NP-MRD: Showing NP-Card for (3r,4as,7as)-3,4a-dimethyl-3-(2-methyl-8-phenyloctyl)-dihydro-4h-furo[3,2-c][1,2]dioxin-6-one (NP0329497)

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Record Information

Version

2.0

Created at

2022-09-12 13:56:30 UTC

Updated at

2022-09-12 13:56:30 UTC

NP-MRD ID

NP0329497

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3r,4as,7as)-3,4a-dimethyl-3-(2-methyl-8-phenyloctyl)-dihydro-4h-furo[3,2-c][1,2]dioxin-6-one

Description

Plakortolide C belongs to the class of organic compounds known as 1,2-dioxanes. These are organic compounds containing 1,2-dioxane, an aliphatic six-member ring with two oxygen atoms in ring positions 1 and 2. (3r,4as,7as)-3,4a-dimethyl-3-(2-methyl-8-phenyloctyl)-dihydro-4h-furo[3,2-c][1,2]dioxin-6-one is found in Plakinastrella onkodes. (3r,4as,7as)-3,4a-dimethyl-3-(2-methyl-8-phenyloctyl)-dihydro-4h-furo[3,2-c][1,2]dioxin-6-one was first documented in 2012 (PMID: 22050345). Based on a literature review a small amount of articles have been published on Plakortolide C.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122215562D          

 27 29  0  0  1  0            999 V2000
    7.0404   -2.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0404   -3.3875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3260   -3.8000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6115   -3.3875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8970   -3.8000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1825   -3.3875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4681   -3.8000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7536   -3.3875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0391   -3.8000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0391   -4.6250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3247   -5.0375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6102   -4.6250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6102   -3.8000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3247   -3.3875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7549   -3.8000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7549   -4.6250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.9424   -4.4817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5674   -4.4817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0977   -5.1137    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.4593   -4.3722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9222   -5.1425    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.1496   -5.9356    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9248   -6.2177    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.4656   -6.3969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8155   -5.8890    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.0030   -6.0322    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4727   -5.4003    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
  9 14  1  0  0  0  0
  2 15  1  0  0  0  0
 16 15  1  6  0  0  0
 16 17  1  1  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  1  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 25 24  1  6  0  0  0
 19 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 16 27  1  0  0  0  0
M  END

     RDKit          3D

 61 63  0  0  0  0  0  0  0  0999 V2000
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   -0.6553   -0.3585    0.0890 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3717   -1.6442   -0.5842 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8343   -1.5562   -1.4670 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1130   -1.1927   -0.7722 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1877   -1.1715   -1.8477 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5465   -0.8337   -1.3400 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5982    0.5328   -0.6941 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9882    0.8077   -0.2179 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3576    0.4430    1.0581 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6719    0.7244    1.4520 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5315    1.3455    0.5618 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1509    1.7047   -0.7096 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8485    1.4237   -1.0942 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.2534    0.5388    0.4298 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.9244   -0.3228   -0.6040 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7500    1.8543    0.2669 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9020    1.9361    1.0243 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9617    2.5417    0.7194 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6458    1.1710    2.2672 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5976    0.1704    1.8318 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4030    0.3239    2.5748 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6231   -0.6529    2.2758 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3882    1.5945   -0.5037 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0783    1.1074   -1.3574 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4229    0.3218   -1.8523 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3257   -0.0387    0.5672 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1714   -2.4562    0.1585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1914   -2.0275   -1.2222 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9932   -2.5910   -1.8922 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6785   -0.9112   -2.3567 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3915   -1.9334   -0.0232 H   0  0  0  0  0  0  0  0  0  0  0  0
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    3.2248   -2.1322   -2.3988 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8623   -1.6319   -0.6335 H   0  0  0  0  0  0  0  0  0  0  0  0
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    6.5529    1.7026   -2.0813 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2744   -1.1304    1.9416 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4781    0.6129    1.7651 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5661   -2.6149    0.6421 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5239   -1.8218   -0.7436 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2997   -2.3279    0.7561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5552    0.6186   -0.8058 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4181    1.5258    0.7696 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8829    0.1667   -0.9491 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3140   -0.4254   -1.5179 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2508   -1.2921   -0.1745 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2628    1.8713    3.0477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5658    0.6559    2.6210 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9918   -0.8607    1.9378 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
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  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
  2 15  1  0
 16 15  1  1
 16 17  1  0
 16 18  1  0
 18 19  1  0
 19 20  1  6
 19 21  1  0
 21 22  1  0
 22 23  2  0
 22 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 14  9  1  0
 27 16  1  0
 25 19  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  2 31  1  1
  3 32  1  0
  3 33  1  0
  4 34  1  0
  4 35  1  0
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 18 55  1  0
 20 56  1  0
 20 57  1  0
 20 58  1  0
 24 59  1  0
 24 60  1  0
 25 61  1  6
M  END


  Mrv1652309122215562D          

 27 29  0  0  1  0            999 V2000
    7.0404   -2.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0404   -3.3875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3260   -3.8000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6115   -3.3875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8970   -3.8000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1825   -3.3875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4681   -3.8000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7536   -3.3875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0391   -3.8000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0391   -4.6250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3247   -5.0375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6102   -4.6250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6102   -3.8000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3247   -3.3875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7549   -3.8000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7549   -4.6250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.9424   -4.4817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5674   -4.4817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0977   -5.1137    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.4593   -4.3722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9222   -5.1425    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.1496   -5.9356    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9248   -6.2177    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.4656   -6.3969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    7.4727   -5.4003    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
  9 14  1  0  0  0  0
  2 15  1  0  0  0  0
 16 15  1  6  0  0  0
 16 17  1  1  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
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 19 21  1  0  0  0  0
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 22 23  2  0  0  0  0
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 25 24  1  6  0  0  0
 19 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 16 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0329497

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(CCCCCCC1=CC=CC=C1)C[C@]1(C)C[C@]2(C)OC(=O)C[C@@H]2OO1

> <INCHI_IDENTIFIER>
InChI=1S/C23H34O4/c1-18(11-7-4-5-8-12-19-13-9-6-10-14-19)16-22(2)17-23(3)20(26-27-22)15-21(24)25-23/h6,9-10,13-14,18,20H,4-5,7-8,11-12,15-17H2,1-3H3/t18?,20-,22+,23-/m0/s1

> <INCHI_KEY>
BJCREQAAFOADRC-OYVLRHCSSA-N

> <FORMULA>
C23H34O4

> <MOLECULAR_WEIGHT>
374.521

> <EXACT_MASS>
374.245709575

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
61

> <JCHEM_AVERAGE_POLARIZABILITY>
43.505450946184574

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3R,4aS,7aS)-3,4a-dimethyl-3-(2-methyl-8-phenyloctyl)-hexahydrofuro[3,2-c][1,2]dioxin-6-one

> <JCHEM_LOGP>
6.0391076046666665

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.846404205036711

> <JCHEM_POLAR_SURFACE_AREA>
44.760000000000005

> <JCHEM_REFRACTIVITY>
104.9845

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(3R,4aS,7aS)-3,4a-dimethyl-3-(2-methyl-8-phenyloctyl)-dihydro-4H-furo[3,2-c][1,2]dioxin-6-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0      13.142  -4.783   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.142  -6.323   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      11.808  -7.093   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.475  -6.323   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.141  -7.093   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.807  -6.323   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.474  -7.093   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.140  -6.323   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.806  -7.093   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.806  -8.633   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.473  -9.403   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.139  -8.633   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.139  -7.093   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.473  -6.323   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      14.476  -7.093   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      14.476  -8.633   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      12.959  -8.366   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      15.992  -8.366   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      16.982  -9.546   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      17.657  -8.161   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      18.521  -9.599   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      18.946 -11.080   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      20.393 -11.606   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      17.669 -11.941   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      16.456 -10.993   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      14.939 -11.260   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0      13.949 -10.080   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   15                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13    9                                                       
CONECT   15    2   16                                                       
CONECT   16   15   17   18   27                                             
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20   21   25                                             
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   19   26                                                  
CONECT   26   25   27                                                       
CONECT   27   26   16                                                       
MASTER        0    0    0    0    0    0    0    0   27    0   58    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₃₄O₄

Average Mass

374.5210 Da

Monoisotopic Mass

374.24571 Da

IUPAC Name

(3R,4aS,7aS)-3,4a-dimethyl-3-(2-methyl-8-phenyloctyl)-hexahydrofuro[3,2-c][1,2]dioxin-6-one

Traditional Name

(3R,4aS,7aS)-3,4a-dimethyl-3-(2-methyl-8-phenyloctyl)-dihydro-4H-furo[3,2-c][1,2]dioxin-6-one

CAS Registry Number

Not Available

SMILES

CC(CCCCCCC1=CC=CC=C1)C[C@]1(C)C[C@]2(C)OC(=O)C[C@@H]2OO1

InChI Identifier

InChI=1S/C23H34O4/c1-18(11-7-4-5-8-12-19-13-9-6-10-14-19)16-22(2)17-23(3)20(26-27-22)15-21(24)25-23/h6,9-10,13-14,18,20H,4-5,7-8,11-12,15-17H2,1-3H3/t18?,20-,22+,23-/m0/s1

InChI Key

BJCREQAAFOADRC-OYVLRHCSSA-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
Plakinastrella onkodes	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 1,2-dioxanes. These are organic compounds containing 1,2-dioxane, an aliphatic six-member ring with two oxygen atoms in ring positions 1 and 2.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Dioxanes

Sub Class

1,2-dioxanes

Direct Parent

1,2-dioxanes

Alternative Parents

Substituents

Ortho-dioxane
Monocyclic benzene moiety
Gamma butyrolactone
Benzenoid
Oxolane
Carboxylic acid ester
Dialkyl peroxide
Lactone
Carboxylic acid derivative
Oxacycle
Monocarboxylic acid or derivatives
Hydrocarbon derivative
Organic oxygen compound
Carbonyl group
Organooxygen compound
Organic oxide
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	6.04	ChemAxon
pKa (Strongest Basic)	-4.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	44.76 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	104.98 m³·mol⁻¹	ChemAxon
Polarizability	43.51 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

8424340

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10248853

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Yong KW, Lambert LK, Hayes PY, De Voss JJ, Garson MJ: Oxidative processes in the Australian marine sponge Plakinastrella clathrata: isolation of plakortolides with oxidatively modified side chains. J Nat Prod. 2012 Mar 23;75(3):351-60. doi: 10.1021/np200619q. Epub 2011 Nov 3. [PubMed:22050345 ]
LOTUS database [Link]

Showing NP-Card for (3r,4as,7as)-3,4a-dimethyl-3-(2-methyl-8-phenyloctyl)-dihydro-4h-furo[3,2-c][1,2]dioxin-6-one (NP0329497)

MOL for NP0329497 ((3r,4as,7as)-3,4a-dimethyl-3-(2-methyl-8-phenyloctyl)-dihydro-4h-furo[3,2-c][1,2]dioxin-6-one)

3D MOL for NP0329497 ((3r,4as,7as)-3,4a-dimethyl-3-(2-methyl-8-phenyloctyl)-dihydro-4h-furo[3,2-c][1,2]dioxin-6-one)

3D SDF for NP0329497 ((3r,4as,7as)-3,4a-dimethyl-3-(2-methyl-8-phenyloctyl)-dihydro-4h-furo[3,2-c][1,2]dioxin-6-one)

3D-SDF for NP0329497 ((3r,4as,7as)-3,4a-dimethyl-3-(2-methyl-8-phenyloctyl)-dihydro-4h-furo[3,2-c][1,2]dioxin-6-one)

PDB for NP0329497 ((3r,4as,7as)-3,4a-dimethyl-3-(2-methyl-8-phenyloctyl)-dihydro-4h-furo[3,2-c][1,2]dioxin-6-one)

3D PDB for NP0329497 ((3r,4as,7as)-3,4a-dimethyl-3-(2-methyl-8-phenyloctyl)-dihydro-4h-furo[3,2-c][1,2]dioxin-6-one)

SMILES for NP0329497 ((3r,4as,7as)-3,4a-dimethyl-3-(2-methyl-8-phenyloctyl)-dihydro-4h-furo[3,2-c][1,2]dioxin-6-one)

INCHI for NP0329497 ((3r,4as,7as)-3,4a-dimethyl-3-(2-methyl-8-phenyloctyl)-dihydro-4h-furo[3,2-c][1,2]dioxin-6-one)

Structure for NP0329497 ((3r,4as,7as)-3,4a-dimethyl-3-(2-methyl-8-phenyloctyl)-dihydro-4h-furo[3,2-c][1,2]dioxin-6-one)

3D Structure for NP0329497 ((3r,4as,7as)-3,4a-dimethyl-3-(2-methyl-8-phenyloctyl)-dihydro-4h-furo[3,2-c][1,2]dioxin-6-one)