NP-MRD: Showing NP-Card for (2r)-1-[(1s,2s,3'r,3as,3bs,4r,4'r,9ar,9br,11as)-4-(acetyloxy)-2-hydroxy-3',9a,11a-trimethyl-7-oxo-3,3a,3b,4,5,9b,10,11-octahydro-2h-spiro[cyclopenta[a]phenanthrene-1,2'-oxetan]-4'-yl]-3-hydroxy-2,3-dimethylbutan-2-yl acetate (NP0210349)

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Record Information

Version

2.0

Created at

2022-09-05 08:07:05 UTC

Updated at

2022-09-05 08:07:05 UTC

NP-MRD ID

NP0210349

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r)-1-[(1s,2s,3'r,3as,3bs,4r,4'r,9ar,9br,11as)-4-(acetyloxy)-2-hydroxy-3',9a,11a-trimethyl-7-oxo-3,3a,3b,4,5,9b,10,11-octahydro-2h-spiro[cyclopenta[a]phenanthrene-1,2'-oxetan]-4'-yl]-3-hydroxy-2,3-dimethylbutan-2-yl acetate

Description

(2R)-1-[(1'R,2S,2'R,3R,4R,9'R,10'S,11'S,13'S,15'S)-9'-(acetyloxy)-13'-hydroxy-2',3,15'-trimethyl-5'-oxospiro[oxetane-2,14'-tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadecane]-3',6'-dien-4-yl]-3-hydroxy-2,3-dimethylbutan-2-yl acetate belongs to the class of organic compounds known as steroid esters. Steroid esters are compounds containing a steroid moiety which bears a carboxylic acid ester group. (2r)-1-[(1s,2s,3'r,3as,3bs,4r,4'r,9ar,9br,11as)-4-(acetyloxy)-2-hydroxy-3',9a,11a-trimethyl-7-oxo-3,3a,3b,4,5,9b,10,11-octahydro-2h-spiro[cyclopenta[a]phenanthrene-1,2'-oxetan]-4'-yl]-3-hydroxy-2,3-dimethylbutan-2-yl acetate is found in Petunia axillaris. Based on a literature review very few articles have been published on (2R)-1-[(1'R,2S,2'R,3R,4R,9'R,10'S,11'S,13'S,15'S)-9'-(acetyloxy)-13'-hydroxy-2',3,15'-trimethyl-5'-oxospiro[oxetane-2,14'-tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadecane]-3',6'-dien-4-yl]-3-hydroxy-2,3-dimethylbutan-2-yl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052210072D          

 40 44  0  0  1  0            999 V2000
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 15 40  1  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652309052210072D          

 40 44  0  0  1  0            999 V2000
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    0.2681   -2.7563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1096   -2.0228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9336   -1.9831    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3368   -1.3290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1609   -1.3687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5385   -2.1022    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9849   -1.4084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3626   -2.1419    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8090   -1.4481    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6330   -1.4879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0106   -2.2214    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5271   -1.5780    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5642   -2.9151    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0861   -3.5541    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8551   -3.2552    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.5489   -3.7016    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8084   -2.4315    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8912   -1.6107    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7120   -1.6935    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.3510   -1.1716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1224   -1.4640    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.8300   -2.2354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8939   -1.7564    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.0264   -2.5707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7978   -2.8631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3874   -3.0926    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4149   -0.6926    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7073    0.0789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1863   -0.9850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6434   -0.4002    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6293   -2.5143    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.1511   -3.1533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7402   -2.8754    0.0000 C   0  0  1  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
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
  7 13  1  0  0  0  0
 13 14  1  1  0  0  0
 13 15  1  0  0  0  0
 15 16  1  6  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  1  0  0  0
 18 20  1  0  0  0  0
 20 21  1  1  0  0  0
 21 22  1  0  0  0  0
 22 23  1  1  0  0  0
 22 24  1  0  0  0  0
 18 24  1  0  0  0  0
 24 25  1  6  0  0  0
 25 26  1  0  0  0  0
 26 27  1  6  0  0  0
 27 28  1  0  0  0  0
 28 29  1  1  0  0  0
 28 30  1  6  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  2  0  0  0  0
 28 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
 34 37  1  0  0  0  0
 26 38  1  0  0  0  0
 24 38  1  0  0  0  0
 38 39  1  1  0  0  0
 40 20  1  1  0  0  0
  5 40  1  0  0  0  0
 15 40  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0210349

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1[C@@H](C[C@@](C)(OC(C)=O)C(C)(C)O)O[C@@]11[C@@H](O)C[C@H]2[C@H]3[C@@H](CC4=CC(=O)C=C[C@]4(C)[C@@H]3CC[C@]12C)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C32H46O8/c1-17-25(16-31(8,28(4,5)37)39-19(3)34)40-32(17)26(36)15-23-27-22(10-12-30(23,32)7)29(6)11-9-21(35)13-20(29)14-24(27)38-18(2)33/h9,11,13,17,22-27,36-37H,10,12,14-16H2,1-8H3/t17-,22-,23+,24-,25-,26+,27+,29+,30+,31-,32-/m1/s1

> <INCHI_KEY>
SBLPFCZXOZMXGI-AWSRRNKMSA-N

> <FORMULA>
C32H46O8

> <MOLECULAR_WEIGHT>
558.712

> <EXACT_MASS>
558.319268441

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
86

> <JCHEM_AVERAGE_POLARIZABILITY>
61.663558218529865

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R)-1-[(1'R,2S,2'R,3R,4R,9'R,10'S,11'S,13'S,15'S)-9'-(acetyloxy)-13'-hydroxy-2',3,15'-trimethyl-5'-oxospiro[oxetane-2,14'-tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecane]-3',6'-dien-4-yl]-3-hydroxy-2,3-dimethylbutan-2-yl acetate

> <JCHEM_LOGP>
2.5735009926666637

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.32370536276331

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.71266390961948

> <JCHEM_PKA_STRONGEST_BASIC>
-3.1990472616487002

> <JCHEM_POLAR_SURFACE_AREA>
119.36000000000003

> <JCHEM_REFRACTIVITY>
149.2193

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2R)-1-[(1'R,2S,2'R,3R,4R,9'R,10'S,11'S,13'S,15'S)-9'-(acetyloxy)-13'-hydroxy-2',3,15'-trimethyl-5'-oxospiro[oxetane-2,14'-tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecane]-3',6'-dien-4-yl]-3-hydroxy-2,3-dimethylbutan-2-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0       2.615  -9.253   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.153  -9.327   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       4.858 -10.696   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       4.987  -8.032   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       4.282  -6.663   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.743  -6.588   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.039  -5.219   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.500  -5.145   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.205  -3.776   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -1.743  -3.702   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       0.629  -2.481   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.167  -2.555   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.872  -3.924   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.705  -2.629   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.410  -3.998   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.243  -2.703   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.782  -2.777   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.487  -4.147   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.451  -2.946   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.653  -5.442   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.627  -6.634   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       9.063  -6.076   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      10.358  -6.910   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       8.976  -4.539   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       9.130  -3.007   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      10.662  -3.161   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      11.855  -2.187   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      13.295  -2.733   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      12.749  -4.173   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      14.735  -3.279   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      14.983  -4.799   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      16.423  -5.345   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      13.790  -5.773   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      13.841  -1.293   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      14.387   0.147   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      15.281  -1.839   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      12.401  -0.747   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      10.508  -4.693   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      11.482  -5.886   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       5.115  -5.367   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   40                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   13                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12    7   14   15                                             
CONECT   14   13                                                            
CONECT   15   13   16   40                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20   24                                             
CONECT   19   18                                                            
CONECT   20   18   21   40                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   18   25   38                                             
CONECT   25   24   26                                                       
CONECT   26   25   27   38                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29   30   34                                             
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31                                                            
CONECT   34   28   35   36   37                                             
CONECT   35   34                                                            
CONECT   36   34                                                            
CONECT   37   34                                                            
CONECT   38   26   24   39                                                  
CONECT   39   38                                                            
CONECT   40   20    5   15                                                  
MASTER        0    0    0    0    0    0    0    0   40    0   88    0
END

View in JSmol

Synonyms

Value	Source
(2R)-1-[(1'r,2S,2'r,3R,4R,9'r,10's,11's,13's,15's)-9'-(Acetyloxy)-13'-hydroxy-2',3,15'-trimethyl-5'-oxospiro[oxetane-2,14'-tetracyclo[8.7.0.0,.0,]heptadecane]-3',6'-dien-4-yl]-3-hydroxy-2,3-dimethylbutan-2-yl acetic acid	Generator

Chemical Formula

C₃₂H₄₆O₈

Average Mass

558.7120 Da

Monoisotopic Mass

558.31927 Da

IUPAC Name

(2R)-1-[(1'R,2S,2'R,3R,4R,9'R,10'S,11'S,13'S,15'S)-9'-(acetyloxy)-13'-hydroxy-2',3,15'-trimethyl-5'-oxospiro[oxetane-2,14'-tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecane]-3',6'-dien-4-yl]-3-hydroxy-2,3-dimethylbutan-2-yl acetate

Traditional Name

CAS Registry Number

Not Available

SMILES

C[C@@H]1[C@@H](C[C@@](C)(OC(C)=O)C(C)(C)O)O[C@@]11[C@@H](O)C[C@H]2[C@H]3[C@@H](CC4=CC(=O)C=C[C@]4(C)[C@@H]3CC[C@]12C)OC(C)=O

InChI Identifier

InChI=1S/C32H46O8/c1-17-25(16-31(8,28(4,5)37)39-19(3)34)40-32(17)26(36)15-23-27-22(10-12-30(23,32)7)29(6)11-9-21(35)13-20(29)14-24(27)38-18(2)33/h9,11,13,17,22-27,36-37H,10,12,14-16H2,1-8H3/t17-,22-,23+,24-,25-,26+,27+,29+,30+,31-,32-/m1/s1

InChI Key

SBLPFCZXOZMXGI-AWSRRNKMSA-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
Petunia axillaris	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as steroid esters. Steroid esters are compounds containing a steroid moiety which bears a carboxylic acid ester group.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroid esters

Direct Parent

Steroid esters

Alternative Parents

Substituents

Steroid ester
3-oxo-delta-1,4-steroid
3-oxosteroid
Hydroxysteroid
Oxosteroid
16-hydroxysteroid
16-beta-hydroxysteroid
Delta-1,4-steroid
Dicarboxylic acid or derivatives
Cyclic alcohol
Tertiary alcohol
Cyclic ketone
Oxetane
Secondary alcohol
Ketone
Carboxylic acid ester
Organoheterocyclic compound
Ether
Oxacycle
Dialkyl ether
Carboxylic acid derivative
Organic oxide
Organic oxygen compound
Hydrocarbon derivative
Carbonyl group
Alcohol
Organooxygen compound
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	2.57	ChemAxon
pKa (Strongest Acidic)	13.71	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	119.36 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	149.22 m³·mol⁻¹	ChemAxon
Polarizability	61.66 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

162971338

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r)-1-[(1s,2s,3'r,3as,3bs,4r,4'r,9ar,9br,11as)-4-(acetyloxy)-2-hydroxy-3',9a,11a-trimethyl-7-oxo-3,3a,3b,4,5,9b,10,11-octahydro-2h-spiro[cyclopenta[a]phenanthrene-1,2'-oxetan]-4'-yl]-3-hydroxy-2,3-dimethylbutan-2-yl acetate (NP0210349)

MOL for NP0210349 ((2r)-1-[(1s,2s,3'r,3as,3bs,4r,4'r,9ar,9br,11as)-4-(acetyloxy)-2-hydroxy-3',9a,11a-trimethyl-7-oxo-3,3a,3b,4,5,9b,10,11-octahydro-2h-spiro[cyclopenta[a]phenanthrene-1,2'-oxetan]-4'-yl]-3-hydroxy-2,3-dimethylbutan-2-yl acetate)

3D MOL for NP0210349 ((2r)-1-[(1s,2s,3'r,3as,3bs,4r,4'r,9ar,9br,11as)-4-(acetyloxy)-2-hydroxy-3',9a,11a-trimethyl-7-oxo-3,3a,3b,4,5,9b,10,11-octahydro-2h-spiro[cyclopenta[a]phenanthrene-1,2'-oxetan]-4'-yl]-3-hydroxy-2,3-dimethylbutan-2-yl acetate)

3D SDF for NP0210349 ((2r)-1-[(1s,2s,3'r,3as,3bs,4r,4'r,9ar,9br,11as)-4-(acetyloxy)-2-hydroxy-3',9a,11a-trimethyl-7-oxo-3,3a,3b,4,5,9b,10,11-octahydro-2h-spiro[cyclopenta[a]phenanthrene-1,2'-oxetan]-4'-yl]-3-hydroxy-2,3-dimethylbutan-2-yl acetate)

3D-SDF for NP0210349 ((2r)-1-[(1s,2s,3'r,3as,3bs,4r,4'r,9ar,9br,11as)-4-(acetyloxy)-2-hydroxy-3',9a,11a-trimethyl-7-oxo-3,3a,3b,4,5,9b,10,11-octahydro-2h-spiro[cyclopenta[a]phenanthrene-1,2'-oxetan]-4'-yl]-3-hydroxy-2,3-dimethylbutan-2-yl acetate)

PDB for NP0210349 ((2r)-1-[(1s,2s,3'r,3as,3bs,4r,4'r,9ar,9br,11as)-4-(acetyloxy)-2-hydroxy-3',9a,11a-trimethyl-7-oxo-3,3a,3b,4,5,9b,10,11-octahydro-2h-spiro[cyclopenta[a]phenanthrene-1,2'-oxetan]-4'-yl]-3-hydroxy-2,3-dimethylbutan-2-yl acetate)

3D PDB for NP0210349 ((2r)-1-[(1s,2s,3'r,3as,3bs,4r,4'r,9ar,9br,11as)-4-(acetyloxy)-2-hydroxy-3',9a,11a-trimethyl-7-oxo-3,3a,3b,4,5,9b,10,11-octahydro-2h-spiro[cyclopenta[a]phenanthrene-1,2'-oxetan]-4'-yl]-3-hydroxy-2,3-dimethylbutan-2-yl acetate)

SMILES for NP0210349 ((2r)-1-[(1s,2s,3'r,3as,3bs,4r,4'r,9ar,9br,11as)-4-(acetyloxy)-2-hydroxy-3',9a,11a-trimethyl-7-oxo-3,3a,3b,4,5,9b,10,11-octahydro-2h-spiro[cyclopenta[a]phenanthrene-1,2'-oxetan]-4'-yl]-3-hydroxy-2,3-dimethylbutan-2-yl acetate)

INCHI for NP0210349 ((2r)-1-[(1s,2s,3'r,3as,3bs,4r,4'r,9ar,9br,11as)-4-(acetyloxy)-2-hydroxy-3',9a,11a-trimethyl-7-oxo-3,3a,3b,4,5,9b,10,11-octahydro-2h-spiro[cyclopenta[a]phenanthrene-1,2'-oxetan]-4'-yl]-3-hydroxy-2,3-dimethylbutan-2-yl acetate)

Structure for NP0210349 ((2r)-1-[(1s,2s,3'r,3as,3bs,4r,4'r,9ar,9br,11as)-4-(acetyloxy)-2-hydroxy-3',9a,11a-trimethyl-7-oxo-3,3a,3b,4,5,9b,10,11-octahydro-2h-spiro[cyclopenta[a]phenanthrene-1,2'-oxetan]-4'-yl]-3-hydroxy-2,3-dimethylbutan-2-yl acetate)

3D Structure for NP0210349 ((2r)-1-[(1s,2s,3'r,3as,3bs,4r,4'r,9ar,9br,11as)-4-(acetyloxy)-2-hydroxy-3',9a,11a-trimethyl-7-oxo-3,3a,3b,4,5,9b,10,11-octahydro-2h-spiro[cyclopenta[a]phenanthrene-1,2'-oxetan]-4'-yl]-3-hydroxy-2,3-dimethylbutan-2-yl acetate)