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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 02:13:31 UTC

Update Date

2021-09-26 22:59:15 UTC

HMDB ID

HMDB0248777

Secondary Accession Numbers

None

Metabolite Identification

Common Name

4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide

Description

4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide belongs to the class of organic compounds known as cinnolines. These are organic aromatic compounds containing a benzene fused to a pyridazine ring. Based on a literature review very few articles have been published on 4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide. This compound has been identified in human blood as reported by (PMID: 31557052 ). 4-amino-8-(2-fluoro-6-methoxyphenyl)-n-propylcinnoline-3-carboxamide is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically 4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide 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


  Mrv1652309112104132D          

 26 28  0  0  0  0            999 V2000
   -2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -3.3000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -3.3000    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
    2.8579   -3.3000    0.0000 C   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   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   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 F   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.0625    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -4.5375    0.0000 N   0  0  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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
  9 14  1  0  0  0  0
 11 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
 20 21  1  0  0  0  0
 16 22  1  0  0  0  0
 22 23  1  0  0  0  0
 10 24  1  0  0  0  0
 24 25  2  0  0  0  0
  7 25  1  0  0  0  0
  8 26  1  0  0  0  0
M  END

HMDB0248777
     RDKit          3D
4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide
 45 47  0  0  0  0  0  0  0  0999 V2000
    6.1284   -0.1748   -0.8075 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6121    0.0865   -2.1656 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4066   -0.5944   -2.6604 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1579   -0.4022   -2.0067 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8559   -0.8041   -0.7156 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6996   -1.4068   -0.0130 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5383   -0.5461   -0.1061 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5934    0.0960   -0.8108 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6077    0.3581   -0.3225 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9017   -0.0300    0.9267 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1684    0.2568    1.4157 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1777    0.9561    0.6294 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2341    2.3331    0.6950 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3699    3.0255    1.4740 F   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1766    3.0588   -0.0333 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0762    2.3973   -0.8394 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0004    1.0207   -0.8888 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0780    0.2845   -0.1781 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9895   -1.0900   -0.2167 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8128   -1.9264   -0.9733 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4482   -0.1520    2.7030 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5038   -0.8198    3.4722 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2557   -1.0955    2.9732 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0381   -0.6944    1.6918 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3049   -0.9638    1.1592 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2868   -1.6351    1.9016 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.2665   -1.2116   -0.5109 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2062    0.2499   -0.8147 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6206    0.3735    0.0142 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4741   -0.0180   -2.8928 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4038    1.2130   -2.2325 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2748   -0.4446   -3.7800 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6114   -1.7252   -2.6207 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3479    0.0962   -2.5271 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2152    4.1382    0.0228 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8280    2.9479   -1.4228 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7050    0.5131   -1.5193 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1897   -2.8224   -1.2594 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1809   -1.5003   -1.9087 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6294   -2.3581   -0.3361 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4365    0.0755    3.0752 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7552   -1.1254    4.4747 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5153   -1.6094    3.5229 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2883   -2.6528    2.1275 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1099   -1.1105    2.2835 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 13 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  1  0
 11 21  2  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
 25  7  1  0
 24 10  1  0
 18 12  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  2 30  1  0
  2 31  1  0
  3 32  1  0
  3 33  1  0
  4 34  1  0
 15 35  1  0
 16 36  1  0
 17 37  1  0
 20 38  1  0
 20 39  1  0
 20 40  1  0
 21 41  1  0
 22 42  1  0
 23 43  1  0
 26 44  1  0
 26 45  1  0
M  END


  Mrv1652309112104132D          

 26 28  0  0  0  0            999 V2000
   -2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -3.3000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -3.3000    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
    2.8579   -3.3000    0.0000 C   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   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   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 F   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.0625    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -4.5375    0.0000 N   0  0  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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
  9 14  1  0  0  0  0
 11 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
 20 21  1  0  0  0  0
 16 22  1  0  0  0  0
 22 23  1  0  0  0  0
 10 24  1  0  0  0  0
 24 25  2  0  0  0  0
  7 25  1  0  0  0  0
  8 26  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0248777

> <DATABASE_NAME>
hmdb

> <SMILES>
CCCNC(=O)C1=C(N)C2=C(N=N1)C(=CC=C2)C1=C(OC)C=CC=C1F

> <INCHI_IDENTIFIER>
InChI=1S/C19H19FN4O2/c1-3-10-22-19(25)18-16(21)12-7-4-6-11(17(12)23-24-18)15-13(20)8-5-9-14(15)26-2/h4-9H,3,10H2,1-2H3,(H2,21,23)(H,22,25)

> <INCHI_KEY>
KYDURMHFWXCKMW-UHFFFAOYSA-N

> <FORMULA>
C19H19FN4O2

> <MOLECULAR_WEIGHT>
354.385

> <EXACT_MASS>
354.149204031

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
36.86101038882218

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide

> <ALOGPS_LOGP>
3.53

> <JCHEM_LOGP>
2.9439576336666664

> <ALOGPS_LOGS>
-4.31

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.382337660367753

> <JCHEM_PKA_STRONGEST_BASIC>
2.897921097880046

> <JCHEM_POLAR_SURFACE_AREA>
90.13

> <JCHEM_REFRACTIVITY>
99.23450000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.72e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0248777
     RDKit          3D
4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide
 45 47  0  0  0  0  0  0  0  0999 V2000
    6.1284   -0.1748   -0.8075 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6121    0.0865   -2.1656 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4066   -0.5944   -2.6604 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1579   -0.4022   -2.0067 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8559   -0.8041   -0.7156 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6996   -1.4068   -0.0130 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5383   -0.5461   -0.1061 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5934    0.0960   -0.8108 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6077    0.3581   -0.3225 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9017   -0.0300    0.9267 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1684    0.2568    1.4157 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1777    0.9561    0.6294 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2341    2.3331    0.6950 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3699    3.0255    1.4740 F   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1766    3.0588   -0.0333 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0762    2.3973   -0.8394 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0004    1.0207   -0.8888 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0780    0.2845   -0.1781 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9895   -1.0900   -0.2167 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8128   -1.9264   -0.9733 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4482   -0.1520    2.7030 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5038   -0.8198    3.4722 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2557   -1.0955    2.9732 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0381   -0.6944    1.6918 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3049   -0.9638    1.1592 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2868   -1.6351    1.9016 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.2665   -1.2116   -0.5109 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2062    0.2499   -0.8147 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6206    0.3735    0.0142 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4741   -0.0180   -2.8928 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4038    1.2130   -2.2325 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2748   -0.4446   -3.7800 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6114   -1.7252   -2.6207 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3479    0.0962   -2.5271 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2152    4.1382    0.0228 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8280    2.9479   -1.4228 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7050    0.5131   -1.5193 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1897   -2.8224   -1.2594 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1809   -1.5003   -1.9087 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6294   -2.3581   -0.3361 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4365    0.0755    3.0752 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7552   -1.1254    4.4747 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5153   -1.6094    3.5229 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2883   -2.6528    2.1275 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1099   -1.1105    2.2835 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 13 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  1  0
 11 21  2  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
 25  7  1  0
 24 10  1  0
 18 12  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  2 30  1  0
  2 31  1  0
  3 32  1  0
  3 33  1  0
  4 34  1  0
 15 35  1  0
 16 36  1  0
 17 37  1  0
 20 38  1  0
 20 39  1  0
 20 40  1  0
 21 41  1  0
 22 42  1  0
 23 43  1  0
 26 44  1  0
 26 45  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      -4.001  -6.930   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.667  -6.160   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.334  -6.930   0.000  0.00  0.00           C+0
HETATM    4  N   UNK     0       0.000  -6.160   0.000  0.00  0.00           N+0
HETATM    5  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       1.334  -8.470   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       2.667  -6.160   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.335  -6.160   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.668  -3.850   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.002  -6.160   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.335  -1.540   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.668   0.770   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.002   0.000   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.002  -1.540   0.000  0.00  0.00           C+0
HETATM   21  F   UNK     0       9.336  -2.310   0.000  0.00  0.00           F+0
HETATM   22  O   UNK     0       4.001  -2.310   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       2.667  -1.540   0.000  0.00  0.00           C+0
HETATM   24  N   UNK     0       4.001  -3.850   0.000  0.00  0.00           N+0
HETATM   25  N   UNK     0       2.667  -4.620   0.000  0.00  0.00           N+0
HETATM   26  N   UNK     0       4.001  -8.470   0.000  0.00  0.00           N+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   25                                                  
CONECT    8    7    9   26                                                  
CONECT    9    8   10   14                                                  
CONECT   10    9   11   24                                                  
CONECT   11   10   12   15                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13    9                                                       
CONECT   15   11   16   20                                                  
CONECT   16   15   17   22                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   15   21                                                  
CONECT   21   20                                                            
CONECT   22   16   23                                                       
CONECT   23   22                                                            
CONECT   24   10   25                                                       
CONECT   25   24    7                                                       
CONECT   26    8                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   56    0
END

COMPND    HMDB0248777
HETATM    1  C1  UNL     1       6.128  -0.175  -0.807  1.00  0.00           C  
HETATM    2  C2  UNL     1       5.612   0.086  -2.166  1.00  0.00           C  
HETATM    3  C3  UNL     1       4.407  -0.594  -2.660  1.00  0.00           C  
HETATM    4  N1  UNL     1       3.158  -0.402  -2.007  1.00  0.00           N  
HETATM    5  C4  UNL     1       2.856  -0.804  -0.716  1.00  0.00           C  
HETATM    6  O1  UNL     1       3.700  -1.407  -0.013  1.00  0.00           O  
HETATM    7  C5  UNL     1       1.538  -0.546  -0.106  1.00  0.00           C  
HETATM    8  N2  UNL     1       0.593   0.096  -0.811  1.00  0.00           N  
HETATM    9  N3  UNL     1      -0.608   0.358  -0.323  1.00  0.00           N  
HETATM   10  C6  UNL     1      -0.902  -0.030   0.927  1.00  0.00           C  
HETATM   11  C7  UNL     1      -2.168   0.257   1.416  1.00  0.00           C  
HETATM   12  C8  UNL     1      -3.178   0.956   0.629  1.00  0.00           C  
HETATM   13  C9  UNL     1      -3.234   2.333   0.695  1.00  0.00           C  
HETATM   14  F1  UNL     1      -2.370   3.025   1.474  1.00  0.00           F  
HETATM   15  C10 UNL     1      -4.177   3.059  -0.033  1.00  0.00           C  
HETATM   16  C11 UNL     1      -5.076   2.397  -0.839  1.00  0.00           C  
HETATM   17  C12 UNL     1      -5.000   1.021  -0.889  1.00  0.00           C  
HETATM   18  C13 UNL     1      -4.078   0.285  -0.178  1.00  0.00           C  
HETATM   19  O2  UNL     1      -3.990  -1.090  -0.217  1.00  0.00           O  
HETATM   20  C14 UNL     1      -4.813  -1.926  -0.973  1.00  0.00           C  
HETATM   21  C15 UNL     1      -2.448  -0.152   2.703  1.00  0.00           C  
HETATM   22  C16 UNL     1      -1.504  -0.820   3.472  1.00  0.00           C  
HETATM   23  C17 UNL     1      -0.256  -1.096   2.973  1.00  0.00           C  
HETATM   24  C18 UNL     1       0.038  -0.694   1.692  1.00  0.00           C  
HETATM   25  C19 UNL     1       1.305  -0.964   1.159  1.00  0.00           C  
HETATM   26  N4  UNL     1       2.287  -1.635   1.902  1.00  0.00           N  
HETATM   27  H1  UNL     1       6.267  -1.212  -0.511  1.00  0.00           H  
HETATM   28  H2  UNL     1       7.206   0.250  -0.815  1.00  0.00           H  
HETATM   29  H3  UNL     1       5.621   0.373   0.014  1.00  0.00           H  
HETATM   30  H4  UNL     1       6.474  -0.018  -2.893  1.00  0.00           H  
HETATM   31  H5  UNL     1       5.404   1.213  -2.232  1.00  0.00           H  
HETATM   32  H6  UNL     1       4.275  -0.445  -3.780  1.00  0.00           H  
HETATM   33  H7  UNL     1       4.611  -1.725  -2.621  1.00  0.00           H  
HETATM   34  H8  UNL     1       2.348   0.096  -2.527  1.00  0.00           H  
HETATM   35  H9  UNL     1      -4.215   4.138   0.023  1.00  0.00           H  
HETATM   36  H10 UNL     1      -5.828   2.948  -1.423  1.00  0.00           H  
HETATM   37  H11 UNL     1      -5.705   0.513  -1.519  1.00  0.00           H  
HETATM   38  H12 UNL     1      -4.190  -2.822  -1.259  1.00  0.00           H  
HETATM   39  H13 UNL     1      -5.181  -1.500  -1.909  1.00  0.00           H  
HETATM   40  H14 UNL     1      -5.629  -2.358  -0.336  1.00  0.00           H  
HETATM   41  H15 UNL     1      -3.437   0.075   3.075  1.00  0.00           H  
HETATM   42  H16 UNL     1      -1.755  -1.125   4.475  1.00  0.00           H  
HETATM   43  H17 UNL     1       0.515  -1.609   3.523  1.00  0.00           H  
HETATM   44  H18 UNL     1       2.288  -2.653   2.128  1.00  0.00           H  
HETATM   45  H19 UNL     1       3.110  -1.111   2.283  1.00  0.00           H  
CONECT    1    2   27   28   29
CONECT    2    3   30   31
CONECT    3    4   32   33
CONECT    4    5   34
CONECT    5    6    6    7
CONECT    7    8    8   25
CONECT    8    9
CONECT    9   10   10
CONECT   10   11   24
CONECT   11   12   21   21
CONECT   12   13   13   18
CONECT   13   14   15
CONECT   15   16   16   35
CONECT   16   17   36
CONECT   17   18   18   37
CONECT   18   19
CONECT   19   20
CONECT   20   38   39   40
CONECT   21   22   41
CONECT   22   23   23   42
CONECT   23   24   43
CONECT   24   25   25
CONECT   25   26
CONECT   26   44   45
END

HMDB0248777
     RDKit          3D
4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide
 45 47  0  0  0  0  0  0  0  0999 V2000
    6.1284   -0.1748   -0.8075 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6121    0.0865   -2.1656 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4066   -0.5944   -2.6604 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1579   -0.4022   -2.0067 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8559   -0.8041   -0.7156 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6996   -1.4068   -0.0130 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5383   -0.5461   -0.1061 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5934    0.0960   -0.8108 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6077    0.3581   -0.3225 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9017   -0.0300    0.9267 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1684    0.2568    1.4157 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1777    0.9561    0.6294 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2341    2.3331    0.6950 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3699    3.0255    1.4740 F   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1766    3.0588   -0.0333 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0762    2.3973   -0.8394 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0004    1.0207   -0.8888 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0780    0.2845   -0.1781 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9895   -1.0900   -0.2167 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8128   -1.9264   -0.9733 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4482   -0.1520    2.7030 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5038   -0.8198    3.4722 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2557   -1.0955    2.9732 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0381   -0.6944    1.6918 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3049   -0.9638    1.1592 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2868   -1.6351    1.9016 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.2665   -1.2116   -0.5109 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2062    0.2499   -0.8147 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6206    0.3735    0.0142 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4741   -0.0180   -2.8928 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4038    1.2130   -2.2325 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2748   -0.4446   -3.7800 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6114   -1.7252   -2.6207 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3479    0.0962   -2.5271 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2152    4.1382    0.0228 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8280    2.9479   -1.4228 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7050    0.5131   -1.5193 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1897   -2.8224   -1.2594 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1809   -1.5003   -1.9087 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6294   -2.3581   -0.3361 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4365    0.0755    3.0752 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7552   -1.1254    4.4747 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5153   -1.6094    3.5229 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2883   -2.6528    2.1275 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1099   -1.1105    2.2835 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 13 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  1  0
 11 21  2  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
 25  7  1  0
 24 10  1  0
 18 12  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  2 30  1  0
  2 31  1  0
  3 32  1  0
  3 33  1  0
  4 34  1  0
 15 35  1  0
 16 36  1  0
 17 37  1  0
 20 38  1  0
 20 39  1  0
 20 40  1  0
 21 41  1  0
 22 42  1  0
 23 43  1  0
 26 44  1  0
 26 45  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
4-Amino-8-(2-fluoro-6-methoxy-phenyl)-N-propylcinnoline-3-carboxamide	HMDB

Chemical Formula

C₁₉H₁₉FN₄O₂

Average Molecular Weight

354.385

Monoisotopic Molecular Weight

354.149204031

IUPAC Name

4-amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide

Traditional Name

4-amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide

CAS Registry Number

Not Available

SMILES

CCCNC(=O)C1=C(N)C2=C(N=N1)C(=CC=C2)C1=C(OC)C=CC=C1F

InChI Identifier

InChI=1S/C19H19FN4O2/c1-3-10-22-19(25)18-16(21)12-7-4-6-11(17(12)23-24-18)15-13(20)8-5-9-14(15)26-2/h4-9H,3,10H2,1-2H3,(H2,21,23)(H,22,25)

InChI Key

KYDURMHFWXCKMW-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cinnolines. These are organic aromatic compounds containing a benzene fused to a pyridazine ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Diazanaphthalenes

Sub Class

Benzodiazines

Direct Parent

Cinnolines

Alternative Parents

Substituents

Cinnoline
2-heteroaryl carboxamide
Phenoxy compound
Anisole
Methoxybenzene
Phenol ether
Alkyl aryl ether
Aminopyridazine
Fluorobenzene
Halobenzene
Aryl fluoride
Aryl halide
Monocyclic benzene moiety
Pyridazine
Benzenoid
Vinylogous amide
Heteroaromatic compound
Amino acid or derivatives
Carboxamide group
Secondary carboxylic acid amide
Carboxylic acid derivative
Ether
Azacycle
Organooxygen compound
Organohalogen compound
Organofluoride
Amine
Organic nitrogen compound
Organic oxide
Primary amine
Hydrocarbon derivative
Organonitrogen compound
Organic oxygen compound
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	3.53	ALOGPS
logP	2.94	ChemAxon
logS	-4.3	ALOGPS
pKa (Strongest Acidic)	14.38	ChemAxon
pKa (Strongest Basic)	2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	90.13 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	99.23 m³·mol⁻¹	ChemAxon
Polarizability	36.86 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	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	184.063	30932474
DeepCCS	[M-H]-	181.705	30932474
DeepCCS	[M-2H]-	215.924	30932474
DeepCCS	[M+Na]+	191.152	30932474
AllCCS	[M+H]+	185.2	32859911
AllCCS	[M+H-H2O]+	182.2	32859911
AllCCS	[M+NH4]+	188.1	32859911
AllCCS	[M+Na]+	188.9	32859911
AllCCS	[M-H]-	186.8	32859911
AllCCS	[M+Na-2H]-	186.7	32859911
AllCCS	[M+HCOO]-	186.8	32859911

Predicted Retention Times

Underivatized

Chromatographic Method	Retention Time	Reference
Predicted by Siyang on May 30, 2022	12.8438 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	1.75 minutes	32390414
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	1982.8 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	275.9 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	178.6 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	183.2 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	139.8 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	433.7 seconds	40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid	517.3 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	81.5 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	1055.4 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	486.2 seconds	40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid	1297.0 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	325.3 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	401.8 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	276.2 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	201.8 seconds	40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water	8.2 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide	CCCNC(=O)C1=C(N)C2=C(N=N1)C(=CC=C2)C1=C(OC)C=CC=C1F	4180.4	Standard polar	33892256
4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide	CCCNC(=O)C1=C(N)C2=C(N=N1)C(=CC=C2)C1=C(OC)C=CC=C1F	3157.9	Standard non polar	33892256
4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide	CCCNC(=O)C1=C(N)C2=C(N=N1)C(=CC=C2)C1=C(OC)C=CC=C1F	3189.0	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide,1TMS,isomer #1	CCCNC(=O)C1=NN=C2C(C3=C(F)C=CC=C3OC)=CC=CC2=C1N[Si](C)(C)C	3031.4	Semi standard non polar	33892256
4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide,1TMS,isomer #1	CCCNC(=O)C1=NN=C2C(C3=C(F)C=CC=C3OC)=CC=CC2=C1N[Si](C)(C)C	2847.3	Standard non polar	33892256
4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide,1TMS,isomer #1	CCCNC(=O)C1=NN=C2C(C3=C(F)C=CC=C3OC)=CC=CC2=C1N[Si](C)(C)C	4297.5	Standard polar	33892256
4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide,1TMS,isomer #2	CCCN(C(=O)C1=NN=C2C(C3=C(F)C=CC=C3OC)=CC=CC2=C1N)[Si](C)(C)C	3066.0	Semi standard non polar	33892256
4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide,1TMS,isomer #2	CCCN(C(=O)C1=NN=C2C(C3=C(F)C=CC=C3OC)=CC=CC2=C1N)[Si](C)(C)C	2878.5	Standard non polar	33892256
4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide,1TMS,isomer #2	CCCN(C(=O)C1=NN=C2C(C3=C(F)C=CC=C3OC)=CC=CC2=C1N)[Si](C)(C)C	4434.2	Standard polar	33892256
4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide,2TMS,isomer #1	CCCN(C(=O)C1=NN=C2C(C3=C(F)C=CC=C3OC)=CC=CC2=C1N[Si](C)(C)C)[Si](C)(C)C	3080.2	Semi standard non polar	33892256
4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide,2TMS,isomer #1	CCCN(C(=O)C1=NN=C2C(C3=C(F)C=CC=C3OC)=CC=CC2=C1N[Si](C)(C)C)[Si](C)(C)C	2943.0	Standard non polar	33892256
4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide,2TMS,isomer #1	CCCN(C(=O)C1=NN=C2C(C3=C(F)C=CC=C3OC)=CC=CC2=C1N[Si](C)(C)C)[Si](C)(C)C	4045.7	Standard polar	33892256
4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide,2TMS,isomer #2	CCCNC(=O)C1=NN=C2C(C3=C(F)C=CC=C3OC)=CC=CC2=C1N([Si](C)(C)C)[Si](C)(C)C	2957.8	Semi standard non polar	33892256
4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide,2TMS,isomer #2	CCCNC(=O)C1=NN=C2C(C3=C(F)C=CC=C3OC)=CC=CC2=C1N([Si](C)(C)C)[Si](C)(C)C	2861.6	Standard non polar	33892256
4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide,2TMS,isomer #2	CCCNC(=O)C1=NN=C2C(C3=C(F)C=CC=C3OC)=CC=CC2=C1N([Si](C)(C)C)[Si](C)(C)C	3975.6	Standard polar	33892256
4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide,3TMS,isomer #1	CCCN(C(=O)C1=NN=C2C(C3=C(F)C=CC=C3OC)=CC=CC2=C1N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	3021.6	Semi standard non polar	33892256
4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide,3TMS,isomer #1	CCCN(C(=O)C1=NN=C2C(C3=C(F)C=CC=C3OC)=CC=CC2=C1N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	2829.0	Standard non polar	33892256
4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide,3TMS,isomer #1	CCCN(C(=O)C1=NN=C2C(C3=C(F)C=CC=C3OC)=CC=CC2=C1N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	3614.9	Standard polar	33892256
4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide,1TBDMS,isomer #1	CCCNC(=O)C1=NN=C2C(C3=C(F)C=CC=C3OC)=CC=CC2=C1N[Si](C)(C)C(C)(C)C	3180.5	Semi standard non polar	33892256
4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide,1TBDMS,isomer #1	CCCNC(=O)C1=NN=C2C(C3=C(F)C=CC=C3OC)=CC=CC2=C1N[Si](C)(C)C(C)(C)C	3048.7	Standard non polar	33892256
4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide,1TBDMS,isomer #1	CCCNC(=O)C1=NN=C2C(C3=C(F)C=CC=C3OC)=CC=CC2=C1N[Si](C)(C)C(C)(C)C	4352.8	Standard polar	33892256
4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide,1TBDMS,isomer #2	CCCN(C(=O)C1=NN=C2C(C3=C(F)C=CC=C3OC)=CC=CC2=C1N)[Si](C)(C)C(C)(C)C	3278.9	Semi standard non polar	33892256
4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide,1TBDMS,isomer #2	CCCN(C(=O)C1=NN=C2C(C3=C(F)C=CC=C3OC)=CC=CC2=C1N)[Si](C)(C)C(C)(C)C	3065.5	Standard non polar	33892256
4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide,1TBDMS,isomer #2	CCCN(C(=O)C1=NN=C2C(C3=C(F)C=CC=C3OC)=CC=CC2=C1N)[Si](C)(C)C(C)(C)C	4436.9	Standard polar	33892256
4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide,2TBDMS,isomer #1	CCCN(C(=O)C1=NN=C2C(C3=C(F)C=CC=C3OC)=CC=CC2=C1N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3422.9	Semi standard non polar	33892256
4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide,2TBDMS,isomer #1	CCCN(C(=O)C1=NN=C2C(C3=C(F)C=CC=C3OC)=CC=CC2=C1N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3332.9	Standard non polar	33892256
4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide,2TBDMS,isomer #1	CCCN(C(=O)C1=NN=C2C(C3=C(F)C=CC=C3OC)=CC=CC2=C1N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4154.0	Standard polar	33892256
4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide,2TBDMS,isomer #2	CCCNC(=O)C1=NN=C2C(C3=C(F)C=CC=C3OC)=CC=CC2=C1N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3320.6	Semi standard non polar	33892256
4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide,2TBDMS,isomer #2	CCCNC(=O)C1=NN=C2C(C3=C(F)C=CC=C3OC)=CC=CC2=C1N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3315.7	Standard non polar	33892256
4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide,2TBDMS,isomer #2	CCCNC(=O)C1=NN=C2C(C3=C(F)C=CC=C3OC)=CC=CC2=C1N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4085.8	Standard polar	33892256
4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide,3TBDMS,isomer #1	CCCN(C(=O)C1=NN=C2C(C3=C(F)C=CC=C3OC)=CC=CC2=C1N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3537.6	Semi standard non polar	33892256
4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide,3TBDMS,isomer #1	CCCN(C(=O)C1=NN=C2C(C3=C(F)C=CC=C3OC)=CC=CC2=C1N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3510.8	Standard non polar	33892256
4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide,3TBDMS,isomer #1	CCCN(C(=O)C1=NN=C2C(C3=C(F)C=CC=C3OC)=CC=CC2=C1N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3816.5	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide GC-MS (Non-derivatized) - 70eV, Positive	splash10-0005-3094000000-8e06a0f38e9f34fdd3d8	2021-09-24	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide 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 - 4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide 10V, Positive-QTOF	splash10-0a4i-0009000000-20e8753933b0a76096ac	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide 20V, Positive-QTOF	splash10-0a4j-0069000000-bd4f35cbeb9b06b733c2	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide 40V, Positive-QTOF	splash10-00r2-0191000000-fedc8e612a6bd6ca5ad4	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide 10V, Negative-QTOF	splash10-0udi-0019000000-1e338fa8d43092d62e8a	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide 20V, Negative-QTOF	splash10-0udi-1049000000-cca2edf9059dd1aca173	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide 40V, Negative-QTOF	splash10-0uec-2090000000-5bf7a3896c698ff9a389	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

26334679

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

23581869

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 4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide (HMDB0248777)

MOL for HMDB0248777 (4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide)

3D MOL for HMDB0248777 (4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide)

3D SDF for HMDB0248777 (4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide)

3D-SDF for HMDB0248777 (4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide)

PDB for HMDB0248777 (4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide)

3D PDB for HMDB0248777 (4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide)

SMILES for HMDB0248777 (4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide)

INCHI for HMDB0248777 (4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide)

Structure for HMDB0248777 (4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide)

3D Structure for HMDB0248777 (4-Amino-8-(2-fluoro-6-methoxyphenyl)-N-propylcinnoline-3-carboxamide)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra