NP-MRD: Showing NP-Card for 3beta-Acetoxy-12beta,13beta-epoxy-11alpha-hydroperoxyursane (NP0074193)

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Record Information

Version

2.0

Created at

2022-04-28 19:21:34 UTC

Updated at

2022-04-28 19:21:34 UTC

NP-MRD ID

NP0074193

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3beta-Acetoxy-12beta,13beta-epoxy-11alpha-hydroperoxyursane

Description

(1S,3R,4S,5R,6S,9S,11S,14R,15S,18R,21R,22S,23R)-4-hydroperoxy-6,10,10,14,15,18,21,22-octamethyl-2-oxahexacyclo[13.8.0.0¹,³.0⁵,¹⁴.0⁶,¹¹.0¹⁸,²³]Tricosan-9-yl acetate belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. 3beta-Acetoxy-12beta,13beta-epoxy-11alpha-hydroperoxyursane is found in Ficus microcarpa . Based on a literature review very few articles have been published on (1S,3R,4S,5R,6S,9S,11S,14R,15S,18R,21R,22S,23R)-4-hydroperoxy-6,10,10,14,15,18,21,22-octamethyl-2-oxahexacyclo[13.8.0.0¹,³.0⁵,¹⁴.0⁶,¹¹.0¹⁸,²³]Tricosan-9-yl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282221212D          

 37 42  0  0  1  0            999 V2000
    8.2204    2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6329    1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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    6.9829    1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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    6.9829    3.0789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579    3.0789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.7454   -0.4934    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    9.4579    1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.8704    0.9355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6954    0.9355    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.4579    0.2211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    8.2492    3.1890    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
  1  6  1  0  0  0  0
  6  7  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
 10  9  1  1  0  0  0
  5 10  1  0  0  0  0
 10 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
  9 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
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 18 13  1  6  0  0  0
 18 19  1  0  0  0  0
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 21 22  1  0  0  0  0
 17 22  1  0  0  0  0
 20 23  1  6  0  0  0
 19 24  1  1  0  0  0
 17 25  1  1  0  0  0
 14 26  1  6  0  0  0
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  9 30  1  1  0  0  0
  5 31  1  1  0  0  0
  2 32  1  1  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 33 35  1  0  0  0  0
  1 36  1  0  0  0  0
  1 37  1  0  0  0  0
M  END

     RDKit          3D

 89 94  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1652304282221212D          

 37 42  0  0  1  0            999 V2000
    8.2204    2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.6829    1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2704    0.9355    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4454    0.9355    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0329    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4454    2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0329    0.2211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829    0.2211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    3.0789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3329    3.0789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0954    0.9355    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579    0.2211    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -0.4934    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8316    3.1850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5704    0.9355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4579    1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.8704    0.9355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6954    0.9355    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.4579    0.2211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9200    2.8017    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2492    3.1890    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
  1  6  1  0  0  0  0
  6  7  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
 10  9  1  1  0  0  0
  5 10  1  0  0  0  0
 10 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
  9 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 13  1  6  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 17 22  1  0  0  0  0
 20 23  1  6  0  0  0
 19 24  1  1  0  0  0
 17 25  1  1  0  0  0
 14 26  1  6  0  0  0
 13 27  1  1  0  0  0
 12 27  1  1  0  0  0
 11 28  1  6  0  0  0
 28 29  1  0  0  0  0
  9 30  1  1  0  0  0
  5 31  1  1  0  0  0
  2 32  1  1  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 33 35  1  0  0  0  0
  1 36  1  0  0  0  0
  1 37  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0074193

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1CC[C@]2(C)CC[C@]3(C)[C@@]4(O[C@@H]4[C@@H](OO)[C@@H]4[C@@]5(C)CC[C@H](OC(C)=O)C(C)(C)[C@H]5CC[C@@]34C)[C@@H]2[C@H]1C

> <INCHI_IDENTIFIER>
InChI=1S/C32H52O5/c1-18-10-13-28(6)16-17-31(9)30(8)15-11-21-27(4,5)22(35-20(3)33)12-14-29(21,7)25(30)23(37-34)26-32(31,36-26)24(28)19(18)2/h18-19,21-26,34H,10-17H2,1-9H3/t18-,19+,21-,22+,23+,24-,25-,26-,28-,29+,30-,31+,32-/m1/s1

> <INCHI_KEY>
MTHXIZRKFSBBNW-JDISTDGYSA-N

> <FORMULA>
C32H52O5

> <MOLECULAR_WEIGHT>
516.763

> <EXACT_MASS>
516.381474774

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
89

> <JCHEM_AVERAGE_POLARIZABILITY>
60.03114012448146

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,3R,4S,5R,6S,9S,11S,14R,15S,18R,21R,22S,23R)-4-hydroperoxy-6,10,10,14,15,18,21,22-octamethyl-2-oxahexacyclo[13.8.0.0^{1,3}.0^{5,14}.0^{6,11}.0^{18,23}]tricosan-9-yl acetate

> <ALOGPS_LOGP>
6.10

> <JCHEM_LOGP>
6.694657133000001

> <ALOGPS_LOGS>
-6.62

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.717857218576555

> <JCHEM_PKA_STRONGEST_BASIC>
-4.193119091323114

> <JCHEM_POLAR_SURFACE_AREA>
68.28999999999999

> <JCHEM_REFRACTIVITY>
142.21949999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.23e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,3R,4S,5R,6S,9S,11S,14R,15S,18R,21R,22S,23R)-4-hydroperoxy-6,10,10,14,15,18,21,22-octamethyl-2-oxahexacyclo[13.8.0.0^{1,3}.0^{5,14}.0^{6,11}.0^{18,23}]tricosan-9-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      15.345   4.414   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      16.115   3.080   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      15.345   1.746   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      13.805   1.746   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      13.035   3.080   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      13.805   4.414   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      13.035   5.747   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      11.495   5.747   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.725   4.414   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      11.495   3.080   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.725   1.746   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.185   1.746   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.415   3.080   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.185   4.414   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.415   5.747   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.875   5.747   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.105   4.414   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.875   3.080   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.105   1.746   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.565   1.746   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.795   3.080   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.565   4.414   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.795   0.413   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.875   0.413   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.335   5.747   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       9.955   5.747   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       7.645   1.746   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0      11.495   0.413   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      10.725  -0.921   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      10.886   5.945   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      12.265   1.746   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      17.655   3.080   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      18.425   1.746   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      19.965   1.746   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      17.655   0.413   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      16.651   5.230   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      15.398   5.953   0.000  0.00  0.00           C+0
CONECT    1    2    6   36   37                                             
CONECT    2    1    3   32                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   10   31                                             
CONECT    6    5    1    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   14   30                                             
CONECT   10    9    5   11                                                  
CONECT   11   10   12   28                                                  
CONECT   12   11   13   27                                                  
CONECT   13   12   14   18   27                                             
CONECT   14   13    9   15   26                                             
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   22   25                                             
CONECT   18   17   13   19                                                  
CONECT   19   18   20   24                                                  
CONECT   20   19   21   23                                                  
CONECT   21   20   22                                                       
CONECT   22   21   17                                                       
CONECT   23   20                                                            
CONECT   24   19                                                            
CONECT   25   17                                                            
CONECT   26   14                                                            
CONECT   27   13   12                                                       
CONECT   28   11   29                                                       
CONECT   29   28                                                            
CONECT   30    9                                                            
CONECT   31    5                                                            
CONECT   32    2   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33                                                            
CONECT   36    1                                                            
CONECT   37    1                                                            
MASTER        0    0    0    0    0    0    0    0   37    0   84    0
END

View in JSmol

Synonyms

Value	Source
(1S,3R,4S,5R,6S,9S,11S,14R,15S,18R,21R,22S,23R)-4-Hydroperoxy-6,10,10,14,15,18,21,22-octamethyl-2-oxahexacyclo[13.8.0.0,.0,.0,.0,]tricosan-9-yl acetic acid	Generator

Chemical Formula

C₃₂H₅₂O₅

Average Mass

516.7630 Da

Monoisotopic Mass

516.38147 Da

IUPAC Name

(1S,3R,4S,5R,6S,9S,11S,14R,15S,18R,21R,22S,23R)-4-hydroperoxy-6,10,10,14,15,18,21,22-octamethyl-2-oxahexacyclo[13.8.0.0^{1,3}.0^{5,14}.0^{6,11}.0^{18,23}]tricosan-9-yl acetate

Traditional Name

(1S,3R,4S,5R,6S,9S,11S,14R,15S,18R,21R,22S,23R)-4-hydroperoxy-6,10,10,14,15,18,21,22-octamethyl-2-oxahexacyclo[13.8.0.0^{1,3}.0^{5,14}.0^{6,11}.0^{18,23}]tricosan-9-yl acetate

CAS Registry Number

Not Available

SMILES

C[C@@H]1CC[C@]2(C)CC[C@]3(C)[C@@]4(O[C@@H]4[C@@H](OO)[C@@H]4[C@@]5(C)CC[C@H](OC(C)=O)C(C)(C)[C@H]5CC[C@@]34C)[C@@H]2[C@H]1C

InChI Identifier

InChI=1S/C32H52O5/c1-18-10-13-28(6)16-17-31(9)30(8)15-11-21-27(4,5)22(35-20(3)33)12-14-29(21,7)25(30)23(37-34)26-32(31,36-26)24(28)19(18)2/h18-19,21-26,34H,10-17H2,1-9H3/t18-,19+,21-,22+,23+,24-,25-,26-,28-,29+,30-,31+,32-/m1/s1

InChI Key

MTHXIZRKFSBBNW-JDISTDGYSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Ficus microcarpa	Plant	KNApSAcK

Chemical Taxonomy

Description

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
Oxepane
Hydroperoxide
Carboxylic acid ester
Alkyl hydroperoxide
Oxacycle
Organoheterocyclic compound
Peroxol
Monocarboxylic acid or derivatives
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
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	6.1	ALOGPS
logP	6.69	ChemAxon
logS	-6.6	ALOGPS
pKa (Strongest Acidic)	11.72	ChemAxon
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	68.29 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	142.22 m³·mol⁻¹	ChemAxon
Polarizability	60.03 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	No	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

163086873

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 3beta-Acetoxy-12beta,13beta-epoxy-11alpha-hydroperoxyursane (NP0074193)

MOL for NP0074193 (3beta-Acetoxy-12beta,13beta-epoxy-11alpha-hydroperoxyursane)

3D MOL for NP0074193 (3beta-Acetoxy-12beta,13beta-epoxy-11alpha-hydroperoxyursane)

3D SDF for NP0074193 (3beta-Acetoxy-12beta,13beta-epoxy-11alpha-hydroperoxyursane)

3D-SDF for NP0074193 (3beta-Acetoxy-12beta,13beta-epoxy-11alpha-hydroperoxyursane)

PDB for NP0074193 (3beta-Acetoxy-12beta,13beta-epoxy-11alpha-hydroperoxyursane)

3D PDB for NP0074193 (3beta-Acetoxy-12beta,13beta-epoxy-11alpha-hydroperoxyursane)

SMILES for NP0074193 (3beta-Acetoxy-12beta,13beta-epoxy-11alpha-hydroperoxyursane)

INCHI for NP0074193 (3beta-Acetoxy-12beta,13beta-epoxy-11alpha-hydroperoxyursane)

Structure for NP0074193 (3beta-Acetoxy-12beta,13beta-epoxy-11alpha-hydroperoxyursane)

3D Structure for NP0074193 (3beta-Acetoxy-12beta,13beta-epoxy-11alpha-hydroperoxyursane)