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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 14:31:16 UTC

Update Date

2021-09-26 23:09:28 UTC

HMDB ID

HMDB0254997

Secondary Accession Numbers

None

Metabolite Identification

Common Name

N-(2,4-Dinitrophenyl)-5-methoxytryptamine

Description

N-(2,4-Dinitrophenyl)-5-methoxytryptamine, also known as 2,4-DNP-MT, belongs to the class of organic compounds known as dinitroanilines. These are organic compounds containing an aniline moiety, which is substituted at 2 positions by a nitro group. Based on a literature review a significant number of articles have been published on N-(2,4-Dinitrophenyl)-5-methoxytryptamine. This compound has been identified in human blood as reported by (PMID: 31557052 ). N-(2,4-dinitrophenyl)-5-methoxytryptamine is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically N-(2,4-Dinitrophenyl)-5-methoxytryptamine 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

  Mrv1652309112116312D          

 26 28  0  0  0  0            999 V2000
    3.4990    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845    0.6979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435    2.1904    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6284    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435    0.8555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3984    0.0709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2054   -0.1006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4604   -0.8853    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2673   -1.0568    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5223   -1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3292   -2.0129    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8813   -1.3998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6263   -0.6152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8194   -0.4437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6882   -1.5714    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
   -4.9432   -2.3560    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2403   -0.9583    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   -1.9702   -2.4545    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
   -2.2252   -3.2391    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1633   -2.2830    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
  1  2  1  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
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  3  8  1  0  0  0  0
  6  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
  5 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 15 20  1  0  0  0  0
 18 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 16 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
M  CHG  4  21   1  23  -1  24   1  26  -1
M  END

HMDB0254997
     RDKit          3D
N-(2,4-Dinitrophenyl)-5-methoxytryptamine
 42 44  0  0  0  0  0  0  0  0999 V2000
   -4.8556   -2.4675   -1.8170 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7680   -2.1028   -1.0146 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6727   -0.7789   -0.5857 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6209    0.1618   -0.9359 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5433    1.4744   -0.5218 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5005    1.9077    0.2705 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1699    3.1053    0.8157 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0293    2.9824    1.5167 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6311    1.6660    1.4082 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4266    1.0158    2.0038 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5867    0.8262    0.9148 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8082    0.1976    1.3834 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8420   -0.0392    0.4449 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6504    0.2936   -0.8945 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6379    0.0545   -1.8216 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8397   -0.5216   -1.4372 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8599   -0.7678   -2.3981 N   0  0  0  0  0  4  0  0  0  0  0  0
    5.6828   -0.4689   -3.5962 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0421   -1.3374   -1.9939 O   0  0  0  0  0  1  0  0  0  0  0  0
    5.0027   -0.8389   -0.1142 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0240   -0.6081    0.8385 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3477   -0.9939    2.1565 N   0  0  0  0  0  4  0  0  0  0  0  0
    3.9249   -0.3556    3.1201 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1543   -2.0774    2.3662 O   0  0  0  0  0  1  0  0  0  0  0  0
   -2.5447    0.9814    0.6295 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6273   -0.3515    0.2066 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8477   -1.7989   -2.7193 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8038   -3.5081   -2.1634 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7832   -2.2950   -1.2416 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4390   -0.1952   -1.5623 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3018    2.1771   -0.8154 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7401    3.9817    0.6913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5096    3.7795    2.0728 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7287    0.0009    2.3767 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0167    1.6052    2.8102 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1192    0.2339    0.1077 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8686    1.8238    0.5271 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8299   -0.0397    2.3894 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7147    0.7493   -1.2324 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5096    0.3055   -2.8678 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9571   -1.2955    0.1867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8752   -1.0580    0.4955 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 17 19  1  0
 16 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  2  0
 22 24  1  0
  9 25  1  0
 25 26  2  0
 26  3  1  0
 25  6  1  0
 21 13  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  4 30  1  0
  5 31  1  0
  7 32  1  0
  8 33  1  0
 10 34  1  0
 10 35  1  0
 11 36  1  0
 11 37  1  0
 12 38  1  0
 14 39  1  0
 15 40  1  0
 20 41  1  0
 26 42  1  0
M  CHG  4  17   1  19  -1  22   1  24  -1
M  END

  Mrv1652309112116312D          

 26 28  0  0  0  0            999 V2000
    3.4990    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845    0.6979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435    2.1904    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6284    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435    0.8555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3984    0.0709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2054   -0.1006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4604   -0.8853    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2673   -1.0568    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5223   -1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3292   -2.0129    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8813   -1.3998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6263   -0.6152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8194   -0.4437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6882   -1.5714    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
   -4.9432   -2.3560    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2403   -0.9583    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   -1.9702   -2.4545    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
   -2.2252   -3.2391    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1633   -2.2830    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
  1  2  1  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
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  3  8  1  0  0  0  0
  6  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
  5 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 15 20  1  0  0  0  0
 18 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 16 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
M  CHG  4  21   1  23  -1  24   1  26  -1
M  END
> <DATABASE_ID>
HMDB0254997

> <DATABASE_NAME>
hmdb

> <SMILES>
COC1=CC2=C(NC=C2CCNC2=C(C=C(C=C2)[N+]([O-])=O)[N+]([O-])=O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C17H16N4O5/c1-26-13-3-5-15-14(9-13)11(10-19-15)6-7-18-16-4-2-12(20(22)23)8-17(16)21(24)25/h2-5,8-10,18-19H,6-7H2,1H3

> <INCHI_KEY>
ODQMCTXUHFTMIE-UHFFFAOYSA-N

> <FORMULA>
C17H16N4O5

> <MOLECULAR_WEIGHT>
356.338

> <EXACT_MASS>
356.112069631

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
35.20641792632671

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
N-[2-(5-methoxy-1H-indol-3-yl)ethyl]-2,4-dinitroaniline

> <ALOGPS_LOGP>
3.88

> <JCHEM_LOGP>
3.930217371666666

> <ALOGPS_LOGS>
-5.16

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
17.622448755554128

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.620248640764494

> <JCHEM_PKA_STRONGEST_BASIC>
-4.341003822401434

> <JCHEM_POLAR_SURFACE_AREA>
123.33000000000001

> <JCHEM_REFRACTIVITY>
95.8101

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.48e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
N-[2-(5-methoxy-1H-indol-3-yl)ethyl]-2,4-dinitroaniline

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0254997
     RDKit          3D
N-(2,4-Dinitrophenyl)-5-methoxytryptamine
 42 44  0  0  0  0  0  0  0  0999 V2000
   -4.8556   -2.4675   -1.8170 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7680   -2.1028   -1.0146 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6727   -0.7789   -0.5857 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6209    0.1618   -0.9359 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5433    1.4744   -0.5218 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5005    1.9077    0.2705 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1699    3.1053    0.8157 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0293    2.9824    1.5167 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6311    1.6660    1.4082 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4266    1.0158    2.0038 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5867    0.8262    0.9148 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8082    0.1976    1.3834 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8420   -0.0392    0.4449 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6504    0.2936   -0.8945 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6379    0.0545   -1.8216 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8397   -0.5216   -1.4372 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8599   -0.7678   -2.3981 N   0  0  0  0  0  4  0  0  0  0  0  0
    5.6828   -0.4689   -3.5962 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0421   -1.3374   -1.9939 O   0  0  0  0  0  1  0  0  0  0  0  0
    5.0027   -0.8389   -0.1142 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0240   -0.6081    0.8385 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3477   -0.9939    2.1565 N   0  0  0  0  0  4  0  0  0  0  0  0
    3.9249   -0.3556    3.1201 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1543   -2.0774    2.3662 O   0  0  0  0  0  1  0  0  0  0  0  0
   -2.5447    0.9814    0.6295 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6273   -0.3515    0.2066 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8477   -1.7989   -2.7193 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8038   -3.5081   -2.1634 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7832   -2.2950   -1.2416 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4390   -0.1952   -1.5623 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3018    2.1771   -0.8154 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7401    3.9817    0.6913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5096    3.7795    2.0728 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7287    0.0009    2.3767 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0167    1.6052    2.8102 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1192    0.2339    0.1077 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8686    1.8238    0.5271 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8299   -0.0397    2.3894 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7147    0.7493   -1.2324 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5096    0.3055   -2.8678 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9571   -1.2955    0.1867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8752   -1.0580    0.4955 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 17 19  1  0
 16 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  2  0
 22 24  1  0
  9 25  1  0
 25 26  2  0
 26  3  1  0
 25  6  1  0
 21 13  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  4 30  1  0
  5 31  1  0
  7 32  1  0
  8 33  1  0
 10 34  1  0
 10 35  1  0
 11 36  1  0
 11 37  1  0
 12 38  1  0
 14 39  1  0
 15 40  1  0
 20 41  1  0
 26 42  1  0
M  CHG  4  17   1  19  -1  22   1  24  -1
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       6.531   2.073   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       5.198   1.303   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       3.864   2.073   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.530   1.303   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.197   2.073   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.197   3.613   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.530   4.383   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.864   3.613   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0      -0.268   4.089   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0      -1.173   2.843   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.268   1.597   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.744   0.132   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.250  -0.188   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0      -2.726  -1.652   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0      -4.232  -1.973   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -4.708  -3.437   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -6.215  -3.757   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -7.245  -2.613   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -6.769  -1.148   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -5.263  -0.828   0.000  0.00  0.00           C+0
HETATM   21  N   UNK     0      -8.751  -2.933   0.000  0.00  0.00           N+1
HETATM   22  O   UNK     0      -9.227  -4.398   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      -9.782  -1.789   0.000  0.00  0.00           O-1
HETATM   24  N   UNK     0      -3.678  -4.582   0.000  0.00  0.00           N+1
HETATM   25  O   UNK     0      -4.154  -6.046   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0      -2.171  -4.262   0.000  0.00  0.00           O-1
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   11                                                  
CONECT    6    5    7    9                                                  
CONECT    7    6    8                                                       
CONECT    8    7    3                                                       
CONECT    9    6   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10    5   12                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   20                                                  
CONECT   16   15   17   24                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   21                                                  
CONECT   19   18   20                                                       
CONECT   20   19   15                                                       
CONECT   21   18   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   16   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   56    0
END

COMPND    HMDB0254997
HETATM    1  C1  UNL     1      -4.856  -2.467  -1.817  1.00  0.00           C  
HETATM    2  O1  UNL     1      -3.768  -2.103  -1.015  1.00  0.00           O  
HETATM    3  C2  UNL     1      -3.673  -0.779  -0.586  1.00  0.00           C  
HETATM    4  C3  UNL     1      -4.621   0.162  -0.936  1.00  0.00           C  
HETATM    5  C4  UNL     1      -4.543   1.474  -0.522  1.00  0.00           C  
HETATM    6  C5  UNL     1      -3.501   1.908   0.271  1.00  0.00           C  
HETATM    7  N1  UNL     1      -3.170   3.105   0.816  1.00  0.00           N  
HETATM    8  C6  UNL     1      -2.029   2.982   1.517  1.00  0.00           C  
HETATM    9  C7  UNL     1      -1.631   1.666   1.408  1.00  0.00           C  
HETATM   10  C8  UNL     1      -0.427   1.016   2.004  1.00  0.00           C  
HETATM   11  C9  UNL     1       0.587   0.826   0.915  1.00  0.00           C  
HETATM   12  N2  UNL     1       1.808   0.198   1.383  1.00  0.00           N  
HETATM   13  C10 UNL     1       2.842  -0.039   0.445  1.00  0.00           C  
HETATM   14  C11 UNL     1       2.650   0.294  -0.894  1.00  0.00           C  
HETATM   15  C12 UNL     1       3.638   0.054  -1.822  1.00  0.00           C  
HETATM   16  C13 UNL     1       4.840  -0.522  -1.437  1.00  0.00           C  
HETATM   17  N3  UNL     1       5.860  -0.768  -2.398  1.00  0.00           N1+
HETATM   18  O2  UNL     1       5.683  -0.469  -3.596  1.00  0.00           O  
HETATM   19  O3  UNL     1       7.042  -1.337  -1.994  1.00  0.00           O1-
HETATM   20  C14 UNL     1       5.003  -0.839  -0.114  1.00  0.00           C  
HETATM   21  C15 UNL     1       4.024  -0.608   0.839  1.00  0.00           C  
HETATM   22  N4  UNL     1       4.348  -0.994   2.157  1.00  0.00           N1+
HETATM   23  O4  UNL     1       3.925  -0.356   3.120  1.00  0.00           O  
HETATM   24  O5  UNL     1       5.154  -2.077   2.366  1.00  0.00           O1-
HETATM   25  C16 UNL     1      -2.545   0.981   0.630  1.00  0.00           C  
HETATM   26  C17 UNL     1      -2.627  -0.352   0.207  1.00  0.00           C  
HETATM   27  H1  UNL     1      -4.848  -1.799  -2.719  1.00  0.00           H  
HETATM   28  H2  UNL     1      -4.804  -3.508  -2.163  1.00  0.00           H  
HETATM   29  H3  UNL     1      -5.783  -2.295  -1.242  1.00  0.00           H  
HETATM   30  H4  UNL     1      -5.439  -0.195  -1.562  1.00  0.00           H  
HETATM   31  H5  UNL     1      -5.302   2.177  -0.815  1.00  0.00           H  
HETATM   32  H6  UNL     1      -3.740   3.982   0.691  1.00  0.00           H  
HETATM   33  H7  UNL     1      -1.510   3.780   2.073  1.00  0.00           H  
HETATM   34  H8  UNL     1      -0.729   0.001   2.377  1.00  0.00           H  
HETATM   35  H9  UNL     1       0.017   1.605   2.810  1.00  0.00           H  
HETATM   36  H10 UNL     1       0.119   0.234   0.108  1.00  0.00           H  
HETATM   37  H11 UNL     1       0.869   1.824   0.527  1.00  0.00           H  
HETATM   38  H12 UNL     1       1.830  -0.040   2.389  1.00  0.00           H  
HETATM   39  H13 UNL     1       1.715   0.749  -1.232  1.00  0.00           H  
HETATM   40  H14 UNL     1       3.510   0.306  -2.868  1.00  0.00           H  
HETATM   41  H15 UNL     1       5.957  -1.295   0.187  1.00  0.00           H  
HETATM   42  H16 UNL     1      -1.875  -1.058   0.496  1.00  0.00           H  
CONECT    1    2   27   28   29
CONECT    2    3
CONECT    3    4    4   26
CONECT    4    5   30
CONECT    5    6    6   31
CONECT    6    7   25
CONECT    7    8   32
CONECT    8    9    9   33
CONECT    9   10   25
CONECT   10   11   34   35
CONECT   11   12   36   37
CONECT   12   13   38
CONECT   13   14   14   21
CONECT   14   15   39
CONECT   15   16   16   40
CONECT   16   17   20
CONECT   17   18   18   19
CONECT   20   21   21   41
CONECT   21   22
CONECT   22   23   23   24
CONECT   25   26   26
CONECT   26   42
END

HMDB0254997
     RDKit          3D
N-(2,4-Dinitrophenyl)-5-methoxytryptamine
 42 44  0  0  0  0  0  0  0  0999 V2000
   -4.8556   -2.4675   -1.8170 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7680   -2.1028   -1.0146 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6727   -0.7789   -0.5857 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6209    0.1618   -0.9359 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5433    1.4744   -0.5218 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5005    1.9077    0.2705 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1699    3.1053    0.8157 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0293    2.9824    1.5167 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6311    1.6660    1.4082 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4266    1.0158    2.0038 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5867    0.8262    0.9148 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8082    0.1976    1.3834 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8420   -0.0392    0.4449 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6504    0.2936   -0.8945 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6379    0.0545   -1.8216 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8397   -0.5216   -1.4372 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8599   -0.7678   -2.3981 N   0  0  0  0  0  4  0  0  0  0  0  0
    5.6828   -0.4689   -3.5962 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0421   -1.3374   -1.9939 O   0  0  0  0  0  1  0  0  0  0  0  0
    5.0027   -0.8389   -0.1142 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0240   -0.6081    0.8385 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3477   -0.9939    2.1565 N   0  0  0  0  0  4  0  0  0  0  0  0
    3.9249   -0.3556    3.1201 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1543   -2.0774    2.3662 O   0  0  0  0  0  1  0  0  0  0  0  0
   -2.5447    0.9814    0.6295 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6273   -0.3515    0.2066 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8477   -1.7989   -2.7193 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8038   -3.5081   -2.1634 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7832   -2.2950   -1.2416 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4390   -0.1952   -1.5623 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3018    2.1771   -0.8154 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7401    3.9817    0.6913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5096    3.7795    2.0728 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7287    0.0009    2.3767 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0167    1.6052    2.8102 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1192    0.2339    0.1077 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8686    1.8238    0.5271 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8299   -0.0397    2.3894 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7147    0.7493   -1.2324 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5096    0.3055   -2.8678 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9571   -1.2955    0.1867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8752   -1.0580    0.4955 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 17 19  1  0
 16 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  2  0
 22 24  1  0
  9 25  1  0
 25 26  2  0
 26  3  1  0
 25  6  1  0
 21 13  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  4 30  1  0
  5 31  1  0
  7 32  1  0
  8 33  1  0
 10 34  1  0
 10 35  1  0
 11 36  1  0
 11 37  1  0
 12 38  1  0
 14 39  1  0
 15 40  1  0
 20 41  1  0
 26 42  1  0
M  CHG  4  17   1  19  -1  22   1  24  -1
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
2,4-DNP-MT	HMDB

Chemical Formula

C₁₇H₁₆N₄O₅

Average Molecular Weight

356.338

Monoisotopic Molecular Weight

356.112069631

IUPAC Name

N-[2-(5-methoxy-1H-indol-3-yl)ethyl]-2,4-dinitroaniline

Traditional Name

N-[2-(5-methoxy-1H-indol-3-yl)ethyl]-2,4-dinitroaniline

CAS Registry Number

Not Available

SMILES

COC1=CC2=C(NC=C2CCNC2=C(C=C(C=C2)[N+]([O-])=O)[N+]([O-])=O)C=C1

InChI Identifier

InChI=1S/C17H16N4O5/c1-26-13-3-5-15-14(9-13)11(10-19-15)6-7-18-16-4-2-12(20(22)23)8-17(16)21(24)25/h2-5,8-10,18-19H,6-7H2,1H3

InChI Key

ODQMCTXUHFTMIE-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as dinitroanilines. These are organic compounds containing an aniline moiety, which is substituted at 2 positions by a nitro group.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Aniline and substituted anilines

Direct Parent

Dinitroanilines

Alternative Parents

Substituents

Dinitroaniline
Tryptamine
3-alkylindole
Nitrobenzene
Indole or derivatives
Indole
Nitroaromatic compound
Phenylalkylamine
Anisole
Aralkylamine
Secondary aliphatic/aromatic amine
Alkyl aryl ether
Substituted pyrrole
Heteroaromatic compound
Pyrrole
Organic nitro compound
C-nitro compound
Azacycle
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Allyl-type 1,3-dipolar organic compound
Secondary amine
Organic oxoazanium
Ether
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organic zwitterion
Organooxygen compound
Organonitrogen compound
Amine
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 31557052)

Source

Exogenous

Exogenous (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	3.88	ALOGPS
logP	3.93	ChemAxon
logS	-5.2	ALOGPS
pKa (Strongest Acidic)	12.62	ChemAxon
pKa (Strongest Basic)	-4.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	123.33 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	95.81 m³·mol⁻¹	ChemAxon
Polarizability	35.21 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	184.716	30932474
DeepCCS	[M-H]-	181.722	30932474
DeepCCS	[M-2H]-	215.67	30932474
DeepCCS	[M+Na]+	192.152	30932474
AllCCS	[M+H]+	181.7	32859911
AllCCS	[M+H-H2O]+	178.7	32859911
AllCCS	[M+NH4]+	184.5	32859911
AllCCS	[M+Na]+	185.3	32859911
AllCCS	[M-H]-	183.3	32859911
AllCCS	[M+Na-2H]-	182.7	32859911
AllCCS	[M+HCOO]-	182.2	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
N-(2,4-Dinitrophenyl)-5-methoxytryptamine	COC1=CC2=C(NC=C2CCNC2=C(C=C(C=C2)[N+]([O-])=O)[N+]([O-])=O)C=C1	4811.4	Standard polar	33892256
N-(2,4-Dinitrophenyl)-5-methoxytryptamine	COC1=CC2=C(NC=C2CCNC2=C(C=C(C=C2)[N+]([O-])=O)[N+]([O-])=O)C=C1	3306.8	Standard non polar	33892256
N-(2,4-Dinitrophenyl)-5-methoxytryptamine	COC1=CC2=C(NC=C2CCNC2=C(C=C(C=C2)[N+]([O-])=O)[N+]([O-])=O)C=C1	3903.3	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
N-(2,4-Dinitrophenyl)-5-methoxytryptamine,1TMS,isomer #1	COC1=CC=C2C(=C1)C(CCNC1=CC=C([N+](=O)[O-])C=C1[N+](=O)[O-])=CN2[Si](C)(C)C	3628.7	Semi standard non polar	33892256
N-(2,4-Dinitrophenyl)-5-methoxytryptamine,1TMS,isomer #1	COC1=CC=C2C(=C1)C(CCNC1=CC=C([N+](=O)[O-])C=C1[N+](=O)[O-])=CN2[Si](C)(C)C	3357.1	Standard non polar	33892256
N-(2,4-Dinitrophenyl)-5-methoxytryptamine,1TMS,isomer #1	COC1=CC=C2C(=C1)C(CCNC1=CC=C([N+](=O)[O-])C=C1[N+](=O)[O-])=CN2[Si](C)(C)C	4338.9	Standard polar	33892256
N-(2,4-Dinitrophenyl)-5-methoxytryptamine,1TMS,isomer #2	COC1=CC=C2[NH]C=C(CCN(C3=CC=C([N+](=O)[O-])C=C3[N+](=O)[O-])[Si](C)(C)C)C2=C1	3455.7	Semi standard non polar	33892256
N-(2,4-Dinitrophenyl)-5-methoxytryptamine,1TMS,isomer #2	COC1=CC=C2[NH]C=C(CCN(C3=CC=C([N+](=O)[O-])C=C3[N+](=O)[O-])[Si](C)(C)C)C2=C1	3336.2	Standard non polar	33892256
N-(2,4-Dinitrophenyl)-5-methoxytryptamine,1TMS,isomer #2	COC1=CC=C2[NH]C=C(CCN(C3=CC=C([N+](=O)[O-])C=C3[N+](=O)[O-])[Si](C)(C)C)C2=C1	4290.8	Standard polar	33892256
N-(2,4-Dinitrophenyl)-5-methoxytryptamine,2TMS,isomer #1	COC1=CC=C2C(=C1)C(CCN(C1=CC=C([N+](=O)[O-])C=C1[N+](=O)[O-])[Si](C)(C)C)=CN2[Si](C)(C)C	3464.4	Semi standard non polar	33892256
N-(2,4-Dinitrophenyl)-5-methoxytryptamine,2TMS,isomer #1	COC1=CC=C2C(=C1)C(CCN(C1=CC=C([N+](=O)[O-])C=C1[N+](=O)[O-])[Si](C)(C)C)=CN2[Si](C)(C)C	3332.7	Standard non polar	33892256
N-(2,4-Dinitrophenyl)-5-methoxytryptamine,2TMS,isomer #1	COC1=CC=C2C(=C1)C(CCN(C1=CC=C([N+](=O)[O-])C=C1[N+](=O)[O-])[Si](C)(C)C)=CN2[Si](C)(C)C	3926.5	Standard polar	33892256
N-(2,4-Dinitrophenyl)-5-methoxytryptamine,1TBDMS,isomer #1	COC1=CC=C2C(=C1)C(CCNC1=CC=C([N+](=O)[O-])C=C1[N+](=O)[O-])=CN2[Si](C)(C)C(C)(C)C	3846.8	Semi standard non polar	33892256
N-(2,4-Dinitrophenyl)-5-methoxytryptamine,1TBDMS,isomer #1	COC1=CC=C2C(=C1)C(CCNC1=CC=C([N+](=O)[O-])C=C1[N+](=O)[O-])=CN2[Si](C)(C)C(C)(C)C	3532.0	Standard non polar	33892256
N-(2,4-Dinitrophenyl)-5-methoxytryptamine,1TBDMS,isomer #1	COC1=CC=C2C(=C1)C(CCNC1=CC=C([N+](=O)[O-])C=C1[N+](=O)[O-])=CN2[Si](C)(C)C(C)(C)C	4318.6	Standard polar	33892256
N-(2,4-Dinitrophenyl)-5-methoxytryptamine,1TBDMS,isomer #2	COC1=CC=C2[NH]C=C(CCN(C3=CC=C([N+](=O)[O-])C=C3[N+](=O)[O-])[Si](C)(C)C(C)(C)C)C2=C1	3735.1	Semi standard non polar	33892256
N-(2,4-Dinitrophenyl)-5-methoxytryptamine,1TBDMS,isomer #2	COC1=CC=C2[NH]C=C(CCN(C3=CC=C([N+](=O)[O-])C=C3[N+](=O)[O-])[Si](C)(C)C(C)(C)C)C2=C1	3516.3	Standard non polar	33892256
N-(2,4-Dinitrophenyl)-5-methoxytryptamine,1TBDMS,isomer #2	COC1=CC=C2[NH]C=C(CCN(C3=CC=C([N+](=O)[O-])C=C3[N+](=O)[O-])[Si](C)(C)C(C)(C)C)C2=C1	4294.0	Standard polar	33892256
N-(2,4-Dinitrophenyl)-5-methoxytryptamine,2TBDMS,isomer #1	COC1=CC=C2C(=C1)C(CCN(C1=CC=C([N+](=O)[O-])C=C1[N+](=O)[O-])[Si](C)(C)C(C)(C)C)=CN2[Si](C)(C)C(C)(C)C	3928.1	Semi standard non polar	33892256
N-(2,4-Dinitrophenyl)-5-methoxytryptamine,2TBDMS,isomer #1	COC1=CC=C2C(=C1)C(CCN(C1=CC=C([N+](=O)[O-])C=C1[N+](=O)[O-])[Si](C)(C)C(C)(C)C)=CN2[Si](C)(C)C(C)(C)C	3676.5	Standard non polar	33892256
N-(2,4-Dinitrophenyl)-5-methoxytryptamine,2TBDMS,isomer #1	COC1=CC=C2C(=C1)C(CCN(C1=CC=C([N+](=O)[O-])C=C1[N+](=O)[O-])[Si](C)(C)C(C)(C)C)=CN2[Si](C)(C)C(C)(C)C	3989.8	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - N-(2,4-Dinitrophenyl)-5-methoxytryptamine GC-MS (Non-derivatized) - 70eV, Positive	splash10-06su-0198000000-22525c23401a4c52052b	2021-09-23	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - N-(2,4-Dinitrophenyl)-5-methoxytryptamine GC-MS (Non-derivatized) - 70eV, Positive	Not Available	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

153402

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

176102

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 N-(2,4-Dinitrophenyl)-5-methoxytryptamine (HMDB0254997)

MOL for HMDB0254997 (N-(2,4-Dinitrophenyl)-5-methoxytryptamine)

3D MOL for HMDB0254997 (N-(2,4-Dinitrophenyl)-5-methoxytryptamine)

3D SDF for HMDB0254997 (N-(2,4-Dinitrophenyl)-5-methoxytryptamine)

3D-SDF for HMDB0254997 (N-(2,4-Dinitrophenyl)-5-methoxytryptamine)

PDB for HMDB0254997 (N-(2,4-Dinitrophenyl)-5-methoxytryptamine)

3D PDB for HMDB0254997 (N-(2,4-Dinitrophenyl)-5-methoxytryptamine)

SMILES for HMDB0254997 (N-(2,4-Dinitrophenyl)-5-methoxytryptamine)

INCHI for HMDB0254997 (N-(2,4-Dinitrophenyl)-5-methoxytryptamine)

Structure for HMDB0254997 (N-(2,4-Dinitrophenyl)-5-methoxytryptamine)

3D Structure for HMDB0254997 (N-(2,4-Dinitrophenyl)-5-methoxytryptamine)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra