MiMeDB: Showing metabocard for Sterenin L (MMDBc0008578)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-15 01:23:30 UTC

Update Date

2022-08-31 06:28:49 UTC

Metabolite ID

MMDBc0008578

Metabolite Identification

Common Name

Sterenin L

Description

Sterenin L belongs to the class of organic compounds known as isoleucine and derivatives. Isoleucine and derivatives are compounds containing isoleucine or a derivative thereof resulting from reaction of isoleucine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom. Based on a literature review very few articles have been published on Sterenin L.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152103232D          

 36 38  0  0  0  0            999 V2000
    2.2295   -0.7827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7709   -7.3851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0084   -8.0996    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2295   -2.4327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9584   -6.6706    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9440   -1.1952    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0084   -6.6706    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8334   -6.6706    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9584   -8.0996    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7209   -8.8140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4834   -5.2417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9910   -3.7426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5959   -7.3851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9440   -2.0202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5459   -7.3851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5459   -8.8140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2459   -5.9562    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0709   -4.5272    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2459   -4.5272    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3084   -8.0996    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0709   -5.9562    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7209   -7.3851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6584   -2.4327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8334   -5.2417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3259   -3.7426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3729   -2.0202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3084   -6.6706    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6584   -3.2577    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.9584   -9.5285    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4834   -8.0996    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0084   -5.2417    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1105   -3.4877    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3729   -1.1952    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0874   -2.4327    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7209   -5.9562    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4834   -6.6706    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  6  1  1  0  0  0  0
  8  7  1  0  0  0  0
 13  2  1  0  0  0  0
 13  3  1  0  0  0  0
 13  7  2  0  0  0  0
 14  4  1  0  0  0  0
 14  6  1  0  0  0  0
 15  5  1  0  0  0  0
 15  9  2  0  0  0  0
 16  9  1  0  0  0  0
 16 10  2  0  0  0  0
 17  8  1  0  0  0  0
 18 11  2  0  0  0  0
 19 12  1  0  0  0  0
 19 18  1  0  0  0  0
 20 10  1  0  0  0  0
 21 11  1  0  0  0  0
 21 17  2  0  0  0  0
 22 15  1  0  0  0  0
 22 20  2  0  0  0  0
 23 14  1  0  0  0  0
 24 17  1  0  0  0  0
 24 19  2  0  0  0  0
 25 18  1  0  0  0  0
 26 23  1  0  0  0  0
 27 22  1  0  0  0  0
 28 12  1  0  0  0  0
 28 23  1  0  0  0  0
 28 25  1  0  0  0  0
 29 16  1  0  0  0  0
 30 20  1  0  0  0  0
 31 24  1  0  0  0  0
 32 25  2  0  0  0  0
 33 26  2  0  0  0  0
 34 26  1  0  0  0  0
 35 27  2  0  0  0  0
 36 21  1  0  0  0  0
 36 27  1  0  0  0  0
M  END


  Mrv1652305152103232D          

 36 38  0  0  0  0            999 V2000
    2.2295   -0.7827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7709   -7.3851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0084   -8.0996    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2295   -2.4327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9584   -6.6706    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9440   -1.1952    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0084   -6.6706    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8334   -6.6706    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9584   -8.0996    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7209   -8.8140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4834   -5.2417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9910   -3.7426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5959   -7.3851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9440   -2.0202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5459   -7.3851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5459   -8.8140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2459   -5.9562    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0709   -4.5272    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2459   -4.5272    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3084   -8.0996    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0709   -5.9562    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7209   -7.3851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6584   -2.4327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8334   -5.2417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3259   -3.7426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3729   -2.0202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3084   -6.6706    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6584   -3.2577    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.9584   -9.5285    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4834   -8.0996    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0084   -5.2417    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1105   -3.4877    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3729   -1.1952    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0874   -2.4327    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7209   -5.9562    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4834   -6.6706    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  6  1  1  0  0  0  0
  8  7  1  0  0  0  0
 13  2  1  0  0  0  0
 13  3  1  0  0  0  0
 13  7  2  0  0  0  0
 14  4  1  0  0  0  0
 14  6  1  0  0  0  0
 15  5  1  0  0  0  0
 15  9  2  0  0  0  0
 16  9  1  0  0  0  0
 16 10  2  0  0  0  0
 17  8  1  0  0  0  0
 18 11  2  0  0  0  0
 19 12  1  0  0  0  0
 19 18  1  0  0  0  0
 20 10  1  0  0  0  0
 21 11  1  0  0  0  0
 21 17  2  0  0  0  0
 22 15  1  0  0  0  0
 22 20  2  0  0  0  0
 23 14  1  0  0  0  0
 24 17  1  0  0  0  0
 24 19  2  0  0  0  0
 25 18  1  0  0  0  0
 26 23  1  0  0  0  0
 27 22  1  0  0  0  0
 28 12  1  0  0  0  0
 28 23  1  0  0  0  0
 28 25  1  0  0  0  0
 29 16  1  0  0  0  0
 30 20  1  0  0  0  0
 31 24  1  0  0  0  0
 32 25  2  0  0  0  0
 33 26  2  0  0  0  0
 34 26  1  0  0  0  0
 35 27  2  0  0  0  0
 36 21  1  0  0  0  0
 36 27  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0008578

> <DATABASE_NAME>
MIME

> <SMILES>
CCC(C)C(N1CC2=C(O)C(CC=C(C)C)=C(OC(=O)C3=C(O)C=C(O)C=C3C)C=C2C1=O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C27H31NO8/c1-6-14(4)23(26(33)34)28-12-19-18(25(28)32)11-21(17(24(19)31)8-7-13(2)3)36-27(35)22-15(5)9-16(29)10-20(22)30/h7,9-11,14,23,29-31H,6,8,12H2,1-5H3,(H,33,34)

> <INCHI_KEY>
JTVABVBUKOFJFR-UHFFFAOYSA-N

> <FORMULA>
C27H31NO8

> <MOLECULAR_WEIGHT>
497.544

> <EXACT_MASS>
497.204966962

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
67

> <JCHEM_AVERAGE_POLARIZABILITY>
51.92139997460251

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-[6-(2,4-dihydroxy-6-methylbenzoyloxy)-4-hydroxy-5-(3-methylbut-2-en-1-yl)-1-oxo-2,3-dihydro-1H-isoindol-2-yl]-3-methylpentanoic acid

> <ALOGPS_LOGP>
3.55

> <JCHEM_LOGP>
6.044004816333334

> <ALOGPS_LOGS>
-4.71

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
7.760964854036603

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.159362934209629

> <JCHEM_PKA_STRONGEST_BASIC>
-1.7498158793745908

> <JCHEM_POLAR_SURFACE_AREA>
144.6

> <JCHEM_REFRACTIVITY>
134.6891

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
9.67e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-[6-(2,4-dihydroxy-6-methylbenzoyloxy)-4-hydroxy-5-(3-methylbut-2-en-1-yl)-1-oxo-3H-isoindol-2-yl]-3-methylpentanoic acid

> <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       4.162  -1.461   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.439 -13.786   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.749 -15.119   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.162  -4.541   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      12.989 -12.452   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.495  -2.231   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.749 -12.452   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.289 -12.452   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      12.989 -15.119   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.679 -16.453   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.369  -9.784   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.583  -6.986   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.979 -13.786   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.495  -3.771   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      12.219 -13.786   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      12.219 -16.453   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.059 -11.118   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.599  -8.451   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.059  -8.451   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.909 -15.119   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.599 -11.118   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      10.679 -13.786   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.829  -4.541   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.289  -9.784   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       8.075  -6.986   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.163  -3.771   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       9.909 -12.452   0.000  0.00  0.00           C+0
HETATM   28  N   UNK     0       6.829  -6.081   0.000  0.00  0.00           N+0
HETATM   29  O   UNK     0      12.989 -17.787   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       8.369 -15.119   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       3.749  -9.784   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       9.540  -6.510   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0       8.163  -2.231   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0       9.496  -4.541   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0      10.679 -11.118   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0       8.369 -12.452   0.000  0.00  0.00           O+0
CONECT    1    6                                                            
CONECT    2   13                                                            
CONECT    3   13                                                            
CONECT    4   14                                                            
CONECT    5   15                                                            
CONECT    6    1   14                                                       
CONECT    7    8   13                                                       
CONECT    8    7   17                                                       
CONECT    9   15   16                                                       
CONECT   10   16   20                                                       
CONECT   11   18   21                                                       
CONECT   12   19   28                                                       
CONECT   13    2    3    7                                                  
CONECT   14    4    6   23                                                  
CONECT   15    5    9   22                                                  
CONECT   16    9   10   29                                                  
CONECT   17    8   21   24                                                  
CONECT   18   11   19   25                                                  
CONECT   19   12   18   24                                                  
CONECT   20   10   22   30                                                  
CONECT   21   11   17   36                                                  
CONECT   22   15   20   27                                                  
CONECT   23   14   26   28                                                  
CONECT   24   17   19   31                                                  
CONECT   25   18   28   32                                                  
CONECT   26   23   33   34                                                  
CONECT   27   22   35   36                                                  
CONECT   28   12   23   25                                                  
CONECT   29   16                                                            
CONECT   30   20                                                            
CONECT   31   24                                                            
CONECT   32   25                                                            
CONECT   33   26                                                            
CONECT   34   26                                                            
CONECT   35   27                                                            
CONECT   36   21   27                                                       
MASTER        0    0    0    0    0    0    0    0   36    0   76    0
END

Synonyms

Not Available

Molecular Formula

C₂₇H₃₁NO₈

Average Mass

497.544

Monoisotopic Mass

497.204966962

IUPAC Name

2-[6-(2,4-dihydroxy-6-methylbenzoyloxy)-4-hydroxy-5-(3-methylbut-2-en-1-yl)-1-oxo-2,3-dihydro-1H-isoindol-2-yl]-3-methylpentanoic acid

Traditional Name

2-[6-(2,4-dihydroxy-6-methylbenzoyloxy)-4-hydroxy-5-(3-methylbut-2-en-1-yl)-1-oxo-3H-isoindol-2-yl]-3-methylpentanoic acid

CAS Registry Number

Not Available

SMILES

CCC(C)C(N1CC2=C(O)C(CC=C(C)C)=C(OC(=O)C3=C(O)C=C(O)C=C3C)C=C2C1=O)C(O)=O

InChI Identifier

InChI=1S/C27H31NO8/c1-6-14(4)23(26(33)34)28-12-19-18(25(28)32)11-21(17(24(19)31)8-7-13(2)3)36-27(35)22-15(5)9-16(29)10-20(22)30/h7,9-11,14,23,29-31H,6,8,12H2,1-5H3,(H,33,34)

InChI Key

JTVABVBUKOFJFR-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as isoleucine and derivatives. Isoleucine and derivatives are compounds containing isoleucine or a derivative thereof resulting from reaction of isoleucine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Isoleucine and derivatives

Alternative Parents

Substituents

Isoleucine or derivatives
Dihydroxybenzoic acid
P-hydroxybenzoic acid ester
O-hydroxybenzoic acid ester
Benzoate ester
Isoindolone
Phenol ester
Salicylic acid or derivatives
Isoindoline
Benzoic acid or derivatives
Isoindole
Isoindole or derivatives
Benzoyl
Resorcinol
M-cresol
1-hydroxy-2-unsubstituted benzenoid
1-hydroxy-4-unsubstituted benzenoid
Toluene
Phenol
Benzenoid
Monocyclic benzene moiety
Vinylogous acid
Tertiary carboxylic acid amide
Carboxamide group
Carboxylic acid ester
Lactam
Carboxylic acid
Organoheterocyclic compound
Azacycle
Monocarboxylic acid or derivatives
Organooxygen compound
Organic nitrogen compound
Organic oxygen compound
Hydrocarbon derivative
Carbonyl group
Organonitrogen compound
Organic oxide
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.0097 g/L	ALOGPS
logP	3.55	ALOGPS
logP	6.04	ChemAxon
logS	-4.7	ALOGPS
pKa (Strongest Acidic)	3.16	ChemAxon
pKa (Strongest Basic)	-1.7	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	144.6 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	134.69 m³·mol⁻¹	ChemAxon
Polarizability	51.92 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

78435348

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

77461068

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 L (MMDBc0008578)

MOL for #<Metabolite:0x00007f923e3a8720>

3D MOL for #<Metabolite:0x00007f923e3a8720>

3D SDF for #<Metabolite:0x00007f923e3a8720>

3D-SDF for #<Metabolite:0x00007f923e3a8720>

PDB for #<Metabolite:0x00007f923e3a8720>

3D PDB for #<Metabolite:0x00007f923e3a8720>

SMILES for #<Metabolite:0x00007f923e3a8720>

INCHI for #<Metabolite:0x00007f923e3a8720>

Structure for #<Metabolite:0x00007f923e3a8720>

3D Structure for #<Metabolite:0x00007f923e3a8720>