NP-MRD: Showing NP-Card for Striatisporolide A (NP0005835)

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Record Information

Version

2.0

Created at

2020-12-09 02:58:52 UTC

Updated at

2021-07-15 16:53:06 UTC

NP-MRD ID

NP0005835

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Striatisporolide A

Provided By

NPAtlas

Description

Striatisporolide A is found in Penicillium striatisporum. Striatisporolide A was first documented in 2005 (PMID: 15844954). Based on a literature review a small amount of articles have been published on Striatisporolide A (PMID: 31960725) (PMID: 31115578) (PMID: 27669209) (PMID: 19675888).

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242118233D          

 31 31  0  0  0  0            999 V2000
   -4.6587    0.2140    0.2615 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3473   -0.2586   -0.3807 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3657   -0.4148    0.7451 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9989   -0.9018    0.2531 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4776    0.0864   -0.6889 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8636   -0.2145   -1.3641 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0434    0.9405   -2.1673 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1689    1.6009   -1.7693 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6627    2.6903   -2.2084 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7782    0.8357   -0.6922 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0446    1.2052    0.0266 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.4265   -1.2315    0.5332 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7486   -2.2565    0.7657 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5981   -1.0965    1.2844 O   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

 31 31  0  0  0  0  0  0  0  0999 V2000
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    1.0434    0.9405   -2.1673 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1689    1.6009   -1.7693 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.1569   -1.9141    1.4779 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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M  END


  Mrv1652306242118233D          

 31 31  0  0  0  0            999 V2000
   -4.6587    0.2140    0.2615 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3473   -0.2586   -0.3807 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3657   -0.4148    0.7451 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9989   -0.9018    0.2531 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4776    0.0864   -0.6889 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8636   -0.2145   -1.3641 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0434    0.9405   -2.1673 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1689    1.6009   -1.7693 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6627    2.6903   -2.2084 O   0  0  0  0  0  0  0  0  0  0  0  0
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    1.7486   -2.2565    0.7657 O   0  0  0  0  0  0  0  0  0  0  0  0
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 15 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0005835

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C11H16O4/c1-3-4-5-6-8-9(10(12)13)7(2)11(14)15-8/h8H,3-6H2,1-2H3,(H,12,13)/t8-/m1/s1

> <INCHI_KEY>
OIUPBOONLQPLQI-UHFFFAOYSA-N

> <FORMULA>
C11H16O4

> <MOLECULAR_WEIGHT>
212.245

> <EXACT_MASS>
212.104858995

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
31

> <JCHEM_AVERAGE_POLARIZABILITY>
22.54898788636233

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R)-4-methyl-5-oxo-2-pentyl-2,5-dihydrofuran-3-carboxylic acid

> <ALOGPS_LOGP>
2.47

> <JCHEM_LOGP>
2.6400233633333334

> <ALOGPS_LOGS>
-2.10

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
13.724137423226374

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.642864537749617

> <JCHEM_PKA_STRONGEST_BASIC>
-6.929534034929951

> <JCHEM_POLAR_SURFACE_AREA>
63.60000000000001

> <JCHEM_REFRACTIVITY>
54.349500000000006

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.70e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R)-4-methyl-5-oxo-2-pentyl-2H-furan-3-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 31 31  0  0  0  0  0  0  0  0999 V2000
   -4.6587    0.2140    0.2615 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3473   -0.2586   -0.3807 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.7782    0.8357   -0.6922 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.3658   -0.8888    1.1876 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.7808   -1.1318   -1.9914 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8548    0.4641   -0.2036 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8840    1.2178    1.1359 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3598    2.1954   -0.2974 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1569   -1.9141    1.4779 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
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  8  9  2  0
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 10 11  1  0
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 13 14  2  0
 13 15  1  0
 12  6  1  0
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  6 27  1  6
 11 28  1  0
 11 29  1  0
 11 30  1  0
 15 31  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      -4.659   0.214   0.262  0.00  0.00           C+0
HETATM    2  C   UNK     0      -3.347  -0.259  -0.381  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.366  -0.415   0.745  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.999  -0.902   0.253  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.478   0.086  -0.689  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.864  -0.215  -1.364  0.00  0.00           C+0
HETATM    7  O   UNK     0       1.043   0.941  -2.167  0.00  0.00           O+0
HETATM    8  C   UNK     0       2.169   1.601  -1.769  0.00  0.00           C+0
HETATM    9  O   UNK     0       2.663   2.690  -2.208  0.00  0.00           O+0
HETATM   10  C   UNK     0       2.778   0.836  -0.692  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.045   1.205   0.027  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.015  -0.240  -0.462  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.426  -1.232   0.533  0.00  0.00           C+0
HETATM   14  O   UNK     0       1.749  -2.256   0.766  0.00  0.00           O+0
HETATM   15  O   UNK     0       3.598  -1.097   1.284  0.00  0.00           O+0
HETATM   16  H   UNK     0      -4.748  -0.395   1.201  0.00  0.00           H+0
HETATM   17  H   UNK     0      -5.508   0.011  -0.409  0.00  0.00           H+0
HETATM   18  H   UNK     0      -4.603   1.279   0.552  0.00  0.00           H+0
HETATM   19  H   UNK     0      -3.564  -1.212  -0.882  0.00  0.00           H+0
HETATM   20  H   UNK     0      -3.086   0.544  -1.110  0.00  0.00           H+0
HETATM   21  H   UNK     0      -2.795  -1.087   1.484  0.00  0.00           H+0
HETATM   22  H   UNK     0      -2.219   0.581   1.204  0.00  0.00           H+0
HETATM   23  H   UNK     0      -1.079  -1.895  -0.207  0.00  0.00           H+0
HETATM   24  H   UNK     0      -0.366  -0.889   1.188  0.00  0.00           H+0
HETATM   25  H   UNK     0      -1.189   0.157  -1.567  0.00  0.00           H+0
HETATM   26  H   UNK     0      -0.381   1.116  -0.274  0.00  0.00           H+0
HETATM   27  H   UNK     0       0.781  -1.132  -1.991  0.00  0.00           H+0
HETATM   28  H   UNK     0       4.855   0.464  -0.204  0.00  0.00           H+0
HETATM   29  H   UNK     0       3.884   1.218   1.136  0.00  0.00           H+0
HETATM   30  H   UNK     0       4.360   2.195  -0.297  0.00  0.00           H+0
HETATM   31  H   UNK     0       4.157  -1.914   1.478  0.00  0.00           H+0
CONECT    1    2   16   17   18                                             
CONECT    2    1    3   19   20                                             
CONECT    3    2    4   21   22                                             
CONECT    4    3    5   23   24                                             
CONECT    5    4    6   25   26                                             
CONECT    6    5    7   12   27                                             
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   12                                                  
CONECT   11   10   28   29   30                                             
CONECT   12   10   13    6                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   31                                                       
CONECT   16    1                                                            
CONECT   17    1                                                            
CONECT   18    1                                                            
CONECT   19    2                                                            
CONECT   20    2                                                            
CONECT   21    3                                                            
CONECT   22    3                                                            
CONECT   23    4                                                            
CONECT   24    4                                                            
CONECT   25    5                                                            
CONECT   26    5                                                            
CONECT   27    6                                                            
CONECT   28   11                                                            
CONECT   29   11                                                            
CONECT   30   11                                                            
CONECT   31   15                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   62    0
END

RDKit          3D

31 31  0  0  0  0  0  0  0  0999 V2000
   -4.6587    0.2140    0.2615 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3473   -0.2586   -0.3807 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3657   -0.4148    0.7451 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9989   -0.9018    0.2531 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4776    0.0864   -0.6889 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8636   -0.2145   -1.3641 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0434    0.9405   -2.1673 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1689    1.6009   -1.7693 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6627    2.6903   -2.2084 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7782    0.8357   -0.6922 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0446    1.2052    0.0266 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0153   -0.2400   -0.4624 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4265   -1.2315    0.5332 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7486   -2.2565    0.7657 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5981   -1.0965    1.2844 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7479   -0.3949    1.2014 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5085    0.0114   -0.4085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6030    1.2790    0.5515 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5637   -1.2122   -0.8823 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0857    0.5441   -1.1096 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7950   -1.0874    1.4837 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2190    0.5809    1.2036 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0795   -1.8947   -0.2066 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3658   -0.8888    1.1876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1894    0.1567   -1.5672 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3805    1.1158   -0.2737 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7808   -1.1318   -1.9914 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8548    0.4641   -0.2036 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8840    1.2178    1.1359 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3598    2.1954   -0.2974 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1569   -1.9141    1.4779 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 10 12  2  0
 12 13  1  0
 13 14  2  0
 13 15  1  0
 12  6  1  0
  1 16  1  0
  1 17  1  0
  1 18  1  0
  2 19  1  0
  2 20  1  0
  3 21  1  0
  3 22  1  0
  4 23  1  0
  4 24  1  0
  5 25  1  0
  5 26  1  0
  6 27  1  6
 11 28  1  0
 11 29  1  0
 11 30  1  0
 15 31  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
4-Methyl-5-oxo-2-pentyl-2,5-dihydrofuran-3-carboxylate	Generator

Chemical Formula

C₁₁H₁₆O₄

Average Mass

212.2450 Da

Monoisotopic Mass

212.10486 Da

IUPAC Name

(2R)-4-methyl-5-oxo-2-pentyl-2,5-dihydrofuran-3-carboxylic acid

Traditional Name

(2R)-4-methyl-5-oxo-2-pentyl-2H-furan-3-carboxylic acid

CAS Registry Number

Not Available

SMILES

CCCCCC1OC(=O)C(C)=C1C(O)=O

InChI Identifier

InChI=1S/C11H16O4/c1-3-4-5-6-8-9(10(12)13)7(2)11(14)15-8/h8H,3-6H2,1-2H3,(H,12,13)

InChI Key

OIUPBOONLQPLQI-UHFFFAOYSA-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
Penicillium striatisporum	NPAtlas	15844954

Chemical Taxonomy

Description

This compound belongs to the class of organic compounds known as butenolides. These are dihydrofurans with a carbonyl group at the C2 carbon atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Dihydrofurans

Sub Class

Furanones

Direct Parent

Butenolides

Alternative Parents

Substituents

Dicarboxylic acid or derivatives
2-furanone
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Lactone
Carboxylic acid ester
Oxacycle
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen 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	2.47	ALOGPS
logP	2.64	ChemAxon
logS	-2.1	ALOGPS
pKa (Strongest Acidic)	3.64	ChemAxon
pKa (Strongest Basic)	-6.9	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	63.6 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	54.35 m³·mol⁻¹	ChemAxon
Polarizability	22.55 Å³	ChemAxon
Number of Rings	1	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

NPA009773

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00043035

Chemspider ID

21615446

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

45359437

PDB ID

Not Available

ChEBI ID

173349

Good Scents ID

Not Available

References

General References

Stewart M, Capon RJ, Lacey E, Tennant S, Gill JH: Calbistrin E and two other new metabolites from an Australian isolate of Penicillium striatisporum. J Nat Prod. 2005 Apr;68(4):581-4. doi: 10.1021/np049614y. [PubMed:15844954 ]
Mei RQ, Nong XH, Wang B, Sun XP, Huang GL, Luo YP, Zheng CJ, Chen GY: A new phenol derivative isolated from mangrove-derived fungus Eupenicillium sp. HJ002. Nat Prod Res. 2020 Jan 21:1-7. doi: 10.1080/14786419.2020.1712388. [PubMed:31960725 ]
Sheng JW, Liu DM, Jing L, Xia GX, Zhang WF, Jiang JR, Tang JB: Striatisporolide A, a butenolide metabolite from Athyrium multidentatum (Doll.) Ching, as a potential antibacterial agent. Mol Med Rep. 2019 Jul;20(1):198-204. doi: 10.3892/mmr.2019.10244. Epub 2019 May 15. [PubMed:31115578 ]
Liu DM, Sheng JW, Wang SH, Zhang WF, Zhang W, Zhang DJ: Cytoproliferative and Cytoprotective Effects of Striatisporolide A Isolated from Rhizomes of Athyrium multidentatum (Doell.) Ching on Human Umbilical Vein Endothelial Cells. Molecules. 2016 Sep 24;21(10). pii: molecules21101280. doi: 10.3390/molecules21101280. [PubMed:27669209 ]
Deska J, Backvall JE: Enzymatic kinetic resolution of primary allenic alcohols. Application to the total synthesis and stereochemical assignment of striatisporolide A. Org Biomol Chem. 2009 Sep 7;7(17):3379-81. doi: 10.1039/b912128p. Epub 2009 Jul 9. [PubMed:19675888 ]

Showing NP-Card for Striatisporolide A (NP0005835)

MOL for NP0005835 (Striatisporolide A)

3D MOL for NP0005835 (Striatisporolide A)

3D SDF for NP0005835 (Striatisporolide A)

3D-SDF for NP0005835 (Striatisporolide A)

PDB for NP0005835 (Striatisporolide A)

3D PDB for NP0005835 (Striatisporolide A)

SMILES for NP0005835 (Striatisporolide A)

INCHI for NP0005835 (Striatisporolide A)

Structure for NP0005835 (Striatisporolide A)

3D Structure for NP0005835 (Striatisporolide A)