NP-MRD: Showing NP-Card for 1-hydroxy-3-{[3'-({1-hydroxy-4-oxo-3h,6h,7h,8h,8ah-pyrrolo[1,2-a]pyrazin-3-yl}methyl)-1'h-[1,5'-biindol]-3-yl]methyl}-3h,6h,7h,8h,8ah-pyrrolo[1,2-a]pyrazin-4-one (NP0291371)

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Record Information

Version

1.0

Created at

2022-09-09 22:26:07 UTC

Updated at

2022-09-09 22:26:07 UTC

NP-MRD ID

NP0291371

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-hydroxy-3-{[3'-({1-hydroxy-4-oxo-3h,6h,7h,8h,8ah-pyrrolo[1,2-a]pyrazin-3-yl}methyl)-1'h-[1,5'-biindol]-3-yl]methyl}-3h,6h,7h,8h,8ah-pyrrolo[1,2-a]pyrazin-4-one

Description

1-Hydroxy-3-{[3-({1-hydroxy-4-oxo-3H,4H,6H,7H,8H,8aH-pyrrolo[1,2-a]pyrazin-3-yl}methyl)-1'H-[1,5'-biindole]-3'-yl]methyl}-3H,4H,6H,7H,8H,8aH-pyrrolo[1,2-a]pyrazin-4-one belongs to the class of organic compounds known as alpha amino acids and derivatives. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon), or a derivative thereof. 1-hydroxy-3-{[3'-({1-hydroxy-4-oxo-3h,6h,7h,8h,8ah-pyrrolo[1,2-a]pyrazin-3-yl}methyl)-1'h-[1,5'-biindol]-3-yl]methyl}-3h,6h,7h,8h,8ah-pyrrolo[1,2-a]pyrazin-4-one is found in Aspergillus taichungensis. Based on a literature review very few articles have been published on 1-hydroxy-3-{[3-({1-hydroxy-4-oxo-3H,4H,6H,7H,8H,8aH-pyrrolo[1,2-a]pyrazin-3-yl}methyl)-1'H-[1,5'-biindole]-3'-yl]methyl}-3H,4H,6H,7H,8H,8aH-pyrrolo[1,2-a]pyrazin-4-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102200262D          

 42 49  0  0  0  0            999 V2000
    8.5469    3.7231    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    9.3084    4.2080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5634    4.9926    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   10.3884    4.9926    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  2 42  1  0  0  0  0
 38 42  1  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652309102200262D          

 42 49  0  0  0  0            999 V2000
    8.5469    3.7231    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5469    2.8981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   12.4468    1.1212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2005    1.4567    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   13.4554    2.2414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9034    2.8545    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.1368    4.6176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.8513    5.0301    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.8513    5.8551    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.1368    6.2676    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4224    5.8551    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4224    5.0301    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4503    4.0365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6433    4.2080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2614    1.6606    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.5469    1.2481    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5469    0.4231    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8324    1.6606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0478    1.4057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5629    2.0731    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0478    2.7405    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8324    2.4856    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 20 24  1  0  0  0  0
 24 25  1  0  0  0  0
 16 25  1  0  0  0  0
 25 26  2  0  0  0  0
 14 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 27 32  1  0  0  0  0
 12 32  1  0  0  0  0
 11 33  1  0  0  0  0
 33 34  2  0  0  0  0
  5 34  1  0  0  0  0
  8 34  1  0  0  0  0
  3 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
  2 42  1  0  0  0  0
 38 42  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0291371

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC1=NC(CC2=CNC3=CC=C(C=C23)N2C=C(CC3N=C(O)C4CCCN4C3=O)C3=CC=CC=C23)C(=O)N2CCCC12

> <INCHI_IDENTIFIER>
InChI=1S/C32H32N6O4/c39-29-27-7-3-11-36(27)31(41)24(34-29)13-18-16-33-23-10-9-20(15-22(18)23)38-17-19(21-5-1-2-6-26(21)38)14-25-32(42)37-12-4-8-28(37)30(40)35-25/h1-2,5-6,9-10,15-17,24-25,27-28,33H,3-4,7-8,11-14H2,(H,34,39)(H,35,40)

> <INCHI_KEY>
JEMUKHUDECTHAQ-UHFFFAOYSA-N

> <FORMULA>
C32H32N6O4

> <MOLECULAR_WEIGHT>
564.646

> <EXACT_MASS>
564.248503534

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
74

> <JCHEM_AVERAGE_POLARIZABILITY>
60.34088263427543

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
1-hydroxy-3-{[3'-({1-hydroxy-4-oxo-3H,4H,6H,7H,8H,8aH-pyrrolo[1,2-a]pyrazin-3-yl}methyl)-1'H-[1,5'-biindole]-3-yl]methyl}-3H,4H,6H,7H,8H,8aH-pyrrolo[1,2-a]pyrazin-4-one

> <JCHEM_LOGP>
3.457028839666668

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
8

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
5.052470594144302

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.450623145224904

> <JCHEM_PKA_STRONGEST_BASIC>
1.6398283306871317

> <JCHEM_POLAR_SURFACE_AREA>
126.52

> <JCHEM_REFRACTIVITY>
165.9578

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
1-hydroxy-3-{[3'-({1-hydroxy-4-oxo-3H,6H,7H,8H,8aH-pyrrolo[1,2-a]pyrazin-3-yl}methyl)-1'H-[1,5'-biindole]-3-yl]methyl}-3H,6H,7H,8H,8aH-pyrrolo[1,2-a]pyrazin-4-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  O   UNK     0      15.954   6.950   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      15.954   5.410   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      17.288   4.640   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      18.622   5.410   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      18.622   6.950   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      17.376   7.855   0.000  0.00  0.00           C+0
HETATM    7  N   UNK     0      17.852   9.320   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0      19.392   9.320   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      20.422  10.464   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      21.928  10.144   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      22.404   8.679   0.000  0.00  0.00           C+0
HETATM   12  N   UNK     0      23.911   8.359   0.000  0.00  0.00           N+0
HETATM   13  C   UNK     0      24.537   6.952   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      26.069   7.113   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      27.099   5.969   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      26.623   4.504   0.000  0.00  0.00           C+0
HETATM   17  N   UNK     0      27.654   3.360   0.000  0.00  0.00           N+0
HETATM   18  C   UNK     0      27.178   1.895   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      28.208   0.751   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      25.671   1.575   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      24.901   0.241   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      23.395   0.561   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      23.234   2.093   0.000  0.00  0.00           C+0
HETATM   24  N   UNK     0      24.641   2.719   0.000  0.00  0.00           N+0
HETATM   25  C   UNK     0      25.117   4.184   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      24.086   5.328   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      26.389   8.619   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      27.722   9.389   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      27.722  10.929   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      26.389  11.699   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      25.055  10.929   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      25.055   9.389   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      21.374   7.535   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      19.867   7.855   0.000  0.00  0.00           C+0
HETATM   35  N   UNK     0      17.288   3.100   0.000  0.00  0.00           N+0
HETATM   36  C   UNK     0      15.954   2.330   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      15.954   0.790   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      14.621   3.100   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      13.156   2.624   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      12.251   3.870   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      13.156   5.116   0.000  0.00  0.00           C+0
HETATM   42  N   UNK     0      14.621   4.640   0.000  0.00  0.00           N+0
CONECT    1    2                                                            
CONECT    2    1    3   42                                                  
CONECT    3    2    4   35                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   34                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   34                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   33                                                  
CONECT   12   11   13   32                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   27                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   25                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   24                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   20   25                                                  
CONECT   25   24   16   26                                                  
CONECT   26   25                                                            
CONECT   27   14   28   32                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   27   12                                                  
CONECT   33   11   34                                                       
CONECT   34   33    5    8                                                  
CONECT   35    3   36                                                       
CONECT   36   35   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   39   42                                                  
CONECT   39   38   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41    2   38                                                  
MASTER        0    0    0    0    0    0    0    0   42    0   98    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₂H₃₂N₆O₄

Average Mass

564.6460 Da

Monoisotopic Mass

564.24850 Da

IUPAC Name

1-hydroxy-3-{[3'-({1-hydroxy-4-oxo-3H,4H,6H,7H,8H,8aH-pyrrolo[1,2-a]pyrazin-3-yl}methyl)-1'H-[1,5'-biindole]-3-yl]methyl}-3H,4H,6H,7H,8H,8aH-pyrrolo[1,2-a]pyrazin-4-one

Traditional Name

1-hydroxy-3-{[3'-({1-hydroxy-4-oxo-3H,6H,7H,8H,8aH-pyrrolo[1,2-a]pyrazin-3-yl}methyl)-1'H-[1,5'-biindole]-3-yl]methyl}-3H,6H,7H,8H,8aH-pyrrolo[1,2-a]pyrazin-4-one

CAS Registry Number

Not Available

SMILES

OC1=NC(CC2=CNC3=CC=C(C=C23)N2C=C(CC3N=C(O)C4CCCN4C3=O)C3=CC=CC=C23)C(=O)N2CCCC12

InChI Identifier

InChI=1S/C32H32N6O4/c39-29-27-7-3-11-36(27)31(41)24(34-29)13-18-16-33-23-10-9-20(15-22(18)23)38-17-19(21-5-1-2-6-26(21)38)14-25-32(42)37-12-4-8-28(37)30(40)35-25/h1-2,5-6,9-10,15-17,24-25,27-28,33H,3-4,7-8,11-14H2,(H,34,39)(H,35,40)

InChI Key

JEMUKHUDECTHAQ-UHFFFAOYSA-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
Aspergillus taichungensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as alpha amino acids and derivatives. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon), or a derivative thereof.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Alpha amino acids and derivatives

Alternative Parents

Substituents

Alpha-amino acid or derivatives
3-alkylindole
Indole
Indole or derivatives
Substituted pyrrole
Benzenoid
Pyrrole
Pyrrolidine
Heteroaromatic compound
Tertiary carboxylic acid amide
Cyclic carboximidic acid
Carboxamide group
Lactam
Organoheterocyclic compound
Azacycle
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Organonitrogen compound
Organopnictogen compound
Organic oxygen compound
Organic nitrogen compound
Carbonyl group
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
logP	3.46	ChemAxon
pKa (Strongest Acidic)	4.45	ChemAxon
pKa (Strongest Basic)	1.64	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	126.52 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	165.96 m³·mol⁻¹	ChemAxon
Polarizability	60.34 Å³	ChemAxon
Number of Rings	8	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	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

162929017

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1-hydroxy-3-{[3'-({1-hydroxy-4-oxo-3h,6h,7h,8h,8ah-pyrrolo[1,2-a]pyrazin-3-yl}methyl)-1'h-[1,5'-biindol]-3-yl]methyl}-3h,6h,7h,8h,8ah-pyrrolo[1,2-a]pyrazin-4-one (NP0291371)

MOL for NP0291371 (1-hydroxy-3-{[3'-({1-hydroxy-4-oxo-3h,6h,7h,8h,8ah-pyrrolo[1,2-a]pyrazin-3-yl}methyl)-1'h-[1,5'-biindol]-3-yl]methyl}-3h,6h,7h,8h,8ah-pyrrolo[1,2-a]pyrazin-4-one)

3D MOL for NP0291371 (1-hydroxy-3-{[3'-({1-hydroxy-4-oxo-3h,6h,7h,8h,8ah-pyrrolo[1,2-a]pyrazin-3-yl}methyl)-1'h-[1,5'-biindol]-3-yl]methyl}-3h,6h,7h,8h,8ah-pyrrolo[1,2-a]pyrazin-4-one)

3D SDF for NP0291371 (1-hydroxy-3-{[3'-({1-hydroxy-4-oxo-3h,6h,7h,8h,8ah-pyrrolo[1,2-a]pyrazin-3-yl}methyl)-1'h-[1,5'-biindol]-3-yl]methyl}-3h,6h,7h,8h,8ah-pyrrolo[1,2-a]pyrazin-4-one)

3D-SDF for NP0291371 (1-hydroxy-3-{[3'-({1-hydroxy-4-oxo-3h,6h,7h,8h,8ah-pyrrolo[1,2-a]pyrazin-3-yl}methyl)-1'h-[1,5'-biindol]-3-yl]methyl}-3h,6h,7h,8h,8ah-pyrrolo[1,2-a]pyrazin-4-one)

PDB for NP0291371 (1-hydroxy-3-{[3'-({1-hydroxy-4-oxo-3h,6h,7h,8h,8ah-pyrrolo[1,2-a]pyrazin-3-yl}methyl)-1'h-[1,5'-biindol]-3-yl]methyl}-3h,6h,7h,8h,8ah-pyrrolo[1,2-a]pyrazin-4-one)

3D PDB for NP0291371 (1-hydroxy-3-{[3'-({1-hydroxy-4-oxo-3h,6h,7h,8h,8ah-pyrrolo[1,2-a]pyrazin-3-yl}methyl)-1'h-[1,5'-biindol]-3-yl]methyl}-3h,6h,7h,8h,8ah-pyrrolo[1,2-a]pyrazin-4-one)

SMILES for NP0291371 (1-hydroxy-3-{[3'-({1-hydroxy-4-oxo-3h,6h,7h,8h,8ah-pyrrolo[1,2-a]pyrazin-3-yl}methyl)-1'h-[1,5'-biindol]-3-yl]methyl}-3h,6h,7h,8h,8ah-pyrrolo[1,2-a]pyrazin-4-one)

INCHI for NP0291371 (1-hydroxy-3-{[3'-({1-hydroxy-4-oxo-3h,6h,7h,8h,8ah-pyrrolo[1,2-a]pyrazin-3-yl}methyl)-1'h-[1,5'-biindol]-3-yl]methyl}-3h,6h,7h,8h,8ah-pyrrolo[1,2-a]pyrazin-4-one)

Structure for NP0291371 (1-hydroxy-3-{[3'-({1-hydroxy-4-oxo-3h,6h,7h,8h,8ah-pyrrolo[1,2-a]pyrazin-3-yl}methyl)-1'h-[1,5'-biindol]-3-yl]methyl}-3h,6h,7h,8h,8ah-pyrrolo[1,2-a]pyrazin-4-one)

3D Structure for NP0291371 (1-hydroxy-3-{[3'-({1-hydroxy-4-oxo-3h,6h,7h,8h,8ah-pyrrolo[1,2-a]pyrazin-3-yl}methyl)-1'h-[1,5'-biindol]-3-yl]methyl}-3h,6h,7h,8h,8ah-pyrrolo[1,2-a]pyrazin-4-one)