NP-MRD: Showing NP-Card for (3r,5s,7r,9s,10s,12r,14s,15s,18r,19r,20r,22s,23r)-9-(acetyloxy)-14-formyl-10,22-dihydroxy-7,18-dimethyl-19-(5-oxo-2h-furan-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0³,¹².0⁵,¹⁰.0¹⁵,²³.0¹⁸,²²]pentacos-1(25)-en-20-yl acetate (NP0261719)

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Record Information

Version

2.0

Created at

2022-09-08 04:14:33 UTC

Updated at

2022-09-08 04:14:33 UTC

NP-MRD ID

NP0261719

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3r,5s,7r,9s,10s,12r,14s,15s,18r,19r,20r,22s,23r)-9-(acetyloxy)-14-formyl-10,22-dihydroxy-7,18-dimethyl-19-(5-oxo-2h-furan-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0³,¹².0⁵,¹⁰.0¹⁵,²³.0¹⁸,²²]pentacos-1(25)-en-20-yl acetate

Description

(3R,5S,7R,9S,10S,12R,14S,15S,18R,19R,20R,22S,23R)-9-(acetyloxy)-14-formyl-10,22-dihydroxy-7,18-dimethyl-19-(5-oxo-2,5-dihydrofuran-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0³,¹².0⁵,¹⁰.0¹⁵,²³.0¹⁸,²²]Pentacos-1(25)-en-20-yl acetate belongs to the class of organic compounds known as steroid esters. Steroid esters are compounds containing a steroid moiety which bears a carboxylic acid ester group. (3r,5s,7r,9s,10s,12r,14s,15s,18r,19r,20r,22s,23r)-9-(acetyloxy)-14-formyl-10,22-dihydroxy-7,18-dimethyl-19-(5-oxo-2h-furan-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0³,¹².0⁵,¹⁰.0¹⁵,²³.0¹⁸,²²]pentacos-1(25)-en-20-yl acetate is found in Asclepias vestita. Based on a literature review very few articles have been published on (3R,5S,7R,9S,10S,12R,14S,15S,18R,19R,20R,22S,23R)-9-(acetyloxy)-14-formyl-10,22-dihydroxy-7,18-dimethyl-19-(5-oxo-2,5-dihydrofuran-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0³,¹².0⁵,¹⁰.0¹⁵,²³.0¹⁸,²²]Pentacos-1(25)-en-20-yl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082206142D          

 45 51  0  0  1  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1652309082206142D          

 45 51  0  0  1  0            999 V2000
   -4.4299    2.1461    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5893    1.3367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3700    1.0700    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9680    0.7939    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1274   -0.0155    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.9081   -0.2822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0675   -1.0917    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.8483   -1.3583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4462   -1.6345    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6655   -1.3678    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0442   -1.9106    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2635   -1.6439    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6422   -2.1867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8615   -1.9200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2402   -2.4628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5405   -2.1961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6999   -1.3867    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0786   -0.8439    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2380   -0.0344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0188    0.2322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6401   -0.3106    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8832    0.4778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4591   -0.2120    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8609    0.5085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6800    0.6070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8394    1.4165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5880    1.7633    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1188    1.8182    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5141    1.2571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8060   -0.9606    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6154   -1.1200    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8821   -1.9007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6915   -2.0602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3393   -2.5220    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2012   -1.5218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4806   -1.1200    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4067   -1.9417    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7021   -1.1106    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5427   -0.3011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1640    0.2417    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3234   -0.5678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1041   -0.8344    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7254   -0.2917    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5061   -0.5583    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.3467    0.2511    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
  2  4  1  0  0  0  0
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  6  0  0  0
  7  9  1  0  0  0  0
 10  9  1  6  0  0  0
 10 11  1  0  0  0  0
 12 11  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 17 16  1  6  0  0  0
 17 18  1  0  0  0  0
 18 19  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  1  0  0  0
 21 23  1  0  0  0  0
 23 24  1  1  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 24 29  1  0  0  0  0
 23 30  1  0  0  0  0
 30 31  1  6  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  2  0  0  0  0
 30 35  1  0  0  0  0
 35 36  1  0  0  0  0
 17 36  1  0  0  0  0
 21 36  1  0  0  0  0
 36 37  1  1  0  0  0
 18 38  1  0  0  0  0
 14 38  1  0  0  0  0
 38 39  1  1  0  0  0
 39 40  2  0  0  0  0
 38 41  1  0  0  0  0
 41 42  1  0  0  0  0
 12 42  1  0  0  0  0
 42 43  1  6  0  0  0
 43 44  1  0  0  0  0
  5 44  1  0  0  0  0
 10 44  1  0  0  0  0
 44 45  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0261719

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1C[C@H](OC(C)=O)[C@]2(O)O[C@@H]3C[C@]4(C=O)[C@H]5CC[C@]6(C)[C@H]([C@@H](C[C@]6(O)[C@@H]5CC=C4C[C@H]3O[C@@H]2O1)OC(C)=O)C1=CC(=O)OC1

> <INCHI_IDENTIFIER>
InChI=1S/C33H42O12/c1-16-9-26(43-18(3)36)33(39)29(41-16)44-23-11-20-5-6-22-21(31(20,15-34)12-24(23)45-33)7-8-30(4)28(19-10-27(37)40-14-19)25(42-17(2)35)13-32(22,30)38/h5,10,15-16,21-26,28-29,38-39H,6-9,11-14H2,1-4H3/t16-,21+,22-,23-,24-,25-,26+,28+,29+,30-,31-,32+,33+/m1/s1

> <INCHI_KEY>
RXIJRFPUSVOGIV-KUMYXRLTSA-N

> <FORMULA>
C33H42O12

> <MOLECULAR_WEIGHT>
630.687

> <EXACT_MASS>
630.267626792

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
87

> <JCHEM_AVERAGE_POLARIZABILITY>
64.6784541833677

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3R,5S,7R,9S,10S,12R,14S,15S,18R,19R,20R,22S,23R)-9-(acetyloxy)-14-formyl-10,22-dihydroxy-7,18-dimethyl-19-(5-oxo-2,5-dihydrofuran-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0^{3,12}.0^{5,10}.0^{15,23}.0^{18,22}]pentacos-1(25)-en-20-yl acetate

> <JCHEM_LOGP>
1.0590283956666648

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
9.427187564282319

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.818401851458962

> <JCHEM_PKA_STRONGEST_BASIC>
-3.2088453572422226

> <JCHEM_POLAR_SURFACE_AREA>
164.12

> <JCHEM_REFRACTIVITY>
154.2255

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(3R,5S,7R,9S,10S,12R,14S,15S,18R,19R,20R,22S,23R)-9-(acetyloxy)-14-formyl-10,22-dihydroxy-7,18-dimethyl-19-(5-oxo-2H-furan-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0^{3,12}.0^{5,10}.0^{15,23}.0^{18,22}]pentacos-1(25)-en-20-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0      -8.269   4.006   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -8.567   2.495   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0     -10.024   1.997   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      -7.407   1.482   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -7.704  -0.029   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -9.162  -0.527   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -9.459  -2.038   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0     -10.917  -2.536   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -8.300  -3.051   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -6.842  -2.553   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -5.683  -3.566   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -4.225  -3.069   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -3.065  -4.082   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.608  -3.584   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.448  -4.597   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.009  -4.099   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.307  -2.588   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.147  -1.575   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.444  -0.064   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.902   0.433   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.061  -0.580   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.515   0.892   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.590  -0.396   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.340   0.949   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.869   1.133   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       7.167   2.644   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       8.564   3.292   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       5.822   3.394   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       4.693   2.347   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.238  -1.793   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       6.749  -2.091   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       7.247  -3.548   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       8.758  -3.846   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       6.233  -4.708   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       4.109  -2.841   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       2.764  -2.091   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       2.626  -3.625   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      -1.311  -2.073   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      -1.013  -0.562   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      -2.173   0.451   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      -2.470  -1.060   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -3.928  -1.558   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      -5.087  -0.544   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0      -6.545  -1.042   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0      -6.247   0.469   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   44                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11   44                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   42                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   38                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   36                                                  
CONECT   18   17   19   38                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23   36                                             
CONECT   22   21                                                            
CONECT   23   21   24   30                                                  
CONECT   24   23   25   29                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   24                                                       
CONECT   30   23   31   35                                                  
CONECT   31   30   32                                                       
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32                                                            
CONECT   35   30   36                                                       
CONECT   36   35   17   21   37                                             
CONECT   37   36                                                            
CONECT   38   18   14   39   41                                             
CONECT   39   38   40                                                       
CONECT   40   39                                                            
CONECT   41   38   42                                                       
CONECT   42   41   12   43                                                  
CONECT   43   42   44                                                       
CONECT   44   43    5   10   45                                             
CONECT   45   44                                                            
MASTER        0    0    0    0    0    0    0    0   45    0  102    0
END

View in JSmol

Synonyms

Value	Source
(3R,5S,7R,9S,10S,12R,14S,15S,18R,19R,20R,22S,23R)-9-(Acetyloxy)-14-formyl-10,22-dihydroxy-7,18-dimethyl-19-(5-oxo-2,5-dihydrofuran-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0,.0,.0,.0,]pentacos-1(25)-en-20-yl acetic acid	Generator

Chemical Formula

C₃₃H₄₂O₁₂

Average Mass

630.6870 Da

Monoisotopic Mass

630.26763 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@@H]1C[C@H](OC(C)=O)[C@]2(O)O[C@@H]3C[C@]4(C=O)[C@H]5CC[C@]6(C)[C@H]([C@@H](C[C@]6(O)[C@@H]5CC=C4C[C@H]3O[C@@H]2O1)OC(C)=O)C1=CC(=O)OC1

InChI Identifier

InChI=1S/C33H42O12/c1-16-9-26(43-18(3)36)33(39)29(41-16)44-23-11-20-5-6-22-21(31(20,15-34)12-24(23)45-33)7-8-30(4)28(19-10-27(37)40-14-19)25(42-17(2)35)13-32(22,30)38/h5,10,15-16,21-26,28-29,38-39H,6-9,11-14H2,1-4H3/t16-,21+,22-,23-,24-,25-,26+,28+,29+,30-,31-,32+,33+/m1/s1

InChI Key

RXIJRFPUSVOGIV-KUMYXRLTSA-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
Asclepias vestita	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as steroid esters. Steroid esters are compounds containing a steroid moiety which bears a carboxylic acid ester group.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroid esters

Direct Parent

Steroid esters

Alternative Parents

Substituents

Steroid ester
19-oxosteroid
Oxosteroid
14-hydroxysteroid
Hydroxysteroid
Delta-5-steroid
Tricarboxylic acid or derivatives
Para-dioxane
2-furanone
Oxane
Cyclic alcohol
Dihydrofuran
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tertiary alcohol
Carboxylic acid ester
Hemiacetal
Lactone
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Acetal
Hydrocarbon derivative
Organic oxygen compound
Carbonyl group
Organic oxide
Aldehyde
Organooxygen compound
Alcohol
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

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

162934390

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3r,5s,7r,9s,10s,12r,14s,15s,18r,19r,20r,22s,23r)-9-(acetyloxy)-14-formyl-10,22-dihydroxy-7,18-dimethyl-19-(5-oxo-2h-furan-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0³,¹².0⁵,¹⁰.0¹⁵,²³.0¹⁸,²²]pentacos-1(25)-en-20-yl acetate (NP0261719)

MOL for NP0261719 ((3r,5s,7r,9s,10s,12r,14s,15s,18r,19r,20r,22s,23r)-9-(acetyloxy)-14-formyl-10,22-dihydroxy-7,18-dimethyl-19-(5-oxo-2h-furan-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0³,¹².0⁵,¹⁰.0¹⁵,²³.0¹⁸,²²]pentacos-1(25)-en-20-yl acetate)

3D MOL for NP0261719 ((3r,5s,7r,9s,10s,12r,14s,15s,18r,19r,20r,22s,23r)-9-(acetyloxy)-14-formyl-10,22-dihydroxy-7,18-dimethyl-19-(5-oxo-2h-furan-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0³,¹².0⁵,¹⁰.0¹⁵,²³.0¹⁸,²²]pentacos-1(25)-en-20-yl acetate)

3D SDF for NP0261719 ((3r,5s,7r,9s,10s,12r,14s,15s,18r,19r,20r,22s,23r)-9-(acetyloxy)-14-formyl-10,22-dihydroxy-7,18-dimethyl-19-(5-oxo-2h-furan-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0³,¹².0⁵,¹⁰.0¹⁵,²³.0¹⁸,²²]pentacos-1(25)-en-20-yl acetate)

3D-SDF for NP0261719 ((3r,5s,7r,9s,10s,12r,14s,15s,18r,19r,20r,22s,23r)-9-(acetyloxy)-14-formyl-10,22-dihydroxy-7,18-dimethyl-19-(5-oxo-2h-furan-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0³,¹².0⁵,¹⁰.0¹⁵,²³.0¹⁸,²²]pentacos-1(25)-en-20-yl acetate)

PDB for NP0261719 ((3r,5s,7r,9s,10s,12r,14s,15s,18r,19r,20r,22s,23r)-9-(acetyloxy)-14-formyl-10,22-dihydroxy-7,18-dimethyl-19-(5-oxo-2h-furan-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0³,¹².0⁵,¹⁰.0¹⁵,²³.0¹⁸,²²]pentacos-1(25)-en-20-yl acetate)

3D PDB for NP0261719 ((3r,5s,7r,9s,10s,12r,14s,15s,18r,19r,20r,22s,23r)-9-(acetyloxy)-14-formyl-10,22-dihydroxy-7,18-dimethyl-19-(5-oxo-2h-furan-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0³,¹².0⁵,¹⁰.0¹⁵,²³.0¹⁸,²²]pentacos-1(25)-en-20-yl acetate)

SMILES for NP0261719 ((3r,5s,7r,9s,10s,12r,14s,15s,18r,19r,20r,22s,23r)-9-(acetyloxy)-14-formyl-10,22-dihydroxy-7,18-dimethyl-19-(5-oxo-2h-furan-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0³,¹².0⁵,¹⁰.0¹⁵,²³.0¹⁸,²²]pentacos-1(25)-en-20-yl acetate)

INCHI for NP0261719 ((3r,5s,7r,9s,10s,12r,14s,15s,18r,19r,20r,22s,23r)-9-(acetyloxy)-14-formyl-10,22-dihydroxy-7,18-dimethyl-19-(5-oxo-2h-furan-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0³,¹².0⁵,¹⁰.0¹⁵,²³.0¹⁸,²²]pentacos-1(25)-en-20-yl acetate)

Structure for NP0261719 ((3r,5s,7r,9s,10s,12r,14s,15s,18r,19r,20r,22s,23r)-9-(acetyloxy)-14-formyl-10,22-dihydroxy-7,18-dimethyl-19-(5-oxo-2h-furan-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0³,¹².0⁵,¹⁰.0¹⁵,²³.0¹⁸,²²]pentacos-1(25)-en-20-yl acetate)

3D Structure for NP0261719 ((3r,5s,7r,9s,10s,12r,14s,15s,18r,19r,20r,22s,23r)-9-(acetyloxy)-14-formyl-10,22-dihydroxy-7,18-dimethyl-19-(5-oxo-2h-furan-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0³,¹².0⁵,¹⁰.0¹⁵,²³.0¹⁸,²²]pentacos-1(25)-en-20-yl acetate)