NP-MRD: Showing NP-Card for 23-Acetoxysoladulcidine (NP0046160)

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Record Information

Version

2.0

Created at

2022-03-17 19:49:27 UTC

Updated at

2022-03-17 19:49:27 UTC

NP-MRD ID

NP0046160

Secondary Accession Numbers

None

Natural Product Identification

Common Name

23-Acetoxysoladulcidine

Description

23-Acetoxysoladulcidine belongs to the class of organic compounds known as spirosolanes and derivatives. These are steroidal alkaloids with a structure containing a spirosolane skeleton. Siporosolane is a polycyclic compound that is characterized by a 1-oxa-6-azaspiro[4.5]Decane moiety where the oxolane ring is fused to a docosahydronaphth[2,1:4',5']Indene ring system. Spirosolane arises from the conversion of a cholestane side-chain into a bicyclic system containing a piperidine and a tetrahydrofuran ring. 23-Acetoxysoladulcidine is a very strong basic compound (based on its pKa). Outside of the human body, 23-acetoxysoladulcidine has been detected, but not quantified in, garden tomato. 23-Acetoxysoladulcidine is found in Lycopersicon esculentum-Lycopersicon hirsutum hybrid and Lycopersicon hirsutum hybrid. This could make 23-acetoxysoladulcidine a potential biomarker for the consumption of these foods.

Structure

MOL SDF PDB SMILES InChI


  Mrv0541 02241210432D          

 34 39  0  0  0  0            999 V2000
    3.2160   -1.6491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4739   -1.3189    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8858   -0.5768    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6476   -1.4847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8135   -2.3097    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4739   -2.8044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2160   -2.4741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8751   -2.8872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8241   -1.7320    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2451   -1.2374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5783   -0.9900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5783   -0.1651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3203    0.2466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0638   -0.1651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7229    0.4124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7229    1.2359    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3820    1.6490    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4649    2.4741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2083    2.8872    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8058    2.8872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1453    2.3911    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9808    1.5662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3203    2.2267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3203    1.0715    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5783    1.4018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0806    0.9885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1636    0.1636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9056    0.4939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6583   -0.4939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4002   -0.7427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0608   -0.0822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7587   -0.5623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1822    0.2015    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2083   -1.3101    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  7  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  3 32  1  0  0  0  0
  4  5  1  0  0  0  0
  4  9  1  0  0  0  0
  4 30  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 29  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 27  1  0  0  0  0
 13 14  1  0  0  0  0
 13 24  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 22  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  2  0  0  0  0
M  END


  Mrv0541 02241210432D          

 34 39  0  0  0  0            999 V2000
    3.2160   -1.6491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4739   -1.3189    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8858   -0.5768    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6476   -1.4847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8135   -2.3097    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4739   -2.8044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2160   -2.4741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8751   -2.8872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8241   -1.7320    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2451   -1.2374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5783   -0.9900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5783   -0.1651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3203    0.2466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0638   -0.1651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7229    0.4124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7229    1.2359    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3820    1.6490    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4649    2.4741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2083    2.8872    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8058    2.8872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1453    2.3911    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9808    1.5662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3203    2.2267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3203    1.0715    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5783    1.4018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0806    0.9885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1636    0.1636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9056    0.4939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6583   -0.4939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4002   -0.7427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0608   -0.0822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7587   -0.5623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1822    0.2015    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2083   -1.3101    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  7  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  3 32  1  0  0  0  0
  4  5  1  0  0  0  0
  4  9  1  0  0  0  0
  4 30  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 29  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 27  1  0  0  0  0
 13 14  1  0  0  0  0
 13 24  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 22  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0046160

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1C2C(CC3C4CCC5CC(O)CCC5(C)C4CCC23C)OC11NCC(C)CC1OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C29H47NO4/c1-16-12-25(33-18(3)31)29(30-15-16)17(2)26-24(34-29)14-23-21-7-6-19-13-20(32)8-10-27(19,4)22(21)9-11-28(23,26)5/h16-17,19-26,30,32H,6-15H2,1-5H3

> <INCHI_KEY>
HQJSCXYJQVACQR-UHFFFAOYSA-N

> <FORMULA>
C29H47NO4

> <MOLECULAR_WEIGHT>
473.6878

> <EXACT_MASS>
473.350508997

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_AVERAGE_POLARIZABILITY>
55.89939740131804

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
16-hydroxy-5',7,9,13-tetramethyl-5-oxaspiro[pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosane-6,2'-piperidine]-3'-yl acetate

> <ALOGPS_LOGP>
4.30

> <JCHEM_LOGP>
4.610380298000001

> <ALOGPS_LOGS>
-5.58

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.2963963211217

> <JCHEM_PKA_STRONGEST_BASIC>
8.540524826782708

> <JCHEM_POLAR_SURFACE_AREA>
67.78999999999999

> <JCHEM_REFRACTIVITY>
131.49939999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.23e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
16-hydroxy-5',7,9,13-tetramethyl-5-oxaspiro[pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosane-6,2'-piperidine]-3'-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0       6.003  -3.078   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.618  -2.462   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       5.387  -1.077   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       3.076  -2.771   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0       3.385  -4.311   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0       4.618  -5.235   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.003  -4.618   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.234  -5.389   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       1.538  -3.233   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       0.458  -2.310   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.079  -1.848   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.079  -0.308   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.465   0.460   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -3.852  -0.308   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -5.083   0.770   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -5.083   2.307   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -6.313   3.078   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -6.468   4.618   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -7.855   5.389   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -5.237   5.389   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -4.005   4.463   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -3.697   2.924   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -2.465   4.157   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -2.465   2.000   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -1.079   2.617   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.150   1.845   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.305   0.305   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       1.690   0.922   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       1.229  -0.922   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.614  -1.386   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       3.847  -0.153   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       7.016  -1.050   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       7.807   0.376   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       7.855  -2.446   0.000  0.00  0.00           O+0
CONECT    1    2    7                                                       
CONECT    2    1    3    4                                                  
CONECT    3    2   32                                                       
CONECT    4    2    5    9   30                                             
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    1    6    8                                                  
CONECT    8    7                                                            
CONECT    9    4   10                                                       
CONECT   10    9   11   29                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   27                                                  
CONECT   13   12   14   24                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   22                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   16   21   23   24                                             
CONECT   23   22                                                            
CONECT   24   13   22   25                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   12   26   28   29                                             
CONECT   28   27                                                            
CONECT   29   10   27   30                                                  
CONECT   30    4   29   31                                                  
CONECT   31   30                                                            
CONECT   32    3   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   78    0
END

View in JSmol

Synonyms

Value	Source
16-Hydroxy-5',7,9,13-tetramethyl-5-oxaspiro[pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosane-6,2'-piperidine]-3'-yl acetic acid	Generator

Chemical Formula

C₂₉H₄₇NO₄

Average Mass

473.6878 Da

Monoisotopic Mass

473.35051 Da

IUPAC Name

16-hydroxy-5',7,9,13-tetramethyl-5-oxaspiro[pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosane-6,2'-piperidine]-3'-yl acetate

Traditional Name

16-hydroxy-5',7,9,13-tetramethyl-5-oxaspiro[pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosane-6,2'-piperidine]-3'-yl acetate

CAS Registry Number

152128-85-3

SMILES

CC1C2C(CC3C4CCC5CC(O)CCC5(C)C4CCC23C)OC11NCC(C)CC1OC(C)=O

InChI Identifier

InChI=1S/C29H47NO4/c1-16-12-25(33-18(3)31)29(30-15-16)17(2)26-24(34-29)14-23-21-7-6-19-13-20(32)8-10-27(19,4)22(21)9-11-28(23,26)5/h16-17,19-26,30,32H,6-15H2,1-5H3

InChI Key

HQJSCXYJQVACQR-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Lycopersicon esculentum-Lycopersicon hirsutum hybrid	Plant	KNApSAcK
Lycopersicon hirsutum hybrid	Plant	KNApSAcK
Solanum lycopersicum	FooDB	Shmuel Yannai Dictionary of Food Compounds with CD-ROM: Additives, Flavors, and Ingredients. Chap...

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as spirosolanes and derivatives. These are steroidal alkaloids with a structure containing a spirosolane skeleton. Siporosolane is a polycyclic compound that is characterized by a 1-oxa-6-azaspiro[4.5]Decane moiety where the oxolane ring is fused to a docosahydronaphth[2,1:4',5']Indene ring system. Spirosolane arises from the conversion of a cholestane side-chain into a bicyclic system containing a piperidine and a tetrahydrofuran ring.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroidal alkaloids

Direct Parent

Spirosolanes and derivatives

Alternative Parents

Substituents

Spirosolane skeleton
3-hydroxysteroid
Hydroxysteroid
Azasteroid
Azaspirodecane
Alkaloid or derivatives
Piperidine
Cyclic alcohol
Tetrahydrofuran
Hemiaminal
Amino acid or derivatives
Carboxylic acid ester
Secondary alcohol
Oxacycle
Secondary aliphatic amine
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Secondary amine
Azacycle
Organoheterocyclic compound
Organic nitrogen compound
Organonitrogen compound
Organooxygen compound
Hydrocarbon derivative
Carbonyl group
Organic oxide
Organopnictogen compound
Organic oxygen compound
Amine
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	4.3	ALOGPS
logP	4.61	ChemAxon
logS	-5.6	ALOGPS
pKa (Strongest Acidic)	18.3	ChemAxon
pKa (Strongest Basic)	8.54	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	67.79 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	131.5 m³·mol⁻¹	ChemAxon
Polarizability	55.9 Å³	ChemAxon
Number of Rings	6	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

HMDB ID

HMDB0031402

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB003476

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

131751167

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for 23-Acetoxysoladulcidine (NP0046160)

MOL for NP0046160 (23-Acetoxysoladulcidine)

3D MOL for NP0046160 (23-Acetoxysoladulcidine)

3D SDF for NP0046160 (23-Acetoxysoladulcidine)

3D-SDF for NP0046160 (23-Acetoxysoladulcidine)

PDB for NP0046160 (23-Acetoxysoladulcidine)

3D PDB for NP0046160 (23-Acetoxysoladulcidine)

SMILES for NP0046160 (23-Acetoxysoladulcidine)

INCHI for NP0046160 (23-Acetoxysoladulcidine)

Structure for NP0046160 (23-Acetoxysoladulcidine)

3D Structure for NP0046160 (23-Acetoxysoladulcidine)