NP-MRD: Showing NP-Card for 3,3,10-trimethyl-6h-pyrano[2,3-c]carbazole (NP0144412)

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Record Information

Version

2.0

Created at

2022-09-01 23:22:48 UTC

Updated at

2022-09-01 23:22:48 UTC

NP-MRD ID

NP0144412

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3,3,10-trimethyl-6h-pyrano[2,3-c]carbazole

Description

Glycomaurin belongs to the class of organic compounds known as indoles and derivatives. These are organic compounds containing an indole, which is a bicyclic ring system made up of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring. 3,3,10-trimethyl-6h-pyrano[2,3-c]carbazole is found in Glycosmis mauritiana. Based on a literature review very few articles have been published on Glycomaurin.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 37 40  0  0  0  0  0  0  0  0999 V2000
   -4.2662    2.5413    0.0643 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8017    1.1194    0.0904 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6768    0.0656    0.1595 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1799   -1.2173    0.1798 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8159   -1.4650    0.1320 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9532   -0.3780    0.0624 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4145    0.9135    0.0403 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6166   -0.9821    0.0269 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5872   -0.4548   -0.0389 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8498    0.9720   -0.0948 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0815    1.4396   -0.1599 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2796    0.6043   -0.1823 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0562    0.9833   -1.4400 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1857    0.9532    1.0023 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0204   -0.7674   -0.1283 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7430   -1.3296   -0.0584 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6126   -2.6380   -0.0116 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3506   -3.3631    0.0628 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8125   -2.4394    0.0811 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0566   -2.6486    0.1385 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2131    2.6596   -0.4831 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3288    2.9044    1.1240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5213    3.1962   -0.4324 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7326    0.3076    0.1949 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8832   -2.0421    0.2346 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7984    1.7907   -0.0126 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0263    1.6857   -0.0838 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1875    2.5489   -0.1993 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4318    0.0768   -1.9452 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8983    1.6530   -1.2018 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3907    1.5066   -2.1791 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2387    0.7917    0.6880 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9443    0.2430    1.8424 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0152    2.0104    1.3307 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5555   -3.2373   -0.0312 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3705   -4.0107    0.9768 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2458   -3.9933   -0.8591 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5 20  1  0
 20 19  2  0
 19 18  1  0
 18 17  1  0
 17 16  2  0
 16 15  1  0
 15 12  1  0
 12 13  1  0
 12 14  1  0
 12 11  1  0
 11 10  2  0
 10  9  1  0
  9  8  2  0
  8  6  1  0
  6  7  2  0
  7  2  1  0
  6  5  1  0
  8 19  1  0
  9 16  1  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
  3 24  1  0
  4 25  1  0
 18 36  1  0
 18 37  1  0
 17 35  1  0
 13 29  1  0
 13 30  1  0
 13 31  1  0
 14 32  1  0
 14 33  1  0
 14 34  1  0
 11 28  1  0
 10 27  1  0
  7 26  1  0
M  END


  Mrv1652309022201222D          

 20 23  0  0  0  0            999 V2000
   -0.8089   -0.8627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5962   -1.6599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1802   -2.2426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9675   -3.0397    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1709   -3.2541    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4131   -2.6713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2004   -1.8742    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1478   -3.0467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9183   -2.7518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0482   -1.9371    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8187   -1.6423    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4593   -2.1621    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8601   -1.4410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2391   -2.4315    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3294   -2.9768    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5589   -3.2717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4290   -4.0864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6585   -4.3812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0179   -3.8614    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2029   -3.9896    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  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
  6  7  2  0  0  0  0
  2  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 12 15  1  0  0  0  0
 15 16  1  0  0  0  0
  9 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
  8 19  1  0  0  0  0
 19 20  2  0  0  0  0
  5 20  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0144412

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=CC=C2N=C3CC=C4OC(C)(C)C=CC4=C3C2=C1

> <INCHI_IDENTIFIER>
InChI=1S/C18H17NO/c1-11-4-5-14-13(10-11)17-12-8-9-18(2,3)20-16(12)7-6-15(17)19-14/h4-5,7-10H,6H2,1-3H3

> <INCHI_KEY>
RUVSOOOCFVUYHV-UHFFFAOYSA-N

> <FORMULA>
C18H17NO

> <MOLECULAR_WEIGHT>
263.34

> <EXACT_MASS>
263.131014171

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
37

> <JCHEM_AVERAGE_POLARIZABILITY>
30.77736795531746

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5,5,15-trimethyl-6-oxa-11-azatetracyclo[8.7.0.0^{2,7}.0^{12,17}]heptadeca-1,3,7,10,12,14,16-heptaene

> <ALOGPS_LOGP>
4.34

> <JCHEM_LOGP>
3.641633074666667

> <ALOGPS_LOGS>
-4.29

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
4.366810943343188

> <JCHEM_POLAR_SURFACE_AREA>
21.59

> <JCHEM_REFRACTIVITY>
86.45270000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.35e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5,5,15-trimethyl-6-oxa-11-azatetracyclo[8.7.0.0^{2,7}.0^{12,17}]heptadeca-1,3,7,10,12,14,16-heptaene

> <JCHEM_VEBER_RULE>
1

$$$$

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      -1.510  -1.610   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.113  -3.098   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.203  -4.186   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.806  -5.674   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.319  -6.074   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.771  -4.986   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.374  -3.499   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.143  -5.687   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.581  -5.137   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.823  -3.616   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.262  -3.066   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.457  -4.036   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.205  -2.690   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.913  -4.539   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       6.215  -5.557   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       4.777  -6.107   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.534  -7.628   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.096  -8.178   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.900  -7.208   0.000  0.00  0.00           C+0
HETATM   20  N   UNK     0       0.379  -7.447   0.000  0.00  0.00           N+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   20                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6    2                                                       
CONECT    8    6    9   19                                                  
CONECT    9    8   10   16                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14   15                                             
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15   12   16                                                       
CONECT   16   15    9   17                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18    8   20                                                  
CONECT   20   19    5                                                       
MASTER        0    0    0    0    0    0    0    0   20    0   46    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₁₇NO

Average Mass

263.3400 Da

Monoisotopic Mass

263.13101 Da

IUPAC Name

5,5,15-trimethyl-6-oxa-11-azatetracyclo[8.7.0.0^{2,7}.0^{12,17}]heptadeca-1,3,7,10,12,14,16-heptaene

Traditional Name

5,5,15-trimethyl-6-oxa-11-azatetracyclo[8.7.0.0^{2,7}.0^{12,17}]heptadeca-1,3,7,10,12,14,16-heptaene

CAS Registry Number

Not Available

SMILES

CC1=CC=C2N=C3CC=C4OC(C)(C)C=CC4=C3C2=C1

InChI Identifier

InChI=1S/C18H17NO/c1-11-4-5-14-13(10-11)17-12-8-9-18(2,3)20-16(12)7-6-15(17)19-14/h4-5,7-10H,6H2,1-3H3

InChI Key

RUVSOOOCFVUYHV-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
Glycosmis mauritiana	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as indoles and derivatives. These are organic compounds containing an indole, which is a bicyclic ring system made up 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

Not Available

Direct Parent

Indoles and derivatives

Alternative Parents

Substituents

Indole or derivatives
Benzenoid
Pyran
Ketimine
Oxacycle
Azacycle
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Organic nitrogen compound
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Imine
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	4.34	ALOGPS
logP	3.64	ChemAxon
logS	-4.3	ALOGPS
pKa (Strongest Basic)	4.37	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	21.59 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	86.45 m³·mol⁻¹	ChemAxon
Polarizability	30.78 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	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

C00024709

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

102081527

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3,3,10-trimethyl-6h-pyrano[2,3-c]carbazole (NP0144412)

MOL for NP0144412 (3,3,10-trimethyl-6h-pyrano[2,3-c]carbazole)

3D MOL for NP0144412 (3,3,10-trimethyl-6h-pyrano[2,3-c]carbazole)

3D SDF for NP0144412 (3,3,10-trimethyl-6h-pyrano[2,3-c]carbazole)

3D-SDF for NP0144412 (3,3,10-trimethyl-6h-pyrano[2,3-c]carbazole)

PDB for NP0144412 (3,3,10-trimethyl-6h-pyrano[2,3-c]carbazole)

3D PDB for NP0144412 (3,3,10-trimethyl-6h-pyrano[2,3-c]carbazole)

SMILES for NP0144412 (3,3,10-trimethyl-6h-pyrano[2,3-c]carbazole)

INCHI for NP0144412 (3,3,10-trimethyl-6h-pyrano[2,3-c]carbazole)

Structure for NP0144412 (3,3,10-trimethyl-6h-pyrano[2,3-c]carbazole)

3D Structure for NP0144412 (3,3,10-trimethyl-6h-pyrano[2,3-c]carbazole)