NP-MRD: Showing NP-Card for (5R,8S,9S,10R,13R,14S,17R,23R*,24R*)-24,25-epoxy-23-hydroxycycloart-3-one (NP0332627)

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Record Information

Version

2.0

Created at

2024-03-14 02:48:11 UTC

Updated at

2025-12-20 06:41:05 UTC

NP-MRD ID

NP0332627

Natural Product DOI

https://doi.org/10.57994/1887

Secondary Accession Numbers

None

Natural Product Identification

Common Name

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

Description

(5R,8S,9S,10R,13R,14S,17R,23R*,24R*)-24,25-epoxy-23-hydroxycycloart-3-one belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. Based on a literature review very few articles have been published on (5R,8S,9S,10R,13R,14S,17R,23R*,24R*)-24,25-epoxy-23-hydroxycycloart-3-one.

Structure

MOL SDF PDB SMILES InChI


  Mrv2104 03142402482D          

 36 41  0  0  1  0            999 V2000
    2.7705    2.6460    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
    3.2485    1.0691    0.0000 C   0  0  0  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
    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  1  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
    2.1561    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  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  2  6  1  0  0  0  0
  6  7  1  0  0  0  0
  8  7  1  0  0  0  0
  8  3  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  6  0  0  0
 14 17  1  1  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
 21  2  1  0  0  0  0
 21 22  1  6  0  0  0
 21 23  1  0  0  0  0
 23  5  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  6  0  0  0
 23 25  1  6  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 21 28  1  0  0  0  0
 26 29  1  1  0  0  0
 26 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 30 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 24 35  1  0  0  0  0
 33 36  2  0  0  0  0
M  END


  Mrv2104 03142402482D          

 36 41  0  0  1  0            999 V2000
    2.7705    2.6460    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
    3.2485    1.0691    0.0000 C   0  0  0  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
    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  1  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
    2.1561    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  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  2  6  1  0  0  0  0
  6  7  1  0  0  0  0
  8  7  1  0  0  0  0
  8  3  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  6  0  0  0
 14 17  1  1  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
 21  2  1  0  0  0  0
 21 22  1  6  0  0  0
 21 23  1  0  0  0  0
 23  5  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  6  0  0  0
 23 25  1  6  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 21 28  1  0  0  0  0
 26 29  1  1  0  0  0
 26 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 30 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 24 35  1  0  0  0  0
 33 36  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0332627

> <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)C1CC[C@@]13C[C@@]11CCC(=O)C(C)(C)[C@]1([H])CC[C@@]23[H]

> <INCHI_IDENTIFIER>
InChI=1S/C29H46O3/c1-17(15-20(30)24-26(4,5)32-24)18-9-12-27(6)19(18)10-13-29-16-28(29)14-11-23(31)25(2,3)21(28)7-8-22(27)29/h17-22,24,30H,7-16H2,1-6H3/t17-,18-,19?,20-,21+,22+,24-,27-,28-,29+/m1/s1

> <INCHI_KEY>
FMISXDCTUFOLFI-HCUWBSPBSA-N

> <FORMULA>
C29H46O3

> <MOLECULAR_WEIGHT>
442.684

> <EXACT_MASS>
442.344695341

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
78

> <JCHEM_AVERAGE_POLARIZABILITY>
53.70093424298837

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

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

> <JCHEM_LOGP>
5.757504119666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.098702080832648

> <JCHEM_PKA_STRONGEST_BASIC>
-3.193027709843801

> <JCHEM_POLAR_SURFACE_AREA>
49.83

> <JCHEM_REFRACTIVITY>
126.93479999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,3R,8R,11S,12R,15R)-15-[(2R,4R)-4-[(2R)-3,3-dimethyloxiran-2-yl]-4-hydroxybutan-2-yl]-7,7,12-trimethylpentacyclo[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       5.172   4.939   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.541   3.444   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.064   1.996   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.071   0.818   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.555   1.089   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       4.025   3.715   0.000  0.00  0.00           C+0
HETATM   22  H   UNK     0       4.548   2.267   0.000  0.00  0.00           H+0
HETATM   23  C   UNK     0       3.032   2.538   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.516   2.809   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.039   1.361   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.993   4.257   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       1.985   5.435   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.501   5.164   0.000  0.00  0.00           C+0
HETATM   29  H   UNK     0       0.470   5.706   0.000  0.00  0.00           H+0
HETATM   30  C   UNK     0      -0.523   4.528   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       0.007   5.974   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -1.855   5.302   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -1.516   3.351   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -0.993   1.903   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       0.523   1.632   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      -3.032   3.622   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    6   21                                             
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4   23                                                       
CONECT    6    2    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    3    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    2   22   23   28                                             
CONECT   22   21                                                            
CONECT   23   21    5   24   25                                             
CONECT   24   23   25   26   35                                             
CONECT   25   24   23                                                       
CONECT   26   24   27   29   30                                             
CONECT   27   26   28                                                       
CONECT   28   27   21                                                       
CONECT   29   26                                                            
CONECT   30   26   31   32   33                                             
CONECT   31   30                                                            
CONECT   32   30                                                            
CONECT   33   30   34   36                                                  
CONECT   34   33   35                                                       
CONECT   35   34   24                                                       
CONECT   36   33                                                            
MASTER        0    0    0    0    0    0    0    0   36    0   82    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₉H₄₆O₃

Average Mass

442.6840 Da

Monoisotopic Mass

442.34470 Da

IUPAC Name

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

Traditional Name

(1S,3R,8R,11S,12R,15R)-15-[(2R,4R)-4-[(2R)-3,3-dimethyloxiran-2-yl]-4-hydroxybutan-2-yl]-7,7,12-trimethylpentacyclo[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)C1CC[C@@]13C[C@@]11CCC(=O)C(C)(C)[C@]1([H])CC[C@@]23[H]

InChI Identifier

InChI=1S/C29H46O3/c1-17(15-20(30)24-26(4,5)32-24)18-9-12-27(6)19(18)10-13-29-16-28(29)14-11-23(31)25(2,3)21(28)7-8-22(27)29/h17-22,24,30H,7-16H2,1-6H3/t17-,18-,19?,20-,21+,22+,24-,27-,28-,29+/m1/s1

InChI Key

FMISXDCTUFOLFI-HCUWBSPBSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CDCL3, experimental)	[email protected]	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
Turraea delphinensis		Not Available

Chemical Taxonomy

Description

This compound belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Triterpenoids

Alternative Parents

Substituents

Triterpenoid
23-hydroxysteroid
3-oxo-5-alpha-steroid
Oxosteroid
Hydroxysteroid
3-oxosteroid
Steroid
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	5.76	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	126.93 m³·mol⁻¹	ChemAxon
Polarizability	53.7 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

Showing NP-Card for (5R,8S,9S,10R,13R,14S,17R,23R*,24R*)-24,25-epoxy-23-hydroxycycloart-3-one (NP0332627)

MOL for NP0332627 ((5R,8S,9S,10R,13R,14S,17R,23R*,24R*)-24,25-epoxy-23-hydroxycycloart-3-one)

3D MOL for NP0332627 ((5R,8S,9S,10R,13R,14S,17R,23R*,24R*)-24,25-epoxy-23-hydroxycycloart-3-one)

3D SDF for NP0332627 ((5R,8S,9S,10R,13R,14S,17R,23R*,24R*)-24,25-epoxy-23-hydroxycycloart-3-one)

3D-SDF for NP0332627 ((5R,8S,9S,10R,13R,14S,17R,23R*,24R*)-24,25-epoxy-23-hydroxycycloart-3-one)

PDB for NP0332627 ((5R,8S,9S,10R,13R,14S,17R,23R*,24R*)-24,25-epoxy-23-hydroxycycloart-3-one)

3D PDB for NP0332627 ((5R,8S,9S,10R,13R,14S,17R,23R*,24R*)-24,25-epoxy-23-hydroxycycloart-3-one)

SMILES for NP0332627 ((5R,8S,9S,10R,13R,14S,17R,23R*,24R*)-24,25-epoxy-23-hydroxycycloart-3-one)

INCHI for NP0332627 ((5R,8S,9S,10R,13R,14S,17R,23R*,24R*)-24,25-epoxy-23-hydroxycycloart-3-one)

Structure for NP0332627 ((5R,8S,9S,10R,13R,14S,17R,23R*,24R*)-24,25-epoxy-23-hydroxycycloart-3-one)

3D Structure for NP0332627 ((5R,8S,9S,10R,13R,14S,17R,23R*,24R*)-24,25-epoxy-23-hydroxycycloart-3-one)

Showing NP-Card for (5R,8S,9S,10R,13R,14S,17R,23R,24R)-24,25-epoxy-23-hydroxycycloart-3-one (NP0332627)

MOL for NP0332627 ((5R,8S,9S,10R,13R,14S,17R,23R,24R)-24,25-epoxy-23-hydroxycycloart-3-one)

3D MOL for NP0332627 ((5R,8S,9S,10R,13R,14S,17R,23R,24R)-24,25-epoxy-23-hydroxycycloart-3-one)

3D SDF for NP0332627 ((5R,8S,9S,10R,13R,14S,17R,23R,24R)-24,25-epoxy-23-hydroxycycloart-3-one)

3D-SDF for NP0332627 ((5R,8S,9S,10R,13R,14S,17R,23R,24R)-24,25-epoxy-23-hydroxycycloart-3-one)

PDB for NP0332627 ((5R,8S,9S,10R,13R,14S,17R,23R,24R)-24,25-epoxy-23-hydroxycycloart-3-one)

3D PDB for NP0332627 ((5R,8S,9S,10R,13R,14S,17R,23R,24R)-24,25-epoxy-23-hydroxycycloart-3-one)

SMILES for NP0332627 ((5R,8S,9S,10R,13R,14S,17R,23R,24R)-24,25-epoxy-23-hydroxycycloart-3-one)

INCHI for NP0332627 ((5R,8S,9S,10R,13R,14S,17R,23R,24R)-24,25-epoxy-23-hydroxycycloart-3-one)

Structure for NP0332627 ((5R,8S,9S,10R,13R,14S,17R,23R,24R)-24,25-epoxy-23-hydroxycycloart-3-one)

3D Structure for NP0332627 ((5R,8S,9S,10R,13R,14S,17R,23R,24R)-24,25-epoxy-23-hydroxycycloart-3-one)