MiMeDB: Showing metabocard for Chaetoviridins K (MMDBc0010835)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-15 02:53:47 UTC

Update Date

2022-08-31 06:32:20 UTC

Metabolite ID

MMDBc0010835

Metabolite Identification

Common Name

Chaetoviridins K

Description

8-chloro-12-hydroxy-5-(3-hydroxy-3-methylpent-1-en-1-yl)-10,13,14-trimethyl-4,11,15-trioxatetracyclo[8.7.0.0²,⁷.0¹²,¹⁷]heptadeca-2,5,7-triene-9,16-dione belongs to the class of organic compounds known as delta valerolactones. These are cyclic organic compounds containing an oxan-2- one moiety. Based on a literature review very few articles have been published on 8-chloro-12-hydroxy-5-(3-hydroxy-3-methylpent-1-en-1-yl)-10,13,14-trimethyl-4,11,15-trioxatetracyclo[8.7.0.0²,⁷.0¹²,¹⁷]heptadeca-2,5,7-triene-9,16-dione.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152104532D          

 31 34  0  0  0  0            999 V2000
   10.4697   -0.2015    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8661   -1.5067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4407    0.0876    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3534   -0.7470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2211   -2.5422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8291    0.3183    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6475    0.2485    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2881   -0.2714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7470   -0.8610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4658    0.1787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4501   -0.9239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2374   -0.1268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8769   -0.0463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9765   -1.1559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3359   -0.6360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5654   -0.9309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8307   -0.5555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8466   -1.9706    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0761   -2.2654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6180    0.2416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0586    0.0235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4355   -1.7456    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2467   -1.1383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4872   -2.4905    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    4.9462   -3.0801    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2020    0.8243    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.7637    0.7940    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7269   -1.7789    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2363    0.4735    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8214    0.4559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6205   -1.8738    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  6  1  1  0  0  0  0
  8  7  2  0  0  0  0
 11  2  1  0  0  0  0
 12  3  1  0  0  0  0
 12 11  1  0  0  0  0
 13  7  1  0  0  0  0
 13  9  2  0  0  0  0
 14  9  1  0  0  0  0
 15 10  2  0  0  0  0
 15 14  1  0  0  0  0
 16 15  1  0  0  0  0
 17 16  1  0  0  0  0
 18 14  2  0  0  0  0
 19 18  1  0  0  0  0
 20 17  1  0  0  0  0
 21  4  1  0  0  0  0
 21  6  1  0  0  0  0
  8 21  1  4  0  0  0
 22  5  1  0  0  0  0
 22 16  1  0  0  0  0
 22 19  1  0  0  0  0
 23 11  1  0  0  0  0
 23 17  1  0  0  0  0
 24 18  1  0  0  0  0
 25 19  2  0  0  0  0
 26 20  2  0  0  0  0
 27 21  1  0  0  0  0
 28 23  1  0  0  0  0
 29 10  1  0  0  0  0
 29 13  1  0  0  0  0
 30 12  1  0  0  0  0
 30 20  1  0  0  0  0
 31 22  1  0  0  0  0
 31 23  1  0  0  0  0
M  END


  Mrv1652305152104532D          

 31 34  0  0  0  0            999 V2000
   10.4697   -0.2015    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8661   -1.5067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4407    0.0876    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3534   -0.7470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2211   -2.5422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8291    0.3183    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6475    0.2485    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2881   -0.2714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7470   -0.8610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4658    0.1787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4501   -0.9239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2374   -0.1268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8769   -0.0463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9765   -1.1559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3359   -0.6360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5654   -0.9309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8307   -0.5555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8466   -1.9706    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0761   -2.2654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6180    0.2416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0586    0.0235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4355   -1.7456    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2467   -1.1383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4872   -2.4905    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    4.9462   -3.0801    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2020    0.8243    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.7637    0.7940    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7269   -1.7789    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2363    0.4735    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8214    0.4559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6205   -1.8738    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  6  1  1  0  0  0  0
  8  7  2  0  0  0  0
 11  2  1  0  0  0  0
 12  3  1  0  0  0  0
 12 11  1  0  0  0  0
 13  7  1  0  0  0  0
 13  9  2  0  0  0  0
 14  9  1  0  0  0  0
 15 10  2  0  0  0  0
 15 14  1  0  0  0  0
 16 15  1  0  0  0  0
 17 16  1  0  0  0  0
 18 14  2  0  0  0  0
 19 18  1  0  0  0  0
 20 17  1  0  0  0  0
 21  4  1  0  0  0  0
 21  6  1  0  0  0  0
  8 21  1  4  0  0  0
 22  5  1  0  0  0  0
 22 16  1  0  0  0  0
 22 19  1  0  0  0  0
 23 11  1  0  0  0  0
 23 17  1  0  0  0  0
 24 18  1  0  0  0  0
 25 19  2  0  0  0  0
 26 20  2  0  0  0  0
 27 21  1  0  0  0  0
 28 23  1  0  0  0  0
 29 10  1  0  0  0  0
 29 13  1  0  0  0  0
 30 12  1  0  0  0  0
 30 20  1  0  0  0  0
 31 22  1  0  0  0  0
 31 23  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0010835

> <DATABASE_NAME>
MIME

> <SMILES>
CCC(C)(O)C=CC1=CC2=C(Cl)C(=O)C3(C)OC4(O)C(C3C2=CO1)C(=O)OC(C)C4C

> <INCHI_IDENTIFIER>
InChI=1S/C23H27ClO7/c1-6-21(4,27)8-7-13-9-14-15(10-29-13)16-17-20(26)30-12(3)11(2)23(17,28)31-22(16,5)19(25)18(14)24/h7-12,16-17,27-28H,6H2,1-5H3

> <INCHI_KEY>
AHSSGPXZWGCGLY-UHFFFAOYSA-N

> <FORMULA>
C23H27ClO7

> <MOLECULAR_WEIGHT>
450.91

> <EXACT_MASS>
450.1445309

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
46.587256299998

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
8-chloro-12-hydroxy-5-(3-hydroxy-3-methylpent-1-en-1-yl)-10,13,14-trimethyl-4,11,15-trioxatetracyclo[8.7.0.0^{2,7}.0^{12,17}]heptadeca-2,5,7-triene-9,16-dione

> <ALOGPS_LOGP>
3.11

> <JCHEM_LOGP>
2.271285420333335

> <ALOGPS_LOGS>
-4.06

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.666240839921603

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.277584174609574

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9448522094869976

> <JCHEM_POLAR_SURFACE_AREA>
102.29000000000002

> <JCHEM_REFRACTIVITY>
116.30690000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.96e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
8-chloro-12-hydroxy-5-(3-hydroxy-3-methylpent-1-en-1-yl)-10,13,14-trimethyl-4,11,15-trioxatetracyclo[8.7.0.0^{2,7}.0^{12,17}]heptadeca-2,5,7-triene-9,16-dione

> <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      19.543  -0.376   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.483  -2.812   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.689   0.163   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      17.460  -1.394   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.879  -4.745   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      18.348   0.594   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      14.275   0.464   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      15.471  -0.507   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      12.594  -1.607   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.203   0.334   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.573  -1.725   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.176  -0.237   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      12.837  -0.086   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      11.156  -2.158   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.960  -1.187   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.522  -1.738   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.151  -1.037   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      10.914  -3.678   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.475  -4.229   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.754   0.451   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      16.909   0.044   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.280  -3.258   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.061  -2.125   0.000  0.00  0.00           C+0
HETATM   24 Cl   UNK     0      12.109  -4.649   0.000  0.00  0.00          Cl+0
HETATM   25  O   UNK     0       9.233  -5.750   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       7.844   1.539   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0      16.359   1.482   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       5.090  -3.321   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      11.641   0.884   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       5.267   0.851   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       6.758  -3.498   0.000  0.00  0.00           O+0
CONECT    1    6                                                            
CONECT    2   11                                                            
CONECT    3   12                                                            
CONECT    4   21                                                            
CONECT    5   22                                                            
CONECT    6    1   21                                                       
CONECT    7    8   13                                                       
CONECT    8    7   21                                                       
CONECT    9   13   14                                                       
CONECT   10   15   29                                                       
CONECT   11    2   12   23                                                  
CONECT   12    3   11   30                                                  
CONECT   13    7    9   29                                                  
CONECT   14    9   15   18                                                  
CONECT   15   10   14   16                                                  
CONECT   16   15   17   22                                                  
CONECT   17   16   20   23                                                  
CONECT   18   14   19   24                                                  
CONECT   19   18   22   25                                                  
CONECT   20   17   26   30                                                  
CONECT   21    4    6    8   27                                             
CONECT   22    5   16   19   31                                             
CONECT   23   11   17   28   31                                             
CONECT   24   18                                                            
CONECT   25   19                                                            
CONECT   26   20                                                            
CONECT   27   21                                                            
CONECT   28   23                                                            
CONECT   29   10   13                                                       
CONECT   30   12   20                                                       
CONECT   31   22   23                                                       
MASTER        0    0    0    0    0    0    0    0   31    0   68    0
END

Synonyms

Not Available

Molecular Formula

C₂₃H₂₇ClO₇

Average Mass

450.91

Monoisotopic Mass

450.1445309

IUPAC Name

8-chloro-12-hydroxy-5-(3-hydroxy-3-methylpent-1-en-1-yl)-10,13,14-trimethyl-4,11,15-trioxatetracyclo[8.7.0.0^{2,7}.0^{12,17}]heptadeca-2,5,7-triene-9,16-dione

Traditional Name

8-chloro-12-hydroxy-5-(3-hydroxy-3-methylpent-1-en-1-yl)-10,13,14-trimethyl-4,11,15-trioxatetracyclo[8.7.0.0^{2,7}.0^{12,17}]heptadeca-2,5,7-triene-9,16-dione

CAS Registry Number

Not Available

SMILES

CCC(C)(O)C=CC1=CC2=C(Cl)C(=O)C3(C)OC4(O)C(C3C2=CO1)C(=O)OC(C)C4C

InChI Identifier

InChI=1S/C23H27ClO7/c1-6-21(4,27)8-7-13-9-14-15(10-29-13)16-17-20(26)30-12(3)11(2)23(17,28)31-22(16,5)19(25)18(14)24/h7-12,16-17,27-28H,6H2,1-5H3

InChI Key

AHSSGPXZWGCGLY-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as delta valerolactones. These are cyclic organic compounds containing an oxan-2- one moiety.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Lactones

Sub Class

Delta valerolactones

Direct Parent

Delta valerolactones

Alternative Parents

Substituents

Cyclohexenone
Delta_valerolactone
Delta valerolactone
Pyran
Oxane
Alpha-haloketone
Alpha-chloroketone
Tetrahydrofuran
Tertiary alcohol
Ketone
Hemiacetal
Carboxylic acid ester
Oxacycle
Chloroalkene
Haloalkene
Vinyl halide
Vinyl chloride
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organochloride
Organohalogen compound
Carbonyl group
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.04 g/L	ALOGPS
logP	3.11	ALOGPS
logP	2.27	ChemAxon
logS	-4.1	ALOGPS
pKa (Strongest Acidic)	11.28	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	102.29 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	116.31 m³·mol⁻¹	ChemAxon
Polarizability	46.59 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

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

Metabolic Reactions

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

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

139585974

PDB ID

Not Available

ChEBI ID

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 Chaetoviridins K (MMDBc0010835)

MOL for #<Metabolite:0x00007f922c021348>

3D MOL for #<Metabolite:0x00007f922c021348>

3D SDF for #<Metabolite:0x00007f922c021348>

3D-SDF for #<Metabolite:0x00007f922c021348>

PDB for #<Metabolite:0x00007f922c021348>

3D PDB for #<Metabolite:0x00007f922c021348>

SMILES for #<Metabolite:0x00007f922c021348>

INCHI for #<Metabolite:0x00007f922c021348>

Structure for #<Metabolite:0x00007f922c021348>

3D Structure for #<Metabolite:0x00007f922c021348>