NP-MRD: Showing NP-Card for 17-Acetoxygrindelic acid (NP0065492)

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Record Information

Version

2.0

Created at

2022-04-28 09:42:52 UTC

Updated at

2022-04-28 09:42:52 UTC

NP-MRD ID

NP0065492

Secondary Accession Numbers

None

Natural Product Identification

Common Name

17-Acetoxygrindelic acid

Description

2-[(1S,4aS,5'S,8aS)-2-[(acetyloxy)methyl]-5,5,5',8a-tetramethyl-4a,5,6,7,8,8a-hexahydro-4H-spiro[naphthalene-1,2'-oxolane]-5'-yl]acetic acid belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. 17-Acetoxygrindelic acid is found in Chrysoma pauciflosculosa, Grindelia hirsutula and Grindelia stricta. Based on a literature review very few articles have been published on 2-[(1S,4aS,5'S,8aS)-2-[(acetyloxy)methyl]-5,5,5',8a-tetramethyl-4a,5,6,7,8,8a-hexahydro-4H-spiro[naphthalene-1,2'-oxolane]-5'-yl]acetic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282211422D          

 27 29  0  0  1  0            999 V2000
    1.6704    0.3724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2728    0.9361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0857    1.7396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2964    1.9794    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6940    1.4157    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8811    0.6122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0954    1.6554    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2824    2.4590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3199    3.0227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1093    2.7829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0718    2.6987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2589    3.5023    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0482    3.7420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2353    4.5455    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6506    3.1783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0066    0.8368    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7404    0.4868    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3042    1.0891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9055    1.8114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4786   -0.2956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2740   -0.1425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0857    0.0050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6193   -0.6243    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3639    0.7817    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2953    0.6934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3529    2.5202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8822    1.9546    0.0000 C   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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
  4 10  1  1  0  0  0
  8 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
  7 16  1  6  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
  7 19  1  0  0  0  0
 17 20  1  1  0  0  0
 17 21  1  6  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
  5 25  1  1  0  0  0
  3 26  1  0  0  0  0
  3 27  1  0  0  0  0
M  END

     RDKit          3D

 61 63  0  0  0  0  0  0  0  0999 V2000
   -2.3563    4.4834    2.1796 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0255    3.6866    0.9735 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0121    4.0402    0.3059 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7341    2.5924    0.5240 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4104    1.8411   -0.6206 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0842    1.1689   -0.5765 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2256    1.5303   -1.5256 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1442    1.0229   -1.7075 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4446   -0.0531   -0.7261 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9131   -0.3878   -0.7212 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1836   -1.0870   -2.0653 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8247    0.8125   -0.7164 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3204   -1.3107    0.3546 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2322   -1.7313    1.2786 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2943   -0.6544    1.7064 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8317    0.2525    0.5900 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0506    1.6788    1.0490 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6922    0.1228    0.4007 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4288    0.0917    1.6697 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0728   -1.2770    1.7222 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7279   -1.8870    0.4101 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1001   -3.2778    0.5772 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9805   -2.1106   -0.4337 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6693   -2.7082   -1.7343 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3859   -3.9243   -1.8794 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6808   -1.9163   -2.8733 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8528   -1.0943   -0.2500 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2118    5.5616    1.8741 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6491    4.3221    3.0037 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4052    4.3882    2.4907 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4742    2.5778   -1.4774 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2250    1.1106   -0.8709 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5453    2.2871   -2.2688 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8973    1.8424   -1.7151 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2593    0.5575   -2.7328 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9418   -0.9876   -1.1235 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0732   -1.7278   -1.9745 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3594   -0.2719   -2.8246 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2719   -1.6449   -2.3722 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8660    0.3766   -0.6123 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8564    1.3471   -1.6778 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7206    1.4595    0.1711 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1661   -0.8853    0.9735 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7724   -2.2674   -0.0470 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6578   -2.6115    0.9030 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7298   -2.0959    2.2298 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4797   -1.1415    2.2647 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8418   -0.0422    2.4700 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2151    2.0204    1.7091 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1968    2.4057    0.2582 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9400    1.6694    1.7480 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2706    0.8111    1.7263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8244    0.3207    2.5859 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7473   -1.9057    2.5472 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1904   -1.2124    1.7826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3552   -3.3779   -0.2342 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5523   -3.2851    1.5346 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8792   -4.0671    0.5230 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5869   -1.1938   -0.4797 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5828   -2.8571    0.1582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5458   -1.3870   -3.0316 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  6
 10 12  1  0
 10 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  1
 16 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  1
 21 23  1  0
 23 24  1  0
 24 26  1  0
 24 25  2  0
 21 27  1  0
 18  6  1  0
 18 27  1  6
 16  9  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  5 31  1  0
  5 32  1  0
  7 33  1  0
  8 34  1  0
  8 35  1  0
  9 36  1  6
 11 37  1  0
 11 38  1  0
 11 39  1  0
 12 40  1  0
 12 41  1  0
 12 42  1  0
 13 43  1  0
 13 44  1  0
 14 45  1  0
 14 46  1  0
 15 47  1  0
 15 48  1  0
 17 49  1  0
 17 50  1  0
 17 51  1  0
 19 52  1  0
 19 53  1  0
 20 54  1  0
 20 55  1  0
 22 56  1  0
 22 57  1  0
 22 58  1  0
 23 59  1  0
 23 60  1  0
 26 61  1  0
M  END


  Mrv1652304282211422D          

 27 29  0  0  1  0            999 V2000
    1.6704    0.3724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2728    0.9361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0857    1.7396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2964    1.9794    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6940    1.4157    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8811    0.6122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0954    1.6554    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2824    2.4590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3199    3.0227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1093    2.7829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0718    2.6987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2589    3.5023    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0482    3.7420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2353    4.5455    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6506    3.1783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0066    0.8368    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7404    0.4868    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3042    1.0891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9055    1.8114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4786   -0.2956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2740   -0.1425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0857    0.0050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6193   -0.6243    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3639    0.7817    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2953    0.6934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3529    2.5202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8822    1.9546    0.0000 C   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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
  4 10  1  1  0  0  0
  8 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
  7 16  1  6  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
  7 19  1  0  0  0  0
 17 20  1  1  0  0  0
 17 21  1  6  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
  5 25  1  1  0  0  0
  3 26  1  0  0  0  0
  3 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0065492

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OCC1=CC[C@H]2C(C)(C)CCC[C@]2(C)[C@@]11CC[C@@](C)(CC(O)=O)O1

> <INCHI_IDENTIFIER>
InChI=1S/C22H34O5/c1-15(23)26-14-16-7-8-17-19(2,3)9-6-10-21(17,5)22(16)12-11-20(4,27-22)13-18(24)25/h7,17H,6,8-14H2,1-5H3,(H,24,25)/t17-,20-,21-,22+/m0/s1

> <INCHI_KEY>
CUIYYSCXUREZKH-AGOPTVSRSA-N

> <FORMULA>
C22H34O5

> <MOLECULAR_WEIGHT>
378.509

> <EXACT_MASS>
378.240624195

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
61

> <JCHEM_AVERAGE_POLARIZABILITY>
42.117127326232165

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-[(1S,4aS,5'S,8aS)-2-[(acetyloxy)methyl]-5,5,5',8a-tetramethyl-4a,5,6,7,8,8a-hexahydro-4H-spiro[naphthalene-1,2'-oxolane]-5'-yl]acetic acid

> <ALOGPS_LOGP>
4.59

> <JCHEM_LOGP>
3.548897674999998

> <ALOGPS_LOGS>
-4.85

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.489661086702973

> <JCHEM_PKA_STRONGEST_BASIC>
-4.244782581452013

> <JCHEM_POLAR_SURFACE_AREA>
72.83

> <JCHEM_REFRACTIVITY>
102.56229999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.29e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,4aS,5'S,8aS)-2-[(acetyloxy)methyl]-5,5,5',8a-tetramethyl-4a,6,7,8-tetrahydro-4H-spiro[naphthalene-1,2'-oxolane]-5'-ylacetic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       3.118   0.695   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.243   1.747   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.893   3.247   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.420   3.695   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.295   2.643   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.645   1.143   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.178   3.090   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.527   4.590   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.597   5.642   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.071   5.195   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.001   5.038   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -2.350   6.538   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -3.823   6.985   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -4.173   8.485   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -4.948   5.933   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       0.012   1.562   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -1.382   0.909   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -2.434   2.033   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.690   3.381   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.893  -0.552   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -2.378  -0.266   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -3.893   0.009   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -4.889  -1.165   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0      -4.413   1.459   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       0.551   1.294   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.392   4.704   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.380   3.649   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4   26   27                                             
CONECT    4    3    5   10                                                  
CONECT    5    4    6    7   25                                             
CONECT    6    5    1                                                       
CONECT    7    5    8   16   19                                             
CONECT    8    7    9   11                                                  
CONECT    9    8   10                                                       
CONECT   10    9    4                                                       
CONECT   11    8   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13                                                            
CONECT   16    7   17                                                       
CONECT   17   16   18   20   21                                             
CONECT   18   17   19                                                       
CONECT   19   18    7                                                       
CONECT   20   17                                                            
CONECT   21   17   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25    5                                                            
CONECT   26    3                                                            
CONECT   27    3                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   58    0
END

View in JSmol

Synonyms

Value	Source
2-[(1S,4AS,5's,8as)-2-[(acetyloxy)methyl]-5,5,5',8a-tetramethyl-4a,5,6,7,8,8a-hexahydro-4H-spiro[naphthalene-1,2'-oxolane]-5'-yl]acetate	Generator

Chemical Formula

C₂₂H₃₄O₅

Average Mass

378.5090 Da

Monoisotopic Mass

378.24062 Da

IUPAC Name

2-[(1S,4aS,5'S,8aS)-2-[(acetyloxy)methyl]-5,5,5',8a-tetramethyl-4a,5,6,7,8,8a-hexahydro-4H-spiro[naphthalene-1,2'-oxolane]-5'-yl]acetic acid

Traditional Name

(1S,4aS,5'S,8aS)-2-[(acetyloxy)methyl]-5,5,5',8a-tetramethyl-4a,6,7,8-tetrahydro-4H-spiro[naphthalene-1,2'-oxolane]-5'-ylacetic acid

CAS Registry Number

Not Available

SMILES

CC(=O)OCC1=CC[C@H]2C(C)(C)CCC[C@]2(C)[C@@]11CC[C@@](C)(CC(O)=O)O1

InChI Identifier

InChI=1S/C22H34O5/c1-15(23)26-14-16-7-8-17-19(2,3)9-6-10-21(17,5)22(16)12-11-20(4,27-22)13-18(24)25/h7,17H,6,8-14H2,1-5H3,(H,24,25)/t17-,20-,21-,22+/m0/s1

InChI Key

CUIYYSCXUREZKH-AGOPTVSRSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Chrysoma pauciflosculosa	LOTUS Database	35616633
Grindelia hirsutula	LOTUS Database	35616633
Grindelia stricta	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Diterpenoids

Alternative Parents

Substituents

Diterpenoid
Grindelane diterpenoid
Dicarboxylic acid or derivatives
Tetrahydrofuran
Carboxylic acid ester
Carboxylic acid derivative
Carboxylic acid
Dialkyl ether
Oxacycle
Ether
Organoheterocyclic compound
Organic oxide
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	4.59	ALOGPS
logP	3.55	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	4.49	ChemAxon
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	72.83 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	102.56 m³·mol⁻¹	ChemAxon
Polarizability	42.12 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

26452079

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 17-Acetoxygrindelic acid (NP0065492)

MOL for NP0065492 (17-Acetoxygrindelic acid)

3D MOL for NP0065492 (17-Acetoxygrindelic acid)

3D SDF for NP0065492 (17-Acetoxygrindelic acid)

3D-SDF for NP0065492 (17-Acetoxygrindelic acid)

PDB for NP0065492 (17-Acetoxygrindelic acid)

3D PDB for NP0065492 (17-Acetoxygrindelic acid)

SMILES for NP0065492 (17-Acetoxygrindelic acid)

INCHI for NP0065492 (17-Acetoxygrindelic acid)

Structure for NP0065492 (17-Acetoxygrindelic acid)

3D Structure for NP0065492 (17-Acetoxygrindelic acid)