MiMeDB: Showing metabocard for Asperteretal E (MMDBc0027524)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-15 17:14:30 UTC

Update Date

2022-08-31 06:52:38 UTC

Metabolite ID

MMDBc0027524

Metabolite Identification

Common Name

Asperteretal E

Description

CHEMBL4213599 belongs to the class of organic compounds known as 2,2-dimethyl-1-benzopyrans. These are organic compounds containing a 1-benzopyran moiety that carries two methyl groups at the 2-position. Based on a literature review very few articles have been published on CHEMBL4213599.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152119142D          

 27 30  0  0  0  0            999 V2000
    2.9559    1.9192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4256    2.8377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0525    0.5770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4941   -0.7820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8372    0.8319    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2787   -0.5271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    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    0.8250    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    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8810   -0.2300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4502    0.2799    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
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0964   -0.4849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7615   -0.4849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8414   -1.2695    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
   -5.2349    0.5348    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0231   -0.2300    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3264   -1.9370    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0164   -1.2695    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  6  4  1  0  0  0  0
  7  5  2  0  0  0  0
  8  3  2  0  0  0  0
 10  9  1  0  0  0  0
 13  3  1  0  0  0  0
 13 11  2  0  0  0  0
 13 12  1  0  0  0  0
 14  4  2  0  0  0  0
 14  5  1  0  0  0  0
 15  9  1  0  0  0  0
 15 11  1  0  0  0  0
 16  6  2  0  0  0  0
 16  7  1  0  0  0  0
 17 12  1  0  0  0  0
 18  8  1  0  0  0  0
 18 15  2  0  0  0  0
 19 14  1  0  0  0  0
 19 17  2  0  0  0  0
 20 17  1  0  0  0  0
 21 19  1  0  0  0  0
 22  1  1  0  0  0  0
 22  2  1  0  0  0  0
 22 10  1  0  0  0  0
 23 16  1  0  0  0  0
 24 20  2  0  0  0  0
 25 21  1  0  0  0  0
 26 20  1  0  0  0  0
 26 21  1  0  0  0  0
 27 18  1  0  0  0  0
 27 22  1  0  0  0  0
M  END


  Mrv1652305152119142D          

 27 30  0  0  0  0            999 V2000
    2.9559    1.9192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4256    2.8377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0525    0.5770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4941   -0.7820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8372    0.8319    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2787   -0.5271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    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    0.8250    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    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8810   -0.2300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4502    0.2799    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
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0964   -0.4849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7615   -0.4849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8414   -1.2695    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
   -5.2349    0.5348    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0231   -0.2300    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3264   -1.9370    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0164   -1.2695    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  6  4  1  0  0  0  0
  7  5  2  0  0  0  0
  8  3  2  0  0  0  0
 10  9  1  0  0  0  0
 13  3  1  0  0  0  0
 13 11  2  0  0  0  0
 13 12  1  0  0  0  0
 14  4  2  0  0  0  0
 14  5  1  0  0  0  0
 15  9  1  0  0  0  0
 15 11  1  0  0  0  0
 16  6  2  0  0  0  0
 16  7  1  0  0  0  0
 17 12  1  0  0  0  0
 18  8  1  0  0  0  0
 18 15  2  0  0  0  0
 19 14  1  0  0  0  0
 19 17  2  0  0  0  0
 20 17  1  0  0  0  0
 21 19  1  0  0  0  0
 22  1  1  0  0  0  0
 22  2  1  0  0  0  0
 22 10  1  0  0  0  0
 23 16  1  0  0  0  0
 24 20  2  0  0  0  0
 25 21  1  0  0  0  0
 26 20  1  0  0  0  0
 26 21  1  0  0  0  0
 27 18  1  0  0  0  0
 27 22  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0027524

> <DATABASE_NAME>
MIME

> <SMILES>
CC1(C)CCC2=C(O1)C=CC(CC1=C(C(O)OC1=O)C1=CC=C(O)C=C1)=C2

> <INCHI_IDENTIFIER>
InChI=1S/C22H22O5/c1-22(2)10-9-15-11-13(3-8-18(15)27-22)12-17-19(21(25)26-20(17)24)14-4-6-16(23)7-5-14/h3-8,11,21,23,25H,9-10,12H2,1-2H3

> <INCHI_KEY>
QCPXFZKWSHOJCI-UHFFFAOYSA-N

> <FORMULA>
C22H22O5

> <MOLECULAR_WEIGHT>
366.413

> <EXACT_MASS>
366.146723808

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
49

> <JCHEM_AVERAGE_POLARIZABILITY>
38.863180123460786

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-[(2,2-dimethyl-3,4-dihydro-2H-1-benzopyran-6-yl)methyl]-5-hydroxy-4-(4-hydroxyphenyl)-2,5-dihydrofuran-2-one

> <ALOGPS_LOGP>
3.77

> <JCHEM_LOGP>
4.382585628666666

> <ALOGPS_LOGS>
-4.55

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.590423171106236

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.15112017481484

> <JCHEM_PKA_STRONGEST_BASIC>
-4.303755587407594

> <JCHEM_POLAR_SURFACE_AREA>
75.99

> <JCHEM_REFRACTIVITY>
101.1191

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.03e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-[(2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl)methyl]-5-hydroxy-4-(4-hydroxyphenyl)-5H-furan-2-one

> <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       5.518   3.583   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.528   5.297   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -5.698   1.077   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -6.522  -1.460   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -7.163   1.553   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -7.987  -0.984   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.001   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  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -5.378  -0.429   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -8.307   0.522   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -3.913  -0.905   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.421  -0.905   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -3.437  -2.370   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -9.772   0.998   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       0.043  -0.429   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0      -4.343  -3.616   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0      -1.897  -2.370   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       2.667   4.620   0.000  0.00  0.00           O+0
CONECT    1   22                                                            
CONECT    2   22                                                            
CONECT    3    8   13                                                       
CONECT    4    6   14                                                       
CONECT    5    7   14                                                       
CONECT    6    4   16                                                       
CONECT    7    5   16                                                       
CONECT    8    3   18                                                       
CONECT    9   10   15                                                       
CONECT   10    9   22                                                       
CONECT   11   13   15                                                       
CONECT   12   13   17                                                       
CONECT   13    3   11   12                                                  
CONECT   14    4    5   19                                                  
CONECT   15    9   11   18                                                  
CONECT   16    6    7   23                                                  
CONECT   17   12   19   20                                                  
CONECT   18    8   15   27                                                  
CONECT   19   14   17   21                                                  
CONECT   20   17   24   26                                                  
CONECT   21   19   25   26                                                  
CONECT   22    1    2   10   27                                             
CONECT   23   16                                                            
CONECT   24   20                                                            
CONECT   25   21                                                            
CONECT   26   20   21                                                       
CONECT   27   18   22                                                       
MASTER        0    0    0    0    0    0    0    0   27    0   60    0
END

Synonyms

Not Available

Molecular Formula

C₂₂H₂₂O₅

Average Mass

366.413

Monoisotopic Mass

366.146723808

IUPAC Name

3-[(2,2-dimethyl-3,4-dihydro-2H-1-benzopyran-6-yl)methyl]-5-hydroxy-4-(4-hydroxyphenyl)-2,5-dihydrofuran-2-one

Traditional Name

3-[(2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl)methyl]-5-hydroxy-4-(4-hydroxyphenyl)-5H-furan-2-one

CAS Registry Number

Not Available

SMILES

CC1(C)CCC2=C(O1)C=CC(CC1=C(C(O)OC1=O)C1=CC=C(O)C=C1)=C2

InChI Identifier

InChI=1S/C22H22O5/c1-22(2)10-9-15-11-13(3-8-18(15)27-22)12-17-19(21(25)26-20(17)24)14-4-6-16(23)7-5-14/h3-8,11,21,23,25H,9-10,12H2,1-2H3

InChI Key

QCPXFZKWSHOJCI-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 2,2-dimethyl-1-benzopyrans. These are organic compounds containing a 1-benzopyran moiety that carries two methyl groups at the 2-position.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

2,2-dimethyl-1-benzopyrans

Alternative Parents

Substituents

2,2-dimethyl-1-benzopyran
1-hydroxy-2-unsubstituted benzenoid
Phenol
Alkyl aryl ether
Benzenoid
2-furanone
Monocyclic benzene moiety
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Dihydrofuran
Lactone
Hemiacetal
Carboxylic acid ester
Oxacycle
Monocarboxylic acid or derivatives
Ether
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
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	0.01 g/L	ALOGPS
logP	3.77	ALOGPS
logP	4.38	ChemAxon
logS	-4.6	ALOGPS
pKa (Strongest Acidic)	9.15	ChemAxon
pKa (Strongest Basic)	-4.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	75.99 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	101.12 m³·mol⁻¹	ChemAxon
Polarizability	38.86 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

65323170

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

145964658

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 Asperteretal E (MMDBc0027524)

MOL for #<Metabolite:0x00005645ca2b5618>

3D MOL for #<Metabolite:0x00005645ca2b5618>

3D SDF for #<Metabolite:0x00005645ca2b5618>

3D-SDF for #<Metabolite:0x00005645ca2b5618>

PDB for #<Metabolite:0x00005645ca2b5618>

3D PDB for #<Metabolite:0x00005645ca2b5618>

SMILES for #<Metabolite:0x00005645ca2b5618>

INCHI for #<Metabolite:0x00005645ca2b5618>

Structure for #<Metabolite:0x00005645ca2b5618>

3D Structure for #<Metabolite:0x00005645ca2b5618>