MiMeDB: Showing metabocard for Alternapyrone D (MMDBc0023895)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2021-05-15 13:47:42 UTC

Update Date

2025-10-07 16:07:22 UTC

Metabolite ID

MMDBc0023895

Metabolite Identification

Common Name

Alternapyrone D

Description

Alternapyrone D is a polyketide compound. There is little literature available on this metabolite, indicating that further research may be needed to fully understand its properties and potential applications.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152115472D          

 35 35  0  0  0  0            999 V2000
   -6.4599    4.8691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3776    8.4414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1401    7.7270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6151    9.1559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8526    9.8704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8526   12.7283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9368    5.9961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6349    4.8691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7474    7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3349    7.7270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1401    9.1559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3776    9.8704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0974    8.4414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8099    6.2980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    5.5836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9651    9.1559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2724    8.4414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2026    9.8704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4401   10.5849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4401   12.0138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9849    6.2980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5099    7.7270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8526   11.2993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6151   10.5849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0974    7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6151   12.0138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2224    5.5836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9849    4.8691    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6776   11.2993    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2724    7.0125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5099    6.2980    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2026   12.7283    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5079    5.1711    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2026   11.2993    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  8  1  1  0  0  0  0
 10  9  1  0  0  0  0
 11  9  1  0  0  0  0
 17  2  1  0  0  0  0
 17 12  2  0  0  0  0
 17 13  1  0  0  0  0
 18  3  1  0  0  0  0
 12 18  1  4  0  0  0
 18 14  2  0  0  0  0
 19  4  1  0  0  0  0
 19 13  1  0  0  0  0
 20  5  1  0  0  0  0
 21  6  1  0  0  0  0
 22 10  1  0  0  0  0
 22 15  1  0  0  0  0
 22 16  1  0  0  0  0
 23 11  1  0  0  0  0
 14 23  1  4  0  0  0
 24 20  1  0  0  0  0
 24 21  2  0  0  0  0
 25 19  1  0  0  0  0
 25 20  2  0  0  0  0
 26 23  1  0  0  0  0
 27 21  1  0  0  0  0
 28  7  1  0  0  0  0
 28  8  1  0  0  0  0
 28 15  1  0  0  0  0
 29 16  1  0  0  0  0
 30 24  1  0  0  0  0
 31 26  2  0  0  0  0
 32 26  1  0  0  0  0
 33 27  2  0  0  0  0
 34 28  1  0  0  0  0
 35 25  1  0  0  0  0
 35 27  1  0  0  0  0
M  END


  Mrv1652305152115472D          

 35 35  0  0  0  0            999 V2000
   -6.4599    4.8691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3776    8.4414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1401    7.7270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6151    9.1559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8526    9.8704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8526   12.7283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9368    5.9961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6349    4.8691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7474    7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3349    7.7270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1401    9.1559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3776    9.8704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0974    8.4414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8099    6.2980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    5.5836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9651    9.1559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2724    8.4414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2026    9.8704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4401   10.5849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4401   12.0138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9849    6.2980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5099    7.7270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8526   11.2993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6151   10.5849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0974    7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6151   12.0138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2224    5.5836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9849    4.8691    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6776   11.2993    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2724    7.0125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5099    6.2980    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2026   12.7283    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5079    5.1711    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2026   11.2993    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  8  1  1  0  0  0  0
 10  9  1  0  0  0  0
 11  9  1  0  0  0  0
 17  2  1  0  0  0  0
 17 12  2  0  0  0  0
 17 13  1  0  0  0  0
 18  3  1  0  0  0  0
 12 18  1  4  0  0  0
 18 14  2  0  0  0  0
 19  4  1  0  0  0  0
 19 13  1  0  0  0  0
 20  5  1  0  0  0  0
 21  6  1  0  0  0  0
 22 10  1  0  0  0  0
 22 15  1  0  0  0  0
 22 16  1  0  0  0  0
 23 11  1  0  0  0  0
 14 23  1  4  0  0  0
 24 20  1  0  0  0  0
 24 21  2  0  0  0  0
 25 19  1  0  0  0  0
 25 20  2  0  0  0  0
 26 23  1  0  0  0  0
 27 21  1  0  0  0  0
 28  7  1  0  0  0  0
 28  8  1  0  0  0  0
 28 15  1  0  0  0  0
 29 16  1  0  0  0  0
 30 24  1  0  0  0  0
 31 26  2  0  0  0  0
 32 26  1  0  0  0  0
 33 27  2  0  0  0  0
 34 28  1  0  0  0  0
 35 25  1  0  0  0  0
 35 27  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0023895

> <DATABASE_NAME>
MIME

> <SMILES>
CCC(C)(O)CC(CO)CCCC(C=C(C)C=C(C)CC(C)C1=C(C)C(O)=C(C)C(=O)O1)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C28H44O7/c1-8-28(7,34)15-22(16-29)10-9-11-23(26(31)32)14-18(3)12-17(2)13-19(4)25-20(5)24(30)21(6)27(33)35-25/h12,14,19,22-23,29-30,34H,8-11,13,15-16H2,1-7H3,(H,31,32)

> <INCHI_KEY>
KAIIOAVNKWEQTI-UHFFFAOYSA-N

> <FORMULA>
C28H44O7

> <MOLECULAR_WEIGHT>
492.653

> <EXACT_MASS>
492.308703757

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
79

> <JCHEM_AVERAGE_POLARIZABILITY>
54.969748224109146

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
8-hydroxy-2-[6-(4-hydroxy-3,5-dimethyl-2-oxo-2H-pyran-6-yl)-2,4-dimethylhepta-1,3-dien-1-yl]-6-(hydroxymethyl)-8-methyldecanoic acid

> <ALOGPS_LOGP>
3.45

> <JCHEM_LOGP>
4.662657371333333

> <ALOGPS_LOGS>
-5.25

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
7.7300160712825585

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.598074076603692

> <JCHEM_PKA_STRONGEST_BASIC>
-2.594683575883468

> <JCHEM_POLAR_SURFACE_AREA>
124.29

> <JCHEM_REFRACTIVITY>
140.99970000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
14

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.76e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
8-hydroxy-2-[6-(4-hydroxy-3,5-dimethyl-6-oxopyran-2-yl)-2,4-dimethylhepta-1,3-dien-1-yl]-6-(hydroxymethyl)-8-methyldecanoic acid

> <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     -12.058   9.089   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.572  15.757   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.262  14.424   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.882  17.091   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.192  18.425   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.192  23.759   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0     -11.082  11.193   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0     -10.518   9.089   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -5.128  13.090   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -6.668  13.090   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -4.358  14.424   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.262  17.091   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.572  18.425   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.048  15.757   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -8.978  11.756   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -6.668  10.423   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.802  17.091   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.508  15.757   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.112  18.425   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.422  19.758   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.422  22.426   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -7.438  11.756   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -2.818  14.424   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       7.192  21.092   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.882  19.758   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -2.048  13.090   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.882  22.426   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -9.748  10.423   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -7.438   9.089   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       8.732  21.092   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0      -0.508  13.090   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0      -2.818  11.756   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0       4.112  23.759   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0      -8.415   9.653   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0       4.112  21.092   0.000  0.00  0.00           O+0
CONECT    1    8                                                            
CONECT    2   17                                                            
CONECT    3   18                                                            
CONECT    4   19                                                            
CONECT    5   20                                                            
CONECT    6   21                                                            
CONECT    7   28                                                            
CONECT    8    1   28                                                       
CONECT    9   10   11                                                       
CONECT   10    9   22                                                       
CONECT   11    9   23                                                       
CONECT   12   17   18                                                       
CONECT   13   17   19                                                       
CONECT   14   18   23                                                       
CONECT   15   22   28                                                       
CONECT   16   22   29                                                       
CONECT   17    2   12   13                                                  
CONECT   18    3   12   14                                                  
CONECT   19    4   13   25                                                  
CONECT   20    5   24   25                                                  
CONECT   21    6   24   27                                                  
CONECT   22   10   15   16                                                  
CONECT   23   11   14   26                                                  
CONECT   24   20   21   30                                                  
CONECT   25   19   20   35                                                  
CONECT   26   23   31   32                                                  
CONECT   27   21   33   35                                                  
CONECT   28    7    8   15   34                                             
CONECT   29   16                                                            
CONECT   30   24                                                            
CONECT   31   26                                                            
CONECT   32   26                                                            
CONECT   33   27                                                            
CONECT   34   28                                                            
CONECT   35   25   27                                                       
MASTER        0    0    0    0    0    0    0    0   35    0   70    0
END

Synonyms

Not Available

Molecular Formula

C₂₈H₄₄O₇

Average Mass

492.653

Monoisotopic Mass

492.308703757

IUPAC Name

8-hydroxy-2-[6-(4-hydroxy-3,5-dimethyl-2-oxo-2H-pyran-6-yl)-2,4-dimethylhepta-1,3-dien-1-yl]-6-(hydroxymethyl)-8-methyldecanoic acid

Traditional Name

8-hydroxy-2-[6-(4-hydroxy-3,5-dimethyl-6-oxopyran-2-yl)-2,4-dimethylhepta-1,3-dien-1-yl]-6-(hydroxymethyl)-8-methyldecanoic acid

CAS Registry Number

Not Available

SMILES

CCC(C)(O)CC(CO)CCCC(C=C(C)C=C(C)CC(C)C1=C(C)C(O)=C(C)C(=O)O1)C(O)=O

InChI Identifier

InChI=1S/C28H44O7/c1-8-28(7,34)15-22(16-29)10-9-11-23(26(31)32)14-18(3)12-17(2)13-19(4)25-20(5)24(30)21(6)27(33)35-25/h12,14,19,22-23,29-30,34H,8-11,13,15-16H2,1-7H3,(H,31,32)

InChI Key

KAIIOAVNKWEQTI-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Diterpene lactones

Alternative Parents

Substituents

Diterpenoid
Diterpene lactone
Medium-chain hydroxy acid
Medium-chain fatty acid
Methyl-branched fatty acid
Pyranone
Hydroxy fatty acid
Heterocyclic fatty acid
Branched fatty acid
Fatty acyl
Fatty acid
Unsaturated fatty acid
Pyran
Heteroaromatic compound
Vinylogous acid
Tertiary alcohol
Lactone
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Carbonyl group
Alcohol
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.0028 g/L	ALOGPS
logP	3.45	ALOGPS
logP	4.66	ChemAxon
logS	-5.2	ALOGPS
pKa (Strongest Acidic)	4.6	ChemAxon
pKa (Strongest Basic)	-2.6	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	124.29 Å²	ChemAxon
Rotatable Bond Count	14	ChemAxon
Refractivity	141 m³·mol⁻¹	ChemAxon
Polarizability	54.97 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Spectrum Type	Description	Splash Key	Deposition Date	View
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TMS_2_5) - 70eV, Positive	Not Available	2022-08-08	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	Not Available	2022-08-10	View Spectrum
MS	Mass Spectrum (Electron Ionization)	Not Available	2022-08-06	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-21	View Spectrum

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
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

78444714

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139591186

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

CMMC Knowledgebase

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 Alternapyrone D (MMDBc0023895)

MOL for #<Metabolite:0x00007f8dbc1d7c60>

3D MOL for #<Metabolite:0x00007f8dbc1d7c60>

3D SDF for #<Metabolite:0x00007f8dbc1d7c60>

3D-SDF for #<Metabolite:0x00007f8dbc1d7c60>

PDB for #<Metabolite:0x00007f8dbc1d7c60>

3D PDB for #<Metabolite:0x00007f8dbc1d7c60>

SMILES for #<Metabolite:0x00007f8dbc1d7c60>

INCHI for #<Metabolite:0x00007f8dbc1d7c60>

Structure for #<Metabolite:0x00007f8dbc1d7c60>

3D Structure for #<Metabolite:0x00007f8dbc1d7c60>