NP-MRD: Showing NP-Card for (3s)-3-methyl-6-{[7-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]methyl}-3,6-dihydropyrazine-2,5-diol (NP0293270)

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Record Information

Version

2.0

Created at

2022-09-10 01:11:49 UTC

Updated at

2022-09-10 01:11:49 UTC

NP-MRD ID

NP0293270

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3s)-3-methyl-6-{[7-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]methyl}-3,6-dihydropyrazine-2,5-diol

Description

Terezine D 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. (3s)-3-methyl-6-{[7-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]methyl}-3,6-dihydropyrazine-2,5-diol was first documented in 2007 (PMID: 17917241). Based on a literature review a small amount of articles have been published on Terezine D (PMID: 30822136) (PMID: 28803474) (PMID: 28744271).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 47 49  0  0  0  0  0  0  0  0999 V2000
   -5.9927    0.8363    0.6880 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4457   -0.1287   -0.3021 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3562   -0.5782   -1.4210 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2229   -0.5938   -0.2368 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3193   -0.1622    0.8540 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0884    0.4896    0.3322 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9464    1.8445    0.3853 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8106    2.4438   -0.0940 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2161    1.6819   -0.6420 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1124    0.3090   -0.7140 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9379   -0.6828   -1.1915 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2645   -0.5581   -1.7853 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3916   -0.3411   -0.8201 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3882    0.9095   -0.1424 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.2046    1.0930    0.8334 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2718    2.2678    1.5460 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1467    0.0016    1.2489 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.3422   -0.0345    0.2975 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3863   -1.2426    1.1292 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5474   -1.4302    0.1570 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8921   -2.6332    0.1471 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2548   -1.8613   -0.9800 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9321   -1.5897   -0.3982 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0579   -0.2534   -0.2164 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5020    1.8223    0.6191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8099    0.4173    1.7039 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0877    0.9637    0.5428 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9596   -1.5040   -1.8697 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4686    0.2330   -2.1789 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3627   -0.7464   -0.9747 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8709   -1.3048   -0.9953 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9912   -1.0530    1.4328 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8016    0.5542    1.5445 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7296    2.4768    0.8092 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6701    3.5048   -0.0666 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1064    2.1599   -1.0244 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3281    0.2921   -2.5288 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5416   -1.4620   -2.4000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3310   -0.3544   -1.4516 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0711    2.8703    1.5254 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5203    0.1299    2.2665 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2674    0.8045   -0.4428 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4070   -1.0124   -0.2194 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2961    0.1045    0.8346 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3429   -3.5325    0.0372 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5372   -2.8808   -1.2092 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6799   -2.2700   -0.1097 H   0  0  0  0  0  0  0  0  0  0  0  0
 18 17  1  0
 17 19  1  0
 19 20  2  0
 20 21  1  0
 20 13  1  0
 13 12  1  0
 12 11  1  0
 11 22  2  0
 22 23  1  0
 23 24  1  0
 24  6  2  0
  6  5  1  0
  5  4  1  0
  4  2  2  3
  2  1  1  0
  2  3  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 15 17  1  0
 10 11  1  0
 10 24  1  0
 18 42  1  0
 18 43  1  0
 18 44  1  0
 17 41  1  1
 21 45  1  0
 13 39  1  6
 12 37  1  0
 12 38  1  0
 22 46  1  0
 23 47  1  0
  5 32  1  0
  5 33  1  0
  4 31  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  3 28  1  0
  3 29  1  0
  3 30  1  0
  7 34  1  0
  8 35  1  0
  9 36  1  0
 16 40  1  0
M  END


  Mrv1652309102203112D          

 24 26  0  0  1  0            999 V2000
    5.4223    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7798   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5249   -1.0396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7179   -1.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4630   -1.9957    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3440   -2.1672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5989   -2.9519    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8960   -1.5541    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7030   -1.7257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6411   -0.7695    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.1659   -0.5980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4208    0.1866    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2949    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7798    1.0799    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.8250    0.0000 C   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
  2  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 13 20  1  0  0  0  0
 20 21  1  0  0  0  0
 11 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
  6 24  2  0  0  0  0
 10 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0293270

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1N=C(O)C(CC2=CNC3=C(CC=C(C)C)C=CC=C23)N=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C19H23N3O2/c1-11(2)7-8-13-5-4-6-15-14(10-20-17(13)15)9-16-19(24)21-12(3)18(23)22-16/h4-7,10,12,16,20H,8-9H2,1-3H3,(H,21,24)(H,22,23)/t12-,16?/m0/s1

> <INCHI_KEY>
IHJVJWQYVQWURS-HKALDPMFSA-N

> <FORMULA>
C19H23N3O2

> <MOLECULAR_WEIGHT>
325.412

> <EXACT_MASS>
325.179026993

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
36.24100754655676

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3S)-3-methyl-6-{[7-(3-methylbut-2-en-1-yl)-1H-indol-3-yl]methyl}-3,6-dihydropyrazine-2,5-diol

> <JCHEM_LOGP>
0.7591463667346916

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
0.6581151056591907

> <JCHEM_PKA_STRONGEST_ACIDIC>
-8.491586371717933

> <JCHEM_PKA_STRONGEST_BASIC>
14.95159626668354

> <JCHEM_POLAR_SURFACE_AREA>
80.97

> <JCHEM_REFRACTIVITY>
95.58650000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(3S)-3-methyl-6-{[7-(3-methylbut-2-en-1-yl)-1H-indol-3-yl]methyl}-3,6-dihydropyrazine-2,5-diol

> <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  C   UNK     0      10.122   4.620   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.788   3.850   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.788   2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.454   4.620   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.121   3.850   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.121   2.310   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.454   1.540   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.454   0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.121  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.787   0.000   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.322  -0.476   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.846  -1.941   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.340  -2.261   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0       0.864  -3.725   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0      -0.642  -4.046   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -1.118  -5.510   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -1.673  -2.901   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -3.179  -3.221   0.000  0.00  0.00           C+0
HETATM   19  N   UNK     0      -1.197  -1.436   0.000  0.00  0.00           N+0
HETATM   20  C   UNK     0       0.310  -1.116   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       0.786   0.348   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       2.417   0.770   0.000  0.00  0.00           C+0
HETATM   23  N   UNK     0       3.322   2.016   0.000  0.00  0.00           N+0
HETATM   24  C   UNK     0       4.787   1.540   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   24                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   24                                                  
CONECT   11   10   12   22                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   20                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   13   21                                                  
CONECT   21   20                                                            
CONECT   22   11   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23    6   10                                                  
MASTER        0    0    0    0    0    0    0    0   24    0   52    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₂₃N₃O₂

Average Mass

325.4120 Da

Monoisotopic Mass

325.17903 Da

IUPAC Name

(3S)-3-methyl-6-{[7-(3-methylbut-2-en-1-yl)-1H-indol-3-yl]methyl}-3,6-dihydropyrazine-2,5-diol

Traditional Name

(3S)-3-methyl-6-{[7-(3-methylbut-2-en-1-yl)-1H-indol-3-yl]methyl}-3,6-dihydropyrazine-2,5-diol

CAS Registry Number

Not Available

SMILES

C[C@@H]1N=C(O)C(CC2=CNC3=C(CC=C(C)C)C=CC=C23)N=C1O

InChI Identifier

InChI=1S/C19H23N3O2/c1-11(2)7-8-13-5-4-6-15-14(10-20-17(13)15)9-16-19(24)21-12(3)18(23)22-16/h4-7,10,12,16,20H,8-9H2,1-3H3,(H,21,24)(H,22,23)/t12-,16?/m0/s1

InChI Key

IHJVJWQYVQWURS-HKALDPMFSA-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

Not Available

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
Dioxopiperazine
2,5-dioxopiperazine
1,4-diazinane
Piperazine
Benzenoid
Substituted pyrrole
Heteroaromatic compound
Pyrrole
Carboxamide group
Lactam
Secondary carboxylic acid amide
Azacycle
Organoheterocyclic compound
Organooxygen compound
Organonitrogen compound
Hydrocarbon derivative
Organic oxide
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	0.76	ChemAxon
pKa (Strongest Acidic)	-8.5	ChemAxon
pKa (Strongest Basic)	14.95	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	80.97 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	95.59 m³·mol⁻¹	ChemAxon
Polarizability	36.24 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

C00029085

Chemspider ID

78436915

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139584661

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Isaka M, Palasarn S, Kocharin K, Hywel-Jones NL: Comparison of the bioactive secondary metabolites from the scale insect pathogens, Anamorph Paecilomyces cinnamomeus, and Teleomorph Torrubiella luteorostrata. J Antibiot (Tokyo). 2007 Sep;60(9):577-81. doi: 10.1038/ja.2007.73. [PubMed:17917241 ]
Zhang PL, Wang G, Xu FQ, Liu JS, Wang JT, Zhang R, Liu HT, Hu JM, Wang GK, Wu PY: Aspergilolide, a steroid lactone produced by an endophytic fungus Aspergillus sp. MBL1612 isolated from Paeonia ostii. Nat Prod Res. 2019 Aug;33(15):2133-2138. doi: 10.1080/14786419.2018.1488706. Epub 2018 Dec 22. [PubMed:30822136 ]
Tanaka S, Shiomi S, Ishikawa H: Bioinspired Indole Prenylation Reactions in Water. J Nat Prod. 2017 Aug 25;80(8):2371-2378. doi: 10.1021/acs.jnatprod.7b00464. Epub 2017 Aug 13. [PubMed:28803474 ]
Wakefield J, Hassan HM, Jaspars M, Ebel R, Rateb ME: Dual Induction of New Microbial Secondary Metabolites by Fungal Bacterial Co-cultivation. Front Microbiol. 2017 Jul 11;8:1284. doi: 10.3389/fmicb.2017.01284. eCollection 2017. [PubMed:28744271 ]
LOTUS database [Link]

Showing NP-Card for (3s)-3-methyl-6-{[7-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]methyl}-3,6-dihydropyrazine-2,5-diol (NP0293270)

MOL for NP0293270 ((3s)-3-methyl-6-{[7-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]methyl}-3,6-dihydropyrazine-2,5-diol)

3D MOL for NP0293270 ((3s)-3-methyl-6-{[7-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]methyl}-3,6-dihydropyrazine-2,5-diol)

3D SDF for NP0293270 ((3s)-3-methyl-6-{[7-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]methyl}-3,6-dihydropyrazine-2,5-diol)

3D-SDF for NP0293270 ((3s)-3-methyl-6-{[7-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]methyl}-3,6-dihydropyrazine-2,5-diol)

PDB for NP0293270 ((3s)-3-methyl-6-{[7-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]methyl}-3,6-dihydropyrazine-2,5-diol)

3D PDB for NP0293270 ((3s)-3-methyl-6-{[7-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]methyl}-3,6-dihydropyrazine-2,5-diol)

SMILES for NP0293270 ((3s)-3-methyl-6-{[7-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]methyl}-3,6-dihydropyrazine-2,5-diol)

INCHI for NP0293270 ((3s)-3-methyl-6-{[7-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]methyl}-3,6-dihydropyrazine-2,5-diol)

Structure for NP0293270 ((3s)-3-methyl-6-{[7-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]methyl}-3,6-dihydropyrazine-2,5-diol)

3D Structure for NP0293270 ((3s)-3-methyl-6-{[7-(3-methylbut-2-en-1-yl)-1h-indol-3-yl]methyl}-3,6-dihydropyrazine-2,5-diol)