MiMeDB: Showing metabocard for Deoxyverrucosidin (MMDBc0007591)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2021-05-15 00:43:13 UTC

Update Date

2025-10-07 16:05:21 UTC

Metabolite ID

MMDBc0007591

Metabolite Identification

Common Name

Deoxyverrucosidin

Description

Deoxyverrucosidin is a fungal metabolite belonging to the class of octaketides. It is characterized by a unique epoxytetrahydrofuran ring and shares a common α-pyrone core with several other nonaketides, such as aurovertins, citreoviridin, and asteltoxin (PMID:40756971 ). The biosynthesis of deoxyverrucosidin involves a unique three-enzyme cascade that facilitates efficient regioselective and stereospecific epoxytetrahydrofuran ring formation (PMID:40756971 ). In biological contexts, deoxyverrucosidin has been identified as a novel down-regulator of GRP78/BiP, a protein that plays a critical role in cellular stress responses (PMID:15895531 ). During a search for compounds that could down-regulate GRP78, researchers isolated deoxyverrucosidin from Penicillium sp. using a luciferase reporter gene assay system (PMID:15895531 ). Additionally, there is a discussion about the potential for other GRP78 inhibitors, including deoxyverrucosidin, to act independently of GRP78 (PMID:23755268 ). Overall, deoxyverrucosidin represents an interesting compound with implications in both chemistry and biology, particularly in the context of stress response mechanisms in cells.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152102432D          

 34 36  0  0  1  0            999 V2000
    2.9570   -3.6161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2425   -2.3786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6715   -4.8536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8149   -3.6161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2438   -6.0911    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4975    1.3909    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9070   -1.4823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1224    1.1050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9583   -4.8536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6715   -2.3786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3859   -3.6161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9570   -1.1411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6715   -3.2036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9570   -1.9661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3859   -4.4411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8149   -4.4411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5294   -5.6786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2425    0.6062    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1004   -4.8536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5294   -4.8536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8149   -6.0911    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4579   -0.4737    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2425   -0.7286    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4579    0.3513    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.8149   -6.9161    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2438   -4.4411    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1004   -5.6786    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7275   -0.0612    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7434   -0.0612    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3859   -1.9661    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1004   -3.2036    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6715   -0.7286    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6592    1.1896    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1224   -1.2274    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 13  1  1  0  0  0  0
 13 10  2  0  0  0  0
 13 11  1  0  0  0  0
 14  2  1  0  0  0  0
 14 10  1  0  0  0  0
 14 12  2  0  0  0  0
 15  3  1  0  0  0  0
 15 11  2  0  0  0  0
 16  4  1  0  0  0  0
 17  5  1  0  0  0  0
 18  6  1  1  0  0  0
 19 15  1  0  0  0  0
 19 16  2  0  0  0  0
 20 16  1  0  0  0  0
 20 17  2  0  0  0  0
 21 17  1  0  0  0  0
 23  7  1  6  0  0  0
 23 12  1  1  0  0  0
 23 22  1  0  0  0  0
 24  8  1  1  0  0  0
 24 18  1  0  0  0  0
 24 22  1  0  0  0  0
 25 21  2  0  0  0  0
 26  9  1  0  0  0  0
 26 20  1  0  0  0  0
 27 19  1  0  0  0  0
 27 21  1  0  0  0  0
 28 18  1  0  0  0  0
 28 23  1  0  0  0  0
 29 22  1  0  0  0  0
 29 24  1  0  0  0  0
 30 10  1  0  0  0  0
 31 11  1  0  0  0  0
 32 12  1  0  0  0  0
 18 33  1  6  0  0  0
 22 34  1  1  0  0  0
M  END


  Mrv1652305152102432D          

 34 36  0  0  1  0            999 V2000
    2.9570   -3.6161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2425   -2.3786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6715   -4.8536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8149   -3.6161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2438   -6.0911    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4975    1.3909    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9070   -1.4823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1224    1.1050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9583   -4.8536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6715   -2.3786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3859   -3.6161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9570   -1.1411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6715   -3.2036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9570   -1.9661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3859   -4.4411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8149   -4.4411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5294   -5.6786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2425    0.6062    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1004   -4.8536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5294   -4.8536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8149   -6.0911    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4579   -0.4737    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2425   -0.7286    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4579    0.3513    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.8149   -6.9161    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2438   -4.4411    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1004   -5.6786    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7275   -0.0612    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7434   -0.0612    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3859   -1.9661    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1004   -3.2036    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6715   -0.7286    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6592    1.1896    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1224   -1.2274    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 13  1  1  0  0  0  0
 13 10  2  0  0  0  0
 13 11  1  0  0  0  0
 14  2  1  0  0  0  0
 14 10  1  0  0  0  0
 14 12  2  0  0  0  0
 15  3  1  0  0  0  0
 15 11  2  0  0  0  0
 16  4  1  0  0  0  0
 17  5  1  0  0  0  0
 18  6  1  1  0  0  0
 19 15  1  0  0  0  0
 19 16  2  0  0  0  0
 20 16  1  0  0  0  0
 20 17  2  0  0  0  0
 21 17  1  0  0  0  0
 23  7  1  6  0  0  0
 23 12  1  1  0  0  0
 23 22  1  0  0  0  0
 24  8  1  1  0  0  0
 24 18  1  0  0  0  0
 24 22  1  0  0  0  0
 25 21  2  0  0  0  0
 26  9  1  0  0  0  0
 26 20  1  0  0  0  0
 27 19  1  0  0  0  0
 27 21  1  0  0  0  0
 28 18  1  0  0  0  0
 28 23  1  0  0  0  0
 29 22  1  0  0  0  0
 29 24  1  0  0  0  0
 30 10  1  0  0  0  0
 31 11  1  0  0  0  0
 32 12  1  0  0  0  0
 18 33  1  6  0  0  0
 22 34  1  1  0  0  0
M  END
> <DATABASE_ID>
MMDBc0007591

> <DATABASE_NAME>
MIME

> <SMILES>
[H]/C(=C(/C)\C(\[H])=C(/C)C1=C(C)C(OC)=C(C)C(=O)O1)/C(/C)=C(\[H])[C@]1(C)O[C@]([H])(C)[C@@]2(C)O[C@@]12[H]

> <INCHI_IDENTIFIER>
InChI=1S/C24H32O5/c1-13(10-14(2)12-23(7)22-24(8,29-22)18(6)28-23)11-15(3)19-16(4)20(26-9)17(5)21(25)27-19/h10-12,18,22H,1-9H3/b13-10+,14-12+,15-11+/t18-,22+,23+,24-/m1/s1

> <INCHI_KEY>
UHXNFXURTCVQIN-YKJJQUFLSA-N

> <FORMULA>
C24H32O5

> <MOLECULAR_WEIGHT>
400.515

> <EXACT_MASS>
400.22497413

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
61

> <JCHEM_AVERAGE_POLARIZABILITY>
45.18474861100708

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
6-[(2E,4E,6E)-4,6-dimethyl-7-[(1S,2S,4R,5R)-2,4,5-trimethyl-3,6-dioxabicyclo[3.1.0]hexan-2-yl]hepta-2,4,6-trien-2-yl]-4-methoxy-3,5-dimethyl-2H-pyran-2-one

> <ALOGPS_LOGP>
5.05

> <JCHEM_LOGP>
3.975772348333332

> <ALOGPS_LOGS>
-4.73

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-3.9049386895761473

> <JCHEM_POLAR_SURFACE_AREA>
57.290000000000006

> <JCHEM_REFRACTIVITY>
117.10519999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.46e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6-[(2E,4E,6E)-4,6-dimethyl-7-[(1S,2S,4R,5R)-2,4,5-trimethyl-3,6-dioxabicyclo[3.1.0]hexan-2-yl]hepta-2,4,6-trien-2-yl]-4-methoxy-3,5-dimethylpyran-2-one

> <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       5.520  -6.750   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.186  -4.440   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.853  -9.060   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.854  -6.750   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      13.522 -11.370   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.662   2.596   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.560  -2.767   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.095   2.063   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      14.855  -9.060   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.853  -4.440   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.187  -6.750   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.520  -2.130   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.853  -5.980   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.520  -3.670   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.187  -8.290   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.854  -8.290   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      12.188 -10.600   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.186   1.132   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.521  -9.060   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      12.188  -9.060   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      10.854 -11.370   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.721  -0.884   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.186  -1.360   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.721   0.656   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      10.854 -12.910   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0      13.522  -8.290   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       9.521 -10.600   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       5.091  -0.114   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       1.388  -0.114   0.000  0.00  0.00           O+0
HETATM   30  H   UNK     0       8.187  -3.670   0.000  0.00  0.00           H+0
HETATM   31  H   UNK     0       9.521  -5.980   0.000  0.00  0.00           H+0
HETATM   32  H   UNK     0       6.853  -1.360   0.000  0.00  0.00           H+0
HETATM   33  H   UNK     0       3.097   2.221   0.000  0.00  0.00           H+0
HETATM   34  H   UNK     0       2.095  -2.291   0.000  0.00  0.00           H+0
CONECT    1   13                                                            
CONECT    2   14                                                            
CONECT    3   15                                                            
CONECT    4   16                                                            
CONECT    5   17                                                            
CONECT    6   18                                                            
CONECT    7   23                                                            
CONECT    8   24                                                            
CONECT    9   26                                                            
CONECT   10   13   14   30                                                  
CONECT   11   13   15   31                                                  
CONECT   12   14   23   32                                                  
CONECT   13    1   10   11                                                  
CONECT   14    2   10   12                                                  
CONECT   15    3   11   19                                                  
CONECT   16    4   19   20                                                  
CONECT   17    5   20   21                                                  
CONECT   18    6   24   28   33                                             
CONECT   19   15   16   27                                                  
CONECT   20   16   17   26                                                  
CONECT   21   17   25   27                                                  
CONECT   22   23   24   29   34                                             
CONECT   23    7   12   22   28                                             
CONECT   24    8   18   22   29                                             
CONECT   25   21                                                            
CONECT   26    9   20                                                       
CONECT   27   19   21                                                       
CONECT   28   18   23                                                       
CONECT   29   22   24                                                       
CONECT   30   10                                                            
CONECT   31   11                                                            
CONECT   32   12                                                            
CONECT   33   18                                                            
CONECT   34   22                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   72    0
END

Synonyms

Not Available

Molecular Formula

C₂₄H₃₂O₅

Average Mass

400.515

Monoisotopic Mass

400.22497413

IUPAC Name

6-[(2E,4E,6E)-4,6-dimethyl-7-[(1S,2S,4R,5R)-2,4,5-trimethyl-3,6-dioxabicyclo[3.1.0]hexan-2-yl]hepta-2,4,6-trien-2-yl]-4-methoxy-3,5-dimethyl-2H-pyran-2-one

Traditional Name

6-[(2E,4E,6E)-4,6-dimethyl-7-[(1S,2S,4R,5R)-2,4,5-trimethyl-3,6-dioxabicyclo[3.1.0]hexan-2-yl]hepta-2,4,6-trien-2-yl]-4-methoxy-3,5-dimethylpyran-2-one

CAS Registry Number

Not Available

SMILES

[H]/C(=C(/C)\C(\[H])=C(/C)C1=C(C)C(OC)=C(C)C(=O)O1)/C(/C)=C(\[H])[C@]1(C)O[C@]([H])(C)[C@@]2(C)O[C@@]12[H]

InChI Identifier

InChI=1S/C24H32O5/c1-13(10-14(2)12-23(7)22-24(8,29-22)18(6)28-23)11-15(3)19-16(4)20(26-9)17(5)21(25)27-19/h10-12,18,22H,1-9H3/b13-10+,14-12+,15-11+/t18-,22+,23+,24-/m1/s1

InChI Key

UHXNFXURTCVQIN-YKJJQUFLSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Terpene lactones

Alternative Parents

Substituents

Terpene lactone
Aromatic monoterpenoid
Bicyclic monoterpenoid
Monoterpenoid
Alkyl aryl ether
Pyranone
Para-dioxane
Pyran
Heteroaromatic compound
Vinylogous ester
Oxolane
Lactone
Oxacycle
Dialkyl ether
Oxirane
Ether
Organoheterocyclic compound
Organic oxide
Hydrocarbon derivative
Organic oxygen compound
Organooxygen compound
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	0.0075 g/L	ALOGPS
logP	5.05	ALOGPS
logP	3.98	ChemAxon
logS	-4.7	ALOGPS
pKa (Strongest Basic)	-3.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	57.29 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	117.11 m³·mol⁻¹	ChemAxon
Polarizability	45.18 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

Microbial Pathways

Pathways

This table shows at most 5 pathways. For the full list of associated pathways:

See All Associated Bacterial Pathways

Name	SMPDB/PathBank	Species

Metabolic Reactions

Reactions

This table shows at most 20 reactions. For the full list of associated reactions:

See All Associated 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	Ascomycota	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

9547897

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11372980

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

CMMC Knowledgebase

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 Deoxyverrucosidin (MMDBc0007591)

MOL for #<Metabolite:0x00007f28947d5bb8>

3D MOL for #<Metabolite:0x00007f28947d5bb8>

3D SDF for #<Metabolite:0x00007f28947d5bb8>

3D-SDF for #<Metabolite:0x00007f28947d5bb8>

PDB for #<Metabolite:0x00007f28947d5bb8>

3D PDB for #<Metabolite:0x00007f28947d5bb8>

SMILES for #<Metabolite:0x00007f28947d5bb8>

INCHI for #<Metabolite:0x00007f28947d5bb8>

Structure for #<Metabolite:0x00007f28947d5bb8>

3D Structure for #<Metabolite:0x00007f28947d5bb8>