NP-MRD: Showing NP-Card for Paecilosetin (NP0005882)

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Record Information

Version

2.0

Created at

2020-12-09 03:00:46 UTC

Updated at

2021-07-15 16:53:14 UTC

NP-MRD ID

NP0005882

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Paecilosetin

Provided By

NPAtlas

Description

Paecilosetin belongs to the class of organic compounds known as pyrrolidine-3-ones. These are pyrrolidines which bear a C=O group at position 3 of the pyrrolidine ring. Paecilosetin is found in Paecilomyces farinosus and Paecilomyces. Paecilosetin was first documented in 2005 (PMID: 15921439). Based on a literature review very few articles have been published on paecilosetin.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242118233D          

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M  END

     RDKit          3D

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M  END


  Mrv1652306242118233D          

 58 60  0  0  0  0            999 V2000
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   -0.6480    2.4677   -1.3182 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6202    3.2715   -0.0401 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3311    1.5665   -0.7004 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3042    0.0733   -2.1038 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2493   -0.9934    0.0204 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7493   -0.6268   -1.7004 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7004   -2.2088   -2.3250 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7841   -3.2981   -2.6061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2694   -2.9304   -0.8702 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0595   -4.2719   -1.2544 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9697   -3.6425   -0.4389 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2468   -2.9693    0.5839 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6557   -1.8733    1.4271 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5106   -2.0886    0.0009 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1799    0.1610    0.9199 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1366    0.6181   -2.4872 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6684   -1.0352   -1.8965 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9730   -0.5448   -1.6897 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6294   -1.4578    1.9998 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5014    2.0460   -0.3093 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8626    0.6078    1.7893 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6805   -1.1299   -0.4530 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6159   -1.8284    2.2296 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9549   -2.9115    0.8922 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6932   -2.5608    0.9593 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8669   -1.4717   -0.9415 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  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
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  1  0  0  0
 16 17  1  0  0  0  0
 16 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 22 26  1  0  0  0  0
 26 27  2  0  0  0  0
 14  4  1  0  0  0  0
 26 18  1  0  0  0  0
 13  7  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
  2 31  1  0  0  0  0
  3 32  1  0  0  0  0
  4 33  1  6  0  0  0
  5 34  1  0  0  0  0
  6 35  1  0  0  0  0
  7 36  1  6  0  0  0
  8 37  1  0  0  0  0
  8 38  1  0  0  0  0
  9 39  1  6  0  0  0
 10 40  1  0  0  0  0
 10 41  1  0  0  0  0
 10 42  1  0  0  0  0
 11 43  1  0  0  0  0
 11 44  1  0  0  0  0
 12 45  1  0  0  0  0
 12 46  1  0  0  0  0
 13 47  1  1  0  0  0
 15 48  1  0  0  0  0
 15 49  1  0  0  0  0
 15 50  1  0  0  0  0
 17 51  1  0  0  0  0
 21 52  1  0  0  0  0
 22 53  1  1  0  0  0
 23 54  1  6  0  0  0
 24 55  1  0  0  0  0
 24 56  1  0  0  0  0
 24 57  1  0  0  0  0
 25 58  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0005882

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]O\C(=C1\C(=O)N([H])[C@@]([H])(C1=O)[C@@]([H])(O[H])C([H])([H])[H])[C@]1(C([H])([H])[H])[C@]([H])(C(\[H])=C(/[H])C([H])([H])[H])C([H])=C([H])[C@]2([H])C([H])([H])[C@]([H])(C([H])([H])[H])C([H])([H])C([H])([H])[C@@]12[H]

> <INCHI_IDENTIFIER>
InChI=1S/C22H31NO4/c1-5-6-15-9-8-14-11-12(2)7-10-16(14)22(15,4)20(26)17-19(25)18(13(3)24)23-21(17)27/h5-6,8-9,12-16,18,24,26H,7,10-11H2,1-4H3,(H,23,27)/b6-5+,20-17+/t12-,13+,14-,15-,16-,18-,22-/m1/s1

> <INCHI_KEY>
MOMBVLIMWZDBMW-SQYLZNHDSA-N

> <FORMULA>
C22H31NO4

> <MOLECULAR_WEIGHT>
373.493

> <EXACT_MASS>
373.225308482

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
41.81094295623219

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3E,5R)-3-{[(1S,2R,4aS,6R,8aR)-1,6-dimethyl-2-[(1E)-prop-1-en-1-yl]-1,2,4a,5,6,7,8,8a-octahydronaphthalen-1-yl](hydroxy)methylidene}-5-[(1S)-1-hydroxyethyl]pyrrolidine-2,4-dione

> <ALOGPS_LOGP>
2.90

> <JCHEM_LOGP>
2.8624925773333327

> <ALOGPS_LOGS>
-4.18

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
10.421546120585782

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.6854050382587245

> <JCHEM_PKA_STRONGEST_BASIC>
-0.9501460514195715

> <JCHEM_POLAR_SURFACE_AREA>
86.63

> <JCHEM_REFRACTIVITY>
107.75369999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.47e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3E,5R)-3-{[(1S,2R,4aS,6R,8aR)-1,6-dimethyl-2-[(1E)-prop-1-en-1-yl]-4a,5,6,7,8,8a-hexahydro-2H-naphthalen-1-yl](hydroxy)methylidene}-5-[(1S)-1-hydroxyethyl]pyrrolidine-2,4-dione

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 58 60  0  0  0  0  0  0  0  0999 V2000
    0.9010    4.5290    1.7953 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3463    3.7269    0.6436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3857    2.6616    0.8204 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9184    1.8916   -0.3719 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3441    2.2378   -0.3514 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2761    1.3793   -0.6901 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7627    0.0428   -1.0885 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9311   -0.9088   -1.0418 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3092   -2.2558   -1.4263 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4469   -3.2607   -1.5640 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5089   -2.6499   -0.2405 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5148   -1.6903    0.3024 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7476   -0.2978   -0.0175 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4454    0.5131   -0.3538 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0363   -0.1060   -1.6710 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5042    0.1207    0.6843 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0696   -0.6507    1.7629 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7853    0.4889    0.6327 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4638    1.2845   -0.3552 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9516    1.8053   -1.3560 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8422    1.3447    0.0677 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.0980    0.3083    1.0482 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4771   -0.9399    0.2865 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6803   -2.1286    1.1626 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6288   -0.6246   -0.4573 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7643    0.0704    1.6599 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5216   -0.3847    2.7969 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0680    5.5593    1.4394 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8035    4.0570    2.2201 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0892    4.5524    2.5736 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5712    4.0581   -0.3795 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6333    2.2975    1.7810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6480    2.4677   -1.3182 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6202    3.2715   -0.0401 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3311    1.5665   -0.7004 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3042    0.0733   -2.1038 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2493   -0.9934    0.0204 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7493   -0.6268   -1.7004 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7004   -2.2088   -2.3250 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7841   -3.2981   -2.6061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2694   -2.9304   -0.8702 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0595   -4.2719   -1.2544 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9697   -3.6425   -0.4389 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2468   -2.9693    0.5839 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6557   -1.8733    1.4271 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5106   -2.0886    0.0009 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1799    0.1610    0.9199 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1366    0.6181   -2.4872 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6684   -1.0352   -1.8965 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9730   -0.5448   -1.6897 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6294   -1.4578    1.9998 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5014    2.0460   -0.3093 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8626    0.6078    1.7893 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6805   -1.1299   -0.4530 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6159   -1.8284    2.2296 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9549   -2.9115    0.8922 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6932   -2.5608    0.9593 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8669   -1.4717   -0.9415 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  1
 16 17  1  0
 16 18  2  0
 18 19  1  0
 19 20  2  0
 19 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 23 25  1  0
 22 26  1  0
 26 27  2  0
 14  4  1  0
 26 18  1  0
 13  7  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  2 31  1  0
  3 32  1  0
  4 33  1  6
  5 34  1  0
  6 35  1  0
  7 36  1  6
  8 37  1  0
  8 38  1  0
  9 39  1  6
 10 40  1  0
 10 41  1  0
 10 42  1  0
 11 43  1  0
 11 44  1  0
 12 45  1  0
 12 46  1  0
 13 47  1  1
 15 48  1  0
 15 49  1  0
 15 50  1  0
 17 51  1  0
 21 52  1  0
 22 53  1  1
 23 54  1  6
 24 55  1  0
 24 56  1  0
 24 57  1  0
 25 58  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0       0.901   4.529   1.795  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.346   3.727   0.644  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.386   2.662   0.820  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.918   1.892  -0.372  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.344   2.238  -0.351  0.00  0.00           C+0
HETATM    6  C   UNK     0      -3.276   1.379  -0.690  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.763   0.043  -1.089  0.00  0.00           C+0
HETATM    8  C   UNK     0      -3.931  -0.909  -1.042  0.00  0.00           C+0
HETATM    9  C   UNK     0      -3.309  -2.256  -1.426  0.00  0.00           C+0
HETATM   10  C   UNK     0      -4.447  -3.261  -1.564  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.509  -2.650  -0.241  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.515  -1.690   0.302  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.748  -0.298  -0.018  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.445   0.513  -0.354  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.036  -0.106  -1.671  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.504   0.121   0.684  0.00  0.00           C+0
HETATM   17  O   UNK     0       0.070  -0.651   1.763  0.00  0.00           O+0
HETATM   18  C   UNK     0       1.785   0.489   0.633  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.464   1.285  -0.355  0.00  0.00           C+0
HETATM   20  O   UNK     0       1.952   1.805  -1.356  0.00  0.00           O+0
HETATM   21  N   UNK     0       3.842   1.345   0.068  0.00  0.00           N+0
HETATM   22  C   UNK     0       4.098   0.308   1.048  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.477  -0.940   0.287  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.680  -2.129   1.163  0.00  0.00           C+0
HETATM   25  O   UNK     0       5.629  -0.625  -0.457  0.00  0.00           O+0
HETATM   26  C   UNK     0       2.764   0.070   1.660  0.00  0.00           C+0
HETATM   27  O   UNK     0       2.522  -0.385   2.797  0.00  0.00           O+0
HETATM   28  H   UNK     0       1.068   5.559   1.439  0.00  0.00           H+0
HETATM   29  H   UNK     0       1.804   4.057   2.220  0.00  0.00           H+0
HETATM   30  H   UNK     0       0.089   4.552   2.574  0.00  0.00           H+0
HETATM   31  H   UNK     0       0.571   4.058  -0.380  0.00  0.00           H+0
HETATM   32  H   UNK     0      -0.633   2.297   1.781  0.00  0.00           H+0
HETATM   33  H   UNK     0      -0.648   2.468  -1.318  0.00  0.00           H+0
HETATM   34  H   UNK     0      -2.620   3.272  -0.040  0.00  0.00           H+0
HETATM   35  H   UNK     0      -4.331   1.567  -0.700  0.00  0.00           H+0
HETATM   36  H   UNK     0      -2.304   0.073  -2.104  0.00  0.00           H+0
HETATM   37  H   UNK     0      -4.249  -0.993   0.020  0.00  0.00           H+0
HETATM   38  H   UNK     0      -4.749  -0.627  -1.700  0.00  0.00           H+0
HETATM   39  H   UNK     0      -2.700  -2.209  -2.325  0.00  0.00           H+0
HETATM   40  H   UNK     0      -4.784  -3.298  -2.606  0.00  0.00           H+0
HETATM   41  H   UNK     0      -5.269  -2.930  -0.870  0.00  0.00           H+0
HETATM   42  H   UNK     0      -4.059  -4.272  -1.254  0.00  0.00           H+0
HETATM   43  H   UNK     0      -1.970  -3.643  -0.439  0.00  0.00           H+0
HETATM   44  H   UNK     0      -3.247  -2.969   0.584  0.00  0.00           H+0
HETATM   45  H   UNK     0      -1.656  -1.873   1.427  0.00  0.00           H+0
HETATM   46  H   UNK     0      -0.511  -2.089   0.001  0.00  0.00           H+0
HETATM   47  H   UNK     0      -2.180   0.161   0.920  0.00  0.00           H+0
HETATM   48  H   UNK     0      -0.137   0.618  -2.487  0.00  0.00           H+0
HETATM   49  H   UNK     0      -0.668  -1.035  -1.897  0.00  0.00           H+0
HETATM   50  H   UNK     0       0.973  -0.545  -1.690  0.00  0.00           H+0
HETATM   51  H   UNK     0       0.629  -1.458   2.000  0.00  0.00           H+0
HETATM   52  H   UNK     0       4.501   2.046  -0.309  0.00  0.00           H+0
HETATM   53  H   UNK     0       4.863   0.608   1.789  0.00  0.00           H+0
HETATM   54  H   UNK     0       3.680  -1.130  -0.453  0.00  0.00           H+0
HETATM   55  H   UNK     0       4.616  -1.828   2.230  0.00  0.00           H+0
HETATM   56  H   UNK     0       3.955  -2.912   0.892  0.00  0.00           H+0
HETATM   57  H   UNK     0       5.693  -2.561   0.959  0.00  0.00           H+0
HETATM   58  H   UNK     0       5.867  -1.472  -0.942  0.00  0.00           H+0
CONECT    1    2   28   29   30                                             
CONECT    2    1    3   31                                                  
CONECT    3    2    4   32                                                  
CONECT    4    3    5   14   33                                             
CONECT    5    4    6   34                                                  
CONECT    6    5    7   35                                                  
CONECT    7    6    8   13   36                                             
CONECT    8    7    9   37   38                                             
CONECT    9    8   10   11   39                                             
CONECT   10    9   40   41   42                                             
CONECT   11    9   12   43   44                                             
CONECT   12   11   13   45   46                                             
CONECT   13   12   14    7   47                                             
CONECT   14   13   15   16    4                                             
CONECT   15   14   48   49   50                                             
CONECT   16   14   17   18                                                  
CONECT   17   16   51                                                       
CONECT   18   16   19   26                                                  
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   52                                                  
CONECT   22   21   23   26   53                                             
CONECT   23   22   24   25   54                                             
CONECT   24   23   55   56   57                                             
CONECT   25   23   58                                                       
CONECT   26   22   27   18                                                  
CONECT   27   26                                                            
CONECT   28    1                                                            
CONECT   29    1                                                            
CONECT   30    1                                                            
CONECT   31    2                                                            
CONECT   32    3                                                            
CONECT   33    4                                                            
CONECT   34    5                                                            
CONECT   35    6                                                            
CONECT   36    7                                                            
CONECT   37    8                                                            
CONECT   38    8                                                            
CONECT   39    9                                                            
CONECT   40   10                                                            
CONECT   41   10                                                            
CONECT   42   10                                                            
CONECT   43   11                                                            
CONECT   44   11                                                            
CONECT   45   12                                                            
CONECT   46   12                                                            
CONECT   47   13                                                            
CONECT   48   15                                                            
CONECT   49   15                                                            
CONECT   50   15                                                            
CONECT   51   17                                                            
CONECT   52   21                                                            
CONECT   53   22                                                            
CONECT   54   23                                                            
CONECT   55   24                                                            
CONECT   56   24                                                            
CONECT   57   24                                                            
CONECT   58   25                                                            
MASTER        0    0    0    0    0    0    0    0   58    0  120    0
END

RDKit          3D

58 60  0  0  0  0  0  0  0  0999 V2000
    0.9010    4.5290    1.7953 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3463    3.7269    0.6436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3857    2.6616    0.8204 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9184    1.8916   -0.3719 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3441    2.2378   -0.3514 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2761    1.3793   -0.6901 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7627    0.0428   -1.0885 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9311   -0.9088   -1.0418 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3092   -2.2558   -1.4263 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4469   -3.2607   -1.5640 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5089   -2.6499   -0.2405 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5148   -1.6903    0.3024 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7476   -0.2978   -0.0175 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4454    0.5131   -0.3538 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0363   -0.1060   -1.6710 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5042    0.1207    0.6843 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0696   -0.6507    1.7629 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7853    0.4889    0.6327 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4638    1.2845   -0.3552 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9516    1.8053   -1.3560 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8422    1.3447    0.0677 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.0980    0.3083    1.0482 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4771   -0.9399    0.2865 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6803   -2.1286    1.1626 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6288   -0.6246   -0.4573 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7643    0.0704    1.6599 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5216   -0.3847    2.7969 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0680    5.5593    1.4394 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8035    4.0570    2.2201 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0892    4.5524    2.5736 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5712    4.0581   -0.3795 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6333    2.2975    1.7810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6480    2.4677   -1.3182 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6202    3.2715   -0.0401 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3311    1.5665   -0.7004 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3042    0.0733   -2.1038 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2493   -0.9934    0.0204 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7493   -0.6268   -1.7004 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7004   -2.2088   -2.3250 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7841   -3.2981   -2.6061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2694   -2.9304   -0.8702 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0595   -4.2719   -1.2544 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9697   -3.6425   -0.4389 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2468   -2.9693    0.5839 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6557   -1.8733    1.4271 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5106   -2.0886    0.0009 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1799    0.1610    0.9199 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1366    0.6181   -2.4872 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6684   -1.0352   -1.8965 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9730   -0.5448   -1.6897 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6294   -1.4578    1.9998 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5014    2.0460   -0.3093 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8626    0.6078    1.7893 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6805   -1.1299   -0.4530 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6159   -1.8284    2.2296 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9549   -2.9115    0.8922 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6932   -2.5608    0.9593 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8669   -1.4717   -0.9415 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  1
 16 17  1  0
 16 18  2  0
 18 19  1  0
 19 20  2  0
 19 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 23 25  1  0
 22 26  1  0
 26 27  2  0
 14  4  1  0
 26 18  1  0
 13  7  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  2 31  1  0
  3 32  1  0
  4 33  1  6
  5 34  1  0
  6 35  1  0
  7 36  1  6
  8 37  1  0
  8 38  1  0
  9 39  1  6
 10 40  1  0
 10 41  1  0
 10 42  1  0
 11 43  1  0
 11 44  1  0
 12 45  1  0
 12 46  1  0
 13 47  1  1
 15 48  1  0
 15 49  1  0
 15 50  1  0
 17 51  1  0
 21 52  1  0
 22 53  1  1
 23 54  1  6
 24 55  1  0
 24 56  1  0
 24 57  1  0
 25 58  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₂₂H₃₁NO₄

Average Mass

373.4930 Da

Monoisotopic Mass

373.22531 Da

IUPAC Name

(3E,5R)-3-{[(1S,2R,4aS,6R,8aR)-1,6-dimethyl-2-[(1E)-prop-1-en-1-yl]-1,2,4a,5,6,7,8,8a-octahydronaphthalen-1-yl](hydroxy)methylidene}-5-[(1S)-1-hydroxyethyl]pyrrolidine-2,4-dione

Traditional Name

(3E,5R)-3-{[(1S,2R,4aS,6R,8aR)-1,6-dimethyl-2-[(1E)-prop-1-en-1-yl]-4a,5,6,7,8,8a-hexahydro-2H-naphthalen-1-yl](hydroxy)methylidene}-5-[(1S)-1-hydroxyethyl]pyrrolidine-2,4-dione

CAS Registry Number

Not Available

SMILES

C\C=C\[C@@H]1C=C[C@@H]2C[C@H](C)CC[C@H]2[C@]1(C)C(\O)=C1/C(=O)NC(C(C)O)C1=O

InChI Identifier

InChI=1S/C22H31NO4/c1-5-6-15-9-8-14-11-12(2)7-10-16(14)22(15,4)20(26)17-19(25)18(13(3)24)23-21(17)27/h5-6,8-9,12-16,18,24,26H,7,10-11H2,1-4H3,(H,23,27)/b6-5+,20-17+/t12-,13?,14-,15-,16-,18?,22-/m1/s1

InChI Key

MOMBVLIMWZDBMW-SQYLZNHDSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Cordyceps farinosa	Fungi	KNApSAcK
Paecilomyces	NPAtlas	15921439

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyrrolidine-3-ones. These are pyrrolidines which bear a C=O group at position 3 of the pyrrolidine ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Pyrrolidines

Sub Class

Pyrrolidones

Direct Parent

Pyrrolidine-3-ones

Alternative Parents

Substituents

2-pyrrolidone
3-pyrrolidone
Vinylogous acid
Carboxamide group
Ketone
Lactam
Cyclic ketone
Secondary carboxylic acid amide
Secondary alcohol
Carboxylic acid derivative
Enol
Azacycle
Organonitrogen compound
Alcohol
Carbonyl group
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organic nitrogen compound
Organic oxygen compound
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
logP	2.9	ALOGPS
logP	2.86	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Acidic)	4.69	ChemAxon
pKa (Strongest Basic)	-0.95	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	86.63 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	107.75 m³·mol⁻¹	ChemAxon
Polarizability	41.81 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	No	ChemAxon

External Links

NPAtlas ID

NPA010570

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00042823

Chemspider ID

78440663

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

54718903

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Lang G, Blunt JW, Cummings NJ, Cole AL, Munro MH: Paecilosetin, a new bioactive fungal metabolite from a New Zealand isolate of Paecilomyces farinosus. J Nat Prod. 2005 May;68(5):810-1. doi: 10.1021/np0500979. [PubMed:15921439 ]

Showing NP-Card for Paecilosetin (NP0005882)

MOL for NP0005882 (Paecilosetin)

3D MOL for NP0005882 (Paecilosetin)

3D SDF for NP0005882 (Paecilosetin)

3D-SDF for NP0005882 (Paecilosetin)

PDB for NP0005882 (Paecilosetin)

3D PDB for NP0005882 (Paecilosetin)

SMILES for NP0005882 (Paecilosetin)

INCHI for NP0005882 (Paecilosetin)

Structure for NP0005882 (Paecilosetin)

3D Structure for NP0005882 (Paecilosetin)