MiMeDB: Showing metabocard for Speradine C (MMDBc0010238)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2021-05-15 02:28:37 UTC

Update Date

2025-10-07 16:05:43 UTC

Metabolite ID

MMDBc0010238

Metabolite Identification

Common Name

Speradine C

Description

Speradine C is a metabolite classified within the category of alkaloids, known for its complex chemical structure and potential biological activities. This compound is synthesized through intricate biosynthetic pathways that reflect the natural processes of alkaloid formation. Recent advancements in synthetic methodologies have facilitated the efficient construction of core skeletons reminiscent of Speradine C, exemplified by a seven-step total synthesis of related compounds such as lamellarins D and H. These synthetic approaches often incorporate bioinspired oxidative coupling reactions, which are pivotal in achieving the desired molecular architecture (PMID: [insert PMID here]). The exploration of Speradine C and its analogs not only enhances our understanding of alkaloid chemistry but also opens avenues for investigating their biological roles and potential therapeutic applications. The ongoing research into the synthesis and function of such metabolites underscores their significance in both natural product chemistry and pharmacology.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152104282D          

 29 32  0  0  1  0            999 V2000
    6.2098   -2.0540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9192   -2.2325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9482   -1.8325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1373    1.4699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5974   -1.1059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0459   -1.6224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4718   -0.2905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9339   -1.4106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7238   -1.7032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7576   -1.3640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8149   -1.3234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4138   -1.2509    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2971    0.0084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4817   -0.7206    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9405   -0.5081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3671   -0.4272    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1361   -0.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4136    0.7402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2116   -1.4611    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6305   -0.0558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5895    0.7799    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.6580   -0.7673    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.1290   -0.6273    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8531    0.0160    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3462    0.6694    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9300    1.3835    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2694    0.4661    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6771   -0.8795    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0609   -0.8736    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  2  0  0  0  0
  7  5  1  0  0  0  0
 10  1  1  0  0  0  0
 10  8  1  0  0  0  0
 11  6  1  0  0  0  0
 11  9  1  0  0  0  0
 12  9  1  0  0  0  0
 13  7  2  0  0  0  0
 14  8  1  0  0  0  0
 15 11  2  0  0  0  0
 15 13  1  0  0  0  0
 16 12  1  0  0  0  0
 17 16  1  0  0  0  0
 19  2  1  0  0  0  0
 19  3  1  0  0  0  0
 19 12  1  0  0  0  0
 20 15  1  0  0  0  0
 20 16  1  0  0  0  0
 20 18  1  0  0  0  0
 21  4  1  0  0  0  0
 21 13  1  0  0  0  0
 21 18  1  0  0  0  0
 22 14  1  0  0  0  0
 22 17  1  0  0  0  0
 22 19  1  0  0  0  0
 23 10  2  0  0  0  0
 24 14  2  0  0  0  0
 25 17  2  0  0  0  0
 26 18  2  0  0  0  0
 27 20  1  0  0  0  0
 12 28  1  1  0  0  0
 16 29  1  1  0  0  0
M  END


  Mrv1652305152104282D          

 29 32  0  0  1  0            999 V2000
    6.2098   -2.0540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9192   -2.2325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9482   -1.8325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1373    1.4699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5974   -1.1059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0459   -1.6224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4718   -0.2905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9339   -1.4106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7238   -1.7032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7576   -1.3640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8149   -1.3234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4138   -1.2509    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2971    0.0084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4817   -0.7206    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9405   -0.5081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3671   -0.4272    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1361   -0.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4136    0.7402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2116   -1.4611    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6305   -0.0558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5895    0.7799    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.6580   -0.7673    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.1290   -0.6273    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8531    0.0160    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3462    0.6694    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9300    1.3835    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2694    0.4661    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6771   -0.8795    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0609   -0.8736    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  2  0  0  0  0
  7  5  1  0  0  0  0
 10  1  1  0  0  0  0
 10  8  1  0  0  0  0
 11  6  1  0  0  0  0
 11  9  1  0  0  0  0
 12  9  1  0  0  0  0
 13  7  2  0  0  0  0
 14  8  1  0  0  0  0
 15 11  2  0  0  0  0
 15 13  1  0  0  0  0
 16 12  1  0  0  0  0
 17 16  1  0  0  0  0
 19  2  1  0  0  0  0
 19  3  1  0  0  0  0
 19 12  1  0  0  0  0
 20 15  1  0  0  0  0
 20 16  1  0  0  0  0
 20 18  1  0  0  0  0
 21  4  1  0  0  0  0
 21 13  1  0  0  0  0
 21 18  1  0  0  0  0
 22 14  1  0  0  0  0
 22 17  1  0  0  0  0
 22 19  1  0  0  0  0
 23 10  2  0  0  0  0
 24 14  2  0  0  0  0
 25 17  2  0  0  0  0
 26 18  2  0  0  0  0
 27 20  1  0  0  0  0
 12 28  1  1  0  0  0
 16 29  1  1  0  0  0
M  END
> <DATABASE_ID>
MMDBc0010238

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@@]12CC3=C4C(=CC=C3)N(C)C(=O)C4(O)[C@]1([H])C(=O)N(C(=O)CC(C)=O)C2(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C20H22N2O5/c1-10(23)8-14(24)22-17(25)16-12(19(22,2)3)9-11-6-5-7-13-15(11)20(16,27)18(26)21(13)4/h5-7,12,16,27H,8-9H2,1-4H3/t12-,16+,20?/m1/s1

> <INCHI_KEY>
KKGFMAANSDFYDF-OIHKITLTSA-N

> <FORMULA>
C20H22N2O5

> <MOLECULAR_WEIGHT>
370.405

> <EXACT_MASS>
370.152871816

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
49

> <JCHEM_AVERAGE_POLARIZABILITY>
37.261525088696665

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R,6R)-1-hydroxy-5,5,13-trimethyl-4-(3-oxobutanoyl)-4,13-diazatetracyclo[6.6.1.0^{2,6}.0^{12,15}]pentadeca-8(15),9,11-triene-3,14-dione

> <ALOGPS_LOGP>
1.16

> <JCHEM_LOGP>
0.3758122336666675

> <ALOGPS_LOGS>
-2.16

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.456483143975108

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.00030452017107

> <JCHEM_PKA_STRONGEST_BASIC>
-4.349397331442092

> <JCHEM_POLAR_SURFACE_AREA>
94.99000000000001

> <JCHEM_REFRACTIVITY>
95.97719999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.56e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R,6R)-1-hydroxy-5,5,13-trimethyl-4-(3-oxobutanoyl)-4,13-diazatetracyclo[6.6.1.0^{2,6}.0^{12,15}]pentadeca-8(15),9,11-triene-3,14-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      11.592  -3.834   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.449  -4.167   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.370  -3.421   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.256   2.744   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.115  -2.064   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.086  -3.028   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.881  -0.542   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.210  -2.633   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.218  -3.179   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.747  -2.546   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.521  -2.470   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.506  -2.335   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.555   0.016   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.366  -1.345   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.756  -0.948   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.419  -0.798   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.854  -0.240   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.639   1.382   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.995  -2.727   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.044  -0.104   0.000  0.00  0.00           C+0
HETATM   21  N   UNK     0       1.100   1.456   0.000  0.00  0.00           N+0
HETATM   22  N   UNK     0       6.828  -1.432   0.000  0.00  0.00           N+0
HETATM   23  O   UNK     0      11.441  -1.171   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       9.059   0.030   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       6.246   1.250   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       3.603   2.583   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       4.236   0.870   0.000  0.00  0.00           O+0
HETATM   28  H   UNK     0       3.131  -1.642   0.000  0.00  0.00           H+0
HETATM   29  H   UNK     0       5.714  -1.631   0.000  0.00  0.00           H+0
CONECT    1   10                                                            
CONECT    2   19                                                            
CONECT    3   19                                                            
CONECT    4   21                                                            
CONECT    5    6    7                                                       
CONECT    6    5   11                                                       
CONECT    7    5   13                                                       
CONECT    8   10   14                                                       
CONECT    9   11   12                                                       
CONECT   10    1    8   23                                                  
CONECT   11    6    9   15                                                  
CONECT   12    9   16   19   28                                             
CONECT   13    7   15   21                                                  
CONECT   14    8   22   24                                                  
CONECT   15   11   13   20                                                  
CONECT   16   12   17   20   29                                             
CONECT   17   16   22   25                                                  
CONECT   18   20   21   26                                                  
CONECT   19    2    3   12   22                                             
CONECT   20   15   16   18   27                                             
CONECT   21    4   13   18                                                  
CONECT   22   14   17   19                                                  
CONECT   23   10                                                            
CONECT   24   14                                                            
CONECT   25   17                                                            
CONECT   26   18                                                            
CONECT   27   20                                                            
CONECT   28   12                                                            
CONECT   29   16                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   64    0
END

Synonyms

Not Available

Molecular Formula

C₂₀H₂₂N₂O₅

Average Mass

370.405

Monoisotopic Mass

370.152871816

IUPAC Name

(2R,6R)-1-hydroxy-5,5,13-trimethyl-4-(3-oxobutanoyl)-4,13-diazatetracyclo[6.6.1.0^{2,6}.0^{12,15}]pentadeca-8(15),9,11-triene-3,14-dione

Traditional Name

(2R,6R)-1-hydroxy-5,5,13-trimethyl-4-(3-oxobutanoyl)-4,13-diazatetracyclo[6.6.1.0^{2,6}.0^{12,15}]pentadeca-8(15),9,11-triene-3,14-dione

CAS Registry Number

Not Available

SMILES

[H][C@@]12CC3=C4C(=CC=C3)N(C)C(=O)C4(O)[C@]1([H])C(=O)N(C(=O)CC(C)=O)C2(C)C

InChI Identifier

InChI=1S/C20H22N2O5/c1-10(23)8-14(24)22-17(25)16-12(19(22,2)3)9-11-6-5-7-13-15(11)20(16,27)18(26)21(13)4/h5-7,12,16,27H,8-9H2,1-4H3/t12-,16+,20?/m1/s1

InChI Key

KKGFMAANSDFYDF-OIHKITLTSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as isoindolones. These are aromatic polycyclic compounds that an isoindole bearing a ketone.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Isoindoles and derivatives

Sub Class

Isoindolines

Direct Parent

Isoindolones

Alternative Parents

Substituents

Tetralin
Isoindolone
Indole or derivatives
N-acylpyrrolidine
Benzenoid
1,3-dicarbonyl compound
2-pyrrolidone
Pyrrolidone
Carboxylic acid imide, n-substituted
Tertiary carboxylic acid amide
Tertiary alcohol
Pyrrolidine
Dicarboximide
Carboxylic acid imide
Lactam
Ketone
Carboxamide group
Azacycle
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Alcohol
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	2.56 g/L	ALOGPS
logP	1.16	ALOGPS
logP	0.38	ChemAxon
logS	-2.2	ALOGPS
pKa (Strongest Acidic)	9	ChemAxon
pKa (Strongest Basic)	-4.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	94.99 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	95.98 m³·mol⁻¹	ChemAxon
Polarizability	37.26 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

Spectrum Type	Description	Splash Key	Deposition Date	View
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2022-08-08	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	Not Available	2022-08-09	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

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	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

32674648

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139585805

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 Speradine C (MMDBc0010238)

MOL for #<Metabolite:0x00007f2af4a17450>

3D MOL for #<Metabolite:0x00007f2af4a17450>

3D SDF for #<Metabolite:0x00007f2af4a17450>

3D-SDF for #<Metabolite:0x00007f2af4a17450>

PDB for #<Metabolite:0x00007f2af4a17450>

3D PDB for #<Metabolite:0x00007f2af4a17450>

SMILES for #<Metabolite:0x00007f2af4a17450>

INCHI for #<Metabolite:0x00007f2af4a17450>

Structure for #<Metabolite:0x00007f2af4a17450>

3D Structure for #<Metabolite:0x00007f2af4a17450>