NP-MRD: Showing NP-Card for 3,3-diisopentenyl-4-acetoxy-N-methyl-2-quinolone (NP0031104)

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Record Information

Version

2.0

Created at

2021-06-19 22:16:48 UTC

Updated at

2021-06-29 23:59:29 UTC

NP-MRD ID

NP0031104

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3,3-diisopentenyl-4-acetoxy-N-methyl-2-quinolone

Provided By

JEOL Database JEOL Logo

Description

3,3-diisopentenyl-4-acetoxy-N-methyl-2-quinolone is found in E. almawillia. 3,3-diisopentenyl-4-acetoxy-N-methyl-2-quinolone was first documented in 2005 (Nunes, F. M., et al.).

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306202100163D          

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M  END

     RDKit          3D

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  Mrv1652306202100163D          

 55 56  0  0  0  0            999 V2000
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    1.9822    2.2279    0.2208 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1447    3.7904    1.4342 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8257    3.3251    1.7223 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6236    3.1880    3.0255 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0757   -0.4075    2.0020 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3119    0.7489    3.3012 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4087    0.7490    1.9050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1918   -1.6703    2.0326 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5096   -1.4568    2.1760 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2756    0.8349    3.0438 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7387    1.1829    5.7371 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3147    2.1218    4.6720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4397    2.2514    4.5006 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0465   -0.8477    4.7564 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7763    0.2571    3.5759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9491   -1.1987    3.0329 H   0  0  0  0  0  0  0  0  0  0  0  0
  9 10  1  0  0  0  0
 17 18  1  0  0  0  0
 10 11  2  0  0  0  0
 18 19  2  3  0  0  0
  8  9  2  0  0  0  0
 16 22  1  1  0  0  0
  6  7  2  0  0  0  0
 22 23  1  0  0  0  0
  7  8  1  0  0  0  0
 23 24  2  3  0  0  0
  6  5  1  0  0  0  0
 24 25  1  0  0  0  0
 11 12  1  0  0  0  0
 19 20  1  0  0  0  0
 12 14  1  0  0  0  0
 19 21  1  0  0  0  0
 14 16  1  0  0  0  0
 24 26  1  0  0  0  0
 16  5  1  0  0  0  0
 12 13  1  0  0  0  0
  6 11  1  0  0  0  0
  5  4  1  0  0  0  0
 14 15  2  0  0  0  0
  4  2  1  0  0  0  0
  2  1  1  0  0  0  0
 16 17  1  0  0  0  0
  2  3  2  0  0  0  0
  8 32  1  0  0  0  0
  9 33  1  0  0  0  0
 10 34  1  0  0  0  0
  7 31  1  0  0  0  0
  5 30  1  1  0  0  0
 17 38  1  0  0  0  0
 17 39  1  0  0  0  0
 18 40  1  0  0  0  0
 22 47  1  0  0  0  0
 22 48  1  0  0  0  0
 23 49  1  0  0  0  0
 25 50  1  0  0  0  0
 25 51  1  0  0  0  0
 25 52  1  0  0  0  0
 20 41  1  0  0  0  0
 20 42  1  0  0  0  0
 20 43  1  0  0  0  0
 21 44  1  0  0  0  0
 21 45  1  0  0  0  0
 21 46  1  0  0  0  0
 26 53  1  0  0  0  0
 26 54  1  0  0  0  0
 26 55  1  0  0  0  0
 13 35  1  0  0  0  0
 13 36  1  0  0  0  0
 13 37  1  0  0  0  0
  1 27  1  0  0  0  0
  1 28  1  0  0  0  0
  1 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0031104

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]C(=C(C([H])([H])[H])C([H])([H])[H])C([H])([H])C1(C(=O)N(C2=C([H])C([H])=C([H])C([H])=C2[C@]1([H])OC(=O)C([H])([H])[H])C([H])([H])[H])C([H])([H])C([H])=C(C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C22H29NO3/c1-15(2)11-13-22(14-12-16(3)4)20(26-17(5)24)18-9-7-8-10-19(18)23(6)21(22)25/h7-12,20H,13-14H2,1-6H3/t20-/m0/s1

> <INCHI_KEY>
RQNRSBKYUUIHSX-FQEVSTJZSA-N

> <FORMULA>
C22H29NO3

> <MOLECULAR_WEIGHT>
355.478

> <EXACT_MASS>
355.214743798

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
40.126728868589254

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(4S)-1-methyl-3,3-bis(3-methylbut-2-en-1-yl)-2-oxo-1,2,3,4-tetrahydroquinolin-4-yl acetate

> <ALOGPS_LOGP>
4.29

> <JCHEM_LOGP>
4.276198524333335

> <ALOGPS_LOGS>
-4.38

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-3.1591140473833943

> <JCHEM_POLAR_SURFACE_AREA>
46.61

> <JCHEM_REFRACTIVITY>
105.2935

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.49e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(4S)-1-methyl-3,3-bis(3-methylbut-2-en-1-yl)-2-oxo-4H-quinolin-4-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 55 56  0  0  0  0  0  0  0  0999 V2000
   -0.1465    2.4946   -3.1321 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3882    2.2632   -1.6721 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7241    3.1342   -0.8830 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1662    0.9572   -1.3710 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3854    0.5504    0.0015 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7723   -0.0316    0.0671 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8660    0.7934    0.3810 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1585    0.2781    0.3957 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3680   -1.0604    0.0855 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2851   -1.8827   -0.2392 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9754   -1.3799   -0.2473 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8533   -2.1893   -0.5850 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0763   -3.5059   -1.1691 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4634   -1.7591   -0.4074 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4224   -2.4324   -0.7977 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6895   -0.4746    0.4122 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1271    0.0404    0.0702 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5298    1.3812    0.6357 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4988    1.6469    1.5344 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7861    3.0675    1.9494 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3661    0.6231    2.2143 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5907   -0.9148    1.9101 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4142    0.1783    2.9339 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6447    0.4085    3.7354 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6217    1.5555    4.7141 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9168   -0.3935    3.7683 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8970    2.2772   -3.3734 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8178    1.8665   -3.7232 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3503    3.5422   -3.3718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3207    1.4187    0.6680 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7093    1.8465    0.6112 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9989    0.9219    0.6421 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3759   -1.4679    0.0921 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4974   -2.9216   -0.4720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7285   -3.4145   -2.0436 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5332   -4.1590   -0.4188 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1450   -3.9764   -1.4962 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2301    0.1218   -1.0215 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8600   -0.7253    0.3470 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9822    2.2279    0.2208 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1447    3.7904    1.4342 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8257    3.3251    1.7223 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6236    3.1880    3.0255 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0757   -0.4075    2.0020 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3119    0.7489    3.3012 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4087    0.7490    1.9050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1918   -1.6703    2.0326 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5096   -1.4568    2.1760 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2756    0.8349    3.0438 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7387    1.1829    5.7371 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3147    2.1218    4.6720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4397    2.2514    4.5006 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0465   -0.8477    4.7564 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7763    0.2571    3.5759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9491   -1.1987    3.0329 H   0  0  0  0  0  0  0  0  0  0  0  0
  9 10  1  0
 17 18  1  0
 10 11  2  0
 18 19  2  3
  8  9  2  0
 16 22  1  1
  6  7  2  0
 22 23  1  0
  7  8  1  0
 23 24  2  3
  6  5  1  0
 24 25  1  0
 11 12  1  0
 19 20  1  0
 12 14  1  0
 19 21  1  0
 14 16  1  0
 24 26  1  0
 16  5  1  0
 12 13  1  0
  6 11  1  0
  5  4  1  0
 14 15  2  0
  4  2  1  0
  2  1  1  0
 16 17  1  0
  2  3  2  0
  8 32  1  0
  9 33  1  0
 10 34  1  0
  7 31  1  0
  5 30  1  1
 17 38  1  0
 17 39  1  0
 18 40  1  0
 22 47  1  0
 22 48  1  0
 23 49  1  0
 25 50  1  0
 25 51  1  0
 25 52  1  0
 20 41  1  0
 20 42  1  0
 20 43  1  0
 21 44  1  0
 21 45  1  0
 21 46  1  0
 26 53  1  0
 26 54  1  0
 26 55  1  0
 13 35  1  0
 13 36  1  0
 13 37  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
M  END

HEADER    PROTEIN                                 20-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-JUN-21         0                                  
HETATM    1  C   UNK     0      -0.147   2.495  -3.132  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.388   2.263  -1.672  0.00  0.00           C+0
HETATM    3  O   UNK     0      -0.724   3.134  -0.883  0.00  0.00           O+0
HETATM    4  O   UNK     0      -0.166   0.957  -1.371  0.00  0.00           O+0
HETATM    5  C   UNK     0      -0.385   0.550   0.002  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.772  -0.032   0.067  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.866   0.793   0.381  0.00  0.00           C+0
HETATM    8  C   UNK     0      -4.159   0.278   0.396  0.00  0.00           C+0
HETATM    9  C   UNK     0      -4.368  -1.060   0.086  0.00  0.00           C+0
HETATM   10  C   UNK     0      -3.285  -1.883  -0.239  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.975  -1.380  -0.247  0.00  0.00           C+0
HETATM   12  N   UNK     0      -0.853  -2.189  -0.585  0.00  0.00           N+0
HETATM   13  C   UNK     0      -1.076  -3.506  -1.169  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.463  -1.759  -0.407  0.00  0.00           C+0
HETATM   15  O   UNK     0       1.422  -2.432  -0.798  0.00  0.00           O+0
HETATM   16  C   UNK     0       0.690  -0.475   0.412  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.127   0.040   0.070  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.530   1.381   0.636  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.499   1.647   1.534  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.786   3.067   1.949  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.366   0.623   2.214  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.591  -0.915   1.910  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.414   0.178   2.934  0.00  0.00           C+0
HETATM   24  C   UNK     0      -0.645   0.409   3.735  0.00  0.00           C+0
HETATM   25  C   UNK     0      -0.622   1.556   4.714  0.00  0.00           C+0
HETATM   26  C   UNK     0      -1.917  -0.394   3.768  0.00  0.00           C+0
HETATM   27  H   UNK     0       0.897   2.277  -3.373  0.00  0.00           H+0
HETATM   28  H   UNK     0      -0.818   1.867  -3.723  0.00  0.00           H+0
HETATM   29  H   UNK     0      -0.350   3.542  -3.372  0.00  0.00           H+0
HETATM   30  H   UNK     0      -0.321   1.419   0.668  0.00  0.00           H+0
HETATM   31  H   UNK     0      -2.709   1.847   0.611  0.00  0.00           H+0
HETATM   32  H   UNK     0      -4.999   0.922   0.642  0.00  0.00           H+0
HETATM   33  H   UNK     0      -5.376  -1.468   0.092  0.00  0.00           H+0
HETATM   34  H   UNK     0      -3.497  -2.922  -0.472  0.00  0.00           H+0
HETATM   35  H   UNK     0      -1.728  -3.414  -2.044  0.00  0.00           H+0
HETATM   36  H   UNK     0      -1.533  -4.159  -0.419  0.00  0.00           H+0
HETATM   37  H   UNK     0      -0.145  -3.976  -1.496  0.00  0.00           H+0
HETATM   38  H   UNK     0       2.230   0.122  -1.022  0.00  0.00           H+0
HETATM   39  H   UNK     0       2.860  -0.725   0.347  0.00  0.00           H+0
HETATM   40  H   UNK     0       1.982   2.228   0.221  0.00  0.00           H+0
HETATM   41  H   UNK     0       3.145   3.790   1.434  0.00  0.00           H+0
HETATM   42  H   UNK     0       4.826   3.325   1.722  0.00  0.00           H+0
HETATM   43  H   UNK     0       3.624   3.188   3.026  0.00  0.00           H+0
HETATM   44  H   UNK     0       4.076  -0.408   2.002  0.00  0.00           H+0
HETATM   45  H   UNK     0       4.312   0.749   3.301  0.00  0.00           H+0
HETATM   46  H   UNK     0       5.409   0.749   1.905  0.00  0.00           H+0
HETATM   47  H   UNK     0      -0.192  -1.670   2.033  0.00  0.00           H+0
HETATM   48  H   UNK     0       1.510  -1.457   2.176  0.00  0.00           H+0
HETATM   49  H   UNK     0       1.276   0.835   3.044  0.00  0.00           H+0
HETATM   50  H   UNK     0      -0.739   1.183   5.737  0.00  0.00           H+0
HETATM   51  H   UNK     0       0.315   2.122   4.672  0.00  0.00           H+0
HETATM   52  H   UNK     0      -1.440   2.251   4.501  0.00  0.00           H+0
HETATM   53  H   UNK     0      -2.046  -0.848   4.756  0.00  0.00           H+0
HETATM   54  H   UNK     0      -2.776   0.257   3.576  0.00  0.00           H+0
HETATM   55  H   UNK     0      -1.949  -1.199   3.033  0.00  0.00           H+0
CONECT    1    2   27   28   29                                             
CONECT    2    4    1    3                                                  
CONECT    3    2                                                            
CONECT    4    5    2                                                       
CONECT    5    6   16    4   30                                             
CONECT    6    7    5   11                                                  
CONECT    7    6    8   31                                                  
CONECT    8    9    7   32                                                  
CONECT    9   10    8   33                                                  
CONECT   10    9   11   34                                                  
CONECT   11   10   12    6                                                  
CONECT   12   11   14   13                                                  
CONECT   13   12   35   36   37                                             
CONECT   14   12   16   15                                                  
CONECT   15   14                                                            
CONECT   16   22   14    5   17                                             
CONECT   17   18   16   38   39                                             
CONECT   18   17   19   40                                                  
CONECT   19   18   20   21                                                  
CONECT   20   19   41   42   43                                             
CONECT   21   19   44   45   46                                             
CONECT   22   16   23   47   48                                             
CONECT   23   22   24   49                                                  
CONECT   24   23   25   26                                                  
CONECT   25   24   50   51   52                                             
CONECT   26   24   53   54   55                                             
CONECT   27    1                                                            
CONECT   28    1                                                            
CONECT   29    1                                                            
CONECT   30    5                                                            
CONECT   31    7                                                            
CONECT   32    8                                                            
CONECT   33    9                                                            
CONECT   34   10                                                            
CONECT   35   13                                                            
CONECT   36   13                                                            
CONECT   37   13                                                            
CONECT   38   17                                                            
CONECT   39   17                                                            
CONECT   40   18                                                            
CONECT   41   20                                                            
CONECT   42   20                                                            
CONECT   43   20                                                            
CONECT   44   21                                                            
CONECT   45   21                                                            
CONECT   46   21                                                            
CONECT   47   22                                                            
CONECT   48   22                                                            
CONECT   49   23                                                            
CONECT   50   25                                                            
CONECT   51   25                                                            
CONECT   52   25                                                            
CONECT   53   26                                                            
CONECT   54   26                                                            
CONECT   55   26                                                            
MASTER        0    0    0    0    0    0    0    0   55    0  112    0
END

RDKit          3D

55 56  0  0  0  0  0  0  0  0999 V2000
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M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₂₉NO₃

Average Mass

355.4780 Da

Monoisotopic Mass

355.21474 Da

IUPAC Name

(4S)-1-methyl-3,3-bis(3-methylbut-2-en-1-yl)-2-oxo-1,2,3,4-tetrahydroquinolin-4-yl acetate

Traditional Name

(4S)-1-methyl-3,3-bis(3-methylbut-2-en-1-yl)-2-oxo-4H-quinolin-4-yl acetate

CAS Registry Number

Not Available

SMILES

[H]C(=C(C([H])([H])[H])C([H])([H])[H])C([H])([H])C1(C(=O)N(C2=C([H])C([H])=C([H])C([H])=C2[C@]1([H])OC(=O)C([H])([H])[H])C([H])([H])[H])C([H])([H])C([H])=C(C([H])([H])[H])C([H])([H])[H]

InChI Identifier

InChI=1S/C22H29NO3/c1-15(2)11-13-22(14-12-16(3)4)20(26-17(5)24)18-9-7-8-10-19(18)23(6)21(22)25/h7-12,20H,13-14H2,1-6H3/t20-/m0/s1

InChI Key

RQNRSBKYUUIHSX-FQEVSTJZSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Esenbeckia almawillia	JEOL database	Nunes, F. M., et al, Magn. Reson. Chem. 43, 180 (2005)

Chemical Taxonomy

Classification

Not classified

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	4.29	ALOGPS
logP	4.28	ChemAxon
logS	-4.4	ALOGPS
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	46.61 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	105.29 m³·mol⁻¹	ChemAxon
Polarizability	40.13 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

Not Available

References

General References

Nunes, F. M., et al. (2005). Nunes, F. M., et al, Magn. Reson. Chem. 43, 180 (2005). Mag. Reson. Chem..

Showing NP-Card for 3,3-diisopentenyl-4-acetoxy-N-methyl-2-quinolone (NP0031104)

MOL for NP0031104 (3,3-diisopentenyl-4-acetoxy-N-methyl-2-quinolone)

3D MOL for NP0031104 (3,3-diisopentenyl-4-acetoxy-N-methyl-2-quinolone)

3D SDF for NP0031104 (3,3-diisopentenyl-4-acetoxy-N-methyl-2-quinolone)

3D-SDF for NP0031104 (3,3-diisopentenyl-4-acetoxy-N-methyl-2-quinolone)

PDB for NP0031104 (3,3-diisopentenyl-4-acetoxy-N-methyl-2-quinolone)

3D PDB for NP0031104 (3,3-diisopentenyl-4-acetoxy-N-methyl-2-quinolone)

SMILES for NP0031104 (3,3-diisopentenyl-4-acetoxy-N-methyl-2-quinolone)

INCHI for NP0031104 (3,3-diisopentenyl-4-acetoxy-N-methyl-2-quinolone)

Structure for NP0031104 (3,3-diisopentenyl-4-acetoxy-N-methyl-2-quinolone)

3D Structure for NP0031104 (3,3-diisopentenyl-4-acetoxy-N-methyl-2-quinolone)