MiMeDB: Showing metabocard for Armochaetoglobin O (MMDBc0006698)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2021-05-15 00:09:04 UTC

Update Date

2025-10-07 16:05:13 UTC

Metabolite ID

MMDBc0006698

Metabolite Identification

Common Name

Armochaetoglobin O

Description

Armochaetoglobin O is a member of the chemical class of metabolites. There is limited literature available on this metabolite, indicating that further research may be necessary to fully understand its properties and biological significance.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152102092D          

 44 49  0  0  1  0            999 V2000
    1.5979   -3.0034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7812   -2.2024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6394    1.7789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3603    0.2946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5987    2.4549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9591    3.1970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1499   -1.6960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3126   -2.3792    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7758    2.3960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2105   -0.9539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4966    3.8802    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2455    0.7644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5034    1.1248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4959   -1.5781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0760    2.5982    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3515    4.0049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1354   -2.3202    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3188   -1.5192    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1770    1.0957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5374    0.3536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4961    3.1926    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3133    3.0792    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2520   -0.2707    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6737    3.8213    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2167   -0.0939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1528    1.8056    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9695    0.4201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3541    1.1546    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6792   -0.7771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0749   -0.3296    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9011    0.7002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1084    0.4714    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0793    4.3934    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.3938   -0.1528    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.9285    1.5247    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5021   -0.7182    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4353   -1.0717    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5520    0.1933    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7750   -3.0623    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9583   -2.2613    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6124   -1.0128    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6573    1.9616    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    0.4125    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8978   -0.3885    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  2  0  0  0  0
  7  8  1  4  0  0  0
  9  5  1  0  0  0  0
 10  7  2  0  0  0  0
 11  6  1  0  0  0  0
 13 12  1  0  0  0  0
 17  1  1  1  0  0  0
 17  8  1  0  0  0  0
 17 14  1  0  0  0  0
 18  2  1  1  0  0  0
 18 14  1  0  0  0  0
 19  3  1  0  0  0  0
 20  4  1  0  0  0  0
 20 19  2  0  0  0  0
 21 15  1  0  0  0  0
 21 16  2  0  0  0  0
 22  9  2  0  0  0  0
 22 21  1  0  0  0  0
 23 10  1  0  0  0  0
 24 11  2  0  0  0  0
 24 22  1  0  0  0  0
 25 12  2  0  0  0  0
 26 15  1  6  0  0  0
 27 13  2  0  0  0  0
 28 19  1  0  0  0  0
 28 26  1  0  0  0  0
 29 18  1  0  0  0  0
 29 25  1  0  0  0  0
 30 20  1  0  0  0  0
 30 23  1  0  0  0  0
 32 23  1  0  0  0  0
 32 27  1  6  0  0  0
 32 28  1  0  0  0  0
 32 31  1  0  0  0  0
 33 16  1  0  0  0  0
 33 24  1  0  0  0  0
 34 25  1  0  0  0  0
 34 27  1  0  0  0  0
 35 26  1  0  0  0  0
 35 31  2  0  0  0  0
 36 29  2  0  0  0  0
 30 37  1  6  0  0  0
 38 31  1  0  0  0  0
 17 39  1  6  0  0  0
 18 40  1  6  0  0  0
 23 41  1  6  0  0  0
 26 42  1  1  0  0  0
 28 43  1  6  0  0  0
 30 44  1  1  0  0  0
M  END


  Mrv1652305152102092D          

 44 49  0  0  1  0            999 V2000
    1.5979   -3.0034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7812   -2.2024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6394    1.7789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3603    0.2946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5987    2.4549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9591    3.1970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1499   -1.6960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3126   -2.3792    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7758    2.3960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2105   -0.9539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4966    3.8802    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2455    0.7644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5034    1.1248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4959   -1.5781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0760    2.5982    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3515    4.0049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1354   -2.3202    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3188   -1.5192    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1770    1.0957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5374    0.3536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4961    3.1926    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3133    3.0792    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2520   -0.2707    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6737    3.8213    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2167   -0.0939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1528    1.8056    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9695    0.4201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3541    1.1546    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6792   -0.7771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0749   -0.3296    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9011    0.7002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1084    0.4714    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0793    4.3934    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.3938   -0.1528    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.9285    1.5247    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5021   -0.7182    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4353   -1.0717    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5520    0.1933    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7750   -3.0623    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9583   -2.2613    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6124   -1.0128    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6573    1.9616    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    0.4125    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8978   -0.3885    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  2  0  0  0  0
  7  8  1  4  0  0  0
  9  5  1  0  0  0  0
 10  7  2  0  0  0  0
 11  6  1  0  0  0  0
 13 12  1  0  0  0  0
 17  1  1  1  0  0  0
 17  8  1  0  0  0  0
 17 14  1  0  0  0  0
 18  2  1  1  0  0  0
 18 14  1  0  0  0  0
 19  3  1  0  0  0  0
 20  4  1  0  0  0  0
 20 19  2  0  0  0  0
 21 15  1  0  0  0  0
 21 16  2  0  0  0  0
 22  9  2  0  0  0  0
 22 21  1  0  0  0  0
 23 10  1  0  0  0  0
 24 11  2  0  0  0  0
 24 22  1  0  0  0  0
 25 12  2  0  0  0  0
 26 15  1  6  0  0  0
 27 13  2  0  0  0  0
 28 19  1  0  0  0  0
 28 26  1  0  0  0  0
 29 18  1  0  0  0  0
 29 25  1  0  0  0  0
 30 20  1  0  0  0  0
 30 23  1  0  0  0  0
 32 23  1  0  0  0  0
 32 27  1  6  0  0  0
 32 28  1  0  0  0  0
 32 31  1  0  0  0  0
 33 16  1  0  0  0  0
 33 24  1  0  0  0  0
 34 25  1  0  0  0  0
 34 27  1  0  0  0  0
 35 26  1  0  0  0  0
 35 31  2  0  0  0  0
 36 29  2  0  0  0  0
 30 37  1  6  0  0  0
 38 31  1  0  0  0  0
 17 39  1  6  0  0  0
 18 40  1  6  0  0  0
 23 41  1  6  0  0  0
 26 42  1  1  0  0  0
 28 43  1  6  0  0  0
 30 44  1  1  0  0  0
M  END
> <DATABASE_ID>
MMDBc0006698

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@@]1(CC2=CNC3=CC=CC=C23)N=C(O)[C@@]23C4=CC=C(N4)C(=O)[C@@]([H])(C)C[C@@]([H])(C)CC=C[C@@]2([H])[C@]([H])(O)C(C)=C(C)[C@@]13[H]

> <INCHI_IDENTIFIER>
InChI=1S/C32H37N3O3/c1-17-8-7-10-23-30(37)20(4)19(3)28-26(15-21-16-33-24-11-6-5-9-22(21)24)35-31(38)32(23,28)27-13-12-25(34-27)29(36)18(2)14-17/h5-7,9-13,16-18,23,26,28,30,33-34,37H,8,14-15H2,1-4H3,(H,35,38)/t17-,18-,23-,26-,28-,30+,32+/m0/s1

> <INCHI_KEY>
KJMPCWQWZNLNTM-MMGNQZIRSA-N

> <FORMULA>
C32H37N3O3

> <MOLECULAR_WEIGHT>
511.666

> <EXACT_MASS>
511.283492063

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
75

> <JCHEM_AVERAGE_POLARIZABILITY>
57.72061174367674

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,5S,6R,9S,10R,14S,16S)-3,9-dihydroxy-5-[(1H-indol-3-yl)methyl]-7,8,14,16-tetramethyl-4,21-diazatetracyclo[16.2.1.0^{2,6}.0^{2,10}]henicosa-1(20),3,7,11,18-pentaen-17-one

> <ALOGPS_LOGP>
5.42

> <JCHEM_LOGP>
4.345484554690948

> <ALOGPS_LOGS>
-5.46

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.353821212256985

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.1029525077726983

> <JCHEM_PKA_STRONGEST_BASIC>
5.500733317451698

> <JCHEM_POLAR_SURFACE_AREA>
101.47

> <JCHEM_REFRACTIVITY>
151.3975

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.77e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R,5S,6R,9S,10R,14S,16S)-3,9-dihydroxy-5-(1H-indol-3-ylmethyl)-7,8,14,16-tetramethyl-4,21-diazatetracyclo[16.2.1.0^{2,6}.0^{2,10}]henicosa-1(20),3,7,11,18-pentaen-17-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 15-MAY-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   15-MAY-21         0                                  
HETATM    1  C   UNK     0       2.983  -5.606   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.192  -4.111   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.060   3.321   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.406   0.550   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.851   4.583   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.524   5.968   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.280  -3.166   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.583  -4.441   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.315   4.473   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.393  -1.781   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.660   7.243   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.192   1.427   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.806   2.100   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.792  -2.946   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.142   4.850   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.656   7.476   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.119  -4.331   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.328  -2.836   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -2.197   2.045   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -2.870   0.660   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.926   5.960   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.452   5.748   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -0.470  -0.505   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.124   7.133   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.138  -0.175   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.285   3.370   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       1.810   0.784   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -0.661   2.155   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       5.001  -1.451   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -2.006  -0.615   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       1.682   1.307   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       0.202   0.880   0.000  0.00  0.00           C+0
HETATM   33  N   UNK     0       2.015   8.201   0.000  0.00  0.00           N+0
HETATM   34  N   UNK     0       2.602  -0.285   0.000  0.00  0.00           N+0
HETATM   35  N   UNK     0       1.733   2.846   0.000  0.00  0.00           N+0
HETATM   36  O   UNK     0       6.537  -1.341   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0      -2.679  -2.001   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0       2.897   0.361   0.000  0.00  0.00           O+0
HETATM   39  H   UNK     0       1.447  -5.716   0.000  0.00  0.00           H+0
HETATM   40  H   UNK     0       3.656  -4.221   0.000  0.00  0.00           H+0
HETATM   41  H   UNK     0      -1.143  -1.891   0.000  0.00  0.00           H+0
HETATM   42  H   UNK     0      -1.227   3.662   0.000  0.00  0.00           H+0
HETATM   43  H   UNK     0      -1.334   0.770   0.000  0.00  0.00           H+0
HETATM   44  H   UNK     0      -3.543  -0.725   0.000  0.00  0.00           H+0
CONECT    1   17                                                            
CONECT    2   18                                                            
CONECT    3   19                                                            
CONECT    4   20                                                            
CONECT    5    6    9                                                       
CONECT    6    5   11                                                       
CONECT    7    8   10                                                       
CONECT    8    7   17                                                       
CONECT    9    5   22                                                       
CONECT   10    7   23                                                       
CONECT   11    6   24                                                       
CONECT   12   13   25                                                       
CONECT   13   12   27                                                       
CONECT   14   17   18                                                       
CONECT   15   21   26                                                       
CONECT   16   21   33                                                       
CONECT   17    1    8   14   39                                             
CONECT   18    2   14   29   40                                             
CONECT   19    3   20   28                                                  
CONECT   20    4   19   30                                                  
CONECT   21   15   16   22                                                  
CONECT   22    9   21   24                                                  
CONECT   23   10   30   32   41                                             
CONECT   24   11   22   33                                                  
CONECT   25   12   29   34                                                  
CONECT   26   15   28   35   42                                             
CONECT   27   13   32   34                                                  
CONECT   28   19   26   32   43                                             
CONECT   29   18   25   36                                                  
CONECT   30   20   23   37   44                                             
CONECT   31   32   35   38                                                  
CONECT   32   23   27   28   31                                             
CONECT   33   16   24                                                       
CONECT   34   25   27                                                       
CONECT   35   26   31                                                       
CONECT   36   29                                                            
CONECT   37   30                                                            
CONECT   38   31                                                            
CONECT   39   17                                                            
CONECT   40   18                                                            
CONECT   41   23                                                            
CONECT   42   26                                                            
CONECT   43   28                                                            
CONECT   44   30                                                            
MASTER        0    0    0    0    0    0    0    0   44    0   98    0
END

Synonyms

Not Available

Molecular Formula

C₃₂H₃₇N₃O₃

Average Mass

511.666

Monoisotopic Mass

511.283492063

IUPAC Name

(2R,5S,6R,9S,10R,14S,16S)-3,9-dihydroxy-5-[(1H-indol-3-yl)methyl]-7,8,14,16-tetramethyl-4,21-diazatetracyclo[16.2.1.0^{2,6}.0^{2,10}]henicosa-1(20),3,7,11,18-pentaen-17-one

Traditional Name

(2R,5S,6R,9S,10R,14S,16S)-3,9-dihydroxy-5-(1H-indol-3-ylmethyl)-7,8,14,16-tetramethyl-4,21-diazatetracyclo[16.2.1.0^{2,6}.0^{2,10}]henicosa-1(20),3,7,11,18-pentaen-17-one

CAS Registry Number

Not Available

SMILES

[H][C@@]1(CC2=CNC3=CC=CC=C23)N=C(O)[C@@]23C4=CC=C(N4)C(=O)[C@@]([H])(C)C[C@@]([H])(C)CC=C[C@@]2([H])[C@]([H])(O)C(C)=C(C)[C@@]13[H]

InChI Identifier

InChI=1S/C32H37N3O3/c1-17-8-7-10-23-30(37)20(4)19(3)28-26(15-21-16-33-24-11-6-5-9-22(21)24)35-31(38)32(23,28)27-13-12-25(34-27)29(36)18(2)14-17/h5-7,9-13,16-18,23,26,28,30,33-34,37H,8,14-15H2,1-4H3,(H,35,38)/t17-,18-,23-,26-,28-,30+,32+/m0/s1

InChI Key

KJMPCWQWZNLNTM-MMGNQZIRSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 3-alkylindoles. 3-Alkylindoles are compounds containing an indole moiety that carries an alkyl chain at the 3-position.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Indoles

Direct Parent

3-alkylindoles

Alternative Parents

Substituents

3-alkylindole
Isoindole or derivatives
Aryl alkyl ketone
Aryl ketone
Benzenoid
Substituted pyrrole
Heteroaromatic compound
Cyclic carboximidic acid
Pyrroline
Pyrrole
Secondary alcohol
Ketone
Azacycle
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Alcohol
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	0.0018 g/L	ALOGPS
logP	5.42	ALOGPS
logP	4.35	ChemAxon
logS	-5.5	ALOGPS
pKa (Strongest Acidic)	3.1	ChemAxon
pKa (Strongest Basic)	5.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	101.47 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	151.4 m³·mol⁻¹	ChemAxon
Polarizability	57.72 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 GC-MS	Predicted GC-MS Spectrum - GC-MS (TMS_2_5) - 70eV, Positive	Not Available	2022-08-08	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	Not Available	2022-08-10	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-20	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	Species

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	1	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

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

139584787

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

CMMC Knowledgebase

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 Armochaetoglobin O (MMDBc0006698)

MOL for #<Metabolite:0x00007f2ab88c01d8>

3D MOL for #<Metabolite:0x00007f2ab88c01d8>

3D SDF for #<Metabolite:0x00007f2ab88c01d8>

3D-SDF for #<Metabolite:0x00007f2ab88c01d8>

PDB for #<Metabolite:0x00007f2ab88c01d8>

3D PDB for #<Metabolite:0x00007f2ab88c01d8>

SMILES for #<Metabolite:0x00007f2ab88c01d8>

INCHI for #<Metabolite:0x00007f2ab88c01d8>

Structure for #<Metabolite:0x00007f2ab88c01d8>

3D Structure for #<Metabolite:0x00007f2ab88c01d8>