NP-MRD: Showing NP-Card for 9a-hydroxy-3-(hydroxymethyl)-2-methyl-3,10a-bis(methylsulfanyl)-1,4,7-trioxo-5ah,6h,10h-pyrazino[1,2-a]indol-6-yl acetate (NP0236498)

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Record Information

Version

2.0

Created at

2022-09-06 19:24:55 UTC

Updated at

2022-09-06 19:24:55 UTC

NP-MRD ID

NP0236498

Secondary Accession Numbers

None

Natural Product Identification

Common Name

9a-hydroxy-3-(hydroxymethyl)-2-methyl-3,10a-bis(methylsulfanyl)-1,4,7-trioxo-5ah,6h,10h-pyrazino[1,2-a]indol-6-yl acetate

Description

9A-hydroxy-3-(hydroxymethyl)-2-methyl-3,10a-bis(methylsulfanyl)-1,4,7-trioxo-1H,2H,3H,4H,5aH,6H,7H,9aH,10H,10aH-pyrazino[1,2-a]indol-6-yl acetate 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. 9a-hydroxy-3-(hydroxymethyl)-2-methyl-3,10a-bis(methylsulfanyl)-1,4,7-trioxo-5ah,6h,10h-pyrazino[1,2-a]indol-6-yl acetate is found in Aspergillus cejpii. Based on a literature review very few articles have been published on 9a-hydroxy-3-(hydroxymethyl)-2-methyl-3,10a-bis(methylsulfanyl)-1,4,7-trioxo-1H,2H,3H,4H,5aH,6H,7H,9aH,10H,10aH-pyrazino[1,2-a]indol-6-yl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062221242D          

 28 30  0  0  0  0            999 V2000
   -0.0877   -0.1482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6407   -0.5356    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    0.6695   -1.3601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1474   -1.2452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4565   -0.4803    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4765   -1.1885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7314   -0.4039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0285   -1.8016    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8535   -1.8016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4056   -1.1885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1506   -0.4039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7027    0.2092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4477    0.9938    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5096    0.0377    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2125   -1.3601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7646   -0.7470    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4675   -2.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9154   -2.7578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1085   -2.5862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2800   -3.3932    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4410   -3.0712    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7736   -2.5862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6021   -3.3932    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    2.2152   -3.9452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9666   -2.7578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7117   -3.5424    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4146   -2.1447    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3924   -2.3162    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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  3  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  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  2  0  0  0  0
 10 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
  9 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
  8 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 22 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
  3 27  1  0  0  0  0
 27 28  1  0  0  0  0
M  END

     RDKit          3D

 50 52  0  0  0  0  0  0  0  0999 V2000
   -3.3865   -2.9281   -0.4137 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3265   -1.1183   -0.3278 S   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9250   -0.5727    0.6893 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9412   -1.2600    2.0445 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8625   -2.6273    1.9589 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6865   -0.9452    0.0013 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3964   -2.1840   -0.0394 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1767   -0.0098   -0.6035 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5185   -0.1709   -1.1600 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5626   -0.4155   -0.1319 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3816   -1.6065    0.6069 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3016   -1.5414    1.9835 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1131   -2.7387    2.8426 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3949   -0.3927    2.5290 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8704   -0.4444   -0.8702 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6561   -1.4063   -0.8497 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1722    0.7565   -1.6343 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1692    1.4823   -2.0750 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7786    1.1492   -1.8406 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0406    1.2614   -3.0290 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0829    2.0905   -0.8417 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2604    1.3610   -0.7418 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1862    1.5839   -2.2838 S   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6866    3.2862   -2.5420 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0195    1.7510    0.4357 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8114    2.8343    1.0089 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0128    0.8598    0.9203 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1594    1.3460    1.6654 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1365   -3.2100   -1.1887 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3703   -3.2911   -0.6536 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7518   -3.2780    0.5803 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8210   -0.8934    2.6127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0407   -0.8722    2.5929 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5123   -3.0246    2.6190 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4819   -0.9480   -1.9515 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6149    0.4546    0.5525 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2884   -3.3904    2.4868 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0651   -3.3447    2.8384 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9728   -2.4263    3.8834 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2233    1.0418   -1.8343 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3778    2.3804   -2.6464 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3823    0.6031   -3.7060 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6006    2.1546    0.1102 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9677    3.0956   -1.2544 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8108    3.4461   -3.6356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9831    4.0249   -2.1631 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6751    3.5187   -2.0662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5448    2.3086    1.2163 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0130    0.6423    1.6026 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8738    1.6077    2.7029 H   0  0  0  0  0  0  0  0  0  0  0  0
 24 23  1  0
 22 23  1  6
 22 21  1  0
 21 19  1  0
 19 20  1  6
 19 18  1  0
 18 17  2  0
 17 15  1  0
 15 16  2  0
 15 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  2  0
 10  9  1  0
  9  8  1  0
  8  6  1  0
  6  7  2  0
  6  3  1  0
  3  4  1  0
  4  5  1  0
  3  2  1  6
  2  1  1  0
  3 27  1  0
 27 28  1  0
 27 25  1  0
 25 26  2  0
  8 22  1  0
 25 22  1  0
  9 19  1  0
 24 45  1  0
 24 46  1  0
 24 47  1  0
 21 43  1  0
 21 44  1  0
 20 42  1  0
 18 41  1  0
 17 40  1  0
 10 36  1  1
 13 37  1  0
 13 38  1  0
 13 39  1  0
  9 35  1  6
  4 32  1  0
  4 33  1  0
  5 34  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
 28 48  1  0
 28 49  1  0
 28 50  1  0
M  END


  Mrv1652309062221242D          

 28 30  0  0  0  0            999 V2000
   -0.0877   -0.1482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6407   -0.5356    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    0.6695   -1.3601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1474   -1.2452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4565   -0.4803    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4765   -1.1885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7314   -0.4039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0285   -1.8016    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8535   -1.8016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4056   -1.1885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1506   -0.4039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7027    0.2092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4477    0.9938    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5096    0.0377    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2125   -1.3601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7646   -0.7470    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4675   -2.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9154   -2.7578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1085   -2.5862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2800   -3.3932    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4410   -3.0712    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7736   -2.5862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6021   -3.3932    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    2.2152   -3.9452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9666   -2.7578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7117   -3.5424    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4146   -2.1447    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3924   -2.3162    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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  3  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  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  2  0  0  0  0
 10 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
  9 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
  8 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 22 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
  3 27  1  0  0  0  0
 27 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0236498

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CSC12CC3(O)C=CC(=O)C(OC(C)=O)C3N1C(=O)C(CO)(SC)N(C)C2=O

> <INCHI_IDENTIFIER>
InChI=1S/C17H22N2O7S2/c1-9(21)26-11-10(22)5-6-15(25)7-16(27-3)13(23)18(2)17(8-20,28-4)14(24)19(16)12(11)15/h5-6,11-12,20,25H,7-8H2,1-4H3

> <INCHI_KEY>
UDENPRNEBPZXPX-UHFFFAOYSA-N

> <FORMULA>
C17H22N2O7S2

> <MOLECULAR_WEIGHT>
430.49

> <EXACT_MASS>
430.086843404

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
50

> <JCHEM_AVERAGE_POLARIZABILITY>
40.307084474226315

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
9a-hydroxy-3-(hydroxymethyl)-2-methyl-3,10a-bis(methylsulfanyl)-1,4,7-trioxo-1H,2H,3H,4H,5aH,6H,7H,9aH,10H,10aH-pyrazino[1,2-a]indol-6-yl acetate

> <JCHEM_LOGP>
0.3605533720000001

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.193511450490341

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.351844856352667

> <JCHEM_PKA_STRONGEST_BASIC>
-3.1540123427222353

> <JCHEM_POLAR_SURFACE_AREA>
124.45

> <JCHEM_REFRACTIVITY>
102.48859999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
9a-hydroxy-3-(hydroxymethyl)-2-methyl-3,10a-bis(methylsulfanyl)-1,4,7-trioxo-5aH,6H,10H-pyrazino[1,2-a]indol-6-yl acetate

> <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      -0.164  -0.277   0.000  0.00  0.00           C+0
HETATM    2  S   UNK     0       1.196  -1.000   0.000  0.00  0.00           S+0
HETATM    3  C   UNK     0       1.250  -2.539   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.275  -2.324   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -0.852  -0.897   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       2.756  -2.219   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       3.232  -0.754   0.000  0.00  0.00           O+0
HETATM    8  N   UNK     0       3.787  -3.363   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0       5.327  -3.363   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.357  -2.219   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       5.881  -0.754   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       6.912   0.390   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.436   1.855   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       8.418   0.070   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       7.863  -2.539   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       8.894  -1.394   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       8.339  -4.003   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.309  -5.148   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.802  -4.828   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       6.123  -6.334   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       4.557  -5.733   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.311  -4.828   0.000  0.00  0.00           C+0
HETATM   23  S   UNK     0       2.991  -6.334   0.000  0.00  0.00           S+0
HETATM   24  C   UNK     0       4.135  -7.364   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.804  -5.148   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       1.328  -6.612   0.000  0.00  0.00           O+0
HETATM   27  N   UNK     0       0.774  -4.003   0.000  0.00  0.00           N+0
HETATM   28  C   UNK     0      -0.732  -4.324   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    6   27                                             
CONECT    4    3    5                                                       
CONECT    5    4                                                            
CONECT    6    3    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   22                                                  
CONECT    9    8   10   19                                                  
CONECT   10    9   11   15                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15   10   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18    9   20   21                                             
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21    8   23   25                                             
CONECT   23   22   24                                                       
CONECT   24   23                                                            
CONECT   25   22   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25    3   28                                                  
CONECT   28   27                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   60    0
END

View in JSmol

Synonyms

Value	Source
9a-Hydroxy-3-(hydroxymethyl)-2-methyl-3,10a-bis(methylsulfanyl)-1,4,7-trioxo-1H,2H,3H,4H,5ah,6H,7H,9ah,10H,10ah-pyrazino[1,2-a]indol-6-yl acetic acid	Generator
9a-Hydroxy-3-(hydroxymethyl)-2-methyl-3,10a-bis(methylsulphanyl)-1,4,7-trioxo-1H,2H,3H,4H,5ah,6H,7H,9ah,10H,10ah-pyrazino[1,2-a]indol-6-yl acetate	Generator
9a-Hydroxy-3-(hydroxymethyl)-2-methyl-3,10a-bis(methylsulphanyl)-1,4,7-trioxo-1H,2H,3H,4H,5ah,6H,7H,9ah,10H,10ah-pyrazino[1,2-a]indol-6-yl acetic acid	Generator

Chemical Formula

C₁₇H₂₂N₂O₇S₂

Average Mass

430.4900 Da

Monoisotopic Mass

430.08684 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CSC12CC3(O)C=CC(=O)C(OC(C)=O)C3N1C(=O)C(CO)(SC)N(C)C2=O

InChI Identifier

InChI=1S/C17H22N2O7S2/c1-9(21)26-11-10(22)5-6-15(25)7-16(27-3)13(23)18(2)17(8-20,28-4)14(24)19(16)12(11)15/h5-6,11-12,20,25H,7-8H2,1-4H3

InChI Key

UDENPRNEBPZXPX-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 cejpii	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
Thiodioxopiperazine
Indole or derivatives
2,5-dioxopiperazine
Dioxopiperazine
Cyclohexenone
Alpha-acyloxy ketone
N-alkylpiperazine
N-methylpiperazine
Piperazine
1,4-diazinane
Tertiary carboxylic acid amide
Tertiary alcohol
Pyrrolidine
Cyclic ketone
Lactam
Ketone
Carboxylic acid ester
Carboxamide group
Azacycle
Organoheterocyclic compound
Dialkylthioether
Sulfenyl compound
Hemithioaminal
Thioether
Monocarboxylic acid or derivatives
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
Organosulfur compound
Organooxygen compound
Organonitrogen compound
Carbonyl group
Alcohol
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

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

162815367

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 9a-hydroxy-3-(hydroxymethyl)-2-methyl-3,10a-bis(methylsulfanyl)-1,4,7-trioxo-5ah,6h,10h-pyrazino[1,2-a]indol-6-yl acetate (NP0236498)

MOL for NP0236498 (9a-hydroxy-3-(hydroxymethyl)-2-methyl-3,10a-bis(methylsulfanyl)-1,4,7-trioxo-5ah,6h,10h-pyrazino[1,2-a]indol-6-yl acetate)

3D MOL for NP0236498 (9a-hydroxy-3-(hydroxymethyl)-2-methyl-3,10a-bis(methylsulfanyl)-1,4,7-trioxo-5ah,6h,10h-pyrazino[1,2-a]indol-6-yl acetate)

3D SDF for NP0236498 (9a-hydroxy-3-(hydroxymethyl)-2-methyl-3,10a-bis(methylsulfanyl)-1,4,7-trioxo-5ah,6h,10h-pyrazino[1,2-a]indol-6-yl acetate)

3D-SDF for NP0236498 (9a-hydroxy-3-(hydroxymethyl)-2-methyl-3,10a-bis(methylsulfanyl)-1,4,7-trioxo-5ah,6h,10h-pyrazino[1,2-a]indol-6-yl acetate)

PDB for NP0236498 (9a-hydroxy-3-(hydroxymethyl)-2-methyl-3,10a-bis(methylsulfanyl)-1,4,7-trioxo-5ah,6h,10h-pyrazino[1,2-a]indol-6-yl acetate)

3D PDB for NP0236498 (9a-hydroxy-3-(hydroxymethyl)-2-methyl-3,10a-bis(methylsulfanyl)-1,4,7-trioxo-5ah,6h,10h-pyrazino[1,2-a]indol-6-yl acetate)

SMILES for NP0236498 (9a-hydroxy-3-(hydroxymethyl)-2-methyl-3,10a-bis(methylsulfanyl)-1,4,7-trioxo-5ah,6h,10h-pyrazino[1,2-a]indol-6-yl acetate)

INCHI for NP0236498 (9a-hydroxy-3-(hydroxymethyl)-2-methyl-3,10a-bis(methylsulfanyl)-1,4,7-trioxo-5ah,6h,10h-pyrazino[1,2-a]indol-6-yl acetate)

Structure for NP0236498 (9a-hydroxy-3-(hydroxymethyl)-2-methyl-3,10a-bis(methylsulfanyl)-1,4,7-trioxo-5ah,6h,10h-pyrazino[1,2-a]indol-6-yl acetate)

3D Structure for NP0236498 (9a-hydroxy-3-(hydroxymethyl)-2-methyl-3,10a-bis(methylsulfanyl)-1,4,7-trioxo-5ah,6h,10h-pyrazino[1,2-a]indol-6-yl acetate)