MiMeDB: Showing metabocard for Stagonosporyne G (MMDBc0025822)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2021-05-15 15:32:10 UTC

Update Date

2025-10-07 16:07:36 UTC

Metabolite ID

MMDBc0025822

Metabolite Identification

Common Name

Stagonosporyne G

Description

Stagonosporyne G is a polyketide, a chemical class characterized by its complex structure formed through the condensation of acetyl and malonyl units. Its chemical structure features a series of carbon chains and functional groups that contribute to its biological activity. Stagonosporyne G is involved in various biochemical pathways, particularly in the context of herbicidal activity, where it has been shown to exhibit significant effects against certain plant species. The compound's mechanism may involve the disruption of metabolic processes in target organisms, leading to herbicidal effects. In a study evaluating multiple compounds for their herbicidal properties, stagonosporyne G was noted for displaying the most significant herbicidal activity, highlighting its potential utility in agricultural applications (PMID:31302342 ). This indicates that Stagonosporyne G may play a role in the development of natural herbicides, contributing to the exploration of environmentally friendly alternatives in pest management strategies.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152117322D          

 18 18  0  0  1  0            999 V2000
   -2.8579   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    0.4125    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.8250    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    1.6500    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    1.6500    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  4  3  3  0  0  0  0
  6  5  2  0  0  0  0
  7  1  2  0  0  0  0
  7  2  1  0  0  0  0
  7  3  1  0  0  0  0
  8  4  1  1  0  0  0
  9  5  1  0  0  0  0
  9  8  1  0  0  0  0
 10  6  1  0  0  0  0
 11  8  1  0  0  0  0
 11 10  1  0  0  0  0
  9 12  1  6  0  0  0
 10 13  1  1  0  0  0
 11 14  1  6  0  0  0
  8 15  1  6  0  0  0
  9 16  1  1  0  0  0
 10 17  1  6  0  0  0
 11 18  1  1  0  0  0
M  END
> <DATABASE_ID>
MMDBc0025822

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@]1(O)C=C[C@]([H])(O)[C@@]([H])(C#CC(C)=C)[C@]1([H])O

> <INCHI_IDENTIFIER>
InChI=1S/C11H14O3/c1-7(2)3-4-8-9(12)5-6-10(13)11(8)14/h5-6,8-14H,1H2,2H3/t8-,9+,10+,11+/m1/s1

> <INCHI_KEY>
ZPYFIPQZEARZFJ-RCWTZXSCSA-N

> <FORMULA>
C11H14O3

> <MOLECULAR_WEIGHT>
194.23

> <EXACT_MASS>
194.094294311

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
28

> <JCHEM_AVERAGE_POLARIZABILITY>
20.4958145251528

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2S,3R,4S)-3-(3-methylbut-3-en-1-yn-1-yl)cyclohex-5-ene-1,2,4-triol

> <ALOGPS_LOGP>
-0.40

> <JCHEM_LOGP>
0.03328009066666637

> <ALOGPS_LOGS>
-2.39

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.189507086029675

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.206222756027671

> <JCHEM_PKA_STRONGEST_BASIC>
-3.1766951786803217

> <JCHEM_POLAR_SURFACE_AREA>
60.69

> <JCHEM_REFRACTIVITY>
54.97839999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.83e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,3R,4S)-3-(3-methylbut-3-en-1-yn-1-yl)cyclohex-5-ene-1,2,4-triol

> <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      -5.335  -1.540   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.001  -3.850   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.667  -1.540   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -4.001  -2.310   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       1.334  -2.310   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0       1.334   3.850   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0      -1.334   2.310   0.000  0.00  0.00           O+0
HETATM   15  H   UNK     0      -1.334   0.770   0.000  0.00  0.00           H+0
HETATM   16  H   UNK     0       0.000  -1.540   0.000  0.00  0.00           H+0
HETATM   17  H   UNK     0       2.667   3.080   0.000  0.00  0.00           H+0
HETATM   18  H   UNK     0       0.000   3.080   0.000  0.00  0.00           H+0
CONECT    1    7                                                            
CONECT    2    7                                                            
CONECT    3    4    7                                                       
CONECT    4    3    8                                                       
CONECT    5    6    9                                                       
CONECT    6    5   10                                                       
CONECT    7    1    2    3                                                  
CONECT    8    4    9   11   15                                             
CONECT    9    5    8   12   16                                             
CONECT   10    6   11   13   17                                             
CONECT   11    8   10   14   18                                             
CONECT   12    9                                                            
CONECT   13   10                                                            
CONECT   14   11                                                            
CONECT   15    8                                                            
CONECT   16    9                                                            
CONECT   17   10                                                            
CONECT   18   11                                                            
MASTER        0    0    0    0    0    0    0    0   18    0   36    0
END

Synonyms

Not Available

Molecular Formula

C₁₁H₁₄O₃

Average Mass

194.23

Monoisotopic Mass

194.094294311

IUPAC Name

(1S,2S,3R,4S)-3-(3-methylbut-3-en-1-yn-1-yl)cyclohex-5-ene-1,2,4-triol

Traditional Name

(1S,2S,3R,4S)-3-(3-methylbut-3-en-1-yn-1-yl)cyclohex-5-ene-1,2,4-triol

CAS Registry Number

Not Available

SMILES

[H][C@]1(O)C=C[C@]([H])(O)[C@@]([H])(C#CC(C)=C)[C@]1([H])O

InChI Identifier

InChI=1S/C11H14O3/c1-7(2)3-4-8-9(12)5-6-10(13)11(8)14/h5-6,8-14H,1H2,2H3/t8-,9+,10+,11+/m1/s1

InChI Key

ZPYFIPQZEARZFJ-RCWTZXSCSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cyclitols and derivatives. Cyclitols and derivatives are compounds containing a cycloalkane moiety with one hydroxyl group on each of three or more ring atoms. These of also include derivatives where the hydrogen atom of one or more of the hydroxyl groups is replaced with another atom.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Alcohols and polyols

Direct Parent

Cyclitols and derivatives

Alternative Parents

Substituents

Cyclitol or derivatives
Secondary alcohol
Polyol
Hydrocarbon derivative
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic homomonocyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.78 g/L	ALOGPS
logP	-0.4	ALOGPS
logP	0.033	ChemAxon
logS	-2.4	ALOGPS
pKa (Strongest Acidic)	13.21	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	60.69 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	54.98 m³·mol⁻¹	ChemAxon
Polarizability	20.5 Å³	ChemAxon
Number of Rings	1	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

Not Available

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		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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

146682448

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

CMMC Knowledgebase

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 Stagonosporyne G (MMDBc0025822)

MOL for #<Metabolite:0x00007f8da77e4cd0>

3D MOL for #<Metabolite:0x00007f8da77e4cd0>

3D SDF for #<Metabolite:0x00007f8da77e4cd0>

3D-SDF for #<Metabolite:0x00007f8da77e4cd0>

PDB for #<Metabolite:0x00007f8da77e4cd0>

3D PDB for #<Metabolite:0x00007f8da77e4cd0>

SMILES for #<Metabolite:0x00007f8da77e4cd0>

INCHI for #<Metabolite:0x00007f8da77e4cd0>

Structure for #<Metabolite:0x00007f8da77e4cd0>

3D Structure for #<Metabolite:0x00007f8da77e4cd0>