NP-MRD: Showing NP-Card for (5R,8S,9S,10R,13R,14S,17R,23R*,24S*)-24,25-epoxy-23-hydroxycycloart-3-one (NP0332626)

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Record Information

Version

2.0

Created at

2024-03-14 02:47:44 UTC

Updated at

2024-11-01 00:37:48 UTC

NP-MRD ID

NP0332626

Natural Product DOI

https://doi.org/10.57994/1886

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(5R,8S,9S,10R,13R,14S,17R,23R*,24S*)-24,25-epoxy-23-hydroxycycloart-3-one

Description

(5R,8S,9S,10R,13R,14S,17R,23R*,24S*)-24,25-epoxy-23-hydroxycycloart-3-one belongs to the class of organic compounds known as cycloartanols and derivatives. These are steroids containing a cycloartanol moiety. Based on a literature review very few articles have been published on (5R,8S,9S,10R,13R,14S,17R,23R*,24S*)-24,25-epoxy-23-hydroxycycloart-3-one.

Structure

MOL SDF PDB SMILES InChI


  Mrv2104 03142402472D          

 37 42  0  0  1  0            999 V2000
    3.6083    0.3268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2485    1.0691    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7167    0.4384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9045    0.5836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9682    1.8451    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6195    2.3514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3024    1.8884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0730    1.0959    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5794    0.4446    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2685   -0.3196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3966    0.5575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9030   -0.0939    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5921   -0.8580    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7202    0.0190    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.3716    0.5253    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6177   -0.7996    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4844   -0.2919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5256   -1.1159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2728   -0.5350    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8833    1.2514    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7705    2.6460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1561    1.9903    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4364    1.2144    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6242    1.3596    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8121    1.5048    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0924    0.7289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5318    2.2807    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0636    2.9114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8758    2.7662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2515    3.0566    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2803    2.4259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0037    3.2005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9938    2.8401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8121    1.7952    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5318    1.0193    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2803    0.8741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6242    1.9404    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  2  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  8  7  1  0  0  0  0
  2  8  1  0  0  0  0
  8  9  1  6  0  0  0
  9 10  1  1  0  0  0
  9 11  1  0  0  0  0
 12 11  1  0  0  0  0
 12 13  1  6  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  1  0  0  0
 14 17  1  6  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
  8 20  1  1  0  0  0
  5 21  1  1  0  0  0
  5 22  1  0  0  0  0
 22 23  1  6  0  0  0
 22 24  1  0  0  0  0
 24  4  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  6  0  0  0
 24 26  1  6  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 22 29  1  0  0  0  0
 27 30  1  1  0  0  0
 27 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 31 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 25 36  1  0  0  0  0
 34 37  2  0  0  0  0
M  END


  Mrv2104 03142402472D          

 37 42  0  0  1  0            999 V2000
    3.6083    0.3268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2485    1.0691    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7167    0.4384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9045    0.5836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9682    1.8451    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6195    2.3514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3024    1.8884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0730    1.0959    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5794    0.4446    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2685   -0.3196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3966    0.5575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9030   -0.0939    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5921   -0.8580    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7202    0.0190    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.3716    0.5253    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6177   -0.7996    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4844   -0.2919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5256   -1.1159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2728   -0.5350    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8833    1.2514    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7705    2.6460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1561    1.9903    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4364    1.2144    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6242    1.3596    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8121    1.5048    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0924    0.7289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5318    2.2807    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0636    2.9114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8758    2.7662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2515    3.0566    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2803    2.4259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0037    3.2005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9938    2.8401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8121    1.7952    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5318    1.0193    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2803    0.8741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6242    1.9404    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  2  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  8  7  1  0  0  0  0
  2  8  1  0  0  0  0
  8  9  1  6  0  0  0
  9 10  1  1  0  0  0
  9 11  1  0  0  0  0
 12 11  1  0  0  0  0
 12 13  1  6  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  1  0  0  0
 14 17  1  6  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
  8 20  1  1  0  0  0
  5 21  1  1  0  0  0
  5 22  1  0  0  0  0
 22 23  1  6  0  0  0
 22 24  1  0  0  0  0
 24  4  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  6  0  0  0
 24 26  1  6  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 22 29  1  0  0  0  0
 27 30  1  1  0  0  0
 27 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 31 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 25 36  1  0  0  0  0
 34 37  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0332626

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@]1(OC1(C)C)[C@H](O)C[C@@H](C)[C@@]1([H])CC[C@@]2(C)[C@]3([H])CC[C@]4([H])[C@]5(C[C@@]35CC[C@]12C)CCC(=O)C4(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C30H48O3/c1-18(16-20(31)24-26(4,5)33-24)19-10-12-28(7)22-9-8-21-25(2,3)23(32)11-13-29(21)17-30(22,29)15-14-27(19,28)6/h18-22,24,31H,8-17H2,1-7H3/t18-,19-,20-,21+,22+,24+,27-,28+,29-,30+/m1/s1

> <INCHI_KEY>
NVAPMTWXAZZIAE-RHQOKDMKSA-N

> <FORMULA>
C30H48O3

> <MOLECULAR_WEIGHT>
456.711

> <EXACT_MASS>
456.360345406

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
81

> <JCHEM_AVERAGE_POLARIZABILITY>
55.65000297966128

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,3R,8R,11S,12S,15R,16R)-15-[(2R,4R)-4-[(2S)-3,3-dimethyloxiran-2-yl]-4-hydroxybutan-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.0^{1,3}.0^{3,8}.0^{12,16}]octadecan-6-one

> <JCHEM_LOGP>
6.057551239666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.098688079599139

> <JCHEM_PKA_STRONGEST_BASIC>
-3.1930338339833377

> <JCHEM_POLAR_SURFACE_AREA>
49.83

> <JCHEM_REFRACTIVITY>
131.4099

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,3R,8R,11S,12S,15R,16R)-15-[(2R,4R)-4-[(2S)-3,3-dimethyloxiran-2-yl]-4-hydroxybutan-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.0^{1,3}.0^{3,8}.0^{12,16}]octadecan-6-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 14-MAR-24   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   14-MAR-24         0                                  
HETATM    1  C   UNK     0       6.736   0.610   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.064   1.996   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.071   0.818   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.555   1.089   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.541   3.444   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.756   4.389   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.031   3.525   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.603   2.046   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.548   0.830   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.968  -0.597   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.074   1.041   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      11.019  -0.175   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      10.439  -1.602   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      12.544   0.035   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      13.760   0.981   0.000  0.00  0.00           O+0
HETATM   16  H   UNK     0      12.353  -1.493   0.000  0.00  0.00           H+0
HETATM   17  C   UNK     0      13.971  -0.545   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      14.048  -2.083   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      15.443  -0.999   0.000  0.00  0.00           C+0
HETATM   20  H   UNK     0       9.115   2.336   0.000  0.00  0.00           H+0
HETATM   21  C   UNK     0       5.172   4.939   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.025   3.715   0.000  0.00  0.00           C+0
HETATM   23  H   UNK     0       4.548   2.267   0.000  0.00  0.00           H+0
HETATM   24  C   UNK     0       3.032   2.538   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.516   2.809   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.039   1.361   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.993   4.257   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       1.985   5.435   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.501   5.164   0.000  0.00  0.00           C+0
HETATM   30  H   UNK     0       0.470   5.706   0.000  0.00  0.00           H+0
HETATM   31  C   UNK     0      -0.523   4.528   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       0.007   5.974   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -1.855   5.302   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -1.516   3.351   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -0.993   1.903   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       0.523   1.632   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      -3.032   3.622   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    5    8                                             
CONECT    3    2    4                                                       
CONECT    4    3   24                                                       
CONECT    5    2    6   21   22                                             
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    2    9   20                                             
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   16   17                                             
CONECT   15   14   17                                                       
CONECT   16   14                                                            
CONECT   17   14   15   18   19                                             
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20    8                                                            
CONECT   21    5                                                            
CONECT   22    5   23   24   29                                             
CONECT   23   22                                                            
CONECT   24   22    4   25   26                                             
CONECT   25   24   26   27   36                                             
CONECT   26   25   24                                                       
CONECT   27   25   28   30   31                                             
CONECT   28   27   29                                                       
CONECT   29   28   22                                                       
CONECT   30   27                                                            
CONECT   31   27   32   33   34                                             
CONECT   32   31                                                            
CONECT   33   31                                                            
CONECT   34   31   35   37                                                  
CONECT   35   34   36                                                       
CONECT   36   35   25                                                       
CONECT   37   34                                                            
MASTER        0    0    0    0    0    0    0    0   37    0   84    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₄₈O₃

Average Mass

456.7110 Da

Monoisotopic Mass

456.36035 Da

IUPAC Name

(1S,3R,8R,11S,12S,15R,16R)-15-[(2R,4R)-4-[(2S)-3,3-dimethyloxiran-2-yl]-4-hydroxybutan-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.0^{1,3}.0^{3,8}.0^{12,16}]octadecan-6-one

Traditional Name

(1S,3R,8R,11S,12S,15R,16R)-15-[(2R,4R)-4-[(2S)-3,3-dimethyloxiran-2-yl]-4-hydroxybutan-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.0^{1,3}.0^{3,8}.0^{12,16}]octadecan-6-one

CAS Registry Number

Not Available

SMILES

[H][C@]1(OC1(C)C)[C@H](O)C[C@@H](C)[C@@]1([H])CC[C@@]2(C)[C@]3([H])CC[C@]4([H])[C@]5(C[C@@]35CC[C@]12C)CCC(=O)C4(C)C

InChI Identifier

InChI=1S/C30H48O3/c1-18(16-20(31)24-26(4,5)33-24)19-10-12-28(7)22-9-8-21-25(2,3)23(32)11-13-29(21)17-30(22,29)15-14-27(19,28)6/h18-22,24,31H,8-17H2,1-7H3/t18-,19-,20-,21+,22+,24+,27-,28+,29-,30+/m1/s1

InChI Key

NVAPMTWXAZZIAE-RHQOKDMKSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
COSY NMR	[¹H, ¹H] NMR Spectrum (2D, 600 MHz, CDCL3, experimental)	kngoto@p.kanazawa-u.ac.jp	Kanazawa University	Kyoko Nakagawa-Goto	2024-03-14	View Spectrum
HMQC NMR	[¹H, ¹³C] NMR Spectrum (2D, 600 MHz, CDCL3, experimental)	kngoto@p.kanazawa-u.ac.jp	Kanazawa University	Kyoko Nakagawa-Goto	2024-03-14	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, CDCL3, experimental)	kngoto@p.kanazawa-u.ac.jp	Kanazawa University	Kyoko Nakagawa-Goto	2024-03-14	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, CDCL3, experimental)	kngoto@p.kanazawa-u.ac.jp	Kanazawa University	Kyoko Nakagawa-Goto	2024-03-14	View Spectrum
HMBC NMR	[¹H, ¹³C] NMR Spectrum (2D, 600 MHz, CDCL3, experimental)	kngoto@p.kanazawa-u.ac.jp	Kanazawa University	Kyoko Nakagawa-Goto	2024-03-14	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CDCL3, experimental)	kngoto@p.kanazawa-u.ac.jp	Kanazawa University	Kyoko Nakagawa-Goto	2024-03-14	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
delphinensis		Not Available

Chemical Taxonomy

Description

This compound belongs to the class of organic compounds known as cycloartanols and derivatives. These are steroids containing a cycloartanol moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Cycloartanols and derivatives

Direct Parent

Cycloartanols and derivatives

Alternative Parents

Substituents

Cycloartanol-skeleton
Triterpenoid
Cycloartane-skeleton
9b,19-cyclo-lanostane-skeleton
Monohydroxy bile acid, alcohol, or derivatives
23-hydroxysteroid
Hydroxy bile acid, alcohol, or derivatives
Bile acid, alcohol, or derivatives
3-oxo-5-alpha-steroid
Oxosteroid
Hydroxysteroid
3-oxosteroid
Cyclic ketone
Secondary alcohol
Ketone
Oxacycle
Organoheterocyclic compound
Ether
Oxirane
Dialkyl ether
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
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
logP	6.06	ChemAxon
pKa (Strongest Acidic)	14.1	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	49.83 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	131.41 m³·mol⁻¹	ChemAxon
Polarizability	55.65 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	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (5R,8S,9S,10R,13R,14S,17R,23R*,24S*)-24,25-epoxy-23-hydroxycycloart-3-one (NP0332626)

MOL for NP0332626 ((5R,8S,9S,10R,13R,14S,17R,23R*,24S*)-24,25-epoxy-23-hydroxycycloart-3-one)

3D MOL for NP0332626 ((5R,8S,9S,10R,13R,14S,17R,23R*,24S*)-24,25-epoxy-23-hydroxycycloart-3-one)

3D SDF for NP0332626 ((5R,8S,9S,10R,13R,14S,17R,23R*,24S*)-24,25-epoxy-23-hydroxycycloart-3-one)

3D-SDF for NP0332626 ((5R,8S,9S,10R,13R,14S,17R,23R*,24S*)-24,25-epoxy-23-hydroxycycloart-3-one)

PDB for NP0332626 ((5R,8S,9S,10R,13R,14S,17R,23R*,24S*)-24,25-epoxy-23-hydroxycycloart-3-one)

3D PDB for NP0332626 ((5R,8S,9S,10R,13R,14S,17R,23R*,24S*)-24,25-epoxy-23-hydroxycycloart-3-one)

SMILES for NP0332626 ((5R,8S,9S,10R,13R,14S,17R,23R*,24S*)-24,25-epoxy-23-hydroxycycloart-3-one)

INCHI for NP0332626 ((5R,8S,9S,10R,13R,14S,17R,23R*,24S*)-24,25-epoxy-23-hydroxycycloart-3-one)

Structure for NP0332626 ((5R,8S,9S,10R,13R,14S,17R,23R*,24S*)-24,25-epoxy-23-hydroxycycloart-3-one)

3D Structure for NP0332626 ((5R,8S,9S,10R,13R,14S,17R,23R*,24S*)-24,25-epoxy-23-hydroxycycloart-3-one)

Showing NP-Card for (5R,8S,9S,10R,13R,14S,17R,23R,24S)-24,25-epoxy-23-hydroxycycloart-3-one (NP0332626)

MOL for NP0332626 ((5R,8S,9S,10R,13R,14S,17R,23R,24S)-24,25-epoxy-23-hydroxycycloart-3-one)

3D MOL for NP0332626 ((5R,8S,9S,10R,13R,14S,17R,23R,24S)-24,25-epoxy-23-hydroxycycloart-3-one)

3D SDF for NP0332626 ((5R,8S,9S,10R,13R,14S,17R,23R,24S)-24,25-epoxy-23-hydroxycycloart-3-one)

3D-SDF for NP0332626 ((5R,8S,9S,10R,13R,14S,17R,23R,24S)-24,25-epoxy-23-hydroxycycloart-3-one)

PDB for NP0332626 ((5R,8S,9S,10R,13R,14S,17R,23R,24S)-24,25-epoxy-23-hydroxycycloart-3-one)

3D PDB for NP0332626 ((5R,8S,9S,10R,13R,14S,17R,23R,24S)-24,25-epoxy-23-hydroxycycloart-3-one)

SMILES for NP0332626 ((5R,8S,9S,10R,13R,14S,17R,23R,24S)-24,25-epoxy-23-hydroxycycloart-3-one)

INCHI for NP0332626 ((5R,8S,9S,10R,13R,14S,17R,23R,24S)-24,25-epoxy-23-hydroxycycloart-3-one)

Structure for NP0332626 ((5R,8S,9S,10R,13R,14S,17R,23R,24S)-24,25-epoxy-23-hydroxycycloart-3-one)

3D Structure for NP0332626 ((5R,8S,9S,10R,13R,14S,17R,23R,24S)-24,25-epoxy-23-hydroxycycloart-3-one)