NP-MRD: Showing NP-Card for (1r,14s,16r,20s,22s)-22-(acetyloxy)-5,8-dimethoxy-24-azapentacyclo[14.7.1.1²,⁶.1⁷,¹¹.0²⁰,²⁴]hexacosa-2,4,6(26),7(25),8,10-hexaen-14-yl acetate (NP0280154)

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Record Information

Version

2.0

Created at

2022-09-09 05:47:29 UTC

Updated at

2022-09-09 05:47:29 UTC

NP-MRD ID

NP0280154

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,14s,16r,20s,22s)-22-(acetyloxy)-5,8-dimethoxy-24-azapentacyclo[14.7.1.1²,⁶.1⁷,¹¹.0²⁰,²⁴]hexacosa-2,4,6(26),7(25),8,10-hexaen-14-yl acetate

Description

(1R,14S,16R,20S,22S)-14-(acetyloxy)-5,8-dimethoxy-24-azapentacyclo[14.7.1.1²,⁶.1⁷,¹¹.0²⁰,²⁴]Hexacosa-2(26),3,5,7,9,11(25)-hexaen-22-yl acetate belongs to the class of organic compounds known as quinolizidines. Quinolizidines are compounds containing a quinolizidine moiety, which is a octahydro-2H-quinolizine derivative. Based on a literature review very few articles have been published on (1R,14S,16R,20S,22S)-14-(acetyloxy)-5,8-dimethoxy-24-azapentacyclo[14.7.1.1²,⁶.1⁷,¹¹.0²⁰,²⁴]Hexacosa-2(26),3,5,7,9,11(25)-hexaen-22-yl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092207472D          

 38 42  0  0  1  0            999 V2000
   10.0564   -0.4946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  6 37  1  0  0  0  0
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 17 38  1  1  0  0  0
M  END

     RDKit          2D

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M  END


  Mrv1652309092207472D          

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    5.8398    4.6796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9384    3.7659    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7032    2.5893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4719    2.2898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6134    0.3490    0.0000 N   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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
  9 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 11 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  1  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 19 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  1  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  2  0  0  0  0
 31 36  1  0  0  0  0
 36 37  1  0  0  0  0
  6 37  1  0  0  0  0
 29 38  1  6  0  0  0
 25 38  1  6  0  0  0
 17 38  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0280154

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C2CC[C@@H](C[C@H]3CCC[C@H]4C[C@@H](C[C@@H](N34)C3=CC=C(OC)C(=C3)C1=C2)OC(C)=O)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C31H39NO6/c1-19(33)37-25-11-8-21-9-12-30(35-3)27(14-21)28-15-22(10-13-31(28)36-4)29-18-26(38-20(2)34)17-24-7-5-6-23(16-25)32(24)29/h9-10,12-15,23-26,29H,5-8,11,16-18H2,1-4H3/t23-,24+,25+,26+,29-/m1/s1

> <INCHI_KEY>
JEJLGHMYBHWNKG-BNUSXPRPSA-N

> <FORMULA>
C31H39NO6

> <MOLECULAR_WEIGHT>
521.654

> <EXACT_MASS>
521.27773798

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
77

> <JCHEM_AVERAGE_POLARIZABILITY>
57.981254690064226

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,14S,16R,20S,22S)-22-(acetyloxy)-5,8-dimethoxy-24-azapentacyclo[14.7.1.1^{2,6}.1^{7,11}.0^{20,24}]hexacosa-2,4,6(26),7(25),8,10-hexaen-14-yl acetate

> <JCHEM_LOGP>
4.3905851369999995

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_BASIC>
9.538492169343517

> <JCHEM_POLAR_SURFACE_AREA>
74.3

> <JCHEM_REFRACTIVITY>
144.58169999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,14S,16R,20S,22S)-22-(acetyloxy)-5,8-dimethoxy-24-azapentacyclo[14.7.1.1^{2,6}.1^{7,11}.0^{20,24}]hexacosa-2,4,6(26),7(25),8,10-hexaen-14-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0      18.772  -0.923   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      17.232  -0.909   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      16.474   0.431   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      17.256   1.758   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      16.498   3.098   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      14.958   3.112   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      14.176   1.786   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      14.934   0.445   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      13.900  -1.021   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      12.660  -1.935   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      11.249  -1.319   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      11.077   0.211   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      12.317   1.125   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      13.728   0.509   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      14.967   1.423   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      16.500   1.273   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.668  -0.469   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.227  -1.944   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.728  -2.299   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       7.286  -3.774   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       5.788  -4.129   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.346  -5.604   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       4.731  -3.009   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       6.671  -1.179   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       7.113   0.297   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.056   1.417   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.498   2.892   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       7.997   3.247   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       9.053   2.127   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       9.707   3.798   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      10.982   4.662   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      10.449   6.106   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      11.434   7.290   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      10.901   8.735   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      12.952   7.030   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      12.513   4.833   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      13.948   4.274   0.000  0.00  0.00           C+0
HETATM   38  N   UNK     0       8.612   0.652   0.000  0.00  0.00           N+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   37                                                  
CONECT    7    6    8                                                       
CONECT    8    7    3    9                                                  
CONECT    9    8   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   17                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13    9   15                                                  
CONECT   15   14   16                                                       
CONECT   16   15                                                            
CONECT   17   11   18   38                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   24                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   19   25                                                       
CONECT   25   24   26   38                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30   38                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32   36                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33                                                            
CONECT   36   31   37                                                       
CONECT   37   36    6                                                       
CONECT   38   29   25   17                                                  
MASTER        0    0    0    0    0    0    0    0   38    0   84    0
END

View in JSmol

Synonyms

Value	Source
(1R,14S,16R,20S,22S)-14-(Acetyloxy)-5,8-dimethoxy-24-azapentacyclo[14.7.1.1,.1,.0,]hexacosa-2(26),3,5,7,9,11(25)-hexaen-22-yl acetic acid	Generator

Chemical Formula

C₃₁H₃₉NO₆

Average Mass

521.6540 Da

Monoisotopic Mass

521.27774 Da

IUPAC Name

(1R,14S,16R,20S,22S)-22-(acetyloxy)-5,8-dimethoxy-24-azapentacyclo[14.7.1.1^{2,6}.1^{7,11}.0^{20,24}]hexacosa-2,4,6(26),7(25),8,10-hexaen-14-yl acetate

Traditional Name

(1R,14S,16R,20S,22S)-22-(acetyloxy)-5,8-dimethoxy-24-azapentacyclo[14.7.1.1^{2,6}.1^{7,11}.0^{20,24}]hexacosa-2,4,6(26),7(25),8,10-hexaen-14-yl acetate

CAS Registry Number

Not Available

SMILES

COC1=CC=C2CC[C@@H](C[C@H]3CCC[C@H]4C[C@@H](C[C@@H](N34)C3=CC=C(OC)C(=C3)C1=C2)OC(C)=O)OC(C)=O

InChI Identifier

InChI=1S/C31H39NO6/c1-19(33)37-25-11-8-21-9-12-30(35-3)27(14-21)28-15-22(10-13-31(28)36-4)29-18-26(38-20(2)34)17-24-7-5-6-23(16-25)32(24)29/h9-10,12-15,23-26,29H,5-8,11,16-18H2,1-4H3/t23-,24+,25+,26+,29-/m1/s1

InChI Key

JEJLGHMYBHWNKG-BNUSXPRPSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as quinolizidines. Quinolizidines are compounds containing a quinolizidine moiety, which is a octahydro-2H-quinolizine derivative.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Quinolizidines

Sub Class

Not Available

Direct Parent

Quinolizidines

Alternative Parents

Substituents

Quinolizidine
Anisole
Alkyl aryl ether
Aralkylamine
Dicarboxylic acid or derivatives
Piperidine
Benzenoid
Amino acid or derivatives
Carboxylic acid ester
Tertiary aliphatic amine
Tertiary amine
Carboxylic acid derivative
Ether
Azacycle
Amine
Hydrocarbon derivative
Organic oxide
Organic nitrogen compound
Carbonyl group
Organopnictogen compound
Organonitrogen compound
Organooxygen compound
Organic oxygen compound
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	4.39	ChemAxon
pKa (Strongest Basic)	9.54	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	74.3 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	144.58 m³·mol⁻¹	ChemAxon
Polarizability	57.98 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

162894734

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,14s,16r,20s,22s)-22-(acetyloxy)-5,8-dimethoxy-24-azapentacyclo[14.7.1.1²,⁶.1⁷,¹¹.0²⁰,²⁴]hexacosa-2,4,6(26),7(25),8,10-hexaen-14-yl acetate (NP0280154)

MOL for NP0280154 ((1r,14s,16r,20s,22s)-22-(acetyloxy)-5,8-dimethoxy-24-azapentacyclo[14.7.1.1²,⁶.1⁷,¹¹.0²⁰,²⁴]hexacosa-2,4,6(26),7(25),8,10-hexaen-14-yl acetate)

3D MOL for NP0280154 ((1r,14s,16r,20s,22s)-22-(acetyloxy)-5,8-dimethoxy-24-azapentacyclo[14.7.1.1²,⁶.1⁷,¹¹.0²⁰,²⁴]hexacosa-2,4,6(26),7(25),8,10-hexaen-14-yl acetate)

3D SDF for NP0280154 ((1r,14s,16r,20s,22s)-22-(acetyloxy)-5,8-dimethoxy-24-azapentacyclo[14.7.1.1²,⁶.1⁷,¹¹.0²⁰,²⁴]hexacosa-2,4,6(26),7(25),8,10-hexaen-14-yl acetate)

3D-SDF for NP0280154 ((1r,14s,16r,20s,22s)-22-(acetyloxy)-5,8-dimethoxy-24-azapentacyclo[14.7.1.1²,⁶.1⁷,¹¹.0²⁰,²⁴]hexacosa-2,4,6(26),7(25),8,10-hexaen-14-yl acetate)

PDB for NP0280154 ((1r,14s,16r,20s,22s)-22-(acetyloxy)-5,8-dimethoxy-24-azapentacyclo[14.7.1.1²,⁶.1⁷,¹¹.0²⁰,²⁴]hexacosa-2,4,6(26),7(25),8,10-hexaen-14-yl acetate)

3D PDB for NP0280154 ((1r,14s,16r,20s,22s)-22-(acetyloxy)-5,8-dimethoxy-24-azapentacyclo[14.7.1.1²,⁶.1⁷,¹¹.0²⁰,²⁴]hexacosa-2,4,6(26),7(25),8,10-hexaen-14-yl acetate)

SMILES for NP0280154 ((1r,14s,16r,20s,22s)-22-(acetyloxy)-5,8-dimethoxy-24-azapentacyclo[14.7.1.1²,⁶.1⁷,¹¹.0²⁰,²⁴]hexacosa-2,4,6(26),7(25),8,10-hexaen-14-yl acetate)

INCHI for NP0280154 ((1r,14s,16r,20s,22s)-22-(acetyloxy)-5,8-dimethoxy-24-azapentacyclo[14.7.1.1²,⁶.1⁷,¹¹.0²⁰,²⁴]hexacosa-2,4,6(26),7(25),8,10-hexaen-14-yl acetate)

Structure for NP0280154 ((1r,14s,16r,20s,22s)-22-(acetyloxy)-5,8-dimethoxy-24-azapentacyclo[14.7.1.1²,⁶.1⁷,¹¹.0²⁰,²⁴]hexacosa-2,4,6(26),7(25),8,10-hexaen-14-yl acetate)

3D Structure for NP0280154 ((1r,14s,16r,20s,22s)-22-(acetyloxy)-5,8-dimethoxy-24-azapentacyclo[14.7.1.1²,⁶.1⁷,¹¹.0²⁰,²⁴]hexacosa-2,4,6(26),7(25),8,10-hexaen-14-yl acetate)