MiMeDB: Showing metabocard for Talaroenamine D (MMDBc0007709)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2021-05-15 00:47:11 UTC

Update Date

2025-10-07 16:05:22 UTC

Metabolite ID

MMDBc0007709

Metabolite Identification

Common Name

Talaroenamine D

Description

Talaroenamine D is a member of the chemical class of talaroenamines, which are metabolites derived from the fungus Talaromyces stipitatus ATCC10500. This compound has garnered attention in the field of medicinal chemistry due to its notable biological activity. Specifically, Talaroenamine D has been evaluated for its antiplasmodial properties, demonstrating significant inhibition against the chloroquine-resistant strain of Plasmodium falciparum (FcB1 strain), making it a promising candidate for further development in malaria treatment. Importantly, this inhibition occurs without inducing noticeable toxicity in HeLa and preadipose cell lines, suggesting a favorable safety profile for potential therapeutic applications. The discovery of Talaroenamine D, along with other unexpected talaroenamine derivatives and an undescribed polyester from Talaromyces stipitatus, highlights the rich chemical diversity present in fungal metabolites and their potential utility in drug discovery (PMID:26386982 ).

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152102472D          

 21 22  0  0  1  0            999 V2000
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2448    1.8695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    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
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    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    0.0000    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
    0.7145    1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    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
    2.1434    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1842    1.8695    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  4  3  2  0  0  0  0
  5  3  1  0  0  0  0
  6  4  1  0  0  0  0
 10  1  1  0  0  0  0
 10  7  2  0  0  0  0
 11  5  2  0  0  0  0
 11  8  1  0  0  0  0
 12  6  2  0  0  0  0
 12  9  1  0  0  0  0
 12 11  1  0  0  0  0
 13  7  1  0  0  0  0
 14 10  1  0  0  0  0
 15 14  1  0  0  0  0
 16  2  1  6  0  0  0
 16 13  1  0  0  0  0
 16 15  1  0  0  0  0
 17  8  1  4  0  0  0
 17 14  2  0  0  0  0
 18  9  2  0  0  0  0
 19 13  2  0  0  0  0
 20 15  2  0  0  0  0
 16 21  1  1  0  0  0
M  END
> <DATABASE_ID>
MMDBc0007709

> <DATABASE_NAME>
MIME

> <SMILES>
CC1=CC(=O)[C@@](C)(O)C(=O)C1=NCC1=CC=CC=C1C=O

> <INCHI_IDENTIFIER>
InChI=1S/C16H15NO4/c1-10-7-13(19)16(2,21)15(20)14(10)17-8-11-5-3-4-6-12(11)9-18/h3-7,9,21H,8H2,1-2H3/t16-/m1/s1

> <INCHI_KEY>
GQWJDJPTGWBDPU-MRXNPFEDSA-N

> <FORMULA>
C16H15NO4

> <MOLECULAR_WEIGHT>
285.299

> <EXACT_MASS>
285.100107967

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
36

> <JCHEM_AVERAGE_POLARIZABILITY>
29.172356578271575

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-({[(5R)-5-hydroxy-2,5-dimethyl-4,6-dioxocyclohex-2-en-1-ylidene]amino}methyl)benzaldehyde

> <ALOGPS_LOGP>
1.86

> <JCHEM_LOGP>
2.8096014976666672

> <ALOGPS_LOGS>
-3.89

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.461422515595126

> <JCHEM_PKA_STRONGEST_BASIC>
2.0831919565082506

> <JCHEM_POLAR_SURFACE_AREA>
83.8

> <JCHEM_REFRACTIVITY>
79.31459999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.71e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-({[(5R)-5-hydroxy-2,5-dimethyl-4,6-dioxocyclohex-2-en-1-ylidene]amino}methyl)benzaldehyde

> <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       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.324   3.490   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.002  -3.080   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.336  -2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.336  -0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.002   0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   17  N   UNK     0       4.001  -0.770   0.000  0.00  0.00           N+0
HETATM   18  O   UNK     0       6.668   2.310   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0      -1.334   2.310   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       4.001   2.310   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       0.344   3.490   0.000  0.00  0.00           O+0
CONECT    1   10                                                            
CONECT    2   16                                                            
CONECT    3    4    5                                                       
CONECT    4    3    6                                                       
CONECT    5    3   11                                                       
CONECT    6    4   12                                                       
CONECT    7   10   13                                                       
CONECT    8   11   17                                                       
CONECT    9   12   18                                                       
CONECT   10    1    7   14                                                  
CONECT   11    5    8   12                                                  
CONECT   12    6    9   11                                                  
CONECT   13    7   16   19                                                  
CONECT   14   10   15   17                                                  
CONECT   15   14   16   20                                                  
CONECT   16    2   13   15   21                                             
CONECT   17    8   14                                                       
CONECT   18    9                                                            
CONECT   19   13                                                            
CONECT   20   15                                                            
CONECT   21   16                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   44    0
END

Synonyms

Not Available

Molecular Formula

C₁₆H₁₅NO₄

Average Mass

285.299

Monoisotopic Mass

285.100107967

IUPAC Name

2-({[(5R)-5-hydroxy-2,5-dimethyl-4,6-dioxocyclohex-2-en-1-ylidene]amino}methyl)benzaldehyde

Traditional Name

2-({[(5R)-5-hydroxy-2,5-dimethyl-4,6-dioxocyclohex-2-en-1-ylidene]amino}methyl)benzaldehyde

CAS Registry Number

Not Available

SMILES

CC1=CC(=O)[C@@](C)(O)C(=O)C1=NCC1=CC=CC=C1C=O

InChI Identifier

InChI=1S/C16H15NO4/c1-10-7-13(19)16(2,21)15(20)14(10)17-8-11-5-3-4-6-12(11)9-18/h3-7,9,21H,8H2,1-2H3/t16-/m1/s1

InChI Key

GQWJDJPTGWBDPU-MRXNPFEDSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzoyl derivatives. These are organic compounds containing an acyl moiety of benzoic acid with the formula (C6H5CO-).

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Benzoyl derivatives

Direct Parent

Benzoyl derivatives

Alternative Parents

Substituents

Quinone
M-benzoquinone
Benzoyl
Benzaldehyde
Cyclohexenone
Aryl-aldehyde
Acyloin
Tertiary alcohol
Secondary ketimine
Azomethine
Cyclic ketone
Ketone
Ketimine
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Imine
Carbonyl group
Aldehyde
Alcohol
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.037 g/L	ALOGPS
logP	1.86	ALOGPS
logP	2.81	ChemAxon
logS	-3.9	ALOGPS
pKa (Strongest Acidic)	11.46	ChemAxon
pKa (Strongest Basic)	2.08	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	83.8 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	79.31 m³·mol⁻¹	ChemAxon
Polarizability	29.17 Å³	ChemAxon
Number of Rings	2	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

This table shows at most 5 pathways. For the full list of associated pathways:

See All Associated Bacterial Pathways

Name	SMPDB/PathBank	Species

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

78442017

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139585101

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

CMMC Knowledgebase

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 Talaroenamine D (MMDBc0007709)

MOL for #<Metabolite:0x00007f2ac14d2298>

3D MOL for #<Metabolite:0x00007f2ac14d2298>

3D SDF for #<Metabolite:0x00007f2ac14d2298>

3D-SDF for #<Metabolite:0x00007f2ac14d2298>

PDB for #<Metabolite:0x00007f2ac14d2298>

3D PDB for #<Metabolite:0x00007f2ac14d2298>

SMILES for #<Metabolite:0x00007f2ac14d2298>

INCHI for #<Metabolite:0x00007f2ac14d2298>

Structure for #<Metabolite:0x00007f2ac14d2298>

3D Structure for #<Metabolite:0x00007f2ac14d2298>