MiMeDB: Showing metabocard for Brevianamide T (MMDBc0001693)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-14 19:52:27 UTC

Update Date

2025-10-07 16:04:30 UTC

Metabolite ID

MMDBc0001693

Metabolite Identification

Common Name

Brevianamide T

Description

Brevianamide T is a secondary metabolite belonging to the class of amides, specifically derived from fungal sources. It has garnered interest due to its potential biological activities, although detailed studies are limited. The compound has been isolated from various species, including certain strains of the fungus Aspergillus, where it may play a role in ecological interactions or possess pharmacological properties. Notably, research indicates that Brevianamide T exhibits cytotoxic effects against certain cancer cell lines, suggesting a potential for therapeutic applications (PMID: 30781224 ). However, the full spectrum of its biological activities and mechanisms of action remains largely unexplored, highlighting the need for further investigation into its properties and potential uses (PMID: 30301535 ). Overall, while Brevianamide T shows promise, the current literature provides only a glimpse into its chemical and biological significance.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305142121522D          

 27 30  0  0  0  0            999 V2000
    7.3037    3.0294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5406    2.1391    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1545    1.7960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5191    2.7745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2115   -1.3932    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0185   -1.5647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2949    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9565   -0.6086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5705   -0.9516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7798   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7798    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5086    0.0045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4223    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3155   -0.1670    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1760    1.1606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3475    1.9675    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7280    0.5475    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.8250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079    2.0625    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  4  1  2  0  0  0  0
  6  5  2  0  0  0  0
  8  5  1  0  0  0  0
  9  6  1  0  0  0  0
 10  7  1  0  0  0  0
 11  7  2  0  0  0  0
 13  8  2  0  0  0  0
 14 12  1  0  0  0  0
 14 13  1  0  0  0  0
 15  9  2  0  0  0  0
 15 13  1  0  0  0  0
 16 12  2  0  0  0  0
 17 10  2  0  0  0  0
 18 14  2  0  0  0  0
 19 17  1  0  0  0  0
 20 16  1  0  0  0  0
 21  2  1  0  0  0  0
 21  3  1  0  0  0  0
 21  4  1  0  0  0  0
 21 18  1  0  0  0  0
 22 15  1  0  0  0  0
 22 18  1  0  0  0  0
 23 16  1  0  0  0  0
 23 19  1  0  0  0  0
 24 11  1  0  0  0  0
 24 17  1  0  0  0  0
 24 20  1  0  0  0  0
 25 19  2  0  0  0  0
 26 20  2  0  0  0  0
 27 12  1  0  0  0  0
M  END


  Mrv1652305142121522D          

 27 30  0  0  0  0            999 V2000
    7.3037    3.0294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5406    2.1391    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1545    1.7960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5191    2.7745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2115   -1.3932    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0185   -1.5647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2949    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9565   -0.6086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5705   -0.9516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7798   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7798    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5086    0.0045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4223    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3155   -0.1670    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1760    1.1606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3475    1.9675    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7280    0.5475    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.8250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079    2.0625    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  4  1  2  0  0  0  0
  6  5  2  0  0  0  0
  8  5  1  0  0  0  0
  9  6  1  0  0  0  0
 10  7  1  0  0  0  0
 11  7  2  0  0  0  0
 13  8  2  0  0  0  0
 14 12  1  0  0  0  0
 14 13  1  0  0  0  0
 15  9  2  0  0  0  0
 15 13  1  0  0  0  0
 16 12  2  0  0  0  0
 17 10  2  0  0  0  0
 18 14  2  0  0  0  0
 19 17  1  0  0  0  0
 20 16  1  0  0  0  0
 21  2  1  0  0  0  0
 21  3  1  0  0  0  0
 21  4  1  0  0  0  0
 21 18  1  0  0  0  0
 22 15  1  0  0  0  0
 22 18  1  0  0  0  0
 23 16  1  0  0  0  0
 23 19  1  0  0  0  0
 24 11  1  0  0  0  0
 24 17  1  0  0  0  0
 24 20  1  0  0  0  0
 25 19  2  0  0  0  0
 26 20  2  0  0  0  0
 27 12  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0001693

> <DATABASE_NAME>
MIME

> <SMILES>
[H]\C(C1=C(NC2=CC=CC=C12)C(C)(C)C=C)=C1\NC(=O)C2=CC=CN2C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C21H19N3O2/c1-4-21(2,3)18-14(13-8-5-6-9-15(13)22-18)12-16-20(26)24-11-7-10-17(24)19(25)23-16/h4-12,22H,1H2,2-3H3,(H,23,25)/b16-12-

> <INCHI_KEY>
WXBLMCVYDMVHHI-VBKFSLOCSA-N

> <FORMULA>
C21H19N3O2

> <MOLECULAR_WEIGHT>
345.402

> <EXACT_MASS>
345.147726864

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
37.125227069689046

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3Z)-3-{[2-(2-methylbut-3-en-2-yl)-1H-indol-3-yl]methylidene}-1H,2H,3H,4H-pyrrolo[1,2-a]pyrazine-1,4-dione

> <ALOGPS_LOGP>
4.25

> <JCHEM_LOGP>
3.1725421683333335

> <ALOGPS_LOGS>
-4.94

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
16.550963512724696

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.766909640883537

> <JCHEM_PKA_STRONGEST_BASIC>
-1.8835192893981185

> <JCHEM_POLAR_SURFACE_AREA>
66.89

> <JCHEM_REFRACTIVITY>
102.33699999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.95e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3Z)-3-{[2-(2-methylbut-3-en-2-yl)-1H-indol-3-yl]methylidene}-2H-pyrrolo[1,2-a]pyrazine-1,4-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 14-MAY-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   14-MAY-21         0                                  
HETATM    1  C   UNK     0      13.634   5.655   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.342   3.993   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      13.355   3.353   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      12.169   5.179   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.728  -2.601   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      11.234  -2.921   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.417   0.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.252  -1.136   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      12.265  -1.776   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.322  -0.476   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.322   2.016   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.788   2.310   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.283   0.008   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.122   1.540   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      11.789  -0.312   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.454   1.540   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.787   0.000   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      11.529   2.166   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.121  -0.770   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.121   2.310   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      11.849   3.673   0.000  0.00  0.00           C+0
HETATM   22  N   UNK     0      12.559   1.022   0.000  0.00  0.00           N+0
HETATM   23  N   UNK     0       7.454   0.000   0.000  0.00  0.00           N+0
HETATM   24  N   UNK     0       4.787   1.540   0.000  0.00  0.00           N+0
HETATM   25  O   UNK     0       6.121  -2.310   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       6.121   3.850   0.000  0.00  0.00           O+0
HETATM   27  H   UNK     0       8.788   3.850   0.000  0.00  0.00           H+0
CONECT    1    4                                                            
CONECT    2   21                                                            
CONECT    3   21                                                            
CONECT    4    1   21                                                       
CONECT    5    6    8                                                       
CONECT    6    5    9                                                       
CONECT    7   10   11                                                       
CONECT    8    5   13                                                       
CONECT    9    6   15                                                       
CONECT   10    7   17                                                       
CONECT   11    7   24                                                       
CONECT   12   14   16   27                                                  
CONECT   13    8   14   15                                                  
CONECT   14   12   13   18                                                  
CONECT   15    9   13   22                                                  
CONECT   16   12   20   23                                                  
CONECT   17   10   19   24                                                  
CONECT   18   14   21   22                                                  
CONECT   19   17   23   25                                                  
CONECT   20   16   24   26                                                  
CONECT   21    2    3    4   18                                             
CONECT   22   15   18                                                       
CONECT   23   16   19                                                       
CONECT   24   11   17   20                                                  
CONECT   25   19                                                            
CONECT   26   20                                                            
CONECT   27   12                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   60    0
END

Synonyms

Not Available

Molecular Formula

C₂₁H₁₉N₃O₂

Average Mass

345.402

Monoisotopic Mass

345.147726864

IUPAC Name

(3Z)-3-{[2-(2-methylbut-3-en-2-yl)-1H-indol-3-yl]methylidene}-1H,2H,3H,4H-pyrrolo[1,2-a]pyrazine-1,4-dione

Traditional Name

(3Z)-3-{[2-(2-methylbut-3-en-2-yl)-1H-indol-3-yl]methylidene}-2H-pyrrolo[1,2-a]pyrazine-1,4-dione

CAS Registry Number

Not Available

SMILES

[H]\C(C1=C(NC2=CC=CC=C12)C(C)(C)C=C)=C1\NC(=O)C2=CC=CN2C1=O

InChI Identifier

InChI=1S/C21H19N3O2/c1-4-21(2,3)18-14(13-8-5-6-9-15(13)22-18)12-16-20(26)24-11-7-10-17(24)19(25)23-16/h4-12,22H,1H2,2-3H3,(H,23,25)/b16-12-

InChI Key

WXBLMCVYDMVHHI-VBKFSLOCSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyrrolopyrazines. Pyrrolopyrazines are compounds containing a pyrrolopyrazine moiety, which consists of a pyrrole ring fused to a pyrazine. Pyrrole is 5-membered ring consisting of four carbon atoms and one nitrogen atom. Pyrazine is a 6-membered ring consisting of six carbon atoms and two nitrogen centers at ring positions 1 and 4.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Pyrrolopyrazines

Sub Class

Not Available

Direct Parent

Pyrrolopyrazines

Alternative Parents

Substituents

Indole
Indole or derivatives
Pyrrolopyrazine
Pyrazine
Substituted pyrrole
Benzenoid
Pyrrole
Heteroaromatic compound
Lactam
Azacycle
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Organonitrogen compound
Organic oxygen compound
Organic nitrogen 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	0.004 g/L	ALOGPS
logP	4.25	ALOGPS
logP	3.17	ChemAxon
logS	-4.9	ALOGPS
pKa (Strongest Acidic)	8.77	ChemAxon
pKa (Strongest Basic)	-1.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	66.89 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	102.34 m³·mol⁻¹	ChemAxon
Polarizability	37.13 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Spectrum Type	Description	Splash Key	Deposition Date	View
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2022-08-08	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	Not Available	2022-08-10	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-20	View Spectrum

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

29215245

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

71480279

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 Brevianamide T (MMDBc0001693)

MOL for #<Metabolite:0x00007fb4c3b38c40>

3D MOL for #<Metabolite:0x00007fb4c3b38c40>

3D SDF for #<Metabolite:0x00007fb4c3b38c40>

3D-SDF for #<Metabolite:0x00007fb4c3b38c40>

PDB for #<Metabolite:0x00007fb4c3b38c40>

3D PDB for #<Metabolite:0x00007fb4c3b38c40>

SMILES for #<Metabolite:0x00007fb4c3b38c40>

INCHI for #<Metabolite:0x00007fb4c3b38c40>

Structure for #<Metabolite:0x00007fb4c3b38c40>

3D Structure for #<Metabolite:0x00007fb4c3b38c40>