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Showing NP-Card for Mukolidine (NP0067029)

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Record Information
Version2.0
Created at2022-04-28 11:13:39 UTC
Updated at2022-04-28 11:13:39 UTC
NP-MRD IDNP0067029
Secondary Accession NumbersNone
Natural Product Identification
Common NameMukolidine
DescriptionMukolidine 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. Mukolidine is an extremely weak basic (essentially neutral) compound (based on its pKa). Outside of the human body, Mukolidine has been detected, but not quantified in, herbs and spices. Mukolidine is found in Murraya koenigii . This could make mukolidine a potential biomarker for the consumption of these foods.
Structure
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MOL3D MOLSDFPDBSMILESInChI

MOL for NP0067029 (Mukolidine)


  Mrv0541 05061312402D          

 17 19  0  0  0  0            999 V2000
    1.7172    2.9069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4820    0.5531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2890    0.3816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2271    1.3377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2800    1.3377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7279    1.9508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2180    0.3816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5771   -0.0600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0250    0.5531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8410    0.9946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6660    0.9946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9210    1.7793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7791    1.9508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5861    1.7793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2535    2.2642    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.3840    0.1115    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5242    2.7354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  3  2  2  0  0  0  0
  4  2  1  0  0  0  0
  6  5  2  0  0  0  0
  9  5  1  0  0  0  0
  9  7  2  0  0  0  0
  9  8  1  0  0  0  0
 10  3  1  0  0  0  0
 11  7  1  0  0  0  0
 11 10  1  0  0  0  0
 12  6  1  0  0  0  0
 12 11  2  0  0  0  0
 13  4  2  0  0  0  0
 14 10  2  0  0  0  0
 14 13  1  0  0  0  0
 15 12  1  0  0  0  0
 15 14  1  0  0  0  0
 16  8  2  0  0  0  0
 17  1  1  0  0  0  0
 17 13  1  0  0  0  0
M  END
Download

3D MOL for NP0067029 (Mukolidine)

     RDKit          3D

 28 30  0  0  0  0  0  0  0  0999 V2000
    4.6085    1.2094    0.2395 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2260    1.2043    0.4060 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3670    0.2581   -0.1176 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8159   -0.7945   -0.8729 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9322   -1.7233   -1.3819 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5828   -1.6213   -1.1482 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1149   -0.5731   -0.3935 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0150    0.3606    0.1168 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2397    1.2430    0.7990 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0584    0.8927    0.7257 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2209    1.4499    1.2392 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4551    0.8592    0.9981 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5782   -0.2910    0.2482 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8809   -0.8919    0.0087 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9859   -1.9371   -0.6735 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4157   -0.8355   -0.2568 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1771   -0.2592   -0.0258 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0684    0.2323    0.0889 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8309    1.8931   -0.6287 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0599    1.6537    1.1687 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8738   -0.9420   -1.1011 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2583   -2.5640   -1.9812 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1367   -2.3446   -1.5407 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6606    2.0612    1.2915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1210    2.3573    1.8304 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3422    1.3030    1.4023 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7822   -0.4616    0.4058 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4996   -1.7387   -0.8472 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
 10 17  2  0
 17 16  1  0
 16 13  2  0
 13 14  1  0
 14 15  2  0
 13 12  1  0
 12 11  2  0
  8  3  1  0
 11 10  1  0
 17  7  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  4 21  1  0
  5 22  1  0
  6 23  1  0
  9 24  1  0
 16 28  1  0
 14 27  1  0
 12 26  1  0
 11 25  1  0
M  END
Download

3D SDF for NP0067029 (Mukolidine)


  Mrv0541 05061312402D          

 17 19  0  0  0  0            999 V2000
    1.7172    2.9069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4820    0.5531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2890    0.3816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2271    1.3377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2800    1.3377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7279    1.9508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2180    0.3816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5771   -0.0600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0250    0.5531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8410    0.9946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6660    0.9946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9210    1.7793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7791    1.9508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5861    1.7793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2535    2.2642    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.3840    0.1115    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5242    2.7354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  3  2  2  0  0  0  0
  4  2  1  0  0  0  0
  6  5  2  0  0  0  0
  9  5  1  0  0  0  0
  9  7  2  0  0  0  0
  9  8  1  0  0  0  0
 10  3  1  0  0  0  0
 11  7  1  0  0  0  0
 11 10  1  0  0  0  0
 12  6  1  0  0  0  0
 12 11  2  0  0  0  0
 13  4  2  0  0  0  0
 14 10  2  0  0  0  0
 14 13  1  0  0  0  0
 15 12  1  0  0  0  0
 15 14  1  0  0  0  0
 16  8  2  0  0  0  0
 17  1  1  0  0  0  0
 17 13  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0067029

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=CC2=C1NC1=C2C=C(C=O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C14H11NO2/c1-17-13-4-2-3-10-11-7-9(8-16)5-6-12(11)15-14(10)13/h2-8,15H,1H3

> <INCHI_KEY>
KSTPFEFAPRYLOZ-UHFFFAOYSA-N

> <FORMULA>
C14H11NO2

> <MOLECULAR_WEIGHT>
225.2426

> <EXACT_MASS>
225.078978601

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_AVERAGE_POLARIZABILITY>
24.128797927244694

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
8-methoxy-9H-carbazole-3-carbaldehyde

> <ALOGPS_LOGP>
3.13

> <JCHEM_LOGP>
2.645716768333333

> <ALOGPS_LOGS>
-4.00

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.43582852693062

> <JCHEM_PKA_STRONGEST_BASIC>
-4.886153623856048

> <JCHEM_POLAR_SURFACE_AREA>
42.09

> <JCHEM_REFRACTIVITY>
66.51939999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.26e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
8-methoxy-9H-carbazole-3-carbaldehyde

> <JCHEM_VEBER_RULE>
0

$$$$
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3D-SDF for NP0067029 (Mukolidine)

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PDB for NP0067029 (Mukolidine)
HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0       3.205   5.426   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.633   1.032   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.139   0.712   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.157   2.497   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      11.723   2.497   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.692   3.641   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.740   0.712   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      12.277  -0.112   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      11.247   1.032   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.170   1.857   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.710   1.857   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.186   3.321   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.188   3.641   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.694   3.321   0.000  0.00  0.00           C+0
HETATM   15  N   UNK     0       7.940   4.227   0.000  0.00  0.00           N+0
HETATM   16  O   UNK     0      13.783   0.208   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       4.712   5.106   0.000  0.00  0.00           O+0
CONECT    1   17                                                            
CONECT    2    3    4                                                       
CONECT    3    2   10                                                       
CONECT    4    2   13                                                       
CONECT    5    6    9                                                       
CONECT    6    5   12                                                       
CONECT    7    9   11                                                       
CONECT    8    9   16                                                       
CONECT    9    5    7    8                                                  
CONECT   10    3   11   14                                                  
CONECT   11    7   10   12                                                  
CONECT   12    6   11   15                                                  
CONECT   13    4   14   17                                                  
CONECT   14   10   13   15                                                  
CONECT   15   12   14                                                       
CONECT   16    8                                                            
CONECT   17    1   13                                                       
MASTER        0    0    0    0    0    0    0    0   17    0   38    0
END

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3D PDB for NP0067029 (Mukolidine)
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SMILES for NP0067029 (Mukolidine)
COC1=CC=CC2=C1NC1=C2C=C(C=O)C=C1
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INCHI for NP0067029 (Mukolidine)
InChI=1S/C14H11NO2/c1-17-13-4-2-3-10-11-7-9(8-16)5-6-12(11)15-14(10)13/h2-8,15H,1H3
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View in JSmol
Synonyms
ValueSource
3-Formyl-8-methoxycarbazoleHMDB
6-Formyl-1-methoxycarbazoleHMDB
8-Methoxy-9H-carbazole-3-carboxaldehyde, 9ciHMDB
Chemical FormulaC14H11NO2
Average Mass225.2426 Da
Monoisotopic Mass225.07898 Da
IUPAC Name8-methoxy-9H-carbazole-3-carbaldehyde
Traditional Name8-methoxy-9H-carbazole-3-carbaldehyde
CAS Registry NumberNot Available
SMILES
COC1=CC=CC2=C1NC1=C2C=C(C=O)C=C1
InChI Identifier
InChI=1S/C14H11NO2/c1-17-13-4-2-3-10-11-7-9(8-16)5-6-12(11)15-14(10)13/h2-8,15H,1H3
InChI KeyKSTPFEFAPRYLOZ-UHFFFAOYSA-N
Experimental Spectra
Not Available
Predicted Spectra
Spectrum TypeDescriptionDepositor IDDepositor OrganizationDepositorDeposition DateView
1D NMR13C NMR Spectrum (1D, 25 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 252 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 1000 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 50 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 200 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 75 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 300 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 101 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 400 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 126 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 500 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 151 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 600 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 176 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 700 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 201 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 800 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 226 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
Chemical Shift Submissions
Not Available
Species
Species of Origin
Species NameSourceReference
Murraya koenigiiPlant
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.
KingdomOrganic compounds  
Super ClassOrganoheterocyclic compounds  
ClassIndoles and derivatives  
Sub ClassCarbazoles  
Direct ParentCarbazoles  
Alternative Parents
Substituents
  • Carbazole
    • 

  • Indole
    • 

  • Anisole
    • 

  • Alkyl aryl ether
    • 

  • Aryl-aldehyde
    • 

  • Benzenoid
    • 

  • Pyrrole
    • 

  • Heteroaromatic compound
    • 

  • Ether
    • 

  • Azacycle
    • 

  • Hydrocarbon derivative
    • 

  • Aldehyde
    • 

  • Organooxygen compound
    • 

  • Organonitrogen compound
    • 

  • Organic oxide
    • 

  • Organopnictogen compound
    • 

  • Organic oxygen compound
    • 

  • Organic nitrogen compound
    • 

  • Aromatic heteropolycyclic compound
Molecular FrameworkAromatic heteropolycyclic compounds
External DescriptorsNot Available
Physical Properties
StateNot Available
Experimental Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Predicted Properties
PropertyValueSource
logP3.13ALOGPS
logP2.65ChemAxon
logS-4ALOGPS
pKa (Strongest Acidic)13.44ChemAxon
pKa (Strongest Basic)-4.9ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count2ChemAxon
Hydrogen Donor Count1ChemAxon
Polar Surface Area42.09 ŲChemAxon
Rotatable Bond Count2ChemAxon
Refractivity66.52 m³·mol⁻¹ChemAxon
Polarizability24.13 ųChemAxon
Number of Rings3ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
HMDB IDHMDB0041443  
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FoodDB IDFDB021394  
KNApSAcK IDC00024716  
Chemspider IDNot Available
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound53465568  
PDB IDNot Available
ChEBI IDNot Available
Good Scents IDNot Available
References
General ReferencesNot Available