NP-MRD: Showing NP-Card for (1s,5s,6r,7s)-1,5-dimethoxy-7-(7-methoxy-2h-1,3-benzodioxol-5-yl)-6-methyl-3-(prop-2-en-1-yl)bicyclo[3.2.1]oct-3-ene-2,8-dione (NP0289275)

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Record Information

Version

2.0

Created at

2022-09-09 19:22:59 UTC

Updated at

2022-09-09 19:22:59 UTC

NP-MRD ID

NP0289275

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,5s,6r,7s)-1,5-dimethoxy-7-(7-methoxy-2h-1,3-benzodioxol-5-yl)-6-methyl-3-(prop-2-en-1-yl)bicyclo[3.2.1]oct-3-ene-2,8-dione

Description

Cinerin A belongs to the class of organic compounds known as benzodioxoles. These are organic compounds containing a benzene ring fused to either isomers of dioxole. Dioxole is a five-membered unsaturated ring of two oxygen atoms and three carbon atoms. (1s,5s,6r,7s)-1,5-dimethoxy-7-(7-methoxy-2h-1,3-benzodioxol-5-yl)-6-methyl-3-(prop-2-en-1-yl)bicyclo[3.2.1]oct-3-ene-2,8-dione is found in Pleurothyrium cinereum. (1s,5s,6r,7s)-1,5-dimethoxy-7-(7-methoxy-2h-1,3-benzodioxol-5-yl)-6-methyl-3-(prop-2-en-1-yl)bicyclo[3.2.1]oct-3-ene-2,8-dione was first documented in 2009 (PMID: 19548690). Based on a literature review very few articles have been published on Cinerin A (PMID: 22674310).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092221232D          

 29 32  0  0  1  0            999 V2000
    7.8415    3.7610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0188    3.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6608    2.9560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8382    2.8943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4257    3.6088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6099    3.7318    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3667    4.5201    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9278    5.1249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4481    2.7902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6254    2.7285    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7484    1.8832    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6254    1.0674    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2705    0.5530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5368    2.1264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0979    1.5216    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    2.3479    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3523    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -0.1271    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.5396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    2.1904    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    0.8555    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0051    3.1706    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2371    3.4720    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  1  1  0  0  0
  7  8  1  0  0  0  0
  6  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  6  0  0  0
 12 13  1  0  0  0  0
 11 14  1  0  0  0  0
  4 14  1  0  0  0  0
 14 15  2  0  0  0  0
 11 16  1  0  0  0  0
 16 17  1  6  0  0  0
 17 18  2  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
 19 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 17 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 22 27  1  0  0  0  0
 16 28  1  0  0  0  0
  6 28  1  0  0  0  0
 28 29  1  1  0  0  0
M  END

     RDKit          2D

 53 56  0  0  0  0  0  0  0  0999 V2000
   -1.0851   11.7235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3351   10.4245    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0851    9.1254    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8351    7.8264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3351    7.8264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9370    6.4418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9407    7.5566    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4079    7.2447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4452    6.5986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8915    7.1720    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8351    5.2283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3679    4.9164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6358    6.0312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0851    6.5273    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3703    6.8903    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9499    4.2246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8351    3.2209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4086    3.6844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7062    2.6807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1328    3.1443    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2475    2.1406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3943    1.2135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0323    0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1470    1.7537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0323   -0.7500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3943   -1.2135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2760    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2489    4.9746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8590    3.6043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3351   13.0225    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5851   11.7235    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1649   10.4245    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3842    9.8754    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2139    8.3754    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0851    9.1254    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8752    6.9328    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7198    8.7119    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2772    5.7504    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6395    7.1459    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7505    5.0275    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2029    7.2748    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6770    2.9127    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2491    5.0326    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3622    1.1369    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2512    3.2553    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2438    1.0259    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5736    1.2902    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6933   -1.9635    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2158   -2.5838    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7213    5.2608    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4691    2.2340    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2293    4.2144    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5733    2.8317    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 21 20  1  0
 20 19  1  0
 19 22  2  0
 22 27  1  0
 27 26  1  0
 26 25  1  0
 25 23  1  0
 23 24  2  0
 24 17  1  0
 17 18  2  0
 17 16  1  0
 16 28  1  0
 28 29  1  0
 28  6  1  0
  6  7  1  1
  7  8  1  0
  6  5  1  0
  5  4  2  0
  4  3  1  0
  3  2  1  0
  2  1  2  3
  4 14  1  0
 14 15  2  0
 14 11  1  0
 11 12  1  6
 12 13  1  0
 11  9  1  0
  9 10  2  0
 18 19  1  0
 11 16  1  0
 23 22  1  0
  9  6  1  0
 21 44  1  0
 21 45  1  0
 21 46  1  0
 26 48  1  0
 26 49  1  0
 24 47  1  0
 18 43  1  0
 16 42  1  1
 28 50  1  6
 29 51  1  0
 29 52  1  0
 29 53  1  0
  8 36  1  0
  8 37  1  0
  8 38  1  0
  5 35  1  0
  3 33  1  0
  3 34  1  0
  2 32  1  0
  1 30  1  0
  1 31  1  0
 13 39  1  0
 13 40  1  0
 13 41  1  0
M  END


  Mrv1652309092221232D          

 29 32  0  0  1  0            999 V2000
    7.8415    3.7610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0188    3.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6608    2.9560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8382    2.8943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4257    3.6088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6099    3.7318    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3667    4.5201    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9278    5.1249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4481    2.7902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6254    2.7285    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7484    1.8832    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6254    1.0674    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2705    0.5530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5368    2.1264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0979    1.5216    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    2.3479    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3523    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -0.1271    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.5396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    2.1904    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    0.8555    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0051    3.1706    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2371    3.4720    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  1  1  0  0  0
  7  8  1  0  0  0  0
  6  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  6  0  0  0
 12 13  1  0  0  0  0
 11 14  1  0  0  0  0
  4 14  1  0  0  0  0
 14 15  2  0  0  0  0
 11 16  1  0  0  0  0
 16 17  1  6  0  0  0
 17 18  2  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
 19 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 17 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 22 27  1  0  0  0  0
 16 28  1  0  0  0  0
  6 28  1  0  0  0  0
 28 29  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0289275

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C2OCOC2=CC(=C1)[C@@H]1[C@@H](C)[C@]2(OC)C=C(CC=C)C(=O)[C@]1(OC)C2=O

> <INCHI_IDENTIFIER>
InChI=1S/C22H24O7/c1-6-7-13-10-21(26-4)12(2)17(22(27-5,19(13)23)20(21)24)14-8-15(25-3)18-16(9-14)28-11-29-18/h6,8-10,12,17H,1,7,11H2,2-5H3/t12-,17+,21-,22+/m1/s1

> <INCHI_KEY>
JRFQBNCUNXLLQL-SLFNRPLXSA-N

> <FORMULA>
C22H24O7

> <MOLECULAR_WEIGHT>
400.427

> <EXACT_MASS>
400.152203113

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
45.011899873830835

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,5S,6R,7S)-1,5-dimethoxy-7-(7-methoxy-2H-1,3-benzodioxol-5-yl)-6-methyl-3-(prop-2-en-1-yl)bicyclo[3.2.1]oct-3-ene-2,8-dione

> <JCHEM_LOGP>
3.5423954686666677

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-3.8431318923566447

> <JCHEM_POLAR_SURFACE_AREA>
80.29

> <JCHEM_REFRACTIVITY>
104.55460000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,5S,6R,7S)-1,5-dimethoxy-7-(7-methoxy-2H-1,3-benzodioxol-5-yl)-6-methyl-3-(prop-2-en-1-yl)bicyclo[3.2.1]oct-3-ene-2,8-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0      14.637   7.020   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.102   6.905   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      12.434   5.518   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.898   5.403   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.128   6.736   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.605   6.966   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       8.151   8.438   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       9.199   9.566   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.303   5.208   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       6.767   5.093   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       8.864   3.515   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       8.634   1.993   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       9.838   1.032   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.335   3.969   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      11.383   2.840   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       7.591   4.383   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.258   3.613   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.258   2.073   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.924   1.303   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       4.924  -0.237   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       6.258  -1.007   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.590   2.073   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.590   3.613   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.924   4.383   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       2.126   4.089   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       1.220   2.843   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       2.126   1.597   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       7.476   5.919   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.043   6.481   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   14                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    9   28                                             
CONECT    7    6    8                                                       
CONECT    8    7                                                            
CONECT    9    6   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   14   16                                             
CONECT   12   11   13                                                       
CONECT   13   12                                                            
CONECT   14   11    4   15                                                  
CONECT   15   14                                                            
CONECT   16   11   17   28                                                  
CONECT   17   16   18   24                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   22                                                  
CONECT   20   19   21                                                       
CONECT   21   20                                                            
CONECT   22   19   23   27                                                  
CONECT   23   22   24   25                                                  
CONECT   24   23   17                                                       
CONECT   25   23   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   22                                                       
CONECT   28   16    6   29                                                  
CONECT   29   28                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₂₄O₇

Average Mass

400.4270 Da

Monoisotopic Mass

400.15220 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

COC1=C2OCOC2=CC(=C1)[C@@H]1[C@@H](C)[C@]2(OC)C=C(CC=C)C(=O)[C@]1(OC)C2=O

InChI Identifier

InChI=1S/C22H24O7/c1-6-7-13-10-21(26-4)12(2)17(22(27-5,19(13)23)20(21)24)14-8-15(25-3)18-16(9-14)28-11-29-18/h6,8-10,12,17H,1,7,11H2,2-5H3/t12-,17+,21-,22+/m1/s1

InChI Key

JRFQBNCUNXLLQL-SLFNRPLXSA-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
Pleurothyrium cinereum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzodioxoles. These are organic compounds containing a benzene ring fused to either isomers of dioxole. Dioxole is a five-membered unsaturated ring of two oxygen atoms and three carbon atoms.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzodioxoles

Sub Class

Not Available

Direct Parent

Benzodioxoles

Alternative Parents

Substituents

Benzodioxole
Anisole
Alkyl aryl ether
Cyclohexenone
Benzenoid
Ketone
Acetal
Dialkyl ether
Ether
Oxacycle
Carbonyl group
Hydrocarbon derivative
Aldehyde
Organic oxygen compound
Organic oxide
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	3.54	ChemAxon
pKa (Strongest Basic)	-3.8	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Rotatable Bond Count	6	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

24643018

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

45487088

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Coy ED, Cuca LE, Sefkow M: Macrophyllin-type bicyclo[3.2.1]octanoid neolignans from the leaves of Pleurothyrium cinereum. J Nat Prod. 2009 Jul;72(7):1245-8. doi: 10.1021/np9000569. [PubMed:19548690 ]
Cuca LE, Coy ED, Alarcon MA, Fernandez A, Aristizabal FA: Cytotoxic effect of some natural compounds isolated from Lauraceae plants and synthetic derivatives. Biomedica. 2011 Jul-Sep;31(3):335-43. doi: 10.1590/S0120-41572011000300006. [PubMed:22674310 ]
LOTUS database [Link]

Showing NP-Card for (1s,5s,6r,7s)-1,5-dimethoxy-7-(7-methoxy-2h-1,3-benzodioxol-5-yl)-6-methyl-3-(prop-2-en-1-yl)bicyclo[3.2.1]oct-3-ene-2,8-dione (NP0289275)

MOL for NP0289275 ((1s,5s,6r,7s)-1,5-dimethoxy-7-(7-methoxy-2h-1,3-benzodioxol-5-yl)-6-methyl-3-(prop-2-en-1-yl)bicyclo[3.2.1]oct-3-ene-2,8-dione)

3D MOL for NP0289275 ((1s,5s,6r,7s)-1,5-dimethoxy-7-(7-methoxy-2h-1,3-benzodioxol-5-yl)-6-methyl-3-(prop-2-en-1-yl)bicyclo[3.2.1]oct-3-ene-2,8-dione)

3D SDF for NP0289275 ((1s,5s,6r,7s)-1,5-dimethoxy-7-(7-methoxy-2h-1,3-benzodioxol-5-yl)-6-methyl-3-(prop-2-en-1-yl)bicyclo[3.2.1]oct-3-ene-2,8-dione)

3D-SDF for NP0289275 ((1s,5s,6r,7s)-1,5-dimethoxy-7-(7-methoxy-2h-1,3-benzodioxol-5-yl)-6-methyl-3-(prop-2-en-1-yl)bicyclo[3.2.1]oct-3-ene-2,8-dione)

PDB for NP0289275 ((1s,5s,6r,7s)-1,5-dimethoxy-7-(7-methoxy-2h-1,3-benzodioxol-5-yl)-6-methyl-3-(prop-2-en-1-yl)bicyclo[3.2.1]oct-3-ene-2,8-dione)

3D PDB for NP0289275 ((1s,5s,6r,7s)-1,5-dimethoxy-7-(7-methoxy-2h-1,3-benzodioxol-5-yl)-6-methyl-3-(prop-2-en-1-yl)bicyclo[3.2.1]oct-3-ene-2,8-dione)

SMILES for NP0289275 ((1s,5s,6r,7s)-1,5-dimethoxy-7-(7-methoxy-2h-1,3-benzodioxol-5-yl)-6-methyl-3-(prop-2-en-1-yl)bicyclo[3.2.1]oct-3-ene-2,8-dione)

INCHI for NP0289275 ((1s,5s,6r,7s)-1,5-dimethoxy-7-(7-methoxy-2h-1,3-benzodioxol-5-yl)-6-methyl-3-(prop-2-en-1-yl)bicyclo[3.2.1]oct-3-ene-2,8-dione)

Structure for NP0289275 ((1s,5s,6r,7s)-1,5-dimethoxy-7-(7-methoxy-2h-1,3-benzodioxol-5-yl)-6-methyl-3-(prop-2-en-1-yl)bicyclo[3.2.1]oct-3-ene-2,8-dione)

3D Structure for NP0289275 ((1s,5s,6r,7s)-1,5-dimethoxy-7-(7-methoxy-2h-1,3-benzodioxol-5-yl)-6-methyl-3-(prop-2-en-1-yl)bicyclo[3.2.1]oct-3-ene-2,8-dione)