MiMeDB: Showing metabocard for Tryptoquialanine B (MMDBc0002725)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-14 21:00:06 UTC

Update Date

2025-10-07 16:04:37 UTC

Metabolite ID

MMDBc0002725

Metabolite Identification

Common Name

Tryptoquialanine B

Description

Tryptoquialanine B is a tryptoquivaline-like metabolite that belongs to the class of secondary metabolites produced by fungi. This compound has been isolated from fungal cultures cultivated on solid medium, highlighting its potential as a novel natural product with unique chemical properties. The biosynthesis of tryptoquialanine B has also been observed on citrus fruits, suggesting a possible ecological role or interaction between the fungi and the fruit hosts (PMID:12381117 ). The structural characteristics and specific biological activities of tryptoquialanine B remain subjects of ongoing research, as understanding these properties could reveal its potential applications in pharmaceuticals or agriculture. The exploration of such metabolites is crucial, as they may exhibit bioactive properties that contribute to the development of new therapeutic agents or natural pesticides. Overall, tryptoquialanine B represents an intriguing area of study within the realm of natural product chemistry and its implications in biological systems.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305142123002D          

 41 46  0  0  1  0            999 V2000
    0.9505    2.4851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8752    0.5124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7580   -0.5983    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1618   -3.8437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4962    1.7974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3432   -3.7413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2568    2.5869    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6598   -3.1859    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9322    1.1953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0225   -2.9811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4534    2.7743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7750    0.4394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7299    2.2148    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3772   -0.1453    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0606   -0.7007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3391   -2.4258    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1288    1.3827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5205   -2.3234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8894    2.1722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0145   -0.3501    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6979   -0.9055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4068    2.6864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8371   -1.7680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8393   -0.3664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7942    1.4090    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4519    0.9110    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1999   -1.5632    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.5165   -1.0079    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.0645    2.1885    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9693    1.4253    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.3812   -1.4608    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4230    3.5113    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6557   -1.8704    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3110   -1.0433    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4713    0.7675    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5586   -0.0430    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1097    0.4130    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6169    3.0320    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1958   -0.2477    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3744   -1.0925    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5837    1.6484    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  4  2  0  0  0  0
  7  5  2  0  0  0  0
  8  4  1  0  0  0  0
  9  5  1  0  0  0  0
 10  6  1  0  0  0  0
 11  7  1  0  0  0  0
 13  1  1  1  0  0  0
 14  2  1  1  0  0  0
 15  3  1  0  0  0  0
 16  8  2  0  0  0  0
 17  9  2  0  0  0  0
 18 10  2  0  0  0  0
 18 16  1  0  0  0  0
 19 11  2  0  0  0  0
 19 17  1  0  0  0  0
 20 12  1  0  0  0  0
 21 14  1  0  0  0  0
 22 13  1  0  0  0  0
 23 16  1  0  0  0  0
 24 20  1  0  0  0  0
 26 12  1  0  0  0  0
 26 17  1  0  0  0  0
 26 25  1  0  0  0  0
 27 18  1  0  0  0  0
 27 21  2  0  0  0  0
 20 28  1  6  0  0  0
 28 21  1  0  0  0  0
 28 23  1  0  0  0  0
 29 19  1  0  0  0  0
 29 22  1  0  0  0  0
 29 25  1  0  0  0  0
 30 13  1  0  0  0  0
 30 25  1  0  0  0  0
 31 15  2  0  0  0  0
 32 22  2  0  0  0  0
 33 23  2  0  0  0  0
 34 24  2  0  0  0  0
 35 30  1  0  0  0  0
 36 14  1  0  0  0  0
 36 15  1  0  0  0  0
 37 24  1  0  0  0  0
 26 37  1  6  0  0  0
 13 38  1  6  0  0  0
 14 39  1  6  0  0  0
 20 40  1  1  0  0  0
 25 41  1  1  0  0  0
M  END


  Mrv1652305142123002D          

 41 46  0  0  1  0            999 V2000
    0.9505    2.4851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8752    0.5124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7580   -0.5983    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1618   -3.8437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4962    1.7974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3432   -3.7413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2568    2.5869    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6598   -3.1859    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9322    1.1953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0225   -2.9811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4534    2.7743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7750    0.4394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7299    2.2148    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3772   -0.1453    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0606   -0.7007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3391   -2.4258    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1288    1.3827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5205   -2.3234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8894    2.1722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0145   -0.3501    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6979   -0.9055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4068    2.6864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8371   -1.7680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8393   -0.3664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7942    1.4090    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4519    0.9110    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1999   -1.5632    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.5165   -1.0079    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.0645    2.1885    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9693    1.4253    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.3812   -1.4608    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4230    3.5113    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6557   -1.8704    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3110   -1.0433    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4713    0.7675    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5586   -0.0430    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1097    0.4130    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6169    3.0320    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1958   -0.2477    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3744   -1.0925    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5837    1.6484    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  4  2  0  0  0  0
  7  5  2  0  0  0  0
  8  4  1  0  0  0  0
  9  5  1  0  0  0  0
 10  6  1  0  0  0  0
 11  7  1  0  0  0  0
 13  1  1  1  0  0  0
 14  2  1  1  0  0  0
 15  3  1  0  0  0  0
 16  8  2  0  0  0  0
 17  9  2  0  0  0  0
 18 10  2  0  0  0  0
 18 16  1  0  0  0  0
 19 11  2  0  0  0  0
 19 17  1  0  0  0  0
 20 12  1  0  0  0  0
 21 14  1  0  0  0  0
 22 13  1  0  0  0  0
 23 16  1  0  0  0  0
 24 20  1  0  0  0  0
 26 12  1  0  0  0  0
 26 17  1  0  0  0  0
 26 25  1  0  0  0  0
 27 18  1  0  0  0  0
 27 21  2  0  0  0  0
 20 28  1  6  0  0  0
 28 21  1  0  0  0  0
 28 23  1  0  0  0  0
 29 19  1  0  0  0  0
 29 22  1  0  0  0  0
 29 25  1  0  0  0  0
 30 13  1  0  0  0  0
 30 25  1  0  0  0  0
 31 15  2  0  0  0  0
 32 22  2  0  0  0  0
 33 23  2  0  0  0  0
 34 24  2  0  0  0  0
 35 30  1  0  0  0  0
 36 14  1  0  0  0  0
 36 15  1  0  0  0  0
 37 24  1  0  0  0  0
 26 37  1  6  0  0  0
 13 38  1  6  0  0  0
 14 39  1  6  0  0  0
 20 40  1  1  0  0  0
 25 41  1  1  0  0  0
M  END
> <DATABASE_ID>
MMDBc0002725

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@@](C)(OC(C)=O)C1=NC2=CC=CC=C2C(=O)N1[C@]1([H])C[C@]2(OC1=O)C1=CC=CC=C1N1C(=O)[C@]([H])(C)N(O)[C@@]21[H]

> <INCHI_IDENTIFIER>
InChI=1S/C26H24N4O7/c1-13-22(32)29-19-11-7-5-9-17(19)26(25(29)30(13)35)12-20(24(34)37-26)28-21(14(2)36-15(3)31)27-18-10-6-4-8-16(18)23(28)33/h4-11,13-14,20,25,35H,12H2,1-3H3/t13-,14-,20+,25-,26-/m0/s1

> <INCHI_KEY>
UNRJSEBGHKFHQK-NHYRABQJSA-N

> <FORMULA>
C26H24N4O7

> <MOLECULAR_WEIGHT>
504.499

> <EXACT_MASS>
504.164499129

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
61

> <JCHEM_AVERAGE_POLARIZABILITY>
51.080132717403245

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S)-1-{3-[(2S,4'R,9S,9aS)-1-hydroxy-2-methyl-3,5'-dioxo-1,2,3,9a-tetrahydrospiro[imidazo[1,2-a]indole-9,2'-oxolane]-4'-yl]-4-oxo-3,4-dihydroquinazolin-2-yl}ethyl acetate

> <ALOGPS_LOGP>
1.53

> <JCHEM_LOGP>
1.4020071773333336

> <ALOGPS_LOGS>
-3.81

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
17.60568359767652

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.922229993953412

> <JCHEM_PKA_STRONGEST_BASIC>
1.585950538012321

> <JCHEM_POLAR_SURFACE_AREA>
129.04999999999998

> <JCHEM_REFRACTIVITY>
128.47330000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
7.84e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S)-1-{3-[(2S,4'R,9S,9aS)-1-hydroxy-2-methyl-3,5'-dioxo-2,9a-dihydrospiro[imidazo[1,2-a]indole-9,2'-oxolane]-4'-yl]-4-oxoquinazolin-2-yl}ethyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 14-MAY-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   14-MAY-21         0                                  
HETATM    1  C   UNK     0       1.774   4.639   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.500   0.956   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.415  -1.117   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.035  -7.175   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.260   3.355   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.507  -6.984   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.813   4.829   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.965  -5.947   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.207   2.231   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.909  -5.565   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.313   5.179   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.180   0.820   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.229   4.134   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.571  -0.271   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.113  -1.308   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.366  -4.528   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.707   2.581   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.838  -4.337   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.260   4.055   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.627  -0.654   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.169  -1.690   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.493   5.015   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.296  -3.300   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       7.167  -0.684   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.216   2.630   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.444   1.701   0.000  0.00  0.00           C+0
HETATM   27  N   UNK     0       2.240  -2.918   0.000  0.00  0.00           N+0
HETATM   28  N   UNK     0       4.697  -1.881   0.000  0.00  0.00           N+0
HETATM   29  N   UNK     0       5.720   4.085   0.000  0.00  0.00           N+0
HETATM   30  N   UNK     0       3.676   2.661   0.000  0.00  0.00           N+0
HETATM   31  O   UNK     0       0.712  -2.727   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       4.523   6.554   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0       6.824  -3.491   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0       8.047  -1.947   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0       2.746   1.433   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0       1.043  -0.080   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0       7.671   0.771   0.000  0.00  0.00           O+0
HETATM   38  H   UNK     0       3.018   5.660   0.000  0.00  0.00           H+0
HETATM   39  H   UNK     0       4.099  -0.462   0.000  0.00  0.00           H+0
HETATM   40  H   UNK     0       6.299  -2.039   0.000  0.00  0.00           H+0
HETATM   41  H   UNK     0       6.689   3.077   0.000  0.00  0.00           H+0
CONECT    1   13                                                            
CONECT    2   14                                                            
CONECT    3   15                                                            
CONECT    4    6    8                                                       
CONECT    5    7    9                                                       
CONECT    6    4   10                                                       
CONECT    7    5   11                                                       
CONECT    8    4   16                                                       
CONECT    9    5   17                                                       
CONECT   10    6   18                                                       
CONECT   11    7   19                                                       
CONECT   12   20   26                                                       
CONECT   13    1   22   30   38                                             
CONECT   14    2   21   36   39                                             
CONECT   15    3   31   36                                                  
CONECT   16    8   18   23                                                  
CONECT   17    9   19   26                                                  
CONECT   18   10   16   27                                                  
CONECT   19   11   17   29                                                  
CONECT   20   12   24   28   40                                             
CONECT   21   14   27   28                                                  
CONECT   22   13   29   32                                                  
CONECT   23   16   28   33                                                  
CONECT   24   20   34   37                                                  
CONECT   25   26   29   30   41                                             
CONECT   26   12   17   25   37                                             
CONECT   27   18   21                                                       
CONECT   28   20   21   23                                                  
CONECT   29   19   22   25                                                  
CONECT   30   13   25   35                                                  
CONECT   31   15                                                            
CONECT   32   22                                                            
CONECT   33   23                                                            
CONECT   34   24                                                            
CONECT   35   30                                                            
CONECT   36   14   15                                                       
CONECT   37   24   26                                                       
CONECT   38   13                                                            
CONECT   39   14                                                            
CONECT   40   20                                                            
CONECT   41   25                                                            
MASTER        0    0    0    0    0    0    0    0   41    0   92    0
END

Synonyms

Not Available

Molecular Formula

C₂₆H₂₄N₄O₇

Average Mass

504.499

Monoisotopic Mass

504.164499129

IUPAC Name

(1S)-1-{3-[(2S,4'R,9S,9aS)-1-hydroxy-2-methyl-3,5'-dioxo-1,2,3,9a-tetrahydrospiro[imidazo[1,2-a]indole-9,2'-oxolane]-4'-yl]-4-oxo-3,4-dihydroquinazolin-2-yl}ethyl acetate

Traditional Name

(1S)-1-{3-[(2S,4'R,9S,9aS)-1-hydroxy-2-methyl-3,5'-dioxo-2,9a-dihydrospiro[imidazo[1,2-a]indole-9,2'-oxolane]-4'-yl]-4-oxoquinazolin-2-yl}ethyl acetate

CAS Registry Number

Not Available

SMILES

[H][C@@](C)(OC(C)=O)C1=NC2=CC=CC=C2C(=O)N1[C@]1([H])C[C@]2(OC1=O)C1=CC=CC=C1N1C(=O)[C@]([H])(C)N(O)[C@@]21[H]

InChI Identifier

InChI=1S/C26H24N4O7/c1-13-22(32)29-19-11-7-5-9-17(19)26(25(29)30(13)35)12-20(24(34)37-26)28-21(14(2)36-15(3)31)27-18-10-6-4-8-16(18)23(28)33/h4-11,13-14,20,25,35H,12H2,1-3H3/t13-,14-,20+,25-,26-/m0/s1

InChI Key

UNRJSEBGHKFHQK-NHYRABQJSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as alpha amino acid esters. These are ester derivatives of alpha amino acids.

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 acid esters

Alternative Parents

Substituents

Alpha-amino acid ester
Diazanaphthalene
Quinazoline
Indole or derivatives
Pyrimidone
Dicarboxylic acid or derivatives
Gamma butyrolactone
Imidazolidinone
Pyrimidine
Benzenoid
Imidazolidine
Heteroaromatic compound
Tertiary carboxylic acid amide
Tetrahydrofuran
Carboxamide group
Lactone
Lactam
Carboxylic acid ester
Azacycle
Oxacycle
Organoheterocyclic compound
N-organohydroxylamine
Organooxygen compound
Organic oxide
Organic nitrogen compound
Organopnictogen compound
Organic oxygen compound
Hydrocarbon derivative
Carbonyl group
Organonitrogen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.078 g/L	ALOGPS
logP	1.53	ALOGPS
logP	1.4	ChemAxon
logS	-3.8	ALOGPS
pKa (Strongest Acidic)	14.92	ChemAxon
pKa (Strongest Basic)	1.59	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	129.05 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	128.47 m³·mol⁻¹	ChemAxon
Polarizability	51.08 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Spectrum Type	Description	Splash Key	Deposition Date	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	Not Available	2022-08-09	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-18	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Protein ID	Protein Name	Protein Type	Uniprot ID	Species

Human Pathways

Pathways

Name	SMPDB/PathBank

Microbial Pathways

Pathways

This table shows at most 5 pathways. For the full list of associated pathways:

See All Associated Bacterial Pathways

Name	SMPDB/PathBank

Metabolic Reactions

Reactions

This table shows at most 20 reactions. For the full list of associated reactions:

See All Associated Reactions

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Evidence Type	Host and Biospecimen	Data Source	Reference

Microbial Sources

Superkingdom/Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
Eukaryota/Fungi	Ascomycota	2	Human feces	Metabolic reconstruction

Exposure Sources

Other Exposures

Source Type	Data Source	Reference

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Units	Age	Sex	Health Condition	Data Source	Reference

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

C00052365

Chemspider ID

9224571

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11049404

PDB ID

Not Available

ChEBI ID

Not Available

CMMC Knowledgebase

Not Available

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

General References

van Santen JA, Poynton EF, Iskakova D, McMann E, Alsup TA, Clark TN, Fergusson CH, Fewer DP, Hughes AH, McCadden CA, Parra J, Soldatou S, Rudolf JD, Janssen EM, Duncan KR, Linington RG: The Natural Products Atlas 2.0: a database of microbially-derived natural products. Nucleic Acids Res. 2022 Jan 7;50(D1):D1317-D1323. doi: 10.1093/nar/gkab941. [PubMed:34718710 ]

Showing metabocard for Tryptoquialanine B (MMDBc0002725)

MOL for #<Metabolite:0x00007fd449000af8>

3D MOL for #<Metabolite:0x00007fd449000af8>

3D SDF for #<Metabolite:0x00007fd449000af8>

3D-SDF for #<Metabolite:0x00007fd449000af8>

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3D PDB for #<Metabolite:0x00007fd449000af8>

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INCHI for #<Metabolite:0x00007fd449000af8>

Structure for #<Metabolite:0x00007fd449000af8>

3D Structure for #<Metabolite:0x00007fd449000af8>