NP-MRD: Showing NP-Card for 5-bromo-1-[(1s)-1-(dimethylamino)-2-(methylsulfanyl)ethyl]-9h-pyrido[3,4-b]indol-6-ol (NP0303464)

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Record Information

Version

2.0

Created at

2022-09-10 17:49:50 UTC

Updated at

2022-09-10 17:49:51 UTC

NP-MRD ID

NP0303464

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-bromo-1-[(1s)-1-(dimethylamino)-2-(methylsulfanyl)ethyl]-9h-pyrido[3,4-b]indol-6-ol

Description

14-Methyleudistomin C belongs to the class of organic compounds known as harmala alkaloids. Harmala alkaloids are compounds with a structure based on harmaline, harmine, harmalol, harman or a derivative of those parents. These parents are beta-carbolines, consisting of a pyrimidine fused to the pyrrole moiety of an indole to form a pyrido[3,4-b]indole. Based on a literature review very few articles have been published on 14-Methyleudistomin C.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 40 42  0  0  0  0  0  0  0  0999 V2000
   -2.5103    1.2467    2.9968 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6504    0.5958    1.8157 S   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2377    0.7459    0.0901 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0613   -0.0380   -0.3848 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8129    0.5743    0.2061 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8104    1.8046    0.7230 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.3100    2.3913    1.2191 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4674    1.6434    1.1632 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5057    0.3707    0.6377 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3480   -0.1859    0.1460 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6012   -1.4131   -0.3125 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9065   -1.7189   -0.1498 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6838   -2.8212   -0.4387 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0295   -2.8447   -0.1480 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6073   -1.7432    0.4430 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9711   -1.7340    0.7511 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8220   -0.6332    0.7332 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6176    0.8944    1.5491 Br  0  0  0  0  0  0  0  0  0  0  0  0
    2.4769   -0.5901    0.4510 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8860    0.1059   -1.8376 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6183    1.4302   -2.2666 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0081   -0.4548   -2.5607 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3025    2.3316    2.8991 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9892    1.1501    4.0224 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5701    0.6247    3.0354 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1542    0.5151   -0.5170 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0982    1.8589   -0.1074 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1429   -1.0761   -0.0721 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2516    3.3903    1.6266 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3640    2.0951    1.5524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1189   -2.0462   -0.7390 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2188   -3.6757   -0.9023 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6747   -3.7000   -0.3625 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5461   -2.5283    0.5510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6178    2.1549   -1.4587 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6319    1.4026   -2.8171 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3497    1.7375   -3.0609 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7803    0.2966   -2.7890 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6038   -0.8359   -3.5311 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4473   -1.3214   -2.0360 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 20  1  0
 20 21  1  0
 20 22  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 19  2  0
 19 17  1  0
 17 18  1  0
 17 15  2  0
 15 16  1  0
 15 14  1  0
 14 13  2  0
 10  5  1  0
 13 12  1  0
 19  9  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  3 26  1  0
  3 27  1  0
  4 28  1  6
 21 35  1  0
 21 36  1  0
 21 37  1  0
 22 38  1  0
 22 39  1  0
 22 40  1  0
  7 29  1  0
  8 30  1  0
 11 31  1  0
 16 34  1  0
 14 33  1  0
 13 32  1  0
M  END


  Mrv1652309102219492D          

 22 24  0  0  1  0            999 V2000
    1.6263   -2.1568    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3408   -2.5693    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    2.3408   -3.3943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0552   -3.8068    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0552   -4.6318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3408   -5.0443    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3408   -5.8693    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0552   -6.2818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7697   -5.8693    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7697   -5.0443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5543   -4.7893    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.0393   -5.4568    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8597   -5.5430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1953   -6.2967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7104   -6.9641    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0459   -7.7178    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8899   -6.8779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4050   -7.5453    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    4.5543   -6.1242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7697   -3.3943    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.7697   -2.5693    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4842   -3.8068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  5 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 12 19  2  0  0  0  0
  9 19  1  0  0  0  0
  4 20  1  1  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0303464

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CSC[C@@H](N(C)C)C1=NC=CC2=C1NC1=C2C(Br)=C(O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C16H18BrN3OS/c1-20(2)11(8-22-3)16-15-9(6-7-18-16)13-10(19-15)4-5-12(21)14(13)17/h4-7,11,19,21H,8H2,1-3H3/t11-/m1/s1

> <INCHI_KEY>
UXXSAQIRPRDAQT-LLVKDONJSA-N

> <FORMULA>
C16H18BrN3OS

> <MOLECULAR_WEIGHT>
380.3

> <EXACT_MASS>
379.035396

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
40

> <JCHEM_AVERAGE_POLARIZABILITY>
36.83029932975735

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5-bromo-1-[(1S)-1-(dimethylamino)-2-(methylsulfanyl)ethyl]-9H-pyrido[3,4-b]indol-6-ol

> <JCHEM_LOGP>
2.37902468140844

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
13.415022544781088

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.5052160048338425

> <JCHEM_PKA_STRONGEST_BASIC>
8.454639230309475

> <JCHEM_POLAR_SURFACE_AREA>
52.15

> <JCHEM_REFRACTIVITY>
95.8107

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
5-bromo-1-[(1S)-1-(dimethylamino)-2-(methylsulfanyl)ethyl]-9H-pyrido[3,4-b]indol-6-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0       3.036  -4.026   0.000  0.00  0.00           C+0
HETATM    2  S   UNK     0       4.369  -4.796   0.000  0.00  0.00           S+0
HETATM    3  C   UNK     0       4.369  -6.336   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.703  -7.106   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.703  -8.646   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0       4.369  -9.416   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0       4.369 -10.956   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.703 -11.726   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.037 -10.956   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.037  -9.416   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0       8.501  -8.940   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0       9.407 -10.186   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.938 -10.347   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      11.565 -11.754   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.659 -13.000   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      11.286 -14.407   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       9.128 -12.839   0.000  0.00  0.00           C+0
HETATM   18 Br   UNK     0       8.223 -14.085   0.000  0.00  0.00          Br+0
HETATM   19  C   UNK     0       8.501 -11.432   0.000  0.00  0.00           C+0
HETATM   20  N   UNK     0       7.037  -6.336   0.000  0.00  0.00           N+0
HETATM   21  C   UNK     0       7.037  -4.796   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.370  -7.106   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   20                                                  
CONECT    5    4    6   10                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   19                                                  
CONECT   10    9    5   11                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   19                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   12    9                                                  
CONECT   20    4   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   48    0
END

View in JSmol

Synonyms

Value	Source
14-Methyleudistomidin C	MeSH

Chemical Formula

C₁₆H₁₈BrN₃OS

Average Mass

380.3000 Da

Monoisotopic Mass

379.03540 Da

IUPAC Name

5-bromo-1-[(1S)-1-(dimethylamino)-2-(methylsulfanyl)ethyl]-9H-pyrido[3,4-b]indol-6-ol

Traditional Name

5-bromo-1-[(1S)-1-(dimethylamino)-2-(methylsulfanyl)ethyl]-9H-pyrido[3,4-b]indol-6-ol

CAS Registry Number

Not Available

SMILES

CSC[C@@H](N(C)C)C1=NC=CC2=C1NC1=C2C(Br)=C(O)C=C1

InChI Identifier

InChI=1S/C16H18BrN3OS/c1-20(2)11(8-22-3)16-15-9(6-7-18-16)13-10(19-15)4-5-12(21)14(13)17/h4-7,11,19,21H,8H2,1-3H3/t11-/m1/s1

InChI Key

UXXSAQIRPRDAQT-LLVKDONJSA-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 harmala alkaloids. Harmala alkaloids are compounds with a structure based on harmaline, harmine, harmalol, harman or a derivative of those parents. These parents are beta-carbolines, consisting of a pyrimidine fused to the pyrrole moiety of an indole to form a pyrido[3,4-b]indole.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Harmala alkaloids

Sub Class

Not Available

Direct Parent

Harmala alkaloids

Alternative Parents

Substituents

Harman
Beta-carboline
Pyridoindole
Hydroxyindole
Indole
Indole or derivatives
2-bromophenol
2-halophenol
Aralkylamine
1-hydroxy-2-unsubstituted benzenoid
Phenol
Aryl halide
Aryl bromide
Benzenoid
Pyridine
Pyrrole
Heteroaromatic compound
Tertiary amine
Tertiary aliphatic amine
Azacycle
Dialkylthioether
Organoheterocyclic compound
Thioether
Sulfenyl compound
Hydrocarbon derivative
Organohalogen compound
Amine
Organobromide
Organonitrogen compound
Organic nitrogen compound
Organooxygen compound
Organosulfur compound
Organic oxygen 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	2.38	ChemAxon
pKa (Strongest Acidic)	7.51	ChemAxon
pKa (Strongest Basic)	8.45	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	52.15 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	95.81 m³·mol⁻¹	ChemAxon
Polarizability	36.83 Å³	ChemAxon
Number of Rings	3	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

8220880

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10045316

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 5-bromo-1-[(1s)-1-(dimethylamino)-2-(methylsulfanyl)ethyl]-9h-pyrido[3,4-b]indol-6-ol (NP0303464)

MOL for NP0303464 (5-bromo-1-[(1s)-1-(dimethylamino)-2-(methylsulfanyl)ethyl]-9h-pyrido[3,4-b]indol-6-ol)

3D MOL for NP0303464 (5-bromo-1-[(1s)-1-(dimethylamino)-2-(methylsulfanyl)ethyl]-9h-pyrido[3,4-b]indol-6-ol)

3D SDF for NP0303464 (5-bromo-1-[(1s)-1-(dimethylamino)-2-(methylsulfanyl)ethyl]-9h-pyrido[3,4-b]indol-6-ol)

3D-SDF for NP0303464 (5-bromo-1-[(1s)-1-(dimethylamino)-2-(methylsulfanyl)ethyl]-9h-pyrido[3,4-b]indol-6-ol)

PDB for NP0303464 (5-bromo-1-[(1s)-1-(dimethylamino)-2-(methylsulfanyl)ethyl]-9h-pyrido[3,4-b]indol-6-ol)

3D PDB for NP0303464 (5-bromo-1-[(1s)-1-(dimethylamino)-2-(methylsulfanyl)ethyl]-9h-pyrido[3,4-b]indol-6-ol)

SMILES for NP0303464 (5-bromo-1-[(1s)-1-(dimethylamino)-2-(methylsulfanyl)ethyl]-9h-pyrido[3,4-b]indol-6-ol)

INCHI for NP0303464 (5-bromo-1-[(1s)-1-(dimethylamino)-2-(methylsulfanyl)ethyl]-9h-pyrido[3,4-b]indol-6-ol)

Structure for NP0303464 (5-bromo-1-[(1s)-1-(dimethylamino)-2-(methylsulfanyl)ethyl]-9h-pyrido[3,4-b]indol-6-ol)

3D Structure for NP0303464 (5-bromo-1-[(1s)-1-(dimethylamino)-2-(methylsulfanyl)ethyl]-9h-pyrido[3,4-b]indol-6-ol)