NP-MRD: Showing NP-Card for Astellolide A (NP0063490)

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Record Information

Version

2.0

Created at

2022-04-28 07:53:42 UTC

Updated at

2024-09-03 04:15:02 UTC

NP-MRD ID

NP0063490

Natural Product DOI

https://doi.org/10.57994/0130

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Astellolide A

Description

Astellolide A belongs to the class of organic compounds known as naphthofurans. Naphthofurans are compounds containing a furan ring fused to a naphthalene moiety. Furan is a 5 membered- ring aromatic ring with four carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings. Astellolide A is found in Aspergillus parasiticus and Aspergillus variecolor. Based on a literature review very few articles have been published on Astellolide A.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282209532D          

 34 37  0  0  1  0            999 V2000
    2.8571    0.8217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2470    1.5487    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8124    2.2499    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9878    2.2242    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5978    1.4972    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0325    0.7959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7732    1.4714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3386    2.1727    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7286    2.8997    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5532    2.9254    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9432    3.6524    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5086    4.3537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6840    4.3279    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8986    5.0807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4640    5.7819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8540    6.5089    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6786    6.5347    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1132    5.8334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7232    5.1064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4626    1.9760    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0926    2.5086    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5232    1.1532    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2406    0.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2079    0.7702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6425    0.0689    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2525   -0.6581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6871   -1.3593    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4279   -0.6838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4981    2.7088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4436    3.5320    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1292    3.9908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8694    3.6264    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0747    4.8140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8155    3.0749    0.0000 C   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
  4  3  1  1  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  4 10  1  0  0  0  0
 10 11  1  1  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 14 19  1  0  0  0  0
  8 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
  7 23  1  0  0  0  0
  5 24  1  1  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
  3 29  1  1  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
  3 34  1  6  0  0  0
M  END

     RDKit          3D

 64 67  0  0  0  0  0  0  0  0999 V2000
   -2.0675   -5.7243    0.3307 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2175   -4.5989   -0.0672 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0158   -4.8264   -0.3009 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6406   -3.2914   -0.2142 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6921   -2.2695   -0.6150 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5489   -1.0062   -0.6568 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6271   -1.4028   -1.7100 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2833   -0.9742    0.6484 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9594    0.3025    0.9862 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5596    1.4583    0.1399 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0775    1.4565   -0.1965 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2132    1.4606    0.9766 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3359    2.5243    1.8485 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0461    3.8160    1.7710 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2160    4.8283    2.8412 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6558    4.2299    0.7651 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8628    2.5842   -1.1118 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0857    2.5609   -2.0264 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8223    1.3530   -2.4297 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5342    0.1290   -1.5916 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5231   -0.1695   -0.6842 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4362   -1.2014   -0.7346 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3345   -1.9447   -1.7439 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4421   -1.4169    0.2995 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3283   -2.4617    0.1996 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2746   -2.6513    1.1879 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3796   -1.8315    2.2918 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4675   -0.7951    2.3487 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5094   -0.5750    1.3814 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8729    0.2200   -1.0900 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2039    3.9132   -2.5399 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9814    4.3651   -3.4256 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7172    4.7256   -1.8884 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6348    3.8590   -1.2508 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5058   -6.4153    0.9917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9387   -5.3323    0.8844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3466   -6.3099   -0.5684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3030   -2.5835   -1.5720 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0339   -2.2596    0.1895 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2180   -1.1273   -2.6961 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8684   -2.4767   -1.6334 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5305   -0.8257   -1.5179 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6503   -1.3624    1.4972 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0973   -1.7668    0.5944 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6627    0.5682    2.0453 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0713    0.1874    1.0271 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1154    1.4269   -0.8187 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8252    2.4340    0.6091 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9052    1.4809    0.6772 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2450    0.5280    1.5926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3204    5.8585    2.4047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1552    4.5313    3.3298 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6126    4.8007    3.5671 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9105    1.5488   -2.5257 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4841    1.1156   -3.4619 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5579   -0.7130   -2.3542 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2822   -3.1459   -0.6685 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9685   -3.4934    1.0814 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1292   -1.9878    3.0676 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5232   -0.1205    3.2177 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8117    0.2734    1.4905 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4446    0.5642   -2.0391 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5259    3.6436   -1.8651 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9090    4.3125   -0.2854 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
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  8  9  1  0
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 11 12  1  1
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 13 14  1  0
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 33 31  1  0
 31 32  2  0
 20 21  1  0
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 22 23  2  0
 22 24  1  0
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 25 26  1  0
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 27 28  1  0
 28 29  2  0
 30  6  1  0
 31 18  1  0
 29 24  1  0
 17 11  1  0
  1 35  1  0
  1 36  1  0
  1 37  1  0
  5 38  1  0
  5 39  1  0
  7 40  1  0
  7 41  1  0
  7 42  1  0
  8 43  1  0
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 10 47  1  0
 10 48  1  0
 12 49  1  0
 12 50  1  0
 15 51  1  0
 15 52  1  0
 15 53  1  0
 30 62  1  6
 20 56  1  6
 19 54  1  0
 19 55  1  0
 34 63  1  0
 34 64  1  0
 25 57  1  0
 26 58  1  0
 27 59  1  0
 28 60  1  0
 29 61  1  0
M  END


  Mrv1652304282209532D          

 34 37  0  0  1  0            999 V2000
    2.8571    0.8217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2470    1.5487    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8124    2.2499    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9878    2.2242    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5978    1.4972    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0325    0.7959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7732    1.4714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3386    2.1727    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7286    2.8997    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5532    2.9254    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9432    3.6524    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5086    4.3537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6840    4.3279    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8986    5.0807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4640    5.7819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8540    6.5089    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6786    6.5347    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1132    5.8334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7232    5.1064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4626    1.9760    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0926    2.5086    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5232    1.1532    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2406    0.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2079    0.7702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6425    0.0689    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2525   -0.6581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6871   -1.3593    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4279   -0.6838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4981    2.7088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4436    3.5320    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1292    3.9908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8694    3.6264    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0747    4.8140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8155    3.0749    0.0000 C   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
  4  3  1  1  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  4 10  1  0  0  0  0
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 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 14 19  1  0  0  0  0
  8 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
  7 23  1  0  0  0  0
  5 24  1  1  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
  3 29  1  1  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
  3 34  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0063490

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC[C@@]1(C)CCC[C@@]2(COC(C)=O)[C@H]1[C@@H](CC1=C2COC1=O)OC(=O)C1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C26H30O8/c1-16(27)32-14-25(3)10-7-11-26(15-33-17(2)28)20-13-31-24(30)19(20)12-21(22(25)26)34-23(29)18-8-5-4-6-9-18/h4-6,8-9,21-22H,7,10-15H2,1-3H3/t21-,22+,25-,26+/m1/s1

> <INCHI_KEY>
ISPOIRCRAAHBEV-GETZNYBYSA-N

> <FORMULA>
C26H30O8

> <MOLECULAR_WEIGHT>
470.518

> <EXACT_MASS>
470.194067926

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
64

> <JCHEM_AVERAGE_POLARIZABILITY>
48.37267174297285

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(5R,5aS,6S,9aR)-6,9a-bis[(acetyloxy)methyl]-6-methyl-3-oxo-1H,3H,4H,5H,5aH,6H,7H,8H,9H,9aH-naphtho[1,2-c]furan-5-yl benzoate

> <ALOGPS_LOGP>
3.23

> <JCHEM_LOGP>
2.9947452923333335

> <ALOGPS_LOGS>
-4.94

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.929423445432203

> <JCHEM_PKA_STRONGEST_BASIC>
-6.34088137197843

> <JCHEM_POLAR_SURFACE_AREA>
105.20000000000002

> <JCHEM_REFRACTIVITY>
120.54899999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.43e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(5R,5aS,6S,9aR)-6,9a-bis[(acetyloxy)methyl]-6-methyl-3-oxo-1H,4H,5H,5aH,7H,8H,9H-naphtho[1,2-c]furan-5-yl benzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       5.333   1.534   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.061   2.891   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.250   4.200   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.711   4.152   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.983   2.795   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.794   1.486   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.443   2.747   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.632   4.056   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.360   5.413   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.899   5.461   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       3.627   6.818   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       2.816   8.127   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       1.277   8.079   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       3.544   9.484   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.733  10.793   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.461  12.150   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.000  12.198   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.811  10.889   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.083   9.532   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.863   3.689   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -2.040   4.683   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      -0.977   2.153   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       0.449   1.571   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.255   1.438   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       3.066   0.129   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       2.338  -1.228   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       3.149  -2.537   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       0.799  -1.276   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.530   5.056   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       6.428   6.593   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       7.708   7.449   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       9.089   6.769   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       7.606   8.986   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       5.256   5.740   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4   29   34                                             
CONECT    4    3    5   10                                                  
CONECT    5    4    6    7   24                                             
CONECT    6    5    1                                                       
CONECT    7    5    8   23                                                  
CONECT    8    7    9   20                                                  
CONECT    9    8   10                                                       
CONECT   10    9    4   11                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   19                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   14                                                       
CONECT   20    8   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22    7                                                       
CONECT   24    5   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26                                                            
CONECT   29    3   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31                                                            
CONECT   34    3                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   74    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₆H₃₀O₈

Average Mass

470.5180 Da

Monoisotopic Mass

470.19407 Da

IUPAC Name

(5R,5aS,6S,9aR)-6,9a-bis[(acetyloxy)methyl]-6-methyl-3-oxo-1H,3H,4H,5H,5aH,6H,7H,8H,9H,9aH-naphtho[1,2-c]furan-5-yl benzoate

Traditional Name

(5R,5aS,6S,9aR)-6,9a-bis[(acetyloxy)methyl]-6-methyl-3-oxo-1H,4H,5H,5aH,7H,8H,9H-naphtho[1,2-c]furan-5-yl benzoate

CAS Registry Number

Not Available

SMILES

CC(=O)OC[C@@]1(C)CCC[C@@]2(COC(C)=O)[C@H]1[C@@H](CC1=C2COC1=O)OC(=O)C1=CC=CC=C1

InChI Identifier

InChI=1S/C26H30O8/c1-16(27)32-14-25(3)10-7-11-26(15-33-17(2)28)20-13-31-24(30)19(20)12-21(22(25)26)34-23(29)18-8-5-4-6-9-18/h4-6,8-9,21-22H,7,10-15H2,1-3H3/t21-,22+,25-,26+/m1/s1

InChI Key

ISPOIRCRAAHBEV-GETZNYBYSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Merangelgri			2022-10-12	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl3, experimental)	merangelgri@uncg.edu	Not Available	Not Available	2023-01-12	View Spectrum
HMBC NMR	[¹H, ¹³C] NMR Spectrum (2D, 126 MHz, CDCl3, experimental)	merangelgri@uncg.edu	Not Available	Not Available	2023-01-12	View Spectrum
HSQC NMR	[¹H, ¹³C] NMR Spectrum (2D, 126 MHz, CDCl3, experimental)	merangelgri@uncg.edu	Not Available	Not Available	2023-01-12	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCl3, experimental)	merangelgri@uncg.edu	Not Available	Not Available	2023-01-12	View Spectrum
COSY NMR	[¹H, ¹H] NMR Spectrum (2D, 500 MHz, CDCl3, experimental)	merangelgri@uncg.edu	Not Available	Not Available	2023-01-12	View Spectrum
HMBC NMR	[¹H, ¹³C] NMR Spectrum (2D, 126 MHz, CDCl3, experimental)	merangelgri@uncg.edu	Not Available	Not Available	2022-12-21	View Spectrum
HSQC NMR	[¹H, ¹³C] NMR Spectrum (2D, 126 MHz, CDCl3, experimental)	merangelgri@uncg.edu	Not Available	Not Available	2022-12-21	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, CDCl3, experimental)	merangelgri@uncg.edu	Not Available	Not Available	2022-12-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl3, experimental)	merangelgri@uncg.edu	Not Available	Not Available	2022-12-21	View Spectrum
COSY NMR	[¹H, ¹H] NMR Spectrum (2D, 500 MHz, CDCl3, experimental)	merangelgri@uncg.edu	Not Available	Not Available	2022-12-21	View Spectrum

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
Aspergillus parasiticus	Fungi	KNApSAcK
Aspergillus stellatus	Fungi	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as naphthofurans. Naphthofurans are compounds containing a furan ring fused to a naphthalene moiety. Furan is a 5 membered- ring aromatic ring with four carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Naphthofurans

Sub Class

Not Available

Direct Parent

Naphthofurans

Alternative Parents

Substituents

Naphthofuran
Tetracarboxylic acid or derivatives
Benzoate ester
Benzoic acid or derivatives
Benzoyl
Monocyclic benzene moiety
Benzenoid
2-furanone
Alpha,beta-unsaturated carboxylic ester
Dihydrofuran
Enoate ester
Carboxylic acid ester
Lactone
Carboxylic acid derivative
Oxacycle
Organic oxygen compound
Carbonyl group
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	3.23	ALOGPS
logP	2.99	ChemAxon
logS	-4.9	ALOGPS
pKa (Strongest Acidic)	12.93	ChemAxon
pKa (Strongest Basic)	-6.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	105.2 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	120.55 m³·mol⁻¹	ChemAxon
Polarizability	48.37 Å³	ChemAxon
Number of Rings	4	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

C00020327

Chemspider ID

78443456

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

101277333

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Astellolide A (NP0063490)

MOL for NP0063490 (Astellolide A)

3D MOL for NP0063490 (Astellolide A)

3D SDF for NP0063490 (Astellolide A)

3D-SDF for NP0063490 (Astellolide A)

PDB for NP0063490 (Astellolide A)

3D PDB for NP0063490 (Astellolide A)

SMILES for NP0063490 (Astellolide A)

INCHI for NP0063490 (Astellolide A)

Structure for NP0063490 (Astellolide A)

3D Structure for NP0063490 (Astellolide A)