NP-MRD: Showing NP-Card for Spiramine E (NP0067263)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-04-28 11:47:27 UTC

Updated at

2022-04-28 11:47:27 UTC

NP-MRD ID

NP0067263

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Spiramine E

Description

2-[(1R,5R,8R,10R,11R,12S,14S,16R,17R)-12-(acetyloxy)-5-methyl-13-methylidene-9-oxa-7-azahexacyclo[8.6.2.2¹¹,¹⁴.0¹,⁸.0⁵,¹⁷.0¹¹,¹⁶]Icosan-7-yl]ethyl acetate belongs to the class of organic compounds known as atisane diterpenoids. These are diterpenoids with a structure based on the atisane skeleton, which is a tetracyclic compound containing the [2,2,2]bicyc1ic ring system with the C15-C16 bridge attached at C12. Spiramine E is found in Spiraea japonica and Spiraea japonica var.acuminata. Based on a literature review very few articles have been published on 2-[(1R,5R,8R,10R,11R,12S,14S,16R,17R)-12-(acetyloxy)-5-methyl-13-methylidene-9-oxa-7-azahexacyclo[8.6.2.2¹¹,¹⁴.0¹,⁸.0⁵,¹⁷.0¹¹,¹⁶]Icosan-7-yl]ethyl acetate.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652304282213472D          

 32 37  0  0  1  0            999 V2000
    5.3197    0.9376    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.9051    0.2812    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.6655   -0.5082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2294   -1.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9897   -1.8999    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5536   -2.5022    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3140   -3.2916    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3571   -2.3150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7086    0.4890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7220    1.3491    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.0541    2.1332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5381    2.8097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7095    2.6455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2043    1.9186    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.8651    1.5054    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9466    1.3644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1984    0.9704    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7007    1.6732    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7300    1.8323    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3236    2.5862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5410    2.8474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0872    2.9382    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9446    3.0289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3666    2.2654    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2394    2.1170    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0614    1.2145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2510    1.1606    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4298    1.2395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0876    1.9902    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9508    0.5678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7274    0.3079    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5292    1.1786    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
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  2  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 14 13  1  6  0  0  0
  1 14  1  0  0  0  0
 14 15  1  0  0  0  0
 10 15  1  0  0  0  0
 15 16  1  1  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
 20 21  2  0  0  0  0
 22 20  1  6  0  0  0
 22 23  1  0  0  0  0
 24 23  1  1  0  0  0
 14 24  1  0  0  0  0
 18 24  1  0  0  0  0
 22 25  1  0  0  0  0
 25 26  1  0  0  0  0
 18 26  1  1  0  0  0
 19 27  1  1  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
 17 31  1  1  0  0  0
  1 31  1  6  0  0  0
 10 32  1  6  0  0  0
M  END


  Mrv1652304282213472D          

 32 37  0  0  1  0            999 V2000
    5.3197    0.9376    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.9051    0.2812    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.6655   -0.5082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2294   -1.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9897   -1.8999    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5536   -2.5022    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3140   -3.2916    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3571   -2.3150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7086    0.4890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7220    1.3491    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.0541    2.1332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5381    2.8097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7095    2.6455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2043    1.9186    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.8651    1.5054    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9466    1.3644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1984    0.9704    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7007    1.6732    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7300    1.8323    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3236    2.5862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5410    2.8474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0872    2.9382    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9446    3.0289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3666    2.2654    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2394    2.1170    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0614    1.2145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2510    1.1606    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4298    1.2395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0876    1.9902    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9508    0.5678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7274    0.3079    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5292    1.1786    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
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  2  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 14 13  1  6  0  0  0
  1 14  1  0  0  0  0
 14 15  1  0  0  0  0
 10 15  1  0  0  0  0
 15 16  1  1  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
 20 21  2  0  0  0  0
 22 20  1  6  0  0  0
 22 23  1  0  0  0  0
 24 23  1  1  0  0  0
 14 24  1  0  0  0  0
 18 24  1  0  0  0  0
 22 25  1  0  0  0  0
 25 26  1  0  0  0  0
 18 26  1  1  0  0  0
 19 27  1  1  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
 17 31  1  1  0  0  0
  1 31  1  6  0  0  0
 10 32  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0067263

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OCCN1C[C@]2(C)CCC[C@@]34[C@H]1O[C@H](C[C@H]23)[C@@]12CC[C@@H](C[C@@H]41)C(=C)[C@@H]2OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C26H37NO5/c1-15-18-6-9-26(22(15)31-17(3)29)20(12-18)25-8-5-7-24(4)14-27(10-11-30-16(2)28)23(25)32-21(26)13-19(24)25/h18-23H,1,5-14H2,2-4H3/t18-,19+,20-,21+,22-,23+,24-,25+,26+/m0/s1

> <INCHI_KEY>
OWDJZYOWYLOEJQ-KZOWRAFGSA-N

> <FORMULA>
C26H37NO5

> <MOLECULAR_WEIGHT>
443.584

> <EXACT_MASS>
443.267173295

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
69

> <JCHEM_AVERAGE_POLARIZABILITY>
57.36992452510072

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-[(1R,5R,8R,10R,11R,12S,14S,16R,17R)-12-(acetyloxy)-5-methyl-13-methylidene-9-oxa-7-azahexacyclo[8.6.2.2^{11,14}.0^{1,8}.0^{5,17}.0^{11,16}]icosan-7-yl]ethyl acetate

> <ALOGPS_LOGP>
3.02

> <JCHEM_LOGP>
2.965833220333335

> <ALOGPS_LOGS>
-4.54

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_BASIC>
6.993408141146883

> <JCHEM_POLAR_SURFACE_AREA>
65.07

> <JCHEM_REFRACTIVITY>
117.65339999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.28e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-[(1R,5R,8R,10R,11R,12S,14S,16R,17R)-12-(acetyloxy)-5-methyl-13-methylidene-9-oxa-7-azahexacyclo[8.6.2.2^{11,14}.0^{1,8}.0^{5,17}.0^{11,16}]icosan-7-yl]ethyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       9.930   1.750   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0      11.023   0.525   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0      10.576  -0.949   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.628  -2.073   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      11.181  -3.547   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      12.233  -4.671   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      11.786  -6.144   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      13.733  -4.321   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      12.523   0.913   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      12.548   2.518   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      13.168   3.982   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      12.204   5.245   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.658   4.938   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.715   3.581   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.948   2.810   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.234   2.547   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.837   1.811   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.908   3.123   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.096   3.420   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.337   4.828   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.877   5.315   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.763   5.485   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.363   5.654   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       8.151   4.229   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.047   3.952   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.715   2.267   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       4.202   2.166   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       2.669   2.314   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       2.030   3.715   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       1.775   1.060   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       8.824   0.575   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      14.054   2.200   0.000  0.00  0.00           C+0
CONECT    1    2   14   31                                                  
CONECT    2    1    3    9                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6                                                            
CONECT    9    2   10                                                       
CONECT   10    9   11   15   32                                             
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13    1   15   24                                             
CONECT   15   14   10   16                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   31                                                  
CONECT   18   17   19   24   26                                             
CONECT   19   18   20   27                                                  
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   25                                                  
CONECT   23   22   24                                                       
CONECT   24   23   14   18                                                  
CONECT   25   22   26                                                       
CONECT   26   25   18                                                       
CONECT   27   19   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28                                                            
CONECT   31   17    1                                                       
CONECT   32   10                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   74    0
END

View in JSmol

Synonyms

Value	Source
2-[(1R,5R,8R,10R,11R,12S,14S,16R,17R)-12-(Acetyloxy)-5-methyl-13-methylidene-9-oxa-7-azahexacyclo[8.6.2.2,.0,.0,.0,]icosan-7-yl]ethyl acetic acid	Generator

Chemical Formula

C₂₆H₃₇NO₅

Average Mass

443.5840 Da

Monoisotopic Mass

443.26717 Da

IUPAC Name

2-[(1R,5R,8R,10R,11R,12S,14S,16R,17R)-12-(acetyloxy)-5-methyl-13-methylidene-9-oxa-7-azahexacyclo[8.6.2.2^{11,14}.0^{1,8}.0^{5,17}.0^{11,16}]icosan-7-yl]ethyl acetate

Traditional Name

2-[(1R,5R,8R,10R,11R,12S,14S,16R,17R)-12-(acetyloxy)-5-methyl-13-methylidene-9-oxa-7-azahexacyclo[8.6.2.2^{11,14}.0^{1,8}.0^{5,17}.0^{11,16}]icosan-7-yl]ethyl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)OCCN1C[C@]2(C)CCC[C@@]34[C@H]1O[C@H](C[C@H]23)[C@@]12CC[C@@H](C[C@@H]41)C(=C)[C@@H]2OC(C)=O

InChI Identifier

InChI=1S/C26H37NO5/c1-15-18-6-9-26(22(15)31-17(3)29)20(12-18)25-8-5-7-24(4)14-27(10-11-30-16(2)28)23(25)32-21(26)13-19(24)25/h18-23H,1,5-14H2,2-4H3/t18-,19+,20-,21+,22-,23+,24-,25+,26+/m0/s1

InChI Key

OWDJZYOWYLOEJQ-KZOWRAFGSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Spiraea japonica	LOTUS Database	35616633
Spiraea japonica var.acuminata	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as atisane diterpenoids. These are diterpenoids with a structure based on the atisane skeleton, which is a tetracyclic compound containing the [2,2,2]bicyc1ic ring system with the C15-C16 bridge attached at C12.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Atisane diterpenoids

Alternative Parents

Substituents

Atisane diterpenoid
Alkaloid or derivatives
Piperidine
Oxane
Dicarboxylic acid or derivatives
Hemiaminal
Carboxylic acid ester
Oxacycle
Azacycle
Organoheterocyclic compound
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	3.02	ALOGPS
logP	2.97	ChemAxon
logS	-4.5	ALOGPS
pKa (Strongest Basic)	6.99	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	65.07 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	117.65 m³·mol⁻¹	ChemAxon
Polarizability	57.37 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

162893852

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Spiramine E (NP0067263)

MOL for NP0067263 (Spiramine E)

3D MOL for NP0067263 (Spiramine E)

3D SDF for NP0067263 (Spiramine E)

3D-SDF for NP0067263 (Spiramine E)

PDB for NP0067263 (Spiramine E)

3D PDB for NP0067263 (Spiramine E)

SMILES for NP0067263 (Spiramine E)

INCHI for NP0067263 (Spiramine E)

Structure for NP0067263 (Spiramine E)

3D Structure for NP0067263 (Spiramine E)