC=C23)C=C14851.3Semi standard non polar33892256
C.I. Acid Green 50,2TMS,isomer #1CN(C)C1=CC=C(C(=C2C=CC(=[N+](C)C)C=C2)C2=C(O[Si](C)(C)C)C(S(=O)(=O)[O-])=CC3=CC(S(=O)(=O)O[Si](C)(C)C)=CC=C23)C=C14456.2Standard non polar33892256
C.I. Acid Green 50,1TBDMS,isomer #1CN(C)C1=CC=C(C(=C2C=CC(=[N+](C)C)C=C2)C2=C(O[Si](C)(C)C(C)(C)C)C(S(=O)(=O)[O-])=CC3=CC(S(=O)(=O)O)=CC=C23)C=C15280.6Semi standard non polar33892256
C.I. Acid Green 50,1TBDMS,isomer #2CN(C)C1=CC=C(C(=C2C=CC(=[N+](C)C)C=C2)C2=C(O)C(S(=O)(=O)[O-])=CC3=CC(S(=O)(=O)O[Si](C)(C)C(C)(C)C)=CC=C23)C=C15225.3Semi standard non polar33892256
C.I. Acid Green 50,2TBDMS,isomer #1CN(C)C1=CC=C(C(=C2C=CC(=[N+](C)C)C=C2)C2=C(O[Si](C)(C)C(C)(C)C)C(S(=O)(=O)[O-])=CC3=CC(S(=O)(=O)O[Si](C)(C)C(C)(C)C)=CC=C23)C=C15290.8Semi standard non polar33892256
C.I. Acid Green 50,2TBDMS,isomer #1CN(C)C1=CC=C(C(=C2C=CC(=[N+](C)C)C=C2)C2=C(O[Si](C)(C)C(C)(C)C)C(S(=O)(=O)[O-])=CC3=CC(S(=O)(=O)O[Si](C)(C)C(C)(C)C)=CC=C23)C=C14931.2Standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - C.I. Acid Green 50 GC-MS (Non-derivatized) - 70eV, Positivesplash10-00di-0011960000-ba095700dac7281fa9c42017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - C.I. Acid Green 50 GC-MS (1 TMS) - 70eV, Positivesplash10-0h9r-5010194000-6d06e15711b4c2ffc33f2017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - C.I. Acid Green 50 GC-MS ("C.I. Acid Green 50,1TMS,#1" TMS) - 70eV, PositiveNot Available2021-10-14Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - C.I. Acid Green 50 GC-MS (TMS_1_2) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - C.I. Acid Green 50 GC-MS (TBDMS_1_1) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - C.I. Acid Green 50 GC-MS (TBDMS_1_2) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - C.I. Acid Green 50 10V, Positive-QTOFsplash10-0a4i-0000090000-27fd80bfa7bdcb9ec6ff2016-08-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - C.I. Acid Green 50 20V, Positive-QTOFsplash10-0aor-0110190000-dedf48fbf291a99bfb062016-08-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - C.I. Acid Green 50 40V, Positive-QTOFsplash10-0f6t-8930010000-eddac4b5897d901135182016-08-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - C.I. Acid Green 50 10V, Negative-QTOFsplash10-0udi-0000090000-b9295d5013cb712cb90b2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - C.I. Acid Green 50 20V, Negative-QTOFsplash10-0udi-0000090000-471198357787b85d9f692016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - C.I. Acid Green 50 40V, Negative-QTOFsplash10-05o0-9010330000-53ccdba4cc419a3ba6982016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - C.I. Acid Green 50 10V, Positive-QTOFsplash10-0a4i-0000390000-5096686c28c0053161862021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - C.I. Acid Green 50 20V, Positive-QTOFsplash10-05di-0000940000-e48077dcd53ad60412fe2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - C.I. Acid Green 50 40V, Positive-QTOFsplash10-0uk9-0143890000-3d9ac09ecce25273800f2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - C.I. Acid Green 50 10V, Negative-QTOFsplash10-0uk9-0000590000-a7024d314ab9b965f0112021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - C.I. Acid Green 50 20V, Negative-QTOFsplash10-0fk9-0000970000-e0066d266d92d42c81b12021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - C.I. Acid Green 50 40V, Negative-QTOFsplash10-0f7o-1009300000-2b76bfda60ee262fe6d32021-09-23Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Biological Properties
Cellular Locations
  • Cytoplasm
  • Extracellular
Biospecimen LocationsNot Available
Tissue LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB011423
KNApSAcK IDNot Available
Chemspider ID82526
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound91394
PDB IDNot Available
ChEBI IDNot Available
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 References
  1. (). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .

Enzymes

General function:
Involved in transferase activity, transferring hexosyl groups
Specific function:
UDPGT is of major importance in the conjugation and subsequent elimination of potentially toxic xenobiotics and endogenous compounds. This isoform glucuronidates bilirubin IX-alpha to form both the IX-alpha-C8 and IX-alpha-C12 monoconjugates and diconjugate. Is also able to catalyze the glucuronidation of 17beta-estradiol, 17alpha-ethinylestradiol, 1-hydroxypyrene, 4-methylumbelliferone, 1-naphthol, paranitrophenol, scopoletin, and umbelliferone.
Gene Name:
UGT1A1
Uniprot ID:
P22309
Molecular weight:
59590.91
Reactions
C.I. Acid Green 50 → 3-[(6-carboxy-3,4,5-trihydroxyoxan-2-yl)oxy]-4-{[4-(dimethylamino)phenyl][4-(dimethyliminiumyl)cyclohexa-2,5-dien-1-ylidene]methyl}-7-sulfonaphthalene-2-sulfonatedetails