NP-MRD: Showing NP-Card for 1-Methoxycarbonyl-beta-carboline (NP0138769)

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Record Information

Version

1.0

Created at

2022-06-29 18:35:21 UTC

Updated at

2022-06-29 18:35:22 UTC

NP-MRD ID

NP0138769

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-Methoxycarbonyl-beta-carboline

Description

Methyl 9H-pyrido[3,4-b]indole-1-carboxylate 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. 1-Methoxycarbonyl-beta-carboline is found in Ailanthus altissima, Ailanthus triphysa, Alstonia constricta, Arenaria kansuensis, Commelina communis, Tetradium glabrifolium, Eurycoma longifolia, Lycium chinense, Nauclea diderrichii, Panax ginseng, Picrasma crenata, Picrasma quassioides, Polygala tenuifolia and Rhazya stricta. Methyl 9H-pyrido[3,4-b]indole-1-carboxylate is a moderately basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241510512D          

 17 19  0  0  0  0            999 V2000
   -0.3502   -4.4985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0953   -3.7139    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7117   -3.5424    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2637   -4.1555    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9666   -2.7578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4146   -2.1447    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6695   -1.3601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4765   -1.1885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0285   -1.8016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8535   -1.8016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4056   -1.1885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2125   -1.3601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4675   -2.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9154   -2.7578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1085   -2.5862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4410   -3.0712    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.7736   -2.5862    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  2  0  0  0  0
  3  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  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
 10 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
  5 17  1  0  0  0  0
  9 17  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0138769

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C1=NC=CC2=C1NC1=C2C=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C13H10N2O2/c1-17-13(16)12-11-9(6-7-14-12)8-4-2-3-5-10(8)15-11/h2-7,15H,1H3

> <INCHI_KEY>
FRNCTTUBAHKEBZ-UHFFFAOYSA-N

> <FORMULA>
C13H10N2O2

> <MOLECULAR_WEIGHT>
226.235

> <EXACT_MASS>
226.07422757

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
27

> <JCHEM_AVERAGE_POLARIZABILITY>
23.50385459839527

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl 9H-pyrido[3,4-b]indole-1-carboxylate

> <ALOGPS_LOGP>
2.65

> <JCHEM_LOGP>
2.0625405519999997

> <ALOGPS_LOGS>
-3.35

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.46161584725252

> <JCHEM_PKA_STRONGEST_BASIC>
2.448854494327162

> <JCHEM_POLAR_SURFACE_AREA>
54.98

> <JCHEM_REFRACTIVITY>
62.9686

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.01e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl 9H-pyrido[3,4-b]indole-1-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0      -0.654  -8.397   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -0.178  -6.933   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       1.328  -6.612   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       2.359  -7.757   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       1.804  -5.148   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0       0.774  -4.003   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0       1.250  -2.539   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.756  -2.219   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.787  -3.363   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.327  -3.363   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.357  -2.219   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.863  -2.539   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.339  -4.003   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.309  -5.148   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.802  -4.828   0.000  0.00  0.00           C+0
HETATM   16  N   UNK     0       4.557  -5.733   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0       3.311  -4.828   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   17                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   17                                                  
CONECT   10    9   11   15                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   10   16                                                  
CONECT   16   15   17                                                       
CONECT   17   16    5    9                                                  
MASTER        0    0    0    0    0    0    0    0   17    0   38    0
END

View in JSmol

Synonyms

Value	Source
Methyl 9H-pyrido[3,4-b]indole-1-carboxylic acid	Generator

Chemical Formula

C₁₃H₁₀N₂O₂

Average Mass

226.2350 Da

Monoisotopic Mass

226.07423 Da

IUPAC Name

methyl 9H-pyrido[3,4-b]indole-1-carboxylate

Traditional Name

methyl 9H-pyrido[3,4-b]indole-1-carboxylate

CAS Registry Number

3464-66-2

SMILES

COC(=O)C1=NC=CC2=C1NC1=C2C=CC=C1

InChI Identifier

InChI=1S/C13H10N2O2/c1-17-13(16)12-11-9(6-7-14-12)8-4-2-3-5-10(8)15-11/h2-7,15H,1H3

InChI Key

FRNCTTUBAHKEBZ-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

Species Name	Source	Reference
Ailanthus altissima	LOTUS Database	35616633
Ailanthus triphysus	LOTUS Database	35616633
Alstonia constricta	LOTUS Database	35616633
Arenaria kansuensis	LOTUS Database	35616633
Commelina communis	LOTUS Database	35616633
Euodia fargesii	LOTUS Database	35616633
Eurycoma longifolia	LOTUS Database	35616633
Lycium chinense	LOTUS Database	35616633
Nauclea diderrichii	LOTUS Database	35616633
Panax ginseng	LOTUS Database	35616633
Picrasma crenata	LOTUS Database	35616633
Picrasma quassioides	LOTUS Database	35616633
Polygala tenuifolia	LOTUS Database	35616633
Rhazya stricta	LOTUS Database	35616633

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
Indole
Indole or derivatives
Pyridine carboxylic acid
Pyridine carboxylic acid or derivatives
Benzenoid
Pyridine
Vinylogous amide
Methyl ester
Pyrrole
Heteroaromatic compound
Carboxylic acid ester
Organoheterocyclic compound
Carboxylic acid derivative
Azacycle
Monocarboxylic acid or derivatives
Organic oxide
Organonitrogen compound
Organic nitrogen compound
Organic oxygen compound
Organooxygen compound
Organopnictogen compound
Hydrocarbon derivative
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	2.65	ALOGPS
logP	2.06	ChemAxon
logS	-3.4	ALOGPS
pKa (Strongest Acidic)	11.46	ChemAxon
pKa (Strongest Basic)	2.45	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	54.98 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	62.97 m³·mol⁻¹	ChemAxon
Polarizability	23.5 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

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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 1-Methoxycarbonyl-beta-carboline (NP0138769)

MOL for NP0138769 (1-Methoxycarbonyl-beta-carboline)

3D MOL for NP0138769 (1-Methoxycarbonyl-beta-carboline)

3D SDF for NP0138769 (1-Methoxycarbonyl-beta-carboline)

3D-SDF for NP0138769 (1-Methoxycarbonyl-beta-carboline)

PDB for NP0138769 (1-Methoxycarbonyl-beta-carboline)

3D PDB for NP0138769 (1-Methoxycarbonyl-beta-carboline)

SMILES for NP0138769 (1-Methoxycarbonyl-beta-carboline)

INCHI for NP0138769 (1-Methoxycarbonyl-beta-carboline)

Structure for NP0138769 (1-Methoxycarbonyl-beta-carboline)

3D Structure for NP0138769 (1-Methoxycarbonyl-beta-carboline)