NP-MRD: Showing NP-Card for O-acetylpolyneurine L (NP0332068)

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Record Information

Version

2.0

Created at

2023-10-31 20:21:24 UTC

Updated at

2024-09-03 04:17:52 UTC

NP-MRD ID

NP0332068

Natural Product DOI

https://doi.org/10.57994/1196

Secondary Accession Numbers

None

Natural Product Identification

Common Name

O-acetylpolyneurine L

Description

O-acetylpolyneurine L belongs to the class of organic compounds known as indoles. Indoles are compounds containing an indole moiety, which consists of pyrrole ring fused to benzene to form 2,3-benzopyrrole. Based on a literature review very few articles have been published on O-acetylpolyneurine L.

Structure

MOL SDF PDB SMILES InChI


  Mrv2104 10312320212D          

 31 34  0  0  1  0            999 V2000
    8.4147    0.0682    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0705   -0.6816    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.8668   -1.4118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8094   -2.1677    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.9723   -2.4247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1500   -2.1710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7108   -1.4532    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8535   -0.6406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5114   -0.1131    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.8365    0.3614    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7793    0.6673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2374    1.2894    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5052    2.0697    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5890    0.8255    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3710   -0.1548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1248   -0.2538    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.5317   -0.8273    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8939   -1.5685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4330   -2.2528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6100   -2.1958    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2478   -1.4545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7087   -0.7703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6771   -2.2833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2590   -1.6563    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.7790   -2.2968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4843   -3.0674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9661   -1.2313    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.6877   -1.6312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3948   -1.2062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7022   -2.4561    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.9255   -0.8685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  9  8  1  0  0  0  0
  9 10  1  1  0  0  0
  9 11  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 11 14  2  0  0  0  0
  9 15  1  0  0  0  0
  2 15  1  0  0  0  0
  8 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
  7 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 17 22  1  0  0  0  0
  4 23  1  0  0  0  0
 24 23  1  0  0  0  0
 24 25  1  1  0  0  0
 25 26  1  0  0  0  0
 24 27  1  6  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  2  0  0  0  0
 24 31  1  0  0  0  0
  2 31  1  0  0  0  0
M  END


  Mrv2104 10312320212D          

 31 34  0  0  1  0            999 V2000
    8.4147    0.0682    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0705   -0.6816    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.8668   -1.4118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8094   -2.1677    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.9723   -2.4247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1500   -2.1710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7108   -1.4532    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8535   -0.6406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5114   -0.1131    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.8365    0.3614    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7793    0.6673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2374    1.2894    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5052    2.0697    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5890    0.8255    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3710   -0.1548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1248   -0.2538    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.5317   -0.8273    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8939   -1.5685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4330   -2.2528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6100   -2.1958    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2478   -1.4545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7087   -0.7703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6771   -2.2833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2590   -1.6563    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.7790   -2.2968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4843   -3.0674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9661   -1.2313    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.6877   -1.6312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3948   -1.2062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7022   -2.4561    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.9255   -0.8685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  9  8  1  0  0  0  0
  9 10  1  1  0  0  0
  9 11  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 11 14  2  0  0  0  0
  9 15  1  0  0  0  0
  2 15  1  0  0  0  0
  8 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
  7 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 17 22  1  0  0  0  0
  4 23  1  0  0  0  0
 24 23  1  0  0  0  0
 24 25  1  1  0  0  0
 25 26  1  0  0  0  0
 24 27  1  6  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  2  0  0  0  0
 24 31  1  0  0  0  0
  2 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0332068

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@]12CN(C[C@](CC)(C1)OC(C)=O)CCC1=C(NC3=C1C=CC=C3)[C@@](O)(C2)C(=O)OC

> <INCHI_IDENTIFIER>
InChI=1S/C23H30N2O5/c1-4-22(30-15(2)26)11-16-12-23(28,21(27)29-3)20-18(9-10-25(13-16)14-22)17-7-5-6-8-19(17)24-20/h5-8,16,24,28H,4,9-14H2,1-3H3/t16-,22-,23-/m0/s1

> <INCHI_KEY>
SIWYHGZUOWYPKF-GMWOSMDTSA-N

> <FORMULA>
C23H30N2O5

> <MOLECULAR_WEIGHT>
414.502

> <EXACT_MASS>
414.215472074

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
44.274899263826

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (13S,15R,17S)-17-(acetyloxy)-17-ethyl-13-hydroxy-1,11-diazatetracyclo[13.3.1.0^{4,12}.0^{5,10}]nonadeca-4(12),5(10),6,8-tetraene-13-carboxylate

> <JCHEM_LOGP>
2.277635662333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
16.53173869967741

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.46340495102487

> <JCHEM_PKA_STRONGEST_BASIC>
7.768740707427909

> <JCHEM_POLAR_SURFACE_AREA>
91.86000000000001

> <JCHEM_REFRACTIVITY>
112.2565

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
methyl (13S,15R,17S)-17-(acetyloxy)-17-ethyl-13-hydroxy-1,11-diazatetracyclo[13.3.1.0^{4,12}.0^{5,10}]nonadeca-4(12),5(10),6,8-tetraene-13-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 31-OCT-23   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   31-OCT-23         0                                  
HETATM    1  H   UNK     0      15.707   0.127   0.000  0.00  0.00           H+0
HETATM    2  C   UNK     0      15.065  -1.272   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      14.685  -2.635   0.000  0.00  0.00           C+0
HETATM    4  N   UNK     0      14.578  -4.046   0.000  0.00  0.00           N+0
HETATM    5  C   UNK     0      13.015  -4.526   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      11.480  -4.052   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.660  -2.713   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      10.927  -1.196   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      12.155  -0.211   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      10.895   0.675   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      12.655   1.246   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      11.643   2.407   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      12.143   3.863   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      14.166   1.541   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      13.759  -0.289   0.000  0.00  0.00           C+0
HETATM   16  N   UNK     0       9.566  -0.474   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0       8.459  -1.544   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.135  -2.928   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.275  -4.205   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.739  -4.099   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.063  -2.715   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.923  -1.438   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      16.197  -4.262   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      17.283  -3.092   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      18.254  -4.287   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      17.704  -5.726   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      18.603  -2.298   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      19.950  -3.045   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      21.270  -2.252   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      19.977  -4.585   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      16.661  -1.621   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   15   31                                             
CONECT    3    2    4                                                       
CONECT    4    3    5   23                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   18                                                  
CONECT    8    7    9   16                                                  
CONECT    9    8   10   11   15                                             
CONECT   10    9                                                            
CONECT   11    9   12   14                                                  
CONECT   12   11   13                                                       
CONECT   13   12                                                            
CONECT   14   11                                                            
CONECT   15    9    2                                                       
CONECT   16    8   17                                                       
CONECT   17   16   18   22                                                  
CONECT   18   17    7   19                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   17                                                       
CONECT   23    4   24                                                       
CONECT   24   23   25   27   31                                             
CONECT   25   24   26                                                       
CONECT   26   25                                                            
CONECT   27   24   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28                                                            
CONECT   31   24    2                                                       
MASTER        0    0    0    0    0    0    0    0   31    0   68    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₃₀N₂O₅

Average Mass

414.5020 Da

Monoisotopic Mass

414.21547 Da

IUPAC Name

methyl (13S,15R,17S)-17-(acetyloxy)-17-ethyl-13-hydroxy-1,11-diazatetracyclo[13.3.1.0^{4,12}.0^{5,10}]nonadeca-4(12),5(10),6,8-tetraene-13-carboxylate

Traditional Name

methyl (13S,15R,17S)-17-(acetyloxy)-17-ethyl-13-hydroxy-1,11-diazatetracyclo[13.3.1.0^{4,12}.0^{5,10}]nonadeca-4(12),5(10),6,8-tetraene-13-carboxylate

CAS Registry Number

Not Available

SMILES

[H][C@]12CN(C[C@](CC)(C1)OC(C)=O)CCC1=C(NC3=C1C=CC=C3)[C@@](O)(C2)C(=O)OC

InChI Identifier

InChI=1S/C23H30N2O5/c1-4-22(30-15(2)26)11-16-12-23(28,21(27)29-3)20-18(9-10-25(13-16)14-22)17-7-5-6-8-19(17)24-20/h5-8,16,24,28H,4,9-14H2,1-3H3/t16-,22-,23-/m0/s1

InChI Key

SIWYHGZUOWYPKF-GMWOSMDTSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
HSQC NMR	[¹H, ¹³C] NMR Spectrum (2D, 600 MHz, CDCl3, experimental)	yylow@um.edu.my	Department of Chemistry, Faculty of Science, Universiti Malaya	Yun-Yee Low	2024-05-04	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, CDCl3, experimental)	yylow@um.edu.my	Department of Chemistry, Faculty of Science, Universiti Malaya	Yun-Yee Low	2024-05-04	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CDCl3, experimental)	yylow@um.edu.my	Department of Chemistry, Faculty of Science, Universiti Malaya	Yun-Yee Low	2024-05-04	View Spectrum
HMBC NMR	[¹H, ¹³C] NMR Spectrum (2D, 600 MHz, CDCl3, experimental)	yylow@um.edu.my	Department of Chemistry, Faculty of Science, Universiti Malaya	Yun-Yee Low	2024-05-04	View Spectrum
COSY NMR	[¹H, ¹H] NMR Spectrum (2D, 600 MHz, CDCl3, experimental)	yylow@um.edu.my	Department of Chemistry, Faculty of Science, Universiti Malaya	Yun-Yee Low	2024-05-04	View Spectrum
NOESY NMR	[¹H, ¹H] NMR Spectrum (2D, 600 MHz, CDCl3, experimental)	yylow@um.edu.my	Department of Chemistry, Faculty of Science, Universiti Malaya	Yun-Yee Low	2024-05-04	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Tabernaemontana polyneura		Not Available

Chemical Taxonomy

Description

This compound belongs to the class of organic compounds known as indoles. These are compounds containing an indole moiety, which consists of pyrrole ring fused to benzene to form 2,3-benzopyrrole.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Indoles

Direct Parent

Indoles

Alternative Parents

Substituents

Indole
Fatty acid ester
Fatty acyl
Benzenoid
Substituted pyrrole
Piperidine
Dicarboxylic acid or derivatives
Heteroaromatic compound
Methyl ester
Tertiary alcohol
Pyrrole
Tertiary aliphatic amine
Tertiary amine
Carboxylic acid ester
Amino acid or derivatives
Azacycle
Secondary amine
Secondary aliphatic amine
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Amine
Alcohol
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	2.28	ChemAxon
pKa (Strongest Acidic)	11.46	ChemAxon
pKa (Strongest Basic)	7.77	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	91.86 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	112.26 m³·mol⁻¹	ChemAxon
Polarizability	44.27 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

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

Showing NP-Card for O-acetylpolyneurine L (NP0332068)

MOL for NP0332068 (O-acetylpolyneurine L)

3D MOL for NP0332068 (O-acetylpolyneurine L)

3D SDF for NP0332068 (O-acetylpolyneurine L)

3D-SDF for NP0332068 (O-acetylpolyneurine L)

PDB for NP0332068 (O-acetylpolyneurine L)

3D PDB for NP0332068 (O-acetylpolyneurine L)

SMILES for NP0332068 (O-acetylpolyneurine L)

INCHI for NP0332068 (O-acetylpolyneurine L)

Structure for NP0332068 (O-acetylpolyneurine L)

3D Structure for NP0332068 (O-acetylpolyneurine L)