NP-MRD: Showing NP-Card for irciformonin K (NP0040493)

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Record Information

Version

2.0

Created at

2021-06-20 22:38:31 UTC

Updated at

2021-06-30 00:14:26 UTC

NP-MRD ID

NP0040493

Secondary Accession Numbers

None

Natural Product Identification

Common Name

irciformonin K

Provided By

JEOL Database JEOL Logo

Description

Irciformonin K belongs to the class of organic compounds known as gamma butyrolactones. Gamma butyrolactones are compounds containing a gamma butyrolactone moiety, which consists of an aliphatic five-member ring with four carbon atoms, one oxygen atom, and bears a ketone group on the carbon adjacent to the oxygen atom. irciformonin K is found in Ircinia formosana. irciformonin K was first documented in 2009 (Shen, Y.-C., et al.). Based on a literature review very few articles have been published on Irciformonin K.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306212100383D          

 57 59  0  0  0  0            999 V2000
    3.4524    1.3375    4.1674 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7082    1.6050    2.7089 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4845    2.7843    2.0932 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9045    4.0313    2.7040 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3698    3.9922    2.7839 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6415    3.9284    1.4836 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9726    4.3128    0.2512 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0968    3.9946   -0.7121 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1145    3.3903    0.0818 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6874    3.3067    1.3707 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3130    2.7982    2.2842 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1922    0.4068    1.9164 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0337   -0.2753    1.2477 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5026   -1.4509    1.6257 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2781   -2.0943    1.0138 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -0.3595   -1.3552   -3.9337 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 13  1  0  0  0  0
  4  3  1  0  0  0  0
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 15 14  1  1  0  0  0
 19 18  1  0  0  0  0
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  3  2  2  0  0  0  0
  5  4  1  0  0  0  0
  2 12  1  0  0  0  0
 26 24  1  0  0  0  0
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 23 22  1  0  0  0  0
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 19 20  1  0  0  0  0
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  2  1  1  0  0  0  0
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 24 25  2  0  0  0  0
  8  7  1  0  0  0  0
 20 21  1  1  0  0  0
  7  6  2  0  0  0  0
 15 16  1  0  0  0  0
  6  5  1  0  0  0  0
 10 11  2  0  0  0  0
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  5 34  1  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652306212100383D          

 57 59  0  0  0  0            999 V2000
    3.4524    1.3375    4.1674 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7082    1.6050    2.7089 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.0272    4.8855    3.3211 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0768    3.1345    3.4028 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8986    4.7901   -0.0319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4973    4.8944   -1.1875 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2396    3.2929   -1.4787 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9084    0.7212    1.1469 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7407   -0.2836    2.5687 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5885    0.2697    0.4162 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9469   -1.9815    2.4655 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4021   -3.3589   -0.3556 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0085   -4.1485    1.1872 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7651   -3.9155   -0.0609 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2752   -1.4801    2.8585 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0436   -3.1888    2.4881 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4568   -2.6705    0.6861 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8922   -1.4188    1.8690 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3059    0.1724    0.8628 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7546    0.8003    0.2091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3483   -0.8390   -0.1429 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3223    0.4117   -1.4026 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3534   -2.5029   -1.6423 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2668   -1.3846   -2.6498 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7329   -1.6946   -2.5556 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3595   -1.3552   -3.9337 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 13  1  0  0  0  0
  4  3  1  0  0  0  0
 13 14  2  0  0  0  0
 15 14  1  1  0  0  0
 19 18  1  0  0  0  0
 18 17  1  0  0  0  0
 17 15  1  0  0  0  0
 20 26  1  0  0  0  0
  6 10  1  0  0  0  0
  3  2  2  0  0  0  0
  5  4  1  0  0  0  0
  2 12  1  0  0  0  0
 26 24  1  0  0  0  0
 24 23  1  0  0  0  0
 23 22  1  0  0  0  0
 22 20  1  0  0  0  0
 19 20  1  0  0  0  0
 10  9  1  0  0  0  0
  2  1  1  0  0  0  0
  9  8  1  0  0  0  0
 24 25  2  0  0  0  0
  8  7  1  0  0  0  0
 20 21  1  1  0  0  0
  7  6  2  0  0  0  0
 15 16  1  0  0  0  0
  6  5  1  0  0  0  0
 10 11  2  0  0  0  0
 15 27  1  0  0  0  0
 19 50  1  1  0  0  0
 19 27  1  0  0  0  0
  5 34  1  0  0  0  0
  5 35  1  0  0  0  0
  4 32  1  0  0  0  0
  4 33  1  0  0  0  0
  3 31  1  0  0  0  0
 12 39  1  0  0  0  0
 12 40  1  0  0  0  0
 13 41  1  0  0  0  0
 14 42  1  0  0  0  0
  8 37  1  0  0  0  0
  8 38  1  0  0  0  0
  7 36  1  0  0  0  0
 18 48  1  0  0  0  0
 18 49  1  0  0  0  0
 17 46  1  0  0  0  0
 17 47  1  0  0  0  0
 23 56  1  0  0  0  0
 23 57  1  0  0  0  0
 22 54  1  0  0  0  0
 22 55  1  0  0  0  0
  1 28  1  0  0  0  0
  1 29  1  0  0  0  0
  1 30  1  0  0  0  0
 21 51  1  0  0  0  0
 21 52  1  0  0  0  0
 21 53  1  0  0  0  0
 16 43  1  0  0  0  0
 16 44  1  0  0  0  0
 16 45  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0040493

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]\C(=C(\[H])[C@@]1(O[C@]([H])(C([H])([H])C1([H])[H])[C@]1(OC(=O)C([H])([H])C1([H])[H])C([H])([H])[H])C([H])([H])[H])C([H])([H])C(=C(/[H])C([H])([H])C([H])([H])C1=C([H])C([H])([H])OC1=O)\C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C22H30O5/c1-16(6-4-8-17-11-15-25-20(17)24)7-5-12-21(2)13-9-18(26-21)22(3)14-10-19(23)27-22/h5-6,11-12,18H,4,7-10,13-15H2,1-3H3/b12-5+,16-6+/t18-,21+,22+/m1/s1

> <INCHI_KEY>
UWXJDRWZPZOIOX-IXTRLJNLSA-N

> <FORMULA>
C22H30O5

> <MOLECULAR_WEIGHT>
374.477

> <EXACT_MASS>
374.209324066

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
57

> <JCHEM_AVERAGE_POLARIZABILITY>
39.860170673843925

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S,2'R,5'R)-2,5'-dimethyl-5'-[(1E,4E)-4-methyl-7-(2-oxo-2,5-dihydrofuran-3-yl)hepta-1,4-dien-1-yl]-[2,2'-bioxolane]-5-one

> <ALOGPS_LOGP>
4.18

> <JCHEM_LOGP>
4.050298414000001

> <ALOGPS_LOGS>
-4.82

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.391819581854332

> <JCHEM_PKA_STRONGEST_BASIC>
-4.232202106967597

> <JCHEM_POLAR_SURFACE_AREA>
61.83000000000001

> <JCHEM_REFRACTIVITY>
105.01969999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.69e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,2'R,5'R)-2,5'-dimethyl-5'-[(1E,4E)-4-methyl-7-(2-oxo-5H-furan-3-yl)hepta-1,4-dien-1-yl]-[2,2'-bioxolane]-5-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 57 59  0  0  0  0  0  0  0  0999 V2000
    3.4524    1.3375    4.1674 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7082    1.6050    2.7089 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4845    2.7843    2.0932 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9045    4.0313    2.7040 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3698    3.9922    2.7839 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6415    3.9284    1.4836 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9726    4.3128    0.2512 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0968    3.9946   -0.7121 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1145    3.3903    0.0818 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6874    3.3067    1.3707 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3130    2.7982    2.2842 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1922    0.4068    1.9164 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0337   -0.2753    1.2477 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5026   -1.4509    1.6257 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2781   -2.0943    1.0138 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6360   -3.4581    0.4227 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1389   -2.1958    2.0369 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0844   -1.8012    1.2389 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5090   -0.7520    0.3047 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3587   -0.4061   -0.9411 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7770    0.0041   -0.5434 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3687   -1.4787   -2.0253 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1612   -1.1559   -2.8776 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0194    0.3110   -2.6414 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7411    1.0530   -3.2894 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7531    0.7270   -1.5986 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7759   -1.2848   -0.0715 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7162    0.5352    4.2829 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0711    2.2084    4.7058 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3802    1.0289    4.6604 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6855    2.8527    1.0239 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3167    4.1861    3.7080 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2344    4.8983    2.1184 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0272    4.8855    3.3211 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0768    3.1345    3.4028 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8986    4.7901   -0.0319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4973    4.8944   -1.1875 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2396    3.2929   -1.4787 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9084    0.7212    1.1469 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7407   -0.2836    2.5687 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5885    0.2697    0.4162 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9469   -1.9815    2.4655 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4021   -3.3589   -0.3556 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0085   -4.1485    1.1872 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7651   -3.9155   -0.0609 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2752   -1.4801    2.8585 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0436   -3.1888    2.4881 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4568   -2.6705    0.6861 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8922   -1.4188    1.8690 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3059    0.1724    0.8628 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7546    0.8003    0.2091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3483   -0.8390   -0.1429 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3223    0.4117   -1.4026 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3534   -2.5029   -1.6423 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2668   -1.3846   -2.6498 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7329   -1.6946   -2.5556 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3595   -1.3552   -3.9337 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 13  1  0
  4  3  1  0
 13 14  2  0
 15 14  1  1
 19 18  1  0
 18 17  1  0
 17 15  1  0
 20 26  1  0
  6 10  1  0
  3  2  2  0
  5  4  1  0
  2 12  1  0
 26 24  1  0
 24 23  1  0
 23 22  1  0
 22 20  1  0
 19 20  1  0
 10  9  1  0
  2  1  1  0
  9  8  1  0
 24 25  2  0
  8  7  1  0
 20 21  1  1
  7  6  2  0
 15 16  1  0
  6  5  1  0
 10 11  2  0
 15 27  1  0
 19 50  1  1
 19 27  1  0
  5 34  1  0
  5 35  1  0
  4 32  1  0
  4 33  1  0
  3 31  1  0
 12 39  1  0
 12 40  1  0
 13 41  1  0
 14 42  1  0
  8 37  1  0
  8 38  1  0
  7 36  1  0
 18 48  1  0
 18 49  1  0
 17 46  1  0
 17 47  1  0
 23 56  1  0
 23 57  1  0
 22 54  1  0
 22 55  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
 21 51  1  0
 21 52  1  0
 21 53  1  0
 16 43  1  0
 16 44  1  0
 16 45  1  0
M  END

HEADER    PROTEIN                                 21-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   21-JUN-21         0                                  
HETATM    1  C   UNK     0       3.452   1.337   4.167  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.708   1.605   2.709  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.485   2.784   2.093  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.905   4.031   2.704  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.370   3.992   2.784  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.642   3.928   1.484  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.973   4.313   0.251  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.097   3.995  -0.712  0.00  0.00           C+0
HETATM    9  O   UNK     0      -1.115   3.390   0.082  0.00  0.00           O+0
HETATM   10  C   UNK     0      -0.687   3.307   1.371  0.00  0.00           C+0
HETATM   11  O   UNK     0      -1.313   2.798   2.284  0.00  0.00           O+0
HETATM   12  C   UNK     0       4.192   0.407   1.916  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.034  -0.275   1.248  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.503  -1.451   1.626  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.278  -2.094   1.014  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.636  -3.458   0.423  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.139  -2.196   2.037  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.084  -1.801   1.239  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.509  -0.752   0.305  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.359  -0.406  -0.941  0.00  0.00           C+0
HETATM   21  C   UNK     0      -2.777   0.004  -0.543  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.369  -1.479  -2.025  0.00  0.00           C+0
HETATM   23  C   UNK     0      -0.161  -1.156  -2.878  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.019   0.311  -2.641  0.00  0.00           C+0
HETATM   25  O   UNK     0       0.741   1.053  -3.289  0.00  0.00           O+0
HETATM   26  O   UNK     0      -0.753   0.727  -1.599  0.00  0.00           O+0
HETATM   27  O   UNK     0       0.776  -1.285  -0.072  0.00  0.00           O+0
HETATM   28  H   UNK     0       2.716   0.535   4.283  0.00  0.00           H+0
HETATM   29  H   UNK     0       3.071   2.208   4.706  0.00  0.00           H+0
HETATM   30  H   UNK     0       4.380   1.029   4.660  0.00  0.00           H+0
HETATM   31  H   UNK     0       3.686   2.853   1.024  0.00  0.00           H+0
HETATM   32  H   UNK     0       3.317   4.186   3.708  0.00  0.00           H+0
HETATM   33  H   UNK     0       3.234   4.898   2.118  0.00  0.00           H+0
HETATM   34  H   UNK     0       1.027   4.886   3.321  0.00  0.00           H+0
HETATM   35  H   UNK     0       1.077   3.135   3.403  0.00  0.00           H+0
HETATM   36  H   UNK     0       1.899   4.790  -0.032  0.00  0.00           H+0
HETATM   37  H   UNK     0      -0.497   4.894  -1.188  0.00  0.00           H+0
HETATM   38  H   UNK     0       0.240   3.293  -1.479  0.00  0.00           H+0
HETATM   39  H   UNK     0       4.908   0.721   1.147  0.00  0.00           H+0
HETATM   40  H   UNK     0       4.741  -0.284   2.569  0.00  0.00           H+0
HETATM   41  H   UNK     0       2.588   0.270   0.416  0.00  0.00           H+0
HETATM   42  H   UNK     0       2.947  -1.982   2.466  0.00  0.00           H+0
HETATM   43  H   UNK     0       2.402  -3.359  -0.356  0.00  0.00           H+0
HETATM   44  H   UNK     0       2.009  -4.149   1.187  0.00  0.00           H+0
HETATM   45  H   UNK     0       0.765  -3.916  -0.061  0.00  0.00           H+0
HETATM   46  H   UNK     0       0.275  -1.480   2.858  0.00  0.00           H+0
HETATM   47  H   UNK     0       0.044  -3.189   2.488  0.00  0.00           H+0
HETATM   48  H   UNK     0      -1.457  -2.671   0.686  0.00  0.00           H+0
HETATM   49  H   UNK     0      -1.892  -1.419   1.869  0.00  0.00           H+0
HETATM   50  H   UNK     0      -0.306   0.172   0.863  0.00  0.00           H+0
HETATM   51  H   UNK     0      -2.755   0.800   0.209  0.00  0.00           H+0
HETATM   52  H   UNK     0      -3.348  -0.839  -0.143  0.00  0.00           H+0
HETATM   53  H   UNK     0      -3.322   0.412  -1.403  0.00  0.00           H+0
HETATM   54  H   UNK     0      -1.353  -2.503  -1.642  0.00  0.00           H+0
HETATM   55  H   UNK     0      -2.267  -1.385  -2.650  0.00  0.00           H+0
HETATM   56  H   UNK     0       0.733  -1.695  -2.556  0.00  0.00           H+0
HETATM   57  H   UNK     0      -0.360  -1.355  -3.934  0.00  0.00           H+0
CONECT    1    2   28   29   30                                             
CONECT    2    3   12    1                                                  
CONECT    3    4    2   31                                                  
CONECT    4    3    5   32   33                                             
CONECT    5    4    6   34   35                                             
CONECT    6   10    7    5                                                  
CONECT    7    8    6   36                                                  
CONECT    8    9    7   37   38                                             
CONECT    9   10    8                                                       
CONECT   10    6    9   11                                                  
CONECT   11   10                                                            
CONECT   12   13    2   39   40                                             
CONECT   13   12   14   41                                                  
CONECT   14   13   15   42                                                  
CONECT   15   14   17   16   27                                             
CONECT   16   15   43   44   45                                             
CONECT   17   18   15   46   47                                             
CONECT   18   19   17   48   49                                             
CONECT   19   18   20   50   27                                             
CONECT   20   26   22   19   21                                             
CONECT   21   20   51   52   53                                             
CONECT   22   23   20   54   55                                             
CONECT   23   24   22   56   57                                             
CONECT   24   26   23   25                                                  
CONECT   25   24                                                            
CONECT   26   20   24                                                       
CONECT   27   15   19                                                       
CONECT   28    1                                                            
CONECT   29    1                                                            
CONECT   30    1                                                            
CONECT   31    3                                                            
CONECT   32    4                                                            
CONECT   33    4                                                            
CONECT   34    5                                                            
CONECT   35    5                                                            
CONECT   36    7                                                            
CONECT   37    8                                                            
CONECT   38    8                                                            
CONECT   39   12                                                            
CONECT   40   12                                                            
CONECT   41   13                                                            
CONECT   42   14                                                            
CONECT   43   16                                                            
CONECT   44   16                                                            
CONECT   45   16                                                            
CONECT   46   17                                                            
CONECT   47   17                                                            
CONECT   48   18                                                            
CONECT   49   18                                                            
CONECT   50   19                                                            
CONECT   51   21                                                            
CONECT   52   21                                                            
CONECT   53   21                                                            
CONECT   54   22                                                            
CONECT   55   22                                                            
CONECT   56   23                                                            
CONECT   57   23                                                            
MASTER        0    0    0    0    0    0    0    0   57    0  118    0
END

RDKit          3D

57 59  0  0  0  0  0  0  0  0999 V2000
    3.4524    1.3375    4.1674 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7082    1.6050    2.7089 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4845    2.7843    2.0932 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9045    4.0313    2.7040 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3698    3.9922    2.7839 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6415    3.9284    1.4836 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9726    4.3128    0.2512 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0968    3.9946   -0.7121 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1145    3.3903    0.0818 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6874    3.3067    1.3707 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3130    2.7982    2.2842 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1922    0.4068    1.9164 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0337   -0.2753    1.2477 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5026   -1.4509    1.6257 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2781   -2.0943    1.0138 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6360   -3.4581    0.4227 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1389   -2.1958    2.0369 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0844   -1.8012    1.2389 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5090   -0.7520    0.3047 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3587   -0.4061   -0.9411 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7770    0.0041   -0.5434 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3687   -1.4787   -2.0253 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1612   -1.1559   -2.8776 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0194    0.3110   -2.6414 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7411    1.0530   -3.2894 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7531    0.7270   -1.5986 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7759   -1.2848   -0.0715 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7162    0.5352    4.2829 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0711    2.2084    4.7058 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3802    1.0289    4.6604 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6855    2.8527    1.0239 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3167    4.1861    3.7080 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2344    4.8983    2.1184 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0272    4.8855    3.3211 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0768    3.1345    3.4028 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8986    4.7901   -0.0319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4973    4.8944   -1.1875 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2396    3.2929   -1.4787 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9084    0.7212    1.1469 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7407   -0.2836    2.5687 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5885    0.2697    0.4162 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9469   -1.9815    2.4655 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4021   -3.3589   -0.3556 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0085   -4.1485    1.1872 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7651   -3.9155   -0.0609 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2752   -1.4801    2.8585 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0436   -3.1888    2.4881 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4568   -2.6705    0.6861 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8922   -1.4188    1.8690 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3059    0.1724    0.8628 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7546    0.8003    0.2091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3483   -0.8390   -0.1429 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3223    0.4117   -1.4026 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3534   -2.5029   -1.6423 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2668   -1.3846   -2.6498 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7329   -1.6946   -2.5556 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3595   -1.3552   -3.9337 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 13  1  0
  4  3  1  0
 13 14  2  0
 15 14  1  1
 19 18  1  0
 18 17  1  0
 17 15  1  0
 20 26  1  0
  6 10  1  0
  3  2  2  0
  5  4  1  0
  2 12  1  0
 26 24  1  0
 24 23  1  0
 23 22  1  0
 22 20  1  0
 19 20  1  0
 10  9  1  0
  2  1  1  0
  9  8  1  0
 24 25  2  0
  8  7  1  0
 20 21  1  1
  7  6  2  0
 15 16  1  0
  6  5  1  0
 10 11  2  0
 15 27  1  0
 19 50  1  1
 19 27  1  0
  5 34  1  0
  5 35  1  0
  4 32  1  0
  4 33  1  0
  3 31  1  0
 12 39  1  0
 12 40  1  0
 13 41  1  0
 14 42  1  0
  8 37  1  0
  8 38  1  0
  7 36  1  0
 18 48  1  0
 18 49  1  0
 17 46  1  0
 17 47  1  0
 23 56  1  0
 23 57  1  0
 22 54  1  0
 22 55  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
 21 51  1  0
 21 52  1  0
 21 53  1  0
 16 43  1  0
 16 44  1  0
 16 45  1  0
M  END

View in JSmol View DFT Assignments 3D Conformers

Synonyms

Not Available

Chemical Formula

C₂₂H₃₀O₅

Average Mass

374.4770 Da

Monoisotopic Mass

374.20932 Da

IUPAC Name

(2S,2'R,5'R)-2,5'-dimethyl-5'-[(1E,4E)-4-methyl-7-(2-oxo-2,5-dihydrofuran-3-yl)hepta-1,4-dien-1-yl]-[2,2'-bioxolane]-5-one

Traditional Name

(2S,2'R,5'R)-2,5'-dimethyl-5'-[(1E,4E)-4-methyl-7-(2-oxo-5H-furan-3-yl)hepta-1,4-dien-1-yl]-[2,2'-bioxolane]-5-one

CAS Registry Number

Not Available

SMILES

[H]\C(=C(\[H])[C@@]1(O[C@]([H])(C([H])([H])C1([H])[H])[C@]1(OC(=O)C([H])([H])C1([H])[H])C([H])([H])[H])C([H])([H])[H])C([H])([H])C(=C(/[H])C([H])([H])C([H])([H])C1=C([H])C([H])([H])OC1=O)\C([H])([H])[H]

InChI Identifier

InChI=1S/C22H30O5/c1-16(6-4-8-17-11-15-25-20(17)24)7-5-12-21(2)13-9-18(26-21)22(3)14-10-19(23)27-22/h5-6,11-12,18H,4,7-10,13-15H2,1-3H3/b12-5+,16-6+/t18-,21+,22+/m1/s1

InChI Key

UWXJDRWZPZOIOX-IXTRLJNLSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 125 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 150 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 175 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 225 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 250 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, chcl3, 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
Ircinia formosana	JEOL database	Shen, Y.-C., et al, Helv. Chem. Acta 92, 2101 (2009)

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as gamma butyrolactones. Gamma butyrolactones are compounds containing a gamma butyrolactone moiety, which consists of an aliphatic five-member ring with four carbon atoms, one oxygen atom, and bears a ketone group on the carbon adjacent to the oxygen atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Lactones

Sub Class

Gamma butyrolactones

Direct Parent

Gamma butyrolactones

Alternative Parents

Substituents

2-furanone
Dicarboxylic acid or derivatives
Gamma butyrolactone
Dihydrofuran
Oxolane
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Carboxylic acid ester
Ether
Dialkyl ether
Carboxylic acid derivative
Oxacycle
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Carbonyl group
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	4.18	ALOGPS
logP	4.05	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	13.39	ChemAxon
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	61.83 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	105.02 m³·mol⁻¹	ChemAxon
Polarizability	39.86 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	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

27024467

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

44541852

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Shen, Y.-C., et al. (2009). Shen, Y.-C., et al, Helv. Chem. Acta 92, 2101 (2009). Helv. Chem. Acta.

Showing NP-Card for irciformonin K (NP0040493)

MOL for NP0040493 (irciformonin K)

3D MOL for NP0040493 (irciformonin K)

3D SDF for NP0040493 (irciformonin K)

3D-SDF for NP0040493 (irciformonin K)

PDB for NP0040493 (irciformonin K)

3D PDB for NP0040493 (irciformonin K)

SMILES for NP0040493 (irciformonin K)

INCHI for NP0040493 (irciformonin K)

Structure for NP0040493 (irciformonin K)

3D Structure for NP0040493 (irciformonin K)