NP-MRD: Showing NP-Card for Clavulone II (NP0078987)

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Record Information

Version

2.0

Created at

2022-04-29 00:03:46 UTC

Updated at

2022-04-29 00:03:46 UTC

NP-MRD ID

NP0078987

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Clavulone II

Description

Clavulone III belongs to the class of organic compounds known as clavulones and derivatives. These are ester derivatives of prostanoids. Thus, clavulone III is considered to be an eicosanoid. Clavulone II is found in Clavularia viridis. Based on a literature review very few articles have been published on clavulone III.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292202032D          

 32 32  0  0  1  0            999 V2000
    9.4389    4.5824    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2185    4.8524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7162    4.1945    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.2443    3.5178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5143    2.7382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9742    2.1146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1641    2.2705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6240    1.6468    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.8139    1.8028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2738    1.1791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4636    1.3350    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1936    2.1146    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9235    0.7114    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1134    0.8673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8940    0.8673    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.7042    0.7114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2443    1.3350    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.9742   -0.0682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4549    3.7575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7969    3.2598    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4270    4.6133    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4197    5.4382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7016    5.8444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9908    5.4256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2727    5.8318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5619    5.4130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8438    5.8191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1330    5.4003    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4426    3.8034    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.1445    4.2370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1199    5.0616    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.8709    3.8460    0.0000 C   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
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
  8 15  1  6  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
  4 19  1  0  0  0  0
  1 19  1  0  0  0  0
 19 20  2  0  0  0  0
  3 21  1  1  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
  3 29  1  6  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
M  END

     RDKit          3D

 66 66  0  0  0  0  0  0  0  0999 V2000
   -5.7866    1.4252    3.3873 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9497    2.6352    2.5456 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3434    2.7168    1.2192 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8625    2.7046    1.1416 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2635    1.4532    1.6437 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8221    1.2942    1.5892 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.4503    3.0065   -2.9036 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2674    2.0283   -1.1066 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9338   -1.2317   -2.1813 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5941   -2.3604   -2.6677 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1728   -2.6057   -2.4168 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6104   -3.6910   -2.8143 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6548   -1.4628   -1.7083 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6140   -1.2577   -1.4162 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6163   -2.2809   -1.6468 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7880   -2.3150   -1.5037 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2104   -2.2415   -1.2886 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5638   -0.8181   -0.8012 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8870   -0.4487    0.4661 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2957    0.9439    0.8364 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0490    1.5679    0.0687 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8459    1.5191    2.0055 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2047    2.8159    2.3922 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8203   -3.1493   -0.4411 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9129   -3.9309   -0.7757 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5356   -4.8847    0.0938 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3188   -3.6980   -2.0028 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7849    1.1852    3.9216 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.1308    1.6499    4.2840 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0869    2.7662    2.3810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7059    3.5511    3.1943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6602    1.7489    0.6631 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7991    3.5247    0.5709 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6100    2.7677    0.0197 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4066    3.6276    1.5941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4226    1.5578    2.8203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8237    0.5814    1.3393 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1435    1.8989    2.1261 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2187    0.1822    0.8103 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2997   -1.5630    0.3377 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2230   -0.1301   -0.0911 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0314    3.7895   -2.3461 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5272    3.4860   -3.2847 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1083    2.6372   -3.6992 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9032   -0.7694   -2.2077 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2403   -3.0865   -3.2144 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9306   -0.3272   -1.0132 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1360   -3.1998   -2.0500 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8742   -3.6110   -1.8615 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7347   -2.2762   -2.2916 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3791   -0.1373   -1.6280 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6403   -0.8871   -0.6269 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7905   -0.4412    0.4133 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1817   -1.1366    1.2741 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9632    3.2875    1.7313 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2895    3.4222    2.4957 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6398    2.7640    3.4381 H   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0
  2  3  1  0
  3  4  1  0
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  9 14  1  0
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 18  9  1  0
  1 33  1  0
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 14 51  1  0
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 28 61  1  0
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 28 63  1  0
 31 64  1  0
 31 65  1  0
 31 66  1  0
M  END


  Mrv1652304292202032D          

 32 32  0  0  1  0            999 V2000
    9.4389    4.5824    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2185    4.8524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7162    4.1945    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.2443    3.5178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5143    2.7382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9742    2.1146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1641    2.2705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6240    1.6468    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.8139    1.8028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2738    1.1791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4636    1.3350    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1936    2.1146    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9235    0.7114    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1134    0.8673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8940    0.8673    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    9.9742   -0.0682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4549    3.7575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7969    3.2598    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4270    4.6133    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4197    5.4382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7016    5.8444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9908    5.4256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2727    5.8318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5619    5.4130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8438    5.8191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1330    5.4003    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4426    3.8034    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.1445    4.2370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1199    5.0616    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.8709    3.8460    0.0000 C   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
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
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 16 18  1  0  0  0  0
  4 19  1  0  0  0  0
  1 19  1  0  0  0  0
 19 20  2  0  0  0  0
  3 21  1  1  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
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  3 29  1  6  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0078987

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCC\C=C/C[C@]1(OC(C)=O)C=CC(=O)\C1=C/C=C/[C@@H](CCC(=O)OC)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C25H34O7/c1-5-6-7-8-9-10-17-25(32-20(3)27)18-16-23(28)22(25)13-11-12-21(31-19(2)26)14-15-24(29)30-4/h9-13,16,18,21H,5-8,14-15,17H2,1-4H3/b10-9-,12-11+,22-13+/t21-,25-/m0/s1

> <INCHI_KEY>
QXSYLWTUKSQQCP-XJHMFZNOSA-N

> <FORMULA>
C25H34O7

> <MOLECULAR_WEIGHT>
446.54

> <EXACT_MASS>
446.230453435

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
66

> <JCHEM_AVERAGE_POLARIZABILITY>
49.755336183256965

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (4R,5E)-4-(acetyloxy)-7-[(1Z,2S)-2-(acetyloxy)-2-[(2Z)-oct-2-en-1-yl]-5-oxocyclopent-3-en-1-ylidene]hept-5-enoate

> <ALOGPS_LOGP>
4.60

> <JCHEM_LOGP>
4.251091236

> <ALOGPS_LOGS>
-5.63

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-6.500635975770406

> <JCHEM_POLAR_SURFACE_AREA>
95.97

> <JCHEM_REFRACTIVITY>
124.41199999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
16

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.05e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
clavulone III

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0      17.619   8.554   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      19.074   9.058   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      20.004   7.830   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      19.123   6.567   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      19.627   5.111   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      18.619   3.947   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      17.106   4.238   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      16.098   3.074   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      14.586   3.365   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      13.578   2.201   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      12.065   2.492   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      11.561   3.947   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0      11.057   1.328   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       9.545   1.619   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      16.602   1.619   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      18.114   1.328   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      19.123   2.492   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      18.619  -0.127   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      17.649   7.014   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      16.421   6.085   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      21.330   8.611   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      21.317  10.151   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      19.976  10.910   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      18.650  10.128   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      17.309  10.886   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      15.982  10.104   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      14.642  10.862   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      13.315  10.081   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      21.360   7.100   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      22.670   7.909   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      22.624   9.448   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      24.026   7.179   0.000  0.00  0.00           C+0
CONECT    1    2   19                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4   21   29                                             
CONECT    4    3    5   19                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   15                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13                                                            
CONECT   15    8   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19    4    1   20                                                  
CONECT   20   19                                                            
CONECT   21    3   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27                                                            
CONECT   29    3   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₃₄O₇

Average Mass

446.5400 Da

Monoisotopic Mass

446.23045 Da

IUPAC Name

methyl (4R,5E)-4-(acetyloxy)-7-[(1Z,2S)-2-(acetyloxy)-2-[(2Z)-oct-2-en-1-yl]-5-oxocyclopent-3-en-1-ylidene]hept-5-enoate

Traditional Name

clavulone III

CAS Registry Number

Not Available

SMILES

CCCCC\C=C/C[C@]1(OC(C)=O)C=CC(=O)\C1=C/C=C/[C@@H](CCC(=O)OC)OC(C)=O

InChI Identifier

InChI=1S/C25H34O7/c1-5-6-7-8-9-10-17-25(32-20(3)27)18-16-23(28)22(25)13-11-12-21(31-19(2)26)14-15-24(29)30-4/h9-13,16,18,21H,5-8,14-15,17H2,1-4H3/b10-9-,12-11+,22-13+/t21-,25-/m0/s1

InChI Key

QXSYLWTUKSQQCP-XJHMFZNOSA-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
Clavularia viridis	-	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as clavulones and derivatives. These are ester derivatives of prostanoids.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Eicosanoids

Direct Parent

Clavulones and derivatives

Alternative Parents

Substituents

Clavulone
Clavulone-skeleton
Fatty alcohol ester
Tricarboxylic acid or derivatives
Fatty acid ester
Fatty acid methyl ester
Methyl ester
Cyclic ketone
Ketone
Carboxylic acid ester
Carboxylic acid derivative
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Carbonyl group
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic homomonocyclic compounds

External Descriptors

acetate ester (CHEBI:34644 )
methyl ester (CHEBI:34644 )
clavulone (CHEBI:34644 )
Clavulones and derivatives (C13813 )
Clavulones and derivatives (LMFA03120003 )

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	4.6	ALOGPS
logP	4.25	ChemAxon
logS	-5.6	ALOGPS
pKa (Strongest Basic)	-6.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	95.97 Å²	ChemAxon
Rotatable Bond Count	16	ChemAxon
Refractivity	124.41 m³·mol⁻¹	ChemAxon
Polarizability	49.76 Å³	ChemAxon
Number of Rings	1	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

C00043398

Chemspider ID

4445438

KEGG Compound ID

C13813

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5282266

PDB ID

Not Available

ChEBI ID

34644

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Clavulone II (NP0078987)

MOL for NP0078987 (Clavulone II)

3D MOL for NP0078987 (Clavulone II)

3D SDF for NP0078987 (Clavulone II)

3D-SDF for NP0078987 (Clavulone II)

PDB for NP0078987 (Clavulone II)

3D PDB for NP0078987 (Clavulone II)

SMILES for NP0078987 (Clavulone II)

INCHI for NP0078987 (Clavulone II)

Structure for NP0078987 (Clavulone II)

3D Structure for NP0078987 (Clavulone II)