MiMeDB: Showing metabocard for Sterenin I (MMDBc0014531)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-15 05:32:58 UTC

Update Date

2022-08-31 06:37:46 UTC

Metabolite ID

MMDBc0014531

Metabolite Identification

Common Name

Sterenin I

Description

Sterenin I belongs to the class of organic compounds known as depsides and depsidones. These are polycyclic compounds that is either a polyphenolic compound composed of two or more monocyclic aromatic units linked by an ester bond (depside), or a compound containing the depsidone structure (depsidone). Based on a literature review very few articles have been published on Sterenin I.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152107322D          

 36 37  0  0  0  0            999 V2000
   10.7171   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.1473   -3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  1  0  0  0  0
 14  1  1  0  0  0  0
 14  2  1  0  0  0  0
 14  5  2  0  0  0  0
 15  3  1  0  0  0  0
 15  7  2  0  0  0  0
 16  4  1  0  0  0  0
 17  8  2  0  0  0  0
 17 10  1  0  0  0  0
 18  7  1  0  0  0  0
 18  9  2  0  0  0  0
 19 11  1  0  0  0  0
 19 12  1  0  0  0  0
 20  6  1  0  0  0  0
 21 13  1  0  0  0  0
 21 17  1  0  0  0  0
 22  9  1  0  0  0  0
 23  8  1  0  0  0  0
 23 20  2  0  0  0  0
 24 15  1  0  0  0  0
 24 22  2  0  0  0  0
 25 20  1  0  0  0  0
 25 21  2  0  0  0  0
 26 24  1  0  0  0  0
 27 10  1  0  0  0  0
 28 16  2  0  0  0  0
 29 18  1  0  0  0  0
 30 19  1  0  0  0  0
 31 22  1  0  0  0  0
 32 25  1  0  0  0  0
 33 26  2  0  0  0  0
 34 11  1  0  0  0  0
 34 13  1  0  0  0  0
 35 12  1  0  0  0  0
 35 16  1  0  0  0  0
 36 23  1  0  0  0  0
 36 26  1  0  0  0  0
M  END


  Mrv1652305152107322D          

 36 37  0  0  0  0            999 V2000
   10.7171   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.1473   -3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  1  0  0  0  0
 14  1  1  0  0  0  0
 14  2  1  0  0  0  0
 14  5  2  0  0  0  0
 15  3  1  0  0  0  0
 15  7  2  0  0  0  0
 16  4  1  0  0  0  0
 17  8  2  0  0  0  0
 17 10  1  0  0  0  0
 18  7  1  0  0  0  0
 18  9  2  0  0  0  0
 19 11  1  0  0  0  0
 19 12  1  0  0  0  0
 20  6  1  0  0  0  0
 21 13  1  0  0  0  0
 21 17  1  0  0  0  0
 22  9  1  0  0  0  0
 23  8  1  0  0  0  0
 23 20  2  0  0  0  0
 24 15  1  0  0  0  0
 24 22  2  0  0  0  0
 25 20  1  0  0  0  0
 25 21  2  0  0  0  0
 26 24  1  0  0  0  0
 27 10  1  0  0  0  0
 28 16  2  0  0  0  0
 29 18  1  0  0  0  0
 30 19  1  0  0  0  0
 31 22  1  0  0  0  0
 32 25  1  0  0  0  0
 33 26  2  0  0  0  0
 34 11  1  0  0  0  0
 34 13  1  0  0  0  0
 35 12  1  0  0  0  0
 35 16  1  0  0  0  0
 36 23  1  0  0  0  0
 36 26  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0014531

> <DATABASE_NAME>
MIME

> <SMILES>
CC(C)=CCC1=C(OC(=O)C2=C(O)C=C(O)C=C2C)C=C(CO)C(COCC(O)COC(C)=O)=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C26H32O10/c1-14(2)5-6-20-23(36-26(33)24-15(3)7-18(29)9-22(24)31)8-17(10-27)21(25(20)32)13-34-11-19(30)12-35-16(4)28/h5,7-9,19,27,29-32H,6,10-13H2,1-4H3

> <INCHI_KEY>
MPUDXKXLMMLLDZ-UHFFFAOYSA-N

> <FORMULA>
C26H32O10

> <MOLECULAR_WEIGHT>
504.532

> <EXACT_MASS>
504.19954723

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
68

> <JCHEM_AVERAGE_POLARIZABILITY>
53.37993245316194

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4-{[3-(acetyloxy)-2-hydroxypropoxy]methyl}-3-hydroxy-5-(hydroxymethyl)-2-(3-methylbut-2-en-1-yl)phenyl 2,4-dihydroxy-6-methylbenzoate

> <ALOGPS_LOGP>
2.60

> <JCHEM_LOGP>
3.8450890776666657

> <ALOGPS_LOGS>
-4.81

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.79508348843789

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.107110583946206

> <JCHEM_PKA_STRONGEST_BASIC>
-2.92759585332436

> <JCHEM_POLAR_SURFACE_AREA>
162.98

> <JCHEM_REFRACTIVITY>
132.8769

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
7.84e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-{[3-(acetyloxy)-2-hydroxypropoxy]methyl}-3-hydroxy-5-(hydroxymethyl)-2-(3-methylbut-2-en-1-yl)phenyl 2,4-dihydroxy-6-methylbenzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 15-MAY-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   15-MAY-21         0                                  
HETATM    1  C   UNK     0      20.005  -8.470   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      22.673  -8.470   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      29.341  -1.540   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.669  -1.540   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      21.339  -6.160   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      22.673  -5.390   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      30.675  -3.850   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      24.006  -1.540   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      29.341  -6.160   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      22.673   0.770   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      17.338  -0.770   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      14.670  -0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      20.005  -0.770   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      21.339  -7.700   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      29.341  -3.080   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      12.003  -0.770   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      22.673  -0.770   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      30.675  -5.390   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      16.004  -1.540   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      22.673  -3.850   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      21.339  -1.540   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      28.007  -5.390   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      24.006  -3.080   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      28.007  -3.850   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      21.339  -3.080   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      26.674  -3.080   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      21.339   1.540   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0      12.003   0.770   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      32.008  -6.160   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      16.004  -3.080   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0      26.674  -6.160   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0      20.005  -3.850   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0      26.674  -1.540   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0      18.672  -1.540   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0      13.337  -1.540   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0      25.340  -3.850   0.000  0.00  0.00           O+0
CONECT    1   14                                                            
CONECT    2   14                                                            
CONECT    3   15                                                            
CONECT    4   16                                                            
CONECT    5    6   14                                                       
CONECT    6    5   20                                                       
CONECT    7   15   18                                                       
CONECT    8   17   23                                                       
CONECT    9   18   22                                                       
CONECT   10   17   27                                                       
CONECT   11   19   34                                                       
CONECT   12   19   35                                                       
CONECT   13   21   34                                                       
CONECT   14    1    2    5                                                  
CONECT   15    3    7   24                                                  
CONECT   16    4   28   35                                                  
CONECT   17    8   10   21                                                  
CONECT   18    7    9   29                                                  
CONECT   19   11   12   30                                                  
CONECT   20    6   23   25                                                  
CONECT   21   13   17   25                                                  
CONECT   22    9   24   31                                                  
CONECT   23    8   20   36                                                  
CONECT   24   15   22   26                                                  
CONECT   25   20   21   32                                                  
CONECT   26   24   33   36                                                  
CONECT   27   10                                                            
CONECT   28   16                                                            
CONECT   29   18                                                            
CONECT   30   19                                                            
CONECT   31   22                                                            
CONECT   32   25                                                            
CONECT   33   26                                                            
CONECT   34   11   13                                                       
CONECT   35   12   16                                                       
CONECT   36   23   26                                                       
MASTER        0    0    0    0    0    0    0    0   36    0   74    0
END

Synonyms

Not Available

Molecular Formula

C₂₆H₃₂O₁₀

Average Mass

504.532

Monoisotopic Mass

504.19954723

IUPAC Name

4-{[3-(acetyloxy)-2-hydroxypropoxy]methyl}-3-hydroxy-5-(hydroxymethyl)-2-(3-methylbut-2-en-1-yl)phenyl 2,4-dihydroxy-6-methylbenzoate

Traditional Name

4-{[3-(acetyloxy)-2-hydroxypropoxy]methyl}-3-hydroxy-5-(hydroxymethyl)-2-(3-methylbut-2-en-1-yl)phenyl 2,4-dihydroxy-6-methylbenzoate

CAS Registry Number

Not Available

SMILES

CC(C)=CCC1=C(OC(=O)C2=C(O)C=C(O)C=C2C)C=C(CO)C(COCC(O)COC(C)=O)=C1O

InChI Identifier

InChI=1S/C26H32O10/c1-14(2)5-6-20-23(36-26(33)24-15(3)7-18(29)9-22(24)31)8-17(10-27)21(25(20)32)13-34-11-19(30)12-35-16(4)28/h5,7-9,19,27,29-32H,6,10-13H2,1-4H3

InChI Key

MPUDXKXLMMLLDZ-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as depsides and depsidones. These are polycyclic compounds that is either a polyphenolic compound composed of two or more monocyclic aromatic units linked by an ester bond (depside), or a compound containing the depsidone structure (depsidone).

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Depsides and depsidones

Sub Class

Not Available

Direct Parent

Depsides and depsidones

Alternative Parents

Substituents

Depside backbone
P-hydroxybenzoic acid ester
O-hydroxybenzoic acid ester
Dihydroxybenzoic acid
Diradylglycerol
1-alkyl,3-acylglycerol
Salicylic acid or derivatives
Phenol ester
Benzoate ester
Benzylether
Benzoic acid or derivatives
Phenoxy compound
Resorcinol
M-cresol
Benzyl alcohol
Benzoyl
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Glycerolipid
Glycerol ether
Toluene
Phenol
Benzenoid
Dicarboxylic acid or derivatives
Monocyclic benzene moiety
Vinylogous acid
Secondary alcohol
Carboxylic acid ester
Ether
Dialkyl ether
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Aromatic alcohol
Primary alcohol
Organooxygen compound
Carbonyl group
Alcohol
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.0078 g/L	ALOGPS
logP	2.6	ALOGPS
logP	3.85	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	8.11	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	162.98 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	132.88 m³·mol⁻¹	ChemAxon
Polarizability	53.38 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Not Available

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Protein ID	Protein Name	Protein Type	Uniprot ID	Species

Human Pathways

Pathways

Name	SMPDB/PathBank

Metabolic Reactions

Reactions

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Evidence Type	Host and Biospecimen	Data Source	Reference

Microbial Sources

Superkingdom/Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
Eukaryota/Fungi	Basidiomycota	1	Human feces	Metabolic reconstruction

Exposure Sources

Other Exposures

Source Type	Data Source	Reference

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Units	Age	Sex	Health Condition	Data Source	Reference

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

78435366

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139587057

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

General References

van Santen JA, Poynton EF, Iskakova D, McMann E, Alsup TA, Clark TN, Fergusson CH, Fewer DP, Hughes AH, McCadden CA, Parra J, Soldatou S, Rudolf JD, Janssen EM, Duncan KR, Linington RG: The Natural Products Atlas 2.0: a database of microbially-derived natural products. Nucleic Acids Res. 2022 Jan 7;50(D1):D1317-D1323. doi: 10.1093/nar/gkab941. [PubMed:34718710 ]

Showing metabocard for Sterenin I (MMDBc0014531)

MOL for #<Metabolite:0x00007f92518e8650>

3D MOL for #<Metabolite:0x00007f92518e8650>

3D SDF for #<Metabolite:0x00007f92518e8650>

3D-SDF for #<Metabolite:0x00007f92518e8650>

PDB for #<Metabolite:0x00007f92518e8650>

3D PDB for #<Metabolite:0x00007f92518e8650>

SMILES for #<Metabolite:0x00007f92518e8650>

INCHI for #<Metabolite:0x00007f92518e8650>

Structure for #<Metabolite:0x00007f92518e8650>

3D Structure for #<Metabolite:0x00007f92518e8650>