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Showing metabocard for Sulfamide (HMDB0258578)

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Record Information
Version5.0
StatusDetected but not Quantified
Creation Date2021-09-11 20:13:06 UTC
Update Date2021-09-26 23:15:34 UTC
HMDB IDHMDB0258578
Secondary Accession NumbersNone
Metabolite Identification
Common NameSulfamide
DescriptionSulfamide, also known as [S(NH2)2O2] or H2nso2nh2, belongs to the class of inorganic compounds known as other non-metal oxides. These are inorganic compounds containing an oxygen atom of an oxidation state of -2, in which the heaviest atom bonded to the oxygen belongs to the class of 'other non-metals'. Based on a literature review a significant number of articles have been published on Sulfamide. This compound has been identified in human blood as reported by (PMID: 31557052 ). Sulfamide is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically Sulfamide is part of the human exposome. The exposome can be defined as the collection of all the exposures of an individual in a lifetime and how those exposures relate to health. An individual's exposure begins before birth and includes insults from environmental and occupational sources.
Structure
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MOL3D MOLSDF3D SDFPDB3D PDBSMILESInChI

MOL for HMDB0258578 (Sulfamide)


  Mrv1652309112122132D          

  5  4  0  0  0  0            999 V2000
    0.8250   -0.8250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    0.0000    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6500   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  2  0  0  0  0
  2  5  1  0  0  0  0
M  END
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3D MOL for HMDB0258578 (Sulfamide)

HMDB0258578
     RDKit          3D
Sulfamide
  9  8  0  0  0  0  0  0  0  0999 V2000
   -1.3851    0.4499   -0.0606 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0693   -0.6704   -0.2910 S   0  0  0  0  0  6  0  0  0  0  0  0
    1.3946    0.0511    0.2493 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.1113   -0.9739   -1.7659 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4178   -1.9095    0.4546 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5206    0.5056    0.9765 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1049    1.3913   -0.4137 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6034    0.8451   -0.3983 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3884    0.3107    1.2490 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  0
  2  5  2  0
  1  6  1  0
  1  7  1  0
  3  8  1  0
  3  9  1  0
M  END
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3D SDF for HMDB0258578 (Sulfamide)


  Mrv1652309112122132D          

  5  4  0  0  0  0            999 V2000
    0.8250   -0.8250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    0.0000    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6500   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  2  0  0  0  0
  2  5  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0258578

> <DATABASE_NAME>
hmdb

> <SMILES>
NS(N)(=O)=O

> <INCHI_IDENTIFIER>
InChI=1S/H4N2O2S/c1-5(2,3)4/h(H4,1,2,3,4)

> <INCHI_KEY>
NVBFHJWHLNUMCV-UHFFFAOYSA-N

> <FORMULA>
H4N2O2S

> <MOLECULAR_WEIGHT>
96.1

> <EXACT_MASS>
95.999348551

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
9

> <JCHEM_AVERAGE_POLARIZABILITY>
7.452621120703073

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
sulfamoylamine

> <JCHEM_LOGP>
-1.9913039173333333

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.368237252372722

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.00070861153997

> <JCHEM_PKA_STRONGEST_BASIC>
-1.5381690363441338

> <JCHEM_POLAR_SURFACE_AREA>
86.18

> <JCHEM_REFRACTIVITY>
16.8416

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
sulfamide

> <JCHEM_VEBER_RULE>
0

$$$$
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3D-SDF for HMDB0258578 (Sulfamide)

HMDB0258578
     RDKit          3D
Sulfamide
  9  8  0  0  0  0  0  0  0  0999 V2000
   -1.3851    0.4499   -0.0606 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0693   -0.6704   -0.2910 S   0  0  0  0  0  6  0  0  0  0  0  0
    1.3946    0.0511    0.2493 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.1113   -0.9739   -1.7659 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4178   -1.9095    0.4546 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5206    0.5056    0.9765 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1049    1.3913   -0.4137 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6034    0.8451   -0.3983 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3884    0.3107    1.2490 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  0
  2  5  2  0
  1  6  1  0
  1  7  1  0
  3  8  1  0
  3  9  1  0
M  END
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PDB for HMDB0258578 (Sulfamide)

HEADER    PROTEIN                                 11-SEP-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-21         0                                  
HETATM    1  N   UNK     0       1.540  -1.540   0.000  0.00  0.00           N+0
HETATM    2  S   UNK     0       1.540   0.000   0.000  0.00  0.00           S+0
HETATM    3  O   UNK     0       1.540   1.540   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       3.080  -0.000   0.000  0.00  0.00           O+0
HETATM    5  N   UNK     0       0.000   0.000   0.000  0.00  0.00           N+0
CONECT    1    2                                                            
CONECT    2    1    3    4    5                                             
CONECT    3    2                                                            
CONECT    4    2                                                            
CONECT    5    2                                                            
MASTER        0    0    0    0    0    0    0    0    5    0    8    0
END
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3D PDB for HMDB0258578 (Sulfamide)

COMPND    HMDB0258578
HETATM    1  N1  UNL     1      -1.385   0.450  -0.061  1.00  0.00           N  
HETATM    2  S1  UNL     1      -0.069  -0.670  -0.291  1.00  0.00           S  
HETATM    3  N2  UNL     1       1.395   0.051   0.249  1.00  0.00           N  
HETATM    4  O1  UNL     1       0.111  -0.974  -1.766  1.00  0.00           O  
HETATM    5  O2  UNL     1      -0.418  -1.909   0.455  1.00  0.00           O  
HETATM    6  H1  UNL     1      -1.521   0.506   0.977  1.00  0.00           H  
HETATM    7  H2  UNL     1      -1.105   1.391  -0.414  1.00  0.00           H  
HETATM    8  H3  UNL     1       1.603   0.845  -0.398  1.00  0.00           H  
HETATM    9  H4  UNL     1       1.388   0.311   1.249  1.00  0.00           H  
CONECT    1    2    6    7
CONECT    2    3    4    4    5
CONECT    2    5
CONECT    3    8    9
END
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SMILES for HMDB0258578 (Sulfamide)

NS(N)(=O)=O
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INCHI for HMDB0258578 (Sulfamide)

InChI=1S/H4N2O2S/c1-5(2,3)4/h(H4,1,2,3,4)
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View in JSmolView Stereo Labels
Synonyms
ValueSource
[S(NH2)2O2]ChEBI
H2NSO2nh2ChEBI
Imidosulfamic acidChEBI
SulfamamideChEBI
Sulfonyl diamideChEBI
Sulfuric diamideChEBI
Sulfuryl amideChEBI
Sulfuryl diamideChEBI
ImidosulfamateGenerator
ImidosulphamateGenerator
Imidosulphamic acidGenerator
SulphamamideGenerator
Sulphonyl diamideGenerator
Sulphuric diamideGenerator
Sulphuryl amideGenerator
Sulphuryl diamideGenerator
SulphamideGenerator
Chemical FormulaH4N2O2S
Average Molecular Weight96.1
Monoisotopic Molecular Weight95.999348551
IUPAC Namesulfamoylamine
Traditional Namesulfamide
CAS Registry NumberNot Available
SMILES
NS(N)(=O)=O
InChI Identifier
InChI=1S/H4N2O2S/c1-5(2,3)4/h(H4,1,2,3,4)
InChI KeyNVBFHJWHLNUMCV-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of inorganic compounds known as other non-metal oxides. These are inorganic compounds containing an oxygen atom of an oxidation state of -2, in which the heaviest atom bonded to the oxygen belongs to the class of 'other non-metals'.
KingdomInorganic compounds
Super ClassHomogeneous non-metal compounds
ClassOther non-metal organides
Sub ClassOther non-metal oxides
Direct ParentOther non-metal oxides
Alternative Parents
Substituents
  • Other non-metal oxide
  • Sulfuric acid diamide
  • Inorganic oxide
Molecular FrameworkNot Available
External Descriptors
Ontology
Physiological effectNot Available
Disposition
Biological locationSource
ProcessNot Available
RoleNot Available
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
logP-2ChemAxon
pKa (Strongest Acidic)13ChemAxon
pKa (Strongest Basic)-1.5ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count3ChemAxon
Hydrogen Donor Count2ChemAxon
Polar Surface Area86.18 ŲChemAxon
Rotatable Bond Count0ChemAxon
Refractivity16.84 m³·mol⁻¹ChemAxon
Polarizability7.45 ųChemAxon
Number of Rings0ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DeepCCS[M+H]+125.70730932474
DeepCCS[M-H]-122.90930932474
DeepCCS[M-2H]-159.35430932474
DeepCCS[M+Na]+133.85130932474

Predicted Retention Times

Underivatized

Chromatographic MethodRetention TimeReference
Predicted by Siyang on May 30, 20228.5652 minutes33406817
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid521.9 seconds40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid361.1 seconds40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid93.2 seconds40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid269.9 seconds40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid112.3 seconds40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid253.8 seconds40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid274.7 seconds40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)748.5 seconds40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid576.9 seconds40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid46.7 seconds40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid612.9 seconds40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid225.6 seconds40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid308.5 seconds40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate658.3 seconds40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA421.2 seconds40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water309.9 seconds40023050

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
SulfamideNS(N)(=O)=O2099.8Standard polar33892256
SulfamideNS(N)(=O)=O1004.9Standard non polar33892256
SulfamideNS(N)(=O)=O1233.9Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
Sulfamide,1TMS,isomer #1C[Si](C)(C)NS(N)(=O)=O1385.3Semi standard non polar33892256
Sulfamide,1TMS,isomer #1C[Si](C)(C)NS(N)(=O)=O1116.3Standard non polar33892256
Sulfamide,1TMS,isomer #1C[Si](C)(C)NS(N)(=O)=O2415.2Standard polar33892256
Sulfamide,2TMS,isomer #1C[Si](C)(C)NS(=O)(=O)N[Si](C)(C)C1445.3Semi standard non polar33892256
Sulfamide,2TMS,isomer #1C[Si](C)(C)NS(=O)(=O)N[Si](C)(C)C1267.0Standard non polar33892256
Sulfamide,2TMS,isomer #1C[Si](C)(C)NS(=O)(=O)N[Si](C)(C)C1849.1Standard polar33892256
Sulfamide,2TMS,isomer #2C[Si](C)(C)N([Si](C)(C)C)S(N)(=O)=O1406.7Semi standard non polar33892256
Sulfamide,2TMS,isomer #2C[Si](C)(C)N([Si](C)(C)C)S(N)(=O)=O1343.7Standard non polar33892256
Sulfamide,2TMS,isomer #2C[Si](C)(C)N([Si](C)(C)C)S(N)(=O)=O2362.8Standard polar33892256
Sulfamide,3TMS,isomer #1C[Si](C)(C)NS(=O)(=O)N([Si](C)(C)C)[Si](C)(C)C1462.6Semi standard non polar33892256
Sulfamide,3TMS,isomer #1C[Si](C)(C)NS(=O)(=O)N([Si](C)(C)C)[Si](C)(C)C1496.7Standard non polar33892256
Sulfamide,3TMS,isomer #1C[Si](C)(C)NS(=O)(=O)N([Si](C)(C)C)[Si](C)(C)C1815.1Standard polar33892256
Sulfamide,4TMS,isomer #1C[Si](C)(C)N([Si](C)(C)C)S(=O)(=O)N([Si](C)(C)C)[Si](C)(C)C1594.4Semi standard non polar33892256
Sulfamide,4TMS,isomer #1C[Si](C)(C)N([Si](C)(C)C)S(=O)(=O)N([Si](C)(C)C)[Si](C)(C)C1747.1Standard non polar33892256
Sulfamide,4TMS,isomer #1C[Si](C)(C)N([Si](C)(C)C)S(=O)(=O)N([Si](C)(C)C)[Si](C)(C)C1842.3Standard polar33892256
Sulfamide,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)NS(N)(=O)=O1632.9Semi standard non polar33892256
Sulfamide,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)NS(N)(=O)=O1453.5Standard non polar33892256
Sulfamide,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)NS(N)(=O)=O2615.6Standard polar33892256
Sulfamide,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)NS(=O)(=O)N[Si](C)(C)C(C)(C)C1931.8Semi standard non polar33892256
Sulfamide,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)NS(=O)(=O)N[Si](C)(C)C(C)(C)C1832.1Standard non polar33892256
Sulfamide,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)NS(=O)(=O)N[Si](C)(C)C(C)(C)C1983.5Standard polar33892256
Sulfamide,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)N([Si](C)(C)C(C)(C)C)S(N)(=O)=O1883.5Semi standard non polar33892256
Sulfamide,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)N([Si](C)(C)C(C)(C)C)S(N)(=O)=O1918.0Standard non polar33892256
Sulfamide,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)N([Si](C)(C)C(C)(C)C)S(N)(=O)=O2469.5Standard polar33892256
Sulfamide,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)NS(=O)(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2171.1Semi standard non polar33892256
Sulfamide,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)NS(=O)(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2290.5Standard non polar33892256
Sulfamide,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)NS(=O)(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2074.3Standard polar33892256
Sulfamide,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)N([Si](C)(C)C(C)(C)C)S(=O)(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2411.1Semi standard non polar33892256
Sulfamide,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)N([Si](C)(C)C(C)(C)C)S(=O)(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2745.3Standard non polar33892256
Sulfamide,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)N([Si](C)(C)C(C)(C)C)S(=O)(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2207.6Standard polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Sulfamide GC-MS (Non-derivatized) - 70eV, Positivesplash10-0002-9000000000-187ddcb20b3f089199002021-09-23Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Sulfamide GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Biological Properties
Cellular LocationsNot Available
Biospecimen Locations
  • Blood
Tissue LocationsNot Available
Pathways
Normal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
BloodDetected but not QuantifiedNot QuantifiedNot SpecifiedNot SpecifiedNormal details
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDNot Available
KNApSAcK IDNot Available
Chemspider ID74243
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkSulfamide
METLIN IDNot Available
PubChem Compound82267
PDB IDNot Available
ChEBI ID29368
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. Barupal DK, Fiehn O: Generating the Blood Exposome Database Using a Comprehensive Text Mining and Database Fusion Approach. Environ Health Perspect. 2019 Sep;127(9):97008. doi: 10.1289/EHP4713. Epub 2019 Sep 26. [PubMed:31557052 ]