NP-MRD: Showing NP-Card for (3s,6r,9s,18s,23as)-6-[(2r)-butan-2-yl]-1,4,7,10,13,16-hexahydroxy-18-[(4-hydroxyphenyl)methyl]-3,9-bis(2-methylpropyl)-3h,6h,9h,12h,15h,18h,21h,22h,23h,23ah-pyrrolo[1,2-a]1,4,7,10,13,16,19-heptaazacyclohenicosan-19-one (NP0236977)

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Record Information

Version

2.0

Created at

2022-09-06 20:00:25 UTC

Updated at

2022-09-06 20:00:25 UTC

NP-MRD ID

NP0236977

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3s,6r,9s,18s,23as)-6-[(2r)-butan-2-yl]-1,4,7,10,13,16-hexahydroxy-18-[(4-hydroxyphenyl)methyl]-3,9-bis(2-methylpropyl)-3h,6h,9h,12h,15h,18h,21h,22h,23h,23ah-pyrrolo[1,2-a]1,4,7,10,13,16,19-heptaazacyclohenicosan-19-one

Description

(3S,6R,9S,18S,23aS)-6-[(2R)-butan-2-yl]-1,4,7,10,13,16-hexahydroxy-18-[(4-hydroxyphenyl)methyl]-3,9-bis(2-methylpropyl)-3H,6H,9H,12H,15H,18H,19H,21H,22H,23H,23aH-pyrrolo[1,2-a]1,4,7,10,13,16,19-heptaazacyclohenicosan-19-one belongs to the class of organic compounds known as cyclic peptides. Cyclic peptides are compounds containing a cyclic moiety bearing a peptide backbone. (3s,6r,9s,18s,23as)-6-[(2r)-butan-2-yl]-1,4,7,10,13,16-hexahydroxy-18-[(4-hydroxyphenyl)methyl]-3,9-bis(2-methylpropyl)-3h,6h,9h,12h,15h,18h,21h,22h,23h,23ah-pyrrolo[1,2-a]1,4,7,10,13,16,19-heptaazacyclohenicosan-19-one is found in Pseudostellaria heterophylla. Based on a literature review very few articles have been published on (3S,6R,9S,18S,23aS)-6-[(2R)-butan-2-yl]-1,4,7,10,13,16-hexahydroxy-18-[(4-hydroxyphenyl)methyl]-3,9-bis(2-methylpropyl)-3H,6H,9H,12H,15H,18H,19H,21H,22H,23H,23aH-pyrrolo[1,2-a]1,4,7,10,13,16,19-heptaazacyclohenicosan-19-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062222002D          

 51 53  0  0  1  0            999 V2000
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M  END

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 47100  1  0
 47101  1  0
 47102  1  0
 48103  1  0
 48104  1  0
 48105  1  0
 51106  1  0
M  END


  Mrv1652309062222002D          

 51 53  0  0  1  0            999 V2000
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    4.4866    1.0947    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    3.1140    1.4922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.2858   -3.0855    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4545   -3.6130    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0017   -4.3026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1781   -4.2552    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7252   -4.9449    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0984   -4.8975    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4692   -4.1605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2929   -4.1131    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0164   -3.4709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8073   -3.5183    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2782   -3.6604    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5350   -4.4444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9844   -5.0588    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3424   -4.6140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8929   -3.9996    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.6660   -4.2877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8031   -5.1012    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3020   -3.7622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1649   -2.9486    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.8721   -2.5238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5937   -2.9239    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8578   -1.6989    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.5650   -1.2741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2866   -1.6742    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9938   -1.2493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3009   -2.4990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1363   -1.2989    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.2451   -0.4811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0077   -0.1664    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  6  0  0  0
  5  3  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  4  0  0  0
  7  9  1  0  0  0  0
  9 10  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
  9 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  4  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 17 21  1  1  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  1  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 31 32  2  0  0  0  0
 26 32  1  0  0  0  0
 24 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  4  0  0  0
 34 36  1  0  0  0  0
 37 36  1  4  0  0  0
 37 38  2  0  0  0  0
 38 39  1  0  0  0  0
 38 40  1  0  0  0  0
 41 40  1  4  0  0  0
 41 42  2  0  0  0  0
 42 43  1  0  0  0  0
 42 44  1  0  0  0  0
 44 45  1  1  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 46 48  1  0  0  0  0
 44 49  1  0  0  0  0
 49 50  2  0  0  0  0
  5 50  1  0  0  0  0
 50 51  1  4  0  0  0
M  END
> <DATABASE_ID>
NP0236977

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@@H](C)[C@H]1N=C(O)[C@H](CC(C)C)N=C(O)[C@@H]2CCCN2C(=O)[C@H](CC2=CC=C(O)C=C2)N=C(O)CN=C(O)CN=C(O)[C@H](CC(C)C)N=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C36H55N7O8/c1-7-22(6)31-35(50)41-25(15-20(2)3)32(47)38-18-29(45)37-19-30(46)39-27(17-23-10-12-24(44)13-11-23)36(51)43-14-8-9-28(43)34(49)40-26(16-21(4)5)33(48)42-31/h10-13,20-22,25-28,31,44H,7-9,14-19H2,1-6H3,(H,37,45)(H,38,47)(H,39,46)(H,40,49)(H,41,50)(H,42,48)/t22-,25+,26+,27+,28+,31-/m1/s1

> <INCHI_KEY>
YOFPLKQHLAVSOC-IOBRMWBLSA-N

> <FORMULA>
C36H55N7O8

> <MOLECULAR_WEIGHT>
713.877

> <EXACT_MASS>
713.411211759

> <JCHEM_ACCEPTOR_COUNT>
14

> <JCHEM_ATOM_COUNT>
106

> <JCHEM_AVERAGE_POLARIZABILITY>
75.49447331118883

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3S,6R,9S,18S,23aS)-6-[(2R)-butan-2-yl]-1,4,7,10,13,16-hexahydroxy-18-[(4-hydroxyphenyl)methyl]-3,9-bis(2-methylpropyl)-3H,6H,9H,12H,15H,18H,19H,21H,22H,23H,23aH-pyrrolo[1,2-a]1,4,7,10,13,16,19-heptaazacyclohenicosan-19-one

> <JCHEM_LOGP>
5.4901741186666655

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
3.6448952812265567

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.2113514829650422

> <JCHEM_PKA_STRONGEST_BASIC>
1.5783882907942768

> <JCHEM_POLAR_SURFACE_AREA>
236.07999999999996

> <JCHEM_REFRACTIVITY>
190.45700000000008

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(3S,6R,9S,18S,23aS)-6-[(2R)-butan-2-yl]-1,4,7,10,13,16-hexahydroxy-18-[(4-hydroxyphenyl)methyl]-3,9-bis(2-methylpropyl)-3H,6H,9H,12H,15H,18H,21H,22H,23H,23aH-pyrrolo[1,2-a]1,4,7,10,13,16,19-heptaazacyclohenicosan-19-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0      12.267   3.682   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.064   2.155   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      10.640   1.568   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.420   2.507   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.437   0.041   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0       9.013  -0.546   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0       7.947   0.564   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       8.375   2.044   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       6.451   0.196   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.384   1.306   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.813   2.785   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.746   3.896   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.308   3.154   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0       6.023  -1.284   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0       4.490  -1.425   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       3.600  -0.168   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       3.846  -2.824   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.375  -3.282   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.356  -4.821   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.441  -5.090   0.000  0.00  0.00           C+0
HETATM   21  N   UNK     0       4.735  -4.081   0.000  0.00  0.00           N+0
HETATM   22  C   UNK     0       3.890  -5.369   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       2.400  -5.760   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       4.582  -6.744   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.736  -8.032   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.199  -7.943   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       1.354  -9.230   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -0.184  -9.142   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -0.876  -7.766   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -2.413  -7.678   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      -0.031  -6.479   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       1.507  -6.567   0.000  0.00  0.00           C+0
HETATM   33  N   UNK     0       6.119  -6.833   0.000  0.00  0.00           N+0
HETATM   34  C   UNK     0       6.599  -8.296   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       5.571  -9.443   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       8.106  -8.613   0.000  0.00  0.00           C+0
HETATM   37  N   UNK     0       9.133  -7.466   0.000  0.00  0.00           N+0
HETATM   38  C   UNK     0      10.577  -8.004   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      10.832  -9.522   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      11.764  -7.023   0.000  0.00  0.00           C+0
HETATM   41  N   UNK     0      11.508  -5.504   0.000  0.00  0.00           N+0
HETATM   42  C   UNK     0      12.828  -4.711   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      14.175  -5.458   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0      12.801  -3.171   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      14.121  -2.378   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      15.468  -3.125   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      16.788  -2.332   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      15.495  -4.665   0.000  0.00  0.00           C+0
HETATM   49  N   UNK     0      11.454  -2.425   0.000  0.00  0.00           N+0
HETATM   50  C   UNK     0      11.658  -0.898   0.000  0.00  0.00           C+0
HETATM   51  O   UNK     0      13.081  -0.311   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   50                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14    9   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   21                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   17   22                                                  
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   33                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   32                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32                                                       
CONECT   32   31   26                                                       
CONECT   33   24   34                                                       
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   43   44                                                  
CONECT   43   42                                                            
CONECT   44   42   45   49                                                  
CONECT   45   44   46                                                       
CONECT   46   45   47   48                                                  
CONECT   47   46                                                            
CONECT   48   46                                                            
CONECT   49   44   50                                                       
CONECT   50   49    5   51                                                  
CONECT   51   50                                                            
MASTER        0    0    0    0    0    0    0    0   51    0  106    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₆H₅₅N₇O₈

Average Mass

713.8770 Da

Monoisotopic Mass

713.41121 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC[C@@H](C)[C@H]1N=C(O)[C@H](CC(C)C)N=C(O)[C@@H]2CCCN2C(=O)[C@H](CC2=CC=C(O)C=C2)N=C(O)CN=C(O)CN=C(O)[C@H](CC(C)C)N=C1O

InChI Identifier

InChI=1S/C36H55N7O8/c1-7-22(6)31-35(50)41-25(15-20(2)3)32(47)38-18-29(45)37-19-30(46)39-27(17-23-10-12-24(44)13-11-23)36(51)43-14-8-9-28(43)34(49)40-26(16-21(4)5)33(48)42-31/h10-13,20-22,25-28,31,44H,7-9,14-19H2,1-6H3,(H,37,45)(H,38,47)(H,39,46)(H,40,49)(H,41,50)(H,42,48)/t22-,25+,26+,27+,28+,31-/m1/s1

InChI Key

YOFPLKQHLAVSOC-IOBRMWBLSA-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, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, 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
Pseudostellaria heterophylla	LOTUS Database	35616633

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
1-hydroxy-2-unsubstituted benzenoid
Phenol
Monocyclic benzene moiety
Benzenoid
Pyrrolidine
Tertiary carboxylic acid amide
Cyclic carboximidic acid
Carboxamide group
Lactam
Organoheterocyclic compound
Azacycle
Polyol
Propargyl-type 1,3-dipolar organic compound
Organic 1,3-dipolar compound
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Organonitrogen compound
Organopnictogen compound
Organic nitrogen compound
Carbonyl group
Organic oxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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

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

162925295

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3s,6r,9s,18s,23as)-6-[(2r)-butan-2-yl]-1,4,7,10,13,16-hexahydroxy-18-[(4-hydroxyphenyl)methyl]-3,9-bis(2-methylpropyl)-3h,6h,9h,12h,15h,18h,21h,22h,23h,23ah-pyrrolo[1,2-a]1,4,7,10,13,16,19-heptaazacyclohenicosan-19-one (NP0236977)

MOL for NP0236977 ((3s,6r,9s,18s,23as)-6-[(2r)-butan-2-yl]-1,4,7,10,13,16-hexahydroxy-18-[(4-hydroxyphenyl)methyl]-3,9-bis(2-methylpropyl)-3h,6h,9h,12h,15h,18h,21h,22h,23h,23ah-pyrrolo[1,2-a]1,4,7,10,13,16,19-heptaazacyclohenicosan-19-one)

3D MOL for NP0236977 ((3s,6r,9s,18s,23as)-6-[(2r)-butan-2-yl]-1,4,7,10,13,16-hexahydroxy-18-[(4-hydroxyphenyl)methyl]-3,9-bis(2-methylpropyl)-3h,6h,9h,12h,15h,18h,21h,22h,23h,23ah-pyrrolo[1,2-a]1,4,7,10,13,16,19-heptaazacyclohenicosan-19-one)

3D SDF for NP0236977 ((3s,6r,9s,18s,23as)-6-[(2r)-butan-2-yl]-1,4,7,10,13,16-hexahydroxy-18-[(4-hydroxyphenyl)methyl]-3,9-bis(2-methylpropyl)-3h,6h,9h,12h,15h,18h,21h,22h,23h,23ah-pyrrolo[1,2-a]1,4,7,10,13,16,19-heptaazacyclohenicosan-19-one)

3D-SDF for NP0236977 ((3s,6r,9s,18s,23as)-6-[(2r)-butan-2-yl]-1,4,7,10,13,16-hexahydroxy-18-[(4-hydroxyphenyl)methyl]-3,9-bis(2-methylpropyl)-3h,6h,9h,12h,15h,18h,21h,22h,23h,23ah-pyrrolo[1,2-a]1,4,7,10,13,16,19-heptaazacyclohenicosan-19-one)

PDB for NP0236977 ((3s,6r,9s,18s,23as)-6-[(2r)-butan-2-yl]-1,4,7,10,13,16-hexahydroxy-18-[(4-hydroxyphenyl)methyl]-3,9-bis(2-methylpropyl)-3h,6h,9h,12h,15h,18h,21h,22h,23h,23ah-pyrrolo[1,2-a]1,4,7,10,13,16,19-heptaazacyclohenicosan-19-one)

3D PDB for NP0236977 ((3s,6r,9s,18s,23as)-6-[(2r)-butan-2-yl]-1,4,7,10,13,16-hexahydroxy-18-[(4-hydroxyphenyl)methyl]-3,9-bis(2-methylpropyl)-3h,6h,9h,12h,15h,18h,21h,22h,23h,23ah-pyrrolo[1,2-a]1,4,7,10,13,16,19-heptaazacyclohenicosan-19-one)

SMILES for NP0236977 ((3s,6r,9s,18s,23as)-6-[(2r)-butan-2-yl]-1,4,7,10,13,16-hexahydroxy-18-[(4-hydroxyphenyl)methyl]-3,9-bis(2-methylpropyl)-3h,6h,9h,12h,15h,18h,21h,22h,23h,23ah-pyrrolo[1,2-a]1,4,7,10,13,16,19-heptaazacyclohenicosan-19-one)

INCHI for NP0236977 ((3s,6r,9s,18s,23as)-6-[(2r)-butan-2-yl]-1,4,7,10,13,16-hexahydroxy-18-[(4-hydroxyphenyl)methyl]-3,9-bis(2-methylpropyl)-3h,6h,9h,12h,15h,18h,21h,22h,23h,23ah-pyrrolo[1,2-a]1,4,7,10,13,16,19-heptaazacyclohenicosan-19-one)

Structure for NP0236977 ((3s,6r,9s,18s,23as)-6-[(2r)-butan-2-yl]-1,4,7,10,13,16-hexahydroxy-18-[(4-hydroxyphenyl)methyl]-3,9-bis(2-methylpropyl)-3h,6h,9h,12h,15h,18h,21h,22h,23h,23ah-pyrrolo[1,2-a]1,4,7,10,13,16,19-heptaazacyclohenicosan-19-one)

3D Structure for NP0236977 ((3s,6r,9s,18s,23as)-6-[(2r)-butan-2-yl]-1,4,7,10,13,16-hexahydroxy-18-[(4-hydroxyphenyl)methyl]-3,9-bis(2-methylpropyl)-3h,6h,9h,12h,15h,18h,21h,22h,23h,23ah-pyrrolo[1,2-a]1,4,7,10,13,16,19-heptaazacyclohenicosan-19-one)