NP-MRD: Showing NP-Card for (+)-Gelomulide G (NP0073485)

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Record Information

Version

2.0

Created at

2022-04-28 18:43:43 UTC

Updated at

2022-04-28 18:43:43 UTC

NP-MRD ID

NP0073485

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-Gelomulide G

Description

(1S,3R,8R,10S,11R,14S,16S,17R)-14-(acetyloxy)-5,11,15,15-tetramethyl-6-oxo-2,7-dioxapentacyclo[8.8.0.0¹,³.0⁴,⁸.0¹¹,¹⁶]Octadec-4-en-17-yl acetate belongs to the class of organic compounds known as naphthofurans. Naphthofurans are compounds containing a furan ring fused to a naphthalene moiety. Furan is a 5 membered- ring aromatic ring with four carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings. (+)-Gelomulide G is found in Gelonium multiflorum A. and Gelonium aequoreum. Based on a literature review very few articles have been published on (1S,3R,8R,10S,11R,14S,16S,17R)-14-(acetyloxy)-5,11,15,15-tetramethyl-6-oxo-2,7-dioxapentacyclo[8.8.0.0¹,³.0⁴,⁸.0¹¹,¹⁶]Octadec-4-en-17-yl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282220432D          

 31 35  0  0  1  0            999 V2000
    0.7475   -0.8930    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4672   -0.1171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3574   -0.1439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5867   -0.9364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3626   -1.2167    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0962   -1.3994    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8637    0.5074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9990    0.5136    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8111    0.3684    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0914   -0.4075    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5596   -1.0382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9035   -0.5527    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4354    0.0780    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1551    0.8539    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3429    0.9991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6869    1.4846    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4066    2.2605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5945    2.4058    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9384    2.8912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2475   -0.0672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5278   -0.8432    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9960   -1.4739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1838   -1.3287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3399   -0.9884    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6202   -1.7643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4323   -1.9095    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0884   -2.3950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4210    0.7393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0132    0.2400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3717   -1.1834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5308    1.1443    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  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
  1  6  1  1  0  0  0
  3  7  1  0  0  0  0
  2  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  6  0  0  0
  1 11  1  0  0  0  0
 10 12  1  0  0  0  0
 13 12  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
  9 15  1  0  0  0  0
 14 16  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 13 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
 12 23  1  0  0  0  0
 21 24  1  1  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 20 28  1  0  0  0  0
 20 29  1  0  0  0  0
 12 30  1  6  0  0  0
  9 31  1  1  0  0  0
  8 31  1  1  0  0  0
M  END

     RDKit          3D

 63 67  0  0  0  0  0  0  0  0999 V2000
    5.0549   -2.4840    2.0259 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5830   -1.8185    0.7831 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3700   -1.5394   -0.1786 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2508   -1.4542    0.5828 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8170   -0.8206   -0.6074 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8482   -1.7580   -1.2798 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5999   -1.9384   -0.4332 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0731   -0.5973   -0.3269 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7307   -0.3199   -1.6595 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8211    0.5284    0.1075 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0349    1.8003   -0.1290 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7017    2.9492    0.4013 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9024    4.0536   -0.3963 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6041    5.2857    0.1173 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4850    4.0196   -1.5796 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2849    1.7701    0.5943 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0645    0.4983    0.5211 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0769    0.6292    1.6379 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4022    0.4125    0.2379 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9550   -0.9844    0.0790 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1677   -1.4723    0.0472 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4481   -0.6825    0.1618 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1148   -2.9295   -0.0029 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0557   -3.7545   -0.0494 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7791   -3.2575    0.0104 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0255   -2.1154   -0.1573 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8458   -2.0169    0.7735 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1880   -0.6713    0.7309 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2135    0.5424   -0.3412 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0824    1.0591    0.8342 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5664    1.4805   -1.4691 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4857   -3.4182    2.2462 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1107   -2.8034    1.8301 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9947   -1.8207    2.9098 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6654   -0.6736   -1.3078 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6107   -1.4755   -2.3185 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3403   -2.7528   -1.3210 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0694   -2.5755   -1.0853 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8613   -2.4092    0.5106 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1351    0.3524   -2.3195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7638    0.0332   -1.5795 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7687   -1.2729   -2.2691 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8211    0.4455    1.2500 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1647    2.0113   -1.1911 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1834    5.5215    1.1180 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3370    6.1146   -0.5486 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6936    5.1211    0.2013 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0484    2.0330    1.6683 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8918    2.6138    0.2218 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9905    1.1690   -0.2661 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3222    0.3292   -0.2857 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8042   -0.6174    1.1884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1925   -1.2293   -0.4610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6914   -2.1372   -1.2385 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2514   -2.1481    1.8081 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1229   -2.8085    0.6129 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6620   -0.5437    1.7116 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0438    1.4256    0.4783 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5116    1.8269    1.3657 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2403    0.2230    1.5635 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3585    0.9470   -2.0871 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1212    2.3941   -1.1216 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7768    1.7104   -2.1698 H   0  0  0  0  0  0  0  0  0  0  0  0
 14 13  1  0
 13 15  2  0
 13 12  1  0
 12 11  1  0
 11 16  1  0
 16 17  1  0
 17 18  1  1
 18 19  1  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 21 23  1  0
 23 24  2  0
 23 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28  8  1  0
  8  9  1  6
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  2  1  0
  2  1  1  0
  2  3  2  0
  5 29  1  0
 29 30  1  1
 29 31  1  0
 29 10  1  0
 10 11  1  0
 19 17  1  0
 26 20  1  0
 10  8  1  0
 28 17  1  0
 14 45  1  0
 14 46  1  0
 14 47  1  0
 11 44  1  6
 16 48  1  0
 16 49  1  0
 19 50  1  6
 22 51  1  0
 22 52  1  0
 22 53  1  0
 26 54  1  6
 27 55  1  0
 27 56  1  0
 28 57  1  1
  9 40  1  0
  9 41  1  0
  9 42  1  0
  7 38  1  0
  7 39  1  0
  6 36  1  0
  6 37  1  0
  5 35  1  6
  1 32  1  0
  1 33  1  0
  1 34  1  0
 30 58  1  0
 30 59  1  0
 30 60  1  0
 31 61  1  0
 31 62  1  0
 31 63  1  0
 10 43  1  1
M  END


  Mrv1652304282220432D          

 31 35  0  0  1  0            999 V2000
    0.7475   -0.8930    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4672   -0.1171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3574   -0.1439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5867   -0.9364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3626   -1.2167    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0962   -1.3994    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8637    0.5074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9990    0.5136    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8111    0.3684    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0914   -0.4075    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5596   -1.0382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9035   -0.5527    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4354    0.0780    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1551    0.8539    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3429    0.9991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6869    1.4846    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4066    2.2605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5945    2.4058    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9384    2.8912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2475   -0.0672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5278   -0.8432    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9960   -1.4739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1838   -1.3287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3399   -0.9884    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6202   -1.7643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4323   -1.9095    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0884   -2.3950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4210    0.7393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0132    0.2400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3717   -1.1834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5308    1.1443    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  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
  1  6  1  1  0  0  0
  3  7  1  0  0  0  0
  2  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  6  0  0  0
  1 11  1  0  0  0  0
 10 12  1  0  0  0  0
 13 12  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
  9 15  1  0  0  0  0
 14 16  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 13 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
 12 23  1  0  0  0  0
 21 24  1  1  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 20 28  1  0  0  0  0
 20 29  1  0  0  0  0
 12 30  1  6  0  0  0
  9 31  1  1  0  0  0
  8 31  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0073485

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)O[C@@H]1C[C@@]23O[C@@H]2C2=C(C)C(=O)O[C@@H]2C[C@H]3[C@]2(C)CC[C@H](OC(C)=O)C(C)(C)[C@@H]12

> <INCHI_IDENTIFIER>
InChI=1S/C24H32O7/c1-11-18-14(30-21(11)27)9-16-23(6)8-7-17(29-13(3)26)22(4,5)19(23)15(28-12(2)25)10-24(16)20(18)31-24/h14-17,19-20H,7-10H2,1-6H3/t14-,15-,16+,17+,19-,20-,23+,24+/m1/s1

> <INCHI_KEY>
KTOGURYEQRFUME-TYGCTQQCSA-N

> <FORMULA>
C24H32O7

> <MOLECULAR_WEIGHT>
432.513

> <EXACT_MASS>
432.21480337

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
63

> <JCHEM_AVERAGE_POLARIZABILITY>
46.29355752699909

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,3R,8R,10S,11R,14S,16S,17R)-14-(acetyloxy)-5,11,15,15-tetramethyl-6-oxo-2,7-dioxapentacyclo[8.8.0.0^{1,3}.0^{4,8}.0^{11,16}]octadec-4-en-17-yl acetate

> <ALOGPS_LOGP>
3.10

> <JCHEM_LOGP>
2.2568149890000004

> <ALOGPS_LOGS>
-4.42

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.095477634952006

> <JCHEM_PKA_STRONGEST_BASIC>
-4.259498946459763

> <JCHEM_POLAR_SURFACE_AREA>
91.43

> <JCHEM_REFRACTIVITY>
108.79079999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.63e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,3R,8R,10S,11R,14S,16S,17R)-14-(acetyloxy)-5,11,15,15-tetramethyl-6-oxo-2,7-dioxapentacyclo[8.8.0.0^{1,3}.0^{4,8}.0^{11,16}]octadec-4-en-17-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       1.395  -1.667   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.872  -0.219   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.667  -0.269   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.095  -1.748   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -2.544  -2.271   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0       0.179  -2.612   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      -1.612   0.947   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.865   0.959   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.381   0.688   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.904  -0.761   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.911  -1.938   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.420  -1.032   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.413   0.146   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.889   1.594   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.374   1.865   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       6.882   2.771   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       6.359   4.220   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       4.843   4.491   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       7.352   5.397   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.929  -0.126   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.452  -1.574   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.459  -2.751   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.943  -2.480   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       9.968  -1.845   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      10.491  -3.293   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      12.007  -3.564   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       9.498  -4.471   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       8.252   1.380   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       9.358   0.448   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       4.427  -2.209   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       2.858   2.136   0.000  0.00  0.00           O+0
CONECT    1    2    6   11                                                  
CONECT    2    1    3    8                                                  
CONECT    3    2    4    7                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    1                                                       
CONECT    7    3                                                            
CONECT    8    2    9   31                                                  
CONECT    9    8   10   15   31                                             
CONECT   10    9   11   12                                                  
CONECT   11   10    1                                                       
CONECT   12   10   13   23   30                                             
CONECT   13   12   14   20                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14    9                                                       
CONECT   16   14   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   13   21   28   29                                             
CONECT   21   20   22   24                                                  
CONECT   22   21   23                                                       
CONECT   23   22   12                                                       
CONECT   24   21   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   20                                                            
CONECT   29   20                                                            
CONECT   30   12                                                            
CONECT   31    9    8                                                       
MASTER        0    0    0    0    0    0    0    0   31    0   70    0
END

View in JSmol

Synonyms

Value	Source
(1S,3R,8R,10S,11R,14S,16S,17R)-14-(Acetyloxy)-5,11,15,15-tetramethyl-6-oxo-2,7-dioxapentacyclo[8.8.0.0,.0,.0,]octadec-4-en-17-yl acetic acid	Generator

Chemical Formula

C₂₄H₃₂O₇

Average Mass

432.5130 Da

Monoisotopic Mass

432.21480 Da

IUPAC Name

(1S,3R,8R,10S,11R,14S,16S,17R)-14-(acetyloxy)-5,11,15,15-tetramethyl-6-oxo-2,7-dioxapentacyclo[8.8.0.0^{1,3}.0^{4,8}.0^{11,16}]octadec-4-en-17-yl acetate

Traditional Name

(1S,3R,8R,10S,11R,14S,16S,17R)-14-(acetyloxy)-5,11,15,15-tetramethyl-6-oxo-2,7-dioxapentacyclo[8.8.0.0^{1,3}.0^{4,8}.0^{11,16}]octadec-4-en-17-yl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)O[C@@H]1C[C@@]23O[C@@H]2C2=C(C)C(=O)O[C@@H]2C[C@H]3[C@]2(C)CC[C@H](OC(C)=O)C(C)(C)[C@@H]12

InChI Identifier

InChI=1S/C24H32O7/c1-11-18-14(30-21(11)27)9-16-23(6)8-7-17(29-13(3)26)22(4,5)19(23)15(28-12(2)25)10-24(16)20(18)31-24/h14-17,19-20H,7-10H2,1-6H3/t14-,15-,16+,17+,19-,20-,23+,24+/m1/s1

InChI Key

KTOGURYEQRFUME-TYGCTQQCSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Gelonium multiflorum A.	Plant	KNApSAcK
Suregada aequorea	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as naphthofurans. Naphthofurans are compounds containing a furan ring fused to a naphthalene moiety. Furan is a 5 membered- ring aromatic ring with four carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Naphthofurans

Sub Class

Not Available

Direct Parent

Naphthofurans

Alternative Parents

Substituents

Naphthofuran
Tricarboxylic acid or derivatives
Oxepane
2-furanone
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Dihydrofuran
Lactone
Carboxylic acid ester
Oxacycle
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
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	3.1	ALOGPS
logP	2.26	ChemAxon
logS	-4.4	ALOGPS
pKa (Strongest Acidic)	12.1	ChemAxon
pKa (Strongest Basic)	-4.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	91.43 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	108.79 m³·mol⁻¹	ChemAxon
Polarizability	46.29 Å³	ChemAxon
Number of Rings	5	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

162837242

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (+)-Gelomulide G (NP0073485)

MOL for NP0073485 ((+)-Gelomulide G)

3D MOL for NP0073485 ((+)-Gelomulide G)

3D SDF for NP0073485 ((+)-Gelomulide G)

3D-SDF for NP0073485 ((+)-Gelomulide G)

PDB for NP0073485 ((+)-Gelomulide G)

3D PDB for NP0073485 ((+)-Gelomulide G)

SMILES for NP0073485 ((+)-Gelomulide G)

INCHI for NP0073485 ((+)-Gelomulide G)

Structure for NP0073485 ((+)-Gelomulide G)

3D Structure for NP0073485 ((+)-Gelomulide G)