NP-MRD: Showing NP-Card for 4-carboxy-4,17,19-trihydroxy-11-methyl-2,13-dioxo-12-oxa-6-thiatricyclo[13.4.0.0³,⁷]nonadeca-1(19),15,17-trien-6-ium-6-olate (NP0198906)

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Record Information

Version

2.0

Created at

2022-09-04 17:26:38 UTC

Updated at

2022-09-04 17:26:39 UTC

NP-MRD ID

NP0198906

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-carboxy-4,17,19-trihydroxy-11-methyl-2,13-dioxo-12-oxa-6-thiatricyclo[13.4.0.0³,⁷]nonadeca-1(19),15,17-trien-6-ium-6-olate

Description

4,17,19-Trihydroxy-11-methyl-2,6,13-trioxo-12-oxa-6λ⁴-thiatricyclo[13.4.0.0³,⁷]Nonadeca-1(19),15,17-triene-4-carboxylic acid belongs to the class of organic compounds known as aryl alkyl ketones. These are ketones have the generic structure RC(=O)R', where R = aryl group and R'=alkyl group. Based on a literature review very few articles have been published on 4,17,19-trihydroxy-11-methyl-2,6,13-trioxo-12-oxa-6λ⁴-thiatricyclo[13.4.0.0³,⁷]Nonadeca-1(19),15,17-triene-4-carboxylic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042219262D          

 29 31  0  0  0  0            999 V2000
    4.4734    5.7056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4358    4.8814    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1307    4.4368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0931    3.6127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7880    3.1680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7504    2.3439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0179    1.9644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3229    2.4090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3606    3.2332    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5904    2.0295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5528    1.2054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2477    0.7607    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8203    0.8259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1254    1.2705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3928    0.8910    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1630    2.0946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8955    2.4741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9331    3.2983    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6656    3.6778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4892    3.7265    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7032    4.5019    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1524    1.1504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3289    1.1017    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1148    0.3263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8098   -0.1184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3823   -0.0532    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9681    1.0269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3377    1.7645    0.0000 S   0  3  0  0  0  0  0  0  0  0  0  0
    7.1516    1.8990    0.0000 O   0  5  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  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 10 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
  2 21  1  0  0  0  0
  7 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 22 27  1  0  0  0  0
 27 28  1  0  0  0  0
  6 28  1  0  0  0  0
 28 29  1  0  0  0  0
M  CHG  2  28   1  29  -1
M  END

     RDKit          3D

 51 53  0  0  0  0  0  0  0  0999 V2000
    4.7673   -1.0855   -0.3066 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2673   -0.8157   -0.1231 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8222   -1.6596    1.0518 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6396   -2.5529    0.6520 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3303   -1.8317    0.8965 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5974   -2.0447   -0.3068 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3814   -0.7714   -0.5915 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2366    0.1960    0.5185 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5908   -0.2871    1.6611 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7545    1.5692    0.4417 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4508    2.5044    1.2123 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5283    2.2222    2.0194 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0939    3.8641    1.2293 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0478    4.3085    0.4862 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3611    5.6419    0.4548 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6358    3.3939   -0.2685 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2995    2.0284   -0.3028 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1900    1.2196   -1.1751 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6194    1.4671   -0.7894 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704    2.4431   -1.2819 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1639    0.5754    0.1202 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8084   -1.2276   -0.8401 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7455   -2.0545   -2.0049 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7102   -0.1380   -1.1247 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9712    0.7389   -0.2759 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3291   -0.0160   -2.3581 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1915   -2.1537    0.2601 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7897   -3.2544    0.2242 S   0  0  0  0  0  3  0  0  0  0  0  0
   -1.4452   -3.8986    1.7110 O   0  0  0  0  0  1  0  0  0  0  0  0
    5.2550   -0.5142    0.5346 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0450   -0.5901   -1.2562 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0014   -2.1518   -0.2702 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7865   -1.1484   -1.0534 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5256   -0.9880    1.8748 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6165   -2.3454    1.4116 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7172   -2.8499   -0.4097 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6563   -3.4702    1.2591 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1630   -2.1503    1.8365 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5846   -0.7652    1.0367 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0516   -2.4142   -1.1807 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1211   -0.3005   -1.5578 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9190    1.3357    2.1307 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6303    4.5901    1.8239 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0697    6.3776    0.9661 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4618    3.7649   -0.8579 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0768    0.1471   -1.1146 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0939    1.6004   -2.2208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9329   -1.5086   -2.8093 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2032   -0.5451   -2.4848 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0601   -2.7596   -0.0888 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3641   -1.6955    1.2405 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  1  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  2  0
 11 12  1  0
 11 13  1  0
 13 14  2  0
 14 15  1  0
 14 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 19 21  1  0
  7 22  1  0
 22 23  1  6
 22 27  1  0
 27 28  1  0
 28 29  1  1
 22 24  1  0
 24 26  1  0
 24 25  2  0
 21  2  1  0
 28  6  1  0
 17 10  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  2 33  1  6
  3 34  1  0
  3 35  1  0
  4 36  1  0
  4 37  1  0
  5 38  1  0
  5 39  1  0
  6 40  1  6
  7 41  1  6
 12 42  1  0
 13 43  1  0
 15 44  1  0
 16 45  1  0
 18 46  1  0
 18 47  1  0
 23 48  1  0
 27 50  1  0
 27 51  1  0
 26 49  1  0
M  CHG  2  28   1  29  -1
M  END


  Mrv1652309042219262D          

 29 31  0  0  0  0            999 V2000
    4.4734    5.7056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4358    4.8814    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1307    4.4368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0931    3.6127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7880    3.1680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7504    2.3439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0179    1.9644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3229    2.4090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3606    3.2332    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5904    2.0295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5528    1.2054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2477    0.7607    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8203    0.8259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1254    1.2705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3928    0.8910    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1630    2.0946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8955    2.4741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9331    3.2983    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6656    3.6778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4892    3.7265    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7032    4.5019    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1524    1.1504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3289    1.1017    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1148    0.3263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8098   -0.1184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3823   -0.0532    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9681    1.0269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3377    1.7645    0.0000 S   0  3  0  0  0  0  0  0  0  0  0  0
    7.1516    1.8990    0.0000 O   0  5  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  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 10 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
  2 21  1  0  0  0  0
  7 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 22 27  1  0  0  0  0
 27 28  1  0  0  0  0
  6 28  1  0  0  0  0
 28 29  1  0  0  0  0
M  CHG  2  28   1  29  -1
M  END
> <DATABASE_ID>
NP0198906

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1CCCC2C(C(=O)C3=C(O)C=C(O)C=C3CC(=O)O1)C(O)(C[S+]2[O-])C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C19H22O9S/c1-9-3-2-4-13-16(19(26,18(24)25)8-29(13)27)17(23)15-10(6-14(22)28-9)5-11(20)7-12(15)21/h5,7,9,13,16,20-21,26H,2-4,6,8H2,1H3,(H,24,25)

> <INCHI_KEY>
XBYWGNYCVAOWKJ-UHFFFAOYSA-N

> <FORMULA>
C19H22O9S

> <MOLECULAR_WEIGHT>
426.44

> <EXACT_MASS>
426.098453462

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
51

> <JCHEM_AVERAGE_POLARIZABILITY>
40.29770682937115

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-carboxy-4,17,19-trihydroxy-11-methyl-2,13-dioxo-12-oxa-6-thiatricyclo[13.4.0.0^{3,7}]nonadeca-1(19),15,17-trien-6-ium-6-olate

> <JCHEM_LOGP>
0.5277447333333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
7.758281544946575

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.0286033992374555

> <JCHEM_PKA_STRONGEST_BASIC>
-4.322116634288551

> <JCHEM_POLAR_SURFACE_AREA>
158.42999999999998

> <JCHEM_REFRACTIVITY>
101.79779999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
4-carboxy-4,17,19-trihydroxy-11-methyl-2,13-dioxo-12-oxa-6-thiatricyclo[13.4.0.0^{3,7}]nonadeca-1(19),15,17-trien-6-ium-6-olate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       8.350  10.650   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.280   9.112   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.577   8.282   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.507   6.744   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.804   5.914   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.734   4.375   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.367   3.667   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.069   4.497   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       8.140   6.035   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       6.702   3.788   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.632   2.250   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       7.929   1.420   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       5.265   1.542   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.967   2.372   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       2.600   1.663   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       4.038   3.910   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.405   4.618   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.475   6.157   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.843   6.865   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       8.380   6.956   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       6.913   8.404   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       9.618   2.147   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       8.081   2.056   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       9.548   0.609   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      10.845  -0.221   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       8.180  -0.099   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      11.141   1.917   0.000  0.00  0.00           C+0
HETATM   28  S   UNK     0      11.830   3.294   0.000  0.00  0.00           S+1
HETATM   29  O   UNK     0      13.350   3.545   0.000  0.00  0.00           O-1
CONECT    1    2                                                            
CONECT    2    1    3   21                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   28                                                  
CONECT    7    6    8   22                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   17                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   10   18                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19    2                                                       
CONECT   22    7   23   24   27                                             
CONECT   23   22                                                            
CONECT   24   22   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24                                                            
CONECT   27   22   28                                                       
CONECT   28   27    6   29                                                  
CONECT   29   28                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   62    0
END

View in JSmol

Synonyms

Value	Source
4,17,19-Trihydroxy-11-methyl-2,6,13-trioxo-12-oxa-6-thiatricyclo[13.4.0.0,]nonadeca-1(19),15,17-triene-4-carboxylate	Generator

Chemical Formula

C₁₉H₂₂O₉S

Average Mass

426.4400 Da

Monoisotopic Mass

426.09845 Da

IUPAC Name

4-carboxy-4,17,19-trihydroxy-11-methyl-2,13-dioxo-12-oxa-6-thiatricyclo[13.4.0.0^{3,7}]nonadeca-1(19),15,17-trien-6-ium-6-olate

Traditional Name

4-carboxy-4,17,19-trihydroxy-11-methyl-2,13-dioxo-12-oxa-6-thiatricyclo[13.4.0.0^{3,7}]nonadeca-1(19),15,17-trien-6-ium-6-olate

CAS Registry Number

Not Available

SMILES

CC1CCCC2C(C(=O)C3=C(O)C=C(O)C=C3CC(=O)O1)C(O)(C[S+]2[O-])C(O)=O

InChI Identifier

InChI=1S/C19H22O9S/c1-9-3-2-4-13-16(19(26,18(24)25)8-29(13)27)17(23)15-10(6-14(22)28-9)5-11(20)7-12(15)21/h5,7,9,13,16,20-21,26H,2-4,6,8H2,1H3,(H,24,25)

InChI Key

XBYWGNYCVAOWKJ-UHFFFAOYSA-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 aryl alkyl ketones. These are ketones have the generic structure RC(=O)R', where R = aryl group and R'=alkyl group.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbonyl compounds

Direct Parent

Aryl alkyl ketones

Alternative Parents

Substituents

Aryl alkyl ketone
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Benzenoid
Hydroxy acid
Dicarboxylic acid or derivatives
Alpha-hydroxy acid
Vinylogous acid
Thiolane
Tertiary alcohol
Sulfoxide
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Sulfinyl compound
Polyol
Carboxylic acid
Carboxylic acid derivative
Organic oxide
Hydrocarbon derivative
Alcohol
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	0.53	ChemAxon
pKa (Strongest Acidic)	3.03	ChemAxon
pKa (Strongest Basic)	-4.3	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	158.43 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	101.8 m³·mol⁻¹	ChemAxon
Polarizability	40.3 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

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

162816075

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4-carboxy-4,17,19-trihydroxy-11-methyl-2,13-dioxo-12-oxa-6-thiatricyclo[13.4.0.0³,⁷]nonadeca-1(19),15,17-trien-6-ium-6-olate (NP0198906)

MOL for NP0198906 (4-carboxy-4,17,19-trihydroxy-11-methyl-2,13-dioxo-12-oxa-6-thiatricyclo[13.4.0.0³,⁷]nonadeca-1(19),15,17-trien-6-ium-6-olate)

3D MOL for NP0198906 (4-carboxy-4,17,19-trihydroxy-11-methyl-2,13-dioxo-12-oxa-6-thiatricyclo[13.4.0.0³,⁷]nonadeca-1(19),15,17-trien-6-ium-6-olate)

3D SDF for NP0198906 (4-carboxy-4,17,19-trihydroxy-11-methyl-2,13-dioxo-12-oxa-6-thiatricyclo[13.4.0.0³,⁷]nonadeca-1(19),15,17-trien-6-ium-6-olate)

3D-SDF for NP0198906 (4-carboxy-4,17,19-trihydroxy-11-methyl-2,13-dioxo-12-oxa-6-thiatricyclo[13.4.0.0³,⁷]nonadeca-1(19),15,17-trien-6-ium-6-olate)

PDB for NP0198906 (4-carboxy-4,17,19-trihydroxy-11-methyl-2,13-dioxo-12-oxa-6-thiatricyclo[13.4.0.0³,⁷]nonadeca-1(19),15,17-trien-6-ium-6-olate)

3D PDB for NP0198906 (4-carboxy-4,17,19-trihydroxy-11-methyl-2,13-dioxo-12-oxa-6-thiatricyclo[13.4.0.0³,⁷]nonadeca-1(19),15,17-trien-6-ium-6-olate)

SMILES for NP0198906 (4-carboxy-4,17,19-trihydroxy-11-methyl-2,13-dioxo-12-oxa-6-thiatricyclo[13.4.0.0³,⁷]nonadeca-1(19),15,17-trien-6-ium-6-olate)

INCHI for NP0198906 (4-carboxy-4,17,19-trihydroxy-11-methyl-2,13-dioxo-12-oxa-6-thiatricyclo[13.4.0.0³,⁷]nonadeca-1(19),15,17-trien-6-ium-6-olate)

Structure for NP0198906 (4-carboxy-4,17,19-trihydroxy-11-methyl-2,13-dioxo-12-oxa-6-thiatricyclo[13.4.0.0³,⁷]nonadeca-1(19),15,17-trien-6-ium-6-olate)

3D Structure for NP0198906 (4-carboxy-4,17,19-trihydroxy-11-methyl-2,13-dioxo-12-oxa-6-thiatricyclo[13.4.0.0³,⁷]nonadeca-1(19),15,17-trien-6-ium-6-olate)