NP-MRD: Showing NP-Card for (2r,3r,7s)-7-hydroxy-4-oxo-2-(3,4,5-trimethoxyphenyl)-5,13-dioxatetracyclo[7.7.0.0³,⁷.0¹¹,¹⁵]hexadeca-1(16),9,11,14-tetraen-3-yl acetate (NP0237458)

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Record Information

Version

2.0

Created at

2022-09-06 20:36:01 UTC

Updated at

2022-09-06 20:36:01 UTC

NP-MRD ID

NP0237458

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,3r,7s)-7-hydroxy-4-oxo-2-(3,4,5-trimethoxyphenyl)-5,13-dioxatetracyclo[7.7.0.0³,⁷.0¹¹,¹⁵]hexadeca-1(16),9,11,14-tetraen-3-yl acetate

Description

Erlangerin D belongs to the class of organic compounds known as lignan lactones. These are lignans that contain a lactone moiety. They include 1-aryltetralin lactones, dibenzylbutyrolactone lignans, and podophyllotoxins, among others. Based on a literature review very few articles have been published on Erlangerin D.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062222362D          

 34 38  0  0  1  0            999 V2000
    5.4957    0.9521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812    1.3646    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    0.9521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -1.1104    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0668   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2803   -1.2680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7652   -1.9354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2803   -2.6029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957   -2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812   -2.7604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668   -2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -2.7604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -2.3479    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5516   -3.1684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8532   -2.6029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3683   -1.9354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8532   -1.2680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3683   -0.6006    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -1.5229    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5516   -0.7025    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7979   -0.3669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7117    0.4536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9729   -0.3669    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.9521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.3646    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    2.1896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.3646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    2.1896    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    2.6021    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  2  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
  7  8  2  0  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
 12 13  2  0  0  0  0
  9 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
  7 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  1  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
  6 23  1  0  0  0  0
 17 23  1  0  0  0  0
 23 24  1  6  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  2  0  0  0  0
  5 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 29 32  2  0  0  0  0
  3 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
M  END

     RDKit          3D

 58 62  0  0  0  0  0  0  0  0999 V2000
   -2.9502    0.0811    4.1883 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6667    0.0222    2.9721 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9391   -0.1500    1.7970 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5692   -0.2591    1.8187 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8162   -0.4327    0.6504 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6333   -0.5296    0.8012 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3497    0.7420    0.5094 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7010    1.9260    0.7662 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3487    3.1125    0.5019 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0044    4.4568    0.6358 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0042    5.1873    0.2314 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0115    4.4594   -0.1711 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6248    3.1308   -0.0112 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2524    1.9434   -0.2595 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6376    0.7410   -0.0084 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3804   -0.5080   -0.3025 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7504   -1.5974    0.4897 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7518   -1.2873    1.8709 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2338   -2.9661    0.3220 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0798   -3.7749    0.2510 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9378   -3.0042    0.4408 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1337   -3.4518    0.8903 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2755   -1.6729    0.0234 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2055   -1.3484   -1.3019 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5616   -2.0295   -2.4127 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3674   -1.3822   -3.7537 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0384   -3.1694   -2.2921 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4775   -0.4944   -0.5517 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8627   -0.3836   -0.5679 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5424   -0.4439   -1.7674 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8122   -0.6210   -2.9907 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6149   -0.2130    0.5721 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9786   -0.1014    0.5822 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6786    1.1214    0.4767 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6304    0.2537    5.0419 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1908    0.8966    4.0894 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3928   -0.8725    4.3097 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0204   -0.2126    2.7608 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9040   -0.7594    1.8768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3097    1.9247    1.1725 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0339    4.7412    1.0250 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9730    4.8201   -0.5588 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2700    1.9967   -0.6688 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2807   -0.7236   -1.3775 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4534   -0.4276    0.0044 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2956   -0.5002    2.0708 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9700   -3.1460   -0.4919 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7493   -3.2970    1.2930 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3017   -1.0909   -3.7979 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7046   -2.0247   -4.5651 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9568   -0.4243   -3.8141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9152   -0.6233   -1.4647 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5036   -0.5596   -3.8557 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3537   -1.6352   -3.0134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0480    0.1614   -3.1132 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3648    1.8230    1.3019 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5122    1.6475   -0.4693 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7592    0.9289    0.6600 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5 28  2  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 29 32  2  0
 32 33  1  0
 33 34  1  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 17 18  1  1
 17 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  2  0
 21 23  1  0
 23 24  1  6
 24 25  1  0
 25 26  1  0
 25 27  2  0
 32  3  1  0
 23  6  1  0
 15  7  1  0
 23 17  1  0
 13  9  1  0
  1 35  1  0
  1 36  1  0
  1 37  1  0
  4 38  1  0
 28 52  1  0
 31 53  1  0
 31 54  1  0
 31 55  1  0
 34 56  1  0
 34 57  1  0
 34 58  1  0
  6 39  1  1
  8 40  1  0
 10 41  1  0
 12 42  1  0
 14 43  1  0
 16 44  1  0
 16 45  1  0
 18 46  1  0
 19 47  1  0
 19 48  1  0
 26 49  1  0
 26 50  1  0
 26 51  1  0
M  END


  Mrv1652309062222362D          

 34 38  0  0  1  0            999 V2000
    5.4957    0.9521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812    1.3646    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    0.9521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -1.1104    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0668   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2803   -1.2680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7652   -1.9354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2803   -2.6029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957   -2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812   -2.7604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668   -2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -2.7604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -2.3479    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5516   -3.1684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8532   -2.6029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3683   -1.9354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8532   -1.2680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3683   -0.6006    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -1.5229    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5516   -0.7025    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7979   -0.3669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7117    0.4536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9729   -0.3669    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.9521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.3646    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    2.1896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.3646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    2.1896    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    2.6021    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  2  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
  7  8  2  0  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
 12 13  2  0  0  0  0
  9 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
  7 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  1  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
  6 23  1  0  0  0  0
 17 23  1  0  0  0  0
 23 24  1  6  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  2  0  0  0  0
  5 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 29 32  2  0  0  0  0
  3 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0237458

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(=CC(OC)=C1OC)[C@@H]1C2=CC3=COC=C3C=C2C[C@]2(O)COC(=O)[C@@]12OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C25H24O9/c1-13(26)34-25-21(14-7-19(29-2)22(31-4)20(8-14)30-3)18-6-17-11-32-10-16(17)5-15(18)9-24(25,28)12-33-23(25)27/h5-8,10-11,21,28H,9,12H2,1-4H3/t21-,24+,25+/m1/s1

> <INCHI_KEY>
TWTFGXAGCDBXLG-ZODMCCGTSA-N

> <FORMULA>
C25H24O9

> <MOLECULAR_WEIGHT>
468.458

> <EXACT_MASS>
468.142032353

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
46.28186452797782

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R,3R,7S)-7-hydroxy-4-oxo-2-(3,4,5-trimethoxyphenyl)-5,13-dioxatetracyclo[7.7.0.0^{3,7}.0^{11,15}]hexadeca-1(16),9,11,14-tetraen-3-yl acetate

> <JCHEM_LOGP>
2.1647568609999994

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.466138354294952

> <JCHEM_PKA_STRONGEST_BASIC>
-2.897639020119908

> <JCHEM_POLAR_SURFACE_AREA>
113.66000000000003

> <JCHEM_REFRACTIVITY>
117.45659999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3R,7S)-7-hydroxy-4-oxo-2-(3,4,5-trimethoxyphenyl)-5,13-dioxatetracyclo[7.7.0.0^{3,7}.0^{11,15}]hexadeca-1(16),9,11,14-tetraen-3-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0      10.259   1.777   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       8.925   2.547   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       7.591   1.777   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.591   0.237   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.258  -0.533   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.258  -2.073   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.591  -2.843   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.925  -2.073   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.259  -2.843   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      11.723  -2.367   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      12.628  -3.613   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      11.723  -4.859   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.259  -4.383   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.925  -5.153   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.591  -4.383   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.258  -5.153   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.924  -4.383   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       4.763  -5.914   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       3.459  -4.859   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       2.554  -3.613   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       3.459  -2.367   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       2.554  -1.121   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       4.924  -2.843   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       4.763  -1.311   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       3.356  -0.685   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.195   0.847   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       1.816  -0.685   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       4.924   0.237   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.924   1.777   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       3.590   2.547   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       3.590   4.087   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       6.258   2.547   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       6.258   4.087   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       7.591   4.857   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   32                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   28                                                  
CONECT    6    5    7   23                                                  
CONECT    7    6    8   15                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   13                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12    9   14                                                  
CONECT   14   13   15                                                       
CONECT   15   14    7   16                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19   23                                             
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21    6   17   24                                             
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28    5   29                                                       
CONECT   29   28   30   32                                                  
CONECT   30   29   31                                                       
CONECT   31   30                                                            
CONECT   32   29    3   33                                                  
CONECT   33   32   34                                                       
CONECT   34   33                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   76    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₂₄O₉

Average Mass

468.4580 Da

Monoisotopic Mass

468.14203 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

COC1=CC(=CC(OC)=C1OC)[C@@H]1C2=CC3=COC=C3C=C2C[C@]2(O)COC(=O)[C@@]12OC(C)=O

InChI Identifier

InChI=1S/C25H24O9/c1-13(26)34-25-21(14-7-19(29-2)22(31-4)20(8-14)30-3)18-6-17-11-32-10-16(17)5-15(18)9-24(25,28)12-33-23(25)27/h5-8,10-11,21,28H,9,12H2,1-4H3/t21-,24+,25+/m1/s1

InChI Key

TWTFGXAGCDBXLG-ZODMCCGTSA-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 lignan lactones. These are lignans that contain a lactone moiety. They include 1-aryltetralin lactones, dibenzylbutyrolactone lignans, and podophyllotoxins, among others.

Kingdom

Organic compounds

Super Class

Lignans, neolignans and related compounds

Class

Lignan lactones

Sub Class

Not Available

Direct Parent

Lignan lactones

Alternative Parents

Substituents

Lignan lactone
1-aryltetralin lignan
Naphthofuran
Tetralin
Isobenzofuran
Phenoxy compound
Methoxybenzene
Phenol ether
Anisole
Alkyl aryl ether
Benzenoid
Gamma butyrolactone
Dicarboxylic acid or derivatives
Monocyclic benzene moiety
Heteroaromatic compound
Tetrahydrofuran
Tertiary alcohol
Furan
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Ether
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
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

C00045925

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

101201269

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r,3r,7s)-7-hydroxy-4-oxo-2-(3,4,5-trimethoxyphenyl)-5,13-dioxatetracyclo[7.7.0.0³,⁷.0¹¹,¹⁵]hexadeca-1(16),9,11,14-tetraen-3-yl acetate (NP0237458)

MOL for NP0237458 ((2r,3r,7s)-7-hydroxy-4-oxo-2-(3,4,5-trimethoxyphenyl)-5,13-dioxatetracyclo[7.7.0.0³,⁷.0¹¹,¹⁵]hexadeca-1(16),9,11,14-tetraen-3-yl acetate)

3D MOL for NP0237458 ((2r,3r,7s)-7-hydroxy-4-oxo-2-(3,4,5-trimethoxyphenyl)-5,13-dioxatetracyclo[7.7.0.0³,⁷.0¹¹,¹⁵]hexadeca-1(16),9,11,14-tetraen-3-yl acetate)

3D SDF for NP0237458 ((2r,3r,7s)-7-hydroxy-4-oxo-2-(3,4,5-trimethoxyphenyl)-5,13-dioxatetracyclo[7.7.0.0³,⁷.0¹¹,¹⁵]hexadeca-1(16),9,11,14-tetraen-3-yl acetate)

3D-SDF for NP0237458 ((2r,3r,7s)-7-hydroxy-4-oxo-2-(3,4,5-trimethoxyphenyl)-5,13-dioxatetracyclo[7.7.0.0³,⁷.0¹¹,¹⁵]hexadeca-1(16),9,11,14-tetraen-3-yl acetate)

PDB for NP0237458 ((2r,3r,7s)-7-hydroxy-4-oxo-2-(3,4,5-trimethoxyphenyl)-5,13-dioxatetracyclo[7.7.0.0³,⁷.0¹¹,¹⁵]hexadeca-1(16),9,11,14-tetraen-3-yl acetate)

3D PDB for NP0237458 ((2r,3r,7s)-7-hydroxy-4-oxo-2-(3,4,5-trimethoxyphenyl)-5,13-dioxatetracyclo[7.7.0.0³,⁷.0¹¹,¹⁵]hexadeca-1(16),9,11,14-tetraen-3-yl acetate)

SMILES for NP0237458 ((2r,3r,7s)-7-hydroxy-4-oxo-2-(3,4,5-trimethoxyphenyl)-5,13-dioxatetracyclo[7.7.0.0³,⁷.0¹¹,¹⁵]hexadeca-1(16),9,11,14-tetraen-3-yl acetate)

INCHI for NP0237458 ((2r,3r,7s)-7-hydroxy-4-oxo-2-(3,4,5-trimethoxyphenyl)-5,13-dioxatetracyclo[7.7.0.0³,⁷.0¹¹,¹⁵]hexadeca-1(16),9,11,14-tetraen-3-yl acetate)

Structure for NP0237458 ((2r,3r,7s)-7-hydroxy-4-oxo-2-(3,4,5-trimethoxyphenyl)-5,13-dioxatetracyclo[7.7.0.0³,⁷.0¹¹,¹⁵]hexadeca-1(16),9,11,14-tetraen-3-yl acetate)

3D Structure for NP0237458 ((2r,3r,7s)-7-hydroxy-4-oxo-2-(3,4,5-trimethoxyphenyl)-5,13-dioxatetracyclo[7.7.0.0³,⁷.0¹¹,¹⁵]hexadeca-1(16),9,11,14-tetraen-3-yl acetate)