NP-MRD: Showing NP-Card for (2e,4e)-5-[(1r,7s,8r,9r)-7-hydroxy-4-(methoxycarbonyl)-9-methyl-11-oxo-10-oxatricyclo[6.3.2.0¹,⁷]tridec-3-en-9-yl]-2-methylpenta-2,4-dienoic acid (NP0200970)

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Record Information

Version

2.0

Created at

2022-09-04 19:55:31 UTC

Updated at

2022-09-04 19:55:31 UTC

NP-MRD ID

NP0200970

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2e,4e)-5-[(1r,7s,8r,9r)-7-hydroxy-4-(methoxycarbonyl)-9-methyl-11-oxo-10-oxatricyclo[6.3.2.0¹,⁷]tridec-3-en-9-yl]-2-methylpenta-2,4-dienoic acid

Description

PSEUDOLARIC ACID C, also known as pseudolarate C, belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety. (2e,4e)-5-[(1r,7s,8r,9r)-7-hydroxy-4-(methoxycarbonyl)-9-methyl-11-oxo-10-oxatricyclo[6.3.2.0¹,⁷]tridec-3-en-9-yl]-2-methylpenta-2,4-dienoic acid is found in Larix kaempferi and Pseudolarix amabilis. (2e,4e)-5-[(1r,7s,8r,9r)-7-hydroxy-4-(methoxycarbonyl)-9-methyl-11-oxo-10-oxatricyclo[6.3.2.0¹,⁷]tridec-3-en-9-yl]-2-methylpenta-2,4-dienoic acid was first documented in 2009 (PMID: 19918938). Based on a literature review a small amount of articles have been published on PSEUDOLARIC ACID C (PMID: 22424731) (PMID: 25322560).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042221552D          

 28 30  0  0  1  0            999 V2000
    5.4198    0.6361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6181    0.4414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0486    1.0384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2808    1.8300    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2469    0.8437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0745    0.0369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3362   -0.3313    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5880    0.0163    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9202    0.7715    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5368    1.5020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7267    1.6578    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3933    0.8180    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6521    0.4557    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8987    1.4701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7236    1.4815    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0998    1.1215    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2836    1.8521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6978    0.9104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2794    1.4955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0769    1.2843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6585    1.8694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4426    2.6656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4560    1.6582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6719    0.8620    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0377    2.2433    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1282    0.2970    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7905   -0.1949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6347   -1.0050    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  9 10  1  0  0  0  0
 11 10  1  6  0  0  0
 11 12  1  0  0  0  0
  8 12  1  0  0  0  0
 12 13  1  6  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
  5 15  1  0  0  0  0
 11 16  1  0  0  0  0
 16 17  1  1  0  0  0
 16 18  1  6  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 16 26  1  0  0  0  0
 26 27  1  0  0  0  0
  8 27  1  0  0  0  0
 27 28  2  0  0  0  0
M  END

     RDKit          3D

 54 56  0  0  0  0  0  0  0  0999 V2000
   -7.0023    1.7695   -0.3648 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8250    0.9956   -0.4396 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1358    0.5252    0.6609 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5728    0.7952    1.8018 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9274   -0.2682    0.5422 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3768   -0.6474    1.6731 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1706   -1.4444    1.9009 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0347   -1.1024    0.9983 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1714   -0.7241    1.8570 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7700    0.5124    1.2550 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2152    0.4613   -0.1772 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2304    0.1064    0.1561 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7300    1.1794    0.8931 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0414   -0.0797   -1.0765 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4187   -0.5830   -0.8162 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9061   -0.6113   -0.9814 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0388   -0.1509   -2.4179 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2834   -0.8866   -0.4591 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2755   -0.0374   -0.6877 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6085   -0.3279   -0.1682 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5878    0.5284   -0.4047 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3259    1.7497   -1.1796 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9098    0.2520    0.1042 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8385    1.0596   -0.1180 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1788   -0.9003    0.8421 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2264   -1.8522   -0.9576 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5968   -2.2164    0.1265 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8938   -3.4073    0.2785 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6968    2.8422   -0.3391 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5755    1.6016    0.5707 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6826    1.5687   -1.2198 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8960   -0.3198    2.5606 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8813   -1.3511    2.9673 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4458   -2.5179    1.7599 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8819   -1.5679    1.9291 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1717   -0.5384    2.9180 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8655    0.5396    1.2688 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3795    1.4361    1.7190 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3166    1.4633   -0.6032 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6243    1.0760    1.8548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5876   -0.6969   -1.8596 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1557    0.9448   -1.5389 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4604   -1.6798   -1.0207 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1376   -0.1310   -1.5541 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4488   -0.7838   -3.1235 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6619    0.8843   -2.5560 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1201   -0.1091   -2.7404 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5306   -1.7680    0.1149 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1111    0.8831   -1.2621 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8385   -1.2069    0.4003 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8600    1.4372   -2.1515 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2727    2.2510   -1.4601 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6071    2.4385   -0.7006 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0416   -1.3911    0.6217 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  1
 12 14  1  0
 14 15  1  0
 11 16  1  0
 16 17  1  0
 16 26  1  0
 26 27  1  0
 27 28  2  0
 16 18  1  1
 18 19  2  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 21 23  1  0
 23 25  1  0
 23 24  2  0
 15  5  1  0
 12  8  1  0
  8 27  1  6
  1 29  1  0
  1 30  1  0
  1 31  1  0
  6 32  1  0
  7 33  1  0
  7 34  1  0
  9 35  1  0
  9 36  1  0
 10 37  1  0
 10 38  1  0
 11 39  1  6
 13 40  1  0
 14 41  1  0
 14 42  1  0
 15 43  1  0
 15 44  1  0
 17 45  1  0
 17 46  1  0
 17 47  1  0
 18 48  1  0
 19 49  1  0
 20 50  1  0
 22 51  1  0
 22 52  1  0
 22 53  1  0
 25 54  1  0
M  END


  Mrv1652309042221552D          

 28 30  0  0  1  0            999 V2000
    5.4198    0.6361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6181    0.4414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0486    1.0384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2808    1.8300    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2469    0.8437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0745    0.0369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3362   -0.3313    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5880    0.0163    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9202    0.7715    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5368    1.5020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7267    1.6578    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3933    0.8180    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6521    0.4557    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8987    1.4701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7236    1.4815    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0998    1.1215    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2836    1.8521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6978    0.9104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2794    1.4955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0769    1.2843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6585    1.8694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4426    2.6656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4560    1.6582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6719    0.8620    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0377    2.2433    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1282    0.2970    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7905   -0.1949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6347   -1.0050    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  9 10  1  0  0  0  0
 11 10  1  6  0  0  0
 11 12  1  0  0  0  0
  8 12  1  0  0  0  0
 12 13  1  6  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
  5 15  1  0  0  0  0
 11 16  1  0  0  0  0
 16 17  1  1  0  0  0
 16 18  1  6  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 16 26  1  0  0  0  0
 26 27  1  0  0  0  0
  8 27  1  0  0  0  0
 27 28  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0200970

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C1=CC[C@]23CC[C@H]([C@@]2(O)CC1)[C@](C)(OC3=O)\C=C\C=C(/C)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C21H26O7/c1-13(16(22)23)5-4-9-19(2)15-8-11-20(18(25)28-19)10-6-14(17(24)27-3)7-12-21(15,20)26/h4-6,9,15,26H,7-8,10-12H2,1-3H3,(H,22,23)/b9-4+,13-5+/t15-,19+,20+,21-/m0/s1

> <INCHI_KEY>
RBXVTEUAOTYIME-GPGKBOPFSA-N

> <FORMULA>
C21H26O7

> <MOLECULAR_WEIGHT>
390.432

> <EXACT_MASS>
390.167853177

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
40.90975020906423

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2E,4E)-5-[(1R,7S,8R,9R)-7-hydroxy-4-(methoxycarbonyl)-9-methyl-11-oxo-10-oxatricyclo[6.3.2.0^{1,7}]tridec-3-en-9-yl]-2-methylpenta-2,4-dienoic acid

> <JCHEM_LOGP>
2.5064813289999996

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
13.803583065825329

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.266633380737903

> <JCHEM_PKA_STRONGEST_BASIC>
-3.3221127688457877

> <JCHEM_POLAR_SURFACE_AREA>
110.13

> <JCHEM_REFRACTIVITY>
101.97999999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2E,4E)-5-[(1R,7S,8R,9R)-7-hydroxy-4-(methoxycarbonyl)-9-methyl-11-oxo-10-oxatricyclo[6.3.2.0^{1,7}]tridec-3-en-9-yl]-2-methylpenta-2,4-dienoic acid

> <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      10.117   1.187   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       8.620   0.824   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       7.557   1.938   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       7.991   3.416   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       6.061   1.575   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.739   0.069   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.361  -0.619   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.964   0.030   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.584   1.440   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.869   2.804   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.356   3.095   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.601   1.527   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       1.217   0.851   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       3.544   2.744   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.084   2.765   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.186   2.093   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.529   3.457   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.302   1.699   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -2.388   2.792   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -3.877   2.397   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -4.963   3.490   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -4.560   4.976   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -6.451   3.095   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -6.854   1.609   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0      -7.537   4.188   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       0.239   0.554   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       1.476  -0.364   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       1.185  -1.876   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   15                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   12   27                                             
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   16                                                  
CONECT   12   11    8   13   14                                             
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14    5                                                       
CONECT   16   11   17   18   26                                             
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23                                                            
CONECT   26   16   27                                                       
CONECT   27   26    8   28                                                  
CONECT   28   27                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   60    0
END

View in JSmol

Synonyms

Value	Source
PSEUDOLARate C	Generator

Chemical Formula

C₂₁H₂₆O₇

Average Mass

390.4320 Da

Monoisotopic Mass

390.16785 Da

IUPAC Name

(2E,4E)-5-[(1R,7S,8R,9R)-7-hydroxy-4-(methoxycarbonyl)-9-methyl-11-oxo-10-oxatricyclo[6.3.2.0^{1,7}]tridec-3-en-9-yl]-2-methylpenta-2,4-dienoic acid

Traditional Name

(2E,4E)-5-[(1R,7S,8R,9R)-7-hydroxy-4-(methoxycarbonyl)-9-methyl-11-oxo-10-oxatricyclo[6.3.2.0^{1,7}]tridec-3-en-9-yl]-2-methylpenta-2,4-dienoic acid

CAS Registry Number

Not Available

SMILES

COC(=O)C1=CC[C@]23CC[C@H]([C@@]2(O)CC1)[C@](C)(OC3=O)\C=C\C=C(/C)C(O)=O

InChI Identifier

InChI=1S/C21H26O7/c1-13(16(22)23)5-4-9-19(2)15-8-11-20(18(25)28-19)10-6-14(17(24)27-3)7-12-21(15,20)26/h4-6,9,15,26H,7-8,10-12H2,1-3H3,(H,22,23)/b9-4+,13-5+/t15-,19+,20+,21-/m0/s1

InChI Key

RBXVTEUAOTYIME-GPGKBOPFSA-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

Species Name	Source	Reference
Larix kaempferi	LOTUS Database	35616633
Pseudolarix amabilis	LOTUS Database	35616633

Chemical Taxonomy

Description

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

Diterpene lactone
Prenyldaucane diterpenoid
Diterpenoid
Tricarboxylic acid or derivatives
Caprolactone
Delta valerolactone
Oxepane
Delta_valerolactone
Oxane
Cyclic alcohol
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Methyl ester
Tertiary alcohol
Carboxylic acid ester
Lactone
Carboxylic acid derivative
Carboxylic acid
Oxacycle
Organoheterocyclic compound
Organic oxide
Alcohol
Hydrocarbon derivative
Organic oxygen compound
Carbonyl group
Organooxygen compound
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	2.51	ChemAxon
pKa (Strongest Acidic)	4.27	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	110.13 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	101.98 m³·mol⁻¹	ChemAxon
Polarizability	40.91 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

C00049280

Chemspider ID

4944957

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

6440704

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

He S, Li S, Yang J, Ye H, Zhong S, Song H, Zhang Y, Peng C, Peng A, Chen L: Application of step-wise gradient high-performance counter-current chromatography for rapid preparative separation and purification of diterpene components from Pseudolarix kaempferi Gordon. J Chromatogr A. 2012 Apr 27;1235:34-8. doi: 10.1016/j.chroma.2012.01.040. Epub 2012 Feb 9. [PubMed:22424731 ]
Liu P, Guo HZ, Sun JH, Xu M, Guo H, Sun SF, Guo DA: [Metabolic pathway and metabolites of total diterpene acid isolated from Pseudolarix kaempferi]. Yao Xue Xue Bao. 2014 Aug;49(8):1169-74. [PubMed:25322560 ]
Ye X, Tang M, Chen L, Peng A, Ma L, Ye H: Rapid separation and identification of major constituents in Pseudolarix kaempferi by ultra-performance liquid chromatography coupled with electrospray and quadrupole time-of-flight tandem mass spectrometry. Rapid Commun Mass Spectrom. 2009 Dec;23(24):3954-62. doi: 10.1002/rcm.4336. [PubMed:19918938 ]
LOTUS database [Link]

Showing NP-Card for (2e,4e)-5-[(1r,7s,8r,9r)-7-hydroxy-4-(methoxycarbonyl)-9-methyl-11-oxo-10-oxatricyclo[6.3.2.0¹,⁷]tridec-3-en-9-yl]-2-methylpenta-2,4-dienoic acid (NP0200970)

MOL for NP0200970 ((2e,4e)-5-[(1r,7s,8r,9r)-7-hydroxy-4-(methoxycarbonyl)-9-methyl-11-oxo-10-oxatricyclo[6.3.2.0¹,⁷]tridec-3-en-9-yl]-2-methylpenta-2,4-dienoic acid)

3D MOL for NP0200970 ((2e,4e)-5-[(1r,7s,8r,9r)-7-hydroxy-4-(methoxycarbonyl)-9-methyl-11-oxo-10-oxatricyclo[6.3.2.0¹,⁷]tridec-3-en-9-yl]-2-methylpenta-2,4-dienoic acid)

3D SDF for NP0200970 ((2e,4e)-5-[(1r,7s,8r,9r)-7-hydroxy-4-(methoxycarbonyl)-9-methyl-11-oxo-10-oxatricyclo[6.3.2.0¹,⁷]tridec-3-en-9-yl]-2-methylpenta-2,4-dienoic acid)

3D-SDF for NP0200970 ((2e,4e)-5-[(1r,7s,8r,9r)-7-hydroxy-4-(methoxycarbonyl)-9-methyl-11-oxo-10-oxatricyclo[6.3.2.0¹,⁷]tridec-3-en-9-yl]-2-methylpenta-2,4-dienoic acid)

PDB for NP0200970 ((2e,4e)-5-[(1r,7s,8r,9r)-7-hydroxy-4-(methoxycarbonyl)-9-methyl-11-oxo-10-oxatricyclo[6.3.2.0¹,⁷]tridec-3-en-9-yl]-2-methylpenta-2,4-dienoic acid)

3D PDB for NP0200970 ((2e,4e)-5-[(1r,7s,8r,9r)-7-hydroxy-4-(methoxycarbonyl)-9-methyl-11-oxo-10-oxatricyclo[6.3.2.0¹,⁷]tridec-3-en-9-yl]-2-methylpenta-2,4-dienoic acid)

SMILES for NP0200970 ((2e,4e)-5-[(1r,7s,8r,9r)-7-hydroxy-4-(methoxycarbonyl)-9-methyl-11-oxo-10-oxatricyclo[6.3.2.0¹,⁷]tridec-3-en-9-yl]-2-methylpenta-2,4-dienoic acid)

INCHI for NP0200970 ((2e,4e)-5-[(1r,7s,8r,9r)-7-hydroxy-4-(methoxycarbonyl)-9-methyl-11-oxo-10-oxatricyclo[6.3.2.0¹,⁷]tridec-3-en-9-yl]-2-methylpenta-2,4-dienoic acid)

Structure for NP0200970 ((2e,4e)-5-[(1r,7s,8r,9r)-7-hydroxy-4-(methoxycarbonyl)-9-methyl-11-oxo-10-oxatricyclo[6.3.2.0¹,⁷]tridec-3-en-9-yl]-2-methylpenta-2,4-dienoic acid)

3D Structure for NP0200970 ((2e,4e)-5-[(1r,7s,8r,9r)-7-hydroxy-4-(methoxycarbonyl)-9-methyl-11-oxo-10-oxatricyclo[6.3.2.0¹,⁷]tridec-3-en-9-yl]-2-methylpenta-2,4-dienoic acid)