MiMeDB: Showing metabocard for Notoamide S (MMDBc0020230)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-15 10:12:22 UTC

Update Date

2022-08-31 06:46:30 UTC

MiMeDB ID

MMDBc0020230

Metabolite Identification

Common Name

Notoamide S

Description

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152112122D          

 34 37  0  0  1  0            999 V2000
    1.0265    1.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1119   -3.1004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8148   -4.4981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6610    0.5048    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2750    0.1618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6395    1.1403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5846   -1.2217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0997   -1.8892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7529   -3.5420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4979   -2.7574    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0770   -2.2428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3320   -3.0274    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0997   -0.5543    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1717   -0.3967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5598   -3.7135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6291   -1.6297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6910   -2.5858    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5428   -0.8092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8861   -0.8092    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3151   -1.6342    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1389   -3.1989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4360   -1.8012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2965   -0.4737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6006   -2.0467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6006   -0.3967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4680    0.3333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8861   -1.6342    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.8485   -1.0868    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3151   -0.8092    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.3939   -3.9836    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6006   -2.8717    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6006    0.4283    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8861    0.0158    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4013   -2.4547    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  1  2  0  0  0  0
  8  7  1  0  0  0  0
 10  9  1  0  0  0  0
 12 11  2  0  0  0  0
 13  7  1  0  0  0  0
 15  2  1  0  0  0  0
 15  3  1  0  0  0  0
 15  9  2  0  0  0  0
 16 11  1  0  0  0  0
 17 10  1  0  0  0  0
 18 14  1  0  0  0  0
 18 16  1  0  0  0  0
 19 14  1  6  0  0  0
 20  8  1  0  0  0  0
 21 12  1  0  0  0  0
 21 17  2  0  0  0  0
 22 16  2  0  0  0  0
 22 17  1  0  0  0  0
 23 18  2  0  0  0  0
 24 20  1  0  0  0  0
 25 19  1  0  0  0  0
 26  4  1  0  0  0  0
 26  5  1  0  0  0  0
 26  6  1  0  0  0  0
 26 23  1  0  0  0  0
 27 19  1  0  0  0  0
 27 24  2  0  0  0  0
 28 22  1  0  0  0  0
 28 23  1  0  0  0  0
 29 13  1  0  0  0  0
 29 20  1  0  0  0  0
 29 25  1  0  0  0  0
 30 21  1  0  0  0  0
 31 24  1  0  0  0  0
 32 25  2  0  0  0  0
 19 33  1  1  0  0  0
 20 34  1  1  0  0  0
M  END


  Mrv1652305152112122D          

 34 37  0  0  1  0            999 V2000
    1.0265    1.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1119   -3.1004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8148   -4.4981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6610    0.5048    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2750    0.1618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6395    1.1403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5846   -1.2217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0997   -1.8892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7529   -3.5420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4979   -2.7574    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0770   -2.2428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3320   -3.0274    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0997   -0.5543    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1717   -0.3967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5598   -3.7135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6291   -1.6297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6910   -2.5858    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5428   -0.8092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8861   -0.8092    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3151   -1.6342    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1389   -3.1989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4360   -1.8012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2965   -0.4737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6006   -2.0467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6006   -0.3967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4680    0.3333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8861   -1.6342    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.8485   -1.0868    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3151   -0.8092    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.3939   -3.9836    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6006   -2.8717    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6006    0.4283    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8861    0.0158    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4013   -2.4547    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  1  2  0  0  0  0
  8  7  1  0  0  0  0
 10  9  1  0  0  0  0
 12 11  2  0  0  0  0
 13  7  1  0  0  0  0
 15  2  1  0  0  0  0
 15  3  1  0  0  0  0
 15  9  2  0  0  0  0
 16 11  1  0  0  0  0
 17 10  1  0  0  0  0
 18 14  1  0  0  0  0
 18 16  1  0  0  0  0
 19 14  1  6  0  0  0
 20  8  1  0  0  0  0
 21 12  1  0  0  0  0
 21 17  2  0  0  0  0
 22 16  2  0  0  0  0
 22 17  1  0  0  0  0
 23 18  2  0  0  0  0
 24 20  1  0  0  0  0
 25 19  1  0  0  0  0
 26  4  1  0  0  0  0
 26  5  1  0  0  0  0
 26  6  1  0  0  0  0
 26 23  1  0  0  0  0
 27 19  1  0  0  0  0
 27 24  2  0  0  0  0
 28 22  1  0  0  0  0
 28 23  1  0  0  0  0
 29 13  1  0  0  0  0
 29 20  1  0  0  0  0
 29 25  1  0  0  0  0
 30 21  1  0  0  0  0
 31 24  1  0  0  0  0
 32 25  2  0  0  0  0
 19 33  1  1  0  0  0
 20 34  1  1  0  0  0
M  END
> <DATABASE_ID>
MMDBc0020230

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@@]12CCCN1C(=O)[C@]([H])(CC1=C(NC3=C1C=CC(O)=C3CC=C(C)C)C(C)(C)C=C)N=C2O

> <INCHI_IDENTIFIER>
InChI=1S/C26H33N3O3/c1-6-26(4,5)23-18(14-19-25(32)29-13-7-8-20(29)24(31)27-19)16-11-12-21(30)17(22(16)28-23)10-9-15(2)3/h6,9,11-12,19-20,28,30H,1,7-8,10,13-14H2,2-5H3,(H,27,31)/t19-,20-/m0/s1

> <INCHI_KEY>
ZGWIWQJHQKPWGB-PMACEKPBSA-N

> <FORMULA>
C26H33N3O3

> <MOLECULAR_WEIGHT>
435.568

> <EXACT_MASS>
435.252191935

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
65

> <JCHEM_AVERAGE_POLARIZABILITY>
49.1994169140673

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3S,8aS)-1-hydroxy-3-{[6-hydroxy-7-(3-methylbut-2-en-1-yl)-2-(2-methylbut-3-en-2-yl)-1H-indol-3-yl]methyl}-3H,4H,6H,7H,8H,8aH-pyrrolo[1,2-a]pyrazin-4-one

> <ALOGPS_LOGP>
4.07

> <JCHEM_LOGP>
4.804959821333334

> <ALOGPS_LOGS>
-4.30

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.839481370530255

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.602304990278273

> <JCHEM_PKA_STRONGEST_BASIC>
1.2141181485600496

> <JCHEM_POLAR_SURFACE_AREA>
88.92000000000002

> <JCHEM_REFRACTIVITY>
127.92329999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.17e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3S,8aS)-1-hydroxy-3-{[6-hydroxy-7-(3-methylbut-2-en-1-yl)-2-(2-methylbut-3-en-2-yl)-1H-indol-3-yl]methyl}-3H,6H,7H,8H,8aH-pyrrolo[1,2-a]pyrazin-4-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       1.916   3.159   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.676  -5.787   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.121  -8.397   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.234   0.942   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.247   0.302   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.060   2.129   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -6.691  -2.281   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -5.786  -3.526   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.139  -6.612   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.663  -5.147   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.144  -4.187   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.620  -5.651   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -5.786  -1.035   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.320  -0.741   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.645  -6.932   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.174  -3.042   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.156  -4.827   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.013  -1.511   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.654  -1.511   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -4.321  -3.051   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.126  -5.971   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.681  -3.362   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.420  -0.884   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -2.988  -3.821   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -2.988  -0.741   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.740   0.622   0.000  0.00  0.00           C+0
HETATM   27  N   UNK     0      -1.654  -3.051   0.000  0.00  0.00           N+0
HETATM   28  N   UNK     0       3.451  -2.029   0.000  0.00  0.00           N+0
HETATM   29  N   UNK     0      -4.321  -1.511   0.000  0.00  0.00           N+0
HETATM   30  O   UNK     0       2.602  -7.436   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0      -2.988  -5.361   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0      -2.988   0.799   0.000  0.00  0.00           O+0
HETATM   33  H   UNK     0      -1.654   0.029   0.000  0.00  0.00           H+0
HETATM   34  H   UNK     0      -4.482  -4.582   0.000  0.00  0.00           H+0
CONECT    1    6                                                            
CONECT    2   15                                                            
CONECT    3   15                                                            
CONECT    4   26                                                            
CONECT    5   26                                                            
CONECT    6    1   26                                                       
CONECT    7    8   13                                                       
CONECT    8    7   20                                                       
CONECT    9   10   15                                                       
CONECT   10    9   17                                                       
CONECT   11   12   16                                                       
CONECT   12   11   21                                                       
CONECT   13    7   29                                                       
CONECT   14   18   19                                                       
CONECT   15    2    3    9                                                  
CONECT   16   11   18   22                                                  
CONECT   17   10   21   22                                                  
CONECT   18   14   16   23                                                  
CONECT   19   14   25   27   33                                             
CONECT   20    8   24   29   34                                             
CONECT   21   12   17   30                                                  
CONECT   22   16   17   28                                                  
CONECT   23   18   26   28                                                  
CONECT   24   20   27   31                                                  
CONECT   25   19   29   32                                                  
CONECT   26    4    5    6   23                                             
CONECT   27   19   24                                                       
CONECT   28   22   23                                                       
CONECT   29   13   20   25                                                  
CONECT   30   21                                                            
CONECT   31   24                                                            
CONECT   32   25                                                            
CONECT   33   19                                                            
CONECT   34   20                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   74    0
END

Synonyms

Not Available

Chemical Formula

C₂₆H₃₃N₃O₃

Average Molecular Weight

435.568

Monoisotopic Molecular Weight

435.252191935

IUPAC Name

(3S,8aS)-1-hydroxy-3-{[6-hydroxy-7-(3-methylbut-2-en-1-yl)-2-(2-methylbut-3-en-2-yl)-1H-indol-3-yl]methyl}-3H,4H,6H,7H,8H,8aH-pyrrolo[1,2-a]pyrazin-4-one

Traditional Name

(3S,8aS)-1-hydroxy-3-{[6-hydroxy-7-(3-methylbut-2-en-1-yl)-2-(2-methylbut-3-en-2-yl)-1H-indol-3-yl]methyl}-3H,6H,7H,8H,8aH-pyrrolo[1,2-a]pyrazin-4-one

CAS Registry Number

Not Available

SMILES

[H][C@@]12CCCN1C(=O)[C@]([H])(CC1=C(NC3=C1C=CC(O)=C3CC=C(C)C)C(C)(C)C=C)N=C2O

InChI Identifier

InChI=1S/C26H33N3O3/c1-6-26(4,5)23-18(14-19-25(32)29-13-7-8-20(29)24(31)27-19)16-11-12-21(30)17(22(16)28-23)10-9-15(2)3/h6,9,11-12,19-20,28,30H,1,7-8,10,13-14H2,2-5H3,(H,27,31)/t19-,20-/m0/s1

InChI Key

ZGWIWQJHQKPWGB-PMACEKPBSA-N

Chemical Taxonomy

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.022 g/L	ALOGPS
logP	4.07	ALOGPS
logP	4.8	ChemAxon
logS	-4.3	ALOGPS
pKa (Strongest Acidic)	4.6	ChemAxon
pKa (Strongest Basic)	1.21	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	88.92 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	127.92 m³·mol⁻¹	ChemAxon
Polarizability	49.2 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	Yes	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
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		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

Proteins

Human Pathways

Pathways

Name	SMPDB/PathBank

Metabolic Reactions

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Related Health Condition	Evidence Type	Measured in Matrix	Data Source	Reference

Microbial Sources

Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
Fungi	Ascomycota	3	Human Feces	Metabolic reconstruction

Exposure Sources

Source Type	Source Sub-type	Species	Data Source	Reference	Details

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Units	Age	Sex	Health Condition	Data Source	Reference

External Links

Not Available

References

Synthesis Reference

Not Available

General References

Bansal P, Morgat A, Axelsen KB, Muthukrishnan V, Coudert E, Aimo L, Hyka-Nouspikel N, Gasteiger E, Kerhornou A, Neto TB, Pozzato M, Blatter MC, Ignatchenko A, Redaschi N, Bridge A: Rhea, the reaction knowledgebase in 2022. Nucleic Acids Res. 2022 Jan 7;50(D1):D693-D700. doi: 10.1093/nar/gkab1016. [PubMed:34755880 ]

Showing metabocard for Notoamide S (MMDBc0020230)

MOL for #<Metabolite:0x000055b76d0d4e48>

3D MOL for #<Metabolite:0x000055b76d0d4e48>

3D SDF for #<Metabolite:0x000055b76d0d4e48>

3D-SDF for #<Metabolite:0x000055b76d0d4e48>

PDB for #<Metabolite:0x000055b76d0d4e48>

3D PDB for #<Metabolite:0x000055b76d0d4e48>

SMILES for #<Metabolite:0x000055b76d0d4e48>

INCHI for #<Metabolite:0x000055b76d0d4e48>

Structure for #<Metabolite:0x000055b76d0d4e48>

3D Structure for #<Metabolite:0x000055b76d0d4e48>