NP-MRD: Showing NP-Card for (1s,3r,4s,5r,8s,11s,13s,14s)-4-(acetyloxy)-8-formyl-14-(furan-3-yl)-6,6,9,13-tetramethyl-18-methylidene-10,16-dioxo-2,7,15-trioxatetracyclo[9.6.1.0¹,¹³.0³,⁹]octadecan-5-yl hexadecanoate (NP0213147)

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Record Information

Version

2.0

Created at

2022-09-05 12:02:28 UTC

Updated at

2022-09-05 12:02:28 UTC

NP-MRD ID

NP0213147

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,3r,4s,5r,8s,11s,13s,14s)-4-(acetyloxy)-8-formyl-14-(furan-3-yl)-6,6,9,13-tetramethyl-18-methylidene-10,16-dioxo-2,7,15-trioxatetracyclo[9.6.1.0¹,¹³.0³,⁹]octadecan-5-yl hexadecanoate

Description

(1S,3R,4S,5R,8S,11S,13S,14R)-4-(acetyloxy)-8-formyl-14-(furan-3-yl)-6,6,9,13-tetramethyl-18-methylidene-10,16-dioxo-2,7,15-trioxatetracyclo[9.6.1.0¹,¹³.0³,⁹]Octadecan-5-yl hexadecanoate belongs to the class of organic compounds known as tricarboxylic acids and derivatives. These are carboxylic acids containing exactly three carboxyl groups. Based on a literature review very few articles have been published on (1S,3R,4S,5R,8S,11S,13S,14R)-4-(acetyloxy)-8-formyl-14-(furan-3-yl)-6,6,9,13-tetramethyl-18-methylidene-10,16-dioxo-2,7,15-trioxatetracyclo[9.6.1.0¹,¹³.0³,⁹]Octadecan-5-yl hexadecanoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052214022D          

 54 58  0  0  1  0            999 V2000
   -2.0744   -4.0952    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8362   -3.7785    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1987   -4.3969    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.8692   -3.7943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5141   -3.0035    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.3354   -3.0819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9960   -2.3176    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.8188   -2.3778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2537   -3.0789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0548   -2.8819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1150   -2.0591    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3511   -1.7476    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6193   -1.5690    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7861   -1.5129    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4171   -0.7751    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3269   -2.2200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6397   -3.0330    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7350   -3.1737    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2944   -3.8945    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5061   -3.6513    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3831   -2.8356    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0281   -2.3212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7961   -2.6226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9052   -1.5054    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1756   -4.1161    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8900   -3.7036    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6045   -4.1161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6045   -4.9411    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3190   -3.7036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0334   -4.1161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7479   -3.7036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4624   -4.1161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1769   -3.7036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8913   -4.1161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6058   -3.7036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3203   -4.1161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0347   -3.7036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7492   -4.1161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4637   -3.7036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1781   -4.1161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8926   -3.7036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6071   -4.1161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3216   -3.7036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2372   -4.9388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0256   -4.6956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6497   -5.6532    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3676   -5.4999    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1833   -5.3770    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6481   -6.0586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2901   -6.8019    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5958   -4.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9083   -5.4260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4505   -4.8994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5823   -5.7138    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  3  2  1  6  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  6  0  0  0
  5  7  1  0  0  0  0
  7  8  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
  8 12  2  0  0  0  0
  7 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17  2  1  6  0  0  0
  5 17  1  0  0  0  0
 17 18  1  0  0  0  0
 19 18  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  1  6  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  2  0  0  0  0
 20 25  1  0  0  0  0
 25 26  1  1  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 25 44  1  0  0  0  0
 44 45  1  0  0  0  0
 44 46  1  0  0  0  0
 44 47  1  0  0  0  0
 47 48  1  0  0  0  0
 48 49  1  6  0  0  0
 49 50  2  0  0  0  0
 48 51  1  0  0  0  0
 19 51  1  0  0  0  0
 51 52  1  0  0  0  0
 51 53  1  0  0  0  0
  3 53  1  0  0  0  0
 53 54  2  0  0  0  0
M  END

     RDKit          3D

116120  0  0  0  0  0  0  0  0999 V2000
   -5.8752   -0.0960   -2.9273 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1450    0.0698   -1.6423 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9452   -0.8715   -0.7976 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.6875    0.0479    0.1543 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1319    1.4330   -0.0734 C   0  0  1  0  0  0  0  0  0  0  0  0
   -8.0499    2.1541   -0.9950 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8744    2.1916    1.1693 C   0  0  2  0  0  0  0  0  0  0  0  0
   -8.1421    2.7678    1.6851 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7963    3.9192    1.2913 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9104    4.0353    2.0633 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9667    3.0270    2.8957 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9336    2.2437    2.7083 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9551    3.2341    0.9135 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4918    3.5064   -0.3863 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1869    4.6778   -0.7146 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3565    2.4191   -1.3888 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7685    1.1506   -0.7270 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.8887    0.7359    0.2478 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0786   -0.3434   -0.1333 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7000   -0.0188    0.2994 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3167    1.1891   -0.3675 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9842    2.3378    0.2856 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6002    3.5385   -0.4957 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9956    2.4002    1.5177 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6394   -1.0221    0.0003 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4307   -0.4281    0.5147 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6654   -0.1701   -0.2930 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.9923    0.6984   -0.5579 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.7198   -0.0747   -2.0789 C   0  0  0  0  0  0  0  0  0  0  0  0
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    6.4444   -1.9381   -2.0458 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2971   -2.6640   -0.8013 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2559   -1.9507    0.4953 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5602   -1.1502    0.7219 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7378   -2.0427    0.7254 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0781   -1.4645    0.9409 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6807   -0.5250   -0.0192 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0213    0.7648   -0.3155 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7920    1.6216    0.8977 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0767    1.9816    1.6088 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7352   -2.3309    0.6794 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4322   -2.1696    2.1755 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5269   -3.1342    0.1394 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7733   -3.1109    0.5190 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9779   -2.8372    0.1375 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.0752   -2.9111   -1.3719 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1169   -3.1914   -2.0463 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6581   -1.5634    0.5335 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.7863   -1.4037    2.0293 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.6394   -0.2733    1.1935 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -8.4321    4.5829    0.4943 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.6403    4.8428    1.9971 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7381    1.3541    3.2533 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.3309    2.3723   -1.8102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1523   -0.4988   -1.2174 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6580    0.2157    1.3759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5018    3.4609   -0.7114 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1007    3.4749   -1.4851 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8332    4.4791    0.0423 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4562   -1.1861   -1.0744 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5936    1.3687    0.8926 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1997   -0.2735    1.1384 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7016    1.4678   -1.2986 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8080    1.1523    0.0430 H   0  0  0  0  0  0  0  0  0  0  0  0
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    7.4538   -1.3232   -1.9515 H   0  0  0  0  0  0  0  0  0  0  0  0
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    7.5793   -0.2741    0.0919 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4428   -0.7674    1.7829 H   0  0  0  0  0  0  0  0  0  0  0  0
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    8.5632   -2.8490    1.5044 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.8409   -2.3125    1.0645 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.0429   -0.9598    1.9773 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.8120   -1.0660   -1.0140 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652309052214022D          

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 41 42  1  0  0  0  0
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 25 44  1  0  0  0  0
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  3 53  1  0  0  0  0
 53 54  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0213147

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCCCCCC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@@H]2O[C@]34CC(=O)O[C@@H](C5=COC=C5)[C@]3(C)C[C@@H](C4=C)C(=O)C2(C)[C@H](OC1(C)C)C=O

> <INCHI_IDENTIFIER>
InChI=1S/C43H62O11/c1-8-9-10-11-12-13-14-15-16-17-18-19-20-21-33(46)51-38-35(50-29(3)45)39-42(7,32(26-44)53-40(38,4)5)36(48)31-24-41(6)37(30-22-23-49-27-30)52-34(47)25-43(41,54-39)28(31)2/h22-23,26-27,31-32,35,37-39H,2,8-21,24-25H2,1,3-7H3/t31-,32+,35+,37-,38+,39-,41-,42?,43-/m0/s1

> <INCHI_KEY>
ZJKRXJKDQHQSET-FCZXANSTSA-N

> <FORMULA>
C43H62O11

> <MOLECULAR_WEIGHT>
754.958

> <EXACT_MASS>
754.429212816

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
116

> <JCHEM_AVERAGE_POLARIZABILITY>
84.82493844658703

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,3R,4S,5R,8S,11S,13S,14R)-4-(acetyloxy)-8-formyl-14-(furan-3-yl)-6,6,9,13-tetramethyl-18-methylidene-10,16-dioxo-2,7,15-trioxatetracyclo[9.6.1.0^{1,13}.0^{3,9}]octadecan-5-yl hexadecanoate

> <JCHEM_LOGP>
8.434750471666668

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
17.921902849494632

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.58702553166366

> <JCHEM_PKA_STRONGEST_BASIC>
-2.853074798628409

> <JCHEM_POLAR_SURFACE_AREA>
144.64000000000001

> <JCHEM_REFRACTIVITY>
198.08310000000006

> <JCHEM_ROTATABLE_BOND_COUNT>
20

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,3R,4S,5R,8S,11S,13S,14R)-4-(acetyloxy)-8-formyl-14-(furan-3-yl)-6,6,9,13-tetramethyl-18-methylidene-10,16-dioxo-2,7,15-trioxatetracyclo[9.6.1.0^{1,13}.0^{3,9}]octadecan-5-yl hexadecanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0      -3.872  -7.644   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.294  -7.053   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -5.971  -8.208   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -7.223  -7.083   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -6.560  -5.607   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -8.093  -5.753   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -7.459  -4.326   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -8.995  -4.439   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -9.807  -5.747   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0     -11.302  -5.380   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0     -11.415  -3.844   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -9.989  -3.262   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -6.756  -2.929   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -5.201  -2.824   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -4.512  -1.447   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -4.344  -4.144   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -4.927  -5.662   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -3.239  -5.924   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -2.416  -7.270   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.945  -6.816   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -0.715  -5.293   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -1.919  -4.333   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -3.353  -4.895   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -1.690  -2.810   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       0.328  -7.683   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       1.661  -6.913   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       2.995  -7.683   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       2.995  -9.223   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       4.329  -6.913   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.662  -7.683   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       6.996  -6.913   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       8.330  -7.683   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       9.663  -6.913   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      10.997  -7.683   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      12.331  -6.913   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      13.664  -7.683   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      14.998  -6.913   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      16.332  -7.683   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      17.666  -6.913   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      18.999  -7.683   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      20.333  -6.913   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      21.667  -7.683   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      23.000  -6.913   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       0.443  -9.219   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       1.914  -8.765   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       1.213 -10.553   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0      -0.686 -10.267   0.000  0.00  0.00           O+0
HETATM   48  C   UNK     0      -2.209 -10.037   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      -3.076 -11.309   0.000  0.00  0.00           C+0
HETATM   50  O   UNK     0      -2.408 -12.697   0.000  0.00  0.00           O+0
HETATM   51  C   UNK     0      -2.979  -8.703   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      -3.562 -10.129   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0      -4.574  -9.146   0.000  0.00  0.00           C+0
HETATM   54  O   UNK     0      -4.820 -10.666   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   17                                                  
CONECT    3    2    4   53                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7   17                                             
CONECT    6    5                                                            
CONECT    7    5    8   13                                                  
CONECT    8    7    9   12                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11    8                                                       
CONECT   13    7   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16    2    5   18                                             
CONECT   18   17   19                                                       
CONECT   19   18   20   51                                                  
CONECT   20   19   21   25                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25   20   26   44                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42                                                            
CONECT   44   25   45   46   47                                             
CONECT   45   44                                                            
CONECT   46   44                                                            
CONECT   47   44   48                                                       
CONECT   48   47   49   51                                                  
CONECT   49   48   50                                                       
CONECT   50   49                                                            
CONECT   51   48   19   52   53                                             
CONECT   52   51                                                            
CONECT   53   51    3   54                                                  
CONECT   54   53                                                            
MASTER        0    0    0    0    0    0    0    0   54    0  116    0
END

View in JSmol

Synonyms

Value	Source
(1S,3R,4S,5R,8S,11S,13S,14R)-4-(Acetyloxy)-8-formyl-14-(furan-3-yl)-6,6,9,13-tetramethyl-18-methylidene-10,16-dioxo-2,7,15-trioxatetracyclo[9.6.1.0,.0,]octadecan-5-yl hexadecanoic acid	Generator

Chemical Formula

C₄₃H₆₂O₁₁

Average Mass

754.9580 Da

Monoisotopic Mass

754.42921 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCCCCCC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@@H]2O[C@]34CC(=O)O[C@@H](C5=COC=C5)[C@]3(C)C[C@@H](C4=C)C(=O)C2(C)[C@H](OC1(C)C)C=O

InChI Identifier

InChI=1S/C43H62O11/c1-8-9-10-11-12-13-14-15-16-17-18-19-20-21-33(46)51-38-35(50-29(3)45)39-42(7,32(26-44)53-40(38,4)5)36(48)31-24-41(6)37(30-22-23-49-27-30)52-34(47)25-43(41,54-39)28(31)2/h22-23,26-27,31-32,35,37-39H,2,8-21,24-25H2,1,3-7H3/t31-,32+,35+,37-,38+,39-,41-,42?,43-/m0/s1

InChI Key

ZJKRXJKDQHQSET-FCZXANSTSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tricarboxylic acids and derivatives. These are carboxylic acids containing exactly three carboxyl groups.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Tricarboxylic acids and derivatives

Direct Parent

Tricarboxylic acids and derivatives

Alternative Parents

Substituents

Tricarboxylic acid or derivatives
Oxepane
Delta_valerolactone
Fatty acid ester
Delta valerolactone
Fatty acyl
Oxane
Heteroaromatic compound
Furan
Lactone
Ketone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Ether
Dialkyl ether
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aldehyde
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

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

163193877

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,3r,4s,5r,8s,11s,13s,14s)-4-(acetyloxy)-8-formyl-14-(furan-3-yl)-6,6,9,13-tetramethyl-18-methylidene-10,16-dioxo-2,7,15-trioxatetracyclo[9.6.1.0¹,¹³.0³,⁹]octadecan-5-yl hexadecanoate (NP0213147)

MOL for NP0213147 ((1s,3r,4s,5r,8s,11s,13s,14s)-4-(acetyloxy)-8-formyl-14-(furan-3-yl)-6,6,9,13-tetramethyl-18-methylidene-10,16-dioxo-2,7,15-trioxatetracyclo[9.6.1.0¹,¹³.0³,⁹]octadecan-5-yl hexadecanoate)

3D MOL for NP0213147 ((1s,3r,4s,5r,8s,11s,13s,14s)-4-(acetyloxy)-8-formyl-14-(furan-3-yl)-6,6,9,13-tetramethyl-18-methylidene-10,16-dioxo-2,7,15-trioxatetracyclo[9.6.1.0¹,¹³.0³,⁹]octadecan-5-yl hexadecanoate)

3D SDF for NP0213147 ((1s,3r,4s,5r,8s,11s,13s,14s)-4-(acetyloxy)-8-formyl-14-(furan-3-yl)-6,6,9,13-tetramethyl-18-methylidene-10,16-dioxo-2,7,15-trioxatetracyclo[9.6.1.0¹,¹³.0³,⁹]octadecan-5-yl hexadecanoate)

3D-SDF for NP0213147 ((1s,3r,4s,5r,8s,11s,13s,14s)-4-(acetyloxy)-8-formyl-14-(furan-3-yl)-6,6,9,13-tetramethyl-18-methylidene-10,16-dioxo-2,7,15-trioxatetracyclo[9.6.1.0¹,¹³.0³,⁹]octadecan-5-yl hexadecanoate)

PDB for NP0213147 ((1s,3r,4s,5r,8s,11s,13s,14s)-4-(acetyloxy)-8-formyl-14-(furan-3-yl)-6,6,9,13-tetramethyl-18-methylidene-10,16-dioxo-2,7,15-trioxatetracyclo[9.6.1.0¹,¹³.0³,⁹]octadecan-5-yl hexadecanoate)

3D PDB for NP0213147 ((1s,3r,4s,5r,8s,11s,13s,14s)-4-(acetyloxy)-8-formyl-14-(furan-3-yl)-6,6,9,13-tetramethyl-18-methylidene-10,16-dioxo-2,7,15-trioxatetracyclo[9.6.1.0¹,¹³.0³,⁹]octadecan-5-yl hexadecanoate)

SMILES for NP0213147 ((1s,3r,4s,5r,8s,11s,13s,14s)-4-(acetyloxy)-8-formyl-14-(furan-3-yl)-6,6,9,13-tetramethyl-18-methylidene-10,16-dioxo-2,7,15-trioxatetracyclo[9.6.1.0¹,¹³.0³,⁹]octadecan-5-yl hexadecanoate)

INCHI for NP0213147 ((1s,3r,4s,5r,8s,11s,13s,14s)-4-(acetyloxy)-8-formyl-14-(furan-3-yl)-6,6,9,13-tetramethyl-18-methylidene-10,16-dioxo-2,7,15-trioxatetracyclo[9.6.1.0¹,¹³.0³,⁹]octadecan-5-yl hexadecanoate)

Structure for NP0213147 ((1s,3r,4s,5r,8s,11s,13s,14s)-4-(acetyloxy)-8-formyl-14-(furan-3-yl)-6,6,9,13-tetramethyl-18-methylidene-10,16-dioxo-2,7,15-trioxatetracyclo[9.6.1.0¹,¹³.0³,⁹]octadecan-5-yl hexadecanoate)

3D Structure for NP0213147 ((1s,3r,4s,5r,8s,11s,13s,14s)-4-(acetyloxy)-8-formyl-14-(furan-3-yl)-6,6,9,13-tetramethyl-18-methylidene-10,16-dioxo-2,7,15-trioxatetracyclo[9.6.1.0¹,¹³.0³,⁹]octadecan-5-yl hexadecanoate)