NP-MRD: Showing NP-Card for (1r,2s,3s,4r)-1-[(1s,3's,3as,3br,5as,9as,9bs,11as)-3',9a,11a-trimethyl-7-oxo-dodecahydro-2h-spiro[cyclopenta[a]phenanthrene-1,2'-oxiran]-3'-yl]-5-(acetyloxy)-4-hydroxy-2,3,4-trimethylpentyl acetate (NP0172874)

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Record Information

Version

2.0

Created at

2022-09-03 09:54:04 UTC

Updated at

2022-09-03 09:54:04 UTC

NP-MRD ID

NP0172874

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2s,3s,4r)-1-[(1s,3's,3as,3br,5as,9as,9bs,11as)-3',9a,11a-trimethyl-7-oxo-dodecahydro-2h-spiro[cyclopenta[a]phenanthrene-1,2'-oxiran]-3'-yl]-5-(acetyloxy)-4-hydroxy-2,3,4-trimethylpentyl acetate

Description

(1R,2S,3S,4R)-5-(acetyloxy)-4-hydroxy-2,3,4-trimethyl-1-[(1'S,2S,2'S,3S,7'S,10'R,11'S,15'S)-2',3,15'-trimethyl-5'-oxospiro[oxirane-2,14'-tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadecane]-3-yl]pentyl acetate belongs to the class of organic compounds known as ergosterols and derivatives. These are steroids containing ergosta-5,7,22-trien-3beta-ol or a derivative thereof, which is based on the 3beta-hydroxylated ergostane skeleton. (1r,2s,3s,4r)-1-[(1s,3's,3as,3br,5as,9as,9bs,11as)-3',9a,11a-trimethyl-7-oxo-dodecahydro-2h-spiro[cyclopenta[a]phenanthrene-1,2'-oxiran]-3'-yl]-5-(acetyloxy)-4-hydroxy-2,3,4-trimethylpentyl acetate is found in Isis hippuris. Based on a literature review very few articles have been published on (1R,2S,3S,4R)-5-(acetyloxy)-4-hydroxy-2,3,4-trimethyl-1-[(1'S,2S,2'S,3S,7'S,10'R,11'S,15'S)-2',3,15'-trimethyl-5'-oxospiro[oxirane-2,14'-tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadecane]-3-yl]pentyl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032211542D          

 40 44  0  0  1  0            999 V2000
   -0.6323   -4.1247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
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 39 40  1  1  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652309032211542D          

 40 44  0  0  1  0            999 V2000
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   -0.3869   -2.7169    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7095   -3.6333    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2386   -3.0003    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0513   -3.1420    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9096   -3.9548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1930   -2.3293    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8641   -3.2837    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1477   -4.0584    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3931   -2.6507    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1095   -1.8760    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2059   -2.7924    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4895   -3.5671    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3023   -3.7088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8314   -3.0758    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5859   -4.4835    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7350   -2.1594    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.4502   -2.5705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2035   -1.5285    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0156   -1.3836    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9565   -0.5608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7208   -0.2502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2524   -0.8812    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.0769   -0.9084    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.5127   -0.2079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3373   -0.2351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7260   -0.9628    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.5506   -0.9900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9393   -1.7177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7638   -1.7449    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.5034   -2.4182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6789   -2.3910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2902   -1.6633    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.8543   -2.3638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4656   -1.6361    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.0298   -2.3366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2052   -2.3094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8165   -1.5817    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.3098   -2.2328    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  1  0  0  0
  6  8  1  1  0  0  0
  6  9  1  0  0  0  0
  9 10  1  6  0  0  0
  9 11  1  0  0  0  0
 11 12  1  6  0  0  0
 11 13  1  0  0  0  0
 13 14  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 18 13  1  6  0  0  0
 18 19  1  1  0  0  0
 18 20  1  0  0  0  0
 21 20  1  1  0  0  0
 18 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 24 23  1  1  0  0  0
 24 25  1  0  0  0  0
 25 26  1  6  0  0  0
 26 27  1  0  0  0  0
 28 27  1  1  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 28 34  1  0  0  0  0
 34 35  1  1  0  0  0
 34 36  1  0  0  0  0
 25 36  1  0  0  0  0
 36 37  1  1  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 24 39  1  0  0  0  0
 21 39  1  0  0  0  0
 39 40  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0172874

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]([C@H](C)[C@@](C)(O)COC(C)=O)[C@@H](OC(C)=O)[C@]1(C)O[C@]11CC[C@H]2[C@@H]3CC[C@H]4CC(=O)CC[C@]4(C)[C@H]3CC[C@]12C

> <INCHI_IDENTIFIER>
InChI=1S/C33H52O7/c1-19(20(2)31(7,37)18-38-21(3)34)28(39-22(4)35)32(8)33(40-32)16-13-27-25-10-9-23-17-24(36)11-14-29(23,5)26(25)12-15-30(27,33)6/h19-20,23,25-28,37H,9-18H2,1-8H3/t19-,20-,23-,25+,26-,27-,28+,29-,30-,31-,32-,33-/m0/s1

> <INCHI_KEY>
RZVOJQTZUNGQBW-KTEPSHEWSA-N

> <FORMULA>
C33H52O7

> <MOLECULAR_WEIGHT>
560.772

> <EXACT_MASS>
560.371304014

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
92

> <JCHEM_AVERAGE_POLARIZABILITY>
62.95814596685896

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2S,3S,4R)-5-(acetyloxy)-4-hydroxy-2,3,4-trimethyl-1-[(1'S,2S,2'S,3S,7'S,10'R,11'S,15'S)-2',3,15'-trimethyl-5'-oxospiro[oxirane-2,14'-tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecane]-3-yl]pentyl acetate

> <ALOGPS_LOGP>
4.73

> <JCHEM_LOGP>
4.666295300666665

> <ALOGPS_LOGS>
-6.42

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.997657339857394

> <JCHEM_PKA_STRONGEST_BASIC>
-3.237224569585906

> <JCHEM_POLAR_SURFACE_AREA>
102.43

> <JCHEM_REFRACTIVITY>
150.195

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.15e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,3S,4R)-5-(acetyloxy)-4-hydroxy-2,3,4-trimethyl-1-[(1'S,2S,2'S,3S,7'S,10'R,11'S,15'S)-2',3,15'-trimethyl-5'-oxospiro[oxirane-2,14'-tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecane]-3-yl]pentyl 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      -1.180  -7.699   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.193  -6.518   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -0.722  -5.072   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       1.324  -6.782   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       2.312  -5.601   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.829  -5.865   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.565  -7.382   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       4.094  -4.348   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       5.346  -6.130   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.876  -7.576   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.334  -4.948   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.804  -3.502   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.851  -5.213   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       8.380  -6.659   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       9.898  -6.923   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.885  -5.742   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      10.427  -8.369   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       8.839  -4.031   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      10.174  -4.798   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       7.846  -2.853   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       9.363  -2.583   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       9.252  -1.047   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      10.679  -0.467   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      11.671  -1.645   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      13.210  -1.696   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      14.024  -0.388   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      15.563  -0.439   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      16.289  -1.797   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      17.828  -1.848   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      18.553  -3.206   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      20.092  -3.257   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      17.740  -4.514   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      16.201  -4.463   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      15.475  -3.105   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      14.661  -4.412   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      13.936  -3.054   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      13.122  -4.362   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      11.583  -4.311   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      10.858  -2.952   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       9.912  -4.168   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    9                                             
CONECT    7    6                                                            
CONECT    8    6                                                            
CONECT    9    6   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   18                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18   13   19   20   21                                             
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   18   22   39                                             
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   39                                                  
CONECT   25   24   26   36                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   34                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   28   35   36                                             
CONECT   35   34                                                            
CONECT   36   34   25   37                                                  
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   24   21   40                                             
CONECT   40   39                                                            
MASTER        0    0    0    0    0    0    0    0   40    0   88    0
END

View in JSmol

Synonyms

Value	Source
(1R,2S,3S,4R)-5-(Acetyloxy)-4-hydroxy-2,3,4-trimethyl-1-[(1's,2S,2's,3S,7's,10'r,11's,15's)-2',3,15'-trimethyl-5'-oxospiro[oxirane-2,14'-tetracyclo[8.7.0.0,.0,]heptadecane]-3-yl]pentyl acetic acid	Generator

Chemical Formula

C₃₃H₅₂O₇

Average Mass

560.7720 Da

Monoisotopic Mass

560.37130 Da

IUPAC Name

Traditional Name

CAS Registry Number

Not Available

SMILES

C[C@@H]([C@H](C)[C@@](C)(O)COC(C)=O)[C@@H](OC(C)=O)[C@]1(C)O[C@]11CC[C@H]2[C@@H]3CC[C@H]4CC(=O)CC[C@]4(C)[C@H]3CC[C@]12C

InChI Identifier

InChI=1S/C33H52O7/c1-19(20(2)31(7,37)18-38-21(3)34)28(39-22(4)35)32(8)33(40-32)16-13-27-25-10-9-23-17-24(36)11-14-29(23,5)26(25)12-15-30(27,33)6/h19-20,23,25-28,37H,9-18H2,1-8H3/t19-,20-,23-,25+,26-,27-,28+,29-,30-,31-,32-,33-/m0/s1

InChI Key

RZVOJQTZUNGQBW-KTEPSHEWSA-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

Species Name	Source	Reference
Isis hippuris	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as ergosterols and derivatives. These are steroids containing ergosta-5,7,22-trien-3beta-ol or a derivative thereof, which is based on the 3beta-hydroxylated ergostane skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Ergostane steroids

Direct Parent

Ergosterols and derivatives

Alternative Parents

Substituents

Ergosterol-skeleton
3-oxosteroid
Oxosteroid
3-oxo-5-alpha-steroid
Dicarboxylic acid or derivatives
Tertiary alcohol
Carboxylic acid ester
Ketone
Cyclic ketone
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Organooxygen compound
Alcohol
Hydrocarbon derivative
Organic oxide
Organic oxygen 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	4.73	ALOGPS
logP	4.67	ChemAxon
logS	-6.4	ALOGPS
pKa (Strongest Acidic)	14	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	102.43 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	150.2 m³·mol⁻¹	ChemAxon
Polarizability	62.96 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

163001207

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,2s,3s,4r)-1-[(1s,3's,3as,3br,5as,9as,9bs,11as)-3',9a,11a-trimethyl-7-oxo-dodecahydro-2h-spiro[cyclopenta[a]phenanthrene-1,2'-oxiran]-3'-yl]-5-(acetyloxy)-4-hydroxy-2,3,4-trimethylpentyl acetate (NP0172874)

MOL for NP0172874 ((1r,2s,3s,4r)-1-[(1s,3's,3as,3br,5as,9as,9bs,11as)-3',9a,11a-trimethyl-7-oxo-dodecahydro-2h-spiro[cyclopenta[a]phenanthrene-1,2'-oxiran]-3'-yl]-5-(acetyloxy)-4-hydroxy-2,3,4-trimethylpentyl acetate)

3D MOL for NP0172874 ((1r,2s,3s,4r)-1-[(1s,3's,3as,3br,5as,9as,9bs,11as)-3',9a,11a-trimethyl-7-oxo-dodecahydro-2h-spiro[cyclopenta[a]phenanthrene-1,2'-oxiran]-3'-yl]-5-(acetyloxy)-4-hydroxy-2,3,4-trimethylpentyl acetate)

3D SDF for NP0172874 ((1r,2s,3s,4r)-1-[(1s,3's,3as,3br,5as,9as,9bs,11as)-3',9a,11a-trimethyl-7-oxo-dodecahydro-2h-spiro[cyclopenta[a]phenanthrene-1,2'-oxiran]-3'-yl]-5-(acetyloxy)-4-hydroxy-2,3,4-trimethylpentyl acetate)

3D-SDF for NP0172874 ((1r,2s,3s,4r)-1-[(1s,3's,3as,3br,5as,9as,9bs,11as)-3',9a,11a-trimethyl-7-oxo-dodecahydro-2h-spiro[cyclopenta[a]phenanthrene-1,2'-oxiran]-3'-yl]-5-(acetyloxy)-4-hydroxy-2,3,4-trimethylpentyl acetate)

PDB for NP0172874 ((1r,2s,3s,4r)-1-[(1s,3's,3as,3br,5as,9as,9bs,11as)-3',9a,11a-trimethyl-7-oxo-dodecahydro-2h-spiro[cyclopenta[a]phenanthrene-1,2'-oxiran]-3'-yl]-5-(acetyloxy)-4-hydroxy-2,3,4-trimethylpentyl acetate)

3D PDB for NP0172874 ((1r,2s,3s,4r)-1-[(1s,3's,3as,3br,5as,9as,9bs,11as)-3',9a,11a-trimethyl-7-oxo-dodecahydro-2h-spiro[cyclopenta[a]phenanthrene-1,2'-oxiran]-3'-yl]-5-(acetyloxy)-4-hydroxy-2,3,4-trimethylpentyl acetate)

SMILES for NP0172874 ((1r,2s,3s,4r)-1-[(1s,3's,3as,3br,5as,9as,9bs,11as)-3',9a,11a-trimethyl-7-oxo-dodecahydro-2h-spiro[cyclopenta[a]phenanthrene-1,2'-oxiran]-3'-yl]-5-(acetyloxy)-4-hydroxy-2,3,4-trimethylpentyl acetate)

INCHI for NP0172874 ((1r,2s,3s,4r)-1-[(1s,3's,3as,3br,5as,9as,9bs,11as)-3',9a,11a-trimethyl-7-oxo-dodecahydro-2h-spiro[cyclopenta[a]phenanthrene-1,2'-oxiran]-3'-yl]-5-(acetyloxy)-4-hydroxy-2,3,4-trimethylpentyl acetate)

Structure for NP0172874 ((1r,2s,3s,4r)-1-[(1s,3's,3as,3br,5as,9as,9bs,11as)-3',9a,11a-trimethyl-7-oxo-dodecahydro-2h-spiro[cyclopenta[a]phenanthrene-1,2'-oxiran]-3'-yl]-5-(acetyloxy)-4-hydroxy-2,3,4-trimethylpentyl acetate)

3D Structure for NP0172874 ((1r,2s,3s,4r)-1-[(1s,3's,3as,3br,5as,9as,9bs,11as)-3',9a,11a-trimethyl-7-oxo-dodecahydro-2h-spiro[cyclopenta[a]phenanthrene-1,2'-oxiran]-3'-yl]-5-(acetyloxy)-4-hydroxy-2,3,4-trimethylpentyl acetate)