NP-MRD: Showing NP-Card for (11r)-11-(2-carbamimidamidoethyl)-8-hydroxy-13-oxo-12,15-dioxa-4-azatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁴]hexadeca-1(16),2,4,6,8,10(14)-hexaene-3-carboxylic acid (NP0154914)

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Record Information

Version

2.0

Created at

2022-09-02 11:53:51 UTC

Updated at

2022-09-02 11:53:51 UTC

NP-MRD ID

NP0154914

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(11r)-11-(2-carbamimidamidoethyl)-8-hydroxy-13-oxo-12,15-dioxa-4-azatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁴]hexadeca-1(16),2,4,6,8,10(14)-hexaene-3-carboxylic acid

Description

3,4-[Oxy(2-carboxy-6-hydroxyquinoline-4,5-diyl)]-5beta-(2-guanidinoethyl)-2,5-dihydrofuran-2-one 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 3,4-[Oxy(2-carboxy-6-hydroxyquinoline-4,5-diyl)]-5beta-(2-guanidinoethyl)-2,5-dihydrofuran-2-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022213532D          

 27 30  0  0  1  0            999 V2000
    6.0213   -2.9519    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.7663   -2.1672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3184   -1.5541    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.9594   -1.9957    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.7044   -1.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8974   -1.0396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6425   -0.2549    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1274    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6425    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8974    1.8646    0.0000 O   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
    2.1434   -0.4125    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   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   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
   -0.0000    0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   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
   -1.4289    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 O   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
    1.4289    0.8250    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
    2.1434    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  7  6  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 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
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 20 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 13 26  2  0  0  0  0
 18 26  1  0  0  0  0
 25 27  1  0  0  0  0
 11 27  1  0  0  0  0
M  END

     RDKit          3D

 41 44  0  0  0  0  0  0  0  0999 V2000
   -5.8771   -2.3049    0.8818 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3192   -1.4419    0.4960 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5967   -0.4465    0.1441 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2303    0.7121   -0.3768 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1829   -0.4635    0.2577 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4840    0.4110    1.1567 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0037    0.2282    1.1202 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4405    0.4992   -0.2829 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8248    1.8728   -0.5027 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7402    2.6739   -0.4516 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7140    3.9438   -0.5024 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4142    1.7731   -0.3243 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0251    0.5084   -0.2947 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0468   -0.5502   -0.1971 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6880   -1.8766   -0.1813 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5724   -2.2992   -0.2528 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7030   -2.8702   -0.0877 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0051   -2.4693   -0.0165 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3904   -1.1410   -0.0325 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6876   -0.8023    0.0371 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.0994    0.4848    0.0191 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5228    0.8222    0.0973 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8305    2.0453    0.0749 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5074   -0.1344    0.1921 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1211    1.4506   -0.0757 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7782    1.1282   -0.1492 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3736   -0.1885   -0.1283 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7815    2.0835   -0.2478 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0029    1.2167    0.0933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9129    1.1060   -1.3015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6511   -1.1353   -0.3352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7733    1.4591    0.9405 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8125    0.2231    2.2057 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6542   -0.7023    1.5715 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5503    1.0414    1.7701 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9433   -0.0444   -1.0725 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4829   -2.1471   -0.3198 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4143   -3.9215   -0.0755 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7786   -3.2171    0.0559 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1941   -0.0087    0.9388 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4072    2.4816   -0.0930 H   0  0  0  0  0  0  0  0  0  0  0  0
  4  3  1  0
  3  2  2  0
  3  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
 12 13  2  0
 13 14  1  0
 14 27  2  0
 27 26  1  0
 26 28  1  0
 26 25  2  0
 25 21  1  0
 21 20  2  0
 20 19  1  0
 19 18  2  0
 18 17  1  0
 17 15  2  0
 15 16  1  0
 21 22  1  0
 22 24  1  0
 22 23  2  0
 13  8  1  0
 15 14  1  0
 28 12  1  0
 19 27  1  0
  4 29  1  0
  4 30  1  0
  2  1  1  0
  5 31  1  0
  6 32  1  0
  6 33  1  0
  7 34  1  0
  7 35  1  0
  8 36  1  6
 25 41  1  0
 18 39  1  0
 17 38  1  0
 16 37  1  0
 24 40  1  0
M  END


  Mrv1652309022213532D          

 27 30  0  0  1  0            999 V2000
    6.0213   -2.9519    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.7663   -2.1672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3184   -1.5541    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.9594   -1.9957    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.7044   -1.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8974   -1.0396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6425   -0.2549    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1274    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6425    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8974    1.8646    0.0000 O   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
    2.1434   -0.4125    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   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   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
   -0.0000    0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   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
   -1.4289    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 O   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
    1.4289    0.8250    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
    2.1434    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  7  6  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 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
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 20 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 13 26  2  0  0  0  0
 18 26  1  0  0  0  0
 25 27  1  0  0  0  0
 11 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0154914

> <DATABASE_NAME>
NP-MRD

> <SMILES>
NC(=N)NCC[C@H]1OC(=O)C2=C1C1=C3C(O2)=CC(=NC3=CC=C1O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C17H14N4O6/c18-17(19)20-4-3-9-13-12-8(22)2-1-6-11(12)10(5-7(21-6)15(23)24)26-14(13)16(25)27-9/h1-2,5,9,22H,3-4H2,(H,23,24)(H4,18,19,20)/t9-/m1/s1

> <INCHI_KEY>
KPSXNCWDIVGTAY-SECBINFHSA-N

> <FORMULA>
C17H14N4O6

> <MOLECULAR_WEIGHT>
370.321

> <EXACT_MASS>
370.091334187

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
41

> <JCHEM_AVERAGE_POLARIZABILITY>
35.79504629282381

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(11R)-11-(2-carbamimidamidoethyl)-8-hydroxy-13-oxo-12,15-dioxa-4-azatetracyclo[7.6.1.0^{5,16}.0^{10,14}]hexadeca-1,3,5,7,9(16),10(14)-hexaene-3-carboxylic acid

> <ALOGPS_LOGP>
0.36

> <JCHEM_LOGP>
-1.4247733425685989

> <ALOGPS_LOGS>
-3.48

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.44570126105069

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.0348320345187463

> <JCHEM_PKA_STRONGEST_BASIC>
11.988190426138047

> <JCHEM_POLAR_SURFACE_AREA>
167.85

> <JCHEM_REFRACTIVITY>
101.78009999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.24e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(11R)-11-(2-carbamimidamidoethyl)-8-hydroxy-13-oxo-12,15-dioxa-4-azatetracyclo[7.6.1.0^{5,16}.0^{10,14}]hexadeca-1,3,5,7,9(16),10(14)-hexaene-3-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  N   UNK     0      11.240  -5.510   0.000  0.00  0.00           N+0
HETATM    2  C   UNK     0      10.764  -4.046   0.000  0.00  0.00           C+0
HETATM    3  N   UNK     0      11.794  -2.901   0.000  0.00  0.00           N+0
HETATM    4  N   UNK     0       9.257  -3.725   0.000  0.00  0.00           N+0
HETATM    5  C   UNK     0       8.782  -2.261   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.275  -1.941   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.799  -0.476   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       7.705   0.770   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       6.799   2.016   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       7.275   3.481   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.001  -0.770   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  O   UNK     0       5.335  -3.080   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   19  N   UNK     0      -0.000   0.000   0.000  0.00  0.00           N+0
HETATM   20  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -2.667   1.540   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      -1.334   3.850   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       4.001   2.310   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   12                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   27                                                  
CONECT   12   11    7   13                                                  
CONECT   13   12   14   26                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   26                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   24                                                  
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   20   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25   13   18                                                  
CONECT   27   25   11                                                       
MASTER        0    0    0    0    0    0    0    0   27    0   60    0
END

View in JSmol

Synonyms

Value	Source
3,4-[Oxy(2-carboxy-6-hydroxyquinoline-4,5-diyl)]-5b-(2-guanidinoethyl)-2,5-dihydrofuran-2-one	Generator
3,4-[Oxy(2-carboxy-6-hydroxyquinoline-4,5-diyl)]-5β-(2-guanidinoethyl)-2,5-dihydrofuran-2-one	Generator

Chemical Formula

C₁₇H₁₄N₄O₆

Average Mass

370.3210 Da

Monoisotopic Mass

370.09133 Da

IUPAC Name

(11R)-11-(2-carbamimidamidoethyl)-8-hydroxy-13-oxo-12,15-dioxa-4-azatetracyclo[7.6.1.0^{5,16}.0^{10,14}]hexadeca-1,3,5,7,9(16),10(14)-hexaene-3-carboxylic acid

Traditional Name

(11R)-11-(2-carbamimidamidoethyl)-8-hydroxy-13-oxo-12,15-dioxa-4-azatetracyclo[7.6.1.0^{5,16}.0^{10,14}]hexadeca-1,3,5,7,9(16),10(14)-hexaene-3-carboxylic acid

CAS Registry Number

Not Available

SMILES

NC(=N)NCC[C@H]1OC(=O)C2=C1C1=C3C(O2)=CC(=NC3=CC=C1O)C(O)=O

InChI Identifier

InChI=1S/C17H14N4O6/c18-17(19)20-4-3-9-13-12-8(22)2-1-6-11(12)10(5-7(21-6)15(23)24)26-14(13)16(25)27-9/h1-2,5,9,22H,3-4H2,(H,23,24)(H4,18,19,20)/t9-/m1/s1

InChI Key

KPSXNCWDIVGTAY-SECBINFHSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

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-2-carboxylic acid
Hydroxyquinoline
Benzopyran
Pyranopyridine
2-benzopyran
Pyridine carboxylic acid
Pyridine carboxylic acid or derivatives
1-hydroxy-2-unsubstituted benzenoid
Phenol
Pyridine
Benzenoid
Heteroaromatic compound
Carboxylic acid ester
Guanidine
Lactone
Azacycle
Oxacycle
Carboxylic acid derivative
Carboxylic acid
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Carboximidamide
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Organonitrogen compound
Organic oxygen compound
Organic nitrogen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental 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

Predicted Properties

Property	Value	Source
logP	0.36	ALOGPS
logP	-1.4	ChemAxon
logS	-3.5	ALOGPS
pKa (Strongest Acidic)	1.03	ChemAxon
pKa (Strongest Basic)	11.99	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	167.85 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	101.78 m³·mol⁻¹	ChemAxon
Polarizability	35.8 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

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

102222291

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (11r)-11-(2-carbamimidamidoethyl)-8-hydroxy-13-oxo-12,15-dioxa-4-azatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁴]hexadeca-1(16),2,4,6,8,10(14)-hexaene-3-carboxylic acid (NP0154914)

MOL for NP0154914 ((11r)-11-(2-carbamimidamidoethyl)-8-hydroxy-13-oxo-12,15-dioxa-4-azatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁴]hexadeca-1(16),2,4,6,8,10(14)-hexaene-3-carboxylic acid)

3D MOL for NP0154914 ((11r)-11-(2-carbamimidamidoethyl)-8-hydroxy-13-oxo-12,15-dioxa-4-azatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁴]hexadeca-1(16),2,4,6,8,10(14)-hexaene-3-carboxylic acid)

3D SDF for NP0154914 ((11r)-11-(2-carbamimidamidoethyl)-8-hydroxy-13-oxo-12,15-dioxa-4-azatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁴]hexadeca-1(16),2,4,6,8,10(14)-hexaene-3-carboxylic acid)

3D-SDF for NP0154914 ((11r)-11-(2-carbamimidamidoethyl)-8-hydroxy-13-oxo-12,15-dioxa-4-azatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁴]hexadeca-1(16),2,4,6,8,10(14)-hexaene-3-carboxylic acid)

PDB for NP0154914 ((11r)-11-(2-carbamimidamidoethyl)-8-hydroxy-13-oxo-12,15-dioxa-4-azatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁴]hexadeca-1(16),2,4,6,8,10(14)-hexaene-3-carboxylic acid)

3D PDB for NP0154914 ((11r)-11-(2-carbamimidamidoethyl)-8-hydroxy-13-oxo-12,15-dioxa-4-azatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁴]hexadeca-1(16),2,4,6,8,10(14)-hexaene-3-carboxylic acid)

SMILES for NP0154914 ((11r)-11-(2-carbamimidamidoethyl)-8-hydroxy-13-oxo-12,15-dioxa-4-azatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁴]hexadeca-1(16),2,4,6,8,10(14)-hexaene-3-carboxylic acid)

INCHI for NP0154914 ((11r)-11-(2-carbamimidamidoethyl)-8-hydroxy-13-oxo-12,15-dioxa-4-azatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁴]hexadeca-1(16),2,4,6,8,10(14)-hexaene-3-carboxylic acid)

Structure for NP0154914 ((11r)-11-(2-carbamimidamidoethyl)-8-hydroxy-13-oxo-12,15-dioxa-4-azatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁴]hexadeca-1(16),2,4,6,8,10(14)-hexaene-3-carboxylic acid)

3D Structure for NP0154914 ((11r)-11-(2-carbamimidamidoethyl)-8-hydroxy-13-oxo-12,15-dioxa-4-azatetracyclo[7.6.1.0⁵,¹⁶.0¹⁰,¹⁴]hexadeca-1(16),2,4,6,8,10(14)-hexaene-3-carboxylic acid)