NP-MRD: Showing NP-Card for 6-hydroxy-7-{[5-({4-hydroxy-5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-4-methoxy-6-methyloxan-2-yl]oxy}-4b-methyl-2-(2-methylfuran-3-yl)-2,3,4,4a,5,6,7,8,10,10a-decahydrophenanthren-1-one (NP0193676)

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Record Information

Version

2.0

Created at

2022-09-04 11:11:47 UTC

Updated at

2022-09-04 11:11:48 UTC

NP-MRD ID

NP0193676

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6-hydroxy-7-{[5-({4-hydroxy-5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-4-methoxy-6-methyloxan-2-yl]oxy}-4b-methyl-2-(2-methylfuran-3-yl)-2,3,4,4a,5,6,7,8,10,10a-decahydrophenanthren-1-one

Description

6-Hydroxy-7-{[5-({4-hydroxy-5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-4-methoxy-6-methyloxan-2-yl]oxy}-4b-methyl-2-(2-methylfuran-3-yl)-1,2,3,4,4a,4b,5,6,7,8,10,10a-dodecahydrophenanthren-1-one belongs to the class of organic compounds known as oligosaccharides. These are carbohydrates made up of 3 to 10 monosaccharide units linked to each other through glycosidic bonds. 6-hydroxy-7-{[5-({4-hydroxy-5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-4-methoxy-6-methyloxan-2-yl]oxy}-4b-methyl-2-(2-methylfuran-3-yl)-2,3,4,4a,5,6,7,8,10,10a-decahydrophenanthren-1-one is found in Cynanchum ascyrifolium, Vincetoxicum atratum and Vincetoxicum sublanceolatum. 6-Hydroxy-7-{[5-({4-hydroxy-5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-4-methoxy-6-methyloxan-2-yl]oxy}-4b-methyl-2-(2-methylfuran-3-yl)-1,2,3,4,4a,4b,5,6,7,8,10,10a-dodecahydrophenanthren-1-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004151518422D          

 53 59  0  0  0  0            999 V2000
    0.2211    3.4618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6039    3.4618    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.8414    4.1763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2539    4.8908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0789    4.8908    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4914    4.1763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3164    4.1763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.3164    2.7474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.2211    4.8908    0.0000 O   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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
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  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
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 17 18  1  0  0  0  0
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 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 17 22  1  0  0  0  0
 22 23  1  0  0  0  0
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 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
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 28 33  1  0  0  0  0
 33 34  2  0  0  0  0
 32 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 35 39  2  0  0  0  0
 39 40  1  0  0  0  0
 29 41  1  0  0  0  0
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 41 42  1  0  0  0  0
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 11 46  1  0  0  0  0
 46 47  1  0  0  0  0
  7 47  1  0  0  0  0
 47 48  1  0  0  0  0
  5 49  1  0  0  0  0
 49 50  1  0  0  0  0
 50 51  1  0  0  0  0
 50 52  1  0  0  0  0
  3 52  1  0  0  0  0
 52 53  1  0  0  0  0
M  END

     RDKit          3D

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M  END


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M  END
> <DATABASE_ID>
NP0193676

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1CC(OC2C(O)CC(OC3C(C)OC(CC3OC)OC3CC4=CCC5C(CCC(C6=C(C)OC=C6)C5=O)C4(C)CC3O)OC2C)OC(C)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C40H60O13/c1-19-24(12-13-47-19)25-10-11-27-26(37(25)44)9-8-23-14-30(29(42)18-40(23,27)5)51-34-17-32(46-7)39(22(4)50-34)53-33-15-28(41)38(21(3)49-33)52-35-16-31(45-6)36(43)20(2)48-35/h8,12-13,20-22,25-36,38-39,41-43H,9-11,14-18H2,1-7H3

> <INCHI_KEY>
MUUBBCBSCRKBGH-UHFFFAOYSA-N

> <FORMULA>
C40H60O13

> <MOLECULAR_WEIGHT>
748.907

> <EXACT_MASS>
748.403391992

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_ATOM_COUNT>
113

> <JCHEM_AVERAGE_POLARIZABILITY>
83.44796719872633

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
6-hydroxy-7-{[5-({4-hydroxy-5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-4-methoxy-6-methyloxan-2-yl]oxy}-4b-methyl-2-(2-methylfuran-3-yl)-1,2,3,4,4a,4b,5,6,7,8,10,10a-dodecahydrophenanthren-1-one

> <ALOGPS_LOGP>
2.74

> <JCHEM_LOGP>
4.008893444999998

> <ALOGPS_LOGS>
-4.00

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.604609101469304

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.029247037416248

> <JCHEM_PKA_STRONGEST_BASIC>
-2.760056422124695

> <JCHEM_POLAR_SURFACE_AREA>
164.73999999999998

> <JCHEM_REFRACTIVITY>
189.5351

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
7.57e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6-hydroxy-7-{[5-({4-hydroxy-5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-4-methoxy-6-methyloxan-2-yl]oxy}-4b-methyl-2-(2-methylfuran-3-yl)-2,3,4,4a,5,6,7,8,10,10a-decahydrophenanthren-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 15-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   15-APR-15         0                                  
HETATM    1  C   UNK     0       0.413   6.462   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -1.127   6.462   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -1.897   7.796   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -3.437   7.796   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -4.207   9.129   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -5.747   9.129   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      -6.517   7.796   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -8.057   7.796   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -8.827   9.129   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -8.827   6.462   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -8.057   5.128   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -8.827   3.795   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -8.057   2.461   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -6.517   2.461   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -5.747   3.795   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -5.747   1.127   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -6.517  -0.206   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -8.057  -0.206   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -8.827   1.127   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0     -10.367   1.127   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0     -11.137   2.461   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -5.747  -1.540   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -4.207  -1.540   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -3.437  -2.874   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -1.897  -2.874   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -1.127  -4.207   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.413  -4.207   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       1.183  -2.874   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       0.413  -1.540   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       1.183  -0.206   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       2.723  -0.206   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       3.493  -1.540   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       2.723  -2.874   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       3.493  -4.207   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       5.033  -1.540   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       5.938  -0.294   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       7.402  -0.770   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       7.402  -2.310   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       5.938  -2.786   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       5.462  -4.251   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -1.127  -1.540   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -0.357  -0.206   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      -1.897  -0.206   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      -3.437  -0.206   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0      -4.207   1.127   0.000  0.00  0.00           O+0
HETATM   46  O   UNK     0      -6.517   5.128   0.000  0.00  0.00           O+0
HETATM   47  C   UNK     0      -5.747   6.462   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      -4.207   6.462   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0      -3.437  10.463   0.000  0.00  0.00           O+0
HETATM   50  C   UNK     0      -1.897  10.463   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      -1.127  11.797   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      -1.127   9.129   0.000  0.00  0.00           C+0
HETATM   53  O   UNK     0       0.413   9.129   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   52                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   49                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   47                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   46                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   19                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18   22                                                  
CONECT   18   17   19                                                       
CONECT   19   18   13   20                                                  
CONECT   20   19   21                                                       
CONECT   21   20                                                            
CONECT   22   17   23                                                       
CONECT   23   22   24   44                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26   41                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   33                                                  
CONECT   29   28   30   41                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33   35                                                  
CONECT   33   32   28   34                                                  
CONECT   34   33                                                            
CONECT   35   32   36   39                                                  
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   35   40                                                  
CONECT   40   39                                                            
CONECT   41   29   25   42   43                                             
CONECT   42   41                                                            
CONECT   43   41   44                                                       
CONECT   44   43   23   45                                                  
CONECT   45   44                                                            
CONECT   46   11   47                                                       
CONECT   47   46    7   48                                                  
CONECT   48   47                                                            
CONECT   49    5   50                                                       
CONECT   50   49   51   52                                                  
CONECT   51   50                                                            
CONECT   52   50    3   53                                                  
CONECT   53   52                                                            
MASTER        0    0    0    0    0    0    0    0   53    0  118    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₀H₆₀O₁₃

Average Mass

748.9070 Da

Monoisotopic Mass

748.40339 Da

IUPAC Name

Traditional Name

CAS Registry Number

Not Available

SMILES

COC1CC(OC2C(O)CC(OC3C(C)OC(CC3OC)OC3CC4=CCC5C(CCC(C6=C(C)OC=C6)C5=O)C4(C)CC3O)OC2C)OC(C)C1O

InChI Identifier

InChI=1S/C40H60O13/c1-19-24(12-13-47-19)25-10-11-27-26(37(25)44)9-8-23-14-30(29(42)18-40(23,27)5)51-34-17-32(46-7)39(22(4)50-34)53-33-15-28(41)38(21(3)49-33)52-35-16-31(45-6)36(43)20(2)48-35/h8,12-13,20-22,25-36,38-39,41-43H,9-11,14-18H2,1-7H3

InChI Key

MUUBBCBSCRKBGH-UHFFFAOYSA-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
Cynanchum ascyrifolium	LOTUS Database	35616633
Vincetoxicum atratum	LOTUS Database	35616633
Vincetoxicum sublanceolatum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oligosaccharides. These are carbohydrates made up of 3 to 10 monosaccharide units linked to each other through glycosidic bonds.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Oligosaccharides

Alternative Parents

Substituents

Oligosaccharide
Hydrophenanthrene
Phenanthrene
Glycosyl compound
O-glycosyl compound
Oxane
Cyclic alcohol
Furan
Heteroaromatic compound
Ketone
Secondary alcohol
Organoheterocyclic compound
Oxacycle
Ether
Dialkyl ether
Acetal
Hydrocarbon derivative
Organic oxide
Carbonyl group
Alcohol
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	2.74	ALOGPS
logP	4.01	ChemAxon
logS	-4	ALOGPS
pKa (Strongest Acidic)	13.03	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	12	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	164.74 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	189.54 m³·mol⁻¹	ChemAxon
Polarizability	83.45 Å³	ChemAxon
Number of Rings	7	ChemAxon
Bioavailability	No	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

73120310

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 6-hydroxy-7-{[5-({4-hydroxy-5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-4-methoxy-6-methyloxan-2-yl]oxy}-4b-methyl-2-(2-methylfuran-3-yl)-2,3,4,4a,5,6,7,8,10,10a-decahydrophenanthren-1-one (NP0193676)

MOL for NP0193676 (6-hydroxy-7-{[5-({4-hydroxy-5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-4-methoxy-6-methyloxan-2-yl]oxy}-4b-methyl-2-(2-methylfuran-3-yl)-2,3,4,4a,5,6,7,8,10,10a-decahydrophenanthren-1-one)

3D MOL for NP0193676 (6-hydroxy-7-{[5-({4-hydroxy-5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-4-methoxy-6-methyloxan-2-yl]oxy}-4b-methyl-2-(2-methylfuran-3-yl)-2,3,4,4a,5,6,7,8,10,10a-decahydrophenanthren-1-one)

3D SDF for NP0193676 (6-hydroxy-7-{[5-({4-hydroxy-5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-4-methoxy-6-methyloxan-2-yl]oxy}-4b-methyl-2-(2-methylfuran-3-yl)-2,3,4,4a,5,6,7,8,10,10a-decahydrophenanthren-1-one)

3D-SDF for NP0193676 (6-hydroxy-7-{[5-({4-hydroxy-5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-4-methoxy-6-methyloxan-2-yl]oxy}-4b-methyl-2-(2-methylfuran-3-yl)-2,3,4,4a,5,6,7,8,10,10a-decahydrophenanthren-1-one)

PDB for NP0193676 (6-hydroxy-7-{[5-({4-hydroxy-5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-4-methoxy-6-methyloxan-2-yl]oxy}-4b-methyl-2-(2-methylfuran-3-yl)-2,3,4,4a,5,6,7,8,10,10a-decahydrophenanthren-1-one)

3D PDB for NP0193676 (6-hydroxy-7-{[5-({4-hydroxy-5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-4-methoxy-6-methyloxan-2-yl]oxy}-4b-methyl-2-(2-methylfuran-3-yl)-2,3,4,4a,5,6,7,8,10,10a-decahydrophenanthren-1-one)

SMILES for NP0193676 (6-hydroxy-7-{[5-({4-hydroxy-5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-4-methoxy-6-methyloxan-2-yl]oxy}-4b-methyl-2-(2-methylfuran-3-yl)-2,3,4,4a,5,6,7,8,10,10a-decahydrophenanthren-1-one)

INCHI for NP0193676 (6-hydroxy-7-{[5-({4-hydroxy-5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-4-methoxy-6-methyloxan-2-yl]oxy}-4b-methyl-2-(2-methylfuran-3-yl)-2,3,4,4a,5,6,7,8,10,10a-decahydrophenanthren-1-one)

Structure for NP0193676 (6-hydroxy-7-{[5-({4-hydroxy-5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-4-methoxy-6-methyloxan-2-yl]oxy}-4b-methyl-2-(2-methylfuran-3-yl)-2,3,4,4a,5,6,7,8,10,10a-decahydrophenanthren-1-one)

3D Structure for NP0193676 (6-hydroxy-7-{[5-({4-hydroxy-5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-4-methoxy-6-methyloxan-2-yl]oxy}-4b-methyl-2-(2-methylfuran-3-yl)-2,3,4,4a,5,6,7,8,10,10a-decahydrophenanthren-1-one)