NP-MRD: Showing NP-Card for Taladuxin L (NP0333666)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2024-07-31 22:48:39 UTC

Updated at

2025-07-31 01:09:32 UTC

NP-MRD ID

NP0333666

Natural Product DOI

https://doi.org/10.57994/3145

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Taladuxin L

Description

Taladuxin L belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety. Based on a literature review very few articles have been published on Taladuxin L.

Structure

MOL SDF PDB SMILES InChI


  Mrv2104 04152301222D          

 40 46  0  0  1  0            999 V2000
    5.6924    0.9837    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9163    0.7040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7704   -0.1080    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9943   -0.3877    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8485   -1.1997    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4787   -1.7320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2549   -1.4524    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3329   -2.5441    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2860    1.2363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5099    0.9566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3640    0.1446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5879   -0.1351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4420   -0.9471    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9576    0.3972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0972    0.2237    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2121    0.3368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2942   -0.3322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0028   -1.1209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8204   -1.2498    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3328   -0.6057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5182   -1.7605    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1220   -0.2583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6017   -0.9295    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4585    0.4970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9708    1.1763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3254    1.9212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1326    1.1262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4722    1.7899    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3339    1.6650    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6085    2.4430    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1770    0.9547    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3630    1.0886    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1940    2.5666    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1034    1.2092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8796    1.4889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0254    2.3009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3951    2.8332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8016    2.5806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4319    2.0483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2080    2.3280    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
  4  3  1  0  0  0  0
  4  5  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  2  0  0  0  0
  2  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
  4 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 15 14  1  6  0  0  0
 15 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
 15 20  1  0  0  0  0
 18 21  2  0  0  0  0
 17 22  2  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
 25 26  1  0  0  0  0
 16 27  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 29 28  1  0  0  0  0
 29 30  1  1  0  0  0
 31 29  1  0  0  0  0
 31 15  1  0  0  0  0
 31 32  1  1  0  0  0
 28 33  2  0  0  0  0
 14 34  2  0  0  0  0
 29 34  1  0  0  0  0
 34 35  1  0  0  0  0
 10 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 38 39  2  0  0  0  0
  9 39  1  0  0  0  0
 39 40  1  0  0  0  0
M  END


  Mrv2104 04152301222D          

 40 46  0  0  1  0            999 V2000
    5.6924    0.9837    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9163    0.7040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7704   -0.1080    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9943   -0.3877    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8485   -1.1997    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4787   -1.7320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2549   -1.4524    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3329   -2.5441    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2860    1.2363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5099    0.9566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3640    0.1446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5879   -0.1351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4420   -0.9471    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9576    0.3972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0972    0.2237    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2121    0.3368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2942   -0.3322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0028   -1.1209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8204   -1.2498    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3328   -0.6057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5182   -1.7605    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1220   -0.2583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6017   -0.9295    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4585    0.4970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9708    1.1763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3254    1.9212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1326    1.1262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4722    1.7899    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3339    1.6650    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6085    2.4430    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1770    0.9547    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3630    1.0886    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1940    2.5666    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1034    1.2092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8796    1.4889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0254    2.3009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3951    2.8332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8016    2.5806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4319    2.0483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2080    2.3280    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
  4  3  1  0  0  0  0
  4  5  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  2  0  0  0  0
  2  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
  4 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 15 14  1  6  0  0  0
 15 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
 15 20  1  0  0  0  0
 18 21  2  0  0  0  0
 17 22  2  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
 25 26  1  0  0  0  0
 16 27  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 29 28  1  0  0  0  0
 29 30  1  1  0  0  0
 31 29  1  0  0  0  0
 31 15  1  0  0  0  0
 31 32  1  1  0  0  0
 28 33  2  0  0  0  0
 14 34  2  0  0  0  0
 29 34  1  0  0  0  0
 34 35  1  0  0  0  0
 10 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 38 39  2  0  0  0  0
  9 39  1  0  0  0  0
 39 40  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0333666

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@@]12[C@H](O)[C@]3(COC(=O)C4=C(O)C=C(C)C(C1=O)=C34)C1=C2C2=C(C)C=C(O)C3=C2C([C@H](CC(O)=O)OC3=O)=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C28H20O11/c1-7-3-9(29)15-18-13(7)19-20-23(33)14-8(2)4-10(30)16-21(14)28(25(20)35,6-38-26(16)36)22(19)24(34)17(18)11(5-12(31)32)39-27(15)37/h3-4,11,20,25,29-30,34-35H,5-6H2,1-2H3,(H,31,32)/t11-,20-,25-,28-/m0/s1

> <INCHI_KEY>
CAKONYRHUGGYOQ-MFPLWRAFSA-N

> <FORMULA>
C28H20O11

> <MOLECULAR_WEIGHT>
532.457

> <EXACT_MASS>
532.100561464

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
50.783165342165674

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-[(1S,5S,14R,24S)-3,9,19,24-tetrahydroxy-11,17-dimethyl-7,15,21-trioxo-6,22-dioxaheptacyclo[12.9.1.1^{1,16}.1^{4,8}.0^{2,13}.0^{12,26}.0^{20,25}]hexacosa-2(13),3,8(26),9,11,16(25),17,19-octaen-5-yl]acetic acid

> <JCHEM_LOGP>
3.4070095116666668

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
7.833223291326623

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.2928383629565112

> <JCHEM_PKA_STRONGEST_BASIC>
-3.3648609868012955

> <JCHEM_POLAR_SURFACE_AREA>
187.88999999999996

> <JCHEM_REFRACTIVITY>
142.96089999999995

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
[(1S,5S,14R,24S)-3,9,19,24-tetrahydroxy-11,17-dimethyl-7,15,21-trioxo-6,22-dioxaheptacyclo[12.9.1.1^{1,16}.1^{4,8}.0^{2,13}.0^{12,26}.0^{20,25}]hexacosa-2(13),3,8(26),9,11,16(25),17,19-octaen-5-yl]acetic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 15-APR-23   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   15-APR-23         0                                  
HETATM    1  O   UNK     0      10.626   1.836   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       9.177   1.314   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       8.905  -0.202   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       7.456  -0.724   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.184  -2.240   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.360  -3.233   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       9.809  -2.711   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0       8.088  -4.749   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       8.001   2.308   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.552   1.786   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.279   0.270   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.831  -0.252   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       4.558  -1.768   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       3.654   0.741   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.048   0.418   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.396   0.629   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.549  -0.620   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.005  -2.092   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       1.531  -2.333   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       2.488  -1.131   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -0.967  -3.286   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -2.094  -0.482   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -2.990  -1.735   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -2.723   0.928   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -1.812   2.196   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -2.474   3.586   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -0.248   2.102   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       0.881   3.341   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.490   3.108   0.000  0.00  0.00           C+0
HETATM   30  H   UNK     0       3.003   4.560   0.000  0.00  0.00           H+0
HETATM   31  C   UNK     0       2.197   1.782   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       0.678   2.032   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0       0.362   4.791   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       3.926   2.257   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       5.375   2.779   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       5.647   4.295   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       4.471   5.289   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       7.096   4.817   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       8.273   3.823   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       9.722   4.346   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    9                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   11                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6                                                            
CONECT    9    2   10   39                                                  
CONECT   10    9   11   35                                                  
CONECT   11   10    4   12                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   34                                                  
CONECT   15   14   16   20   31                                             
CONECT   16   15   17   27                                                  
CONECT   17   16   18   22                                                  
CONECT   18   17   19   21                                                  
CONECT   19   18   20                                                       
CONECT   20   19   15                                                       
CONECT   21   18                                                            
CONECT   22   17   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   16   25   28                                                  
CONECT   28   27   29   33                                                  
CONECT   29   28   30   31   34                                             
CONECT   30   29                                                            
CONECT   31   29   15   32                                                  
CONECT   32   31                                                            
CONECT   33   28                                                            
CONECT   34   14   29   35                                                  
CONECT   35   34   10   36                                                  
CONECT   36   35   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   39                                                       
CONECT   39   38    9   40                                                  
CONECT   40   39                                                            
MASTER        0    0    0    0    0    0    0    0   40    0   92    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₈H₂₀O₁₁

Average Mass

532.4570 Da

Monoisotopic Mass

532.10056 Da

IUPAC Name

2-[(1S,5S,14R,24S)-3,9,19,24-tetrahydroxy-11,17-dimethyl-7,15,21-trioxo-6,22-dioxaheptacyclo[12.9.1.1^{1,16}.1^{4,8}.0^{2,13}.0^{12,26}.0^{20,25}]hexacosa-2(13),3,8(26),9,11,16(25),17,19-octaen-5-yl]acetic acid

Traditional Name

[(1S,5S,14R,24S)-3,9,19,24-tetrahydroxy-11,17-dimethyl-7,15,21-trioxo-6,22-dioxaheptacyclo[12.9.1.1^{1,16}.1^{4,8}.0^{2,13}.0^{12,26}.0^{20,25}]hexacosa-2(13),3,8(26),9,11,16(25),17,19-octaen-5-yl]acetic acid

CAS Registry Number

Not Available

SMILES

[H][C@@]12[C@H](O)[C@]3(COC(=O)C4=C(O)C=C(C)C(C1=O)=C34)C1=C2C2=C(C)C=C(O)C3=C2C([C@H](CC(O)=O)OC3=O)=C1O

InChI Identifier

InChI=1S/C28H20O11/c1-7-3-9(29)15-18-13(7)19-20-23(33)14-8(2)4-10(30)16-21(14)28(25(20)35,6-38-26(16)36)22(19)24(34)17(18)11(5-12(31)32)39-27(15)37/h3-4,11,20,25,29-30,34-35H,5-6H2,1-2H3,(H,31,32)/t11-,20-,25-,28-/m0/s1

InChI Key

CAKONYRHUGGYOQ-MFPLWRAFSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D_DEPT NMR	¹³C NMR Spectrum (1D, 101 MHz, C2D6OS, experimental)	zyzenghanxiao@126.com	Huazhong University of Science and Technology	hanxiao zeng	2024-07-31	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, C2D6OS, experimental)	zyzenghanxiao@126.com	Huazhong University of Science and Technology	hanxiao zeng	2024-07-31	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, C2D6OS, experimental)	zyzenghanxiao@126.com	Huazhong University of Science and Technology	hanxiao zeng	2024-07-31	View Spectrum
ROESY NMR	[¹H, ¹H] NMR Spectrum (2D, 400 MHz, C2D6OS, experimental)	zyzenghanxiao@126.com	Huazhong University of Science and Technology	hanxiao zeng	2024-07-31	View Spectrum
HMBC NMR	[¹H, ¹³C] NMR Spectrum (2D, 400 MHz, C2D6OS, experimental)	zyzenghanxiao@126.com	Huazhong University of Science and Technology	hanxiao zeng	2024-07-31	View Spectrum
COSY NMR	[¹H, ¹H] NMR Spectrum (2D, 400 MHz, C2D6OS, experimental)	zyzenghanxiao@126.com	Huazhong University of Science and Technology	hanxiao zeng	2024-07-31	View Spectrum
HSQC NMR	[¹H, ¹³C] NMR Spectrum (2D, 400 MHz, C2D6OS, experimental)	zyzenghanxiao@126.com	Huazhong University of Science and Technology	hanxiao zeng	2024-07-31	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, C2D6OS, experimental)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View

Chemical Shift Submissions

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹H NMR Spectrum (1D, 400, C2D6OS, simulated)	zyzenghanxiao@126.com	Huazhong University of Science and Technology	hanxiao zeng	2024-07-31	View Spectrum

Species

Species of Origin

Species Name	Source	Reference
Talaromyces sp. TJ403-AL05		Not Available

Chemical Taxonomy

Description

This compound belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Diterpene lactones

Alternative Parents

Substituents

Diterpenoid
Diterpene lactone
Dibenzocycloheptene
2-naphthol
2-benzopyran
Tetralin
Naphthalene
Isochromane
Benzopyran
Tricarboxylic acid or derivatives
Indane
Aryl alkyl ketone
Aryl ketone
1-hydroxy-2-unsubstituted benzenoid
Cyclohexenone
B'-hydroxy-alpha,beta-unsaturated-ketone
Delta_valerolactone
Fatty acid ester
Dihydropyranone
Delta valerolactone
Fatty acyl
Alpha-branched alpha,beta-unsaturated-ketone
Benzenoid
Pyran
Oxane
Beta-hydroxy ketone
Vinylogous acid
Alpha,beta-unsaturated ketone
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Enone
Acryloyl-group
Secondary alcohol
Lactone
Ketone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
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	3.41	ChemAxon
pKa (Strongest Acidic)	3.29	ChemAxon
pKa (Strongest Basic)	-3.4	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	187.89 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	142.96 m³·mol⁻¹	ChemAxon
Polarizability	50.78 Å³	ChemAxon
Number of Rings	7	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Taladuxin L (NP0333666)

MOL for NP0333666 (Taladuxin L)

3D MOL for NP0333666 (Taladuxin L)

3D SDF for NP0333666 (Taladuxin L)

3D-SDF for NP0333666 (Taladuxin L)

PDB for NP0333666 (Taladuxin L)

3D PDB for NP0333666 (Taladuxin L)

SMILES for NP0333666 (Taladuxin L)

INCHI for NP0333666 (Taladuxin L)

Structure for NP0333666 (Taladuxin L)

3D Structure for NP0333666 (Taladuxin L)