MiMeDB: Showing metabocard for (+)-floridamide (MMDBc0024392)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2021-05-15 14:12:58 UTC

Update Date

2025-10-07 16:07:27 UTC

Metabolite ID

MMDBc0024392

Metabolite Identification

Common Name

(+)-floridamide

Description

(+)-floridamide is a cyclic depsipeptide, a class of compounds characterized by the presence of both amino acid and hydroxy acid residues linked by ester bonds. This compound was identified through a bioassay-guided investigation focused on cancer cell cytotoxicity, which highlighted its potential as a bioactive natural product derived from the marine cyanobacterium Moorea producens collected in Key West, Florida (PMID:27426414 ). The chemical structure of (+)-floridamide features a unique arrangement of its constituent amino acids and hydroxy acids, contributing to its biological activity. While the specific biological pathways involving (+)-floridamide remain to be fully elucidated, its classification as a depsipeptide suggests potential interactions with various cellular processes, possibly influencing signaling pathways related to cell proliferation and apoptosis. Further studies are necessary to explore its mechanisms of action and potential therapeutic applications.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152116122D          

 43 45  0  0  0  0            999 V2000
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0467   -3.0308    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3289   -3.5195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5657   -5.0182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9012   -4.2645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7452   -4.9320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -0.4125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -2.4750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -4.1250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.5375   -1.1513    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  8  1  1  0  0  0  0
  9  8  1  0  0  0  0
 11  9  1  0  0  0  0
 12 10  2  0  0  0  0
 13 10  1  0  0  0  0
 15 12  1  0  0  0  0
 16 13  2  0  0  0  0
 17 14  1  0  0  0  0
 18 11  1  0  0  0  0
 19 14  1  0  0  0  0
 21  2  1  0  0  0  0
 21  3  1  0  0  0  0
 22  4  1  0  0  0  0
 23 15  2  0  0  0  0
 23 16  1  0  0  0  0
 23 20  1  0  0  0  0
 24 17  1  0  0  0  0
 25 20  1  0  0  0  0
 26 18  1  0  0  0  0
 27 21  1  0  0  0  0
 28 22  1  0  0  0  0
 29 25  1  0  0  0  0
 30 24  1  0  0  0  0
 31 27  1  0  0  0  0
 33  5  1  0  0  0  0
 33  6  1  0  0  0  0
 33 26  1  0  0  0  0
 33 32  1  0  0  0  0
 34 22  1  4  0  0  0
 34 29  2  0  0  0  0
 35 27  1  4  0  0  0
 35 28  2  0  0  0  0
 36  7  1  0  0  0  0
 36 25  1  0  0  0  0
 36 30  1  0  0  0  0
 37 19  1  0  0  0  0
 37 24  1  0  0  0  0
 37 32  1  0  0  0  0
 38 28  1  0  0  0  0
 39 29  1  0  0  0  0
 40 30  2  0  0  0  0
 41 31  2  0  0  0  0
 42 32  2  0  0  0  0
 43 26  1  0  0  0  0
 43 31  1  0  0  0  0
M  END


  Mrv1652305152116122D          

 43 45  0  0  0  0            999 V2000
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0467   -3.0308    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3289   -3.5195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5657   -5.0182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9012   -4.2645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7452   -4.9320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -0.4125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -2.4750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -4.1250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.5375   -1.1513    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  8  1  1  0  0  0  0
  9  8  1  0  0  0  0
 11  9  1  0  0  0  0
 12 10  2  0  0  0  0
 13 10  1  0  0  0  0
 15 12  1  0  0  0  0
 16 13  2  0  0  0  0
 17 14  1  0  0  0  0
 18 11  1  0  0  0  0
 19 14  1  0  0  0  0
 21  2  1  0  0  0  0
 21  3  1  0  0  0  0
 22  4  1  0  0  0  0
 23 15  2  0  0  0  0
 23 16  1  0  0  0  0
 23 20  1  0  0  0  0
 24 17  1  0  0  0  0
 25 20  1  0  0  0  0
 26 18  1  0  0  0  0
 27 21  1  0  0  0  0
 28 22  1  0  0  0  0
 29 25  1  0  0  0  0
 30 24  1  0  0  0  0
 31 27  1  0  0  0  0
 33  5  1  0  0  0  0
 33  6  1  0  0  0  0
 33 26  1  0  0  0  0
 33 32  1  0  0  0  0
 34 22  1  4  0  0  0
 34 29  2  0  0  0  0
 35 27  1  4  0  0  0
 35 28  2  0  0  0  0
 36  7  1  0  0  0  0
 36 25  1  0  0  0  0
 36 30  1  0  0  0  0
 37 19  1  0  0  0  0
 37 24  1  0  0  0  0
 37 32  1  0  0  0  0
 38 28  1  0  0  0  0
 39 29  1  0  0  0  0
 40 30  2  0  0  0  0
 41 31  2  0  0  0  0
 42 32  2  0  0  0  0
 43 26  1  0  0  0  0
 43 31  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0024392

> <DATABASE_NAME>
MIME

> <SMILES>
CCCCCC1OC(=O)C(N=C(O)C(C)N=C(O)C(CC2=CC=CC=C2)N(C)C(=O)C2CCCN2C(=O)C1(C)C)C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C33H50N4O6/c1-8-9-11-18-26-33(5,6)32(42)37-19-14-17-24(37)30(40)36(7)25(20-23-15-12-10-13-16-23)29(39)34-22(4)28(38)35-27(21(2)3)31(41)43-26/h10,12-13,15-16,21-22,24-27H,8-9,11,14,17-20H2,1-7H3,(H,34,39)(H,35,38)

> <INCHI_KEY>
KDCDMMXOSHLPFR-UHFFFAOYSA-N

> <FORMULA>
C33H50N4O6

> <MOLECULAR_WEIGHT>
598.785

> <EXACT_MASS>
598.373035346

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
93

> <JCHEM_AVERAGE_POLARIZABILITY>
66.32710185859845

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3-benzyl-4,7-dihydroxy-2,6,13,13-tetramethyl-12-pentyl-9-(propan-2-yl)-1H,2H,3H,6H,9H,10H,12H,13H,14H,16H,17H,18H,18aH-pyrrolo[2,1-l]1-oxa-4,7,10,13-tetraazacyclohexadecane-1,10,14-trione

> <ALOGPS_LOGP>
4.04

> <JCHEM_LOGP>
4.586440672295042

> <ALOGPS_LOGS>
-4.88

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
4.2473801123228565

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.886455852083563

> <JCHEM_PKA_STRONGEST_BASIC>
5.275705157916389

> <JCHEM_POLAR_SURFACE_AREA>
132.1

> <JCHEM_REFRACTIVITY>
163.80780000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
7.88e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-benzyl-4,7-dihydroxy-9-isopropyl-2,6,13,13-tetramethyl-12-pentyl-3H,6H,9H,12H,16H,17H,18H,18aH-pyrrolo[2,1-l]1-oxa-4,7,10,13-tetraazacyclohexadecane-1,10,14-trione

> <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       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.337   1.540   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      12.003  -0.770   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      18.672   1.540   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      13.154  -5.657   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      13.681  -6.570   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      20.005  -5.390   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.336  -5.390   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      24.006  -1.540   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.669  -4.620   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      22.673  -0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      24.006  -3.080   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      17.856  -9.367   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      21.339  -1.540   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      22.673  -3.850   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      18.482  -7.960   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      12.003  -5.390   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      16.324  -9.206   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      20.005  -3.850   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      13.337  -0.000   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      18.672  -0.000   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      21.339  -3.080   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      17.338  -6.930   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      18.672  -3.080   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      13.337  -4.620   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      14.670  -0.770   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      17.338  -0.770   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      20.005  -2.310   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      17.338  -5.390   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      14.670  -2.310   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      14.670  -6.930   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      14.670  -5.390   0.000  0.00  0.00           C+0
HETATM   34  N   UNK     0      20.005  -0.770   0.000  0.00  0.00           N+0
HETATM   35  N   UNK     0      16.004  -0.000   0.000  0.00  0.00           N+0
HETATM   36  N   UNK     0      18.672  -4.620   0.000  0.00  0.00           N+0
HETATM   37  N   UNK     0      16.004  -7.700   0.000  0.00  0.00           N+0
HETATM   38  O   UNK     0      17.338  -2.310   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0      21.537  -2.149   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0      16.004  -4.620   0.000  0.00  0.00           O+0
HETATM   41  O   UNK     0      16.004  -3.080   0.000  0.00  0.00           O+0
HETATM   42  O   UNK     0      13.337  -7.700   0.000  0.00  0.00           O+0
HETATM   43  O   UNK     0      13.337  -3.080   0.000  0.00  0.00           O+0
CONECT    1    8                                                            
CONECT    2   21                                                            
CONECT    3   21                                                            
CONECT    4   22                                                            
CONECT    5   33                                                            
CONECT    6   33                                                            
CONECT    7   36                                                            
CONECT    8    1    9                                                       
CONECT    9    8   11                                                       
CONECT   10   12   13                                                       
CONECT   11    9   18                                                       
CONECT   12   10   15                                                       
CONECT   13   10   16                                                       
CONECT   14   17   19                                                       
CONECT   15   12   23                                                       
CONECT   16   13   23                                                       
CONECT   17   14   24                                                       
CONECT   18   11   26                                                       
CONECT   19   14   37                                                       
CONECT   20   23   25                                                       
CONECT   21    2    3   27                                                  
CONECT   22    4   28   34                                                  
CONECT   23   15   16   20                                                  
CONECT   24   17   30   37                                                  
CONECT   25   20   29   36                                                  
CONECT   26   18   33   43                                                  
CONECT   27   21   31   35                                                  
CONECT   28   22   35   38                                                  
CONECT   29   25   34   39                                                  
CONECT   30   24   36   40                                                  
CONECT   31   27   41   43                                                  
CONECT   32   33   37   42                                                  
CONECT   33    5    6   26   32                                             
CONECT   34   22   29                                                       
CONECT   35   27   28                                                       
CONECT   36    7   25   30                                                  
CONECT   37   19   24   32                                                  
CONECT   38   28                                                            
CONECT   39   29                                                            
CONECT   40   30                                                            
CONECT   41   31                                                            
CONECT   42   32                                                            
CONECT   43   26   31                                                       
MASTER        0    0    0    0    0    0    0    0   43    0   90    0
END

Synonyms

Not Available

Molecular Formula

C₃₃H₅₀N₄O₆

Average Mass

598.785

Monoisotopic Mass

598.373035346

IUPAC Name

3-benzyl-4,7-dihydroxy-2,6,13,13-tetramethyl-12-pentyl-9-(propan-2-yl)-1H,2H,3H,6H,9H,10H,12H,13H,14H,16H,17H,18H,18aH-pyrrolo[2,1-l]1-oxa-4,7,10,13-tetraazacyclohexadecane-1,10,14-trione

Traditional Name

3-benzyl-4,7-dihydroxy-9-isopropyl-2,6,13,13-tetramethyl-12-pentyl-3H,6H,9H,12H,16H,17H,18H,18aH-pyrrolo[2,1-l]1-oxa-4,7,10,13-tetraazacyclohexadecane-1,10,14-trione

CAS Registry Number

Not Available

SMILES

CCCCCC1OC(=O)C(N=C(O)C(C)N=C(O)C(CC2=CC=CC=C2)N(C)C(=O)C2CCCN2C(=O)C1(C)C)C(C)C

InChI Identifier

InChI=1S/C33H50N4O6/c1-8-9-11-18-26-33(5,6)32(42)37-19-14-17-24(37)30(40)36(7)25(20-23-15-12-10-13-16-23)29(39)34-22(4)28(38)35-27(21(2)3)31(41)43-26/h10,12-13,15-16,21-22,24-27H,8-9,11,14,17-20H2,1-7H3,(H,34,39)(H,35,38)

InChI Key

KDCDMMXOSHLPFR-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cyclic depsipeptides. These are natural or synthetic compounds having sequences of amino and hydroxy carboxylic acid residues (usually α-amino and α-hydroxy acids) connected in a ring. The residues are commonly but not necessarily regularly alternating.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Peptidomimetics

Sub Class

Depsipeptides

Direct Parent

Cyclic depsipeptides

Alternative Parents

Substituents

Cyclic depsipeptide
Alpha-amino acid ester
Macrolactam
Macrolide
Alpha-amino acid or derivatives
Monocyclic benzene moiety
Benzenoid
Cyclic carboximidic acid
Tertiary carboxylic acid amide
Pyrrolidine
Carboxamide group
Carboxylic acid ester
Lactam
Lactone
Carboxylic acid derivative
Oxacycle
Azacycle
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Monocarboxylic acid or derivatives
Organic oxygen compound
Hydrocarbon derivative
Organopnictogen compound
Carbonyl group
Organic oxide
Organic nitrogen compound
Organonitrogen compound
Organooxygen 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	0.0079 g/L	ALOGPS
logP	4.04	ALOGPS
logP	4.59	ChemAxon
logS	-4.9	ALOGPS
pKa (Strongest Acidic)	2.89	ChemAxon
pKa (Strongest Basic)	5.28	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	132.1 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	163.81 m³·mol⁻¹	ChemAxon
Polarizability	66.33 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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_1) - 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
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-22	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
Bacteria	Cyanobacteria	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

61360277

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139591603

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 (+)-floridamide (MMDBc0024392)

MOL for #<Metabolite:0x00007f8dc81d2ec0>

3D MOL for #<Metabolite:0x00007f8dc81d2ec0>

3D SDF for #<Metabolite:0x00007f8dc81d2ec0>

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PDB for #<Metabolite:0x00007f8dc81d2ec0>

3D PDB for #<Metabolite:0x00007f8dc81d2ec0>

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INCHI for #<Metabolite:0x00007f8dc81d2ec0>

Structure for #<Metabolite:0x00007f8dc81d2ec0>

3D Structure for #<Metabolite:0x00007f8dc81d2ec0>