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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-08-29 02:32:22 UTC

Update Date

2021-09-26 22:48:55 UTC

HMDB ID

HMDB0242280

Secondary Accession Numbers

None

Metabolite Identification

Common Name

(1-(5-Fluoropentyl)-1H-indol-3-yl)(4-methylnaphthalen-1-yl)methanone

Description

(1-(5-Fluoropentyl)-1H-indol-3-yl)(4-methylnaphthalen-1-yl)methanone, also known as 1-(5-fluoropentyl)-3-(4-methyl-1-naphthoyl)indole, belongs to the class of organic compounds known as naphthoylindoles. These are polycyclic compounds containing an indole moiety that is N-linked to the carboxamide group attached to naphthalene. Based on a literature review very few articles have been published on (1-(5-Fluoropentyl)-1H-indol-3-yl)(4-methylnaphthalen-1-yl)methanone. This compound has been identified in human blood as reported by (PMID: 31557052 ). (1-(5-fluoropentyl)-1h-indol-3-yl)(4-methylnaphthalen-1-yl)methanone is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically (1-(5-Fluoropentyl)-1H-indol-3-yl)(4-methylnaphthalen-1-yl)methanone 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

  Mrv1652308292104422D          

 28 31  0  0  0  0            999 V2000
   -1.9468   -4.3198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4317   -3.6523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2522   -3.7386    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7371   -3.0711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4016   -2.3174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5811   -2.2312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2455   -1.4775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4250   -1.3913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9401   -2.0587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2757   -2.8124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0961   -2.8986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8865   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7070   -1.7362    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5509   -0.8963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7439   -0.7248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6577    0.0957    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4114    0.4312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6663    1.2159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4733    1.3874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0253    0.7743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7704   -0.0103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9634   -0.1819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9432    0.5082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2288    0.0957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5143    0.5082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2002    0.0957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9146    0.5082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6291    0.0957    0.0000 F   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
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
  2 11  1  0  0  0  0
  6 11  1  0  0  0  0
  5 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  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
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 17 22  1  0  0  0  0
 14 22  1  0  0  0  0
 16 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
M  END

HMDB0242280
     RDKit          3D
(1-(5-Fluoropentyl)-1H-indol-3-yl)(4-methylnaphthalen-1-yl)methanone
 52 55  0  0  0  0  0  0  0  0999 V2000
   -6.9066   -0.5924    0.3065 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4715   -0.4905    0.7048 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8999   -1.3634    1.6018 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5710   -1.2272    1.9332 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7706   -0.2156    1.3795 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3637   -0.1217    1.7277 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1603    0.1217    2.9781 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2419   -0.2728    0.8546 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8221    0.5730    0.7150 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6794    0.0867   -0.1798 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.9044    0.6931   -0.5975 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1143    0.2812    0.2148 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2909    1.0297   -0.3822 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5889    0.7370    0.3067 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6595    1.5683   -0.4125 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8934    1.3834    0.1282 F   0  0  0  0  0  0  0  0  0  0  0  0
    1.1998   -1.0971   -0.6535 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6769   -2.0079   -1.5779 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9918   -3.1634   -1.8943 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2039   -3.3738   -1.2415 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7048   -2.4874   -0.3180 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0044   -1.3283   -0.0091 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3588    0.6420    0.4906 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6579    1.6608   -0.0877 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2338    2.5408   -0.9802 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5552    2.3842   -1.2948 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3274    1.3779   -0.7489 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7137    0.5170    0.1414 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9943   -0.6704   -0.8167 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3690   -1.5100    0.7285 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4706    0.2814    0.7016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4864   -2.1464    2.0408 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0678   -1.8746    2.6247 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9434    1.4969    1.2551 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7876    1.7991   -0.5031 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0464    0.4863   -1.6696 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2626   -0.8002    0.2682 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0075    0.6575    1.2617 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4055    0.8449   -1.4617 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0754    2.1205   -0.2493 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5865    1.0037    1.3836 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8486   -0.3339    0.1290 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5965    1.3124   -1.5065 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2923    2.6249   -0.3434 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6195   -1.8053   -2.0683 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3819   -3.8630   -2.6184 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7714   -4.2725   -1.4634 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6482   -2.6330    0.2102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6286    1.7615    0.1854 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6628    3.3407   -1.4269 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0428    3.0575   -1.9919 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3876    1.2667   -1.0121 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  6  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  1  0
 14 15  1  0
 15 16  1  0
 10 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
  5 23  1  0
 23 24  2  0
 24 25  1  0
 25 26  2  0
 26 27  1  0
 27 28  2  0
 28  2  1  0
 22  8  1  0
 28 23  1  0
 22 17  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  3 32  1  0
  4 33  1  0
  9 34  1  0
 11 35  1  0
 11 36  1  0
 12 37  1  0
 12 38  1  0
 13 39  1  0
 13 40  1  0
 14 41  1  0
 14 42  1  0
 15 43  1  0
 15 44  1  0
 18 45  1  0
 19 46  1  0
 20 47  1  0
 21 48  1  0
 24 49  1  0
 25 50  1  0
 26 51  1  0
 27 52  1  0
M  END

  Mrv1652308292104422D          

 28 31  0  0  0  0            999 V2000
   -1.9468   -4.3198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4317   -3.6523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2522   -3.7386    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7371   -3.0711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4016   -2.3174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5811   -2.2312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2455   -1.4775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4250   -1.3913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9401   -2.0587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2757   -2.8124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0961   -2.8986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8865   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7070   -1.7362    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5509   -0.8963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7439   -0.7248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6577    0.0957    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4114    0.4312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6663    1.2159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4733    1.3874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0253    0.7743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7704   -0.0103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9634   -0.1819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9432    0.5082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2288    0.0957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5143    0.5082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2002    0.0957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9146    0.5082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6291    0.0957    0.0000 F   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
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
  2 11  1  0  0  0  0
  6 11  1  0  0  0  0
  5 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  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
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 17 22  1  0  0  0  0
 14 22  1  0  0  0  0
 16 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0242280

> <DATABASE_NAME>
hmdb

> <SMILES>
CC1=CC=C(C(=O)C2=CN(CCCCCF)C3=CC=CC=C23)C2=CC=CC=C12

> <INCHI_IDENTIFIER>
InChI=1S/C25H24FNO/c1-18-13-14-22(20-10-4-3-9-19(18)20)25(28)23-17-27(16-8-2-7-15-26)24-12-6-5-11-21(23)24/h3-6,9-14,17H,2,7-8,15-16H2,1H3

> <INCHI_KEY>
IGBHZHCGWLHBAE-UHFFFAOYSA-N

> <FORMULA>
C25H24FNO

> <MOLECULAR_WEIGHT>
373.471

> <EXACT_MASS>
373.18419256

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
42.69682083029761

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
1-(5-fluoropentyl)-3-(4-methylnaphthalene-1-carbonyl)-1H-indole

> <ALOGPS_LOGP>
5.76

> <JCHEM_LOGP>
6.480815894999999

> <ALOGPS_LOGS>
-5.96

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-7.6185092848164775

> <JCHEM_POLAR_SURFACE_AREA>
22.0

> <JCHEM_REFRACTIVITY>
112.8193

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.13e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-(5-fluoropentyl)-3-(4-methylnaphthalene-1-carbonyl)indole

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0242280
     RDKit          3D
(1-(5-Fluoropentyl)-1H-indol-3-yl)(4-methylnaphthalen-1-yl)methanone
 52 55  0  0  0  0  0  0  0  0999 V2000
   -6.9066   -0.5924    0.3065 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4715   -0.4905    0.7048 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8999   -1.3634    1.6018 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5710   -1.2272    1.9332 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7706   -0.2156    1.3795 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3637   -0.1217    1.7277 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1603    0.1217    2.9781 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2419   -0.2728    0.8546 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8221    0.5730    0.7150 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6794    0.0867   -0.1798 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.9044    0.6931   -0.5975 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1143    0.2812    0.2148 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2909    1.0297   -0.3822 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5889    0.7370    0.3067 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6595    1.5683   -0.4125 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8934    1.3834    0.1282 F   0  0  0  0  0  0  0  0  0  0  0  0
    1.1998   -1.0971   -0.6535 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6769   -2.0079   -1.5779 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9918   -3.1634   -1.8943 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2039   -3.3738   -1.2415 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7048   -2.4874   -0.3180 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0044   -1.3283   -0.0091 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3588    0.6420    0.4906 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6579    1.6608   -0.0877 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2338    2.5408   -0.9802 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5552    2.3842   -1.2948 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3274    1.3779   -0.7489 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7137    0.5170    0.1414 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9943   -0.6704   -0.8167 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3690   -1.5100    0.7285 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4706    0.2814    0.7016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4864   -2.1464    2.0408 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0678   -1.8746    2.6247 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9434    1.4969    1.2551 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7876    1.7991   -0.5031 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0464    0.4863   -1.6696 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2626   -0.8002    0.2682 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0075    0.6575    1.2617 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4055    0.8449   -1.4617 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0754    2.1205   -0.2493 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5865    1.0037    1.3836 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8486   -0.3339    0.1290 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5965    1.3124   -1.5065 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2923    2.6249   -0.3434 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6195   -1.8053   -2.0683 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3819   -3.8630   -2.6184 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7714   -4.2725   -1.4634 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6482   -2.6330    0.2102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6286    1.7615    0.1854 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6628    3.3407   -1.4269 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0428    3.0575   -1.9919 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3876    1.2667   -1.0121 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  6  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  1  0
 14 15  1  0
 15 16  1  0
 10 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
  5 23  1  0
 23 24  2  0
 24 25  1  0
 25 26  2  0
 26 27  1  0
 27 28  2  0
 28  2  1  0
 22  8  1  0
 28 23  1  0
 22 17  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  3 32  1  0
  4 33  1  0
  9 34  1  0
 11 35  1  0
 11 36  1  0
 12 37  1  0
 12 38  1  0
 13 39  1  0
 13 40  1  0
 14 41  1  0
 14 42  1  0
 15 43  1  0
 15 44  1  0
 18 45  1  0
 19 46  1  0
 20 47  1  0
 21 48  1  0
 24 49  1  0
 25 50  1  0
 26 51  1  0
 27 52  1  0
M  END

HEADER    PROTEIN                                 29-AUG-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-AUG-21         0                                  
HETATM    1  C   UNK     0      -3.634  -8.064   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.539  -6.818   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -6.071  -6.979   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -6.976  -5.733   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -6.350  -4.326   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -4.818  -4.165   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -4.192  -2.758   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.660  -2.597   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.755  -3.843   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.381  -5.250   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -3.913  -5.411   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -7.255  -3.080   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -8.786  -3.241   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -6.628  -1.673   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -5.122  -1.353   0.000  0.00  0.00           C+0
HETATM   16  N   UNK     0      -4.961   0.179   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0      -6.368   0.805   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -6.844   2.270   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -8.350   2.590   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -9.381   1.445   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -8.905  -0.019   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -7.398  -0.339   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -3.627   0.949   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -2.294   0.179   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -0.960   0.949   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.374   0.179   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       1.707   0.949   0.000  0.00  0.00           C+0
HETATM   28  F   UNK     0       3.041   0.179   0.000  0.00  0.00           F+0
CONECT    1    2                                                            
CONECT    2    1    3   11                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   12                                                  
CONECT    6    5    7   11                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10    2    6                                                  
CONECT   12    5   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   22                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   23                                                  
CONECT   17   16   18   22                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   17   14                                                  
CONECT   23   16   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   62    0
END

COMPND    HMDB0242280
HETATM    1  C1  UNL     1      -6.907  -0.592   0.307  1.00  0.00           C  
HETATM    2  C2  UNL     1      -5.471  -0.490   0.705  1.00  0.00           C  
HETATM    3  C3  UNL     1      -4.900  -1.363   1.602  1.00  0.00           C  
HETATM    4  C4  UNL     1      -3.571  -1.227   1.933  1.00  0.00           C  
HETATM    5  C5  UNL     1      -2.771  -0.216   1.380  1.00  0.00           C  
HETATM    6  C6  UNL     1      -1.364  -0.122   1.728  1.00  0.00           C  
HETATM    7  O1  UNL     1      -1.160   0.122   2.978  1.00  0.00           O  
HETATM    8  C7  UNL     1      -0.242  -0.273   0.855  1.00  0.00           C  
HETATM    9  C8  UNL     1       0.822   0.573   0.715  1.00  0.00           C  
HETATM   10  N1  UNL     1       1.679   0.087  -0.180  1.00  0.00           N  
HETATM   11  C9  UNL     1       2.904   0.693  -0.598  1.00  0.00           C  
HETATM   12  C10 UNL     1       4.114   0.281   0.215  1.00  0.00           C  
HETATM   13  C11 UNL     1       5.291   1.030  -0.382  1.00  0.00           C  
HETATM   14  C12 UNL     1       6.589   0.737   0.307  1.00  0.00           C  
HETATM   15  C13 UNL     1       7.660   1.568  -0.412  1.00  0.00           C  
HETATM   16  F1  UNL     1       8.893   1.383   0.128  1.00  0.00           F  
HETATM   17  C14 UNL     1       1.200  -1.097  -0.654  1.00  0.00           C  
HETATM   18  C15 UNL     1       1.677  -2.008  -1.578  1.00  0.00           C  
HETATM   19  C16 UNL     1       0.992  -3.163  -1.894  1.00  0.00           C  
HETATM   20  C17 UNL     1      -0.204  -3.374  -1.241  1.00  0.00           C  
HETATM   21  C18 UNL     1      -0.705  -2.487  -0.318  1.00  0.00           C  
HETATM   22  C19 UNL     1      -0.004  -1.328  -0.009  1.00  0.00           C  
HETATM   23  C20 UNL     1      -3.359   0.642   0.491  1.00  0.00           C  
HETATM   24  C21 UNL     1      -2.658   1.661  -0.088  1.00  0.00           C  
HETATM   25  C22 UNL     1      -3.234   2.541  -0.980  1.00  0.00           C  
HETATM   26  C23 UNL     1      -4.555   2.384  -1.295  1.00  0.00           C  
HETATM   27  C24 UNL     1      -5.327   1.378  -0.749  1.00  0.00           C  
HETATM   28  C25 UNL     1      -4.714   0.517   0.141  1.00  0.00           C  
HETATM   29  H1  UNL     1      -6.994  -0.670  -0.817  1.00  0.00           H  
HETATM   30  H2  UNL     1      -7.369  -1.510   0.728  1.00  0.00           H  
HETATM   31  H3  UNL     1      -7.471   0.281   0.702  1.00  0.00           H  
HETATM   32  H4  UNL     1      -5.486  -2.146   2.041  1.00  0.00           H  
HETATM   33  H5  UNL     1      -3.068  -1.875   2.625  1.00  0.00           H  
HETATM   34  H6  UNL     1       0.943   1.497   1.255  1.00  0.00           H  
HETATM   35  H7  UNL     1       2.788   1.799  -0.503  1.00  0.00           H  
HETATM   36  H8  UNL     1       3.046   0.486  -1.670  1.00  0.00           H  
HETATM   37  H9  UNL     1       4.263  -0.800   0.268  1.00  0.00           H  
HETATM   38  H10 UNL     1       4.007   0.657   1.262  1.00  0.00           H  
HETATM   39  H11 UNL     1       5.406   0.845  -1.462  1.00  0.00           H  
HETATM   40  H12 UNL     1       5.075   2.121  -0.249  1.00  0.00           H  
HETATM   41  H13 UNL     1       6.586   1.004   1.384  1.00  0.00           H  
HETATM   42  H14 UNL     1       6.849  -0.334   0.129  1.00  0.00           H  
HETATM   43  H15 UNL     1       7.596   1.312  -1.506  1.00  0.00           H  
HETATM   44  H16 UNL     1       7.292   2.625  -0.343  1.00  0.00           H  
HETATM   45  H17 UNL     1       2.619  -1.805  -2.068  1.00  0.00           H  
HETATM   46  H18 UNL     1       1.382  -3.863  -2.618  1.00  0.00           H  
HETATM   47  H19 UNL     1      -0.771  -4.273  -1.463  1.00  0.00           H  
HETATM   48  H20 UNL     1      -1.648  -2.633   0.210  1.00  0.00           H  
HETATM   49  H21 UNL     1      -1.629   1.761   0.185  1.00  0.00           H  
HETATM   50  H22 UNL     1      -2.663   3.341  -1.427  1.00  0.00           H  
HETATM   51  H23 UNL     1      -5.043   3.058  -1.992  1.00  0.00           H  
HETATM   52  H24 UNL     1      -6.388   1.267  -1.012  1.00  0.00           H  
CONECT    1    2   29   30   31
CONECT    2    3    3   28
CONECT    3    4   32
CONECT    4    5    5   33
CONECT    5    6   23
CONECT    6    7    7    8
CONECT    8    9    9   22
CONECT    9   10   34
CONECT   10   11   17
CONECT   11   12   35   36
CONECT   12   13   37   38
CONECT   13   14   39   40
CONECT   14   15   41   42
CONECT   15   16   43   44
CONECT   17   18   18   22
CONECT   18   19   45
CONECT   19   20   20   46
CONECT   20   21   47
CONECT   21   22   22   48
CONECT   23   24   24   28
CONECT   24   25   49
CONECT   25   26   26   50
CONECT   26   27   51
CONECT   27   28   28   52
END

HMDB0242280
     RDKit          3D
(1-(5-Fluoropentyl)-1H-indol-3-yl)(4-methylnaphthalen-1-yl)methanone
 52 55  0  0  0  0  0  0  0  0999 V2000
   -6.9066   -0.5924    0.3065 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4715   -0.4905    0.7048 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8999   -1.3634    1.6018 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5710   -1.2272    1.9332 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7706   -0.2156    1.3795 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3637   -0.1217    1.7277 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1603    0.1217    2.9781 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2419   -0.2728    0.8546 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8221    0.5730    0.7150 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6794    0.0867   -0.1798 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.9044    0.6931   -0.5975 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1143    0.2812    0.2148 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2909    1.0297   -0.3822 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5889    0.7370    0.3067 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6595    1.5683   -0.4125 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8934    1.3834    0.1282 F   0  0  0  0  0  0  0  0  0  0  0  0
    1.1998   -1.0971   -0.6535 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6769   -2.0079   -1.5779 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9918   -3.1634   -1.8943 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2039   -3.3738   -1.2415 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7048   -2.4874   -0.3180 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0044   -1.3283   -0.0091 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3588    0.6420    0.4906 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6579    1.6608   -0.0877 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2338    2.5408   -0.9802 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5552    2.3842   -1.2948 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3274    1.3779   -0.7489 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7137    0.5170    0.1414 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9943   -0.6704   -0.8167 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3690   -1.5100    0.7285 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4706    0.2814    0.7016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4864   -2.1464    2.0408 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0678   -1.8746    2.6247 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9434    1.4969    1.2551 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7876    1.7991   -0.5031 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0464    0.4863   -1.6696 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2626   -0.8002    0.2682 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0075    0.6575    1.2617 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4055    0.8449   -1.4617 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0754    2.1205   -0.2493 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5865    1.0037    1.3836 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8486   -0.3339    0.1290 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5965    1.3124   -1.5065 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2923    2.6249   -0.3434 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6195   -1.8053   -2.0683 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3819   -3.8630   -2.6184 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7714   -4.2725   -1.4634 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6482   -2.6330    0.2102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6286    1.7615    0.1854 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6628    3.3407   -1.4269 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0428    3.0575   -1.9919 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3876    1.2667   -1.0121 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  6  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  1  0
 14 15  1  0
 15 16  1  0
 10 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
  5 23  1  0
 23 24  2  0
 24 25  1  0
 25 26  2  0
 26 27  1  0
 27 28  2  0
 28  2  1  0
 22  8  1  0
 28 23  1  0
 22 17  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  3 32  1  0
  4 33  1  0
  9 34  1  0
 11 35  1  0
 11 36  1  0
 12 37  1  0
 12 38  1  0
 13 39  1  0
 13 40  1  0
 14 41  1  0
 14 42  1  0
 15 43  1  0
 15 44  1  0
 18 45  1  0
 19 46  1  0
 20 47  1  0
 21 48  1  0
 24 49  1  0
 25 50  1  0
 26 51  1  0
 27 52  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
(1-(5-Fluoropentyl)-1H-indol-3-yl)(4-methyl-1-naphthalenyl)methanone	HMDB
1-(5-Fluoropentyl)-3-(4-methyl-1-naphthoyl)indole	HMDB

Chemical Formula

C₂₅H₂₄FNO

Average Molecular Weight

373.471

Monoisotopic Molecular Weight

373.18419256

IUPAC Name

1-(5-fluoropentyl)-3-(4-methylnaphthalene-1-carbonyl)-1H-indole

Traditional Name

1-(5-fluoropentyl)-3-(4-methylnaphthalene-1-carbonyl)indole

CAS Registry Number

Not Available

SMILES

CC1=CC=C(C(=O)C2=CN(CCCCCF)C3=CC=CC=C23)C2=CC=CC=C12

InChI Identifier

InChI=1S/C25H24FNO/c1-18-13-14-22(20-10-4-3-9-19(18)20)25(28)23-17-27(16-8-2-7-15-26)24-12-6-5-11-21(23)24/h3-6,9-14,17H,2,7-8,15-16H2,1H3

InChI Key

IGBHZHCGWLHBAE-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as naphthoylindoles. These are polycyclic compounds containing an indole moiety that is N-linked to the carboxamide group attached to naphthalene.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Naphthoylindoles

Direct Parent

Naphthoylindoles

Alternative Parents

Substituents

Naphthoylindole
Benzoylindole
1-naphthalenecarboxylic acid or derivatives
Indolecarboxylic acid derivative
N-alkylindole
Naphthalene
Indole
Aryl ketone
Benzenoid
Substituted pyrrole
Heteroaromatic compound
Vinylogous amide
Pyrrole
Ketone
Azacycle
Organohalogen compound
Organonitrogen compound
Organooxygen compound
Alkyl fluoride
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Organic nitrogen compound
Alkyl halide
Organofluoride
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	5.76	ALOGPS
logP	6.48	ChemAxon
logS	-6	ALOGPS
pKa (Strongest Basic)	-7.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	22 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	112.82 m³·mol⁻¹	ChemAxon
Polarizability	42.7 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M-2H]-	224.595	30932474
DeepCCS	[M+Na]+	200.461	30932474
AllCCS	[M+H]+	193.0	32859911
AllCCS	[M+H-H2O]+	190.2	32859911
AllCCS	[M+NH4]+	195.6	32859911
AllCCS	[M+Na]+	196.4	32859911
AllCCS	[M-H]-	195.2	32859911
AllCCS	[M+Na-2H]-	194.8	32859911
AllCCS	[M+HCOO]-	194.5	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
(1-(5-Fluoropentyl)-1H-indol-3-yl)(4-methylnaphthalen-1-yl)methanone	CC1=CC=C(C(=O)C2=CN(CCCCCF)C3=CC=CC=C23)C2=CC=CC=C12	4627.2	Standard polar	33892256
(1-(5-Fluoropentyl)-1H-indol-3-yl)(4-methylnaphthalen-1-yl)methanone	CC1=CC=C(C(=O)C2=CN(CCCCCF)C3=CC=CC=C23)C2=CC=CC=C12	3216.8	Standard non polar	33892256
(1-(5-Fluoropentyl)-1H-indol-3-yl)(4-methylnaphthalen-1-yl)methanone	CC1=CC=C(C(=O)C2=CN(CCCCCF)C3=CC=CC=C23)C2=CC=CC=C12	3416.3	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - (1-(5-Fluoropentyl)-1H-indol-3-yl)(4-methylnaphthalen-1-yl)methanone GC-MS (Non-derivatized) - 70eV, Positive	splash10-004i-4239000000-a8e663fde9731f5720d9	2021-09-24	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (1-(5-Fluoropentyl)-1H-indol-3-yl)(4-methylnaphthalen-1-yl)methanone 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 - (1-(5-Fluoropentyl)-1H-indol-3-yl)(4-methylnaphthalen-1-yl)methanone 10V, Positive-QTOF	splash10-00di-0109000000-dae5df6de9430bdcea24	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (1-(5-Fluoropentyl)-1H-indol-3-yl)(4-methylnaphthalen-1-yl)methanone 20V, Positive-QTOF	splash10-00xr-0917000000-26f5ef0ab2e30a417465	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (1-(5-Fluoropentyl)-1H-indol-3-yl)(4-methylnaphthalen-1-yl)methanone 40V, Positive-QTOF	splash10-0006-0900000000-763b5c9cf3d0baaa8524	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (1-(5-Fluoropentyl)-1H-indol-3-yl)(4-methylnaphthalen-1-yl)methanone 10V, Negative-QTOF	splash10-00e9-0089000000-a9018002047852e266bd	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (1-(5-Fluoropentyl)-1H-indol-3-yl)(4-methylnaphthalen-1-yl)methanone 20V, Negative-QTOF	splash10-00e9-0069000000-1f537fbb8faa2dcf06f7	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (1-(5-Fluoropentyl)-1H-indol-3-yl)(4-methylnaphthalen-1-yl)methanone 40V, Negative-QTOF	splash10-001i-0391000000-9019246616b5b1d873cd	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

28289977

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

66570720

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 (1-(5-Fluoropentyl)-1H-indol-3-yl)(4-methylnaphthalen-1-yl)methanone (HMDB0242280)

MOL for HMDB0242280 ((1-(5-Fluoropentyl)-1H-indol-3-yl)(4-methylnaphthalen-1-yl)methanone)

3D MOL for HMDB0242280 ((1-(5-Fluoropentyl)-1H-indol-3-yl)(4-methylnaphthalen-1-yl)methanone)

3D SDF for HMDB0242280 ((1-(5-Fluoropentyl)-1H-indol-3-yl)(4-methylnaphthalen-1-yl)methanone)

3D-SDF for HMDB0242280 ((1-(5-Fluoropentyl)-1H-indol-3-yl)(4-methylnaphthalen-1-yl)methanone)

PDB for HMDB0242280 ((1-(5-Fluoropentyl)-1H-indol-3-yl)(4-methylnaphthalen-1-yl)methanone)

3D PDB for HMDB0242280 ((1-(5-Fluoropentyl)-1H-indol-3-yl)(4-methylnaphthalen-1-yl)methanone)

SMILES for HMDB0242280 ((1-(5-Fluoropentyl)-1H-indol-3-yl)(4-methylnaphthalen-1-yl)methanone)

INCHI for HMDB0242280 ((1-(5-Fluoropentyl)-1H-indol-3-yl)(4-methylnaphthalen-1-yl)methanone)

Structure for HMDB0242280 ((1-(5-Fluoropentyl)-1H-indol-3-yl)(4-methylnaphthalen-1-yl)methanone)

3D Structure for HMDB0242280 ((1-(5-Fluoropentyl)-1H-indol-3-yl)(4-methylnaphthalen-1-yl)methanone)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

GC-MS Spectra

MS/MS Spectra