MiMeDB: Showing metabocard for Cyclo-[phenylalanyl-prolyl-leucyl-prolyl] (MMDBc0007417)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-15 00:36:23 UTC

Update Date

2022-08-31 06:27:07 UTC

Metabolite ID

MMDBc0007417

Metabolite Identification

Common Name

Cyclo-[phenylalanyl-prolyl-leucyl-prolyl]

Description

Cyclo-[phenylalanyl-prolyl-leucyl-prolyl] belongs to the class of organic compounds known as cyclic peptides. Cyclic peptides are compounds containing a cyclic moiety bearing a peptide backbone. Based on a literature review a significant number of articles have been published on Cyclo-[phenylalanyl-prolyl-leucyl-prolyl].

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152102362D          

 37 40  0  0  1  0            999 V2000
    1.2893    3.5382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4266    2.3991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8426   -3.3297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1849   -3.8278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7400   -2.5111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6271    0.1993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3446   -0.3460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4247   -3.5073    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9798   -2.1906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1571    0.4574    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4395   -0.6041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9210    0.6259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6385   -0.7726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8444    2.2215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4380   -2.3682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1868    2.7196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3222   -2.6887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7419    1.4029    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5406   -1.5496    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3350    0.5273    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6175   -0.6740    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1631    1.1850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1194   -1.3317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3996    0.9048    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1171   -1.0515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9817    1.0824    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.3008   -1.2291    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2970    0.0862    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0145   -0.2329    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1574    1.9452    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4399   -2.0919    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1598    1.2253    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8773   -1.3720    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5021    1.7234    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1982   -2.0477    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7332    1.2498    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0157   -1.3966    0.0000 H   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
  8  4  1  0  0  0  0
  9  5  2  0  0  0  0
 10  7  1  0  0  0  0
 11  6  1  0  0  0  0
 12  6  1  0  0  0  0
 13  7  1  0  0  0  0
 16  1  1  0  0  0  0
 16  2  1  0  0  0  0
 16 14  1  0  0  0  0
 17  8  2  0  0  0  0
 17  9  1  0  0  0  0
 17 15  1  0  0  0  0
 18 14  1  1  0  0  0
 19 15  1  1  0  0  0
 20 10  1  0  0  0  0
 21 11  1  0  0  0  0
 22 20  1  0  0  0  0
 23 21  1  0  0  0  0
 24 18  1  0  0  0  0
 25 19  1  0  0  0  0
 26 18  1  0  0  0  0
 26 22  2  0  0  0  0
 27 19  1  0  0  0  0
 27 23  2  0  0  0  0
 28 12  1  0  0  0  0
 28 21  1  0  0  0  0
 28 24  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
 22 30  1  4  0  0  0
 23 31  1  4  0  0  0
 32 24  2  0  0  0  0
 33 25  2  0  0  0  0
 18 34  1  6  0  0  0
 19 35  1  6  0  0  0
 20 36  1  6  0  0  0
 21 37  1  6  0  0  0
M  END


  Mrv1652305152102362D          

 37 40  0  0  1  0            999 V2000
    1.2893    3.5382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4266    2.3991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8426   -3.3297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1849   -3.8278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7400   -2.5111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6271    0.1993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3446   -0.3460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4247   -3.5073    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9798   -2.1906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1571    0.4574    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4395   -0.6041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9210    0.6259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6385   -0.7726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8444    2.2215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4380   -2.3682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1868    2.7196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3222   -2.6887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7419    1.4029    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5406   -1.5496    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3350    0.5273    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6175   -0.6740    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1631    1.1850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1194   -1.3317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3996    0.9048    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1171   -1.0515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9817    1.0824    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.3008   -1.2291    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2970    0.0862    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0145   -0.2329    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1574    1.9452    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4399   -2.0919    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1598    1.2253    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8773   -1.3720    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5021    1.7234    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1982   -2.0477    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7332    1.2498    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0157   -1.3966    0.0000 H   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
  8  4  1  0  0  0  0
  9  5  2  0  0  0  0
 10  7  1  0  0  0  0
 11  6  1  0  0  0  0
 12  6  1  0  0  0  0
 13  7  1  0  0  0  0
 16  1  1  0  0  0  0
 16  2  1  0  0  0  0
 16 14  1  0  0  0  0
 17  8  2  0  0  0  0
 17  9  1  0  0  0  0
 17 15  1  0  0  0  0
 18 14  1  1  0  0  0
 19 15  1  1  0  0  0
 20 10  1  0  0  0  0
 21 11  1  0  0  0  0
 22 20  1  0  0  0  0
 23 21  1  0  0  0  0
 24 18  1  0  0  0  0
 25 19  1  0  0  0  0
 26 18  1  0  0  0  0
 26 22  2  0  0  0  0
 27 19  1  0  0  0  0
 27 23  2  0  0  0  0
 28 12  1  0  0  0  0
 28 21  1  0  0  0  0
 28 24  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
 22 30  1  4  0  0  0
 23 31  1  4  0  0  0
 32 24  2  0  0  0  0
 33 25  2  0  0  0  0
 18 34  1  6  0  0  0
 19 35  1  6  0  0  0
 20 36  1  6  0  0  0
 21 37  1  6  0  0  0
M  END
> <DATABASE_ID>
MMDBc0007417

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@@]12CCCN1C(=O)[C@]([H])(CC(C)C)N=C(O)[C@]1([H])CCCN1C(=O)[C@]([H])(CC1=CC=CC=C1)N=C2O

> <INCHI_IDENTIFIER>
InChI=1S/C25H34N4O4/c1-16(2)14-18-24(32)28-12-6-11-21(28)23(31)27-19(15-17-8-4-3-5-9-17)25(33)29-13-7-10-20(29)22(30)26-18/h3-5,8-9,16,18-21H,6-7,10-15H2,1-2H3,(H,26,30)(H,27,31)/t18-,19-,20-,21-/m0/s1

> <INCHI_KEY>
DGVAQUZMNFTFKE-TUFLPTIASA-N

> <FORMULA>
C25H34N4O4

> <MOLECULAR_WEIGHT>
454.571

> <EXACT_MASS>
454.258005591

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
67

> <JCHEM_AVERAGE_POLARIZABILITY>
48.393875434955035

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3S,6S,12S,15S)-3-benzyl-5,14-dihydroxy-12-(2-methylpropyl)-1,4,10,13-tetraazatricyclo[13.3.0.0^{6,10}]octadeca-4,13-diene-2,11-dione

> <ALOGPS_LOGP>
1.98

> <JCHEM_LOGP>
2.0521718420600643

> <ALOGPS_LOGS>
-3.64

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
5.43020211169366

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.668979289775579

> <JCHEM_PKA_STRONGEST_BASIC>
3.131207482680218

> <JCHEM_POLAR_SURFACE_AREA>
105.80000000000001

> <JCHEM_REFRACTIVITY>
123.90379999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.04e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3S,6S,12S,15S)-3-benzyl-5,14-dihydroxy-12-(2-methylpropyl)-1,4,10,13-tetraazatricyclo[13.3.0.0^{6,10}]octadeca-4,13-diene-2,11-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       2.407   6.605   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.796   4.478   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.439  -6.215   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.212  -7.145   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -3.248  -4.687   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.771   0.372   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.510  -0.646   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.793  -6.547   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.829  -4.089   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.160   0.854   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.420  -1.128   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.452   1.168   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.192  -1.442   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.443   4.147   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.818  -4.421   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.215   5.077   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.601  -5.019   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.252   2.619   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.009  -2.893   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.625   0.984   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.886  -1.258   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.304   2.212   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.956  -2.486   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.479   1.689   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -0.219  -1.963   0.000  0.00  0.00           C+0
HETATM   26  N   UNK     0       1.832   2.020   0.000  0.00  0.00           N+0
HETATM   27  N   UNK     0       2.428  -2.294   0.000  0.00  0.00           N+0
HETATM   28  N   UNK     0       4.288   0.161   0.000  0.00  0.00           N+0
HETATM   29  N   UNK     0      -0.027  -0.435   0.000  0.00  0.00           N+0
HETATM   30  O   UNK     0      -0.294   3.631   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       4.554  -3.905   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       5.898   2.287   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0      -1.638  -2.561   0.000  0.00  0.00           O+0
HETATM   34  H   UNK     0       4.671   3.217   0.000  0.00  0.00           H+0
HETATM   35  H   UNK     0       2.237  -3.822   0.000  0.00  0.00           H+0
HETATM   36  H   UNK     0      -1.369   2.333   0.000  0.00  0.00           H+0
HETATM   37  H   UNK     0       5.629  -2.607   0.000  0.00  0.00           H+0
CONECT    1   16                                                            
CONECT    2   16                                                            
CONECT    3    4    5                                                       
CONECT    4    3    8                                                       
CONECT    5    3    9                                                       
CONECT    6   11   12                                                       
CONECT    7   10   13                                                       
CONECT    8    4   17                                                       
CONECT    9    5   17                                                       
CONECT   10    7   20                                                       
CONECT   11    6   21                                                       
CONECT   12    6   28                                                       
CONECT   13    7   29                                                       
CONECT   14   16   18                                                       
CONECT   15   17   19                                                       
CONECT   16    1    2   14                                                  
CONECT   17    8    9   15                                                  
CONECT   18   14   24   26   34                                             
CONECT   19   15   25   27   35                                             
CONECT   20   10   22   29   36                                             
CONECT   21   11   23   28   37                                             
CONECT   22   20   26   30                                                  
CONECT   23   21   27   31                                                  
CONECT   24   18   28   32                                                  
CONECT   25   19   29   33                                                  
CONECT   26   18   22                                                       
CONECT   27   19   23                                                       
CONECT   28   12   21   24                                                  
CONECT   29   13   20   25                                                  
CONECT   30   22                                                            
CONECT   31   23                                                            
CONECT   32   24                                                            
CONECT   33   25                                                            
CONECT   34   18                                                            
CONECT   35   19                                                            
CONECT   36   20                                                            
CONECT   37   21                                                            
MASTER        0    0    0    0    0    0    0    0   37    0   80    0
END

Synonyms

Not Available

Molecular Formula

C₂₅H₃₄N₄O₄

Average Mass

454.571

Monoisotopic Mass

454.258005591

IUPAC Name

(3S,6S,12S,15S)-3-benzyl-5,14-dihydroxy-12-(2-methylpropyl)-1,4,10,13-tetraazatricyclo[13.3.0.0^{6,10}]octadeca-4,13-diene-2,11-dione

Traditional Name

(3S,6S,12S,15S)-3-benzyl-5,14-dihydroxy-12-(2-methylpropyl)-1,4,10,13-tetraazatricyclo[13.3.0.0^{6,10}]octadeca-4,13-diene-2,11-dione

CAS Registry Number

Not Available

SMILES

[H][C@@]12CCCN1C(=O)[C@]([H])(CC(C)C)N=C(O)[C@]1([H])CCCN1C(=O)[C@]([H])(CC1=CC=CC=C1)N=C2O

InChI Identifier

InChI=1S/C25H34N4O4/c1-16(2)14-18-24(32)28-12-6-11-21(28)23(31)27-19(15-17-8-4-3-5-9-17)25(33)29-13-7-10-20(29)22(30)26-18/h3-5,8-9,16,18-21H,6-7,10-15H2,1-2H3,(H,26,30)(H,27,31)/t18-,19-,20-,21-/m0/s1

InChI Key

DGVAQUZMNFTFKE-TUFLPTIASA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cyclic peptides. Cyclic peptides are compounds containing a cyclic moiety bearing a peptide backbone.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Cyclic peptides

Alternative Parents

Substituents

Cyclic alpha peptide
Macrolactam
Alpha-amino acid or derivatives
Monocyclic benzene moiety
Benzenoid
Pyrrolidine
Tertiary carboxylic acid amide
Secondary carboxylic acid amide
Lactam
Carboxamide group
Azacycle
Organoheterocyclic compound
Organic nitrogen compound
Organooxygen compound
Organonitrogen compound
Hydrocarbon derivative
Organic oxide
Carbonyl group
Organic oxygen 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	0.1 g/L	ALOGPS
logP	1.98	ALOGPS
logP	2.05	ChemAxon
logS	-3.6	ALOGPS
pKa (Strongest Acidic)	4.67	ChemAxon
pKa (Strongest Basic)	3.13	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	105.8 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	123.9 m³·mol⁻¹	ChemAxon
Polarizability	48.39 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
Bacteria	Proteobacteria	1	Human feces; 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

27023277

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

24851291

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 Cyclo-[phenylalanyl-prolyl-leucyl-prolyl] (MMDBc0007417)

MOL for #<Metabolite:0x00007fec9d4140d8>

3D MOL for #<Metabolite:0x00007fec9d4140d8>

3D SDF for #<Metabolite:0x00007fec9d4140d8>

3D-SDF for #<Metabolite:0x00007fec9d4140d8>

PDB for #<Metabolite:0x00007fec9d4140d8>

3D PDB for #<Metabolite:0x00007fec9d4140d8>

SMILES for #<Metabolite:0x00007fec9d4140d8>

INCHI for #<Metabolite:0x00007fec9d4140d8>

Structure for #<Metabolite:0x00007fec9d4140d8>

3D Structure for #<Metabolite:0x00007fec9d4140d8>