NP-MRD: Showing NP-Card for (1r,3br,4s,5r,5as,7r,9s,9ar,9br,11as)-4,9-bis(acetyloxy)-1-(furan-3-yl)-5-hydroxy-3b,6,6,9a,11a-pentamethyl-1h,2h,4h,5h,5ah,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl propanoate (NP0289939)

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Record Information

Version

2.0

Created at

2022-09-09 20:22:14 UTC

Updated at

2022-09-09 20:22:14 UTC

NP-MRD ID

NP0289939

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,3br,4s,5r,5as,7r,9s,9ar,9br,11as)-4,9-bis(acetyloxy)-1-(furan-3-yl)-5-hydroxy-3b,6,6,9a,11a-pentamethyl-1h,2h,4h,5h,5ah,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl propanoate

Description

CHEMBL2386297 belongs to the class of organic compounds known as limonoids. These are highly oxygenated, modified terpenoids with a prototypical structure either containing or derived from a precursor with a 4,4,8-trimethyl-17-furanylsteroid skeleton. All naturally occurring citrus limonoids contain a furan ring attached to the D-ring, at C-17, as well as oxygen containing functional groups at C-3, C-4, C-7, C-16 and C-17. (1r,3br,4s,5r,5as,7r,9s,9ar,9br,11as)-4,9-bis(acetyloxy)-1-(furan-3-yl)-5-hydroxy-3b,6,6,9a,11a-pentamethyl-1h,2h,4h,5h,5ah,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl propanoate is found in Turraea pubescens. Based on a literature review very few articles have been published on CHEMBL2386297.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092222222D          

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M  END

     RDKit          3D

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M  END


  Mrv1652309092222222D          

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    2.0745   -2.8623    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6700   -0.9702    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9503   -1.7461    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3897   -0.1943    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9215    0.4364    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6412    1.2123    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7336    0.2912    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2655    0.9219    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9852    1.6978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1730    1.8430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5170    2.3285    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0139   -0.4847    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5458    0.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8261   -0.6299    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4774   -0.1236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1602   -0.5866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9309   -1.3791    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.4373   -2.0304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2618   -2.0036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5421   -2.7795    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8908   -3.2859    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2080   -2.8229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1064   -1.4059    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.4662   -2.1482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5745   -2.0366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7624   -1.8914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4821   -1.1154    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5776   -0.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6944    0.7676    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9658    0.5044    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  2  0  0  0  0
  3  5  1  0  0  0  0
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  2  0  0  0  0
  8 13  1  0  0  0  0
 13 14  1  6  0  0  0
 15 13  1  6  0  0  0
 15 16  1  0  0  0  0
 16 17  1  1  0  0  0
 16 18  1  0  0  0  0
 18 19  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  2  0  0  0  0
 18 23  1  0  0  0  0
 23 24  1  6  0  0  0
 23 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  1  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 29 33  2  0  0  0  0
 28 34  1  0  0  0  0
 25 34  1  0  0  0  0
 34 35  1  1  0  0  0
 34 36  1  0  0  0  0
 36 37  1  0  0  0  0
 38 37  1  6  0  0  0
 23 38  1  0  0  0  0
 13 38  1  0  0  0  0
 15 39  1  0  0  0  0
  6 39  1  0  0  0  0
 39 40  1  0  0  0  0
 39 41  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0289939

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC(=O)O[C@@H]1C[C@H](OC(C)=O)[C@]2(C)[C@H]3CC[C@@]4(C)[C@@H](CC=C4[C@]3(C)[C@H](OC(C)=O)[C@H](O)[C@H]2C1(C)C)C1=COC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C33H46O8/c1-9-26(36)41-24-16-25(39-18(2)34)33(8)23-12-14-31(6)21(20-13-15-38-17-20)10-11-22(31)32(23,7)29(40-19(3)35)27(37)28(33)30(24,4)5/h11,13,15,17,21,23-25,27-29,37H,9-10,12,14,16H2,1-8H3/t21-,23-,24+,25-,27+,28-,29+,31-,32-,33-/m0/s1

> <INCHI_KEY>
OLAITLNVWDKEJN-DHGKALFUSA-N

> <FORMULA>
C33H46O8

> <MOLECULAR_WEIGHT>
570.723

> <EXACT_MASS>
570.319268441

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
87

> <JCHEM_AVERAGE_POLARIZABILITY>
61.77287917540574

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2R,3S,5R,7S,8R,9S,10R,14R,15S)-3,9-bis(acetyloxy)-14-(furan-3-yl)-8-hydroxy-2,6,6,10,15-pentamethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-11-en-5-yl propanoate

> <JCHEM_LOGP>
4.125623863333333

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.859742554028877

> <JCHEM_PKA_STRONGEST_BASIC>
-2.804437075448131

> <JCHEM_POLAR_SURFACE_AREA>
112.27

> <JCHEM_REFRACTIVITY>
150.82080000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,3S,5R,7S,8R,9S,10R,14R,15S)-3,9-bis(acetyloxy)-14-(furan-3-yl)-8-hydroxy-2,6,6,10,15-pentamethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-11-en-5-yl propanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0       0.841  -4.801   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.833  -3.624   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.310  -2.175   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -0.206  -1.904   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0       2.303  -0.998   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       3.819  -1.269   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.342  -2.717   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.858  -2.988   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       6.381  -4.437   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       5.388  -5.614   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.912  -7.062   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       3.872  -5.343   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       6.851  -1.811   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.374  -3.259   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.327  -0.363   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.320   0.815   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       6.797   2.263   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       8.836   0.544   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       9.829   1.721   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       9.306   3.169   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.790   3.440   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      10.298   4.347   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       9.359  -0.905   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      10.352   0.273   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      10.875  -1.176   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      12.091  -0.231   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      13.366  -1.095   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      12.938  -2.574   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      13.883  -3.790   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      15.422  -3.740   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      15.945  -5.188   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      14.730  -6.134   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      13.455  -5.269   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      11.399  -2.624   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      12.070  -4.010   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      10.406  -3.802   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       8.890  -3.531   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       8.367  -2.082   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       4.811  -0.092   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       5.029   1.433   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       3.670   0.942   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7   39                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   13                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10                                                            
CONECT   13    8   14   15   38                                             
CONECT   14   13                                                            
CONECT   15   13   16   39                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   23                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   18   24   25   38                                             
CONECT   24   23                                                            
CONECT   25   23   26   34                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   34                                                  
CONECT   29   28   30   33                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   29                                                       
CONECT   34   28   25   35   36                                             
CONECT   35   34                                                            
CONECT   36   34   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   23   13                                                  
CONECT   39   15    6   40   41                                             
CONECT   40   39                                                            
CONECT   41   39                                                            
MASTER        0    0    0    0    0    0    0    0   41    0   90    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₃H₄₆O₈

Average Mass

570.7230 Da

Monoisotopic Mass

570.31927 Da

IUPAC Name

(1R,2R,3S,5R,7S,8R,9S,10R,14R,15S)-3,9-bis(acetyloxy)-14-(furan-3-yl)-8-hydroxy-2,6,6,10,15-pentamethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-11-en-5-yl propanoate

Traditional Name

(1R,2R,3S,5R,7S,8R,9S,10R,14R,15S)-3,9-bis(acetyloxy)-14-(furan-3-yl)-8-hydroxy-2,6,6,10,15-pentamethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-11-en-5-yl propanoate

CAS Registry Number

Not Available

SMILES

CCC(=O)O[C@@H]1C[C@H](OC(C)=O)[C@]2(C)[C@H]3CC[C@@]4(C)[C@@H](CC=C4[C@]3(C)[C@H](OC(C)=O)[C@H](O)[C@H]2C1(C)C)C1=COC=C1

InChI Identifier

InChI=1S/C33H46O8/c1-9-26(36)41-24-16-25(39-18(2)34)33(8)23-12-14-31(6)21(20-13-15-38-17-20)10-11-22(31)32(23,7)29(40-19(3)35)27(37)28(33)30(24,4)5/h11,13,15,17,21,23-25,27-29,37H,9-10,12,14,16H2,1-8H3/t21-,23-,24+,25-,27+,28-,29+,31-,32-,33-/m0/s1

InChI Key

OLAITLNVWDKEJN-DHGKALFUSA-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
Turraea pubescens	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as limonoids. These are highly oxygenated, modified terpenoids with a prototypical structure either containing or derived from a precursor with a 4,4,8-trimethyl-17-furanylsteroid skeleton. All naturally occurring citrus limonoids contain a furan ring attached to the D-ring, at C-17, as well as oxygen containing functional groups at C-3, C-4, C-7, C-16 and C-17.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Limonoids

Alternative Parents

Substituents

Limonoid skeleton
17-furanylsteroid skeleton
Steroid ester
6-hydroxysteroid
Hydroxysteroid
Steroid
Tricarboxylic acid or derivatives
Cyclic alcohol
Heteroaromatic compound
Furan
Carboxylic acid ester
Secondary alcohol
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Carbonyl group
Alcohol
Organooxygen 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	4.13	ChemAxon
pKa (Strongest Acidic)	13.86	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	112.27 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	150.82 m³·mol⁻¹	ChemAxon
Polarizability	61.77 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

30825505

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

71725942

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,3br,4s,5r,5as,7r,9s,9ar,9br,11as)-4,9-bis(acetyloxy)-1-(furan-3-yl)-5-hydroxy-3b,6,6,9a,11a-pentamethyl-1h,2h,4h,5h,5ah,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl propanoate (NP0289939)

MOL for NP0289939 ((1r,3br,4s,5r,5as,7r,9s,9ar,9br,11as)-4,9-bis(acetyloxy)-1-(furan-3-yl)-5-hydroxy-3b,6,6,9a,11a-pentamethyl-1h,2h,4h,5h,5ah,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl propanoate)

3D MOL for NP0289939 ((1r,3br,4s,5r,5as,7r,9s,9ar,9br,11as)-4,9-bis(acetyloxy)-1-(furan-3-yl)-5-hydroxy-3b,6,6,9a,11a-pentamethyl-1h,2h,4h,5h,5ah,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl propanoate)

3D SDF for NP0289939 ((1r,3br,4s,5r,5as,7r,9s,9ar,9br,11as)-4,9-bis(acetyloxy)-1-(furan-3-yl)-5-hydroxy-3b,6,6,9a,11a-pentamethyl-1h,2h,4h,5h,5ah,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl propanoate)

3D-SDF for NP0289939 ((1r,3br,4s,5r,5as,7r,9s,9ar,9br,11as)-4,9-bis(acetyloxy)-1-(furan-3-yl)-5-hydroxy-3b,6,6,9a,11a-pentamethyl-1h,2h,4h,5h,5ah,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl propanoate)

PDB for NP0289939 ((1r,3br,4s,5r,5as,7r,9s,9ar,9br,11as)-4,9-bis(acetyloxy)-1-(furan-3-yl)-5-hydroxy-3b,6,6,9a,11a-pentamethyl-1h,2h,4h,5h,5ah,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl propanoate)

3D PDB for NP0289939 ((1r,3br,4s,5r,5as,7r,9s,9ar,9br,11as)-4,9-bis(acetyloxy)-1-(furan-3-yl)-5-hydroxy-3b,6,6,9a,11a-pentamethyl-1h,2h,4h,5h,5ah,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl propanoate)

SMILES for NP0289939 ((1r,3br,4s,5r,5as,7r,9s,9ar,9br,11as)-4,9-bis(acetyloxy)-1-(furan-3-yl)-5-hydroxy-3b,6,6,9a,11a-pentamethyl-1h,2h,4h,5h,5ah,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl propanoate)

INCHI for NP0289939 ((1r,3br,4s,5r,5as,7r,9s,9ar,9br,11as)-4,9-bis(acetyloxy)-1-(furan-3-yl)-5-hydroxy-3b,6,6,9a,11a-pentamethyl-1h,2h,4h,5h,5ah,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl propanoate)

Structure for NP0289939 ((1r,3br,4s,5r,5as,7r,9s,9ar,9br,11as)-4,9-bis(acetyloxy)-1-(furan-3-yl)-5-hydroxy-3b,6,6,9a,11a-pentamethyl-1h,2h,4h,5h,5ah,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl propanoate)

3D Structure for NP0289939 ((1r,3br,4s,5r,5as,7r,9s,9ar,9br,11as)-4,9-bis(acetyloxy)-1-(furan-3-yl)-5-hydroxy-3b,6,6,9a,11a-pentamethyl-1h,2h,4h,5h,5ah,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl propanoate)