NP-MRD: Showing NP-Card for (24S)-24-Ethylbrassinone (NP0336499)

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Record Information

Version

2.0

Created at

2024-09-11 06:32:41 UTC

Updated at

2024-09-11 06:32:41 UTC

NP-MRD ID

NP0336499

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(24S)-24-Ethylbrassinone

Description

(24S)-24-Ethylbrassinone belongs to the class of organic compounds known as stigmastanes and derivatives. These are sterol lipids with a structure based on the stigmastane skeleton, which consists of a cholestane moiety bearing an ethyl group at the carbon atom C24. Based on a literature review very few articles have been published on (24S)-24-Ethylbrassinone.

Structure

MOL SDF PDB SMILES InChI


  Mrv2104 05262309042D          

 36 39  0  0  0  0            999 V2000
   -3.1048   -0.5971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8193   -1.0096    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.8193   -1.8346    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1048   -2.2471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3904   -1.8346    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3904   -1.0096    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6759   -0.5971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6759   -2.2471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9614   -1.8346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9614   -1.0096    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9614    0.6404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6759    0.2279    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4675    0.6404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2470    0.2279    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2470   -0.5971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1819   -0.5971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1819    0.2279    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5338   -2.2471    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3904   -0.1846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2470    1.0529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1820    1.8779    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4675    1.4654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8964    1.4654    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6109    1.8779    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3254    1.4654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0398    1.8779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3254    0.6404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2470    1.8779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5338   -0.5971    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3904   -2.6596    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6759   -3.0721    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9614   -0.1846    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1820    2.7029    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8963    0.6404    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6109    2.7029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3253    3.1154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  6  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3 18  1  6  0  0  0
  4  5  1  0  0  0  0
  6  5  1  0  0  0  0
  5  8  1  0  0  0  0
  7  6  1  0  0  0  0
  6 19  1  1  0  0  0
 12  7  1  0  0  0  0
  7 10  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 15  1  0  0  0  0
 11 12  1  0  0  0  0
 11 14  1  0  0  0  0
 13 14  1  0  0  0  0
 22 13  1  1  0  0  0
 13 17  1  0  0  0  0
 14 15  1  0  0  0  0
 14 20  1  1  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 22 28  1  6  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
  2 29  1  6  0  0  0
  5 30  1  6  0  0  0
  8 31  2  0  0  0  0
 10 32  1  1  0  0  0
 21 33  1  1  0  0  0
 23 34  1  1  0  0  0
 24 35  1  1  0  0  0
 35 36  1  0  0  0  0
M  END


  Mrv2104 05262309042D          

 36 39  0  0  0  0            999 V2000
   -3.1048   -0.5971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8193   -1.0096    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.8193   -1.8346    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1048   -2.2471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3904   -1.8346    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3904   -1.0096    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6759   -0.5971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6759   -2.2471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9614   -1.8346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9614   -1.0096    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9614    0.6404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6759    0.2279    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4675    0.6404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2470    0.2279    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2470   -0.5971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1819   -0.5971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1819    0.2279    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5338   -2.2471    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3904   -0.1846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2470    1.0529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1820    1.8779    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4675    1.4654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8964    1.4654    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6109    1.8779    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3254    1.4654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0398    1.8779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3254    0.6404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2470    1.8779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5338   -0.5971    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3904   -2.6596    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6759   -3.0721    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9614   -0.1846    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1820    2.7029    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8963    0.6404    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6109    2.7029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3253    3.1154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  6  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3 18  1  6  0  0  0
  4  5  1  0  0  0  0
  6  5  1  0  0  0  0
  5  8  1  0  0  0  0
  7  6  1  0  0  0  0
  6 19  1  1  0  0  0
 12  7  1  0  0  0  0
  7 10  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 15  1  0  0  0  0
 11 12  1  0  0  0  0
 11 14  1  0  0  0  0
 13 14  1  0  0  0  0
 22 13  1  1  0  0  0
 13 17  1  0  0  0  0
 14 15  1  0  0  0  0
 14 20  1  1  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 22 28  1  6  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
  2 29  1  6  0  0  0
  5 30  1  6  0  0  0
  8 31  2  0  0  0  0
 10 32  1  1  0  0  0
 21 33  1  1  0  0  0
 23 34  1  1  0  0  0
 24 35  1  1  0  0  0
 35 36  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0336499

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@@]12CC(=O)[C@@]3([H])C[C@H](O)[C@H](O)C[C@]3(C)C1CC[C@]1(C)C(CCC21)C(C)[C@@H](O)[C@H](O)[C@@H](CC)C(C)C

> <INCHI_IDENTIFIER>
InChI=1/C29H50O5/c1-7-17(15(2)3)27(34)26(33)16(4)19-8-9-20-18-12-23(30)22-13-24(31)25(32)14-29(22,6)21(18)10-11-28(19,20)5/h15-22,24-27,31-34H,7-14H2,1-6H3/t16?,17-,18-,19?,20?,21?,22+,24-,25+,26+,27+,28+,29+/s2

> <INCHI_KEY>
WADMTJKRYLAHQV-JLHHFALONA-N

> <FORMULA>
C29H50O5

> <MOLECULAR_WEIGHT>
478.714

> <EXACT_MASS>
478.36582471

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
84

> <JCHEM_AVERAGE_POLARIZABILITY>
56.411773604544024

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3bS,5aS,7S,8R,9aR,11aS)-1-[(3R,4R,5S)-5-ethyl-3,4-dihydroxy-6-methylheptan-2-yl]-7,8-dihydroxy-9a,11a-dimethyl-hexadecahydro-1H-cyclopenta[a]phenanthren-5-one

> <JCHEM_LOGP>
3.9461874490000004

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.049297505843867

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.451752114126071

> <JCHEM_PKA_STRONGEST_BASIC>
-3.1530299910083177

> <JCHEM_POLAR_SURFACE_AREA>
97.99000000000001

> <JCHEM_REFRACTIVITY>
133.8219

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(3bS,5aS,7S,8R,9aR,11aS)-1-[(3R,4R,5S)-5-ethyl-3,4-dihydroxy-6-methylheptan-2-yl]-7,8-dihydroxy-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthren-5-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 26-MAY-23   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   26-MAY-23         0                                  
HETATM    1  C   UNK     0      -5.796  -1.115   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -7.129  -1.885   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -7.129  -3.425   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -5.796  -4.195   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -4.462  -3.425   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -4.462  -1.885   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -3.128  -1.115   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -3.128  -4.195   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.795  -3.425   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.795  -1.885   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.795   1.195   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -3.128   0.425   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.873   1.195   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.461   0.425   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.461  -1.115   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.206  -1.115   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.206   0.425   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -8.463  -4.195   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -4.462  -0.345   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.461   1.965   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.206   3.505   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.873   2.735   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.540   2.735   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.874   3.505   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.207   2.735   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       7.541   3.505   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.207   1.195   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -0.461   3.505   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -8.463  -1.115   0.000  0.00  0.00           O+0
HETATM   30  H   UNK     0      -4.462  -4.965   0.000  0.00  0.00           H+0
HETATM   31  O   UNK     0      -3.128  -5.735   0.000  0.00  0.00           O+0
HETATM   32  H   UNK     0      -1.795  -0.345   0.000  0.00  0.00           H+0
HETATM   33  O   UNK     0       2.206   5.045   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0       3.540   1.195   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       4.874   5.045   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       6.207   5.815   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3   29                                                  
CONECT    3    2    4   18                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    8   30                                             
CONECT    6    1    5    7   19                                             
CONECT    7    6   12   10                                                  
CONECT    8    5    9   31                                                  
CONECT    9    8   10                                                       
CONECT   10    7    9   15   32                                             
CONECT   11   12   14                                                       
CONECT   12    7   11                                                       
CONECT   13   14   22   17                                                  
CONECT   14   11   13   15   20                                             
CONECT   15   10   14   16                                                  
CONECT   16   15   17                                                       
CONECT   17   13   16                                                       
CONECT   18    3                                                            
CONECT   19    6                                                            
CONECT   20   14                                                            
CONECT   21   22   23   33                                                  
CONECT   22   13   21   28                                                  
CONECT   23   21   24   34                                                  
CONECT   24   23   25   35                                                  
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   22                                                            
CONECT   29    2                                                            
CONECT   30    5                                                            
CONECT   31    8                                                            
CONECT   32   10                                                            
CONECT   33   21                                                            
CONECT   34   23                                                            
CONECT   35   24   36                                                       
CONECT   36   35                                                            
MASTER        0    0    0    0    0    0    0    0   36    0   78    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₉H₅₀O₅

Average Mass

478.7140 Da

Monoisotopic Mass

478.36582 Da

IUPAC Name

(3bS,5aS,7S,8R,9aR,11aS)-1-[(3R,4R,5S)-5-ethyl-3,4-dihydroxy-6-methylheptan-2-yl]-7,8-dihydroxy-9a,11a-dimethyl-hexadecahydro-1H-cyclopenta[a]phenanthren-5-one

Traditional Name

(3bS,5aS,7S,8R,9aR,11aS)-1-[(3R,4R,5S)-5-ethyl-3,4-dihydroxy-6-methylheptan-2-yl]-7,8-dihydroxy-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthren-5-one

CAS Registry Number

Not Available

SMILES

[H][C@@]12CC(=O)[C@@]3([H])C[C@H](O)[C@H](O)C[C@]3(C)C1CC[C@]1(C)C(CCC21)C(C)[C@@H](O)[C@H](O)[C@@H](CC)C(C)C

InChI Identifier

InChI=1/C29H50O5/c1-7-17(15(2)3)27(34)26(33)16(4)19-8-9-20-18-12-23(30)22-13-24(31)25(32)14-29(22,6)21(18)10-11-28(19,20)5/h15-22,24-27,31-34H,7-14H2,1-6H3/t16?,17-,18-,19?,20?,21?,22+,24-,25+,26+,27+,28+,29+/s2

InChI Key

WADMTJKRYLAHQV-JLHHFALONA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

This compound belongs to the class of organic compounds known as stigmastanes and derivatives. These are sterol lipids with a structure based on the stigmastane skeleton, which consists of a cholestane moiety bearing an ethyl group at the carbon atom C24.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Stigmastanes and derivatives

Direct Parent

Stigmastanes and derivatives

Alternative Parents

Substituents

C24-propyl-sterol-skeleton
Triterpenoid
Stigmastane-skeleton
Tetrahydroxy bile acid, alcohol, or derivatives
Ecdysteroid
Hydroxy bile acid, alcohol, or derivatives
23-hydroxysteroid
Bile acid, alcohol, or derivatives
22-hydroxysteroid
3-hydroxysteroid
6-oxosteroid
3-alpha-hydroxysteroid
Oxosteroid
2-hydroxysteroid
Hydroxysteroid
Cyclic alcohol
Secondary alcohol
Ketone
Organooxygen compound
Organic oxygen compound
Hydrocarbon derivative
Carbonyl group
Organic oxide
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic 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	3.95	ChemAxon
pKa (Strongest Acidic)	13.45	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	97.99 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	133.82 m³·mol⁻¹	ChemAxon
Polarizability	56.41 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (24S)-24-Ethylbrassinone (NP0336499)

MOL for NP0336499 ((24S)-24-Ethylbrassinone)

3D MOL for NP0336499 ((24S)-24-Ethylbrassinone)

3D SDF for NP0336499 ((24S)-24-Ethylbrassinone)

3D-SDF for NP0336499 ((24S)-24-Ethylbrassinone)

PDB for NP0336499 ((24S)-24-Ethylbrassinone)

3D PDB for NP0336499 ((24S)-24-Ethylbrassinone)

SMILES for NP0336499 ((24S)-24-Ethylbrassinone)

INCHI for NP0336499 ((24S)-24-Ethylbrassinone)

Structure for NP0336499 ((24S)-24-Ethylbrassinone)

3D Structure for NP0336499 ((24S)-24-Ethylbrassinone)