NP-MRD: Showing NP-Card for {17-hydroxy-2,7,7,10-tetramethyl-6,8-dioxapentacyclo[14.3.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰]icosan-17-yl}methyl acetate (NP0171572)

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Record Information

Version

1.0

Created at

2022-09-03 08:08:55 UTC

Updated at

2022-09-03 08:08:55 UTC

NP-MRD ID

NP0171572

Secondary Accession Numbers

None

Natural Product Identification

Common Name

{17-hydroxy-2,7,7,10-tetramethyl-6,8-dioxapentacyclo[14.3.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰]icosan-17-yl}methyl acetate

Description

{17-Hydroxy-2,7,7,10-tetramethyl-6,8-dioxapentacyclo[14.3.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰]Icosan-17-yl}methyl acetate belongs to the class of organic compounds known as oxasteroids and derivatives. These are steroid derivatives where a carbon atom of the steroid is replaced by an oxygen atom. Based on a literature review very few articles have been published on {17-hydroxy-2,7,7,10-tetramethyl-6,8-dioxapentacyclo[14.3.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰]Icosan-17-yl}methyl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032210082D          

 30 34  0  0  0  0            999 V2000
   -3.5112   -0.8018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6867   -0.8294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2506   -0.1291    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2983   -1.5572    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4737   -1.5847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0376   -0.8844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8072   -0.5872    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4061   -1.4673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3877   -1.1461    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5427   -0.2755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1842   -0.1868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8799   -0.0194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4523    0.7454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4241    0.6024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1043    1.0909    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8651    0.7562    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9696   -0.0676    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7389   -0.3654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6122    0.4498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3816    0.1519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1509   -0.1459    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2777   -0.9611    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0585   -0.6947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6756   -1.6838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6350   -1.4785    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8657   -1.1806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2231   -1.6980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4537   -1.4001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3270   -0.5849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6827   -1.1002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  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
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
  6 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 10 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 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
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 22 25  1  0  0  0  0
 25 26  1  0  0  0  0
 18 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 17 29  1  0  0  0  0
 10 29  1  0  0  0  0
 29 30  1  0  0  0  0
M  END

     RDKit          3D

 70 74  0  0  0  0  0  0  0  0999 V2000
   -7.6030   -1.5661    0.5547 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7012   -0.6341   -0.1957 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0118    0.5431   -0.4300 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.7449    1.6597   -0.3878 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.2250    2.4110    0.6437 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.4532    0.5170    0.5006 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7794    0.3193   -0.1871 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0004    1.1801   -1.3813 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8809    0.6991    0.8212 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7462   -0.3649    0.9015 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2936   -0.7624   -0.3002 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9755   -2.1126   -0.0327 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3530    0.1516   -0.8273 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3016   -1.0564   -1.2660 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0766   -1.1066   -0.5528 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9915   -1.7712   -1.3049 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6820   -1.0505   -1.3180 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.3802   -1.5053   -0.1510 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.8834    2.4645    0.6986 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7616    1.6845    2.3058 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6407    0.8401    1.9857 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3365    3.2207    1.4255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6128    2.9107   -0.2913 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5915    2.4891   -0.4321 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7756    2.4505    1.3156 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6379    0.2279    1.5821 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7731    0.6728   -2.0344 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1524    1.3672   -2.0290 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5138    2.1426   -1.0831 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3670    1.6403    0.5604 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652309032210082D          

 30 34  0  0  0  0            999 V2000
   -3.5112   -0.8018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6867   -0.8294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2506   -0.1291    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    0.6827   -1.1002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END
> <DATABASE_ID>
NP0171572

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OCC1(O)CCC23CC1CC2CCC1C2(C)COC(C)(C)OC2CCC31C

> <INCHI_IDENTIFIER>
InChI=1S/C25H40O5/c1-16(26)28-15-25(27)11-10-24-13-18(25)12-17(24)6-7-19-22(4)14-29-21(2,3)30-20(22)8-9-23(19,24)5/h17-20,27H,6-15H2,1-5H3

> <INCHI_KEY>
WTLPSBZUQMYRGQ-UHFFFAOYSA-N

> <FORMULA>
C25H40O5

> <MOLECULAR_WEIGHT>
420.59

> <EXACT_MASS>
420.287574388

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
70

> <JCHEM_AVERAGE_POLARIZABILITY>
48.139404080013044

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
{17-hydroxy-2,7,7,10-tetramethyl-6,8-dioxapentacyclo[14.3.1.0^{1,14}.0^{2,11}.0^{5,10}]icosan-17-yl}methyl acetate

> <ALOGPS_LOGP>
3.57

> <JCHEM_LOGP>
3.2336345869999987

> <ALOGPS_LOGS>
-5.72

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.769299170934087

> <JCHEM_PKA_STRONGEST_BASIC>
-3.3371085426334295

> <JCHEM_POLAR_SURFACE_AREA>
64.99000000000001

> <JCHEM_REFRACTIVITY>
113.7434

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.96e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
{17-hydroxy-2,7,7,10-tetramethyl-6,8-dioxapentacyclo[14.3.1.0^{1,14}.0^{2,11}.0^{5,10}]icosan-17-yl}methyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0      -6.554  -1.497   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.015  -1.548   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -4.201  -0.241   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      -4.290  -2.907   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -2.751  -2.958   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.937  -1.651   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -3.373  -1.096   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -0.758  -2.739   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.724  -2.139   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.013  -0.514   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.344  -0.349   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.643  -0.036   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.844   1.391   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.792   1.125   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.061   2.036   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.481   1.412   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.677  -0.126   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.113  -0.682   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.876   0.840   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.312   0.284   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       7.748  -0.272   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       7.985  -1.794   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.442  -1.297   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       8.728  -3.143   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       6.785  -2.760   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       5.349  -2.204   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.150  -3.170   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.714  -2.614   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.477  -1.092   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       1.274  -2.054   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8   12                                             
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   14   29                                             
CONECT   11   10   12                                                       
CONECT   12   11    6   13                                                  
CONECT   13   12   14                                                       
CONECT   14   13   10   15                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   29                                                  
CONECT   18   17   19   20   26                                             
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24   25                                             
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25   22   26                                                       
CONECT   26   25   18   27                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   17   10   30                                             
CONECT   30   29                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   68    0
END

View in JSmol

Synonyms

Value	Source
{17-hydroxy-2,7,7,10-tetramethyl-6,8-dioxapentacyclo[14.3.1.0,.0,.0,]icosan-17-yl}methyl acetic acid	Generator

Chemical Formula

C₂₅H₄₀O₅

Average Mass

420.5900 Da

Monoisotopic Mass

420.28757 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(=O)OCC1(O)CCC23CC1CC2CCC1C2(C)COC(C)(C)OC2CCC31C

InChI Identifier

InChI=1S/C25H40O5/c1-16(26)28-15-25(27)11-10-24-13-18(25)12-17(24)6-7-19-22(4)14-29-21(2,3)30-20(22)8-9-23(19,24)5/h17-20,27H,6-15H2,1-5H3

InChI Key

WTLPSBZUQMYRGQ-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oxasteroids and derivatives. These are steroid derivatives where a carbon atom of the steroid is replaced by an oxygen atom.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Oxasteroids and derivatives

Direct Parent

Oxasteroids and derivatives

Alternative Parents

Substituents

2-oxasteroid
Sesquiterpenoid
Chamigrane sesquiterpenoid
Ketal
Meta-dioxane
Tertiary alcohol
Cyclic alcohol
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Acetal
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
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

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

162814148

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for {17-hydroxy-2,7,7,10-tetramethyl-6,8-dioxapentacyclo[14.3.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰]icosan-17-yl}methyl acetate (NP0171572)

MOL for NP0171572 ({17-hydroxy-2,7,7,10-tetramethyl-6,8-dioxapentacyclo[14.3.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰]icosan-17-yl}methyl acetate)

3D MOL for NP0171572 ({17-hydroxy-2,7,7,10-tetramethyl-6,8-dioxapentacyclo[14.3.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰]icosan-17-yl}methyl acetate)

3D SDF for NP0171572 ({17-hydroxy-2,7,7,10-tetramethyl-6,8-dioxapentacyclo[14.3.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰]icosan-17-yl}methyl acetate)

3D-SDF for NP0171572 ({17-hydroxy-2,7,7,10-tetramethyl-6,8-dioxapentacyclo[14.3.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰]icosan-17-yl}methyl acetate)

PDB for NP0171572 ({17-hydroxy-2,7,7,10-tetramethyl-6,8-dioxapentacyclo[14.3.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰]icosan-17-yl}methyl acetate)

3D PDB for NP0171572 ({17-hydroxy-2,7,7,10-tetramethyl-6,8-dioxapentacyclo[14.3.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰]icosan-17-yl}methyl acetate)

SMILES for NP0171572 ({17-hydroxy-2,7,7,10-tetramethyl-6,8-dioxapentacyclo[14.3.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰]icosan-17-yl}methyl acetate)

INCHI for NP0171572 ({17-hydroxy-2,7,7,10-tetramethyl-6,8-dioxapentacyclo[14.3.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰]icosan-17-yl}methyl acetate)

Structure for NP0171572 ({17-hydroxy-2,7,7,10-tetramethyl-6,8-dioxapentacyclo[14.3.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰]icosan-17-yl}methyl acetate)

3D Structure for NP0171572 ({17-hydroxy-2,7,7,10-tetramethyl-6,8-dioxapentacyclo[14.3.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰]icosan-17-yl}methyl acetate)