NP-MRD: Showing NP-Card for (1s,3r,4ar,6r,6as,6bs,7ar,10s,10as,12ar,12bs)-10-(furan-3-yl)-3,6-dihydroxy-4,4,6a,10a,12b-pentamethyl-8-oxo-dodecahydrochryseno[4,4a-b]oxiren-1-yl acetate (NP0218593)

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Record Information

Version

2.0

Created at

2022-09-05 19:18:03 UTC

Updated at

2022-09-05 19:18:03 UTC

NP-MRD ID

NP0218593

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,3r,4ar,6r,6as,6bs,7ar,10s,10as,12ar,12bs)-10-(furan-3-yl)-3,6-dihydroxy-4,4,6a,10a,12b-pentamethyl-8-oxo-dodecahydrochryseno[4,4a-b]oxiren-1-yl acetate

Description

(1S,2S,4R,7R,8S,11R,12S,13S,15R,17R,19R)-7-(furan-3-yl)-15,19-dihydroxy-1,8,12,16,16-pentamethyl-5-oxo-3-oxapentacyclo[9.8.0.0²,⁴.0²,⁸.0¹²,¹⁷]Nonadecan-13-yl acetate belongs to the class of organic compounds known as oxepanes. Oxepanes are compounds containing an oxepane ring, which is a seven-member saturated aliphatic heterocycle with one oxygen and six carbon atoms. (1s,3r,4ar,6r,6as,6bs,7ar,10s,10as,12ar,12bs)-10-(furan-3-yl)-3,6-dihydroxy-4,4,6a,10a,12b-pentamethyl-8-oxo-dodecahydrochryseno[4,4a-b]oxiren-1-yl acetate is found in Khaya senegalensis. Based on a literature review very few articles have been published on (1S,2S,4R,7R,8S,11R,12S,13S,15R,17R,19R)-7-(furan-3-yl)-15,19-dihydroxy-1,8,12,16,16-pentamethyl-5-oxo-3-oxapentacyclo[9.8.0.0²,⁴.0²,⁸.0¹²,¹⁷]Nonadecan-13-yl acetate.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309052221182D          

 36 41  0  0  1  0            999 V2000
    4.2251   -2.5498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4951   -1.7702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3052   -1.6143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9550   -1.1466    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2251   -0.3671    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0352   -0.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3052    0.5684    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.1154    0.7243    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7651    1.1921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4731    1.6156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4709    1.9628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9550    1.0361    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4149    1.6598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6048    1.5039    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0647    2.1275    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3347    0.7243    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2644    1.5463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8748    0.1007    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6048   -0.6789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7946   -0.8348    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2546   -0.2111    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9845   -0.9907    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4444   -0.3671    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1744   -1.1466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6463   -1.8233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1486   -2.4812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6310   -2.2112    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6150   -1.3863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0957    0.2566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1744    1.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3657    1.6598    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9845    1.1921    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7946    1.3480    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5246    0.5684    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6850    0.2566    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4149   -0.5230    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
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  6  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
  9 12  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 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
 21 22  1  6  0  0  0
 21 23  1  0  0  0  0
 23 24  1  6  0  0  0
 24 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
 24 28  2  0  0  0  0
 23 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  6  0  0  0
 34 33  1  6  0  0  0
 32 34  1  0  0  0  0
 21 34  1  0  0  0  0
 16 34  1  0  0  0  0
 18 35  1  0  0  0  0
  5 35  1  0  0  0  0
 12 35  1  0  0  0  0
 35 36  1  1  0  0  0
M  END


  Mrv1652309052221182D          

 36 41  0  0  1  0            999 V2000
    4.2251   -2.5498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4951   -1.7702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3052   -1.6143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9550   -1.1466    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2251   -0.3671    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0352   -0.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3052    0.5684    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.1154    0.7243    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7651    1.1921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4731    1.6156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4709    1.9628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9550    1.0361    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4149    1.6598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6048    1.5039    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0647    2.1275    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3347    0.7243    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2644    1.5463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8748    0.1007    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6048   -0.6789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7946   -0.8348    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2546   -0.2111    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9845   -0.9907    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4444   -0.3671    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1744   -1.1466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6463   -1.8233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1486   -2.4812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6310   -2.2112    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6150   -1.3863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0957    0.2566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1744    1.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3657    1.6598    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9845    1.1921    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7946    1.3480    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5246    0.5684    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6850    0.2566    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4149   -0.5230    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
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  6  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
  9 12  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 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
 21 22  1  6  0  0  0
 21 23  1  0  0  0  0
 23 24  1  6  0  0  0
 24 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
 24 28  2  0  0  0  0
 23 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  6  0  0  0
 34 33  1  6  0  0  0
 32 34  1  0  0  0  0
 21 34  1  0  0  0  0
 16 34  1  0  0  0  0
 18 35  1  0  0  0  0
  5 35  1  0  0  0  0
 12 35  1  0  0  0  0
 35 36  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0218593

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)O[C@H]1C[C@@H](O)C(C)(C)[C@H]2C[C@@H](O)[C@]3(C)[C@H](CC[C@@]4(C)[C@@H](CC(=O)[C@@H]5O[C@]345)C3=COC=C3)[C@@]12C

> <INCHI_IDENTIFIER>
InChI=1S/C29H40O7/c1-15(30)35-23-13-21(32)25(2,3)20-12-22(33)28(6)19(27(20,23)5)7-9-26(4)17(16-8-10-34-14-16)11-18(31)24-29(26,28)36-24/h8,10,14,17,19-24,32-33H,7,9,11-13H2,1-6H3/t17-,19+,20+,21+,22+,23-,24-,26-,27+,28-,29-/m0/s1

> <INCHI_KEY>
GTODYYAOVGMZSU-RAMIVWMLSA-N

> <FORMULA>
C29H40O7

> <MOLECULAR_WEIGHT>
500.632

> <EXACT_MASS>
500.277403628

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
76

> <JCHEM_AVERAGE_POLARIZABILITY>
54.10585187597761

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2S,4R,7R,8S,11R,12S,13S,15R,17R,19R)-7-(furan-3-yl)-15,19-dihydroxy-1,8,12,16,16-pentamethyl-5-oxo-3-oxapentacyclo[9.8.0.0^{2,4}.0^{2,8}.0^{12,17}]nonadecan-13-yl acetate

> <JCHEM_LOGP>
2.809777760333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.91081091802953

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.308928316978854

> <JCHEM_PKA_STRONGEST_BASIC>
-2.861110590310806

> <JCHEM_POLAR_SURFACE_AREA>
109.5

> <JCHEM_REFRACTIVITY>
130.047

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,4R,7R,8S,11R,12S,13S,15R,17R,19R)-7-(furan-3-yl)-15,19-dihydroxy-1,8,12,16,16-pentamethyl-5-oxo-3-oxapentacyclo[9.8.0.0^{2,4}.0^{2,8}.0^{12,17}]nonadecan-13-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       7.887  -4.760   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.391  -3.304   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       9.903  -3.013   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       7.383  -2.140   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       7.887  -0.685   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.399  -0.394   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.903   1.061   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      11.415   1.352   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       8.895   2.225   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.216   3.016   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.346   3.664   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.383   1.934   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.375   3.098   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.862   2.807   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       3.854   3.971   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       4.358   1.352   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.227   2.886   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.366   0.188   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.862  -1.267   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.350  -1.558   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.342  -0.394   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.838  -1.849   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.830  -0.685   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.326  -2.140   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.206  -3.403   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.277  -4.632   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -1.178  -4.128   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      -1.148  -2.588   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -0.179   0.479   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       0.326   1.934   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      -0.683   3.098   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       1.838   2.225   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       3.350   2.516   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       2.846   1.061   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       6.879   0.479   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       6.375  -0.976   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   35                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   11   12                                             
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    9   13   35                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   18   34                                             
CONECT   17   16                                                            
CONECT   18   16   19   35                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23   34                                             
CONECT   22   21                                                            
CONECT   23   21   24   29                                                  
CONECT   24   23   25   28                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   24                                                       
CONECT   29   23   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33   34                                                  
CONECT   33   32   34                                                       
CONECT   34   33   32   21   16                                             
CONECT   35   18    5   12   36                                             
CONECT   36   35                                                            
MASTER        0    0    0    0    0    0    0    0   36    0   82    0
END

View in JSmol

Synonyms

Value	Source
(1S,2S,4R,7R,8S,11R,12S,13S,15R,17R,19R)-7-(Furan-3-yl)-15,19-dihydroxy-1,8,12,16,16-pentamethyl-5-oxo-3-oxapentacyclo[9.8.0.0,.0,.0,]nonadecan-13-yl acetic acid	Generator

Chemical Formula

C₂₉H₄₀O₇

Average Mass

500.6320 Da

Monoisotopic Mass

500.27740 Da

IUPAC Name

(1S,2S,4R,7R,8S,11R,12S,13S,15R,17R,19R)-7-(furan-3-yl)-15,19-dihydroxy-1,8,12,16,16-pentamethyl-5-oxo-3-oxapentacyclo[9.8.0.0^{2,4}.0^{2,8}.0^{12,17}]nonadecan-13-yl acetate

Traditional Name

(1S,2S,4R,7R,8S,11R,12S,13S,15R,17R,19R)-7-(furan-3-yl)-15,19-dihydroxy-1,8,12,16,16-pentamethyl-5-oxo-3-oxapentacyclo[9.8.0.0^{2,4}.0^{2,8}.0^{12,17}]nonadecan-13-yl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)O[C@H]1C[C@@H](O)C(C)(C)[C@H]2C[C@@H](O)[C@]3(C)[C@H](CC[C@@]4(C)[C@@H](CC(=O)[C@@H]5O[C@]345)C3=COC=C3)[C@@]12C

InChI Identifier

InChI=1S/C29H40O7/c1-15(30)35-23-13-21(32)25(2,3)20-12-22(33)28(6)19(27(20,23)5)7-9-26(4)17(16-8-10-34-14-16)11-18(31)24-29(26,28)36-24/h8,10,14,17,19-24,32-33H,7,9,11-13H2,1-6H3/t17-,19+,20+,21+,22+,23-,24-,26-,27+,28-,29-/m0/s1

InChI Key

GTODYYAOVGMZSU-RAMIVWMLSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Khaya senegalensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oxepanes. Oxepanes are compounds containing an oxepane ring, which is a seven-member saturated aliphatic heterocycle with one oxygen and six carbon atoms.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Oxepanes

Sub Class

Not Available

Direct Parent

Oxepanes

Alternative Parents

Substituents

Oxepane
Cyclic alcohol
Furan
Heteroaromatic compound
Carboxylic acid ester
Ketone
Secondary alcohol
Monocarboxylic acid or derivatives
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Oxacycle
Organooxygen compound
Organic oxide
Organic oxygen compound
Alcohol
Hydrocarbon derivative
Carbonyl group
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	2.81	ChemAxon
pKa (Strongest Acidic)	14.31	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	109.5 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	130.05 m³·mol⁻¹	ChemAxon
Polarizability	54.11 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

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

163032761

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,3r,4ar,6r,6as,6bs,7ar,10s,10as,12ar,12bs)-10-(furan-3-yl)-3,6-dihydroxy-4,4,6a,10a,12b-pentamethyl-8-oxo-dodecahydrochryseno[4,4a-b]oxiren-1-yl acetate (NP0218593)

MOL for NP0218593 ((1s,3r,4ar,6r,6as,6bs,7ar,10s,10as,12ar,12bs)-10-(furan-3-yl)-3,6-dihydroxy-4,4,6a,10a,12b-pentamethyl-8-oxo-dodecahydrochryseno[4,4a-b]oxiren-1-yl acetate)

3D MOL for NP0218593 ((1s,3r,4ar,6r,6as,6bs,7ar,10s,10as,12ar,12bs)-10-(furan-3-yl)-3,6-dihydroxy-4,4,6a,10a,12b-pentamethyl-8-oxo-dodecahydrochryseno[4,4a-b]oxiren-1-yl acetate)

3D SDF for NP0218593 ((1s,3r,4ar,6r,6as,6bs,7ar,10s,10as,12ar,12bs)-10-(furan-3-yl)-3,6-dihydroxy-4,4,6a,10a,12b-pentamethyl-8-oxo-dodecahydrochryseno[4,4a-b]oxiren-1-yl acetate)

3D-SDF for NP0218593 ((1s,3r,4ar,6r,6as,6bs,7ar,10s,10as,12ar,12bs)-10-(furan-3-yl)-3,6-dihydroxy-4,4,6a,10a,12b-pentamethyl-8-oxo-dodecahydrochryseno[4,4a-b]oxiren-1-yl acetate)

PDB for NP0218593 ((1s,3r,4ar,6r,6as,6bs,7ar,10s,10as,12ar,12bs)-10-(furan-3-yl)-3,6-dihydroxy-4,4,6a,10a,12b-pentamethyl-8-oxo-dodecahydrochryseno[4,4a-b]oxiren-1-yl acetate)

3D PDB for NP0218593 ((1s,3r,4ar,6r,6as,6bs,7ar,10s,10as,12ar,12bs)-10-(furan-3-yl)-3,6-dihydroxy-4,4,6a,10a,12b-pentamethyl-8-oxo-dodecahydrochryseno[4,4a-b]oxiren-1-yl acetate)

SMILES for NP0218593 ((1s,3r,4ar,6r,6as,6bs,7ar,10s,10as,12ar,12bs)-10-(furan-3-yl)-3,6-dihydroxy-4,4,6a,10a,12b-pentamethyl-8-oxo-dodecahydrochryseno[4,4a-b]oxiren-1-yl acetate)

INCHI for NP0218593 ((1s,3r,4ar,6r,6as,6bs,7ar,10s,10as,12ar,12bs)-10-(furan-3-yl)-3,6-dihydroxy-4,4,6a,10a,12b-pentamethyl-8-oxo-dodecahydrochryseno[4,4a-b]oxiren-1-yl acetate)

Structure for NP0218593 ((1s,3r,4ar,6r,6as,6bs,7ar,10s,10as,12ar,12bs)-10-(furan-3-yl)-3,6-dihydroxy-4,4,6a,10a,12b-pentamethyl-8-oxo-dodecahydrochryseno[4,4a-b]oxiren-1-yl acetate)

3D Structure for NP0218593 ((1s,3r,4ar,6r,6as,6bs,7ar,10s,10as,12ar,12bs)-10-(furan-3-yl)-3,6-dihydroxy-4,4,6a,10a,12b-pentamethyl-8-oxo-dodecahydrochryseno[4,4a-b]oxiren-1-yl acetate)