NP-MRD: Showing NP-Card for (22alpha)-Hydroxy-5alpha-campestan-3-one (NP0334801)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2024-09-10 20:01:29 UTC

Updated at

2024-09-10 20:01:29 UTC

NP-MRD ID

NP0334801

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(22alpha)-Hydroxy-5alpha-campestan-3-one

Description

DG(18:2(9Z,12Z)/22:4(7Z,10Z,13Z,16Z)/0:0) Belongs to the class of organic compounds known as 1,2-diacylglycerols. These are diacylglycerols containing a glycerol acylated at positions 1 and 2. Mono- and diacylglycerols are common food additives used to blend together certain ingredients, such as oil and water, which would not otherwise blend well. DG(18:2(9Z,12Z)/22:4(7Z,10Z,13Z,16Z)/0:0) Is an extremely weak basic (essentially neutral) compound (based on its pKa). Within humans, DG(18:2(9Z,12Z)/22:4(7Z,10Z,13Z,16Z)/0:0) Participates in a number of enzymatic reactions. In particular, DG(18:2(9Z,12Z)/22:4(7Z,10Z,13Z,16Z)/0:0) Can be biosynthesized from PA(18:2(9Z,12Z)/22:4(7Z,10Z,13Z,16Z)); which is mediated by the enzyme phosphatidate phosphatase. In addition, DG(18:2(9Z,12Z)/22:4(7Z,10Z,13Z,16Z)/0:0) And linoleoyl-CoA can be converted into TG(18:2(9Z,12Z)/22:4(7Z,10Z,13Z,16Z)/18:2(9Z,12Z)); which is mediated by the enzyme diacylglycerol O-acyltransferase. In humans, DG(18:2(9Z,12Z)/22:4(7Z,10Z,13Z,16Z)/0:0) Is involved in the metabolic disorder called de novo triacylglycerol biosynthesis pathway. Diacylglycerols can have many different combinations of fatty acids attached at both the C-1 and C-2 positions. Glycerol-3-phosphate is first acylated with acyl-coenzyme A (acyl-CoA) to form lysophosphatidic acid, which is then acylated with another molecule of acyl-CoA to yield phosphatidic acid. It is a glyceride consisting of two fatty acid chains covalently bonded to a glycerol molecule through ester linkages. The linoleic acid moiety is derived from seed oils, while the adrenic acid moiety is derived from animal fats. Diacylglycerols are precursors to triacylglycerols (triglyceride), which are formed by the addition of a third fatty acid to the diacylglycerol under the catalysis of diglyceride acyltransferase. DG(18:2(9Z,12Z)/22:4(7Z,10Z,13Z,16Z)/0:0) Is a diglyceride, or a diacylglycerol (DAG). Synthesis of diacylglycerol begins with glycerol-3-phosphate, which is derived primarily from dihydroxyacetone phosphate, a product of glycolysis (usually in the cytoplasm of liver or adipose tissue cells). Phosphatidic acid is then de-phosphorylated to form diacylglycerol. DG(18:2(9Z,12Z)/22:4(7Z,10Z,13Z,16Z)/0:0), In particular, consists of one chain of linoleic acid at the C-1 position and one chain of adrenic acid at the C-2 position. Since diacylglycerols are synthesized via phosphatidic acid, they will usually contain a saturated fatty acid at the C-1 position on the glycerol moiety and an unsaturated fatty acid at the C-2 position. Dacylglycerols are often found in bakery products, beverages, ice cream, chewing gum, shortening, whipped toppings, margarine, and confections.

Structure

MOL SDF PDB SMILES InChI


  Mrv0541 02241203392D          

 31 34  0  0  1  0            999 V2000
    8.8850   -8.8514    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.8850   -9.6764    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.1704   -8.4389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1704  -10.0889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4560   -8.8514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4560   -9.6764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3139   -8.8514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3139   -9.6764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5994   -8.4389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5994  -10.0889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0285   -7.6139    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.0285   -8.4389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3139   -7.2014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5995   -7.6139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8131   -7.3589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2980   -8.0264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8132   -8.6938    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8849   -8.0264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9955   -6.7933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8849  -10.5014    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.0680   -6.5743    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.8750   -6.4028    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.5160   -5.9612    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4270   -7.0159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.1300   -5.6182    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.2340   -6.8444    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   14.7860   -7.4575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.4890   -6.0598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.5310   -8.2421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.5930   -7.2861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7415  -10.0888    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  3  1  1  0  0  0  0
  4  2  1  0  0  0  0
  5  3  1  0  0  0  0
  6  4  1  0  0  0  0
  6  5  1  0  0  0  0
  8  7  1  0  0  0  0
 10  8  1  0  0  0  0
  1  9  1  0  0  0  0
  2 10  1  0  0  0  0
  2  1  1  0  0  0  0
 13 11  1  0  0  0  0
  7 12  1  0  0  0  0
 14 13  1  0  0  0  0
  9  7  1  0  0  0  0
  9 14  1  0  0  0  0
 15 11  1  0  0  0  0
 12 11  1  0  0  0  0
 16 15  1  0  0  0  0
 17 12  1  0  0  0  0
 17 16  1  0  0  0  0
  1 18  1  1  0  0  0
 11 19  1  1  0  0  0
  2 20  1  6  0  0  0
 21 15  1  0  0  0  0
 22 21  1  0  0  0  0
 21 23  1  6  0  0  0
 24 22  1  0  0  0  0
 22 25  1  1  0  0  0
 26 24  1  0  0  0  0
 27 26  1  0  0  0  0
 26 28  1  1  0  0  0
 29 27  1  0  0  0  0
 30 27  1  0  0  0  0
  6 31  2  0  0  0  0
M  END


  Mrv0541 02241203392D          

 31 34  0  0  1  0            999 V2000
    8.8850   -8.8514    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.8850   -9.6764    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.1704   -8.4389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1704  -10.0889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4560   -8.8514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4560   -9.6764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3139   -8.8514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3139   -9.6764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5994   -8.4389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5994  -10.0889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0285   -7.6139    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.0285   -8.4389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3139   -7.2014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5995   -7.6139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8131   -7.3589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2980   -8.0264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8132   -8.6938    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8849   -8.0264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9955   -6.7933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8849  -10.5014    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.0680   -6.5743    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.8750   -6.4028    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.5160   -5.9612    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4270   -7.0159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.1300   -5.6182    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.2340   -6.8444    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   14.7860   -7.4575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.4890   -6.0598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.5310   -8.2421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.5930   -7.2861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7415  -10.0888    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  3  1  1  0  0  0  0
  4  2  1  0  0  0  0
  5  3  1  0  0  0  0
  6  4  1  0  0  0  0
  6  5  1  0  0  0  0
  8  7  1  0  0  0  0
 10  8  1  0  0  0  0
  1  9  1  0  0  0  0
  2 10  1  0  0  0  0
  2  1  1  0  0  0  0
 13 11  1  0  0  0  0
  7 12  1  0  0  0  0
 14 13  1  0  0  0  0
  9  7  1  0  0  0  0
  9 14  1  0  0  0  0
 15 11  1  0  0  0  0
 12 11  1  0  0  0  0
 16 15  1  0  0  0  0
 17 12  1  0  0  0  0
 17 16  1  0  0  0  0
  1 18  1  1  0  0  0
 11 19  1  1  0  0  0
  2 20  1  6  0  0  0
 21 15  1  0  0  0  0
 22 21  1  0  0  0  0
 21 23  1  6  0  0  0
 24 22  1  0  0  0  0
 22 25  1  1  0  0  0
 26 24  1  0  0  0  0
 27 26  1  0  0  0  0
 26 28  1  1  0  0  0
 29 27  1  0  0  0  0
 30 27  1  0  0  0  0
  6 31  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0334801

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@@]12CCC3C4CCC([C@H](C)[C@@H](O)C[C@@H](C)C(C)C)[C@@]4(C)CCC3[C@@]1(C)CCC(=O)C2

> <INCHI_IDENTIFIER>
InChI=1S/C28H48O2/c1-17(2)18(3)15-26(30)19(4)23-9-10-24-22-8-7-20-16-21(29)11-13-27(20,5)25(22)12-14-28(23,24)6/h17-20,22-26,30H,7-16H2,1-6H3/t18-,19+,20+,22?,23?,24?,25?,26+,27+,28-/m1/s1

> <INCHI_KEY>
XGIZPVUTLMXXTK-UKPMHFJNSA-N

> <FORMULA>
C28H48O2

> <MOLECULAR_WEIGHT>
416.6795

> <EXACT_MASS>
416.36543078

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_AVERAGE_POLARIZABILITY>
52.326343948441064

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,7S,15S)-14-[(2S,3S,5R)-3-hydroxy-5,6-dimethylheptan-2-yl]-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-5-one

> <ALOGPS_LOGP>
5.39

> <JCHEM_LOGP>
6.704223613

> <ALOGPS_LOGS>
-6.77

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
19.835650000816642

> <JCHEM_PKA_STRONGEST_BASIC>
-0.683686596604406

> <JCHEM_POLAR_SURFACE_AREA>
37.3

> <JCHEM_REFRACTIVITY>
124.87949999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
7.09e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,7S,15S)-14-[(2S,3S,5R)-3-hydroxy-5,6-dimethylheptan-2-yl]-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-5-one

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0      16.585 -16.523   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      16.585 -18.063   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      15.251 -15.753   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      15.251 -18.833   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      13.918 -16.523   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      13.918 -18.063   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      19.253 -16.523   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      19.253 -18.063   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      17.919 -15.753   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      17.919 -18.833   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      20.587 -14.213   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      20.587 -15.753   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      19.253 -13.443   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      17.919 -14.213   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      22.051 -13.737   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      22.956 -14.983   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      22.051 -16.228   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      16.585 -14.983   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      20.525 -12.681   0.000  0.00  0.00           C+0
HETATM   20  H   UNK     0      16.585 -19.603   0.000  0.00  0.00           H+0
HETATM   21  C   UNK     0      22.527 -12.272   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      24.033 -11.952   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      21.497 -11.128   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      25.064 -13.096   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      24.509 -10.487   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      26.570 -12.776   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      27.601 -13.921   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      27.046 -11.312   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      27.125 -15.385   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      29.107 -13.601   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      12.584 -18.832   0.000  0.00  0.00           O+0
CONECT    1    3    9    2   18                                             
CONECT    2    4   10    1   20                                             
CONECT    3    1    5                                                       
CONECT    4    2    6                                                       
CONECT    5    3    6                                                       
CONECT    6    4    5   31                                                  
CONECT    7    8   12    9                                                  
CONECT    8    7   10                                                       
CONECT    9    1    7   14                                                  
CONECT   10    8    2                                                       
CONECT   11   13   15   12   19                                             
CONECT   12    7   11   17                                                  
CONECT   13   11   14                                                       
CONECT   14   13    9                                                       
CONECT   15   11   16   21                                                  
CONECT   16   15   17                                                       
CONECT   17   12   16                                                       
CONECT   18    1                                                            
CONECT   19   11                                                            
CONECT   20    2                                                            
CONECT   21   15   22   23                                                  
CONECT   22   21   24   25                                                  
CONECT   23   21                                                            
CONECT   24   22   26                                                       
CONECT   25   22                                                            
CONECT   26   24   27   28                                                  
CONECT   27   26   29   30                                                  
CONECT   28   26                                                            
CONECT   29   27                                                            
CONECT   30   27                                                            
CONECT   31    6                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   68    0
END

View in JSmol

Synonyms

Value	Source
(22a)-Hydroxy-5a-campestan-3-one	Generator
(22Α)-hydroxy-5α-campestan-3-one	Generator

Chemical Formula

C₂₈H₄₈O₂

Average Mass

416.6795 Da

Monoisotopic Mass

416.36543 Da

IUPAC Name

(2S,7S,15S)-14-[(2S,3S,5R)-3-hydroxy-5,6-dimethylheptan-2-yl]-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-5-one

Traditional Name

(2S,7S,15S)-14-[(2S,3S,5R)-3-hydroxy-5,6-dimethylheptan-2-yl]-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-5-one

CAS Registry Number

Not Available

SMILES

[H][C@@]12CCC3C4CCC([C@H](C)[C@@H](O)C[C@@H](C)C(C)C)[C@@]4(C)CCC3[C@@]1(C)CCC(=O)C2

InChI Identifier

InChI=1S/C28H48O2/c1-17(2)18(3)15-26(30)19(4)23-9-10-24-22-8-7-20-16-21(29)11-13-27(20,5)25(22)12-14-28(23,24)6/h17-20,22-26,30H,7-16H2,1-6H3/t18-,19+,20+,22?,23?,24?,25?,26+,27+,28-/m1/s1

InChI Key

XGIZPVUTLMXXTK-UKPMHFJNSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 1,2-diacylglycerols. These are diacylglycerols containing a glycerol acylated at positions 1 and 2.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Glycerolipids

Sub Class

Diradylglycerols

Direct Parent

1,2-diacylglycerols

Alternative Parents

Substituents

1,2-acyl-sn-glycerol
Fatty acid ester
Fatty acyl
Dicarboxylic acid or derivatives
Carboxylic acid ester
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic 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	5.39	ALOGPS
logP	6.7	ChemAxon
logS	-6.8	ALOGPS
pKa (Strongest Acidic)	19.84	ChemAxon
pKa (Strongest Basic)	-0.68	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	37.3 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	124.88 m³·mol⁻¹	ChemAxon
Polarizability	52.33 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB024456

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 (22alpha)-Hydroxy-5alpha-campestan-3-one (NP0334801)

MOL for NP0334801 ((22alpha)-Hydroxy-5alpha-campestan-3-one)

3D MOL for NP0334801 ((22alpha)-Hydroxy-5alpha-campestan-3-one)

3D SDF for NP0334801 ((22alpha)-Hydroxy-5alpha-campestan-3-one)

3D-SDF for NP0334801 ((22alpha)-Hydroxy-5alpha-campestan-3-one)

PDB for NP0334801 ((22alpha)-Hydroxy-5alpha-campestan-3-one)

3D PDB for NP0334801 ((22alpha)-Hydroxy-5alpha-campestan-3-one)

SMILES for NP0334801 ((22alpha)-Hydroxy-5alpha-campestan-3-one)

INCHI for NP0334801 ((22alpha)-Hydroxy-5alpha-campestan-3-one)

Structure for NP0334801 ((22alpha)-Hydroxy-5alpha-campestan-3-one)

3D Structure for NP0334801 ((22alpha)-Hydroxy-5alpha-campestan-3-one)