NP-MRD: Showing NP-Card for (1s,2s,6r,8s,11s,12r,13s,16s,17s,19r,20s)-17-(acetyloxy)-19-hydroxy-1,9,11,16-tetramethyl-8-(2-oxo-5h-furan-3-yl)-5,14-dioxapentacyclo[11.6.1.0²,¹¹.0⁶,¹⁰.0¹⁶,²⁰]icos-9-en-12-yl (2e)-2-methylbut-2-enoate (NP0182541)

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Record Information

Version

2.0

Created at

2022-09-03 21:15:28 UTC

Updated at

2022-09-03 21:15:28 UTC

NP-MRD ID

NP0182541

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2s,6r,8s,11s,12r,13s,16s,17s,19r,20s)-17-(acetyloxy)-19-hydroxy-1,9,11,16-tetramethyl-8-(2-oxo-5h-furan-3-yl)-5,14-dioxapentacyclo[11.6.1.0²,¹¹.0⁶,¹⁰.0¹⁶,²⁰]icos-9-en-12-yl (2e)-2-methylbut-2-enoate

Description

(1S,2S,6R,8S,11S,12R,13S,16S,17S,19R,20S)-17-(acetyloxy)-19-hydroxy-1,9,11,16-tetramethyl-8-(2-oxo-2,5-dihydrofuran-3-yl)-5,14-dioxapentacyclo[11.6.1.0²,¹¹.0⁶,¹⁰.0¹⁶,²⁰]Icos-9-en-12-yl (2E)-2-methylbut-2-enoate 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,2S,6R,8S,11S,12R,13S,16S,17S,19R,20S)-17-(acetyloxy)-19-hydroxy-1,9,11,16-tetramethyl-8-(2-oxo-2,5-dihydrofuran-3-yl)-5,14-dioxapentacyclo[11.6.1.0²,¹¹.0⁶,¹⁰.0¹⁶,²⁰]Icos-9-en-12-yl (2E)-2-methylbut-2-enoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032223152D          

 42 47  0  0  1  0            999 V2000
    5.8786   -2.1501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3143   -1.5483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5110   -1.7360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2719   -2.5256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.1858   -0.3445    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6215    0.2573    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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    2.4202   -0.6530    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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  8 41  1  0  0  0  0
 41 42  1  6  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652309032223152D          

 42 47  0  0  1  0            999 V2000
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    2.4202   -0.6530    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6099   -0.4978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5072    0.3208    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8011   -0.1060    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8301    0.7922    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0833    0.4415    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5937    0.9129    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3405    0.5623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5240    1.7350    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8998    1.6142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6466    1.9649    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6870    2.7889    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4930    1.4610    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6193    2.2763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539    0.6714    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2964    1.6488    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4151    2.4652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1275    2.8814    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8970    2.5839    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1442    1.7969    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.9373    1.5696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9662    0.7451    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.6503    0.2839    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4255    0.5662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9335   -0.0838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4723   -0.7679    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6792   -0.5406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0292   -1.0486    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1910    0.4628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9638   -0.3303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6830    1.1128    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8606    1.0469    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3784    0.4046    0.0000 C   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
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  8  7  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  6  0  0  0
 12 14  1  0  0  0  0
 14 15  1  1  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  2  0  0  0  0
 14 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  1  0  0  0
 20 22  1  0  0  0  0
 22 23  1  6  0  0  0
 22 24  1  0  0  0  0
 24  9  1  6  0  0  0
 12 24  1  0  0  0  0
 22 25  1  0  0  0  0
 25 26  1  6  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  6  0  0  0
 30 31  1  0  0  0  0
 31 32  1  6  0  0  0
 32 33  2  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
 32 36  1  0  0  0  0
 36 37  2  0  0  0  0
 31 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  2  0  0  0  0
 29 40  1  0  0  0  0
 40 41  1  0  0  0  0
 25 41  1  0  0  0  0
  8 41  1  0  0  0  0
 41 42  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0182541

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C=C(/C)C(=O)O[C@H]1[C@H]2OC[C@]3(C)[C@@H]2[C@@](C)([C@H](O)C[C@@H]3OC(C)=O)[C@@H]2CCO[C@@H]3C[C@@H](C(C)=C3[C@@]12C)C1=CCOC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C33H44O9/c1-8-16(2)29(36)42-28-26-27-31(5,15-40-26)24(41-18(4)34)14-23(35)32(27,6)22-10-12-38-21-13-20(19-9-11-39-30(19)37)17(3)25(21)33(22,28)7/h8-9,20-24,26-28,35H,10-15H2,1-7H3/b16-8+/t20-,21+,22-,23+,24-,26-,27+,28-,31-,32+,33-/m0/s1

> <INCHI_KEY>
POBWGJYVMWYKSK-SBYDWGRLSA-N

> <FORMULA>
C33H44O9

> <MOLECULAR_WEIGHT>
584.706

> <EXACT_MASS>
584.298532997

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
86

> <JCHEM_AVERAGE_POLARIZABILITY>
62.39333041174156

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2S,6R,8S,11S,12R,13S,16S,17S,19R,20S)-17-(acetyloxy)-19-hydroxy-1,9,11,16-tetramethyl-8-(2-oxo-2,5-dihydrofuran-3-yl)-5,14-dioxapentacyclo[11.6.1.0^{2,11}.0^{6,10}.0^{16,20}]icos-9-en-12-yl (2E)-2-methylbut-2-enoate

> <JCHEM_LOGP>
3.00076371

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.623682501635052

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.308668592479222

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9733487520091932

> <JCHEM_POLAR_SURFACE_AREA>
117.59

> <JCHEM_REFRACTIVITY>
153.5728

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,6R,8S,11S,12R,13S,16S,17S,19R,20S)-17-(acetyloxy)-19-hydroxy-1,9,11,16-tetramethyl-8-(2-oxo-5H-furan-3-yl)-5,14-dioxapentacyclo[11.6.1.0^{2,11}.0^{6,10}.0^{16,20}]icos-9-en-12-yl (2E)-2-methylbut-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0      10.973  -4.014   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.920  -2.890   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.420  -3.241   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.974  -4.714   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.367  -2.117   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       5.868  -2.467   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       7.814  -0.643   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       6.760   0.480   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.261   0.130   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       4.518  -1.219   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       3.005  -0.929   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.813   0.599   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.495  -0.198   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.550   1.479   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       0.156   0.824   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -1.108   1.704   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -2.502   1.050   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -0.978   3.239   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       1.680   3.013   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.074   3.668   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       3.149   5.206   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       4.654   2.727   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.889   4.249   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.207   1.253   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.153   3.078   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.375   4.602   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       7.705   5.379   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       9.141   4.823   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       9.603   3.354   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      11.083   2.930   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      11.137   1.391   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      12.414   0.530   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      13.861   1.057   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      14.809  -0.156   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      13.948  -1.433   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      12.468  -1.009   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      11.255  -1.957   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       9.690   0.864   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       9.266  -0.617   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       8.742   2.077   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       7.207   1.954   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       8.173   0.755   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   41                                                  
CONECT    9    8   10   24                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14   24                                             
CONECT   13   12                                                            
CONECT   14   12   15   19                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19   14   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   24   25                                             
CONECT   23   22                                                            
CONECT   24   22    9   12                                                  
CONECT   25   22   26   41                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30   40                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32   38                                                  
CONECT   32   31   33   36                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   32   37                                                  
CONECT   37   36                                                            
CONECT   38   31   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38   29   41                                                  
CONECT   41   40   25    8   42                                             
CONECT   42   41                                                            
MASTER        0    0    0    0    0    0    0    0   42    0   94    0
END

View in JSmol

Synonyms

Value	Source
(1S,2S,6R,8S,11S,12R,13S,16S,17S,19R,20S)-17-(Acetyloxy)-19-hydroxy-1,9,11,16-tetramethyl-8-(2-oxo-2,5-dihydrofuran-3-yl)-5,14-dioxapentacyclo[11.6.1.0,.0,.0,]icos-9-en-12-yl (2E)-2-methylbut-2-enoic acid	Generator

Chemical Formula

C₃₃H₄₄O₉

Average Mass

584.7060 Da

Monoisotopic Mass

584.29853 Da

IUPAC Name

Traditional Name

(1S,2S,6R,8S,11S,12R,13S,16S,17S,19R,20S)-17-(acetyloxy)-19-hydroxy-1,9,11,16-tetramethyl-8-(2-oxo-5H-furan-3-yl)-5,14-dioxapentacyclo[11.6.1.0^{2,11}.0^{6,10}.0^{16,20}]icos-9-en-12-yl (2E)-2-methylbut-2-enoate

CAS Registry Number

Not Available

SMILES

C\C=C(/C)C(=O)O[C@H]1[C@H]2OC[C@]3(C)[C@@H]2[C@@](C)([C@H](O)C[C@@H]3OC(C)=O)[C@@H]2CCO[C@@H]3C[C@@H](C(C)=C3[C@@]12C)C1=CCOC1=O

InChI Identifier

InChI=1S/C33H44O9/c1-8-16(2)29(36)42-28-26-27-31(5,15-40-26)24(41-18(4)34)14-23(35)32(27,6)22-10-12-38-21-13-20(19-9-11-39-30(19)37)17(3)25(21)33(22,28)7/h8-9,20-24,26-28,35H,10-15H2,1-7H3/b16-8+/t20-,21+,22-,23+,24-,26-,27+,28-,31-,32+,33-/m0/s1

InChI Key

POBWGJYVMWYKSK-SBYDWGRLSA-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
Fatty acid ester
Oxepane
2-furanone
Fatty acyl
Cyclic alcohol
Dihydrofuran
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tetrahydrofuran
Carboxylic acid ester
Secondary alcohol
Lactone
Dialkyl ether
Oxacycle
Ether
Organoheterocyclic compound
Alcohol
Hydrocarbon derivative
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	ChemAxon
pKa (Strongest Acidic)	13.31	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	117.59 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	153.57 m³·mol⁻¹	ChemAxon
Polarizability	62.39 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

162932908

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,2s,6r,8s,11s,12r,13s,16s,17s,19r,20s)-17-(acetyloxy)-19-hydroxy-1,9,11,16-tetramethyl-8-(2-oxo-5h-furan-3-yl)-5,14-dioxapentacyclo[11.6.1.0²,¹¹.0⁶,¹⁰.0¹⁶,²⁰]icos-9-en-12-yl (2e)-2-methylbut-2-enoate (NP0182541)

MOL for NP0182541 ((1s,2s,6r,8s,11s,12r,13s,16s,17s,19r,20s)-17-(acetyloxy)-19-hydroxy-1,9,11,16-tetramethyl-8-(2-oxo-5h-furan-3-yl)-5,14-dioxapentacyclo[11.6.1.0²,¹¹.0⁶,¹⁰.0¹⁶,²⁰]icos-9-en-12-yl (2e)-2-methylbut-2-enoate)

3D MOL for NP0182541 ((1s,2s,6r,8s,11s,12r,13s,16s,17s,19r,20s)-17-(acetyloxy)-19-hydroxy-1,9,11,16-tetramethyl-8-(2-oxo-5h-furan-3-yl)-5,14-dioxapentacyclo[11.6.1.0²,¹¹.0⁶,¹⁰.0¹⁶,²⁰]icos-9-en-12-yl (2e)-2-methylbut-2-enoate)

3D SDF for NP0182541 ((1s,2s,6r,8s,11s,12r,13s,16s,17s,19r,20s)-17-(acetyloxy)-19-hydroxy-1,9,11,16-tetramethyl-8-(2-oxo-5h-furan-3-yl)-5,14-dioxapentacyclo[11.6.1.0²,¹¹.0⁶,¹⁰.0¹⁶,²⁰]icos-9-en-12-yl (2e)-2-methylbut-2-enoate)

3D-SDF for NP0182541 ((1s,2s,6r,8s,11s,12r,13s,16s,17s,19r,20s)-17-(acetyloxy)-19-hydroxy-1,9,11,16-tetramethyl-8-(2-oxo-5h-furan-3-yl)-5,14-dioxapentacyclo[11.6.1.0²,¹¹.0⁶,¹⁰.0¹⁶,²⁰]icos-9-en-12-yl (2e)-2-methylbut-2-enoate)

PDB for NP0182541 ((1s,2s,6r,8s,11s,12r,13s,16s,17s,19r,20s)-17-(acetyloxy)-19-hydroxy-1,9,11,16-tetramethyl-8-(2-oxo-5h-furan-3-yl)-5,14-dioxapentacyclo[11.6.1.0²,¹¹.0⁶,¹⁰.0¹⁶,²⁰]icos-9-en-12-yl (2e)-2-methylbut-2-enoate)

3D PDB for NP0182541 ((1s,2s,6r,8s,11s,12r,13s,16s,17s,19r,20s)-17-(acetyloxy)-19-hydroxy-1,9,11,16-tetramethyl-8-(2-oxo-5h-furan-3-yl)-5,14-dioxapentacyclo[11.6.1.0²,¹¹.0⁶,¹⁰.0¹⁶,²⁰]icos-9-en-12-yl (2e)-2-methylbut-2-enoate)

SMILES for NP0182541 ((1s,2s,6r,8s,11s,12r,13s,16s,17s,19r,20s)-17-(acetyloxy)-19-hydroxy-1,9,11,16-tetramethyl-8-(2-oxo-5h-furan-3-yl)-5,14-dioxapentacyclo[11.6.1.0²,¹¹.0⁶,¹⁰.0¹⁶,²⁰]icos-9-en-12-yl (2e)-2-methylbut-2-enoate)

INCHI for NP0182541 ((1s,2s,6r,8s,11s,12r,13s,16s,17s,19r,20s)-17-(acetyloxy)-19-hydroxy-1,9,11,16-tetramethyl-8-(2-oxo-5h-furan-3-yl)-5,14-dioxapentacyclo[11.6.1.0²,¹¹.0⁶,¹⁰.0¹⁶,²⁰]icos-9-en-12-yl (2e)-2-methylbut-2-enoate)

Structure for NP0182541 ((1s,2s,6r,8s,11s,12r,13s,16s,17s,19r,20s)-17-(acetyloxy)-19-hydroxy-1,9,11,16-tetramethyl-8-(2-oxo-5h-furan-3-yl)-5,14-dioxapentacyclo[11.6.1.0²,¹¹.0⁶,¹⁰.0¹⁶,²⁰]icos-9-en-12-yl (2e)-2-methylbut-2-enoate)

3D Structure for NP0182541 ((1s,2s,6r,8s,11s,12r,13s,16s,17s,19r,20s)-17-(acetyloxy)-19-hydroxy-1,9,11,16-tetramethyl-8-(2-oxo-5h-furan-3-yl)-5,14-dioxapentacyclo[11.6.1.0²,¹¹.0⁶,¹⁰.0¹⁶,²⁰]icos-9-en-12-yl (2e)-2-methylbut-2-enoate)