NP-MRD: Showing NP-Card for (1r,2s,8r)-14-oxa-7-azatetracyclo[6.6.1.0¹,¹¹.0²,⁷]pentadeca-9,11-dien-13-one (NP0164752)

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Record Information

Version

2.0

Created at

2022-09-02 23:41:44 UTC

Updated at

2022-09-02 23:41:45 UTC

NP-MRD ID

NP0164752

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2s,8r)-14-oxa-7-azatetracyclo[6.6.1.0¹,¹¹.0²,⁷]pentadeca-9,11-dien-13-one

Description

Virosecurinin belongs to the class of organic compounds known as indolizidines. These are polycyclic compounds containing an indolizidine, which is a bicyclic heterocycle containing a saturated six-member ring fused to a saturated five-member ring, one of the bridging atoms being nitrogen. (1r,2s,8r)-14-oxa-7-azatetracyclo[6.6.1.0¹,¹¹.0²,⁷]pentadeca-9,11-dien-13-one is found in Flueggea virosa. Based on a literature review very few articles have been published on Virosecurinin.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 31 34  0  0  0  0  0  0  0  0999 V2000
   -2.0060   -2.4924    2.9897 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7679   -1.7112    2.0342 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7525   -1.4185    0.9819 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2143   -0.5833    0.1428 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5742    0.1185   -1.0859 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8029    1.1324   -1.4787 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5918    1.5740   -0.7476 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7706    1.2197    0.7379 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8117   -0.2889    0.6167 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6019   -0.9958    1.7723 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1999   -0.5251   -0.4796 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3214   -1.4122   -0.0455 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6753   -0.8493   -0.3620 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6643    0.5621    0.2423 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7167    1.3650   -0.5742 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5655    0.7137   -1.0506 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7644   -1.8002    0.8701 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4491   -0.2184   -1.6169 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0864    1.6605   -2.3897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3698    2.6321   -0.8763 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7560    1.6247    1.0484 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0611    1.5798    1.3427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3559   -1.1039   -1.2797 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2796   -2.4344   -0.4810 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2115   -1.5700    1.0656 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4699   -1.4619    0.0547 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7433   -0.7690   -1.4785 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2922    0.4655    1.2896 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6881    0.9314    0.2226 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2967    1.7455   -1.4681 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4899    2.3095    0.0029 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2 10  1  0
  9 10  1  1
  9  8  1  0
  8  7  1  0
  7  6  1  0
  6  5  2  0
  5  4  1  0
  4  3  2  0
  7 16  1  0
 16 15  1  0
 15 14  1  0
 14 13  1  0
 13 12  1  0
 12 11  1  0
  3  2  1  0
 11 16  1  0
  4  9  1  0
 11  9  1  0
  8 21  1  0
  8 22  1  0
  7 20  1  1
  6 19  1  0
  5 18  1  0
  3 17  1  0
 15 30  1  0
 15 31  1  0
 14 28  1  0
 14 29  1  0
 13 26  1  0
 13 27  1  0
 12 24  1  0
 12 25  1  0
 11 23  1  6
M  END


  Mrv1652309032201412D          

 16 19  0  0  1  0            999 V2000
    0.6745   -1.9760    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1729   -1.3186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9304   -0.5260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6085   -0.0420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6393    0.8266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4190    1.1771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1148    0.6685    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6803    0.0633    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3331   -0.5551    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0052   -1.3381    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2154   -0.7305    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6056   -1.4574    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4302   -1.4828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8646   -0.7814    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4743   -0.0545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6497   -0.0291    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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  1  1  0  0  0
  9  8  1  1  0  0  0
  4  9  1  0  0  0  0
  9 10  1  0  0  0  0
  2 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 11 16  1  1  0  0  0
  7 16  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0164752

> <DATABASE_NAME>
NP-MRD

> <SMILES>
O=C1O[C@]23C[C@H](C=CC2=C1)N1CCCC[C@@H]31

> <INCHI_IDENTIFIER>
InChI=1S/C13H15NO2/c15-12-7-9-4-5-10-8-13(9,16-12)11-3-1-2-6-14(10)11/h4-5,7,10-11H,1-3,6,8H2/t10-,11-,13+/m0/s1

> <INCHI_KEY>
SWZMSZQQJRKFBP-GMXVVIOVSA-N

> <FORMULA>
C13H15NO2

> <MOLECULAR_WEIGHT>
217.268

> <EXACT_MASS>
217.110278727

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
31

> <JCHEM_AVERAGE_POLARIZABILITY>
22.990976169981543

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,2S,8R)-14-oxa-7-azatetracyclo[6.6.1.0^{1,11}.0^{2,7}]pentadeca-9,11-dien-13-one

> <ALOGPS_LOGP>
1.35

> <JCHEM_LOGP>
1.4055138189999998

> <ALOGPS_LOGS>
-0.74

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_BASIC>
9.504628886284035

> <JCHEM_POLAR_SURFACE_AREA>
29.54

> <JCHEM_REFRACTIVITY>
61.31910000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.98e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,8R)-14-oxa-7-azatetracyclo[6.6.1.0^{1,11}.0^{2,7}]pentadeca-9,11-dien-13-one

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  O   UNK     0       1.259  -3.689   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       2.189  -2.461   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.737  -0.982   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.002  -0.078   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.060   1.543   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.516   2.197   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.814   1.248   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.003   0.118   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.355  -1.036   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       3.743  -2.498   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       6.002  -1.364   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.730  -2.720   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.270  -2.768   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.081  -1.459   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.352  -0.102   0.000  0.00  0.00           C+0
HETATM   16  N   UNK     0       6.813  -0.054   0.000  0.00  0.00           N+0
CONECT    1    2                                                            
CONECT    2    1    3   10                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    9                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   16                                                  
CONECT    8    7    9                                                       
CONECT    9    8    4   10   11                                             
CONECT   10    9    2                                                       
CONECT   11    9   12   16                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   11    7                                                  
MASTER        0    0    0    0    0    0    0    0   16    0   38    0
END

View in JSmol

Synonyms

Value	Source
Viro-securinine	MeSH
Viroallosecurinine	MeSH
Virosecurinine	MeSH

Chemical Formula

C₁₃H₁₅NO₂

Average Mass

217.2680 Da

Monoisotopic Mass

217.11028 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

O=C1O[C@]23C[C@H](C=CC2=C1)N1CCCC[C@@H]31

InChI Identifier

InChI=1S/C13H15NO2/c15-12-7-9-4-5-10-8-13(9,16-12)11-3-1-2-6-14(10)11/h4-5,7,10-11H,1-3,6,8H2/t10-,11-,13+/m0/s1

InChI Key

SWZMSZQQJRKFBP-GMXVVIOVSA-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

Species Name	Source	Reference
Flueggea virosa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as indolizidines. These are polycyclic compounds containing an indolizidine, which is a bicyclic heterocycle containing a saturated six-member ring fused to a saturated five-member ring, one of the bridging atoms being nitrogen.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indolizidines

Sub Class

Not Available

Direct Parent

Indolizidines

Alternative Parents

Substituents

Indolizidine
Azepine
2-furanone
Piperidine
N-alkylpyrrolidine
Dihydrofuran
Pyrrolidine
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Amino acid or derivatives
Carboxylic acid ester
Lactone
Tertiary amine
Tertiary aliphatic amine
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Oxacycle
Azacycle
Organooxygen compound
Organonitrogen compound
Organic oxide
Organopnictogen compound
Amine
Carbonyl group
Hydrocarbon derivative
Organic nitrogen compound
Organic oxygen compound
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	1.35	ALOGPS
logS	-0.74	ALOGPS

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00058808

Chemspider ID

809063

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

928095

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,2s,8r)-14-oxa-7-azatetracyclo[6.6.1.0¹,¹¹.0²,⁷]pentadeca-9,11-dien-13-one (NP0164752)

MOL for NP0164752 ((1r,2s,8r)-14-oxa-7-azatetracyclo[6.6.1.0¹,¹¹.0²,⁷]pentadeca-9,11-dien-13-one)

3D MOL for NP0164752 ((1r,2s,8r)-14-oxa-7-azatetracyclo[6.6.1.0¹,¹¹.0²,⁷]pentadeca-9,11-dien-13-one)

3D SDF for NP0164752 ((1r,2s,8r)-14-oxa-7-azatetracyclo[6.6.1.0¹,¹¹.0²,⁷]pentadeca-9,11-dien-13-one)

3D-SDF for NP0164752 ((1r,2s,8r)-14-oxa-7-azatetracyclo[6.6.1.0¹,¹¹.0²,⁷]pentadeca-9,11-dien-13-one)

PDB for NP0164752 ((1r,2s,8r)-14-oxa-7-azatetracyclo[6.6.1.0¹,¹¹.0²,⁷]pentadeca-9,11-dien-13-one)

3D PDB for NP0164752 ((1r,2s,8r)-14-oxa-7-azatetracyclo[6.6.1.0¹,¹¹.0²,⁷]pentadeca-9,11-dien-13-one)

SMILES for NP0164752 ((1r,2s,8r)-14-oxa-7-azatetracyclo[6.6.1.0¹,¹¹.0²,⁷]pentadeca-9,11-dien-13-one)

INCHI for NP0164752 ((1r,2s,8r)-14-oxa-7-azatetracyclo[6.6.1.0¹,¹¹.0²,⁷]pentadeca-9,11-dien-13-one)

Structure for NP0164752 ((1r,2s,8r)-14-oxa-7-azatetracyclo[6.6.1.0¹,¹¹.0²,⁷]pentadeca-9,11-dien-13-one)

3D Structure for NP0164752 ((1r,2s,8r)-14-oxa-7-azatetracyclo[6.6.1.0¹,¹¹.0²,⁷]pentadeca-9,11-dien-13-one)