NP-MRD: Showing NP-Card for 15-hydroxy-14-methoxy-4,8,11,15-tetramethyl-9-oxo-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadecan-4-yl acetate (NP0148532)

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Record Information

Version

2.0

Created at

2022-09-02 04:17:47 UTC

Updated at

2022-09-02 04:17:47 UTC

NP-MRD ID

NP0148532

Secondary Accession Numbers

None

Natural Product Identification

Common Name

15-hydroxy-14-methoxy-4,8,11,15-tetramethyl-9-oxo-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadecan-4-yl acetate

Description

15-Hydroxy-14-methoxy-4,8,11,15-tetramethyl-9-oxo-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]Octadecan-4-yl acetate belongs to the class of organic compounds known as lactones. These are cyclic esters of hydroxy carboxylic acids, containing a 1-oxacycloalkan-2-one structure, or analogues having unsaturation or heteroatoms replacing one or more carbon atoms of the ring. 15-hydroxy-14-methoxy-4,8,11,15-tetramethyl-9-oxo-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadecan-4-yl acetate is found in Briareum asbestinum. 15-Hydroxy-14-methoxy-4,8,11,15-tetramethyl-9-oxo-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]Octadecan-4-yl acetate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004191523092D          

 30 33  0  0  0  0            999 V2000
    6.6572    0.7417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3662   -0.0303    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5521   -0.1642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3871   -0.9830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7127   -1.4902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8689   -1.4741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3240   -2.1622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5497   -2.2663    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7671   -2.5415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6594   -3.3594    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0775   -2.0698    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3710   -2.4959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9782   -1.2064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2211   -0.8326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1145   -0.0053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7818    0.5012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1616    1.0453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1909    1.2177    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7749    1.9301    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9499    1.9262    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1840    2.6466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5632    0.2445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4180    0.6191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2827    0.8586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1205    0.5806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3101    1.3836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8681    0.9296    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5208   -0.0294    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3543   -0.8201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5909   -0.6365    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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  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
 16 22  1  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
  3 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 23 28  1  0  0  0  0
 28 29  1  0  0  0  0
  6 29  1  0  0  0  0
 29 30  1  0  0  0  0
 13 30  1  0  0  0  0
 22 30  1  0  0  0  0
M  END

     RDKit          3D

 66 69  0  0  0  0  0  0  0  0999 V2000
    4.0172    2.4140   -1.3320 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9185    1.6627   -1.0186 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1069    0.7507    0.0293 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1345   -0.5947   -0.5433 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5997   -1.7911    0.1065 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2163   -2.2329   -0.4600 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3322   -2.2062   -1.9687 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8185   -3.4688    0.0371 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5090   -3.9145    0.1690 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5233   -5.0439    0.7736 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8062   -3.3621   -0.2321 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0701   -3.4367   -1.7156 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9655   -1.9943    0.3266 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3378   -1.3669    0.0268 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4979   -0.2181    0.9405 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4465    0.9012    0.7726 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4579    1.5528    2.1817 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9805    1.7445   -0.1707 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5852    2.9562   -0.6126 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2878    3.7200   -1.6942 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5888    3.5024   -0.1216 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1419    0.2923    0.5997 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0457   -0.9927   -0.2416 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3839   -1.1856    0.0976 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8684   -0.0047   -0.4317 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0120    1.0180    0.0233 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9152    1.7640    0.9108 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2883    1.1879    1.1567 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9903    2.4327    1.7736 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3348    0.3351    2.2720 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3554    3.0073   -0.4877 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8818    1.7913   -1.6990 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7942    3.0847   -2.2015 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1903    0.9738    0.3254 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2162   -0.8673   -0.8109 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7399   -0.5900   -1.6134 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2212   -2.7118   -0.0399 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4458   -1.7392    1.2013 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3777   -2.4696   -2.3088 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9839   -1.2508   -2.4114 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6979   -3.0027   -2.4506 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6069   -3.9997    0.2459 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4021   -4.2417   -2.1319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7458   -2.5014   -2.1900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1015   -3.7258   -1.9598 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8306   -2.0403    1.4194 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3274   -1.0030   -1.0262 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1461   -2.0702    0.2024 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4897    0.2598    0.8271 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4295   -0.6255    1.9928 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9297    0.8183    2.8265 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8825    2.4749    2.1925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4870    1.6320    2.5615 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8547    4.5253   -1.1824 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5182    4.1599   -2.3330 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9596    3.0155   -2.2083 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7933   -0.0527    1.6308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1764   -0.7576   -1.2985 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4168   -1.2535    1.2061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2604    1.5307   -0.9447 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9842    2.8140    0.4933 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4456    1.8814    1.9095 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5202    2.5620    2.7791 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7225    3.3405    1.1898 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0547    2.2599    1.9131 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2005    0.3501    2.7270 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  6
  6  8  1  0
  8  9  1  0
  9 10  2  0
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 11 12  1  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 16 18  1  6
 18 19  1  0
 19 20  1  0
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 16 22  1  0
 22 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 28 30  1  1
 26 25  1  0
 25 24  1  0
 24 23  1  0
 28  3  1  0
 24  6  1  0
 23 13  1  0
 23 22  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  3 34  1  1
  4 35  1  0
  4 36  1  0
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  5 38  1  0
  7 39  1  0
  7 40  1  0
  7 41  1  0
 11 42  1  1
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 17 52  1  0
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 26 60  1  6
 27 61  1  0
 27 62  1  0
 29 63  1  0
 29 64  1  0
 29 65  1  0
 30 66  1  0
 24 59  1  1
 23 58  1  6
M  END


  Mrv1533004191523092D          

 30 33  0  0  0  0            999 V2000
    6.6572    0.7417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3662   -0.0303    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5521   -0.1642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3871   -0.9830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7127   -1.4902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8689   -1.4741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3240   -2.1622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5497   -2.2663    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7671   -2.5415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6594   -3.3594    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0775   -2.0698    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3710   -2.4959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9782   -1.2064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2211   -0.8326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1145   -0.0053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7818    0.5012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1616    1.0453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1909    1.2177    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7749    1.9301    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9499    1.9262    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1840    2.6466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5632    0.2445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4180    0.6191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2827    0.8586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1205    0.5806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3101    1.3836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8681    0.9296    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5208   -0.0294    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3543   -0.8201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5909   -0.6365    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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
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 16 17  1  0  0  0  0
 16 18  1  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
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 22 23  1  0  0  0  0
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  6 29  1  0  0  0  0
 29 30  1  0  0  0  0
 13 30  1  0  0  0  0
 22 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0148532

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1CCC2(C)OC(=O)C(C)C3CCC(C)(OC(C)=O)C4C(CC1(C)O)OC2C34

> <INCHI_IDENTIFIER>
InChI=1S/C23H36O7/c1-12-14-7-9-22(4,29-13(2)24)18-15-11-21(3,26)16(27-6)8-10-23(5,30-20(12)25)19(28-15)17(14)18/h12,14-19,26H,7-11H2,1-6H3

> <INCHI_KEY>
BFRZTCFDEPTFFN-UHFFFAOYSA-N

> <FORMULA>
C23H36O7

> <MOLECULAR_WEIGHT>
424.534

> <EXACT_MASS>
424.246103499

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
66

> <JCHEM_AVERAGE_POLARIZABILITY>
45.559692484725765

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
15-hydroxy-14-methoxy-4,8,11,15-tetramethyl-9-oxo-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadecan-4-yl acetate

> <ALOGPS_LOGP>
2.26

> <JCHEM_LOGP>
1.5796140196666664

> <ALOGPS_LOGS>
-3.81

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.973167139986092

> <JCHEM_PKA_STRONGEST_BASIC>
-3.2479366929700833

> <JCHEM_POLAR_SURFACE_AREA>
91.29

> <JCHEM_REFRACTIVITY>
107.8161

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.51e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
15-hydroxy-14-methoxy-4,8,11,15-tetramethyl-9-oxo-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadecan-4-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 19-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-APR-15         0                                  
HETATM    1  C   UNK     0      12.427   1.385   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      11.884  -0.056   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      10.364  -0.307   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.056  -1.835   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.797  -2.782   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.222  -2.752   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.071  -4.036   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       6.626  -4.230   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       5.165  -4.744   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       4.964  -6.271   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       3.878  -3.864   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.559  -4.659   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.693  -2.252   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.279  -1.554   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.080  -0.010   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.326   0.936   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.168   1.951   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       4.090   2.273   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       3.313   3.603   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       1.773   3.596   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       4.077   4.940   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.785   0.456   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.380   1.156   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       7.994   1.603   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       9.558   1.084   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       9.912   2.583   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      10.954   1.735   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       6.572  -0.055   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       6.261  -1.531   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       4.836  -1.188   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   25                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8   29                                             
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   30                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18   22                                             
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19                                                            
CONECT   22   16   23   30                                                  
CONECT   23   22   24   28                                                  
CONECT   24   23   25                                                       
CONECT   25   24    3   26   27                                             
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   23   29                                                       
CONECT   29   28    6   30                                                  
CONECT   30   29   13   22                                                  
MASTER        0    0    0    0    0    0    0    0   30    0   66    0
END

View in JSmol

Synonyms

Value	Source
15-Hydroxy-14-methoxy-4,8,11,15-tetramethyl-9-oxo-10,18-dioxatetracyclo[9.7.0.0,.0,]octadecan-4-yl acetic acid	Generator
15-Hydroxy-14-methoxy-4,8,11,15-tetramethyl-9-oxo-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadecan-4-yl acetic acid	Generator

Chemical Formula

C₂₃H₃₆O₇

Average Mass

424.5340 Da

Monoisotopic Mass

424.24610 Da

IUPAC Name

15-hydroxy-14-methoxy-4,8,11,15-tetramethyl-9-oxo-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadecan-4-yl acetate

Traditional Name

15-hydroxy-14-methoxy-4,8,11,15-tetramethyl-9-oxo-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadecan-4-yl acetate

CAS Registry Number

Not Available

SMILES

COC1CCC2(C)OC(=O)C(C)C3CCC(C)(OC(C)=O)C4C(CC1(C)O)OC2C34

InChI Identifier

InChI=1S/C23H36O7/c1-12-14-7-9-22(4,29-13(2)24)18-15-11-21(3,26)16(27-6)8-10-23(5,30-20(12)25)19(28-15)17(14)18/h12,14-19,26H,7-11H2,1-6H3

InChI Key

BFRZTCFDEPTFFN-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, 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
Briareum asbestinum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as lactones. These are cyclic esters of hydroxy carboxylic acids, containing a 1-oxacycloalkan-2-one structure, or analogues having unsaturation or heteroatoms replacing one or more carbon atoms of the ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Lactones

Sub Class

Not Available

Direct Parent

Lactones

Alternative Parents

Substituents

Caprolactone
Oxepane
Dicarboxylic acid or derivatives
Tertiary alcohol
Tetrahydrofuran
Carboxylic acid ester
Lactone
Ether
Dialkyl ether
Carboxylic acid derivative
Oxacycle
Organooxygen compound
Organic oxide
Alcohol
Carbonyl group
Organic oxygen compound
Hydrocarbon derivative
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	2.26	ALOGPS
logP	1.58	ChemAxon
logS	-3.8	ALOGPS
pKa (Strongest Acidic)	13.97	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	91.29 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	107.82 m³·mol⁻¹	ChemAxon
Polarizability	45.56 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	No	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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

73837521

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 15-hydroxy-14-methoxy-4,8,11,15-tetramethyl-9-oxo-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadecan-4-yl acetate (NP0148532)

MOL for NP0148532 (15-hydroxy-14-methoxy-4,8,11,15-tetramethyl-9-oxo-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadecan-4-yl acetate)

3D MOL for NP0148532 (15-hydroxy-14-methoxy-4,8,11,15-tetramethyl-9-oxo-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadecan-4-yl acetate)

3D SDF for NP0148532 (15-hydroxy-14-methoxy-4,8,11,15-tetramethyl-9-oxo-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadecan-4-yl acetate)

3D-SDF for NP0148532 (15-hydroxy-14-methoxy-4,8,11,15-tetramethyl-9-oxo-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadecan-4-yl acetate)

PDB for NP0148532 (15-hydroxy-14-methoxy-4,8,11,15-tetramethyl-9-oxo-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadecan-4-yl acetate)

3D PDB for NP0148532 (15-hydroxy-14-methoxy-4,8,11,15-tetramethyl-9-oxo-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadecan-4-yl acetate)

SMILES for NP0148532 (15-hydroxy-14-methoxy-4,8,11,15-tetramethyl-9-oxo-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadecan-4-yl acetate)

INCHI for NP0148532 (15-hydroxy-14-methoxy-4,8,11,15-tetramethyl-9-oxo-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadecan-4-yl acetate)

Structure for NP0148532 (15-hydroxy-14-methoxy-4,8,11,15-tetramethyl-9-oxo-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadecan-4-yl acetate)

3D Structure for NP0148532 (15-hydroxy-14-methoxy-4,8,11,15-tetramethyl-9-oxo-10,18-dioxatetracyclo[9.7.0.0²,⁷.0³,¹⁷]octadecan-4-yl acetate)