NP-MRD: Showing NP-Card for (1r,3as,3br,5as,7s,9as,9bs,11ar)-7-{[(2s,3s,4s,6s)-3,4-dihydroxy-6-methyloxan-2-yl]oxy}-3a,5a-dihydroxy-11a-methyl-11-oxo-1-(6-oxopyran-3-yl)-dodecahydrocyclopenta[a]phenanthrene-9a-carbaldehyde (NP0253029)

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Record Information

Version

2.0

Created at

2022-09-07 16:46:26 UTC

Updated at

2022-09-07 16:46:26 UTC

NP-MRD ID

NP0253029

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,3as,3br,5as,7s,9as,9bs,11ar)-7-{[(2s,3s,4s,6s)-3,4-dihydroxy-6-methyloxan-2-yl]oxy}-3a,5a-dihydroxy-11a-methyl-11-oxo-1-(6-oxopyran-3-yl)-dodecahydrocyclopenta[a]phenanthrene-9a-carbaldehyde

Description

(1S,2S,5S,7S,10R,11S,14R,15R)-5-{[(2S,3S,4S,6S)-3,4-dihydroxy-6-methyloxan-2-yl]oxy}-7,11-dihydroxy-15-methyl-16-oxo-14-(2-oxo-2H-pyran-5-yl)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadecane-2-carbaldehyde belongs to the class of organic compounds known as bufanolides and derivatives. These are steroid lactones containing a pyran-2-one moiety linked to the C17 atom of a cyclopenta[a]phenanthrene derivative. (1r,3as,3br,5as,7s,9as,9bs,11ar)-7-{[(2s,3s,4s,6s)-3,4-dihydroxy-6-methyloxan-2-yl]oxy}-3a,5a-dihydroxy-11a-methyl-11-oxo-1-(6-oxopyran-3-yl)-dodecahydrocyclopenta[a]phenanthrene-9a-carbaldehyde is found in Kalanchoe laciniata. Based on a literature review very few articles have been published on (1S,2S,5S,7S,10R,11S,14R,15R)-5-{[(2S,3S,4S,6S)-3,4-dihydroxy-6-methyloxan-2-yl]oxy}-7,11-dihydroxy-15-methyl-16-oxo-14-(2-oxo-2H-pyran-5-yl)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadecane-2-carbaldehyde.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072218462D          

 40 45  0  0  1  0            999 V2000
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   -2.0022   -3.2741    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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   -1.1901   -3.1289    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9098   -2.3529    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0976   -2.2077    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1827   -1.4318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  2  1  1  1  0  0  0
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 10 39  1  0  0  0  0
  8 40  1  0  0  0  0
  2 40  1  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652309072218462D          

 40 45  0  0  1  0            999 V2000
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    2.6190   -0.9961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4311   -0.8509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7114   -0.0750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9629   -1.4816    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3228   -0.7393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7875   -1.5084    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2939   -0.8571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9830   -0.0929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4893    0.5584    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3066    0.4455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8129    1.0969    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6175   -0.3186    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1111   -0.9700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0168   -2.3009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3340   -2.7639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6826   -2.2576    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4850   -3.0585    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8705   -2.4028    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5902   -3.1787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7781   -3.3239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2463   -2.6932    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9660   -3.4691    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4342   -2.8384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6582   -3.7596    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  6  0  0  0
  4  6  1  0  0  0  0
  6  7  1  6  0  0  0
  6  8  1  0  0  0  0
  8  9  1  6  0  0  0
 10  9  1  1  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  1  0  0  0
 14 15  2  0  0  0  0
 13 16  1  0  0  0  0
 16 17  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  1  0  0  0
 20 22  1  0  0  0  0
 22 23  1  1  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 23 29  2  0  0  0  0
 22 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 20 32  1  0  0  0  0
 32 33  1  1  0  0  0
 32 34  1  0  0  0  0
 16 34  1  0  0  0  0
 34 35  1  6  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 13 37  1  0  0  0  0
 37 38  1  1  0  0  0
 37 39  1  0  0  0  0
 10 39  1  0  0  0  0
  8 40  1  0  0  0  0
  2 40  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0253029

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1C[C@H](O)[C@H](O)[C@H](O[C@H]2CC[C@]3(C=O)[C@H]4CC(=O)[C@]5(C)[C@H](CC[C@]5(O)[C@@H]4CC[C@]3(O)C2)C2=COC(=O)C=C2)O1

> <INCHI_IDENTIFIER>
InChI=1S/C30H40O10/c1-16-11-22(32)25(35)26(39-16)40-18-5-8-28(15-31)21-12-23(33)27(2)19(17-3-4-24(34)38-14-17)7-10-30(27,37)20(21)6-9-29(28,36)13-18/h3-4,14-16,18-22,25-26,32,35-37H,5-13H2,1-2H3/t16-,18-,19+,20+,21-,22-,25-,26-,27-,28-,29-,30-/m0/s1

> <INCHI_KEY>
MZEHMNFHHVLJSI-WBXLJUSXSA-N

> <FORMULA>
C30H40O10

> <MOLECULAR_WEIGHT>
560.64

> <EXACT_MASS>
560.262147488

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
80

> <JCHEM_AVERAGE_POLARIZABILITY>
57.988780872232645

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2S,5S,7S,10R,11S,14R,15R)-5-{[(2S,3S,4S,6S)-3,4-dihydroxy-6-methyloxan-2-yl]oxy}-7,11-dihydroxy-15-methyl-16-oxo-14-(2-oxo-2H-pyran-5-yl)tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecane-2-carbaldehyde

> <JCHEM_LOGP>
0.376829719999998

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.718220888565462

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.422493593350726

> <JCHEM_PKA_STRONGEST_BASIC>
-3.1927191828368535

> <JCHEM_POLAR_SURFACE_AREA>
159.81999999999996

> <JCHEM_REFRACTIVITY>
141.23069999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,5S,7S,10R,11S,14R,15R)-5-{[(2S,3S,4S,6S)-3,4-dihydroxy-6-methyloxan-2-yl]oxy}-7,11-dihydroxy-15-methyl-16-oxo-14-(6-oxopyran-3-yl)tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecane-2-carbaldehyde

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0      -0.759  -9.644   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.752  -8.466   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.268  -8.737   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.261  -7.560   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -5.777  -7.831   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -3.737  -6.112   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -4.730  -4.934   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -2.221  -5.841   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -1.698  -4.392   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -0.182  -4.121   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.341  -2.673   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.857  -2.402   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.850  -3.579   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.373  -2.131   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       2.380  -0.953   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       4.366  -3.308   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.889  -1.859   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.405  -1.588   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       6.928  -0.140   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       7.398  -2.766   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.069  -1.380   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.937  -2.816   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.882  -1.600   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.302  -0.173   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      10.247   1.042   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      11.772   0.832   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      12.717   2.047   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0      12.353  -0.595   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      11.407  -1.811   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       9.365  -4.295   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       8.090  -5.159   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       6.874  -4.214   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       6.505  -5.709   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       5.358  -4.485   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       4.835  -5.934   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       3.319  -6.205   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       2.326  -5.027   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       1.803  -6.476   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       0.810  -5.298   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      -1.229  -7.018   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   40                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   40                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   39                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   16   37                                             
CONECT   14   13   15                                                       
CONECT   15   14                                                            
CONECT   16   13   17   34                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   22   32                                             
CONECT   21   20                                                            
CONECT   22   20   23   30                                                  
CONECT   23   22   24   29                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   23                                                       
CONECT   30   22   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   20   33   34                                             
CONECT   33   32                                                            
CONECT   34   32   16   35                                                  
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   13   38   39                                             
CONECT   38   37                                                            
CONECT   39   37   10                                                       
CONECT   40    8    2                                                       
MASTER        0    0    0    0    0    0    0    0   40    0   90    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₄₀O₁₀

Average Mass

560.6400 Da

Monoisotopic Mass

560.26215 Da

IUPAC Name

Traditional Name

(1S,2S,5S,7S,10R,11S,14R,15R)-5-{[(2S,3S,4S,6S)-3,4-dihydroxy-6-methyloxan-2-yl]oxy}-7,11-dihydroxy-15-methyl-16-oxo-14-(6-oxopyran-3-yl)tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecane-2-carbaldehyde

CAS Registry Number

Not Available

SMILES

C[C@H]1C[C@H](O)[C@H](O)[C@H](O[C@H]2CC[C@]3(C=O)[C@H]4CC(=O)[C@]5(C)[C@H](CC[C@]5(O)[C@@H]4CC[C@]3(O)C2)C2=COC(=O)C=C2)O1

InChI Identifier

InChI=1S/C30H40O10/c1-16-11-22(32)25(35)26(39-16)40-18-5-8-28(15-31)21-12-23(33)27(2)19(17-3-4-24(34)38-14-17)7-10-30(27,37)20(21)6-9-29(28,36)13-18/h3-4,14-16,18-22,25-26,32,35-37H,5-13H2,1-2H3/t16-,18-,19+,20+,21-,22-,25-,26-,27-,28-,29-,30-/m0/s1

InChI Key

MZEHMNFHHVLJSI-WBXLJUSXSA-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
Kalanchoe laciniata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as bufanolides and derivatives. These are steroid lactones containing a pyran-2-one moiety linked to the C17 atom of a cyclopenta[a]phenanthrene derivative.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroid lactones

Direct Parent

Bufanolides and derivatives

Alternative Parents

Substituents

Bufanolide-skeleton
Steroidal glycoside
19-oxosteroid
14-hydroxysteroid
5-hydroxysteroid
Hydroxysteroid
12-oxosteroid
Oxosteroid
Pyranone
Pyran
Oxane
Heteroaromatic compound
Tertiary alcohol
Cyclic alcohol
Secondary alcohol
Lactone
Ketone
Oxacycle
Organoheterocyclic compound
Acetal
Organic oxide
Alcohol
Aldehyde
Carbonyl group
Organooxygen compound
Hydrocarbon derivative
Organic oxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	0.38	ChemAxon
pKa (Strongest Acidic)	12.42	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	159.82 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	141.23 m³·mol⁻¹	ChemAxon
Polarizability	57.99 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

10167077

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11994610

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,3as,3br,5as,7s,9as,9bs,11ar)-7-{[(2s,3s,4s,6s)-3,4-dihydroxy-6-methyloxan-2-yl]oxy}-3a,5a-dihydroxy-11a-methyl-11-oxo-1-(6-oxopyran-3-yl)-dodecahydrocyclopenta[a]phenanthrene-9a-carbaldehyde (NP0253029)

MOL for NP0253029 ((1r,3as,3br,5as,7s,9as,9bs,11ar)-7-{[(2s,3s,4s,6s)-3,4-dihydroxy-6-methyloxan-2-yl]oxy}-3a,5a-dihydroxy-11a-methyl-11-oxo-1-(6-oxopyran-3-yl)-dodecahydrocyclopenta[a]phenanthrene-9a-carbaldehyde)

3D MOL for NP0253029 ((1r,3as,3br,5as,7s,9as,9bs,11ar)-7-{[(2s,3s,4s,6s)-3,4-dihydroxy-6-methyloxan-2-yl]oxy}-3a,5a-dihydroxy-11a-methyl-11-oxo-1-(6-oxopyran-3-yl)-dodecahydrocyclopenta[a]phenanthrene-9a-carbaldehyde)

3D SDF for NP0253029 ((1r,3as,3br,5as,7s,9as,9bs,11ar)-7-{[(2s,3s,4s,6s)-3,4-dihydroxy-6-methyloxan-2-yl]oxy}-3a,5a-dihydroxy-11a-methyl-11-oxo-1-(6-oxopyran-3-yl)-dodecahydrocyclopenta[a]phenanthrene-9a-carbaldehyde)

3D-SDF for NP0253029 ((1r,3as,3br,5as,7s,9as,9bs,11ar)-7-{[(2s,3s,4s,6s)-3,4-dihydroxy-6-methyloxan-2-yl]oxy}-3a,5a-dihydroxy-11a-methyl-11-oxo-1-(6-oxopyran-3-yl)-dodecahydrocyclopenta[a]phenanthrene-9a-carbaldehyde)

PDB for NP0253029 ((1r,3as,3br,5as,7s,9as,9bs,11ar)-7-{[(2s,3s,4s,6s)-3,4-dihydroxy-6-methyloxan-2-yl]oxy}-3a,5a-dihydroxy-11a-methyl-11-oxo-1-(6-oxopyran-3-yl)-dodecahydrocyclopenta[a]phenanthrene-9a-carbaldehyde)

3D PDB for NP0253029 ((1r,3as,3br,5as,7s,9as,9bs,11ar)-7-{[(2s,3s,4s,6s)-3,4-dihydroxy-6-methyloxan-2-yl]oxy}-3a,5a-dihydroxy-11a-methyl-11-oxo-1-(6-oxopyran-3-yl)-dodecahydrocyclopenta[a]phenanthrene-9a-carbaldehyde)

SMILES for NP0253029 ((1r,3as,3br,5as,7s,9as,9bs,11ar)-7-{[(2s,3s,4s,6s)-3,4-dihydroxy-6-methyloxan-2-yl]oxy}-3a,5a-dihydroxy-11a-methyl-11-oxo-1-(6-oxopyran-3-yl)-dodecahydrocyclopenta[a]phenanthrene-9a-carbaldehyde)

INCHI for NP0253029 ((1r,3as,3br,5as,7s,9as,9bs,11ar)-7-{[(2s,3s,4s,6s)-3,4-dihydroxy-6-methyloxan-2-yl]oxy}-3a,5a-dihydroxy-11a-methyl-11-oxo-1-(6-oxopyran-3-yl)-dodecahydrocyclopenta[a]phenanthrene-9a-carbaldehyde)

Structure for NP0253029 ((1r,3as,3br,5as,7s,9as,9bs,11ar)-7-{[(2s,3s,4s,6s)-3,4-dihydroxy-6-methyloxan-2-yl]oxy}-3a,5a-dihydroxy-11a-methyl-11-oxo-1-(6-oxopyran-3-yl)-dodecahydrocyclopenta[a]phenanthrene-9a-carbaldehyde)

3D Structure for NP0253029 ((1r,3as,3br,5as,7s,9as,9bs,11ar)-7-{[(2s,3s,4s,6s)-3,4-dihydroxy-6-methyloxan-2-yl]oxy}-3a,5a-dihydroxy-11a-methyl-11-oxo-1-(6-oxopyran-3-yl)-dodecahydrocyclopenta[a]phenanthrene-9a-carbaldehyde)