NP-MRD: Showing NP-Card for 7-{[(1r,2s,4as,8as)-1,2,4a-trimethyl-5-methylidene-hexahydro-2h-naphthalen-1-yl]methyl}-5-(acetyloxy)-1,3-benzoxazol-6-yl acetate (NP0258024)

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Record Information

Version

2.0

Created at

2022-09-07 23:18:51 UTC

Updated at

2022-09-07 23:18:51 UTC

NP-MRD ID

NP0258024

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7-{[(1r,2s,4as,8as)-1,2,4a-trimethyl-5-methylidene-hexahydro-2h-naphthalen-1-yl]methyl}-5-(acetyloxy)-1,3-benzoxazol-6-yl acetate

Description

Nakijinol B Diacetate, also known as nakijinol b diacetic acid, belongs to the class of organic compounds known as benzoxazoles. These are organic compounds containing a benzene fused to an oxazole ring Oxazole is five-membered aromatic ring with a nitrogen and an oxygen atoms at the 1- and 3-position, respectively. 7-{[(1r,2s,4as,8as)-1,2,4a-trimethyl-5-methylidene-hexahydro-2h-naphthalen-1-yl]methyl}-5-(acetyloxy)-1,3-benzoxazol-6-yl acetate is found in Dactylospongia elegans. 7-{[(1r,2s,4as,8as)-1,2,4a-trimethyl-5-methylidene-hexahydro-2h-naphthalen-1-yl]methyl}-5-(acetyloxy)-1,3-benzoxazol-6-yl acetate was first documented in 2011 (PMID: 21155589). Based on a literature review very few articles have been published on Nakijinol B Diacetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082201182D          

 32 35  0  0  1  0            999 V2000
    3.9384   -4.2793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3756   -3.5796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2001   -3.6084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6373   -2.9088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2499   -2.1803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4254   -2.1515    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9883   -2.8512    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5511   -3.5508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1638   -2.8224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7764   -2.0940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2136   -1.3943    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8263   -0.6659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0381   -1.4231    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0957   -0.6001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7526   -1.0106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7526   -0.1856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4671    0.2269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1815   -0.1856    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1815   -1.0106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4671   -1.4231    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8960   -1.4231    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4671    1.0519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1815    1.4644    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1815    2.2894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8960    2.7019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4671    2.7019    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7526    1.4644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0381    1.0519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2535    1.3068    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.7686    0.6394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2535   -0.0280    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0381    0.2269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  2  7  1  0  0  0  0
  7  8  1  6  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
 11 13  1  0  0  0  0
  6 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  1  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 17 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  2  0  0  0  0
 22 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 16 32  2  0  0  0  0
 28 32  1  0  0  0  0
M  END

     RDKit          3D

 65 68  0  0  0  0  0  0  0  0999 V2000
   -5.4672   -0.8375    0.0328 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3891   -0.1785   -0.3116 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2601    0.3708   -1.6645 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5872    1.7249   -1.6924 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.1038    0.4591   -0.1236 C   0  0  2  0  0  0  0  0  0  0  0  0
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   -2.9614   -1.3233    1.2821 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7009   -1.9291    0.8173 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4775   -1.0688    0.7579 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4386   -1.3656    1.9228 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7447    0.4097    0.5648 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7713    0.9679    1.9478 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2843    1.0405   -0.2810 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7000    1.0464    0.1040 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6225    0.2289   -0.5001 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2579   -0.6943   -1.5104 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4878   -2.0476   -1.3040 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1054   -3.0128   -2.3664 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0147   -2.3699   -0.2099 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9910    0.2282   -0.1905 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8781   -0.6298   -0.8432 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5372   -0.2776   -2.0094 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4864   -1.1536   -2.7391 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3154    0.8641   -2.4835 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3629    1.1186    0.7796 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4609    1.9529    1.4038 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6276    2.9008    2.3758 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4071    3.4045    2.5935 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5196    2.8377    1.8325 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1358    1.9379    1.0868 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2676   -0.9906   -0.6770 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6112   -1.2487    1.0224 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7115   -0.3689   -2.2844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2706    0.4715   -2.1082 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3209    2.4746   -1.3333 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4423    1.9601   -2.7672 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2365    2.5921   -0.2787 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4901    1.7806   -1.7038 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0105   -0.3389   -0.9319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3154    1.8937    1.8914 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9155    0.4492    2.7445 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8673    1.1936    1.4872 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1039   -1.3133    2.4019 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7727   -2.0575    0.9762 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4643   -2.7810    1.5194 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8974   -2.4596   -0.1623 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0537   -1.3960   -0.1576 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6995   -2.4612    1.8118 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0745   -1.3074    2.9078 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3842   -0.8345    1.8573 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5495    0.4396    2.5925 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1645    0.6645    2.4608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9656    2.0199    2.0645 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2013    0.6044   -1.3366 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0754    2.1277   -0.4953 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6870   -3.9553   -2.2938 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2289   -2.5497   -3.3735 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0262   -3.2442   -2.2647 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2054   -2.2254   -2.6422 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4999   -0.9521   -2.2839 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5510   -0.8367   -3.7867 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4280    1.1461    1.0499 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2475    4.2008    3.3415 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 11  1  0
 11 10  1  0
 10  9  1  0
  9  7  1  0
  7  8  1  1
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  2  3
  6 13  1  0
 13 14  1  1
 13 15  1  0
 15 16  1  0
 16 32  2  0
 32 31  1  0
 31 30  1  0
 30 29  2  0
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 23 24  1  0
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 17 18  1  0
 18 19  1  0
 19 20  1  0
 19 21  2  0
 13 11  1  0
 17 16  1  0
  2  7  1  0
 28 32  1  0
 12 50  1  0
 12 51  1  0
 12 52  1  0
 11 49  1  6
 10 47  1  0
 10 48  1  0
  9 45  1  0
  9 46  1  0
  8 42  1  0
  8 43  1  0
  8 44  1  0
  6 41  1  6
  5 39  1  0
  5 40  1  0
  4 37  1  0
  4 38  1  0
  3 35  1  0
  3 36  1  0
  1 33  1  0
  1 34  1  0
 14 53  1  0
 14 54  1  0
 14 55  1  0
 15 56  1  0
 15 57  1  0
 30 65  1  0
 27 64  1  0
 25 61  1  0
 25 62  1  0
 25 63  1  0
 20 58  1  0
 20 59  1  0
 20 60  1  0
M  END


  Mrv1652309082201182D          

 32 35  0  0  1  0            999 V2000
    3.9384   -4.2793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3756   -3.5796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2001   -3.6084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6373   -2.9088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2499   -2.1803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4254   -2.1515    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9883   -2.8512    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5511   -3.5508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1638   -2.8224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7764   -2.0940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2136   -1.3943    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8263   -0.6659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0381   -1.4231    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0957   -0.6001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7526   -1.0106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7526   -0.1856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4671    0.2269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1815   -0.1856    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1815   -1.0106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4671   -1.4231    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8960   -1.4231    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4671    1.0519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1815    1.4644    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1815    2.2894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8960    2.7019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4671    2.7019    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7526    1.4644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0381    1.0519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2535    1.3068    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.7686    0.6394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2535   -0.0280    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0381    0.2269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  2  7  1  0  0  0  0
  7  8  1  6  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
 11 13  1  0  0  0  0
  6 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  1  0  0  0
 15 16  1  0  0  0  0
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 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
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 24 26  2  0  0  0  0
 22 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 16 32  2  0  0  0  0
 28 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0258024

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1CC[C@@]2(C)[C@@H](CCCC2=C)[C@]1(C)CC1=C2OC=NC2=CC(OC(C)=O)=C1OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C26H33NO5/c1-15-8-7-9-22-25(15,5)11-10-16(2)26(22,6)13-19-23-20(27-14-30-23)12-21(31-17(3)28)24(19)32-18(4)29/h12,14,16,22H,1,7-11,13H2,2-6H3/t16-,22+,25+,26+/m0/s1

> <INCHI_KEY>
LBTUMRYFDFRELU-NDHSLDTFSA-N

> <FORMULA>
C26H33NO5

> <MOLECULAR_WEIGHT>
439.552

> <EXACT_MASS>
439.235873167

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
65

> <JCHEM_AVERAGE_POLARIZABILITY>
47.399707522748216

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
7-{[(1R,2S,4aS,8aS)-1,2,4a-trimethyl-5-methylidene-decahydronaphthalen-1-yl]methyl}-5-(acetyloxy)-1,3-benzoxazol-6-yl acetate

> <JCHEM_LOGP>
4.919881505

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
1.100528190555832

> <JCHEM_POLAR_SURFACE_AREA>
78.63000000000001

> <JCHEM_REFRACTIVITY>
120.10239999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
7-{[(1R,2S,4aS,8aS)-1,2,4a-trimethyl-5-methylidene-hexahydro-2H-naphthalen-1-yl]methyl}-5-(acetyloxy)-1,3-benzoxazol-6-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0       7.352  -7.988   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.168  -6.682   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.707  -6.736   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.523  -5.430   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.800  -4.070   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.261  -4.016   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.445  -5.322   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.629  -6.628   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.906  -5.268   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.183  -3.909   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.999  -2.603   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.276  -1.243   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.538  -2.656   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.645  -1.120   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.872  -1.886   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.872  -0.346   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.205   0.424   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      11.539  -0.346   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      11.539  -1.886   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      10.205  -2.656   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      12.873  -2.656   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      10.205   1.964   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      11.539   2.734   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      11.539   4.274   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      12.873   5.044   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      10.205   5.044   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       8.872   2.734   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       7.538   1.964   0.000  0.00  0.00           C+0
HETATM   29  N   UNK     0       6.073   2.439   0.000  0.00  0.00           N+0
HETATM   30  C   UNK     0       5.168   1.194   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       6.073  -0.052   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       7.538   0.424   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   13                                                  
CONECT    7    6    2    8    9                                             
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11    6   14   15                                             
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17   32                                                  
CONECT   17   16   18   22                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19                                                            
CONECT   22   17   23   27                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24                                                            
CONECT   27   22   28                                                       
CONECT   28   27   29   32                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   16   28                                                  
MASTER        0    0    0    0    0    0    0    0   32    0   70    0
END

View in JSmol

Synonyms

Value	Source
Nakijinol b diacetic acid	Generator

Chemical Formula

C₂₆H₃₃NO₅

Average Mass

439.5520 Da

Monoisotopic Mass

439.23587 Da

IUPAC Name

7-{[(1R,2S,4aS,8aS)-1,2,4a-trimethyl-5-methylidene-decahydronaphthalen-1-yl]methyl}-5-(acetyloxy)-1,3-benzoxazol-6-yl acetate

Traditional Name

7-{[(1R,2S,4aS,8aS)-1,2,4a-trimethyl-5-methylidene-hexahydro-2H-naphthalen-1-yl]methyl}-5-(acetyloxy)-1,3-benzoxazol-6-yl acetate

CAS Registry Number

Not Available

SMILES

C[C@H]1CC[C@@]2(C)[C@@H](CCCC2=C)[C@]1(C)CC1=C2OC=NC2=CC(OC(C)=O)=C1OC(C)=O

InChI Identifier

InChI=1S/C26H33NO5/c1-15-8-7-9-22-25(15,5)11-10-16(2)26(22,6)13-19-23-20(27-14-30-23)12-21(31-17(3)28)24(19)32-18(4)29/h12,14,16,22H,1,7-11,13H2,2-6H3/t16-,22+,25+,26+/m0/s1

InChI Key

LBTUMRYFDFRELU-NDHSLDTFSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Dactylospongia elegans	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzoxazoles. These are organic compounds containing a benzene fused to an oxazole ring Oxazole is five-membered aromatic ring with a nitrogen and an oxygen atoms at the 1- and 3-position, respectively.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzoxazoles

Sub Class

Not Available

Direct Parent

Benzoxazoles

Alternative Parents

Substituents

Benzoxazole
Dicarboxylic acid or derivatives
Benzenoid
Azole
Oxazole
Heteroaromatic compound
Carboxylic acid ester
Oxacycle
Azacycle
Carboxylic acid derivative
Organopnictogen compound
Organooxygen compound
Organonitrogen compound
Organic oxygen compound
Carbonyl group
Organic nitrogen compound
Hydrocarbon derivative
Organic oxide
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	4.92	ChemAxon
pKa (Strongest Basic)	1.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	78.63 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	120.1 m³·mol⁻¹	ChemAxon
Polarizability	47.4 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

Not Available

Chemspider ID

26383903

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

50994613

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Ovenden SP, Nielson JL, Liptrot CH, Willis RH, Tapiolas DM, Wright AD, Motti CA: Sesquiterpene benzoxazoles and sesquiterpene quinones from the marine sponge Dactylospongia elegans. J Nat Prod. 2011 Jan 28;74(1):65-8. doi: 10.1021/np100669p. Epub 2010 Dec 14. [PubMed:21155589 ]
LOTUS database [Link]

Showing NP-Card for 7-{[(1r,2s,4as,8as)-1,2,4a-trimethyl-5-methylidene-hexahydro-2h-naphthalen-1-yl]methyl}-5-(acetyloxy)-1,3-benzoxazol-6-yl acetate (NP0258024)

MOL for NP0258024 (7-{[(1r,2s,4as,8as)-1,2,4a-trimethyl-5-methylidene-hexahydro-2h-naphthalen-1-yl]methyl}-5-(acetyloxy)-1,3-benzoxazol-6-yl acetate)

3D MOL for NP0258024 (7-{[(1r,2s,4as,8as)-1,2,4a-trimethyl-5-methylidene-hexahydro-2h-naphthalen-1-yl]methyl}-5-(acetyloxy)-1,3-benzoxazol-6-yl acetate)

3D SDF for NP0258024 (7-{[(1r,2s,4as,8as)-1,2,4a-trimethyl-5-methylidene-hexahydro-2h-naphthalen-1-yl]methyl}-5-(acetyloxy)-1,3-benzoxazol-6-yl acetate)

3D-SDF for NP0258024 (7-{[(1r,2s,4as,8as)-1,2,4a-trimethyl-5-methylidene-hexahydro-2h-naphthalen-1-yl]methyl}-5-(acetyloxy)-1,3-benzoxazol-6-yl acetate)

PDB for NP0258024 (7-{[(1r,2s,4as,8as)-1,2,4a-trimethyl-5-methylidene-hexahydro-2h-naphthalen-1-yl]methyl}-5-(acetyloxy)-1,3-benzoxazol-6-yl acetate)

3D PDB for NP0258024 (7-{[(1r,2s,4as,8as)-1,2,4a-trimethyl-5-methylidene-hexahydro-2h-naphthalen-1-yl]methyl}-5-(acetyloxy)-1,3-benzoxazol-6-yl acetate)

SMILES for NP0258024 (7-{[(1r,2s,4as,8as)-1,2,4a-trimethyl-5-methylidene-hexahydro-2h-naphthalen-1-yl]methyl}-5-(acetyloxy)-1,3-benzoxazol-6-yl acetate)

INCHI for NP0258024 (7-{[(1r,2s,4as,8as)-1,2,4a-trimethyl-5-methylidene-hexahydro-2h-naphthalen-1-yl]methyl}-5-(acetyloxy)-1,3-benzoxazol-6-yl acetate)

Structure for NP0258024 (7-{[(1r,2s,4as,8as)-1,2,4a-trimethyl-5-methylidene-hexahydro-2h-naphthalen-1-yl]methyl}-5-(acetyloxy)-1,3-benzoxazol-6-yl acetate)

3D Structure for NP0258024 (7-{[(1r,2s,4as,8as)-1,2,4a-trimethyl-5-methylidene-hexahydro-2h-naphthalen-1-yl]methyl}-5-(acetyloxy)-1,3-benzoxazol-6-yl acetate)