NP-MRD: Showing NP-Card for 10-hydroxy-3,3-dimethyl-11h-pyrano[3,2-a]carbazole-5-carbaldehyde (NP0201683)

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Record Information

Version

2.0

Created at

2022-09-04 20:46:19 UTC

Updated at

2022-09-04 20:46:19 UTC

NP-MRD ID

NP0201683

Secondary Accession Numbers

None

Natural Product Identification

Common Name

10-hydroxy-3,3-dimethyl-11h-pyrano[3,2-a]carbazole-5-carbaldehyde

Description

Clauszoline G 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. 10-hydroxy-3,3-dimethyl-11h-pyrano[3,2-a]carbazole-5-carbaldehyde is found in Clausena excavata. Clauszoline G is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 37 40  0  0  0  0  0  0  0  0999 V2000
   -4.2521    0.8213   -1.1774 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3744    0.4132   -0.0094 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3029    0.0152    1.1460 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5821    1.6109    0.3666 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2640    1.6064    0.4240 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5632    0.3742    0.1048 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2205   -0.7858   -0.2545 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5901   -1.9649   -0.5618 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3300   -3.1649   -0.9361 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7951   -4.2432   -1.2190 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8062   -1.9775   -0.5032 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5053   -0.8429   -0.1493 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8259    0.3184    0.1508 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6966    1.2966    0.4678 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.9447    0.7643    0.3720 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1892    1.3174    0.5847 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2494    2.6489    0.9662 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3561    0.5646    0.4226 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2486   -0.7465    0.0448 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0042   -1.2894   -0.1650 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8417   -0.5431   -0.0045 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5995   -0.7200   -0.2972 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3239    0.8999   -0.8824 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1937    0.0969   -2.0149 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9685    1.8108   -1.5935 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3446    0.3656    0.9497 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3050   -1.0658    1.3186 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9079    0.4944    2.0744 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1605    2.5180    0.5988 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7448    2.5138    0.7053 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4079   -3.0935   -0.9639 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3512   -2.8839   -0.7367 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4575    2.2763    0.7358 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4130    3.1812    1.0803 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2856    1.0466    0.6011 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1683   -1.3249   -0.0787 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8872   -2.3089   -0.4602 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2 22  1  0
 22  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
  8 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 21  2  0
 21 20  1  0
 20 19  2  0
 19 18  1  0
 18 16  2  0
 16 17  1  0
 13  6  2  0
  6  5  1  0
  5  4  2  0
  4  2  1  0
  6  7  1  0
 21 12  1  0
 16 15  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  3 26  1  0
  3 27  1  0
  3 28  1  0
  9 31  1  0
 11 32  1  0
 14 33  1  0
 20 37  1  0
 19 36  1  0
 18 35  1  0
 17 34  1  0
  5 30  1  0
  4 29  1  0
M  END


  Mrv1652310091718352D          

 22 25  0  0  0  0            999 V2000
    0.6585   -0.0337    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7191    1.0252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4665    0.8585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7333    1.2366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5058    0.0344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5144   -0.3244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6908   -0.2772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8724    1.7448    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6777    2.5288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0487    1.7920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0392    0.7906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9671    0.3654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2434    1.0079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8117   -0.4116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7907    0.3182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0784   -0.0335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5961    1.1022    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3198    0.4596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3068   -0.3254    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.8541    2.5760    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8509   -1.2356    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7724    1.1494    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  4  3  2  0  0  0  0
  5  3  1  0  0  0  0
  7  6  2  0  0  0  0
 10  8  1  0  0  0  0
 10  9  1  0  0  0  0
 11  4  1  0  0  0  0
 12  6  1  0  0  0  0
 13  8  2  0  0  0  0
 13 11  1  0  0  0  0
 14  5  2  0  0  0  0
 15 12  2  0  0  0  0
 15 13  1  0  0  0  0
 16 11  2  0  0  0  0
 16 14  1  0  0  0  0
 17 10  2  0  0  0  0
 17 12  1  0  0  0  0
 18  1  1  0  0  0  0
 18  2  1  0  0  0  0
 18  7  1  0  0  0  0
 19 15  1  0  0  0  0
 19 16  1  0  0  0  0
 20  9  2  0  0  0  0
 21 14  1  0  0  0  0
 22 17  1  0  0  0  0
 22 18  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0201683

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)OC2=C(C=O)C=C3C(NC4=C3C=CC=C4O)=C2C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C18H15NO3/c1-18(2)7-6-12-15-13(8-10(9-20)17(12)22-18)11-4-3-5-14(21)16(11)19-15/h3-9,19,21H,1-2H3

> <INCHI_KEY>
FKSZZYVPIDFKQY-UHFFFAOYSA-N

> <FORMULA>
C18H15NO3

> <MOLECULAR_WEIGHT>
293.322

> <EXACT_MASS>
293.105193347

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
37

> <JCHEM_AVERAGE_POLARIZABILITY>
31.814151504537946

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
15-hydroxy-5,5-dimethyl-6-oxa-17-azatetracyclo[8.7.0.0^{2,7}.0^{11,16}]heptadeca-1,3,7,9,11(16),12,14-heptaene-8-carbaldehyde

> <ALOGPS_LOGP>
4.12

> <JCHEM_LOGP>
3.4004461143333327

> <ALOGPS_LOGS>
-4.52

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.859844447776947

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.314470867607325

> <JCHEM_PKA_STRONGEST_BASIC>
-4.9478897481891115

> <JCHEM_POLAR_SURFACE_AREA>
62.32000000000001

> <JCHEM_REFRACTIVITY>
86.43050000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.78e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
15-hydroxy-5,5-dimethyl-6-oxa-17-azatetracyclo[8.7.0.0^{2,7}.0^{11,16}]heptadeca-1,3,7,9,11(16),12,14-heptaene-8-carbaldehyde

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-OCT-17   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-OCT-17         0                                  
HETATM    1  C   UNK     0       1.229  -0.063   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.342   1.914   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      12.071   1.603   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.702   2.308   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      12.144   0.064   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.694  -0.606   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.156  -0.517   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.228   3.257   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.998   4.720   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.691   3.345   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.407   1.476   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.539   0.682   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.921   1.881   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.849  -0.768   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.076   0.594   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.480  -0.063   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.846   2.057   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.464   0.858   0.000  0.00  0.00           C+0
HETATM   19  N   UNK     0       8.039  -0.607   0.000  0.00  0.00           N+0
HETATM   20  O   UNK     0       3.461   4.809   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      10.922  -2.307   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       3.309   2.146   0.000  0.00  0.00           O+0
CONECT    1   18                                                            
CONECT    2   18                                                            
CONECT    3    4    5                                                       
CONECT    4    3   11                                                       
CONECT    5    3   14                                                       
CONECT    6    7   12                                                       
CONECT    7    6   18                                                       
CONECT    8   10   13                                                       
CONECT    9   10   20                                                       
CONECT   10    8    9   17                                                  
CONECT   11    4   13   16                                                  
CONECT   12    6   15   17                                                  
CONECT   13    8   11   15                                                  
CONECT   14    5   16   21                                                  
CONECT   15   12   13   19                                                  
CONECT   16   11   14   19                                                  
CONECT   17   10   12   22                                                  
CONECT   18    1    2    7   22                                             
CONECT   19   15   16                                                       
CONECT   20    9                                                            
CONECT   21   14                                                            
CONECT   22   17   18                                                       
MASTER        0    0    0    0    0    0    0    0   22    0   50    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₁₅NO₃

Average Mass

293.3220 Da

Monoisotopic Mass

293.10519 Da

IUPAC Name

15-hydroxy-5,5-dimethyl-6-oxa-17-azatetracyclo[8.7.0.0^{2,7}.0^{11,16}]heptadeca-1,3,7,9,11(16),12,14-heptaene-8-carbaldehyde

Traditional Name

15-hydroxy-5,5-dimethyl-6-oxa-17-azatetracyclo[8.7.0.0^{2,7}.0^{11,16}]heptadeca-1,3,7,9,11(16),12,14-heptaene-8-carbaldehyde

CAS Registry Number

Not Available

SMILES

CC1(C)OC2=C(C=O)C=C3C(NC4=C3C=CC=C4O)=C2C=C1

InChI Identifier

InChI=1S/C18H15NO3/c1-18(2)7-6-12-15-13(8-10(9-20)17(12)22-18)11-4-3-5-14(21)16(11)19-15/h3-9,19,21H,1-2H3

InChI Key

FKSZZYVPIDFKQY-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
Clausena excavata	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
Benzopyran
1-benzopyran
Hydroxyindole
Indole
Alkyl aryl ether
1-hydroxy-4-unsubstituted benzenoid
Phenol
Aryl-aldehyde
1-hydroxy-2-unsubstituted benzenoid
Benzenoid
Pyrrole
Heteroaromatic compound
Ether
Azacycle
Oxacycle
Organic oxygen compound
Organic oxide
Organic nitrogen compound
Organooxygen compound
Organonitrogen compound
Aldehyde
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	4.12	ALOGPS
logP	3.4	ChemAxon
logS	-4.5	ALOGPS
pKa (Strongest Acidic)	9.31	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	62.32 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	86.43 m³·mol⁻¹	ChemAxon
Polarizability	31.81 Å³	ChemAxon
Number of Rings	4	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

HMDB0170774

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

10756117

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 10-hydroxy-3,3-dimethyl-11h-pyrano[3,2-a]carbazole-5-carbaldehyde (NP0201683)

MOL for NP0201683 (10-hydroxy-3,3-dimethyl-11h-pyrano[3,2-a]carbazole-5-carbaldehyde)

3D MOL for NP0201683 (10-hydroxy-3,3-dimethyl-11h-pyrano[3,2-a]carbazole-5-carbaldehyde)

3D SDF for NP0201683 (10-hydroxy-3,3-dimethyl-11h-pyrano[3,2-a]carbazole-5-carbaldehyde)

3D-SDF for NP0201683 (10-hydroxy-3,3-dimethyl-11h-pyrano[3,2-a]carbazole-5-carbaldehyde)

PDB for NP0201683 (10-hydroxy-3,3-dimethyl-11h-pyrano[3,2-a]carbazole-5-carbaldehyde)

3D PDB for NP0201683 (10-hydroxy-3,3-dimethyl-11h-pyrano[3,2-a]carbazole-5-carbaldehyde)

SMILES for NP0201683 (10-hydroxy-3,3-dimethyl-11h-pyrano[3,2-a]carbazole-5-carbaldehyde)

INCHI for NP0201683 (10-hydroxy-3,3-dimethyl-11h-pyrano[3,2-a]carbazole-5-carbaldehyde)

Structure for NP0201683 (10-hydroxy-3,3-dimethyl-11h-pyrano[3,2-a]carbazole-5-carbaldehyde)

3D Structure for NP0201683 (10-hydroxy-3,3-dimethyl-11h-pyrano[3,2-a]carbazole-5-carbaldehyde)