NP-MRD: Showing NP-Card for 10-(2-hydroxypropan-2-yl)-4,6,14,19,19-pentamethyl-11-oxahexacyclo[13.9.0.0¹,²³.0⁴,¹⁴.0⁵,¹².0¹⁸,²³]tetracosan-20-one (NP0286145)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-09 14:35:52 UTC

Updated at

2022-09-09 14:35:52 UTC

NP-MRD ID

NP0286145

Secondary Accession Numbers

None

Natural Product Identification

Common Name

10-(2-hydroxypropan-2-yl)-4,6,14,19,19-pentamethyl-11-oxahexacyclo[13.9.0.0¹,²³.0⁴,¹⁴.0⁵,¹².0¹⁸,²³]tetracosan-20-one

Description

10-(2-Hydroxypropan-2-yl)-4,6,14,19,19-pentamethyl-11-oxahexacyclo[13.9.0.0¹,²³.0⁴,¹⁴.0⁵,¹².0¹⁸,²³]Tetracosan-20-one belongs to the class of organic compounds known as cycloartanols and derivatives. These are steroids containing a cycloartanol moiety. 10-(2-hydroxypropan-2-yl)-4,6,14,19,19-pentamethyl-11-oxahexacyclo[13.9.0.0¹,²³.0⁴,¹⁴.0⁵,¹².0¹⁸,²³]tetracosan-20-one is found in Parthenium argentatum. Based on a literature review very few articles have been published on 10-(2-hydroxypropan-2-yl)-4,6,14,19,19-pentamethyl-11-oxahexacyclo[13.9.0.0¹,²³.0⁴,¹⁴.0⁵,¹².0¹⁸,²³]Tetracosan-20-one.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309092216352D          

 34 39  0  0  0  0            999 V2000
    5.5328    3.2311    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9918    2.5456    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8008    2.7074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4872    2.2498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6490    1.4408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1914    0.7544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6504    0.0689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1095   -0.6166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3359    0.5279    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9649   -0.3902    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3824    0.5926    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6959    1.0502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9766    0.6464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3702    1.2058    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1058    0.4243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5487    1.1294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2041    0.3799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3826    0.3035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9058    0.9768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0843    0.9004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3021    0.1047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3385    0.5477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6075    1.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2140    1.4973    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9521    2.3232    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7736    2.3996    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2504    1.7263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5950    2.4759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0719    1.8027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4165    2.5522    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2379    2.6286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7148    1.9553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1359    2.6648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5342    1.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  7 10  1  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 20 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 19 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 16 29  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 14 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
  2 34  1  0  0  0  0
 12 34  1  0  0  0  0
M  END


  Mrv1652309092216352D          

 34 39  0  0  0  0            999 V2000
    5.5328    3.2311    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9918    2.5456    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8008    2.7074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4872    2.2498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6490    1.4408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1914    0.7544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6504    0.0689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1095   -0.6166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3359    0.5279    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9649   -0.3902    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3824    0.5926    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6959    1.0502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9766    0.6464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3702    1.2058    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1058    0.4243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5487    1.1294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2041    0.3799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3826    0.3035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9058    0.9768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0843    0.9004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3021    0.1047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3385    0.5477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6075    1.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2140    1.4973    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9521    2.3232    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7736    2.3996    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2504    1.7263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5950    2.4759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0719    1.8027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4165    2.5522    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2379    2.6286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7148    1.9553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1359    2.6648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5342    1.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  7 10  1  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 20 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 19 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 16 29  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 14 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
  2 34  1  0  0  0  0
 12 34  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0286145

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1CCCC(OC2CC3(C)C4CCC5C6(CC46CCC3(C)C12)CCC(=O)C5(C)C)C(C)(C)O

> <INCHI_IDENTIFIER>
InChI=1S/C31H50O3/c1-19-9-8-10-24(27(4,5)33)34-20-17-29(7)22-12-11-21-26(2,3)23(32)13-14-30(21)18-31(22,30)16-15-28(29,6)25(19)20/h19-22,24-25,33H,8-18H2,1-7H3

> <INCHI_KEY>
BRSJEZNEKATFHB-UHFFFAOYSA-N

> <FORMULA>
C31H50O3

> <MOLECULAR_WEIGHT>
470.738

> <EXACT_MASS>
470.37599547

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
84

> <JCHEM_AVERAGE_POLARIZABILITY>
56.55406512716843

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
10-(2-hydroxypropan-2-yl)-4,6,14,19,19-pentamethyl-11-oxahexacyclo[13.9.0.0^{1,23}.0^{4,14}.0^{5,12}.0^{18,23}]tetracosan-20-one

> <JCHEM_LOGP>
6.2682587146666675

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
19.881774692397315

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.32616408735565

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0935352996793144

> <JCHEM_POLAR_SURFACE_AREA>
46.53

> <JCHEM_REFRACTIVITY>
136.24189999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
10-(2-hydroxypropan-2-yl)-4,6,14,19,19-pentamethyl-11-oxahexacyclo[13.9.0.0^{1,23}.0^{4,14}.0^{5,12}.0^{18,23}]tetracosan-20-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0      10.328   6.031   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      11.185   4.752   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      12.695   5.054   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      13.976   4.200   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      14.278   2.689   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      13.424   1.408   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      14.281   0.129   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      15.138  -1.151   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      15.560   0.985   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      13.001  -0.728   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0      11.914   1.106   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      10.632   1.960   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.290   1.207   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.158   2.251   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.664   0.792   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.624   2.108   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.981   0.709   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.448   0.567   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.557   1.823   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.024   1.681   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.431   0.195   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.632   1.022   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.134   2.938   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -0.399   2.795   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       1.777   4.337   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.311   4.479   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.201   3.222   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.844   4.622   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       5.734   3.365   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       6.377   4.764   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       7.911   4.907   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       8.801   3.650   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       9.587   4.974   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      10.330   3.471   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   34                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   11                                                  
CONECT    7    6    8    9   10                                             
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    7                                                            
CONECT   11    6   12                                                       
CONECT   12   11   13   34                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16   32                                             
CONECT   15   14                                                            
CONECT   16   14   17   29                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   27                                                  
CONECT   20   19   21   22   23                                             
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   20   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   19   28   29                                             
CONECT   28   27   29                                                       
CONECT   29   28   16   27   30                                             
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   14   33   34                                             
CONECT   33   32                                                            
CONECT   34   32    2   12                                                  
MASTER        0    0    0    0    0    0    0    0   34    0   78    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₁H₅₀O₃

Average Mass

470.7380 Da

Monoisotopic Mass

470.37600 Da

IUPAC Name

10-(2-hydroxypropan-2-yl)-4,6,14,19,19-pentamethyl-11-oxahexacyclo[13.9.0.0^{1,23}.0^{4,14}.0^{5,12}.0^{18,23}]tetracosan-20-one

Traditional Name

10-(2-hydroxypropan-2-yl)-4,6,14,19,19-pentamethyl-11-oxahexacyclo[13.9.0.0^{1,23}.0^{4,14}.0^{5,12}.0^{18,23}]tetracosan-20-one

CAS Registry Number

Not Available

SMILES

CC1CCCC(OC2CC3(C)C4CCC5C6(CC46CCC3(C)C12)CCC(=O)C5(C)C)C(C)(C)O

InChI Identifier

InChI=1S/C31H50O3/c1-19-9-8-10-24(27(4,5)33)34-20-17-29(7)22-12-11-21-26(2,3)23(32)13-14-30(21)18-31(22,30)16-15-28(29,6)25(19)20/h19-22,24-25,33H,8-18H2,1-7H3

InChI Key

BRSJEZNEKATFHB-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Parthenium argentatum	LOTUS Database	35616633

Chemical Taxonomy

Description

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
Cycloartane-skeleton
Triterpenoid
3-oxosteroid
Oxosteroid
Tertiary alcohol
Ketone
Cyclic ketone
Oxacycle
Ether
Dialkyl ether
Organoheterocyclic compound
Organooxygen compound
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
Carbonyl group
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	6.27	ChemAxon
pKa (Strongest Acidic)	14.33	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	46.53 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	136.24 m³·mol⁻¹	ChemAxon
Polarizability	56.55 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

162871798

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 10-(2-hydroxypropan-2-yl)-4,6,14,19,19-pentamethyl-11-oxahexacyclo[13.9.0.0¹,²³.0⁴,¹⁴.0⁵,¹².0¹⁸,²³]tetracosan-20-one (NP0286145)

MOL for NP0286145 (10-(2-hydroxypropan-2-yl)-4,6,14,19,19-pentamethyl-11-oxahexacyclo[13.9.0.0¹,²³.0⁴,¹⁴.0⁵,¹².0¹⁸,²³]tetracosan-20-one)

3D MOL for NP0286145 (10-(2-hydroxypropan-2-yl)-4,6,14,19,19-pentamethyl-11-oxahexacyclo[13.9.0.0¹,²³.0⁴,¹⁴.0⁵,¹².0¹⁸,²³]tetracosan-20-one)

3D SDF for NP0286145 (10-(2-hydroxypropan-2-yl)-4,6,14,19,19-pentamethyl-11-oxahexacyclo[13.9.0.0¹,²³.0⁴,¹⁴.0⁵,¹².0¹⁸,²³]tetracosan-20-one)

3D-SDF for NP0286145 (10-(2-hydroxypropan-2-yl)-4,6,14,19,19-pentamethyl-11-oxahexacyclo[13.9.0.0¹,²³.0⁴,¹⁴.0⁵,¹².0¹⁸,²³]tetracosan-20-one)

PDB for NP0286145 (10-(2-hydroxypropan-2-yl)-4,6,14,19,19-pentamethyl-11-oxahexacyclo[13.9.0.0¹,²³.0⁴,¹⁴.0⁵,¹².0¹⁸,²³]tetracosan-20-one)

3D PDB for NP0286145 (10-(2-hydroxypropan-2-yl)-4,6,14,19,19-pentamethyl-11-oxahexacyclo[13.9.0.0¹,²³.0⁴,¹⁴.0⁵,¹².0¹⁸,²³]tetracosan-20-one)

SMILES for NP0286145 (10-(2-hydroxypropan-2-yl)-4,6,14,19,19-pentamethyl-11-oxahexacyclo[13.9.0.0¹,²³.0⁴,¹⁴.0⁵,¹².0¹⁸,²³]tetracosan-20-one)

INCHI for NP0286145 (10-(2-hydroxypropan-2-yl)-4,6,14,19,19-pentamethyl-11-oxahexacyclo[13.9.0.0¹,²³.0⁴,¹⁴.0⁵,¹².0¹⁸,²³]tetracosan-20-one)

Structure for NP0286145 (10-(2-hydroxypropan-2-yl)-4,6,14,19,19-pentamethyl-11-oxahexacyclo[13.9.0.0¹,²³.0⁴,¹⁴.0⁵,¹².0¹⁸,²³]tetracosan-20-one)

3D Structure for NP0286145 (10-(2-hydroxypropan-2-yl)-4,6,14,19,19-pentamethyl-11-oxahexacyclo[13.9.0.0¹,²³.0⁴,¹⁴.0⁵,¹².0¹⁸,²³]tetracosan-20-one)