NP-MRD: Showing NP-Card for ethyl 2-{4,9,11,19,19-pentamethyl-5,10,21,24-tetraoxo-2,6,18,25-tetraoxaheptacyclo[12.10.1.1¹,⁸.0³,⁷.0¹⁴,²³.0¹⁶,²⁰.0¹¹,²⁶]hexacosa-16(20),22-dien-17-yl}acetate (NP0214782)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-05 14:10:57 UTC

Updated at

2022-09-05 14:10:57 UTC

NP-MRD ID

NP0214782

Secondary Accession Numbers

None

Natural Product Identification

Common Name

ethyl 2-{4,9,11,19,19-pentamethyl-5,10,21,24-tetraoxo-2,6,18,25-tetraoxaheptacyclo[12.10.1.1¹,⁸.0³,⁷.0¹⁴,²³.0¹⁶,²⁰.0¹¹,²⁶]hexacosa-16(20),22-dien-17-yl}acetate

Description

Ethyl 2-{4,9,11,19,19-pentamethyl-5,10,21,24-tetraoxo-2,6,18,25-tetraoxaheptacyclo[12.10.1.1¹,⁸.0³,⁷.0¹⁴,²³.0¹⁶,²⁰.0¹¹,²⁶]Hexacosa-16(20),22-dien-17-yl}acetate belongs to the class of organic compounds known as furopyrans. These are organic polycyclic compounds containing a furan ring fused to a pyran ring. Furan is a five-membered aromatic ring with four carbon atoms and one oxygen atom. Pyran a six-membered heterocyclic, non-aromatic ring, made up of five carbon atoms and one oxygen atom and containing two double bonds. ethyl 2-{4,9,11,19,19-pentamethyl-5,10,21,24-tetraoxo-2,6,18,25-tetraoxaheptacyclo[12.10.1.1¹,⁸.0³,⁷.0¹⁴,²³.0¹⁶,²⁰.0¹¹,²⁶]hexacosa-16(20),22-dien-17-yl}acetate is found in Schisandra rubriflora. Ethyl 2-{4,9,11,19,19-pentamethyl-5,10,21,24-tetraoxo-2,6,18,25-tetraoxaheptacyclo[12.10.1.1¹,⁸.0³,⁷.0¹⁴,²³.0¹⁶,²⁰.0¹¹,²⁶]Hexacosa-16(20),22-dien-17-yl}acetate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004191518022D          

 41 47  0  0  0  0            999 V2000
   11.2460   -2.5333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1844   -1.7106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4411   -1.3526    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.3796   -0.5299    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0612   -0.0652    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.6363   -0.1719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5747    0.6508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2041    1.1842    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.8913    1.9476    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6832    2.1789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7440    2.7594    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0686    1.8860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8729    1.0846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1102    0.7742    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3180    1.1055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3752    0.2320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8216   -0.4005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9747   -0.3049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2749   -1.0734    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5430    0.4380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7303    0.2171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6599   -0.6242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9561   -1.0547    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4260   -0.9386    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6172   -1.7411    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1392    0.8072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3155    0.7604    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0165    1.5294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2187    1.7395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6555    2.0513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6087    2.8750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3493    1.6050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1506    1.8290    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8188    1.2851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5475    1.1227    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2774    2.0536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9076    2.7911    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1612    1.9621    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7418    2.5704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5734    2.5489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9526    3.2816    0.0000 O   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  2  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
  9 12  1  0  0  0  0
 12 13  2  0  0  0  0
  7 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
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 18 24  1  0  0  0  0
 24 25  2  0  0  0  0
 21 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 26 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 20 34  1  0  0  0  0
 34 35  1  0  0  0  0
 15 35  1  0  0  0  0
 34 36  1  0  0  0  0
 36 37  2  0  0  0  0
 36 38  1  0  0  0  0
 15 38  1  0  0  0  0
 38 39  2  0  0  0  0
 39 40  1  0  0  0  0
 12 40  1  0  0  0  0
 40 41  2  0  0  0  0
M  END

     RDKit          3D

 77 83  0  0  0  0  0  0  0  0999 V2000
    3.6719    2.0497    2.1896 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7202    2.8221    0.9022 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6768    2.0457   -0.2556 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5665    1.0759   -0.6227 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5311    0.8700    0.2029 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5344    0.2593   -1.8476 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0244   -1.1356   -1.6614 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7882   -1.8054   -0.7401 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9757   -2.6491   -0.0604 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1744   -4.0645   -0.5757 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1945   -2.6073    1.4454 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5976   -2.2666   -0.3909 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6300   -1.2730   -1.2554 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5495   -0.4542   -1.7853 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3781   -0.1773   -0.8841 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8011    0.5619    0.3469 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0155    0.3719    1.5571 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4934    0.6317    1.4669 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2002   -0.5660    1.9499 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9274    1.7538    2.3682 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3752    2.0724    3.3751 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1375    2.3728    1.7861 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4127    1.8644    2.3870 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0223    2.1425    0.3080 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2110    1.6694   -0.4088 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.9192    0.5885    0.0574 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6393    0.0657   -1.0173 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6176   -0.7250   -1.0116 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0658    0.6003   -2.3032 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.7507   -0.5520   -3.1902 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8276    1.3300   -1.8165 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7024    0.6775   -2.0344 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7989    0.4088   -1.0504 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5239    0.5442   -1.6750 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7776   -1.0698   -0.8914 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6634   -1.9431   -0.9641 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3786   -1.3918   -0.5994 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0236   -2.5659   -0.1547 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4109   -2.9329    0.1727 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5578   -3.8621    0.9726 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8092    1.2238    0.1503 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7336    2.8008    3.0121 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5593    1.3844    2.2412 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7332    1.4936    2.2911 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8368    3.5260    0.8668 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6156    3.4953    0.9288 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5929    0.1636   -2.2175 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0141    0.8041   -2.6668 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1742   -1.6974   -2.6501 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4445   -4.2888   -1.3785 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1836   -4.2214   -0.9797 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0064   -4.7810    0.2461 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2669   -2.3942    1.6978 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5149   -1.8635    1.8756 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9269   -3.6242    1.8232 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9539    0.5431   -2.0951 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1029   -0.8822   -2.7283 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0139    1.6110    0.0763 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8165    0.1297    0.5800 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3773    1.0913    2.3324 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2180   -0.6378    1.9865 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5491   -1.4909    2.0177 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1194   -0.8733    1.4819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4734   -0.4487    3.0508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0855    3.4675    2.0690 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4643    0.7951    2.5462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2458    2.2350    1.7946 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5122    2.3499    3.4017 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8129    3.1714   -0.1329 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9454    2.5288   -0.4777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7912    1.2866   -2.7843 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3706   -0.4730   -4.1151 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6736   -0.6483   -3.4358 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0527   -1.5210   -2.7251 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8143    2.2982   -2.4028 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7434   -3.2890   -0.0272 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9690    1.9984    0.0548 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  2  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
  9 11  1  0
  9 12  1  0
 12 13  2  0
 13 14  1  0
 15 14  1  6
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  1
 18 41  1  0
 41 24  1  0
 24 22  1  0
 22 23  1  0
 22 20  1  0
 20 21  2  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  2  0
 27 29  1  0
 29 30  1  0
 29 31  1  0
 31 32  1  0
 33 32  1  6
 33 34  1  0
 33 35  1  0
 35 36  2  0
 35 37  1  0
 37 38  2  0
 38 39  1  0
 39 40  2  0
 13  7  1  0
 34 15  1  0
 39 12  1  0
 37 15  1  0
 20 18  1  0
 31 25  1  0
 33 41  1  0
  1 42  1  0
  1 43  1  0
  1 44  1  0
  2 45  1  0
  2 46  1  0
  6 47  1  0
  6 48  1  0
  7 49  1  6
 10 50  1  0
 10 51  1  0
 10 52  1  0
 11 53  1  0
 11 54  1  0
 11 55  1  0
 14 56  1  0
 14 57  1  0
 16 58  1  0
 16 59  1  0
 17 60  1  0
 17 61  1  0
 19 62  1  0
 19 63  1  0
 19 64  1  0
 41 77  1  6
 24 69  1  6
 22 65  1  6
 23 66  1  0
 23 67  1  0
 23 68  1  0
 25 70  1  6
 29 71  1  6
 30 72  1  0
 30 73  1  0
 30 74  1  0
 31 75  1  6
 38 76  1  0
M  END


  Mrv1533004191518022D          

 41 47  0  0  0  0            999 V2000
   11.2460   -2.5333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1844   -1.7106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4411   -1.3526    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.3796   -0.5299    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0612   -0.0652    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.6363   -0.1719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5747    0.6508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2041    1.1842    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.8913    1.9476    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6832    2.1789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7440    2.7594    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0686    1.8860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8729    1.0846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1102    0.7742    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3180    1.1055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3752    0.2320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8216   -0.4005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9747   -0.3049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2749   -1.0734    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5430    0.4380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7303    0.2171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6599   -0.6242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9561   -1.0547    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4260   -0.9386    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6172   -1.7411    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1392    0.8072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3155    0.7604    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0165    1.5294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2187    1.7395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6555    2.0513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6087    2.8750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3493    1.6050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1506    1.8290    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8188    1.2851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5475    1.1227    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2774    2.0536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9076    2.7911    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1612    1.9621    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7418    2.5704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5734    2.5489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9526    3.2816    0.0000 O   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  2  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
  9 12  1  0  0  0  0
 12 13  2  0  0  0  0
  7 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
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 18 24  1  0  0  0  0
 24 25  2  0  0  0  0
 21 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 26 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 20 34  1  0  0  0  0
 34 35  1  0  0  0  0
 15 35  1  0  0  0  0
 34 36  1  0  0  0  0
 36 37  2  0  0  0  0
 36 38  1  0  0  0  0
 15 38  1  0  0  0  0
 38 39  2  0  0  0  0
 39 40  1  0  0  0  0
 12 40  1  0  0  0  0
 40 41  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0214782

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCOC(=O)CC1OC(C)(C)C2=C1CC13CCC4(C)C5C(C(C)C4=O)C4OC(=O)C(C)C4OC5(O1)C(=O)C3=CC2=O

> <INCHI_IDENTIFIER>
InChI=1S/C31H36O10/c1-7-37-19(33)11-18-15-12-30-9-8-29(6)24-20(13(2)25(29)34)23-22(14(3)27(36)38-23)40-31(24,41-30)26(35)16(30)10-17(32)21(15)28(4,5)39-18/h10,13-14,18,20,22-24H,7-9,11-12H2,1-6H3

> <INCHI_KEY>
NGRMPILGZOCJFL-UHFFFAOYSA-N

> <FORMULA>
C31H36O10

> <MOLECULAR_WEIGHT>
568.619

> <EXACT_MASS>
568.230847359

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
77

> <JCHEM_AVERAGE_POLARIZABILITY>
58.07901156462687

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
ethyl 2-{4,9,11,19,19-pentamethyl-5,10,21,24-tetraoxo-2,6,18,25-tetraoxaheptacyclo[12.10.1.1¹,⁸.0³,⁷.0¹⁴,²³.0¹⁶,²⁰.0¹¹,²⁶]hexacosa-16(20),22-dien-17-yl}acetate

> <ALOGPS_LOGP>
3.03

> <JCHEM_LOGP>
3.549705920666665

> <ALOGPS_LOGS>
-4.17

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.306537084176433

> <JCHEM_PKA_STRONGEST_BASIC>
-3.8922828748513694

> <JCHEM_POLAR_SURFACE_AREA>
131.5

> <JCHEM_REFRACTIVITY>
141.9267

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.82e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
ethyl 2-{4,9,11,19,19-pentamethyl-5,10,21,24-tetraoxo-2,6,18,25-tetraoxaheptacyclo[12.10.1.1¹,⁸.0³,⁷.0¹⁴,²³.0¹⁶,²⁰.0¹¹,²⁶]hexacosa-16(20),22-dien-17-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      20.993  -4.729   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      20.878  -3.193   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      19.490  -2.525   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      19.375  -0.989   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      20.648  -0.122   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      17.988  -0.321   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      17.873   1.215   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      19.048   2.211   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      18.464   3.636   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      19.942   4.067   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      18.189   5.151   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      16.928   3.521   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      16.563   2.025   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      15.139   1.445   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      13.660   2.064   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      13.767   0.433   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      12.734  -0.748   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      11.153  -0.569   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      11.713  -2.004   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      10.347   0.818   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.830   0.405   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.699  -1.165   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.385  -1.969   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      10.129  -1.752   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      10.485  -3.250   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       7.726   1.507   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       6.189   1.419   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       5.631   2.855   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       4.142   3.247   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       6.824   3.829   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       6.736   5.367   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       8.119   2.996   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       9.614   3.414   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      10.862   2.399   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      12.222   2.096   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      11.718   3.833   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      11.027   5.210   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      13.368   3.663   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      14.451   4.798   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      16.004   4.758   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      16.711   6.126   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8   13                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11   12                                             
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    9   13   40                                                  
CONECT   13   12    7   14                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   35   38                                             
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20   24                                             
CONECT   19   18                                                            
CONECT   20   18   21   34                                                  
CONECT   21   20   22   26                                                  
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   18   25                                                  
CONECT   25   24                                                            
CONECT   26   21   27   32                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   26   33                                                  
CONECT   33   32   34                                                       
CONECT   34   33   20   35   36                                             
CONECT   35   34   15                                                       
CONECT   36   34   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   15   39                                                  
CONECT   39   38   40                                                       
CONECT   40   39   12   41                                                  
CONECT   41   40                                                            
MASTER        0    0    0    0    0    0    0    0   41    0   94    0
END

View in JSmol

Synonyms

Value	Source
Ethyl 2-{4,9,11,19,19-pentamethyl-5,10,21,24-tetraoxo-2,6,18,25-tetraoxaheptacyclo[12.10.1.1,.0,.0,.0,.0,]hexacosa-16(20),22-dien-17-yl}acetic acid	Generator
Ethyl 2-{4,9,11,19,19-pentamethyl-5,10,21,24-tetraoxo-2,6,18,25-tetraoxaheptacyclo[12.10.1.1¹,⁸.0³,⁷.0¹⁴,²³.0¹⁶,²⁰.0¹¹,²⁶]hexacosa-16(20),22-dien-17-yl}acetic acid	Generator

Chemical Formula

C₃₁H₃₆O₁₀

Average Mass

568.6190 Da

Monoisotopic Mass

568.23085 Da

IUPAC Name

ethyl 2-{4,9,11,19,19-pentamethyl-5,10,21,24-tetraoxo-2,6,18,25-tetraoxaheptacyclo[12.10.1.1¹,⁸.0³,⁷.0¹⁴,²³.0¹⁶,²⁰.0¹¹,²⁶]hexacosa-16(20),22-dien-17-yl}acetate

Traditional Name

ethyl 2-{4,9,11,19,19-pentamethyl-5,10,21,24-tetraoxo-2,6,18,25-tetraoxaheptacyclo[12.10.1.1¹,⁸.0³,⁷.0¹⁴,²³.0¹⁶,²⁰.0¹¹,²⁶]hexacosa-16(20),22-dien-17-yl}acetate

CAS Registry Number

Not Available

SMILES

CCOC(=O)CC1OC(C)(C)C2=C1CC13CCC4(C)C5C(C(C)C4=O)C4OC(=O)C(C)C4OC5(O1)C(=O)C3=CC2=O

InChI Identifier

InChI=1S/C31H36O10/c1-7-37-19(33)11-18-15-12-30-9-8-29(6)24-20(13(2)25(29)34)23-22(14(3)27(36)38-23)40-31(24,41-30)26(35)16(30)10-17(32)21(15)28(4,5)39-18/h10,13-14,18,20,22-24H,7-9,11-12H2,1-6H3

InChI Key

NGRMPILGZOCJFL-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
Schisandra rubriflora	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as furopyrans. These are organic polycyclic compounds containing a furan ring fused to a pyran ring. Furan is a five-membered aromatic ring with four carbon atoms and one oxygen atom. Pyran a six-membered heterocyclic, non-aromatic ring, made up of five carbon atoms and one oxygen atom and containing two double bonds.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Furopyrans

Sub Class

Not Available

Direct Parent

Furopyrans

Alternative Parents

Substituents

Furopyran
Ketal
Oxepane
Dicarboxylic acid or derivatives
3-furanone
Gamma butyrolactone
Pyran
Oxane
Dihydrofuran
Furan
Oxolane
Ketone
Carboxylic acid ester
Lactone
Oxacycle
Ether
Acetal
Dialkyl ether
Carboxylic acid derivative
Hydrocarbon derivative
Aldehyde
Organic oxide
Organic oxygen compound
Carbonyl group
Organooxygen compound
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	3.03	ALOGPS
logP	3.55	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Acidic)	18.31	ChemAxon
pKa (Strongest Basic)	-3.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	131.5 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	141.93 m³·mol⁻¹	ChemAxon
Polarizability	58.08 Å³	ChemAxon
Number of Rings	7	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

73316336

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for ethyl 2-{4,9,11,19,19-pentamethyl-5,10,21,24-tetraoxo-2,6,18,25-tetraoxaheptacyclo[12.10.1.1¹,⁸.0³,⁷.0¹⁴,²³.0¹⁶,²⁰.0¹¹,²⁶]hexacosa-16(20),22-dien-17-yl}acetate (NP0214782)

MOL for NP0214782 (ethyl 2-{4,9,11,19,19-pentamethyl-5,10,21,24-tetraoxo-2,6,18,25-tetraoxaheptacyclo[12.10.1.1¹,⁸.0³,⁷.0¹⁴,²³.0¹⁶,²⁰.0¹¹,²⁶]hexacosa-16(20),22-dien-17-yl}acetate)

3D MOL for NP0214782 (ethyl 2-{4,9,11,19,19-pentamethyl-5,10,21,24-tetraoxo-2,6,18,25-tetraoxaheptacyclo[12.10.1.1¹,⁸.0³,⁷.0¹⁴,²³.0¹⁶,²⁰.0¹¹,²⁶]hexacosa-16(20),22-dien-17-yl}acetate)

3D SDF for NP0214782 (ethyl 2-{4,9,11,19,19-pentamethyl-5,10,21,24-tetraoxo-2,6,18,25-tetraoxaheptacyclo[12.10.1.1¹,⁸.0³,⁷.0¹⁴,²³.0¹⁶,²⁰.0¹¹,²⁶]hexacosa-16(20),22-dien-17-yl}acetate)

3D-SDF for NP0214782 (ethyl 2-{4,9,11,19,19-pentamethyl-5,10,21,24-tetraoxo-2,6,18,25-tetraoxaheptacyclo[12.10.1.1¹,⁸.0³,⁷.0¹⁴,²³.0¹⁶,²⁰.0¹¹,²⁶]hexacosa-16(20),22-dien-17-yl}acetate)

PDB for NP0214782 (ethyl 2-{4,9,11,19,19-pentamethyl-5,10,21,24-tetraoxo-2,6,18,25-tetraoxaheptacyclo[12.10.1.1¹,⁸.0³,⁷.0¹⁴,²³.0¹⁶,²⁰.0¹¹,²⁶]hexacosa-16(20),22-dien-17-yl}acetate)

3D PDB for NP0214782 (ethyl 2-{4,9,11,19,19-pentamethyl-5,10,21,24-tetraoxo-2,6,18,25-tetraoxaheptacyclo[12.10.1.1¹,⁸.0³,⁷.0¹⁴,²³.0¹⁶,²⁰.0¹¹,²⁶]hexacosa-16(20),22-dien-17-yl}acetate)

SMILES for NP0214782 (ethyl 2-{4,9,11,19,19-pentamethyl-5,10,21,24-tetraoxo-2,6,18,25-tetraoxaheptacyclo[12.10.1.1¹,⁸.0³,⁷.0¹⁴,²³.0¹⁶,²⁰.0¹¹,²⁶]hexacosa-16(20),22-dien-17-yl}acetate)

INCHI for NP0214782 (ethyl 2-{4,9,11,19,19-pentamethyl-5,10,21,24-tetraoxo-2,6,18,25-tetraoxaheptacyclo[12.10.1.1¹,⁸.0³,⁷.0¹⁴,²³.0¹⁶,²⁰.0¹¹,²⁶]hexacosa-16(20),22-dien-17-yl}acetate)

Structure for NP0214782 (ethyl 2-{4,9,11,19,19-pentamethyl-5,10,21,24-tetraoxo-2,6,18,25-tetraoxaheptacyclo[12.10.1.1¹,⁸.0³,⁷.0¹⁴,²³.0¹⁶,²⁰.0¹¹,²⁶]hexacosa-16(20),22-dien-17-yl}acetate)

3D Structure for NP0214782 (ethyl 2-{4,9,11,19,19-pentamethyl-5,10,21,24-tetraoxo-2,6,18,25-tetraoxaheptacyclo[12.10.1.1¹,⁸.0³,⁷.0¹⁴,²³.0¹⁶,²⁰.0¹¹,²⁶]hexacosa-16(20),22-dien-17-yl}acetate)