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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 03:45:51 UTC

Update Date

2021-09-26 23:00:00 UTC

HMDB ID

HMDB0249259

Secondary Accession Numbers

None

Metabolite Identification

Common Name

2,2'-Dipicolylamine

Description

bis[(pyridin-2-yl)methyl]amine belongs to the class of organic compounds known as 2-pyridylmethylamines. These are aromatic heterocyclic compounds contaning a pyridine ring which is substituted at the 2-position with a methylamine. Based on a literature review very few articles have been published on bis[(pyridin-2-yl)methyl]amine. This compound has been identified in human blood as reported by (PMID: 31557052 ). 2,2'-dipicolylamine is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically 2,2'-Dipicolylamine 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

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI

HMDB0249259
     RDKit          3D
2,2'-Dipicolylamine
 28 29  0  0  0  0  0  0  0  0999 V2000
    4.9907   -0.2131    0.7181 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9425   -1.1187    0.7141 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7204   -0.7331    0.3011 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4183    0.5764   -0.1488 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1146    0.7844   -0.7311 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0409    0.4221    0.0397 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9410   -0.3641   -0.8184 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3569   -0.3988   -0.4057 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0327    0.8414   -0.5867 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3488    0.9188   -0.2920 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0122   -0.1666    0.1706 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3558   -1.4014    0.3573 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0415   -1.4419    0.0525 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4340    1.4321   -0.1333 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.6815    1.0779    0.2802 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9812   -0.5219    1.0327 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1161   -2.1318    1.0372 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8918   -1.4404    0.3089 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9732    0.5169   -1.7819 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9841    1.9443   -0.7632 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0489    0.1472    0.9943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8265   -0.1733   -1.8707 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5778   -1.4563   -0.6024 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4593    1.6826   -0.9556 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8743    1.8636   -0.4368 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0571   -0.1562    0.4366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8838   -2.2857    0.7314 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5112    1.7955    0.2797 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
  4 14  1  0
 14 15  2  0
 15  1  1  0
 13  8  1  0
  1 16  1  0
  2 17  1  0
  3 18  1  0
  5 19  1  0
  5 20  1  0
  6 21  1  0
  7 22  1  0
  7 23  1  0
  9 24  1  0
 10 25  1  0
 11 26  1  0
 12 27  1  0
 15 28  1  0
M  END


  Mrv1652309112105462D          

 15 16  0  0  0  0            999 V2000
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 10 15  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0249259

> <DATABASE_NAME>
hmdb

> <SMILES>
C(NCC1=CC=CC=N1)C1=CC=CC=N1

> <INCHI_IDENTIFIER>
InChI=1S/C12H13N3/c1-3-7-14-11(5-1)9-13-10-12-6-2-4-8-15-12/h1-8,13H,9-10H2

> <INCHI_KEY>
KXZQYLBVMZGIKC-UHFFFAOYSA-N

> <FORMULA>
C12H13N3

> <MOLECULAR_WEIGHT>
199.257

> <EXACT_MASS>
199.110947431

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
28

> <JCHEM_AVERAGE_POLARIZABILITY>
21.931831461919916

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
bis[(pyridin-2-yl)methyl]amine

> <ALOGPS_LOGP>
1.13

> <JCHEM_LOGP>
0.9836666896666663

> <ALOGPS_LOGS>
-2.67

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_BASIC>
6.9486110836540185

> <JCHEM_POLAR_SURFACE_AREA>
37.81

> <JCHEM_REFRACTIVITY>
58.56040000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.28e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
bis(pyridin-2-ylmethyl)amine

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0249259
     RDKit          3D
2,2'-Dipicolylamine
 28 29  0  0  0  0  0  0  0  0999 V2000
    4.9907   -0.2131    0.7181 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9425   -1.1187    0.7141 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7204   -0.7331    0.3011 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4183    0.5764   -0.1488 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1146    0.7844   -0.7311 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0409    0.4221    0.0397 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9410   -0.3641   -0.8184 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3569   -0.3988   -0.4057 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0327    0.8414   -0.5867 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3488    0.9188   -0.2920 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0122   -0.1666    0.1706 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3558   -1.4014    0.3573 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0415   -1.4419    0.0525 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4340    1.4321   -0.1333 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.6815    1.0779    0.2802 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9812   -0.5219    1.0327 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1161   -2.1318    1.0372 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8918   -1.4404    0.3089 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9732    0.5169   -1.7819 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9841    1.9443   -0.7632 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0489    0.1472    0.9943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8265   -0.1733   -1.8707 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5778   -1.4563   -0.6024 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4593    1.6826   -0.9556 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8743    1.8636   -0.4368 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0571   -0.1562    0.4366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8838   -2.2857    0.7314 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5112    1.7955    0.2797 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
  4 14  1  0
 14 15  2  0
 15  1  1  0
 13  8  1  0
  1 16  1  0
  2 17  1  0
  3 18  1  0
  5 19  1  0
  5 20  1  0
  6 21  1  0
  7 22  1  0
  7 23  1  0
  9 24  1  0
 10 25  1  0
 11 26  1  0
 12 27  1  0
 15 28  1  0
M  END

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  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM    4  N   UNK     0       4.001  -5.390   0.000  0.00  0.00           N+0
HETATM    5  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM    8  N   UNK     0       6.668  -2.310   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.002  -0.000   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.336   2.310   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.669   1.540   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.669  -0.000   0.000  0.00  0.00           C+0
HETATM   15  N   UNK     0       9.336  -0.770   0.000  0.00  0.00           N+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   15                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   10                                                       
MASTER        0    0    0    0    0    0    0    0   15    0   32    0
END

COMPND    HMDB0249259
HETATM    1  C1  UNL     1       4.991  -0.213   0.718  1.00  0.00           C  
HETATM    2  C2  UNL     1       3.942  -1.119   0.714  1.00  0.00           C  
HETATM    3  C3  UNL     1       2.720  -0.733   0.301  1.00  0.00           C  
HETATM    4  C4  UNL     1       2.418   0.576  -0.149  1.00  0.00           C  
HETATM    5  C5  UNL     1       1.115   0.784  -0.731  1.00  0.00           C  
HETATM    6  N1  UNL     1      -0.041   0.422   0.040  1.00  0.00           N  
HETATM    7  C6  UNL     1      -0.941  -0.364  -0.818  1.00  0.00           C  
HETATM    8  C7  UNL     1      -2.357  -0.399  -0.406  1.00  0.00           C  
HETATM    9  C8  UNL     1      -3.033   0.841  -0.587  1.00  0.00           C  
HETATM   10  C9  UNL     1      -4.349   0.919  -0.292  1.00  0.00           C  
HETATM   11  C10 UNL     1      -5.012  -0.167   0.171  1.00  0.00           C  
HETATM   12  C11 UNL     1      -4.356  -1.401   0.357  1.00  0.00           C  
HETATM   13  N2  UNL     1      -3.041  -1.442   0.052  1.00  0.00           N  
HETATM   14  N3  UNL     1       3.434   1.432  -0.133  1.00  0.00           N  
HETATM   15  C12 UNL     1       4.682   1.078   0.280  1.00  0.00           C  
HETATM   16  H1  UNL     1       5.981  -0.522   1.033  1.00  0.00           H  
HETATM   17  H2  UNL     1       4.116  -2.132   1.037  1.00  0.00           H  
HETATM   18  H3  UNL     1       1.892  -1.440   0.309  1.00  0.00           H  
HETATM   19  H4  UNL     1       0.973   0.517  -1.782  1.00  0.00           H  
HETATM   20  H5  UNL     1       0.984   1.944  -0.763  1.00  0.00           H  
HETATM   21  H6  UNL     1       0.049   0.147   0.994  1.00  0.00           H  
HETATM   22  H7  UNL     1      -0.826  -0.173  -1.871  1.00  0.00           H  
HETATM   23  H8  UNL     1      -0.578  -1.456  -0.602  1.00  0.00           H  
HETATM   24  H9  UNL     1      -2.459   1.683  -0.956  1.00  0.00           H  
HETATM   25  H10 UNL     1      -4.874   1.864  -0.437  1.00  0.00           H  
HETATM   26  H11 UNL     1      -6.057  -0.156   0.437  1.00  0.00           H  
HETATM   27  H12 UNL     1      -4.884  -2.286   0.731  1.00  0.00           H  
HETATM   28  H13 UNL     1       5.511   1.796   0.280  1.00  0.00           H  
CONECT    1    2    2   15   16
CONECT    2    3   17
CONECT    3    4    4   18
CONECT    4    5   14
CONECT    5    6   19   20
CONECT    6    7   21
CONECT    7    8   22   23
CONECT    8    9    9   13
CONECT    9   10   24
CONECT   10   11   11   25
CONECT   11   12   26
CONECT   12   13   13   27
CONECT   14   15   15
CONECT   15   28
END

View in JSmol View Stereo Labels

Synonyms

Value	Source
Bis(pyridin-2-ylmethyl)amine	MeSH
Bis-pma CPD	MeSH

Chemical Formula

C₁₂H₁₃N₃

Average Molecular Weight

199.257

Monoisotopic Molecular Weight

199.110947431

IUPAC Name

bis[(pyridin-2-yl)methyl]amine

Traditional Name

bis(pyridin-2-ylmethyl)amine

CAS Registry Number

Not Available

SMILES

C(NCC1=CC=CC=N1)C1=CC=CC=N1

InChI Identifier

InChI=1S/C12H13N3/c1-3-7-14-11(5-1)9-13-10-12-6-2-4-8-15-12/h1-8,13H,9-10H2

InChI Key

KXZQYLBVMZGIKC-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 2-pyridylmethylamines. These are aromatic heterocyclic compounds contaning a pyridine ring which is substituted at the 2-position with a methylamine.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Pyridines and derivatives

Sub Class

2-pyridylmethylamines

Direct Parent

2-pyridylmethylamines

Alternative Parents

Substituents

2-pyridylmethylamine
Aralkylamine
Heteroaromatic compound
Azacycle
Secondary amine
Secondary aliphatic amine
Organic nitrogen compound
Organopnictogen compound
Hydrocarbon derivative
Organonitrogen compound
Amine
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 31557052)

Process

Not Available

Role

Not Available

Physical Properties

State

Not Available

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	1.13	ALOGPS
logP	0.98	ChemAxon
logS	-2.7	ALOGPS
pKa (Strongest Basic)	6.95	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	37.81 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	58.56 m³·mol⁻¹	ChemAxon
Polarizability	21.93 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	136.839	30932474
DeepCCS	[M-H]-	133.515	30932474
DeepCCS	[M-2H]-	170.522	30932474
DeepCCS	[M+Na]+	146.06	30932474
AllCCS	[M+H]+	145.6	32859911
AllCCS	[M+H-H2O]+	141.2	32859911
AllCCS	[M+NH4]+	149.6	32859911
AllCCS	[M+Na]+	150.8	32859911
AllCCS	[M-H]-	149.6	32859911
AllCCS	[M+Na-2H]-	149.8	32859911
AllCCS	[M+HCOO]-	150.1	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
2,2'-Dipicolylamine	C(NCC1=CC=CC=N1)C1=CC=CC=N1	2621.4	Standard polar	33892256
2,2'-Dipicolylamine	C(NCC1=CC=CC=N1)C1=CC=CC=N1	1771.9	Standard non polar	33892256
2,2'-Dipicolylamine	C(NCC1=CC=CC=N1)C1=CC=CC=N1	1842.3	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
2,2'-Dipicolylamine,1TMS,isomer #1	C[Si](C)(C)N(CC1=CC=CC=N1)CC1=CC=CC=N1	1898.4	Semi standard non polar	33892256
2,2'-Dipicolylamine,1TMS,isomer #1	C[Si](C)(C)N(CC1=CC=CC=N1)CC1=CC=CC=N1	1909.9	Standard non polar	33892256
2,2'-Dipicolylamine,1TMS,isomer #1	C[Si](C)(C)N(CC1=CC=CC=N1)CC1=CC=CC=N1	2570.7	Standard polar	33892256
2,2'-Dipicolylamine,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)N(CC1=CC=CC=N1)CC1=CC=CC=N1	2114.9	Semi standard non polar	33892256
2,2'-Dipicolylamine,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)N(CC1=CC=CC=N1)CC1=CC=CC=N1	2132.1	Standard non polar	33892256
2,2'-Dipicolylamine,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)N(CC1=CC=CC=N1)CC1=CC=CC=N1	2683.8	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 2,2'-Dipicolylamine GC-MS (Non-derivatized) - 70eV, Positive	splash10-0007-9700000000-7c00fd6f01d6c609ce62	2021-09-24	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2,2'-Dipicolylamine GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,2'-Dipicolylamine 10V, Positive-QTOF	splash10-0udi-2090000000-2144d0a61b6accc0c53e	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,2'-Dipicolylamine 20V, Positive-QTOF	splash10-0f6x-9060000000-91d22045ddb031f52792	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,2'-Dipicolylamine 40V, Positive-QTOF	splash10-0006-9000000000-a05f58aedc58dcfe6adc	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,2'-Dipicolylamine 10V, Negative-QTOF	splash10-0002-0900000000-4f9b47b48bda71211297	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,2'-Dipicolylamine 20V, Negative-QTOF	splash10-0005-5900000000-b81c7c6606e8a181d026	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2,2'-Dipicolylamine 40V, Negative-QTOF	splash10-0005-7900000000-1a3f137e85c7dab3ac44	2021-10-12	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Blood

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Detected but not Quantified	Not Quantified	Not Specified	Not Specified	Normal	31557052	details

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

66400

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

73759

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

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 ]

Showing metabocard for 2,2'-Dipicolylamine (HMDB0249259)

MOL for HMDB0249259 (2,2'-Dipicolylamine)

3D MOL for HMDB0249259 (2,2'-Dipicolylamine)

3D SDF for HMDB0249259 (2,2'-Dipicolylamine)

3D-SDF for HMDB0249259 (2,2'-Dipicolylamine)

PDB for HMDB0249259 (2,2'-Dipicolylamine)

3D PDB for HMDB0249259 (2,2'-Dipicolylamine)

SMILES for HMDB0249259 (2,2'-Dipicolylamine)

INCHI for HMDB0249259 (2,2'-Dipicolylamine)

Structure for HMDB0249259 (2,2'-Dipicolylamine)

3D Structure for HMDB0249259 (2,2'-Dipicolylamine)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra