MiMeDB: Showing metabocard for Fengycin C (MMDBc0020208)

Microbial

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-15 10:10:45 UTC

Update Date

2022-08-12 20:01:20 UTC

Metabolite ID

MMDBc0020208

Metabolite Identification

Common Name

Fengycin C

Description

Plipastatin belongs to the class of organic compounds known as cyclic depsipeptides. These are natural or synthetic compounds having sequences of amino and hydroxy carboxylic acid residues (usually α-amino and α-hydroxy acids) connected in a ring. The residues are commonly but not necessarily regularly alternating. Based on a literature review a significant number of articles have been published on Plipastatin.

Structure

MOL SDF PDB SMILES InChI

Synonyms

Value	Source
Plipastatin a2	MeSH
Plipastatin b2	MeSH
Plipastatins	MeSH
Plipastatin a1	MeSH
Plipastatin b1	MeSH
Fengycin	MeSH
Fengycin C	MeSH

Molecular Formula

C₇₂H₁₁₀N₁₂O₂₀

Average Mass

1463.736

Monoisotopic Mass

1462.79593399

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

Not Available

InChI Identifier

InChI=1S/C72H110N12O20/c1-6-8-9-10-11-12-13-14-15-16-17-20-48(87)41-58(89)76-51(32-35-59(90)91)65(96)77-50(21-18-37-73)64(95)80-55-40-46-25-29-49(30-26-46)104-72(103)61(42(3)7-2)82-67(98)54(39-45-23-27-47(86)28-24-45)81-66(97)52(31-34-57(74)88)78-69(100)56-22-19-38-84(56)71(102)43(4)75-63(94)53(33-36-60(92)93)79-70(101)62(44(5)85)83-68(55)99/h23-30,42-44,48,50-56,61-62,85-87H,6-22,31-41,73H2,1-5H3,(H2,74,88)(H,75,94)(H,76,89)(H,77,96)(H,78,100)(H,79,101)(H,80,95)(H,81,97)(H,82,98)(H,83,99)(H,90,91)(H,92,93)

InChI Key

CUOJDWBMJMRDHN-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cyclic depsipeptides. These are natural or synthetic compounds having sequences of amino and hydroxy carboxylic acid residues (usually α-amino and α-hydroxy acids) connected in a ring. The residues are commonly but not necessarily regularly alternating.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Peptidomimetics

Sub Class

Depsipeptides

Direct Parent

Cyclic depsipeptides

Alternative Parents

Substituents

Cyclic depsipeptide
Glutamic acid or derivatives
Macrolide lactam
Macrolactam
Alpha-amino acid ester
N-acyl-alpha amino acid or derivatives
Alpha-amino acid amide
N-substituted-alpha-amino acid
Alpha-amino acid or derivatives
Tricarboxylic acid or derivatives
1-hydroxy-2-unsubstituted benzenoid
Phenol
Benzenoid
Monocyclic benzene moiety
Fatty amide
N-acyl-amine
Fatty acyl
Tertiary carboxylic acid amide
Pyrrolidine
Carboxamide group
Secondary carboxylic acid amide
Secondary alcohol
Primary carboxylic acid amide
Amino acid
Lactam
Amino acid or derivatives
Lactone
Carboxylic acid ester
Oxacycle
Azacycle
Carboxylic acid derivative
Organoheterocyclic compound
Carboxylic acid
Organopnictogen compound
Organic oxygen compound
Organic nitrogen compound
Carbonyl group
Alcohol
Hydrocarbon derivative
Amine
Organic oxide
Primary amine
Organooxygen compound
Organonitrogen compound
Primary aliphatic amine
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Not Available

Spectra

Spectrum Type	Description	Splash Key	Deposition Date	View

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
Bacteria	Firmicutes	2	Human feces; Human	Metabolic reconstruction; Microbial culture
Bacteria/Eubacteria	Firmicutes	3	Human feces; Human	Metabolic reconstruction; Microbial culture
Bacteria	Actinobacteria	6	Human	Microbial culture
Bacteria/Eubacteria	Bacteroidetes	1		Microbial culture
Bacteria/Eubacteria	Proteobacteria	1		Microbial culture

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

4590478

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5491283

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

CMMC Knowledgebase

Not Available

General References

Showing metabocard for Fengycin C (MMDBc0020208)

MOL for #<Metabolite:0x00007f8d964dc328>

3D MOL for #<Metabolite:0x00007f8d964dc328>

3D SDF for #<Metabolite:0x00007f8d964dc328>

3D-SDF for #<Metabolite:0x00007f8d964dc328>

PDB for #<Metabolite:0x00007f8d964dc328>

3D PDB for #<Metabolite:0x00007f8d964dc328>

SMILES for #<Metabolite:0x00007f8d964dc328>

INCHI for #<Metabolite:0x00007f8d964dc328>

Structure for #<Metabolite:0x00007f8d964dc328>

3D Structure for #<Metabolite:0x00007f8d964dc328>