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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 16:29:59 UTC

Update Date

2021-09-26 23:11:40 UTC

HMDB ID

HMDB0256179

Secondary Accession Numbers

None

Metabolite Identification

Common Name

3-Quinolinecarboxylic acid, 7-(3-amino-1-pyrrolidinyl)-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-

Description

7-(3-aminopyrrolidin-1-yl)-1-cyclopropyl-6,8-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid belongs to the class of organic compounds known as quinoline carboxylic acids. These are quinolines in which the quinoline ring system is substituted by a carboxyl group at one or more positions. Based on a literature review very few articles have been published on 7-(3-aminopyrrolidin-1-yl)-1-cyclopropyl-6,8-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid. This compound has been identified in human blood as reported by (PMID: 31557052 ). 3-quinolinecarboxylic acid, 7-(3-amino-1-pyrrolidinyl)-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo- is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically 3-Quinolinecarboxylic acid, 7-(3-amino-1-pyrrolidinyl)-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo- 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


  Mrv1652309112118302D          

 25 28  0  0  0  0            999 V2000
    1.8414   -3.1895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164   -3.1895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    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
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.0405   -1.3144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5925   -1.9275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1800   -2.6420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3731   -2.4705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5156   -3.3957    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 O   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
  1  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
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  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
  4 14  1  0  0  0  0
 13 15  1  0  0  0  0
 12 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 16 20  1  0  0  0  0
 19 21  1  0  0  0  0
 11 22  1  0  0  0  0
  6 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
M  END

HMDB0256179
     RDKit          3D
3-Quinolinecarboxylic acid, 7-(3-amino-1-pyrrolidinyl)-1-cyclopropyl-6,8-difl...
 42 45  0  0  0  0  0  0  0  0999 V2000
    5.5551   -1.4334   -0.4921 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.5444   -0.4083   -0.7723 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5702    0.6029    0.3542 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2131    0.4768    1.0382 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3599    0.0136   -0.0500 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.0415    0.4667   -0.3064 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8585    1.5478   -1.1390 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9333    2.1622   -1.7002 F   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4283    2.0090   -1.4040 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5184    1.3838   -0.8332 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8012    1.8361   -1.0887 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9972    2.8278   -1.8501 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8833    1.2264   -0.5281 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2255    1.6740   -0.7752 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1935    1.0925   -0.2454 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4521    2.7755   -1.6201 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6662    0.1412    0.3047 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4280   -0.3259    0.5749 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1634   -1.4585    1.4361 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2775   -2.5216    1.5073 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0143   -2.7820    0.7779 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3703    0.2856    0.0152 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0794   -0.1274    0.2423 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1328   -1.1759    1.0526 F   0  0  0  0  0  0  0  0  0  0  0  0
    3.1622   -0.9679   -0.7543 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4796   -1.0010   -0.7919 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6245   -1.4960    0.5603 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8188    0.0421   -1.7513 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7157    1.6115   -0.0816 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4075    0.4231    1.0540 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2994   -0.3463    1.7563 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8860    1.4272    1.4601 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5694    2.8528   -2.0539 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2509    3.7141   -1.2876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4919   -0.3843    0.7834 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7210   -1.2668    2.4359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2085   -2.3695    0.9679 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3982   -3.0918    2.4478 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1070   -2.8058   -0.3281 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3008   -3.5376    1.1573 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7611   -1.1785   -1.7679 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1827   -1.9143   -0.1720 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  1  0
  6  7  2  0
  7  8  1  0
  7  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 13 17  2  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 18 22  1  0
 22 23  2  0
 23 24  1  0
  5 25  1  0
 25  2  1  0
 23  6  1  0
 22 10  1  0
 21 19  1  0
  1 26  1  0
  1 27  1  0
  2 28  1  0
  3 29  1  0
  3 30  1  0
  4 31  1  0
  4 32  1  0
  9 33  1  0
 16 34  1  0
 17 35  1  0
 19 36  1  0
 20 37  1  0
 20 38  1  0
 21 39  1  0
 21 40  1  0
 25 41  1  0
 25 42  1  0
M  END


  Mrv1652309112118302D          

 25 28  0  0  0  0            999 V2000
    1.8414   -3.1895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164   -3.1895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    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
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.0405   -1.3144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5925   -1.9275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1800   -2.6420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3731   -2.4705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5156   -3.3957    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 O   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
  1  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
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  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
  4 14  1  0  0  0  0
 13 15  1  0  0  0  0
 12 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 16 20  1  0  0  0  0
 19 21  1  0  0  0  0
 11 22  1  0  0  0  0
  6 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0256179

> <DATABASE_NAME>
hmdb

> <SMILES>
NC1CCN(C1)C1=C(F)C=C2C(=O)C(=CN(C3CC3)C2=C1F)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C17H17F2N3O3/c18-12-5-10-14(13(19)15(12)21-4-3-8(20)6-21)22(9-1-2-9)7-11(16(10)23)17(24)25/h5,7-9H,1-4,6,20H2,(H,24,25)

> <INCHI_KEY>
UHBXZNXCIZHGFF-UHFFFAOYSA-N

> <FORMULA>
C17H17F2N3O3

> <MOLECULAR_WEIGHT>
349.338

> <EXACT_MASS>
349.123797745

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
33.73017963798965

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
7-(3-aminopyrrolidin-1-yl)-1-cyclopropyl-6,8-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid

> <ALOGPS_LOGP>
-0.20

> <JCHEM_LOGP>
-0.8821097470762507

> <ALOGPS_LOGS>
-2.68

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.6519824982596045

> <JCHEM_PKA_STRONGEST_BASIC>
9.629816368376785

> <JCHEM_POLAR_SURFACE_AREA>
86.87000000000002

> <JCHEM_REFRACTIVITY>
87.91680000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.35e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
7-(3-aminopyrrolidin-1-yl)-1-cyclopropyl-6,8-difluoro-4-oxoquinoline-3-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0256179
     RDKit          3D
3-Quinolinecarboxylic acid, 7-(3-amino-1-pyrrolidinyl)-1-cyclopropyl-6,8-difl...
 42 45  0  0  0  0  0  0  0  0999 V2000
    5.5551   -1.4334   -0.4921 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.5444   -0.4083   -0.7723 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5702    0.6029    0.3542 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2131    0.4768    1.0382 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3599    0.0136   -0.0500 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.0415    0.4667   -0.3064 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8585    1.5478   -1.1390 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9333    2.1622   -1.7002 F   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4283    2.0090   -1.4040 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5184    1.3838   -0.8332 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8012    1.8361   -1.0887 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9972    2.8278   -1.8501 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8833    1.2264   -0.5281 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2255    1.6740   -0.7752 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1935    1.0925   -0.2454 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4521    2.7755   -1.6201 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6662    0.1412    0.3047 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4280   -0.3259    0.5749 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1634   -1.4585    1.4361 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2775   -2.5216    1.5073 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0143   -2.7820    0.7779 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3703    0.2856    0.0152 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0794   -0.1274    0.2423 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1328   -1.1759    1.0526 F   0  0  0  0  0  0  0  0  0  0  0  0
    3.1622   -0.9679   -0.7543 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4796   -1.0010   -0.7919 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6245   -1.4960    0.5603 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8188    0.0421   -1.7513 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7157    1.6115   -0.0816 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4075    0.4231    1.0540 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2994   -0.3463    1.7563 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8860    1.4272    1.4601 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5694    2.8528   -2.0539 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2509    3.7141   -1.2876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4919   -0.3843    0.7834 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7210   -1.2668    2.4359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2085   -2.3695    0.9679 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3982   -3.0918    2.4478 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1070   -2.8058   -0.3281 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3008   -3.5376    1.1573 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7611   -1.1785   -1.7679 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1827   -1.9143   -0.1720 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  1  0
  6  7  2  0
  7  8  1  0
  7  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 13 17  2  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 18 22  1  0
 22 23  2  0
 23 24  1  0
  5 25  1  0
 25  2  1  0
 23  6  1  0
 22 10  1  0
 21 19  1  0
  1 26  1  0
  1 27  1  0
  2 28  1  0
  3 29  1  0
  3 30  1  0
  4 31  1  0
  4 32  1  0
  9 33  1  0
 16 34  1  0
 17 35  1  0
 19 36  1  0
 20 37  1  0
 20 38  1  0
 21 39  1  0
 21 40  1  0
 25 41  1  0
 25 42  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       3.437  -5.954   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.897  -5.954   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    4  N   UNK     0       2.667  -3.080   0.000  0.00  0.00           N+0
HETATM    5  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       2.667   1.540   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   15  F   UNK     0       5.335  -4.620   0.000  0.00  0.00           F+0
HETATM   16  N   UNK     0       8.002  -3.080   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0       9.409  -2.454   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      10.439  -3.598   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.669  -4.932   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.163  -4.612   0.000  0.00  0.00           C+0
HETATM   21  N   UNK     0      10.296  -6.339   0.000  0.00  0.00           N+0
HETATM   22  F   UNK     0       8.002  -0.000   0.000  0.00  0.00           F+0
HETATM   23  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -1.334  -0.770   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       0.000   1.540   0.000  0.00  0.00           O+0
CONECT    1    2    3                                                       
CONECT    2    1    3                                                       
CONECT    3    2    1    4                                                  
CONECT    4    3    5   14                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   23                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   22                                                  
CONECT   12   11   13   16                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13    9    4                                                  
CONECT   15   13                                                            
CONECT   16   12   17   20                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19   16                                                       
CONECT   21   19                                                            
CONECT   22   11                                                            
CONECT   23    6   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   56    0
END

COMPND    HMDB0256179
HETATM    1  N1  UNL     1       5.555  -1.433  -0.492  1.00  0.00           N  
HETATM    2  C1  UNL     1       4.544  -0.408  -0.772  1.00  0.00           C  
HETATM    3  C2  UNL     1       4.570   0.603   0.354  1.00  0.00           C  
HETATM    4  C3  UNL     1       3.213   0.477   1.038  1.00  0.00           C  
HETATM    5  N2  UNL     1       2.360   0.014  -0.050  1.00  0.00           N  
HETATM    6  C4  UNL     1       1.041   0.467  -0.306  1.00  0.00           C  
HETATM    7  C5  UNL     1       0.858   1.548  -1.139  1.00  0.00           C  
HETATM    8  F1  UNL     1       1.933   2.162  -1.700  1.00  0.00           F  
HETATM    9  C6  UNL     1      -0.428   2.009  -1.404  1.00  0.00           C  
HETATM   10  C7  UNL     1      -1.518   1.384  -0.833  1.00  0.00           C  
HETATM   11  C8  UNL     1      -2.801   1.836  -1.089  1.00  0.00           C  
HETATM   12  O1  UNL     1      -2.997   2.828  -1.850  1.00  0.00           O  
HETATM   13  C9  UNL     1      -3.883   1.226  -0.528  1.00  0.00           C  
HETATM   14  C10 UNL     1      -5.226   1.674  -0.775  1.00  0.00           C  
HETATM   15  O2  UNL     1      -6.193   1.092  -0.245  1.00  0.00           O  
HETATM   16  O3  UNL     1      -5.452   2.775  -1.620  1.00  0.00           O  
HETATM   17  C11 UNL     1      -3.666   0.141   0.305  1.00  0.00           C  
HETATM   18  N3  UNL     1      -2.428  -0.326   0.575  1.00  0.00           N  
HETATM   19  C12 UNL     1      -2.163  -1.459   1.436  1.00  0.00           C  
HETATM   20  C13 UNL     1      -3.277  -2.522   1.507  1.00  0.00           C  
HETATM   21  C14 UNL     1      -2.014  -2.782   0.778  1.00  0.00           C  
HETATM   22  C15 UNL     1      -1.370   0.286   0.015  1.00  0.00           C  
HETATM   23  C16 UNL     1      -0.079  -0.127   0.242  1.00  0.00           C  
HETATM   24  F2  UNL     1       0.133  -1.176   1.053  1.00  0.00           F  
HETATM   25  C17 UNL     1       3.162  -0.968  -0.754  1.00  0.00           C  
HETATM   26  H1  UNL     1       6.480  -1.001  -0.792  1.00  0.00           H  
HETATM   27  H2  UNL     1       5.625  -1.496   0.560  1.00  0.00           H  
HETATM   28  H3  UNL     1       4.819   0.042  -1.751  1.00  0.00           H  
HETATM   29  H4  UNL     1       4.716   1.612  -0.082  1.00  0.00           H  
HETATM   30  H5  UNL     1       5.407   0.423   1.054  1.00  0.00           H  
HETATM   31  H6  UNL     1       3.299  -0.346   1.756  1.00  0.00           H  
HETATM   32  H7  UNL     1       2.886   1.427   1.460  1.00  0.00           H  
HETATM   33  H8  UNL     1      -0.569   2.853  -2.054  1.00  0.00           H  
HETATM   34  H9  UNL     1      -5.251   3.714  -1.288  1.00  0.00           H  
HETATM   35  H10 UNL     1      -4.492  -0.384   0.783  1.00  0.00           H  
HETATM   36  H11 UNL     1      -1.721  -1.267   2.436  1.00  0.00           H  
HETATM   37  H12 UNL     1      -4.209  -2.370   0.968  1.00  0.00           H  
HETATM   38  H13 UNL     1      -3.398  -3.092   2.448  1.00  0.00           H  
HETATM   39  H14 UNL     1      -2.107  -2.806  -0.328  1.00  0.00           H  
HETATM   40  H15 UNL     1      -1.301  -3.538   1.157  1.00  0.00           H  
HETATM   41  H16 UNL     1       2.761  -1.179  -1.768  1.00  0.00           H  
HETATM   42  H17 UNL     1       3.183  -1.914  -0.172  1.00  0.00           H  
CONECT    1    2   26   27
CONECT    2    3   25   28
CONECT    3    4   29   30
CONECT    4    5   31   32
CONECT    5    6   25
CONECT    6    7    7   23
CONECT    7    8    9
CONECT    9   10   10   33
CONECT   10   11   22
CONECT   11   12   12   13
CONECT   13   14   17   17
CONECT   14   15   15   16
CONECT   16   34
CONECT   17   18   35
CONECT   18   19   22
CONECT   19   20   21   36
CONECT   20   21   37   38
CONECT   21   39   40
CONECT   22   23   23
CONECT   23   24
CONECT   25   41   42
END

HMDB0256179
     RDKit          3D
3-Quinolinecarboxylic acid, 7-(3-amino-1-pyrrolidinyl)-1-cyclopropyl-6,8-difl...
 42 45  0  0  0  0  0  0  0  0999 V2000
    5.5551   -1.4334   -0.4921 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.5444   -0.4083   -0.7723 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5702    0.6029    0.3542 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2131    0.4768    1.0382 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3599    0.0136   -0.0500 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.0415    0.4667   -0.3064 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8585    1.5478   -1.1390 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9333    2.1622   -1.7002 F   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4283    2.0090   -1.4040 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5184    1.3838   -0.8332 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8012    1.8361   -1.0887 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9972    2.8278   -1.8501 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8833    1.2264   -0.5281 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2255    1.6740   -0.7752 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1935    1.0925   -0.2454 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4521    2.7755   -1.6201 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6662    0.1412    0.3047 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4280   -0.3259    0.5749 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1634   -1.4585    1.4361 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2775   -2.5216    1.5073 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0143   -2.7820    0.7779 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3703    0.2856    0.0152 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0794   -0.1274    0.2423 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1328   -1.1759    1.0526 F   0  0  0  0  0  0  0  0  0  0  0  0
    3.1622   -0.9679   -0.7543 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4796   -1.0010   -0.7919 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6245   -1.4960    0.5603 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8188    0.0421   -1.7513 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7157    1.6115   -0.0816 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4075    0.4231    1.0540 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2994   -0.3463    1.7563 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8860    1.4272    1.4601 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5694    2.8528   -2.0539 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2509    3.7141   -1.2876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4919   -0.3843    0.7834 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7210   -1.2668    2.4359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2085   -2.3695    0.9679 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3982   -3.0918    2.4478 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1070   -2.8058   -0.3281 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3008   -3.5376    1.1573 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7611   -1.1785   -1.7679 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1827   -1.9143   -0.1720 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  1  0
  6  7  2  0
  7  8  1  0
  7  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 13 17  2  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 18 22  1  0
 22 23  2  0
 23 24  1  0
  5 25  1  0
 25  2  1  0
 23  6  1  0
 22 10  1  0
 21 19  1  0
  1 26  1  0
  1 27  1  0
  2 28  1  0
  3 29  1  0
  3 30  1  0
  4 31  1  0
  4 32  1  0
  9 33  1  0
 16 34  1  0
 17 35  1  0
 19 36  1  0
 20 37  1  0
 20 38  1  0
 21 39  1  0
 21 40  1  0
 25 41  1  0
 25 42  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
7-(3-Aminopyrrolidin-1-yl)-1-cyclopropyl-6,8-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylate	Generator

Chemical Formula

C₁₇H₁₇F₂N₃O₃

Average Molecular Weight

349.338

Monoisotopic Molecular Weight

349.123797745

IUPAC Name

7-(3-aminopyrrolidin-1-yl)-1-cyclopropyl-6,8-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid

Traditional Name

7-(3-aminopyrrolidin-1-yl)-1-cyclopropyl-6,8-difluoro-4-oxoquinoline-3-carboxylic acid

CAS Registry Number

Not Available

SMILES

NC1CCN(C1)C1=C(F)C=C2C(=O)C(=CN(C3CC3)C2=C1F)C(O)=O

InChI Identifier

InChI=1S/C17H17F2N3O3/c18-12-5-10-14(13(19)15(12)21-4-3-8(20)6-21)22(9-1-2-9)7-11(16(10)23)17(24)25/h5,7-9H,1-4,6,20H2,(H,24,25)

InChI Key

UHBXZNXCIZHGFF-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as quinoline carboxylic acids. These are quinolines in which the quinoline ring system is substituted by a carboxyl group at one or more positions.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Quinolines and derivatives

Sub Class

Quinoline carboxylic acids

Direct Parent

Quinoline carboxylic acids

Alternative Parents

Substituents

Quinoline-3-carboxylic acid
Fluoroquinolone
Aminoquinoline
Haloquinoline
Dihydroquinolone
Dihydroquinoline
Pyridine carboxylic acid
Pyridine carboxylic acid or derivatives
Dialkylarylamine
Tertiary aliphatic/aromatic amine
Benzenoid
Pyridine
Aryl fluoride
Aryl halide
Heteroaromatic compound
Vinylogous amide
Pyrrolidine
Tertiary amine
Amino acid
Amino acid or derivatives
Azacycle
Carboxylic acid derivative
Carboxylic acid
Monocarboxylic acid or derivatives
Primary aliphatic amine
Organic oxide
Organopnictogen compound
Organic oxygen compound
Organic nitrogen compound
Hydrocarbon derivative
Primary amine
Amine
Organohalogen compound
Organofluoride
Organonitrogen compound
Organooxygen 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)

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	-0.2	ALOGPS
logP	-0.88	ChemAxon
logS	-2.7	ALOGPS
pKa (Strongest Acidic)	5.65	ChemAxon
pKa (Strongest Basic)	9.63	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	86.87 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	87.92 m³·mol⁻¹	ChemAxon
Polarizability	33.73 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	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]+	183.806	30932474
DeepCCS	[M-H]-	181.425	30932474
DeepCCS	[M-2H]-	215.74	30932474
DeepCCS	[M+Na]+	191.258	30932474
AllCCS	[M+H]+	178.1	32859911
AllCCS	[M+H-H2O]+	175.2	32859911
AllCCS	[M+NH4]+	180.7	32859911
AllCCS	[M+Na]+	181.5	32859911
AllCCS	[M-H]-	179.5	32859911
AllCCS	[M+Na-2H]-	179.1	32859911
AllCCS	[M+HCOO]-	178.7	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
3-Quinolinecarboxylic acid, 7-(3-amino-1-pyrrolidinyl)-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-	NC1CCN(C1)C1=C(F)C=C2C(=O)C(=CN(C3CC3)C2=C1F)C(O)=O	3702.1	Standard polar	33892256
3-Quinolinecarboxylic acid, 7-(3-amino-1-pyrrolidinyl)-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-	NC1CCN(C1)C1=C(F)C=C2C(=O)C(=CN(C3CC3)C2=C1F)C(O)=O	2425.4	Standard non polar	33892256
3-Quinolinecarboxylic acid, 7-(3-amino-1-pyrrolidinyl)-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-	NC1CCN(C1)C1=C(F)C=C2C(=O)C(=CN(C3CC3)C2=C1F)C(O)=O	3330.6	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
3-Quinolinecarboxylic acid, 7-(3-amino-1-pyrrolidinyl)-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-,2TMS,isomer #1	C[Si](C)(C)NC1CCN(C2=C(F)C=C3C(=O)C(C(=O)O[Si](C)(C)C)=CN(C4CC4)C3=C2F)C1	3156.3	Semi standard non polar	33892256
3-Quinolinecarboxylic acid, 7-(3-amino-1-pyrrolidinyl)-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-,2TMS,isomer #1	C[Si](C)(C)NC1CCN(C2=C(F)C=C3C(=O)C(C(=O)O[Si](C)(C)C)=CN(C4CC4)C3=C2F)C1	2787.3	Standard non polar	33892256
3-Quinolinecarboxylic acid, 7-(3-amino-1-pyrrolidinyl)-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-,2TMS,isomer #1	C[Si](C)(C)NC1CCN(C2=C(F)C=C3C(=O)C(C(=O)O[Si](C)(C)C)=CN(C4CC4)C3=C2F)C1	3532.9	Standard polar	33892256
3-Quinolinecarboxylic acid, 7-(3-amino-1-pyrrolidinyl)-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-,2TMS,isomer #2	C[Si](C)(C)N(C1CCN(C2=C(F)C=C3C(=O)C(C(=O)O)=CN(C4CC4)C3=C2F)C1)[Si](C)(C)C	3147.3	Semi standard non polar	33892256
3-Quinolinecarboxylic acid, 7-(3-amino-1-pyrrolidinyl)-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-,2TMS,isomer #2	C[Si](C)(C)N(C1CCN(C2=C(F)C=C3C(=O)C(C(=O)O)=CN(C4CC4)C3=C2F)C1)[Si](C)(C)C	2839.8	Standard non polar	33892256
3-Quinolinecarboxylic acid, 7-(3-amino-1-pyrrolidinyl)-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-,2TMS,isomer #2	C[Si](C)(C)N(C1CCN(C2=C(F)C=C3C(=O)C(C(=O)O)=CN(C4CC4)C3=C2F)C1)[Si](C)(C)C	3676.2	Standard polar	33892256
3-Quinolinecarboxylic acid, 7-(3-amino-1-pyrrolidinyl)-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-,3TMS,isomer #1	C[Si](C)(C)OC(=O)C1=CN(C2CC2)C2=C(F)C(N3CCC(N([Si](C)(C)C)[Si](C)(C)C)C3)=C(F)C=C2C1=O	3077.1	Semi standard non polar	33892256
3-Quinolinecarboxylic acid, 7-(3-amino-1-pyrrolidinyl)-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-,3TMS,isomer #1	C[Si](C)(C)OC(=O)C1=CN(C2CC2)C2=C(F)C(N3CCC(N([Si](C)(C)C)[Si](C)(C)C)C3)=C(F)C=C2C1=O	2973.3	Standard non polar	33892256
3-Quinolinecarboxylic acid, 7-(3-amino-1-pyrrolidinyl)-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-,3TMS,isomer #1	C[Si](C)(C)OC(=O)C1=CN(C2CC2)C2=C(F)C(N3CCC(N([Si](C)(C)C)[Si](C)(C)C)C3)=C(F)C=C2C1=O	3373.7	Standard polar	33892256
3-Quinolinecarboxylic acid, 7-(3-amino-1-pyrrolidinyl)-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC1CCN(C2=C(F)C=C3C(=O)C(C(=O)O[Si](C)(C)C(C)(C)C)=CN(C4CC4)C3=C2F)C1	3521.3	Semi standard non polar	33892256
3-Quinolinecarboxylic acid, 7-(3-amino-1-pyrrolidinyl)-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC1CCN(C2=C(F)C=C3C(=O)C(C(=O)O[Si](C)(C)C(C)(C)C)=CN(C4CC4)C3=C2F)C1	3266.1	Standard non polar	33892256
3-Quinolinecarboxylic acid, 7-(3-amino-1-pyrrolidinyl)-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC1CCN(C2=C(F)C=C3C(=O)C(C(=O)O[Si](C)(C)C(C)(C)C)=CN(C4CC4)C3=C2F)C1	3651.7	Standard polar	33892256
3-Quinolinecarboxylic acid, 7-(3-amino-1-pyrrolidinyl)-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)N(C1CCN(C2=C(F)C=C3C(=O)C(C(=O)O)=CN(C4CC4)C3=C2F)C1)[Si](C)(C)C(C)(C)C	3630.5	Semi standard non polar	33892256
3-Quinolinecarboxylic acid, 7-(3-amino-1-pyrrolidinyl)-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)N(C1CCN(C2=C(F)C=C3C(=O)C(C(=O)O)=CN(C4CC4)C3=C2F)C1)[Si](C)(C)C(C)(C)C	3262.3	Standard non polar	33892256
3-Quinolinecarboxylic acid, 7-(3-amino-1-pyrrolidinyl)-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)N(C1CCN(C2=C(F)C=C3C(=O)C(C(=O)O)=CN(C4CC4)C3=C2F)C1)[Si](C)(C)C(C)(C)C	3691.8	Standard polar	33892256
3-Quinolinecarboxylic acid, 7-(3-amino-1-pyrrolidinyl)-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)C1=CN(C2CC2)C2=C(F)C(N3CCC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C3)=C(F)C=C2C1=O	3719.4	Semi standard non polar	33892256
3-Quinolinecarboxylic acid, 7-(3-amino-1-pyrrolidinyl)-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)C1=CN(C2CC2)C2=C(F)C(N3CCC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C3)=C(F)C=C2C1=O	3576.9	Standard non polar	33892256
3-Quinolinecarboxylic acid, 7-(3-amino-1-pyrrolidinyl)-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)C1=CN(C2CC2)C2=C(F)C(N3CCC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C3)=C(F)C=C2C1=O	3542.4	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 3-Quinolinecarboxylic acid, 7-(3-amino-1-pyrrolidinyl)-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo- GC-MS (Non-derivatized) - 70eV, Positive	splash10-05ai-0049000000-58cf15a328e73e9c44aa	2021-09-23	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3-Quinolinecarboxylic acid, 7-(3-amino-1-pyrrolidinyl)-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo- GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3-Quinolinecarboxylic acid, 7-(3-amino-1-pyrrolidinyl)-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo- GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3-Quinolinecarboxylic acid, 7-(3-amino-1-pyrrolidinyl)-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo- GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3-Quinolinecarboxylic acid, 7-(3-amino-1-pyrrolidinyl)-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo- GC-MS (TBDMS_1_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3-Quinolinecarboxylic acid, 7-(3-amino-1-pyrrolidinyl)-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo- GC-MS (TBDMS_1_2) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-10-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-10-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-10-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-10-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-10-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-10-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-10-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-10-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-10-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-10-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-10-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-10-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-10-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-10-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-10-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-10-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-10-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-10-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-10-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-10-25	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

109465

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

122796

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 3-Quinolinecarboxylic acid, 7-(3-amino-1-pyrrolidinyl)-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo- (HMDB0256179)

MOL for HMDB0256179 (3-Quinolinecarboxylic acid, 7-(3-amino-1-pyrrolidinyl)-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-)

3D MOL for HMDB0256179 (3-Quinolinecarboxylic acid, 7-(3-amino-1-pyrrolidinyl)-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-)

3D SDF for HMDB0256179 (3-Quinolinecarboxylic acid, 7-(3-amino-1-pyrrolidinyl)-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-)

3D-SDF for HMDB0256179 (3-Quinolinecarboxylic acid, 7-(3-amino-1-pyrrolidinyl)-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-)

PDB for HMDB0256179 (3-Quinolinecarboxylic acid, 7-(3-amino-1-pyrrolidinyl)-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-)

3D PDB for HMDB0256179 (3-Quinolinecarboxylic acid, 7-(3-amino-1-pyrrolidinyl)-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-)

SMILES for HMDB0256179 (3-Quinolinecarboxylic acid, 7-(3-amino-1-pyrrolidinyl)-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-)

INCHI for HMDB0256179 (3-Quinolinecarboxylic acid, 7-(3-amino-1-pyrrolidinyl)-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-)

Structure for HMDB0256179 (3-Quinolinecarboxylic acid, 7-(3-amino-1-pyrrolidinyl)-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-)

3D Structure for HMDB0256179 (3-Quinolinecarboxylic acid, 7-(3-amino-1-pyrrolidinyl)-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

NMR Spectra