NP-MRD: Showing NP-Card for 14-ethyl-2-hydroxy-3-(1h-indol-3-yl)-18-methyl-15,16-dithia-10,12,18-triazapentacyclo[12.2.2.0¹,¹².0³,¹¹.0⁴,⁹]octadeca-4,6,8-triene-13,17-dione (NP0159208)

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Record Information

Version

2.0

Created at

2022-09-02 16:55:30 UTC

Updated at

2022-09-02 16:55:30 UTC

NP-MRD ID

NP0159208

Secondary Accession Numbers

None

Natural Product Identification

Common Name

14-ethyl-2-hydroxy-3-(1h-indol-3-yl)-18-methyl-15,16-dithia-10,12,18-triazapentacyclo[12.2.2.0¹,¹².0³,¹¹.0⁴,⁹]octadeca-4,6,8-triene-13,17-dione

Description

14-Ethyl-2-hydroxy-3-(1H-indol-3-yl)-18-methyl-15,16-dithia-10,12,18-triazapentacyclo[12.2.2.0¹,¹².0³,¹¹.0⁴,⁹]Octadeca-4,6,8-triene-13,17-dione belongs to the class of organic compounds known as pyrroloindoles. Pyrroloindoles are compounds containing a pyrroloindole moiety, which is a tricyclic heterocycle which consists of a pyrrole ring fused to an indole. Pyrrole is 5-membered ring consisting of four carbon atoms and one nitrogen atom. Indole is a bicyclic compound consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring. Based on a literature review very few articles have been published on 14-ethyl-2-hydroxy-3-(1H-indol-3-yl)-18-methyl-15,16-dithia-10,12,18-triazapentacyclo[12.2.2.0¹,¹².0³,¹¹.0⁴,⁹]Octadeca-4,6,8-triene-13,17-dione.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022218552D          

 33 39  0  0  0  0            999 V2000
   -1.3838   -0.5860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5755   -0.7510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0284   -0.1335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6196    0.2417    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    0.5632    0.9870    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    1.2330    1.3231    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2750    1.4689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0370    2.2327    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2789    0.7310    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0905    0.8795    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0254    1.6342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1418    2.4509    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6952    1.1172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0035    1.8825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8038    2.0828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8605    2.9059    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.0953    3.2142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8124    3.9891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9998    4.1316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4701    3.4991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7530    2.7241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5656    2.5817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5154    1.0277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1306    1.5774    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9142    1.3193    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0826    0.5117    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4673   -0.0379    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6837    0.2201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9676   -0.1896    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3567    0.3649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4883    0.4446    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.9065   -0.2855    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2036   -1.0552    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
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  6 31  1  0  0  0  0
 31 32  1  0  0  0  0
  3 32  1  0  0  0  0
 32 33  2  0  0  0  0
M  END

     RDKit          3D

 55 61  0  0  0  0  0  0  0  0999 V2000
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    4.6513    1.1385    0.4126 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4590    0.5270   -0.2064 C   0  0  2  0  0  0  0  0  0  0  0  0
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   -0.5614   -0.4293   -1.3429 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8597   -1.4835   -2.2249 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1812   -0.6974    0.0203 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4451    0.0149    0.1463 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6698   -0.5788    0.3317 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6119    0.3802    0.3975 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9997    1.5706    0.2567 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4975    2.8751    0.2509 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6293    3.9224    0.0886 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2621    3.7150   -0.0704 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7647    2.4300   -0.0655 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6579    1.3794    0.0996 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4179   -2.1590    0.1379 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1945   -3.0556   -0.6101 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2693   -4.4001   -0.3240 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5372   -4.8594    0.7526 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7757   -3.9883    1.4881 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.0910   -0.1743    0.3502 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4057    0.1281    0.7872 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.6517    0.2437    0.5346 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5583    3.0161    0.3753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0568    4.9332    0.0892 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5943    4.5560   -0.1968 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7221    2.1887   -0.1780 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7697   -2.7052   -1.4530 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8720   -5.0820   -0.9086 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6073   -5.9211    0.9643 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2088   -4.3606    2.3266 H   0  0  0  0  0  0  0  0  0  0  0  0
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 10 41  1  0
M  END


  Mrv1652309022218552D          

 33 39  0  0  0  0            999 V2000
   -1.3838   -0.5860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5755   -0.7510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0284   -0.1335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6196    0.2417    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    0.5632    0.9870    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    1.2330    1.3231    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2750    1.4689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0370    2.2327    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2789    0.7310    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0905    0.8795    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0254    1.6342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1418    2.4509    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6952    1.1172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0035    1.8825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8038    2.0828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8605    2.9059    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.0953    3.2142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8124    3.9891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9998    4.1316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.9142    1.3193    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0826    0.5117    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.6837    0.2201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.3567    0.3649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4883    0.4446    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.9065   -0.2855    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2036   -1.0552    0.0000 O   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
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
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M  END
> <DATABASE_ID>
NP0159208

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC12SSC3(C(O)C4(C(NC5=CC=CC=C45)N3C1=O)C1=CNC3=CC=CC=C13)C(=O)N2C

> <INCHI_IDENTIFIER>
InChI=1S/C24H22N4O3S2/c1-3-22-20(30)28-19-23(14-9-5-7-11-17(14)26-19,15-12-25-16-10-6-4-8-13(15)16)18(29)24(28,33-32-22)21(31)27(22)2/h4-12,18-19,25-26,29H,3H2,1-2H3

> <INCHI_KEY>
HURRRPHPMBYTBV-UHFFFAOYSA-N

> <FORMULA>
C24H22N4O3S2

> <MOLECULAR_WEIGHT>
478.59

> <EXACT_MASS>
478.113332932

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
48.47235888336387

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
14-ethyl-2-hydroxy-3-(1H-indol-3-yl)-18-methyl-15,16-dithia-10,12,18-triazapentacyclo[12.2.2.0^{1,12}.0^{3,11}.0^{4,9}]octadeca-4,6,8-triene-13,17-dione

> <ALOGPS_LOGP>
3.36

> <JCHEM_LOGP>
3.6920780483333324

> <ALOGPS_LOGS>
-3.87

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.576517102485717

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.041238252912255

> <JCHEM_PKA_STRONGEST_BASIC>
1.5575012658939438

> <JCHEM_POLAR_SURFACE_AREA>
88.66999999999999

> <JCHEM_REFRACTIVITY>
140.16810000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.52e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
14-ethyl-2-hydroxy-3-(1H-indol-3-yl)-18-methyl-15,16-dithia-10,12,18-triazapentacyclo[12.2.2.0^{1,12}.0^{3,11}.0^{4,9}]octadeca-4,6,8-triene-13,17-dione

> <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  C   UNK     0      -2.583  -1.094   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.074  -1.402   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.053  -0.249   0.000  0.00  0.00           C+0
HETATM    4  S   UNK     0       1.157   0.451   0.000  0.00  0.00           S+0
HETATM    5  S   UNK     0       1.051   1.842   0.000  0.00  0.00           S+0
HETATM    6  C   UNK     0       2.302   2.470   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.513   2.742   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -0.069   4.168   0.000  0.00  0.00           O+0
HETATM    9  N   UNK     0      -0.521   1.365   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0      -2.036   1.642   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.781   3.050   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       3.998   4.575   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       5.031   2.085   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.607   3.514   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.100   3.888   0.000  0.00  0.00           C+0
HETATM   16  N   UNK     0       7.206   5.424   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0       5.778   6.000   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.250   7.446   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.733   7.712   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.744   6.532   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.272   5.085   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.789   4.819   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.562   1.918   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       7.711   2.944   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       9.173   2.463   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       9.487   0.955   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       8.339  -0.071   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.876   0.411   0.000  0.00  0.00           C+0
HETATM   29  N   UNK     0       5.540  -0.354   0.000  0.00  0.00           N+0
HETATM   30  C   UNK     0       4.399   0.681   0.000  0.00  0.00           C+0
HETATM   31  N   UNK     0       2.778   0.830   0.000  0.00  0.00           N+0
HETATM   32  C   UNK     0       1.692  -0.533   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       2.247  -1.970   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    9   32                                             
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   11   31                                             
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7    3   10                                                  
CONECT   10    9                                                            
CONECT   11    6   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   23   30                                             
CONECT   14   13   15   22                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   22                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   14   17                                                  
CONECT   23   13   24   28                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   23   29                                                  
CONECT   29   28   30                                                       
CONECT   30   29   13   31                                                  
CONECT   31   30    6   32                                                  
CONECT   32   31    3   33                                                  
CONECT   33   32                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   78    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₂₂N₄O₃S₂

Average Mass

478.5900 Da

Monoisotopic Mass

478.11333 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CCC12SSC3(C(O)C4(C(NC5=CC=CC=C45)N3C1=O)C1=CNC3=CC=CC=C13)C(=O)N2C

InChI Identifier

InChI=1S/C24H22N4O3S2/c1-3-22-20(30)28-19-23(14-9-5-7-11-17(14)26-19,15-12-25-16-10-6-4-8-13(15)16)18(29)24(28,33-32-22)21(31)27(22)2/h4-12,18-19,25-26,29H,3H2,1-2H3

InChI Key

HURRRPHPMBYTBV-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 pyrroloindoles. Pyrroloindoles are compounds containing a pyrroloindole moiety, which is a tricyclic heterocycle which consists of a pyrrole ring fused to an indole. Pyrrole is 5-membered ring consisting of four carbon atoms and one nitrogen atom. Indole is a bicyclic compound consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Pyrroloindoles

Direct Parent

Pyrroloindoles

Alternative Parents

Substituents

Pyrroloindole
3-alkylindole
Epipolythiodioxopiperazine
Alpha-amino acid or derivatives
Thiodioxopiperazine
Dihydroindole
Indole
2,5-dioxopiperazine
Dioxopiperazine
N-alkylpiperazine
N-methylpiperazine
Secondary aliphatic/aromatic amine
Dithiazinane
Benzenoid
Substituted pyrrole
Piperazine
1,4-diazinane
Heteroaromatic compound
Tertiary carboxylic acid amide
Pyrrolidine
Pyrrole
Secondary alcohol
Organic disulfide
Lactam
Carboxamide group
Amino acid or derivatives
Azacycle
Secondary amine
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Amine
Alcohol
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	3.36	ALOGPS
logP	3.69	ChemAxon
logS	-3.9	ALOGPS

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

162873334

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 14-ethyl-2-hydroxy-3-(1h-indol-3-yl)-18-methyl-15,16-dithia-10,12,18-triazapentacyclo[12.2.2.0¹,¹².0³,¹¹.0⁴,⁹]octadeca-4,6,8-triene-13,17-dione (NP0159208)

MOL for NP0159208 (14-ethyl-2-hydroxy-3-(1h-indol-3-yl)-18-methyl-15,16-dithia-10,12,18-triazapentacyclo[12.2.2.0¹,¹².0³,¹¹.0⁴,⁹]octadeca-4,6,8-triene-13,17-dione)

3D MOL for NP0159208 (14-ethyl-2-hydroxy-3-(1h-indol-3-yl)-18-methyl-15,16-dithia-10,12,18-triazapentacyclo[12.2.2.0¹,¹².0³,¹¹.0⁴,⁹]octadeca-4,6,8-triene-13,17-dione)

3D SDF for NP0159208 (14-ethyl-2-hydroxy-3-(1h-indol-3-yl)-18-methyl-15,16-dithia-10,12,18-triazapentacyclo[12.2.2.0¹,¹².0³,¹¹.0⁴,⁹]octadeca-4,6,8-triene-13,17-dione)

3D-SDF for NP0159208 (14-ethyl-2-hydroxy-3-(1h-indol-3-yl)-18-methyl-15,16-dithia-10,12,18-triazapentacyclo[12.2.2.0¹,¹².0³,¹¹.0⁴,⁹]octadeca-4,6,8-triene-13,17-dione)

PDB for NP0159208 (14-ethyl-2-hydroxy-3-(1h-indol-3-yl)-18-methyl-15,16-dithia-10,12,18-triazapentacyclo[12.2.2.0¹,¹².0³,¹¹.0⁴,⁹]octadeca-4,6,8-triene-13,17-dione)

3D PDB for NP0159208 (14-ethyl-2-hydroxy-3-(1h-indol-3-yl)-18-methyl-15,16-dithia-10,12,18-triazapentacyclo[12.2.2.0¹,¹².0³,¹¹.0⁴,⁹]octadeca-4,6,8-triene-13,17-dione)

SMILES for NP0159208 (14-ethyl-2-hydroxy-3-(1h-indol-3-yl)-18-methyl-15,16-dithia-10,12,18-triazapentacyclo[12.2.2.0¹,¹².0³,¹¹.0⁴,⁹]octadeca-4,6,8-triene-13,17-dione)

INCHI for NP0159208 (14-ethyl-2-hydroxy-3-(1h-indol-3-yl)-18-methyl-15,16-dithia-10,12,18-triazapentacyclo[12.2.2.0¹,¹².0³,¹¹.0⁴,⁹]octadeca-4,6,8-triene-13,17-dione)

Structure for NP0159208 (14-ethyl-2-hydroxy-3-(1h-indol-3-yl)-18-methyl-15,16-dithia-10,12,18-triazapentacyclo[12.2.2.0¹,¹².0³,¹¹.0⁴,⁹]octadeca-4,6,8-triene-13,17-dione)

3D Structure for NP0159208 (14-ethyl-2-hydroxy-3-(1h-indol-3-yl)-18-methyl-15,16-dithia-10,12,18-triazapentacyclo[12.2.2.0¹,¹².0³,¹¹.0⁴,⁹]octadeca-4,6,8-triene-13,17-dione)