NP-MRD: Showing NP-Card for 2-[2-amino-1-(6-bromo-1h-indol-3-yl)ethyl]-3-(2-aminoethyl)-1h-indol-5-ol (NP0154547)

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Record Information

Version

2.0

Created at

2022-09-02 11:28:43 UTC

Updated at

2022-09-02 11:28:43 UTC

NP-MRD ID

NP0154547

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-[2-amino-1-(6-bromo-1h-indol-3-yl)ethyl]-3-(2-aminoethyl)-1h-indol-5-ol

Description

(+/-)-Gelliusine E belongs to the class of organic compounds known as serotonins. Serotonins are compounds containing a serotonin moiety, which consists of an indole that bears an aminoethyl a position 2 and a hydroxyl group at position 5. 2-[2-amino-1-(6-bromo-1h-indol-3-yl)ethyl]-3-(2-aminoethyl)-1h-indol-5-ol was first documented in 2021 (PMID: 34528793). Based on a literature review very few articles have been published on (+/-)-Gelliusine E.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022213282D          

 26 29  0  0  0  0            999 V2000
    3.1461   -1.7782    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4010   -0.9936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8490   -0.3805    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1039    0.4041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6190    1.0716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7940    1.0716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3815    0.3571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5565    0.3571    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.3815    1.7860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5610    1.8723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3895    2.6792    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1040    3.0917    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2755    3.8987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0601    4.1536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2317    4.9606    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    2.6732    3.6016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5017    2.7946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7171    2.5397    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1039    1.7390    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8886    1.4841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6030    1.8966    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3175    1.4841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3175    0.6591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0320    0.2466    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6030    0.2466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8886    0.6591    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  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  6  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  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
  9 18  1  0  0  0  0
 12 18  1  0  0  0  0
  5 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  2  0  0  0  0
  4 26  1  0  0  0  0
 20 26  1  0  0  0  0
M  END

     RDKit          3D

 47 50  0  0  0  0  0  0  0  0999 V2000
   -2.0907   -1.4021   -2.5531 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1565   -0.6561   -1.9780 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8037    0.6232   -1.3065 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8877    0.5585   -0.1803 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5423    0.5125   -0.1399 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4813    0.5640   -1.2187 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9098    1.9897   -1.3000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9374    2.1048   -2.3156 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4812   -0.4527   -0.9505 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3213   -1.8026   -1.3306 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3828   -2.5134   -0.9613 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.2566   -1.6925   -0.3441 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5100   -1.9243    0.2226 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2161   -0.8948    0.7977 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9433   -1.2082    1.5799 Br  0  0  0  0  0  0  0  0  0  0  0  0
    4.6543    0.3609    0.7976 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4139    0.6074    0.2408 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7199   -0.4379   -0.3316 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1331    0.4283    1.1639 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1992    0.4196    1.9805 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2975    0.3490    3.3535 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5482    0.3605    3.9130 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6650    0.4406    3.1125 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9436    0.4518    3.6939 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5371    0.5105    1.7344 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2993    0.5003    1.1586 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1361   -1.4984   -3.5900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9988   -2.3279   -2.1126 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9311   -0.4634   -2.7855 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7473   -1.2876   -1.2392 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4172    1.3195   -2.0864 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7635    1.1241   -0.9692 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0125    0.2726   -2.2135 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0461    2.5877   -1.8007 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0483    2.5376   -0.3882 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0272    3.1203   -2.5574 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6933    1.6097   -3.1758 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4587   -2.1966   -1.8481 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5636   -3.5480   -1.1027 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8833   -2.9331    0.1841 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1750    1.2102    1.2414 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9649    1.5680    0.2301 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8631    0.3752    1.5202 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3877    0.2881    3.9232 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6242    0.3051    4.9909 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4240   -0.4345    3.8510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4052    0.5741    1.0900 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  5 19  1  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 23 25  1  0
 25 26  2  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  6  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 14 16  2  0
 16 17  1  0
 17 18  2  0
 26  4  1  0
 18  9  1  0
 26 20  1  0
 18 12  1  0
  1 27  1  0
  1 28  1  0
  2 29  1  0
  2 30  1  0
  3 31  1  0
  3 32  1  0
 19 43  1  0
 21 44  1  0
 22 45  1  0
 24 46  1  0
 25 47  1  0
  6 33  1  6
  7 34  1  0
  7 35  1  0
  8 36  1  0
  8 37  1  0
 10 38  1  0
 11 39  1  0
 13 40  1  0
 16 41  1  0
 17 42  1  0
M  END


  Mrv1652309022213282D          

 26 29  0  0  0  0            999 V2000
    3.1461   -1.7782    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4010   -0.9936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8490   -0.3805    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1039    0.4041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6190    1.0716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7940    1.0716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3815    0.3571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5565    0.3571    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.3815    1.7860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5610    1.8723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3895    2.6792    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1040    3.0917    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2755    3.8987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0601    4.1536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2317    4.9606    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    2.6732    3.6016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5017    2.7946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7171    2.5397    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1039    1.7390    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8886    1.4841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6030    1.8966    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3175    1.4841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3175    0.6591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0320    0.2466    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6030    0.2466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8886    0.6591    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  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  6  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  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
  9 18  1  0  0  0  0
 12 18  1  0  0  0  0
  5 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  2  0  0  0  0
  4 26  1  0  0  0  0
 20 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0154547

> <DATABASE_NAME>
NP-MRD

> <SMILES>
NCCC1=C(NC2=CC=C(O)C=C12)C(CN)C1=CNC2=CC(Br)=CC=C12

> <INCHI_IDENTIFIER>
InChI=1S/C20H21BrN4O/c21-11-1-3-13-17(10-24-19(13)7-11)16(9-23)20-14(5-6-22)15-8-12(26)2-4-18(15)25-20/h1-4,7-8,10,16,24-26H,5-6,9,22-23H2

> <INCHI_KEY>
XDYZPDVYNZANQI-UHFFFAOYSA-N

> <FORMULA>
C20H21BrN4O

> <MOLECULAR_WEIGHT>
413.319

> <EXACT_MASS>
412.089874

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
41.182235263934

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-[2-amino-1-(6-bromo-1H-indol-3-yl)ethyl]-3-(2-aminoethyl)-1H-indol-5-ol

> <ALOGPS_LOGP>
2.62

> <JCHEM_LOGP>
1.93448176435602

> <ALOGPS_LOGS>
-4.89

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
2

> <JCHEM_PKA>
16.136127576710496

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.163902596698634

> <JCHEM_PKA_STRONGEST_BASIC>
10.19882023546322

> <JCHEM_POLAR_SURFACE_AREA>
103.85000000000001

> <JCHEM_REFRACTIVITY>
108.7908

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.36e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-[2-amino-1-(6-bromo-1H-indol-3-yl)ethyl]-3-(2-aminoethyl)-1H-indol-5-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  N   UNK     0       5.873  -3.319   0.000  0.00  0.00           N+0
HETATM    2  C   UNK     0       6.349  -1.855   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.318  -0.710   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.794   0.754   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.889   2.000   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.349   2.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.579   0.667   0.000  0.00  0.00           C+0
HETATM    8  N   UNK     0       1.039   0.667   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0       2.579   3.334   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.047   3.495   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0       0.727   5.001   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0       2.061   5.771   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.381   7.278   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.846   7.753   0.000  0.00  0.00           C+0
HETATM   15 Br   UNK     0       4.166   9.260   0.000  0.00  0.00          Br+0
HETATM   16  C   UNK     0       4.990   6.723   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.670   5.217   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.205   4.741   0.000  0.00  0.00           C+0
HETATM   19  N   UNK     0       5.794   3.246   0.000  0.00  0.00           N+0
HETATM   20  C   UNK     0       7.259   2.770   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.592   3.540   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       9.926   2.770   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.926   1.230   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      11.260   0.460   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       8.592   0.460   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       7.259   1.230   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   26                                                  
CONECT    5    4    6   19                                                  
CONECT    6    5    7    9                                                  
CONECT    7    6    8                                                       
CONECT    8    7                                                            
CONECT    9    6   10   18                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   18                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17    9   12                                                  
CONECT   19    5   20                                                       
CONECT   20   19   21   26                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25    4   20                                                  
MASTER        0    0    0    0    0    0    0    0   26    0   58    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₁BrN₄O

Average Mass

413.3190 Da

Monoisotopic Mass

412.08987 Da

IUPAC Name

2-[2-amino-1-(6-bromo-1H-indol-3-yl)ethyl]-3-(2-aminoethyl)-1H-indol-5-ol

Traditional Name

2-[2-amino-1-(6-bromo-1H-indol-3-yl)ethyl]-3-(2-aminoethyl)-1H-indol-5-ol

CAS Registry Number

Not Available

SMILES

NCCC1=C(NC2=CC=C(O)C=C12)C(CN)C1=CNC2=CC(Br)=CC=C12

InChI Identifier

InChI=1S/C20H21BrN4O/c21-11-1-3-13-17(10-24-19(13)7-11)16(9-23)20-14(5-6-22)15-8-12(26)2-4-18(15)25-20/h1-4,7-8,10,16,24-26H,5-6,9,22-23H2

InChI Key

XDYZPDVYNZANQI-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as serotonins. Serotonins are compounds containing a serotonin moiety, which consists of an indole that bears an aminoethyl a position 2 and a hydroxyl group at position 5.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Tryptamines and derivatives

Direct Parent

Serotonins

Alternative Parents

Substituents

Serotonin
Hydroxyindole
3-alkylindole
Indole
2-arylethylamine
1-hydroxy-2-unsubstituted benzenoid
Phenol
Aralkylamine
Aryl bromide
Aryl halide
Benzenoid
Substituted pyrrole
Heteroaromatic compound
Pyrrole
Azacycle
Primary amine
Amine
Organooxygen compound
Organonitrogen compound
Organobromide
Organohalogen compound
Primary aliphatic amine
Hydrocarbon derivative
Organic oxygen compound
Organic nitrogen compound
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	2.62	ALOGPS
logP	1.93	ChemAxon
logS	-4.9	ALOGPS
pKa (Strongest Acidic)	9.16	ChemAxon
pKa (Strongest Basic)	10.2	ChemAxon
Physiological Charge	2	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	103.85 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	108.79 m³·mol⁻¹	ChemAxon
Polarizability	41.18 Å³	ChemAxon
Number of Rings	4	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

Not Available

Chemspider ID

8562462

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10387020

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Chantana C, Sirion U, Iawsipo P, Jaratjaroonphong J: Short Total Synthesis of (+/-)-Gelliusine E and 2,3'-Bis(indolyl)ethylamines via PTSA-Catalyzed Transindolylation. J Org Chem. 2021 Oct 1;86(19):13360-13370. doi: 10.1021/acs.joc.1c01461. Epub 2021 Sep 16. [PubMed:34528793 ]
LOTUS database [Link]

Showing NP-Card for 2-[2-amino-1-(6-bromo-1h-indol-3-yl)ethyl]-3-(2-aminoethyl)-1h-indol-5-ol (NP0154547)

MOL for NP0154547 (2-[2-amino-1-(6-bromo-1h-indol-3-yl)ethyl]-3-(2-aminoethyl)-1h-indol-5-ol)

3D MOL for NP0154547 (2-[2-amino-1-(6-bromo-1h-indol-3-yl)ethyl]-3-(2-aminoethyl)-1h-indol-5-ol)

3D SDF for NP0154547 (2-[2-amino-1-(6-bromo-1h-indol-3-yl)ethyl]-3-(2-aminoethyl)-1h-indol-5-ol)

3D-SDF for NP0154547 (2-[2-amino-1-(6-bromo-1h-indol-3-yl)ethyl]-3-(2-aminoethyl)-1h-indol-5-ol)

PDB for NP0154547 (2-[2-amino-1-(6-bromo-1h-indol-3-yl)ethyl]-3-(2-aminoethyl)-1h-indol-5-ol)

3D PDB for NP0154547 (2-[2-amino-1-(6-bromo-1h-indol-3-yl)ethyl]-3-(2-aminoethyl)-1h-indol-5-ol)

SMILES for NP0154547 (2-[2-amino-1-(6-bromo-1h-indol-3-yl)ethyl]-3-(2-aminoethyl)-1h-indol-5-ol)

INCHI for NP0154547 (2-[2-amino-1-(6-bromo-1h-indol-3-yl)ethyl]-3-(2-aminoethyl)-1h-indol-5-ol)

Structure for NP0154547 (2-[2-amino-1-(6-bromo-1h-indol-3-yl)ethyl]-3-(2-aminoethyl)-1h-indol-5-ol)

3D Structure for NP0154547 (2-[2-amino-1-(6-bromo-1h-indol-3-yl)ethyl]-3-(2-aminoethyl)-1h-indol-5-ol)