NP-MRD: Showing NP-Card for Keenamide A (NP0076750)

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Record Information

Version

2.0

Created at

2022-04-28 21:56:32 UTC

Updated at

2022-04-28 21:56:32 UTC

NP-MRD ID

NP0076750

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Keenamide A

Description

(1R,4S,10S,16S,19S)-4,19-bis[(2S)-butan-2-yl]-2,11,14,17-tetrahydroxy-16-{[(2-methylbut-3-en-2-yl)oxy]methyl}-21-thia-3,6,12,15,18,23-hexaazatricyclo[18.2.1.0⁶,¹⁰]Tricosa-2,11,14,17,20(23)-pentaen-5-one belongs to the class of organic compounds known as cyclic peptides. Cyclic peptides are compounds containing a cyclic moiety bearing a peptide backbone. Keenamide A is found in Didemnum molle. Based on a literature review very few articles have been published on (1R,4S,10S,16S,19S)-4,19-bis[(2S)-butan-2-yl]-2,11,14,17-tetrahydroxy-16-{[(2-methylbut-3-en-2-yl)oxy]methyl}-21-thia-3,6,12,15,18,23-hexaazatricyclo[18.2.1.0⁶,¹⁰]Tricosa-2,11,14,17,20(23)-pentaen-5-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282223562D          

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M  END

     RDKit          3D

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M  END


  Mrv1652304282223562D          

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    5.5292   -5.2568    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.2457   -4.8478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9581   -5.2639    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2498   -4.0228    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.9663   -3.6139    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.6787   -4.0299    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.3952   -3.6210    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1076   -4.0370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6746   -4.8549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9704   -2.7889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2580   -2.3729    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.2621   -1.5479    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.1165   -1.4621    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5255   -2.1786    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    5.5497   -1.1318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5538   -0.3068    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8332   -1.5408    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.1207   -1.1247    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5171   -1.5041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6918   -1.1176    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4001   -2.3587    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.2326   -1.5509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4126   -1.4606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0733   -2.2126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1248   -0.2998    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4124    0.1163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4165    0.9413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8413    0.1092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5251   -6.0818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2375   -6.4978    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2334   -7.3228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4084   -7.3187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2293   -8.1478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9417   -8.5638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0584   -7.3269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 14 17  1  6  0  0  0
 13 18  1  0  0  0  0
 18 19  2  0  0  0  0
 20 19  1  6  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 18 22  1  0  0  0  0
 20 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
  1 29  1  6  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
  1 32  1  0  0  0  0
 26 33  1  6  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 33 36  1  6  0  0  0
  9 37  1  6  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 39 41  1  0  0  0  0
 41 42  2  0  0  0  0
 39 43  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0076750

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@H](C)[C@@H]1NC(=O)[C@H](COC(C)(C)C=C)NC(=O)CNC(=O)[C@@H]2CCCN2C(=O)[C@@H](NC(=O)[C@@H]2CSC1=N2)[C@@H](C)CC

> <INCHI_IDENTIFIER>
InChI=1S/C30H48N6O6S/c1-8-17(4)23-28-33-20(16-43-28)26(39)35-24(18(5)9-2)29(41)36-13-11-12-21(36)27(40)31-14-22(37)32-19(25(38)34-23)15-42-30(6,7)10-3/h10,17-21,23-24H,3,8-9,11-16H2,1-2,4-7H3,(H,31,40)(H,32,37)(H,34,38)(H,35,39)/t17-,18-,19-,20-,21-,23-,24-/m0/s1

> <INCHI_KEY>
KFDMDQKSGAFMNV-DJKVCXMVSA-N

> <FORMULA>
C30H48N6O6S

> <MOLECULAR_WEIGHT>
620.81

> <EXACT_MASS>
620.335604464

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
91

> <JCHEM_AVERAGE_POLARIZABILITY>
66.23513021008445

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,4S,10S,16S,19S)-4,19-bis[(2S)-butan-2-yl]-16-{[(2-methylbut-3-en-2-yl)oxy]methyl}-21-thia-3,6,12,15,18,23-hexaazatricyclo[18.2.1.0^{6,10}]tricos-20(23)-ene-2,5,11,14,17-pentone

> <ALOGPS_LOGP>
1.99

> <JCHEM_LOGP>
1.105642545

> <ALOGPS_LOGS>
-4.29

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.05497091269053

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.541132997145409

> <JCHEM_PKA_STRONGEST_BASIC>
1.8205566802429063

> <JCHEM_POLAR_SURFACE_AREA>
158.3

> <JCHEM_REFRACTIVITY>
163.47269999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.20e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,4S,10S,16S,19S)-4,19-bis[(2S)-butan-2-yl]-16-{[(2-methylbut-3-en-2-yl)oxy]methyl}-21-thia-3,6,12,15,18,23-hexaazatricyclo[18.2.1.0^{6,10}]tricos-20(23)-ene-2,5,11,14,17-pentone

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       5.009  -5.166   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.002  -6.706   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       3.664  -7.470   0.000  0.00  0.00           O+0
HETATM    4  N   UNK     0       6.332  -7.483   0.000  0.00  0.00           N+0
HETATM    5  C   UNK     0       6.324  -9.023   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.654  -9.799   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       7.646 -11.339   0.000  0.00  0.00           O+0
HETATM    8  N   UNK     0       8.991  -9.036   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0      10.321  -9.813   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      11.659  -9.049   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      12.988  -9.826   0.000  0.00  0.00           O+0
HETATM   12  N   UNK     0      11.666  -7.509   0.000  0.00  0.00           N+0
HETATM   13  C   UNK     0      13.004  -6.746   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      14.334  -7.523   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      15.671  -6.759   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      17.001  -7.536   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      14.326  -9.063   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      13.011  -5.206   0.000  0.00  0.00           C+0
HETATM   19  N   UNK     0      11.682  -4.429   0.000  0.00  0.00           N+0
HETATM   20  C   UNK     0      11.689  -2.889   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      13.284  -2.729   0.000  0.00  0.00           C+0
HETATM   22  S   UNK     0      14.048  -4.067   0.000  0.00  0.00           S+0
HETATM   23  C   UNK     0      10.359  -2.113   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      10.367  -0.573   0.000  0.00  0.00           O+0
HETATM   25  N   UNK     0       9.022  -2.876   0.000  0.00  0.00           N+0
HETATM   26  C   UNK     0       7.692  -2.100   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.565  -2.808   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       5.025  -2.086   0.000  0.00  0.00           O+0
HETATM   29  N   UNK     0       6.347  -4.403   0.000  0.00  0.00           N+0
HETATM   30  C   UNK     0       6.034  -2.895   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.503  -2.726   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       3.870  -4.130   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       7.700  -0.560   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       6.370   0.217   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       6.377   1.757   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       9.037   0.204   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      10.313 -11.353   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      11.643 -12.129   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0      11.636 -13.669   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      10.096 -13.662   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      11.628 -15.209   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      12.958 -15.986   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      13.176 -13.677   0.000  0.00  0.00           C+0
CONECT    1    2   29   32                                                  
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10   37                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   18                                                  
CONECT   14   13   15   17                                                  
CONECT   15   14   16                                                       
CONECT   16   15                                                            
CONECT   17   14                                                            
CONECT   18   13   19   22                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   23                                                  
CONECT   21   20   22                                                       
CONECT   22   21   18                                                       
CONECT   23   20   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   27   33                                                  
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27    1   30                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31    1                                                       
CONECT   33   26   34   36                                                  
CONECT   34   33   35                                                       
CONECT   35   34                                                            
CONECT   36   33                                                            
CONECT   37    9   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40   41   43                                             
CONECT   40   39                                                            
CONECT   41   39   42                                                       
CONECT   42   41                                                            
CONECT   43   39                                                            
MASTER        0    0    0    0    0    0    0    0   43    0   90    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₄₈N₆O₆S

Average Mass

620.8100 Da

Monoisotopic Mass

620.33560 Da

IUPAC Name

(1R,4S,10S,16S,19S)-4,19-bis[(2S)-butan-2-yl]-16-{[(2-methylbut-3-en-2-yl)oxy]methyl}-21-thia-3,6,12,15,18,23-hexaazatricyclo[18.2.1.0^{6,10}]tricos-20(23)-ene-2,5,11,14,17-pentone

Traditional Name

(1R,4S,10S,16S,19S)-4,19-bis[(2S)-butan-2-yl]-16-{[(2-methylbut-3-en-2-yl)oxy]methyl}-21-thia-3,6,12,15,18,23-hexaazatricyclo[18.2.1.0^{6,10}]tricos-20(23)-ene-2,5,11,14,17-pentone

CAS Registry Number

Not Available

SMILES

CC[C@H](C)[C@@H]1NC(=O)[C@H](COC(C)(C)C=C)NC(=O)CNC(=O)[C@@H]2CCCN2C(=O)[C@@H](NC(=O)[C@@H]2CSC1=N2)[C@@H](C)CC

InChI Identifier

InChI=1S/C30H48N6O6S/c1-8-17(4)23-28-33-20(16-43-28)26(39)35-24(18(5)9-2)29(41)36-13-11-12-21(36)27(40)31-14-22(37)32-19(25(38)34-23)15-42-30(6,7)10-3/h10,17-21,23-24H,3,8-9,11-16H2,1-2,4-7H3,(H,31,40)(H,32,37)(H,34,38)(H,35,39)/t17-,18-,19-,20-,21-,23-,24-/m0/s1

InChI Key

KFDMDQKSGAFMNV-DJKVCXMVSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Didemnum molle	Animalia	KNApSAcK

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
Alpha-amino acid or derivatives
Imidothiolactone
Cyclic carboximidic acid
Meta-thiazoline
Tertiary carboxylic acid amide
Pyrrolidine
Lactam
Carboxamide group
Azacycle
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Polyol
Ether
Dialkyl ether
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	1.99	ALOGPS
logP	1.11	ChemAxon
logS	-4.3	ALOGPS
pKa (Strongest Acidic)	10.54	ChemAxon
pKa (Strongest Basic)	1.82	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	158.3 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	163.47 m³·mol⁻¹	ChemAxon
Polarizability	66.24 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

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

163104705

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Keenamide A (NP0076750)

MOL for NP0076750 (Keenamide A)

3D MOL for NP0076750 (Keenamide A)

3D SDF for NP0076750 (Keenamide A)

3D-SDF for NP0076750 (Keenamide A)

PDB for NP0076750 (Keenamide A)

3D PDB for NP0076750 (Keenamide A)

SMILES for NP0076750 (Keenamide A)

INCHI for NP0076750 (Keenamide A)

Structure for NP0076750 (Keenamide A)

3D Structure for NP0076750 (Keenamide A)