NP-MRD: Showing NP-Card for (3S,5S,8R,9S,10S,12S,13S,14R,17R,20R)-12β-O-phenylacetyltenacigenin A (NP0331751)

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Record Information

Version

1.0

Created at

2023-08-01 08:34:01 UTC

Updated at

2024-05-09 01:52:16 UTC

NP-MRD ID

NP0331751

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3S,5S,8R,9S,10S,12S,13S,14R,17R,20R)-12β-O-phenylacetyltenacigenin A

Description

Not Available

Structure

MOL SDF PDB SMILES InChI


  Mrv2104 08012308342D          

 36 42  0  0  1  0            999 V2000
   -2.9533   -0.7634    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1524   -0.5652    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9236    0.2275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1228    0.4256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5507   -0.1688    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3305    0.6262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7795   -0.9615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2600   -1.6273    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6165   -1.4126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0577   -0.5838    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2922    0.0591    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2574    0.8834    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1933   -0.4471    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1788   -1.2681    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7009    0.5000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4063    1.2706    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9263    1.9110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6317    2.6816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1517    3.3221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8571    4.0927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3771    4.7331    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1918    4.6030    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4864    3.8324    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9664    3.1919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7410    1.7809    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5932    0.1759    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0499    0.8630    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9242   -0.1824    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5011    0.4074    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6813   -0.8513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8292   -0.1547    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0855   -0.8227    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1688   -1.4283    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7021   -1.3104    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3422   -2.2349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5804   -1.1597    0.0000 C   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
  5  4  1  0  0  0  0
  5  6  1  1  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
 10  9  1  0  0  0  0
 11 10  1  0  0  0  0
 11  5  1  0  0  0  0
 11 12  1  1  0  0  0
 11 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  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 19 24  1  0  0  0  0
 17 25  2  0  0  0  0
 15 26  1  0  0  0  0
 26 27  1  6  0  0  0
 28 26  1  0  0  0  0
 10 28  1  0  0  0  0
 28 29  1  1  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 32 31  1  1  0  0  0
 26 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 14  1  0  0  0  0
 33 34  1  0  0  0  0
 10 34  1  6  0  0  0
 33 35  1  6  0  0  0
  7 36  1  0  0  0  0
  2 36  1  0  0  0  0
M  END


  Mrv2104 08012308342D          

 36 42  0  0  1  0            999 V2000
   -2.9533   -0.7634    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1524   -0.5652    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9236    0.2275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1228    0.4256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5507   -0.1688    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3305    0.6262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7795   -0.9615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2600   -1.6273    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6165   -1.4126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0577   -0.5838    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2922    0.0591    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2574    0.8834    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1933   -0.4471    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1788   -1.2681    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7009    0.5000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4063    1.2706    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9263    1.9110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6317    2.6816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1517    3.3221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8571    4.0927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3771    4.7331    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1918    4.6030    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4864    3.8324    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9664    3.1919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7410    1.7809    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5932    0.1759    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0499    0.8630    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9242   -0.1824    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5011    0.4074    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6813   -0.8513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8292   -0.1547    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0855   -0.8227    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1688   -1.4283    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7021   -1.3104    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3422   -2.2349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5804   -1.1597    0.0000 C   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
  5  4  1  0  0  0  0
  5  6  1  1  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
 10  9  1  0  0  0  0
 11 10  1  0  0  0  0
 11  5  1  0  0  0  0
 11 12  1  1  0  0  0
 11 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  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 19 24  1  0  0  0  0
 17 25  2  0  0  0  0
 15 26  1  0  0  0  0
 26 27  1  6  0  0  0
 28 26  1  0  0  0  0
 10 28  1  0  0  0  0
 28 29  1  1  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 32 31  1  1  0  0  0
 26 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 14  1  0  0  0  0
 33 34  1  0  0  0  0
 10 34  1  6  0  0  0
 33 35  1  6  0  0  0
  7 36  1  0  0  0  0
  2 36  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0331751

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@]12[C@@H]3O[C@]4(C)O[C@@]1(CCC1C[C@@H](O)CC[C@]21C)[C@@]1(O)CC[C@@H]4[C@@]1(C)[C@H]3OC(=O)CC1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C29H38O6/c1-25-12-10-19(30)16-18(25)9-13-28-23(25)22-24(33-21(31)15-17-7-5-4-6-8-17)26(2)20(11-14-29(26,28)32)27(3,34-22)35-28/h4-8,18-20,22-24,30,32H,9-16H2,1-3H3/t18?,19-,20+,22-,23+,24-,25-,26-,27+,28+,29+/m0/s1

> <INCHI_KEY>
JLZMRNKMXYCMPT-DVYNSGFOSA-N

> <FORMULA>
C29H38O6

> <MOLECULAR_WEIGHT>
482.617

> <EXACT_MASS>
482.266838944

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
73

> <JCHEM_AVERAGE_POLARIZABILITY>
52.80400105000322

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2S,3S,6S,11R,13R,14R,17R,18S,19R)-6,17-dihydroxy-3,13,18-trimethyl-12,20-dioxahexacyclo[11.6.1.0^{2,11}.0^{3,8}.0^{11,17}.0^{14,18}]icosan-19-yl 2-phenylacetate

> <JCHEM_LOGP>
3.3823262463333323

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
18.296394135279364

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.240373584106553

> <JCHEM_PKA_STRONGEST_BASIC>
-1.3561532131946852

> <JCHEM_POLAR_SURFACE_AREA>
85.22

> <JCHEM_REFRACTIVITY>
128.07950000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,3S,6S,11R,13R,14R,17R,18S,19R)-6,17-dihydroxy-3,13,18-trimethyl-12,20-dioxahexacyclo[11.6.1.0^{2,11}.0^{3,8}.0^{11,17}.0^{14,18}]icosan-19-yl 2-phenylacetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 01-AUG-23   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   01-AUG-23         0                                  
HETATM    1  O   UNK     0      -5.513  -1.425   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      -4.018  -1.055   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.591   0.425   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.096   0.794   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.028  -0.315   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.617   1.169   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.455  -1.795   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.485  -3.038   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.151  -2.637   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.974  -1.090   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.545   0.110   0.000  0.00  0.00           C+0
HETATM   12  H   UNK     0       0.480   1.649   0.000  0.00  0.00           H+0
HETATM   13  C   UNK     0       0.361  -0.835   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       0.334  -2.367   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       1.308   0.933   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       0.758   2.372   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       1.729   3.567   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.179   5.006   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.150   6.201   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.600   7.640   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.571   8.835   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.091   8.592   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.641   7.154   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.671   5.958   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       3.250   3.324   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       2.974   0.328   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       3.827   1.611   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.592  -0.340   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       4.669   0.760   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       5.005  -1.589   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       5.281  -0.289   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       3.893  -1.536   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       2.182  -2.666   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       3.177  -2.446   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       2.505  -4.172   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -2.950  -2.165   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   36                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7   11                                             
CONECT    6    5                                                            
CONECT    7    5    8   36                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   28   34                                             
CONECT   11   10    5   12   13                                             
CONECT   12   11                                                            
CONECT   13   11   14   15                                                  
CONECT   14   13   33                                                       
CONECT   15   13   16   26                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   25                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   24                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   19                                                       
CONECT   25   17                                                            
CONECT   26   15   27   28   32                                             
CONECT   27   26                                                            
CONECT   28   26   10   29   30                                             
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   26   33                                                  
CONECT   33   32   14   34   35                                             
CONECT   34   33   10                                                       
CONECT   35   33                                                            
CONECT   36    7    2                                                       
MASTER        0    0    0    0    0    0    0    0   36    0   84    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₉H₃₈O₆

Average Mass

482.6170 Da

Monoisotopic Mass

482.26684 Da

IUPAC Name

(1S,2S,3S,6S,11R,13R,14R,17R,18S,19R)-6,17-dihydroxy-3,13,18-trimethyl-12,20-dioxahexacyclo[11.6.1.0^{2,11}.0^{3,8}.0^{11,17}.0^{14,18}]icosan-19-yl 2-phenylacetate

Traditional Name

(1S,2S,3S,6S,11R,13R,14R,17R,18S,19R)-6,17-dihydroxy-3,13,18-trimethyl-12,20-dioxahexacyclo[11.6.1.0^{2,11}.0^{3,8}.0^{11,17}.0^{14,18}]icosan-19-yl 2-phenylacetate

CAS Registry Number

Not Available

SMILES

[H][C@]12[C@@H]3O[C@]4(C)O[C@@]1(CCC1C[C@@H](O)CC[C@]21C)[C@@]1(O)CC[C@@H]4[C@@]1(C)[C@H]3OC(=O)CC1=CC=CC=C1

InChI Identifier

InChI=1S/C29H38O6/c1-25-12-10-19(30)16-18(25)9-13-28-23(25)22-24(33-21(31)15-17-7-5-4-6-8-17)26(2)20(11-14-29(26,28)32)27(3,34-22)35-28/h4-8,18-20,22-24,30,32H,9-16H2,1-3H3/t18?,19-,20+,22-,23+,24-,25-,26-,27+,28+,29+/m0/s1

InChI Key

JLZMRNKMXYCMPT-DVYNSGFOSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D_DEPT NMR	¹³C NMR Spectrum (1D, 101 MHz, CDCl3, experimental)	xht8710@163.com	Not Available	Not Available	2024-05-09	View Spectrum
NOESY NMR	[¹H, ¹H] NMR Spectrum (2D, 400 MHz, CDCl3, experimental)	xht8710@163.com	Not Available	Not Available	2023-08-01	View Spectrum
COSY NMR	[¹H, ¹H] NMR Spectrum (2D, 400 MHz, CDCl3, experimental)	xht8710@163.com	Not Available	Not Available	2023-08-01	View Spectrum
HMBC NMR	[¹H, ¹³C] NMR Spectrum (2D, 400 MHz, CDCl3, experimental)	xht8710@163.com	Not Available	Not Available	2023-08-01	View Spectrum
HSQC NMR	[¹H, ¹³C] NMR Spectrum (2D, 400 MHz, CDCl3, experimental)	xht8710@163.com	Not Available	Not Available	2023-08-01	View Spectrum
1D NMR	[¹³C, ] NMR Spectrum (2D, 101 MHz, CDCl3, experimental)	xht8710@163.com	Not Available	Not Available	2023-08-01	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 400 MHz, CDCl3, experimental)	xht8710@163.com	Not Available	Not Available	2023-08-01	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹H NMR Spectrum (1D, 400, CDCl₃, simulated)	Not Available	Not Available	Not Available	2024-05-09	View Spectrum

Species

Species of Origin

Species Name	Source	Reference
tenacissima		Not Available

Chemical Taxonomy

Classification

Not classified

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	3.38	ChemAxon
pKa (Strongest Acidic)	13.24	ChemAxon
pKa (Strongest Basic)	-1.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	85.22 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	128.08 m³·mol⁻¹	ChemAxon
Polarizability	52.8 Å³	ChemAxon
Number of Rings	7	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

Not Available

References

General References

Liu JL, Xu HT, Mu DD, Han X, Du TT, Wang YL, Wei XH, Chou GX: C(21) steroids from the roots of Marsdenia tenacissima. Phytochemistry. 2023 Sep;213:113782. doi: 10.1016/j.phytochem.2023.113782. Epub 2023 Jul 13. [PubMed:37451564 ]

Showing NP-Card for (3S,5S,8R,9S,10S,12S,13S,14R,17R,20R)-12β-O-phenylacetyltenacigenin A (NP0331751)

MOL for NP0331751 ((3S,5S,8R,9S,10S,12S,13S,14R,17R,20R)-12β-O-phenylacetyltenacigenin A)

3D MOL for NP0331751 ((3S,5S,8R,9S,10S,12S,13S,14R,17R,20R)-12β-O-phenylacetyltenacigenin A)

3D SDF for NP0331751 ((3S,5S,8R,9S,10S,12S,13S,14R,17R,20R)-12β-O-phenylacetyltenacigenin A)

3D-SDF for NP0331751 ((3S,5S,8R,9S,10S,12S,13S,14R,17R,20R)-12β-O-phenylacetyltenacigenin A)

PDB for NP0331751 ((3S,5S,8R,9S,10S,12S,13S,14R,17R,20R)-12β-O-phenylacetyltenacigenin A)

3D PDB for NP0331751 ((3S,5S,8R,9S,10S,12S,13S,14R,17R,20R)-12β-O-phenylacetyltenacigenin A)

SMILES for NP0331751 ((3S,5S,8R,9S,10S,12S,13S,14R,17R,20R)-12β-O-phenylacetyltenacigenin A)

INCHI for NP0331751 ((3S,5S,8R,9S,10S,12S,13S,14R,17R,20R)-12β-O-phenylacetyltenacigenin A)

Structure for NP0331751 ((3S,5S,8R,9S,10S,12S,13S,14R,17R,20R)-12β-O-phenylacetyltenacigenin A)

3D Structure for NP0331751 ((3S,5S,8R,9S,10S,12S,13S,14R,17R,20R)-12β-O-phenylacetyltenacigenin A)