NP-MRD: Showing NP-Card for Mooniine A (NP0082377)

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Record Information

Version

2.0

Created at

2022-04-29 03:24:46 UTC

Updated at

2022-04-29 03:24:46 UTC

NP-MRD ID

NP0082377

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Mooniine A

Description

Mooniine A is found in Erythroxylum moonii .

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292205242D          

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M  END

     RDKit          3D

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M  END


  Mrv1652304292205242D          

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    5.7358    5.8040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2215    5.1589    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4050    4.3546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1483    5.3907    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.9188    6.5473    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4540    7.2289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6314    7.1673    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8120    7.9722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3473    8.6538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0255    1.3508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6130    2.0653    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6130    0.6363    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7880    0.6363    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4300    1.3796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6257    1.5632    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9807    1.0488    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9807    0.2238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6257   -0.2905    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4300   -0.1070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3940    0.6363    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5690    0.6363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4339   -0.0576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1483   -0.4701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1483   -1.2951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4339   -1.7076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7194   -1.2951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7194   -0.4701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  1  4  1  0  0  0  0
  4  5  1  1  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  5 10  1  0  0  0  0
  3 11  1  6  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 14 13  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 14 20  1  0  0  0  0
 19 21  1  1  0  0  0
 16 21  1  1  0  0  0
 17 22  1  1  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
  2 27  1  1  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 30 29  1  6  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 30 36  1  0  0  0  0
 35 37  1  1  0  0  0
 32 37  1  1  0  0  0
 37 38  1  0  0  0  0
  1 39  1  6  0  0  0
 39 40  2  0  0  0  0
 40 41  1  0  0  0  0
 41 42  2  0  0  0  0
 42 43  1  0  0  0  0
 43 44  2  0  0  0  0
 39 44  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0082377

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC(=O)O[C@@H]1C[C@H]2C[C@H](C[C@@H]1N2)OC(=O)[C@H]1[C@@H]([C@H]([C@@H]1C1=CC=CC=C1)C1=CC=CC=C1)C(=O)O[C@@H]1C[C@@H]2CC[C@H](C1)N2C

> <INCHI_IDENTIFIER>
InChI=1S/C36H44N2O6/c1-3-30(39)44-29-17-23-16-26(20-28(29)37-23)42-35(40)33-31(21-10-6-4-7-11-21)32(22-12-8-5-9-13-22)34(33)36(41)43-27-18-24-14-15-25(19-27)38(24)2/h4-13,23-29,31-34,37H,3,14-20H2,1-2H3/t23-,24-,25+,26-,27+,28+,29-,31+,32+,33-,34-/m1/s1

> <INCHI_KEY>
RIVCLOHZRRTVNF-LTGPJTOPSA-N

> <FORMULA>
C36H44N2O6

> <MOLECULAR_WEIGHT>
600.756

> <EXACT_MASS>
600.319937145

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
88

> <JCHEM_AVERAGE_POLARIZABILITY>
65.93450922400805

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
1-(1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl 2-(1R,3R,5S,6R)-6-(propanoyloxy)-8-azabicyclo[3.2.1]octan-3-yl (1R,2R,3S,4S)-3,4-diphenylcyclobutane-1,2-dicarboxylate

> <ALOGPS_LOGP>
4.29

> <JCHEM_LOGP>
4.072389111

> <ALOGPS_LOGS>
-5.57

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
2

> <JCHEM_PKA_STRONGEST_BASIC>
9.977437792843252

> <JCHEM_POLAR_SURFACE_AREA>
94.16999999999999

> <JCHEM_REFRACTIVITY>
164.1757999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.60e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-(1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl 2-(1R,3R,5S,6R)-6-(propanoyloxy)-8-azabicyclo[3.2.1]octan-3-yl (1R,2R,3S,4S)-3,4-diphenylcyclobutane-1,2-dicarboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0      10.143   1.433   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.054   2.522   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      10.143   3.610   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.232   2.522   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      12.772   2.522   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      13.542   3.855   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      15.082   3.855   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      15.852   2.522   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      15.082   1.188   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      13.542   1.188   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.143   5.150   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       8.810   5.920   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0      11.477   5.920   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      11.477   7.460   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      12.864   8.129   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      13.207   9.630   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      12.247  10.834   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      10.707  10.834   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.747   9.630   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      10.089   8.129   0.000  0.00  0.00           C+0
HETATM   21  N   UNK     0      11.477  10.063   0.000  0.00  0.00           N+0
HETATM   22  O   UNK     0      12.915  12.222   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      12.048  13.494   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      10.512  13.379   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      12.716  14.881   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      11.848  16.154   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       7.514   2.522   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       6.744   3.855   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       6.744   1.188   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       5.204   1.188   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.536   2.575   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       3.035   2.918   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       1.831   1.958   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       1.831   0.418   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       3.035  -0.542   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       4.536  -0.200   0.000  0.00  0.00           C+0
HETATM   37  N   UNK     0       2.602   1.188   0.000  0.00  0.00           N+0
HETATM   38  C   UNK     0       1.062   1.188   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      10.143  -0.107   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      11.477  -0.877   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      11.477  -2.417   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      10.143  -3.187   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       8.810  -2.417   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       8.810  -0.877   0.000  0.00  0.00           C+0
CONECT    1    2    4   39                                                  
CONECT    2    1    3   27                                                  
CONECT    3    2    4   11                                                  
CONECT    4    3    1    5                                                  
CONECT    5    4    6   10                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9    5                                                       
CONECT   11    3   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15   20                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   21                                                  
CONECT   17   16   18   22                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19   14                                                       
CONECT   21   19   16                                                       
CONECT   22   17   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25                                                            
CONECT   27    2   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30                                                       
CONECT   30   29   31   36                                                  
CONECT   31   30   32                                                       
CONECT   32   31   33   37                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36   37                                                  
CONECT   36   35   30                                                       
CONECT   37   35   32   38                                                  
CONECT   38   37                                                            
CONECT   39    1   40   44                                                  
CONECT   40   39   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   44                                                       
CONECT   44   43   39                                                       
MASTER        0    0    0    0    0    0    0    0   44    0  100    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₆H₄₄N₂O₆

Average Mass

600.7560 Da

Monoisotopic Mass

600.31994 Da

IUPAC Name

1-(1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl 2-(1R,3R,5S,6R)-6-(propanoyloxy)-8-azabicyclo[3.2.1]octan-3-yl (1R,2R,3S,4S)-3,4-diphenylcyclobutane-1,2-dicarboxylate

Traditional Name

1-(1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl 2-(1R,3R,5S,6R)-6-(propanoyloxy)-8-azabicyclo[3.2.1]octan-3-yl (1R,2R,3S,4S)-3,4-diphenylcyclobutane-1,2-dicarboxylate

CAS Registry Number

Not Available

SMILES

CCC(=O)O[C@@H]1C[C@H]2C[C@H](C[C@@H]1N2)OC(=O)[C@H]1[C@@H]([C@H]([C@@H]1C1=CC=CC=C1)C1=CC=CC=C1)C(=O)O[C@@H]1C[C@@H]2CC[C@H](C1)N2C

InChI Identifier

InChI=1S/C36H44N2O6/c1-3-30(39)44-29-17-23-16-26(20-28(29)37-23)42-35(40)33-31(21-10-6-4-7-11-21)32(22-12-8-5-9-13-22)34(33)36(41)43-27-18-24-14-15-25(19-27)38(24)2/h4-13,23-29,31-34,37H,3,14-20H2,1-2H3/t23-,24-,25+,26-,27+,28+,29-,31+,32+,33-,34-/m1/s1

InChI Key

RIVCLOHZRRTVNF-LTGPJTOPSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Erythroxylum moonii	Plant	KNApSAcK

Chemical Taxonomy

Classification

Not classified

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	4.29	ALOGPS
logP	4.07	ChemAxon
logS	-5.6	ALOGPS
pKa (Strongest Basic)	9.98	ChemAxon
Physiological Charge	2	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	94.17 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	164.18 m³·mol⁻¹	ChemAxon
Polarizability	65.93 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	Yes	ChemAxon

External Links

Not Available

References

General References

Not Available

Showing NP-Card for Mooniine A (NP0082377)

MOL for NP0082377 (Mooniine A)

3D MOL for NP0082377 (Mooniine A)

3D SDF for NP0082377 (Mooniine A)

3D-SDF for NP0082377 (Mooniine A)

PDB for NP0082377 (Mooniine A)

3D PDB for NP0082377 (Mooniine A)

SMILES for NP0082377 (Mooniine A)

INCHI for NP0082377 (Mooniine A)

Structure for NP0082377 (Mooniine A)

3D Structure for NP0082377 (Mooniine A)