NP-MRD: Showing NP-Card for (1r,2s,9z,11s,18r)-11-hydroxy-2-[(1e,3e,5s)-5-hydroxy-4-methyl-6-methylidenedeca-1,3-dien-1-yl]-10,14-dimethyl-6-methylidene-3,21-dioxabicyclo[16.2.1]henicos-9-ene-4,13,16-trione (NP0236537)

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Record Information

Version

2.0

Created at

2022-09-06 19:27:39 UTC

Updated at

2022-09-06 19:27:39 UTC

NP-MRD ID

NP0236537

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2s,9z,11s,18r)-11-hydroxy-2-[(1e,3e,5s)-5-hydroxy-4-methyl-6-methylidenedeca-1,3-dien-1-yl]-10,14-dimethyl-6-methylidene-3,21-dioxabicyclo[16.2.1]henicos-9-ene-4,13,16-trione

Description

Amphidinolide U belongs to the class of organic compounds known as macrolides and analogues. These are organic compounds containing a lactone ring of at least twelve members. Based on a literature review very few articles have been published on Amphidinolide U.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309062221272D          

 41 42  0  0  1  0            999 V2000
   -0.0000   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2297   -4.5330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0366   -4.7045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4491   -3.9900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2696   -3.9038    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8971   -3.3770    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6607   -3.0646    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8070    0.1715    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2195   -0.5429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0000   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.0625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8579   -5.7750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    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  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  6  0  0  0
  8 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
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  6  0  0  0
 19 23  1  1  0  0  0
 22 24  1  0  0  0  0
 24 25  1  6  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 30 31  1  6  0  0  0
 30 32  1  0  0  0  0
 32 33  2  0  0  0  0
 32 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 24 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  2  0  0  0  0
 39 41  1  0  0  0  0
  2 41  1  0  0  0  0
M  END


  Mrv1652309062221272D          

 41 42  0  0  1  0            999 V2000
   -0.0000   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2297   -4.5330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0366   -4.7045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4491   -3.9900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2696   -3.9038    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8971   -3.3770    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6607   -3.0646    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8070    0.1715    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2195   -0.5429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0000   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.0625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8579   -5.7750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    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  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  6  0  0  0
  8 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
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  6  0  0  0
 19 23  1  1  0  0  0
 22 24  1  0  0  0  0
 24 25  1  6  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 30 31  1  6  0  0  0
 30 32  1  0  0  0  0
 32 33  2  0  0  0  0
 32 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 24 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  2  0  0  0  0
 39 41  1  0  0  0  0
  2 41  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0236537

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCC(=C)[C@H](O)C(\C)=C\C=C\[C@@H]1OC(=O)CC(=C)CC\C=C(C)/[C@@H](O)CC(=O)C(C)CC(=O)C[C@H]2CC[C@H]1O2

> <INCHI_IDENTIFIER>
InChI=1S/C34H50O7/c1-7-8-12-24(4)34(39)25(5)14-10-15-31-32-17-16-28(40-32)20-27(35)19-26(6)30(37)21-29(36)23(3)13-9-11-22(2)18-33(38)41-31/h10,13-15,26,28-29,31-32,34,36,39H,2,4,7-9,11-12,16-21H2,1,3,5-6H3/b15-10+,23-13-,25-14+/t26?,28-,29+,31+,32-,34+/m1/s1

> <INCHI_KEY>
BJKVTFDJZUKVOD-DJFFXAFJSA-N

> <FORMULA>
C34H50O7

> <MOLECULAR_WEIGHT>
570.767

> <EXACT_MASS>
570.35565395

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
91

> <JCHEM_AVERAGE_POLARIZABILITY>
65.29790275998172

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2S,9Z,11S,18R)-11-hydroxy-2-[(1E,3E,5S)-5-hydroxy-4-methyl-6-methylidenedeca-1,3-dien-1-yl]-10,14-dimethyl-6-methylidene-3,21-dioxabicyclo[16.2.1]henicos-9-ene-4,13,16-trione

> <JCHEM_LOGP>
5.640072136333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
17.24002527444017

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.445446445724262

> <JCHEM_PKA_STRONGEST_BASIC>
-1.4076612857864053

> <JCHEM_POLAR_SURFACE_AREA>
110.13

> <JCHEM_REFRACTIVITY>
163.43310000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,9Z,11S,18R)-11-hydroxy-2-[(1E,3E,5S)-5-hydroxy-4-methyl-6-methylidenedeca-1,3-dien-1-yl]-10,14-dimethyl-6-methylidene-3,21-dioxabicyclo[16.2.1]henicos-9-ene-4,13,16-trione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0      -0.000  -9.240   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.334  -8.470   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.667  -9.240   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.162  -8.462   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -5.668  -8.782   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -6.438  -7.448   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -7.970  -7.287   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -5.408  -6.304   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -6.833  -5.721   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -4.001  -3.850   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -2.667  -4.620   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -5.335  -1.540   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.667  -1.540   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -4.001   0.770   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -1.334   0.770   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.000  -0.000   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.506   0.320   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.276  -1.013   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -0.000  -1.540   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       1.334  -3.850   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.667  -6.160   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.001  -8.470   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.667  -9.240   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.335  -9.240   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       5.335 -10.780   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       6.668  -8.470   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       8.002  -9.240   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       9.336  -8.470   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      10.669  -9.240   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      12.003  -8.470   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      -0.000  -4.620   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0      -0.000  -6.160   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       1.334  -6.930   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      -1.334  -6.930   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   41                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20   23                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22   19                                                       
CONECT   24   22   25   38                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36                                                            
CONECT   38   24   39                                                       
CONECT   39   38   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39    2                                                       
MASTER        0    0    0    0    0    0    0    0   41    0   84    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₄H₅₀O₇

Average Mass

570.7670 Da

Monoisotopic Mass

570.35565 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CCCCC(=C)[C@H](O)C(\C)=C\C=C\[C@@H]1OC(=O)CC(=C)CC\C=C(C)/[C@@H](O)CC(=O)C(C)CC(=O)C[C@H]2CC[C@H]1O2

InChI Identifier

InChI=1S/C34H50O7/c1-7-8-12-24(4)34(39)25(5)14-10-15-31-32-17-16-28(40-32)20-27(35)19-26(6)30(37)21-29(36)23(3)13-9-11-22(2)18-33(38)41-31/h10,13-15,26,28-29,31-32,34,36,39H,2,4,7-9,11-12,16-21H2,1,3,5-6H3/b15-10+,23-13-,25-14+/t26?,28-,29+,31+,32-,34+/m1/s1

InChI Key

BJKVTFDJZUKVOD-DJFFXAFJSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as macrolides and analogues. These are organic compounds containing a lactone ring of at least twelve members.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Macrolides and analogues

Sub Class

Not Available

Direct Parent

Macrolides and analogues

Alternative Parents

Substituents

Macrolide
Fatty alcohol
Fatty acyl
Tetrahydrofuran
Cyclic ketone
Secondary alcohol
Lactone
Ketone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Ether
Dialkyl ether
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
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

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

74104932

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

100993431

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,2s,9z,11s,18r)-11-hydroxy-2-[(1e,3e,5s)-5-hydroxy-4-methyl-6-methylidenedeca-1,3-dien-1-yl]-10,14-dimethyl-6-methylidene-3,21-dioxabicyclo[16.2.1]henicos-9-ene-4,13,16-trione (NP0236537)

MOL for NP0236537 ((1r,2s,9z,11s,18r)-11-hydroxy-2-[(1e,3e,5s)-5-hydroxy-4-methyl-6-methylidenedeca-1,3-dien-1-yl]-10,14-dimethyl-6-methylidene-3,21-dioxabicyclo[16.2.1]henicos-9-ene-4,13,16-trione)

3D MOL for NP0236537 ((1r,2s,9z,11s,18r)-11-hydroxy-2-[(1e,3e,5s)-5-hydroxy-4-methyl-6-methylidenedeca-1,3-dien-1-yl]-10,14-dimethyl-6-methylidene-3,21-dioxabicyclo[16.2.1]henicos-9-ene-4,13,16-trione)

3D SDF for NP0236537 ((1r,2s,9z,11s,18r)-11-hydroxy-2-[(1e,3e,5s)-5-hydroxy-4-methyl-6-methylidenedeca-1,3-dien-1-yl]-10,14-dimethyl-6-methylidene-3,21-dioxabicyclo[16.2.1]henicos-9-ene-4,13,16-trione)

3D-SDF for NP0236537 ((1r,2s,9z,11s,18r)-11-hydroxy-2-[(1e,3e,5s)-5-hydroxy-4-methyl-6-methylidenedeca-1,3-dien-1-yl]-10,14-dimethyl-6-methylidene-3,21-dioxabicyclo[16.2.1]henicos-9-ene-4,13,16-trione)

PDB for NP0236537 ((1r,2s,9z,11s,18r)-11-hydroxy-2-[(1e,3e,5s)-5-hydroxy-4-methyl-6-methylidenedeca-1,3-dien-1-yl]-10,14-dimethyl-6-methylidene-3,21-dioxabicyclo[16.2.1]henicos-9-ene-4,13,16-trione)

3D PDB for NP0236537 ((1r,2s,9z,11s,18r)-11-hydroxy-2-[(1e,3e,5s)-5-hydroxy-4-methyl-6-methylidenedeca-1,3-dien-1-yl]-10,14-dimethyl-6-methylidene-3,21-dioxabicyclo[16.2.1]henicos-9-ene-4,13,16-trione)

SMILES for NP0236537 ((1r,2s,9z,11s,18r)-11-hydroxy-2-[(1e,3e,5s)-5-hydroxy-4-methyl-6-methylidenedeca-1,3-dien-1-yl]-10,14-dimethyl-6-methylidene-3,21-dioxabicyclo[16.2.1]henicos-9-ene-4,13,16-trione)

INCHI for NP0236537 ((1r,2s,9z,11s,18r)-11-hydroxy-2-[(1e,3e,5s)-5-hydroxy-4-methyl-6-methylidenedeca-1,3-dien-1-yl]-10,14-dimethyl-6-methylidene-3,21-dioxabicyclo[16.2.1]henicos-9-ene-4,13,16-trione)

Structure for NP0236537 ((1r,2s,9z,11s,18r)-11-hydroxy-2-[(1e,3e,5s)-5-hydroxy-4-methyl-6-methylidenedeca-1,3-dien-1-yl]-10,14-dimethyl-6-methylidene-3,21-dioxabicyclo[16.2.1]henicos-9-ene-4,13,16-trione)

3D Structure for NP0236537 ((1r,2s,9z,11s,18r)-11-hydroxy-2-[(1e,3e,5s)-5-hydroxy-4-methyl-6-methylidenedeca-1,3-dien-1-yl]-10,14-dimethyl-6-methylidene-3,21-dioxabicyclo[16.2.1]henicos-9-ene-4,13,16-trione)