MiMeDB: Showing metabocard for (+)-penicamide A (MMDBc0026438)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-15 16:05:01 UTC

Update Date

2022-08-31 06:52:04 UTC

Metabolite ID

MMDBc0026438

Metabolite Identification

Common Name

(+)-penicamide A

Description

(+)-penicamide A belongs to the class of organic compounds known as quinazolines. Quinazolines are compounds containing a quinazoline moiety, which is made up of two fused six-member aromatic rings, a benzene ring and a pyrimidine ring (+)-penicamide A is a moderately basic compound (based on its pKa).

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152118052D          

 23 26  0  0  1  0            999 V2000
    5.1926   -1.4584    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9226    2.1275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1631    0.5684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6230    1.1921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8931   -0.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8129    1.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3023   -0.3671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0323    1.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6525   -0.8348    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1926    0.7243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1124   -0.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7622    0.2566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0829   -0.3671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3825    0.5684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5428    0.2566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8424    1.1921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8129   -1.1466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4627   -0.6789    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.0028   -1.3025    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.7327    0.1007    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9521    0.1007    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3530   -1.7702    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1124    1.9716    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
 11  7  2  0  0  0  0
 11  9  1  0  0  0  0
 12  7  1  0  0  0  0
 12  8  2  0  0  0  0
 13  5  2  0  0  0  0
 14 10  1  0  0  0  0
 14 11  1  0  0  0  0
 15  6  2  0  0  0  0
 15 13  1  0  0  0  0
 16  8  1  0  0  0  0
 16 14  2  0  0  0  0
 17 13  1  0  0  0  0
 18  1  1  6  0  0  0
 18  9  1  0  0  0  0
 19 17  2  0  0  0  0
 19 18  1  0  0  0  0
 20 10  1  0  0  0  0
 20 15  1  0  0  0  0
 20 18  1  0  0  0  0
 21 12  1  0  0  0  0
 22 17  1  0  0  0  0
 23  2  1  0  0  0  0
 23 16  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0026438

> <DATABASE_NAME>
MIME

> <SMILES>
COC1=C2CN3C4=CC=CC=C4C(O)=N[C@@]3(C)CC2=CC(O)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C18H18N2O3/c1-18-9-11-7-12(21)8-16(23-2)14(11)10-20(18)15-6-4-3-5-13(15)17(22)19-18/h3-8,21H,9-10H2,1-2H3,(H,19,22)/t18-/m1/s1

> <INCHI_KEY>
IUJJCTODHWNTJY-GOSISDBHSA-N

> <FORMULA>
C18H18N2O3

> <MOLECULAR_WEIGHT>
310.353

> <EXACT_MASS>
310.131742448

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
41

> <JCHEM_AVERAGE_POLARIZABILITY>
32.99448535939937

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(11aS)-7-methoxy-11a-methyl-11,11a-dihydro-6H-5a,12-diazatetraphene-9,13-diol

> <ALOGPS_LOGP>
2.72

> <JCHEM_LOGP>
3.4520495846666654

> <ALOGPS_LOGS>
-3.23

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
9.399742512815896

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.212804301575494

> <JCHEM_PKA_STRONGEST_BASIC>
1.5607713861528492

> <JCHEM_POLAR_SURFACE_AREA>
65.29

> <JCHEM_REFRACTIVITY>
89.2505

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.82e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(11aS)-7-methoxy-11a-methyl-6,11-dihydro-5a,12-diazatetraphene-9,13-diol

> <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       9.693  -2.722   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.189   3.971   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      15.238   1.061   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      14.230   2.225   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      14.734  -0.394   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      12.717   1.934   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.164  -0.685   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.660   1.934   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.685  -1.558   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.693   1.352   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.677  -0.394   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.156   0.479   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      13.221  -0.685   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.181   1.061   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      12.213   0.479   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.172   2.225   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      12.717  -2.140   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      10.197  -1.267   0.000  0.00  0.00           C+0
HETATM   19  N   UNK     0      11.205  -2.431   0.000  0.00  0.00           N+0
HETATM   20  N   UNK     0      10.701   0.188   0.000  0.00  0.00           N+0
HETATM   21  O   UNK     0       3.644   0.188   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      13.726  -3.304   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       7.677   3.680   0.000  0.00  0.00           O+0
CONECT    1   18                                                            
CONECT    2   23                                                            
CONECT    3    4    5                                                       
CONECT    4    3    6                                                       
CONECT    5    3   13                                                       
CONECT    6    4   15                                                       
CONECT    7   11   12                                                       
CONECT    8   12   16                                                       
CONECT    9   11   18                                                       
CONECT   10   14   20                                                       
CONECT   11    7    9   14                                                  
CONECT   12    7    8   21                                                  
CONECT   13    5   15   17                                                  
CONECT   14   10   11   16                                                  
CONECT   15    6   13   20                                                  
CONECT   16    8   14   23                                                  
CONECT   17   13   19   22                                                  
CONECT   18    1    9   19   20                                             
CONECT   19   17   18                                                       
CONECT   20   10   15   18                                                  
CONECT   21   12                                                            
CONECT   22   17                                                            
CONECT   23    2   16                                                       
MASTER        0    0    0    0    0    0    0    0   23    0   52    0
END

Synonyms

Not Available

Molecular Formula

C₁₈H₁₈N₂O₃

Average Mass

310.353

Monoisotopic Mass

310.131742448

IUPAC Name

(11aS)-7-methoxy-11a-methyl-11,11a-dihydro-6H-5a,12-diazatetraphene-9,13-diol

Traditional Name

(11aS)-7-methoxy-11a-methyl-6,11-dihydro-5a,12-diazatetraphene-9,13-diol

CAS Registry Number

Not Available

SMILES

COC1=C2CN3C4=CC=CC=C4C(O)=N[C@@]3(C)CC2=CC(O)=C1

InChI Identifier

InChI=1S/C18H18N2O3/c1-18-9-11-7-12(21)8-16(23-2)14(11)10-20(18)15-6-4-3-5-13(15)17(22)19-18/h3-8,21H,9-10H2,1-2H3,(H,19,22)/t18-/m1/s1

InChI Key

IUJJCTODHWNTJY-GOSISDBHSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as quinazolines. Quinazolines are compounds containing a quinazoline moiety, which is made up of two fused six-member aromatic rings, a benzene ring and a pyrimidine ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Diazanaphthalenes

Sub Class

Benzodiazines

Direct Parent

Quinazolines

Alternative Parents

Substituents

Tetrahydroisoquinoline
Quinazoline
Dialkylarylamine
Anisole
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Benzenoid
Vinylogous amide
Secondary carboxylic acid amide
Lactam
Carboxamide group
Azacycle
Ether
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
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	0.18 g/L	ALOGPS
logP	2.72	ALOGPS
logP	3.45	ChemAxon
logS	-3.2	ALOGPS
pKa (Strongest Acidic)	8.21	ChemAxon
pKa (Strongest Basic)	1.56	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	65.29 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	89.25 m³·mol⁻¹	ChemAxon
Polarizability	32.99 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

Not Available

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	2	Human feces; Human sputum; Human	Metabolic reconstruction

Exposure Sources

Source Type	Source Sub-type	Species	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

81131466

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

146683059

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 (+)-penicamide A (MMDBc0026438)

MOL for #<Metabolite:0x000055e8c805ba70>

3D MOL for #<Metabolite:0x000055e8c805ba70>

3D SDF for #<Metabolite:0x000055e8c805ba70>

3D-SDF for #<Metabolite:0x000055e8c805ba70>

PDB for #<Metabolite:0x000055e8c805ba70>

3D PDB for #<Metabolite:0x000055e8c805ba70>

SMILES for #<Metabolite:0x000055e8c805ba70>

INCHI for #<Metabolite:0x000055e8c805ba70>

Structure for #<Metabolite:0x000055e8c805ba70>

3D Structure for #<Metabolite:0x000055e8c805ba70>