NP-MRD: Showing NP-Card for 3',5,5'-tribromo-7'-methoxy-1h,1'h-3,4'-biindole (NP0288141)

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Record Information

Version

2.0

Created at

2022-09-09 17:43:38 UTC

Updated at

2022-09-09 17:43:38 UTC

NP-MRD ID

NP0288141

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3',5,5'-tribromo-7'-methoxy-1h,1'h-3,4'-biindole

Description

UNII-1RLR9NIC1V belongs to the class of organic compounds known as indoles. Indoles are compounds containing an indole moiety, which consists of pyrrole ring fused to benzene to form 2,3-benzopyrrole. UNII-1RLR9NIC1V is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 34 37  0  0  0  0  0  0  0  0999 V2000
    5.1232   -1.0724    1.2133 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3371   -0.0970    0.6156 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9939   -0.2365    0.2978 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2747   -1.3834    0.5452 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9198   -1.5113    0.2196 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0470   -3.0999    0.5704 Br  0  0  0  0  0  0  0  0  0  0  0  0
    0.2792   -0.4510   -0.3708 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1310   -0.5268   -0.7320 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6369   -0.9615   -1.9409 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9776   -0.8816   -1.8816 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3782   -0.4191   -0.7020 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6113   -0.1544   -0.1412 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6954    0.3346    1.1447 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5275    0.5536    1.8574 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6893    1.2292    3.6287 Br  0  0  0  0  0  0  0  0  0  0  0  0
   -2.2866    0.2981    1.3216 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2324   -0.1902    0.0344 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9807    0.7063   -0.6271 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5942    1.9138   -1.2045 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1609    2.2812   -1.8338 Br  0  0  0  0  0  0  0  0  0  0  0  0
    1.7082    2.7061   -1.2044 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7541    2.0556   -0.6613 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3366    0.8207   -0.2960 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0956   -2.0286    0.6150 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1864   -0.7391    1.1509 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8040   -1.2409    2.2527 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7569   -2.2193    1.0043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0423   -1.3110   -2.7989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6095   -1.1507   -2.6664 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5290   -0.3284   -0.7065 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6812    0.5262    1.5399 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3753    0.4657    1.8691 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7309    3.7144   -1.5908 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7357    2.3976   -0.5225 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3 23  2  0
 23 22  1  0
 22 21  1  0
 21 19  2  0
 19 20  1  0
 19 18  1  0
 18  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 14 16  1  0
 16 17  2  0
  7  5  1  0
  5  6  1  0
  5  4  2  0
  4  3  1  0
 18 23  1  0
 17  8  1  0
 17 11  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
 22 34  1  0
 21 33  1  0
  9 28  1  0
 10 29  1  0
 12 30  1  0
 13 31  1  0
 16 32  1  0
  4 27  1  0
M  END


  Mrv1533004251510412D          

 23 26  0  0  0  0            999 V2000
    3.9571    3.1077    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6716    2.6952    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6716    1.8702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3861    1.4577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3861    0.6327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1006    0.2202    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    4.6716    0.2202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6716   -0.6048    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3391   -1.0897    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0841   -1.8743    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.2591   -1.8743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7071   -2.4874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9001   -2.3159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6452   -1.5313    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8382   -1.3597    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    3.1972   -0.9182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0042   -1.0897    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9571    0.6327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1725    0.3778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9176   -0.4068    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    2.6876    1.0452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1725    1.7127    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9571    1.4577    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
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  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
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
  8 17  1  0  0  0  0
 11 17  1  0  0  0  0
  7 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
  3 23  2  0  0  0  0
 18 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0288141

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C2NC=C(Br)C2=C(C2=CNC3=CC=C(Br)C=C23)C(Br)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C17H11Br3N2O/c1-23-14-5-11(19)15(16-12(20)7-22-17(14)16)10-6-21-13-3-2-8(18)4-9(10)13/h2-7,21-22H,1H3

> <INCHI_KEY>
HEYVTLDTOFVUNA-UHFFFAOYSA-N

> <FORMULA>
C17H11Br3N2O

> <MOLECULAR_WEIGHT>
499.0

> <EXACT_MASS>
495.842152

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
34

> <JCHEM_AVERAGE_POLARIZABILITY>
38.57518518754324

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3,5-dibromo-4-(5-bromo-1H-indol-3-yl)-7-methoxy-1H-indole

> <ALOGPS_LOGP>
6.11

> <JCHEM_LOGP>
5.966581774333333

> <ALOGPS_LOGS>
-6.44

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.56496792853553

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.96711204386136

> <JCHEM_PKA_STRONGEST_BASIC>
-4.889789573990847

> <JCHEM_POLAR_SURFACE_AREA>
40.81

> <JCHEM_REFRACTIVITY>
102.6988

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.81e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3,5-dibromo-4-(5-bromo-1H-indol-3-yl)-7-methoxy-1H-indole

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0       7.387   5.801   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       8.720   5.031   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       8.720   3.491   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.054   2.721   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.054   1.181   0.000  0.00  0.00           C+0
HETATM    6 Br   UNK     0      11.388   0.411   0.000  0.00  0.00          Br+0
HETATM    7  C   UNK     0       8.720   0.411   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.720  -1.129   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.966  -2.034   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0       9.490  -3.499   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0       7.950  -3.499   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.920  -4.643   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.414  -4.323   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.938  -2.858   0.000  0.00  0.00           C+0
HETATM   15 Br   UNK     0       3.431  -2.538   0.000  0.00  0.00          Br+0
HETATM   16  C   UNK     0       5.968  -1.714   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.474  -2.034   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.387   1.181   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.922   0.705   0.000  0.00  0.00           C+0
HETATM   20 Br   UNK     0       5.446  -0.759   0.000  0.00  0.00          Br+0
HETATM   21  C   UNK     0       5.017   1.951   0.000  0.00  0.00           C+0
HETATM   22  N   UNK     0       5.922   3.197   0.000  0.00  0.00           N+0
HETATM   23  C   UNK     0       7.387   2.721   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   23                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   18                                                  
CONECT    8    7    9   17                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   17                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16    8   11                                                  
CONECT   18    7   19   23                                                  
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22    3   18                                                  
MASTER        0    0    0    0    0    0    0    0   23    0   52    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₇H₁₁Br₃N₂O

Average Mass

499.0000 Da

Monoisotopic Mass

495.84215 Da

IUPAC Name

3,5-dibromo-4-(5-bromo-1H-indol-3-yl)-7-methoxy-1H-indole

Traditional Name

3,5-dibromo-4-(5-bromo-1H-indol-3-yl)-7-methoxy-1H-indole

CAS Registry Number

Not Available

SMILES

COC1=C2NC=C(Br)C2=C(C2=CNC3=CC=C(Br)C=C23)C(Br)=C1

InChI Identifier

InChI=1S/C17H11Br3N2O/c1-23-14-5-11(19)15(16-12(20)7-22-17(14)16)10-6-21-13-3-2-8(18)4-9(10)13/h2-7,21-22H,1H3

InChI Key

HEYVTLDTOFVUNA-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 indoles. Indoles are compounds containing an indole moiety, which consists of pyrrole ring fused to benzene to form 2,3-benzopyrrole.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Indoles

Direct Parent

Indoles

Alternative Parents

Substituents

Indole
Anisole
Phenol ether
Alkyl aryl ether
Aryl bromide
Aryl halide
Benzenoid
Substituted pyrrole
Heteroaromatic compound
Pyrrole
Azacycle
Ether
Organohalogen compound
Organooxygen compound
Organic oxygen compound
Organic nitrogen compound
Hydrocarbon derivative
Organobromide
Organonitrogen 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	6.11	ALOGPS
logP	5.97	ChemAxon
logS	-6.4	ALOGPS
pKa (Strongest Acidic)	13.97	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	40.81 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	102.7 m³·mol⁻¹	ChemAxon
Polarizability	38.58 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

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

21674191

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3',5,5'-tribromo-7'-methoxy-1h,1'h-3,4'-biindole (NP0288141)

MOL for NP0288141 (3',5,5'-tribromo-7'-methoxy-1h,1'h-3,4'-biindole)

3D MOL for NP0288141 (3',5,5'-tribromo-7'-methoxy-1h,1'h-3,4'-biindole)

3D SDF for NP0288141 (3',5,5'-tribromo-7'-methoxy-1h,1'h-3,4'-biindole)

3D-SDF for NP0288141 (3',5,5'-tribromo-7'-methoxy-1h,1'h-3,4'-biindole)

PDB for NP0288141 (3',5,5'-tribromo-7'-methoxy-1h,1'h-3,4'-biindole)

3D PDB for NP0288141 (3',5,5'-tribromo-7'-methoxy-1h,1'h-3,4'-biindole)

SMILES for NP0288141 (3',5,5'-tribromo-7'-methoxy-1h,1'h-3,4'-biindole)

INCHI for NP0288141 (3',5,5'-tribromo-7'-methoxy-1h,1'h-3,4'-biindole)

Structure for NP0288141 (3',5,5'-tribromo-7'-methoxy-1h,1'h-3,4'-biindole)

3D Structure for NP0288141 (3',5,5'-tribromo-7'-methoxy-1h,1'h-3,4'-biindole)