NP-MRD: Showing NP-Card for 1-(1-methoxy-3-methylcarbazol-9-yl)-3,3,5-trimethyl-1h,2h,11h-pyrano[3,2-a]carbazol-2-ol (NP0256861)

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Record Information

Version

2.0

Created at

2022-09-07 21:49:27 UTC

Updated at

2022-09-07 21:49:27 UTC

NP-MRD ID

NP0256861

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-(1-methoxy-3-methylcarbazol-9-yl)-3,3,5-trimethyl-1h,2h,11h-pyrano[3,2-a]carbazol-2-ol

Description

3-(1-Methoxy-3-methyl-9H-carbazol-9-yl)-5,5,8-trimethyl-6-oxa-17-azatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]Heptadeca-1(10),2(7),8,11,13,15-hexaen-4-ol belongs to the class of organic compounds known as carbazoles. Carbazoles are compounds containing a three ring system containing a pyrrole ring fused on either side to a benzene ring. 1-(1-methoxy-3-methylcarbazol-9-yl)-3,3,5-trimethyl-1h,2h,11h-pyrano[3,2-a]carbazol-2-ol is found in Murraya euchrestifolia. 3-(1-Methoxy-3-methyl-9H-carbazol-9-yl)-5,5,8-trimethyl-6-oxa-17-azatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]Heptadeca-1(10),2(7),8,11,13,15-hexaen-4-ol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004191519442D          

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M  END

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  Mrv1533004191519442D          

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 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 28 33  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 27 35  2  0  0  0  0
 35 36  1  0  0  0  0
 16 36  1  0  0  0  0
 23 36  2  0  0  0  0
 15 37  1  0  0  0  0
  3 37  1  0  0  0  0
  8 37  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0256861

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(C)=CC2=C1N(C1C(O)C(C)(C)OC3=C1C1=C(C=C3C)C3=C(N1)C=CC=C3)C1=C2C=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C32H30N2O3/c1-17-14-22-20-11-7-9-13-24(20)34(28(22)25(15-17)36-5)29-26-27-21(19-10-6-8-12-23(19)33-27)16-18(2)30(26)37-32(3,4)31(29)35/h6-16,29,31,33,35H,1-5H3

> <INCHI_KEY>
BDBDIRCWZPEVGI-UHFFFAOYSA-N

> <FORMULA>
C32H30N2O3

> <MOLECULAR_WEIGHT>
490.603

> <EXACT_MASS>
490.225642834

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
67

> <JCHEM_AVERAGE_POLARIZABILITY>
55.9404547574818

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
1-(1-methoxy-3-methyl-9H-carbazol-9-yl)-3,3,5-trimethyl-1H,2H,3H,11H-pyrano[3,2-a]carbazol-2-ol

> <ALOGPS_LOGP>
6.47

> <JCHEM_LOGP>
6.823233870666667

> <ALOGPS_LOGS>
-5.75

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.965049047977736

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.16246540406663

> <JCHEM_PKA_STRONGEST_BASIC>
-3.598661353828448

> <JCHEM_POLAR_SURFACE_AREA>
59.410000000000004

> <JCHEM_REFRACTIVITY>
146.1252

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
8.69e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-(1-methoxy-3-methylcarbazol-9-yl)-3,3,5-trimethyl-1H,2H,11H-pyrano[3,2-a]carbazol-2-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 19-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-APR-15         0                                  
HETATM    1  C   UNK     0       6.837   0.810   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       8.343   0.490   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       8.819  -0.974   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.789  -2.119   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.264  -3.584   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.234  -4.728   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.771  -3.904   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      10.801  -2.759   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      12.341  -2.759   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      13.372  -3.904   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      14.878  -3.584   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      15.354  -2.119   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      14.323  -0.974   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      12.817  -1.295   0.000  0.00  0.00           C+0
HETATM   15  N   UNK     0      11.571  -0.389   0.000  0.00  0.00           N+0
HETATM   16  C   UNK     0      11.571   1.151   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.238   1.921   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       8.904   1.151   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      10.238   3.461   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.721   3.193   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.711   4.908   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      11.571   4.231   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      12.905   3.461   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      14.239   4.231   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      14.239   5.771   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      15.572   3.461   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      15.572   1.921   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      16.717   0.890   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      18.248   1.051   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      19.153  -0.195   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      18.527  -1.602   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      16.996  -1.763   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      16.090  -0.517   0.000  0.00  0.00           C+0
HETATM   34  N   UNK     0      14.559  -0.356   0.000  0.00  0.00           N+0
HETATM   35  C   UNK     0      14.239   1.151   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      12.905   1.921   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      10.325  -1.295   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   37                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   37                                                  
CONECT    9    8   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13    9   15                                                  
CONECT   15   14   16   37                                                  
CONECT   16   15   17   36                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   21   22                                             
CONECT   20   19                                                            
CONECT   21   19                                                            
CONECT   22   19   23                                                       
CONECT   23   22   24   36                                                  
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   28   35                                                  
CONECT   28   27   29   33                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   28   34                                                  
CONECT   34   33   35                                                       
CONECT   35   34   27   36                                                  
CONECT   36   35   16   23                                                  
CONECT   37   15    3    8                                                  
MASTER        0    0    0    0    0    0    0    0   37    0   86    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₂H₃₀N₂O₃

Average Mass

490.6030 Da

Monoisotopic Mass

490.22564 Da

IUPAC Name

1-(1-methoxy-3-methyl-9H-carbazol-9-yl)-3,3,5-trimethyl-1H,2H,3H,11H-pyrano[3,2-a]carbazol-2-ol

Traditional Name

1-(1-methoxy-3-methylcarbazol-9-yl)-3,3,5-trimethyl-1H,2H,11H-pyrano[3,2-a]carbazol-2-ol

CAS Registry Number

Not Available

SMILES

COC1=CC(C)=CC2=C1N(C1C(O)C(C)(C)OC3=C1C1=C(C=C3C)C3=C(N1)C=CC=C3)C1=C2C=CC=C1

InChI Identifier

InChI=1S/C32H30N2O3/c1-17-14-22-20-11-7-9-13-24(20)34(28(22)25(15-17)36-5)29-26-27-21(19-10-6-8-12-23(19)33-27)16-18(2)30(26)37-32(3,4)31(29)35/h6-16,29,31,33,35H,1-5H3

InChI Key

BDBDIRCWZPEVGI-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
Murraya euchrestifolia	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as carbazoles. Carbazoles are compounds containing a three ring system containing a pyrrole ring fused on either side to a benzene ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Carbazoles

Direct Parent

Carbazoles

Alternative Parents

Substituents

Carbazole
2,2-dimethyl-1-benzopyran
N-alkylindole
Chromane
Benzopyran
1-benzopyran
Indole
Anisole
Phenol ether
Alkyl aryl ether
Benzenoid
Substituted pyrrole
Heteroaromatic compound
Pyrrole
Secondary alcohol
Azacycle
Ether
Oxacycle
Organooxygen compound
Organonitrogen compound
Alcohol
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	6.47	ALOGPS
logP	6.82	ChemAxon
logS	-5.8	ALOGPS
pKa (Strongest Acidic)	13.16	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	59.41 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	146.13 m³·mol⁻¹	ChemAxon
Polarizability	55.94 Å³	ChemAxon
Number of Rings	7	ChemAxon
Bioavailability	No	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

14634647

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1-(1-methoxy-3-methylcarbazol-9-yl)-3,3,5-trimethyl-1h,2h,11h-pyrano[3,2-a]carbazol-2-ol (NP0256861)

MOL for NP0256861 (1-(1-methoxy-3-methylcarbazol-9-yl)-3,3,5-trimethyl-1h,2h,11h-pyrano[3,2-a]carbazol-2-ol)

3D MOL for NP0256861 (1-(1-methoxy-3-methylcarbazol-9-yl)-3,3,5-trimethyl-1h,2h,11h-pyrano[3,2-a]carbazol-2-ol)

3D SDF for NP0256861 (1-(1-methoxy-3-methylcarbazol-9-yl)-3,3,5-trimethyl-1h,2h,11h-pyrano[3,2-a]carbazol-2-ol)

3D-SDF for NP0256861 (1-(1-methoxy-3-methylcarbazol-9-yl)-3,3,5-trimethyl-1h,2h,11h-pyrano[3,2-a]carbazol-2-ol)

PDB for NP0256861 (1-(1-methoxy-3-methylcarbazol-9-yl)-3,3,5-trimethyl-1h,2h,11h-pyrano[3,2-a]carbazol-2-ol)

3D PDB for NP0256861 (1-(1-methoxy-3-methylcarbazol-9-yl)-3,3,5-trimethyl-1h,2h,11h-pyrano[3,2-a]carbazol-2-ol)

SMILES for NP0256861 (1-(1-methoxy-3-methylcarbazol-9-yl)-3,3,5-trimethyl-1h,2h,11h-pyrano[3,2-a]carbazol-2-ol)

INCHI for NP0256861 (1-(1-methoxy-3-methylcarbazol-9-yl)-3,3,5-trimethyl-1h,2h,11h-pyrano[3,2-a]carbazol-2-ol)

Structure for NP0256861 (1-(1-methoxy-3-methylcarbazol-9-yl)-3,3,5-trimethyl-1h,2h,11h-pyrano[3,2-a]carbazol-2-ol)

3D Structure for NP0256861 (1-(1-methoxy-3-methylcarbazol-9-yl)-3,3,5-trimethyl-1h,2h,11h-pyrano[3,2-a]carbazol-2-ol)