NP-MRD: Showing NP-Card for (3r,5s,7r,9s,10s,12r,14s,15s,18r,19r,20r,22s,23r)-14-formyl-9,10,22-trihydroxy-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 (NP0298114)

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Record Information

Version

2.0

Created at

2022-09-10 09:04:51 UTC

Updated at

2022-09-10 09:04:51 UTC

NP-MRD ID

NP0298114

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3r,5s,7r,9s,10s,12r,14s,15s,18r,19r,20r,22s,23r)-14-formyl-9,10,22-trihydroxy-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)-14-formyl-9,10,22-trihydroxy-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)-14-formyl-9,10,22-trihydroxy-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)-14-formyl-9,10,22-trihydroxy-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


  Mrv1652309102211042D          

 42 48  0  0  1  0            999 V2000
    2.3538   -3.1753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1633   -3.3347    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7060   -2.7134    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4299   -4.1154    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2394   -4.2748    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8441   -3.7137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5647   -4.1154    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.6386   -3.2937    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3454   -3.8488    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.5048   -3.0393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2855   -2.7726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9068   -3.3154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6876   -3.0488    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3089   -3.5915    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.0896   -3.3249    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.7109   -3.8677    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.4916   -3.6010    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.1129   -4.1438    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
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 39 40  2  0  0  0  0
 39 41  1  0  0  0  0
 41 42  1  0  0  0  0
 37 42  1  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652309102211042D          

 42 48  0  0  1  0            999 V2000
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    6.3454   -3.8488    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.5048   -3.0393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2855   -2.7726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9068   -3.3154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6876   -3.0488    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3089   -3.5915    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.0896   -3.3249    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.7109   -3.8677    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.4916   -3.6010    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.1129   -4.1438    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.8936   -3.8771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9535   -4.9532    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1727   -5.2199    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.0133   -6.0293    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.5515   -4.6771    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.3920   -5.4866    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.7707   -4.9438    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.1494   -4.4010    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.3687   -4.6677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7474   -4.1249    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.5880   -4.9343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2093   -5.4771    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9667   -4.3915    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.8073   -5.2010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0266   -5.4677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4053   -4.9249    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1621   -5.7132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5862   -5.0234    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1844   -5.7440    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5313   -6.4925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9265   -7.0537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0250   -7.8728    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2059   -6.6519    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3653   -5.8425    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
  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  1  0  0  0
  7  9  1  0  0  0  0
  9 10  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  1  0  0  0
 16 15  1  6  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  6  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  6  0  0  0
 21 23  1  0  0  0  0
 16 23  1  0  0  0  0
 23 24  1  1  0  0  0
 23 25  1  0  0  0  0
 26 25  1  6  0  0  0
 14 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 12 28  1  0  0  0  0
 28 29  1  1  0  0  0
 29 30  2  0  0  0  0
 28 31  1  0  0  0  0
  9 31  1  0  0  0  0
 31 32  1  1  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
  7 34  1  0  0  0  0
 34 35  1  1  0  0  0
 34 36  1  0  0  0  0
  5 36  1  0  0  0  0
 36 37  1  1  0  0  0
 37 38  2  0  0  0  0
 38 39  1  0  0  0  0
 39 40  2  0  0  0  0
 39 41  1  0  0  0  0
 41 42  1  0  0  0  0
 37 42  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0298114

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1C[C@H](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/C31H40O11/c1-15-8-24(34)31(37)27(39-15)41-21-10-18-4-5-20-19(29(18,14-32)11-22(21)42-31)6-7-28(3)26(17-9-25(35)38-13-17)23(40-16(2)33)12-30(20,28)36/h4,9,14-15,19-24,26-27,34,36-37H,5-8,10-13H2,1-3H3/t15-,19+,20-,21-,22-,23-,24+,26+,27+,28-,29-,30+,31+/m1/s1

> <INCHI_KEY>
DXQPSTQSSWLUJC-MQXAYUHBSA-N

> <FORMULA>
C31H40O11

> <MOLECULAR_WEIGHT>
588.65

> <EXACT_MASS>
588.257062108

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
82

> <JCHEM_AVERAGE_POLARIZABILITY>
61.183443825167956

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3R,5S,7R,9S,10S,12R,14S,15S,18R,19R,20R,22S,23R)-14-formyl-9,10,22-trihydroxy-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>
0.6179029853333317

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
9.460862758822215

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.818482001062218

> <JCHEM_PKA_STRONGEST_BASIC>
-3.2088453572422226

> <JCHEM_POLAR_SURFACE_AREA>
158.05

> <JCHEM_REFRACTIVITY>
145.074

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(3R,5S,7R,9S,10S,12R,14S,15S,18R,19R,20R,22S,23R)-14-formyl-9,10,22-trihydroxy-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                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0       4.394  -5.927   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.905  -6.225   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       6.918  -5.065   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       6.403  -7.682   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       7.914  -7.980   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.042  -6.932   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.387  -7.682   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      10.525  -6.148   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      11.845  -7.184   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      12.142  -5.673   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      13.600  -5.176   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      14.759  -6.189   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      16.217  -5.691   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      17.377  -6.704   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      18.834  -6.206   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      19.994  -7.220   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      21.451  -6.722   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      22.611  -7.735   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      24.068  -7.237   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      22.313  -9.246   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      20.856  -9.744   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      20.558 -11.255   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      19.696  -8.731   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      19.398 -10.242   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0      18.239  -9.228   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      17.079  -8.215   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      15.622  -8.713   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      14.462  -7.700   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      14.164  -9.211   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      15.324 -10.224   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      13.005  -8.198   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      12.707  -9.709   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      11.250 -10.206   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      10.090  -9.193   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       9.636 -10.665   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       8.561  -9.377   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       7.811 -10.722   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       8.458 -12.119   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       7.329 -13.167   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       7.513 -14.696   0.000  0.00  0.00           O+0
HETATM   41  O   UNK     0       5.984 -12.417   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       6.282 -10.906   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   36                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9   34                                             
CONECT    8    7                                                            
CONECT    9    7   10   31                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   28                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   26                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   23                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   16   24   25                                             
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   14   27                                                  
CONECT   27   26   28                                                       
CONECT   28   27   12   29   31                                             
CONECT   29   28   30                                                       
CONECT   30   29                                                            
CONECT   31   28    9   32                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33    7   35   36                                             
CONECT   35   34                                                            
CONECT   36   34    5   37                                                  
CONECT   37   36   38   42                                                  
CONECT   38   37   39                                                       
CONECT   39   38   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   42                                                       
CONECT   42   41   37                                                       
MASTER        0    0    0    0    0    0    0    0   42    0   96    0
END

View in JSmol

Synonyms

Value	Source
(3R,5S,7R,9S,10S,12R,14S,15S,18R,19R,20R,22S,23R)-14-Formyl-9,10,22-trihydroxy-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

C₃₁H₄₀O₁₁

Average Mass

588.6500 Da

Monoisotopic Mass

588.25706 Da

IUPAC Name

Traditional Name

(3R,5S,7R,9S,10S,12R,14S,15S,18R,19R,20R,22S,23R)-14-formyl-9,10,22-trihydroxy-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

CAS Registry Number

Not Available

SMILES

C[C@@H]1C[C@H](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/C31H40O11/c1-15-8-24(34)31(37)27(39-15)41-21-10-18-4-5-20-19(29(18,14-32)11-22(21)42-31)6-7-28(3)26(17-9-25(35)38-13-17)23(40-16(2)33)12-30(20,28)36/h4,9,14-15,19-24,26-27,34,36-37H,5-8,10-13H2,1-3H3/t15-,19+,20-,21-,22-,23-,24+,26+,27+,28-,29-,30+,31+/m1/s1

InChI Key

DXQPSTQSSWLUJC-MQXAYUHBSA-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
14-hydroxysteroid
Oxosteroid
Hydroxysteroid
Delta-5-steroid
Para-dioxane
2-furanone
Dicarboxylic acid or derivatives
Oxane
Cyclic alcohol
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tertiary alcohol
Dihydrofuran
Carboxylic acid ester
Secondary alcohol
Hemiacetal
Lactone
Acetal
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Polyol
Hydrocarbon derivative
Organic oxygen compound
Carbonyl group
Organic oxide
Alcohol
Organooxygen compound
Aldehyde
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	0.62	ChemAxon
pKa (Strongest Acidic)	6.82	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	158.05 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	145.07 m³·mol⁻¹	ChemAxon
Polarizability	61.18 Å³	ChemAxon
Number of Rings	7	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

162952955

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)-14-formyl-9,10,22-trihydroxy-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 (NP0298114)

MOL for NP0298114 ((3r,5s,7r,9s,10s,12r,14s,15s,18r,19r,20r,22s,23r)-14-formyl-9,10,22-trihydroxy-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 NP0298114 ((3r,5s,7r,9s,10s,12r,14s,15s,18r,19r,20r,22s,23r)-14-formyl-9,10,22-trihydroxy-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 NP0298114 ((3r,5s,7r,9s,10s,12r,14s,15s,18r,19r,20r,22s,23r)-14-formyl-9,10,22-trihydroxy-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 NP0298114 ((3r,5s,7r,9s,10s,12r,14s,15s,18r,19r,20r,22s,23r)-14-formyl-9,10,22-trihydroxy-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 NP0298114 ((3r,5s,7r,9s,10s,12r,14s,15s,18r,19r,20r,22s,23r)-14-formyl-9,10,22-trihydroxy-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 NP0298114 ((3r,5s,7r,9s,10s,12r,14s,15s,18r,19r,20r,22s,23r)-14-formyl-9,10,22-trihydroxy-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 NP0298114 ((3r,5s,7r,9s,10s,12r,14s,15s,18r,19r,20r,22s,23r)-14-formyl-9,10,22-trihydroxy-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 NP0298114 ((3r,5s,7r,9s,10s,12r,14s,15s,18r,19r,20r,22s,23r)-14-formyl-9,10,22-trihydroxy-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 NP0298114 ((3r,5s,7r,9s,10s,12r,14s,15s,18r,19r,20r,22s,23r)-14-formyl-9,10,22-trihydroxy-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 NP0298114 ((3r,5s,7r,9s,10s,12r,14s,15s,18r,19r,20r,22s,23r)-14-formyl-9,10,22-trihydroxy-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)