MiMeDB: Showing metabocard for Spirotryprostatin A (MMDBc0001046)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-14 18:41:57 UTC

Update Date

2025-10-07 16:04:25 UTC

Metabolite ID

MMDBc0001046

Metabolite Identification

Common Name

Spirotryprostatin A

Description

Spirotryprostatin A is a member of the alkaloid chemical class, characterized by its complex bicyclic structure. It is synthesized through a series of chemical reactions, including enantioselective total synthesis that utilizes starting materials such as 2-iodo-5-methoxyaniline and γ-butyrolactone (PMID:36445815 ). The compound has garnered attention for its antifungal properties, as demonstrated by the synthesis and evaluation of various derivatives that exhibit broad-spectrum antifungal activity against multiple plant pathogens (PMID:38398616 ). Notably, molecular docking studies indicate that spirotryprostatin A derivatives interact with the binding site of succinate dehydrogenase (SDH), suggesting potential mechanisms of action (PMID:38398616 ). Additionally, spirotryprostatin A is biosynthesized from fumitremorgin C via the fumiquinazoline biosynthetic pathway, specifically through the action of the FqzB enzyme, which catalyzes the epoxidation process (PMID:33332106 ). The understanding of substrate recognition and tolerance exhibited by FqzB further elucidates the biochemical pathways involved in the formation of spirotryprostatin A (PMID:33332106 ).

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305142120412D          

 32 36  0  0  1  0            999 V2000
    1.5572   -0.9599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8373   -1.5950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1288    0.1358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2437    0.2236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5970   -0.2887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0156   -0.4109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2766   -0.0442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9562    0.9970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7473   -0.1689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6507    0.8692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9313    1.8038    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3806   -0.9079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7027    0.0458    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2246    0.7792    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9117    1.2359    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0901    0.1680    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2443    1.3471    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2906    0.5182    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4451    1.5521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8892   -0.0370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8654    2.0648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5780    1.2915    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6897    2.0304    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1320    0.9626    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4663    0.5526    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.2231    2.3467    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1112   -0.8316    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4087    2.7519    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4417   -0.3209    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2278   -0.6454    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6672    0.7576    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8857   -0.2007    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  4  1  0  0  0  0
  7  6  2  0  0  0  0
  8  4  1  0  0  0  0
 12  1  1  0  0  0  0
 12  2  1  0  0  0  0
 12  9  2  0  0  0  0
 13  6  1  0  0  0  0
 13 10  2  0  0  0  0
 14  7  1  0  0  0  0
 15 10  1  0  0  0  0
 15 14  2  0  0  0  0
 16  5  1  0  0  0  0
 17 11  1  0  0  0  0
 18  9  1  6  0  0  0
 19 17  1  0  0  0  0
 20 16  1  0  0  0  0
 22 11  1  6  0  0  0
 22 14  1  0  0  0  0
 22 18  1  0  0  0  0
 22 21  1  0  0  0  0
 23 15  1  0  0  0  0
 23 21  2  0  0  0  0
 24  8  1  0  0  0  0
 24 16  1  0  0  0  0
 24 19  1  0  0  0  0
 25 17  1  0  0  0  0
 25 18  1  0  0  0  0
 25 20  1  0  0  0  0
 26 19  2  0  0  0  0
 27 20  2  0  0  0  0
 28 21  1  0  0  0  0
 29  3  1  0  0  0  0
 29 13  1  0  0  0  0
 16 30  1  1  0  0  0
 17 31  1  1  0  0  0
 18 32  1  1  0  0  0
M  END


  Mrv1652305142120412D          

 32 36  0  0  1  0            999 V2000
    1.5572   -0.9599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8373   -1.5950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1288    0.1358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2437    0.2236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5970   -0.2887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0156   -0.4109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2766   -0.0442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9562    0.9970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7473   -0.1689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6507    0.8692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9313    1.8038    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3806   -0.9079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7027    0.0458    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2246    0.7792    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9117    1.2359    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0901    0.1680    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2443    1.3471    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2906    0.5182    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4451    1.5521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8892   -0.0370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8654    2.0648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5780    1.2915    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6897    2.0304    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1320    0.9626    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4663    0.5526    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.2231    2.3467    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1112   -0.8316    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4087    2.7519    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4417   -0.3209    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2278   -0.6454    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6672    0.7576    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8857   -0.2007    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  4  1  0  0  0  0
  7  6  2  0  0  0  0
  8  4  1  0  0  0  0
 12  1  1  0  0  0  0
 12  2  1  0  0  0  0
 12  9  2  0  0  0  0
 13  6  1  0  0  0  0
 13 10  2  0  0  0  0
 14  7  1  0  0  0  0
 15 10  1  0  0  0  0
 15 14  2  0  0  0  0
 16  5  1  0  0  0  0
 17 11  1  0  0  0  0
 18  9  1  6  0  0  0
 19 17  1  0  0  0  0
 20 16  1  0  0  0  0
 22 11  1  6  0  0  0
 22 14  1  0  0  0  0
 22 18  1  0  0  0  0
 22 21  1  0  0  0  0
 23 15  1  0  0  0  0
 23 21  2  0  0  0  0
 24  8  1  0  0  0  0
 24 16  1  0  0  0  0
 24 19  1  0  0  0  0
 25 17  1  0  0  0  0
 25 18  1  0  0  0  0
 25 20  1  0  0  0  0
 26 19  2  0  0  0  0
 27 20  2  0  0  0  0
 28 21  1  0  0  0  0
 29  3  1  0  0  0  0
 29 13  1  0  0  0  0
 16 30  1  1  0  0  0
 17 31  1  1  0  0  0
 18 32  1  1  0  0  0
M  END
> <DATABASE_ID>
MMDBc0001046

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@@]12CCCN1C(=O)[C@]1([H])C[C@@]3(C(O)=NC4=C3C=CC(OC)=C4)[C@]([H])(C=C(C)C)N1C2=O

> <INCHI_IDENTIFIER>
InChI=1S/C22H25N3O4/c1-12(2)9-18-22(14-7-6-13(29-3)10-15(14)23-21(22)28)11-17-19(26)24-8-4-5-16(24)20(27)25(17)18/h6-7,9-10,16-18H,4-5,8,11H2,1-3H3,(H,23,28)/t16-,17-,18-,22-/m0/s1

> <INCHI_KEY>
MQJKGSIAJNXSCM-ORGXJRBJSA-N

> <FORMULA>
C22H25N3O4

> <MOLECULAR_WEIGHT>
395.459

> <EXACT_MASS>
395.184506297

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
42.251060093350645

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3S,3'S,6'S,9'S)-2-hydroxy-6-methoxy-6'-(2-methylprop-1-en-1-yl)-1',7'-diazaspiro[indole-3,5'-tricyclo[7.3.0.0^{3,7}]dodecane]-2',8'-dione

> <ALOGPS_LOGP>
1.48

> <JCHEM_LOGP>
1.992618054666667

> <ALOGPS_LOGS>
-3.28

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
19.313322795768908

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.181626470431944

> <JCHEM_PKA_STRONGEST_BASIC>
0.8437008073510442

> <JCHEM_POLAR_SURFACE_AREA>
82.44

> <JCHEM_REFRACTIVITY>
108.88089999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.07e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3S,3'S,6'S,9'S)-2-hydroxy-6-methoxy-6'-(2-methylprop-1-en-1-yl)-1',7'-diazaspiro[indole-3,5'-tricyclo[7.3.0.0^{3,7}]dodecane]-2',8'-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       2.907  -1.792   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.296  -2.977   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      11.440   0.254   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.321   0.417   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.114  -0.539   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.496  -0.767   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.116  -0.082   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.785   1.861   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.128  -0.315   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.681   1.622   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.605   3.367   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.444  -1.695   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.778   0.086   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.019   1.454   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.302   2.307   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.168   0.314   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.323   2.515   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.276   0.967   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.831   2.897   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.660  -0.069   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.349   3.854   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.812   2.411   0.000  0.00  0.00           C+0
HETATM   23  N   UNK     0       6.887   3.790   0.000  0.00  0.00           N+0
HETATM   24  N   UNK     0      -0.246   1.797   0.000  0.00  0.00           N+0
HETATM   25  N   UNK     0       2.737   1.031   0.000  0.00  0.00           N+0
HETATM   26  O   UNK     0       0.417   4.380   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       2.074  -1.552   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       4.496   5.137   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      10.158  -0.599   0.000  0.00  0.00           O+0
HETATM   30  H   UNK     0       0.425  -1.205   0.000  0.00  0.00           H+0
HETATM   31  H   UNK     0       1.245   1.414   0.000  0.00  0.00           H+0
HETATM   32  H   UNK     0       3.520  -0.375   0.000  0.00  0.00           H+0
CONECT    1   12                                                            
CONECT    2   12                                                            
CONECT    3   29                                                            
CONECT    4    5    8                                                       
CONECT    5    4   16                                                       
CONECT    6    7   13                                                       
CONECT    7    6   14                                                       
CONECT    8    4   24                                                       
CONECT    9   12   18                                                       
CONECT   10   13   15                                                       
CONECT   11   17   22                                                       
CONECT   12    1    2    9                                                  
CONECT   13    6   10   29                                                  
CONECT   14    7   15   22                                                  
CONECT   15   10   14   23                                                  
CONECT   16    5   20   24   30                                             
CONECT   17   11   19   25   31                                             
CONECT   18    9   22   25   32                                             
CONECT   19   17   24   26                                                  
CONECT   20   16   25   27                                                  
CONECT   21   22   23   28                                                  
CONECT   22   11   14   18   21                                             
CONECT   23   15   21                                                       
CONECT   24    8   16   19                                                  
CONECT   25   17   18   20                                                  
CONECT   26   19                                                            
CONECT   27   20                                                            
CONECT   28   21                                                            
CONECT   29    3   13                                                       
CONECT   30   16                                                            
CONECT   31   17                                                            
CONECT   32   18                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   72    0
END

Synonyms

Not Available

Molecular Formula

C₂₂H₂₅N₃O₄

Average Mass

395.459

Monoisotopic Mass

395.184506297

IUPAC Name

(3S,3'S,6'S,9'S)-2-hydroxy-6-methoxy-6'-(2-methylprop-1-en-1-yl)-1',7'-diazaspiro[indole-3,5'-tricyclo[7.3.0.0^{3,7}]dodecane]-2',8'-dione

Traditional Name

(3S,3'S,6'S,9'S)-2-hydroxy-6-methoxy-6'-(2-methylprop-1-en-1-yl)-1',7'-diazaspiro[indole-3,5'-tricyclo[7.3.0.0^{3,7}]dodecane]-2',8'-dione

CAS Registry Number

Not Available

SMILES

[H][C@@]12CCCN1C(=O)[C@]1([H])C[C@@]3(C(O)=NC4=C3C=CC(OC)=C4)[C@]([H])(C=C(C)C)N1C2=O

InChI Identifier

InChI=1S/C22H25N3O4/c1-12(2)9-18-22(14-7-6-13(29-3)10-15(14)23-21(22)28)11-17-19(26)24-8-4-5-16(24)20(27)25(17)18/h6-7,9-10,16-18H,4-5,8,11H2,1-3H3,(H,23,28)/t16-,17-,18-,22-/m0/s1

InChI Key

MQJKGSIAJNXSCM-ORGXJRBJSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as alpha amino acids and derivatives. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon), or a derivative thereof.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Alpha amino acids and derivatives

Alternative Parents

Substituents

Alpha-amino acid or derivatives
Indole or derivatives
Dihydroindole
Anisole
Dioxopiperazine
Phenol ether
2,5-dioxopiperazine
N-alkylpiperazine
Alkyl aryl ether
Benzenoid
1,4-diazinane
Piperazine
Tertiary carboxylic acid amide
Pyrrolidine
Carboxamide group
Secondary carboxylic acid amide
Lactam
Ether
Azacycle
Organoheterocyclic compound
Organic oxide
Organic oxygen compound
Organic nitrogen compound
Hydrocarbon derivative
Carbonyl group
Organonitrogen 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	0.21 g/L	ALOGPS
logP	1.48	ALOGPS
logP	1.99	ChemAxon
logS	-3.3	ALOGPS
pKa (Strongest Acidic)	4.18	ChemAxon
pKa (Strongest Basic)	0.84	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	82.44 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	108.88 m³·mol⁻¹	ChemAxon
Polarizability	42.25 Å³	ChemAxon
Number of Rings	5	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
MS	Mass Spectrum (Electron Ionization)	Not Available	2022-08-06	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

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	3	Human feces; Human supragingival plaque	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

C00026639

Chemspider ID

8583811

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Spirotryprostatin A

METLIN ID

Not Available

PubChem Compound

10408374

PDB ID

Not Available

ChEBI ID

Not Available

CMMC Knowledgebase

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 Spirotryprostatin A (MMDBc0001046)

MOL for #<Metabolite:0x00007fd4361e84c8>

3D MOL for #<Metabolite:0x00007fd4361e84c8>

3D SDF for #<Metabolite:0x00007fd4361e84c8>

3D-SDF for #<Metabolite:0x00007fd4361e84c8>

PDB for #<Metabolite:0x00007fd4361e84c8>

3D PDB for #<Metabolite:0x00007fd4361e84c8>

SMILES for #<Metabolite:0x00007fd4361e84c8>

INCHI for #<Metabolite:0x00007fd4361e84c8>

Structure for #<Metabolite:0x00007fd4361e84c8>

3D Structure for #<Metabolite:0x00007fd4361e84c8>