NP-MRD: Showing NP-Card for (1s,9s)-7,11-diazatricyclo[7.3.1.0²,⁷]tridec-4-en-6-one (NP0224301)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-06 02:37:41 UTC

Updated at

2022-09-06 02:37:42 UTC

NP-MRD ID

NP0224301

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,9s)-7,11-diazatricyclo[7.3.1.0²,⁷]tridec-4-en-6-one

Description

Dihydrocytisine belongs to the class of organic compounds known as piperidines. Piperidines are compounds containing a piperidine ring, which is a saturated aliphatic six-member ring with one nitrogen atom and five carbon atoms. (1s,9s)-7,11-diazatricyclo[7.3.1.0²,⁷]tridec-4-en-6-one is found in Lupinus hintonii. Based on a literature review very few articles have been published on Dihydrocytisine.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 30 32  0  0  0  0  0  0  0  0999 V2000
    2.2746    2.0576    1.9605 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1290    1.1238    1.1416 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2779    0.6548    0.4005 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1405   -0.3259   -0.4673 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8549   -0.9684   -0.7181 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8142   -0.8413    0.3249 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5539   -0.8611   -0.0834 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5721   -1.6809   -0.6106 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7700   -0.7951   -0.4914 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5965    0.3043    0.4435 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4239    1.2509    0.1779 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7004    0.4405   -0.8964 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3652    1.2058    1.3002 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8587    0.5330    0.9412 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.2623    1.1126    0.5584 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0623   -0.6514   -1.0102 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4241   -0.7178   -1.7165 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0824   -2.0770   -0.8098 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1347   -1.4956    1.1895 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9881   -0.8102    0.9871 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4846   -1.9086   -1.7105 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7807   -2.6470   -0.1271 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1183   -0.5121   -1.4055 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5029    0.9503    0.2050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7365    0.0505    1.4913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6945    2.2415   -0.1233 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2454    0.8937   -1.1931 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3190    0.3722   -1.7767 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8110    0.8193    2.2369 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435    2.2813    1.5051 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 14  2  1  0
 14  6  1  0
 12  7  1  0
  3 15  1  0
  4 16  1  0
  5 17  1  0
  5 18  1  0
  6 19  1  1
  7 20  1  1
  8 21  1  0
  8 22  1  0
  9 23  1  0
 10 24  1  0
 10 25  1  0
 11 26  1  6
 12 27  1  0
 12 28  1  0
 13 29  1  0
 13 30  1  0
M  END


  Mrv1652309062204372D          

 14 16  0  0  1  0            999 V2000
   -0.8328    2.0583    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7736    1.2354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4567    0.7727    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3975   -0.0502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6553   -0.4104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0277    0.0523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6514   -0.4877    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4743   -0.4286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0143    0.1951    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9552    1.0180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3315    1.5580    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7357    0.6202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5086    1.4989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0314    0.8752    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  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  1  0  0  0
  7 12  1  6  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
  2 14  1  0  0  0  0
  6 14  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0224301

> <DATABASE_NAME>
NP-MRD

> <SMILES>
O=C1C=CCC2[C@@H]3CNC[C@H](C3)CN12

> <INCHI_IDENTIFIER>
InChI=1S/C11H16N2O/c14-11-3-1-2-10-9-4-8(5-12-6-9)7-13(10)11/h1,3,8-10,12H,2,4-7H2/t8-,9-,10?/m0/s1

> <INCHI_KEY>
KSXAIQGMVVISIG-XMCUXHSSSA-N

> <FORMULA>
C11H16N2O

> <MOLECULAR_WEIGHT>
192.262

> <EXACT_MASS>
192.126263143

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
30

> <JCHEM_AVERAGE_POLARIZABILITY>
59.00534953192571

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,9S)-7,11-diazatricyclo[7.3.1.0^{2,7}]tridec-4-en-6-one

> <JCHEM_LOGP>
-0.21943033733333345

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.567279007605013

> <JCHEM_PKA_STRONGEST_BASIC>
10.26751360748212

> <JCHEM_POLAR_SURFACE_AREA>
32.34

> <JCHEM_REFRACTIVITY>
55.434900000000006

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,9S)-7,11-diazatricyclo[7.3.1.0^{2,7}]tridec-4-en-6-one

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  O   UNK     0      -1.555   3.842   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      -1.444   2.306   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.719   1.442   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.609  -0.094   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.223  -0.766   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.052   0.098   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.216  -0.910   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.752  -0.800   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0       3.760   0.364   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0       3.650   1.900   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.485   2.908   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.373   1.158   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.949   2.798   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0      -0.059   1.634   0.000  0.00  0.00           N+0
CONECT    1    2                                                            
CONECT    2    1    3   14                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   14                                                  
CONECT    7    6    8   12                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11    7                                                       
CONECT   13   11   14                                                       
CONECT   14   13    2    6                                                  
MASTER        0    0    0    0    0    0    0    0   14    0   32    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₁H₁₆N₂O

Average Mass

192.2620 Da

Monoisotopic Mass

192.12626 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

O=C1C=CCC2[C@@H]3CNC[C@H](C3)CN12

InChI Identifier

InChI=1S/C11H16N2O/c14-11-3-1-2-10-9-4-8(5-12-6-9)7-13(10)11/h1,3,8-10,12H,2,4-7H2/t8-,9-,10?/m0/s1

InChI Key

KSXAIQGMVVISIG-XMCUXHSSSA-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
Lupinus hintonii	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as piperidines. Piperidines are compounds containing a piperidine ring, which is a saturated aliphatic six-member ring with one nitrogen atom and five carbon atoms.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Piperidines

Sub Class

Not Available

Direct Parent

Piperidines

Alternative Parents

Substituents

Piperidine
Tertiary carboxylic acid amide
Amino acid or derivatives
Carboxamide group
Lactam
Carboxylic acid derivative
Secondary aliphatic amine
Secondary amine
Azacycle
Organonitrogen compound
Organic oxide
Amine
Organic oxygen compound
Organooxygen compound
Hydrocarbon derivative
Organic nitrogen 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

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

91747228

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,9s)-7,11-diazatricyclo[7.3.1.0²,⁷]tridec-4-en-6-one (NP0224301)

MOL for NP0224301 ((1s,9s)-7,11-diazatricyclo[7.3.1.0²,⁷]tridec-4-en-6-one)

3D MOL for NP0224301 ((1s,9s)-7,11-diazatricyclo[7.3.1.0²,⁷]tridec-4-en-6-one)

3D SDF for NP0224301 ((1s,9s)-7,11-diazatricyclo[7.3.1.0²,⁷]tridec-4-en-6-one)

3D-SDF for NP0224301 ((1s,9s)-7,11-diazatricyclo[7.3.1.0²,⁷]tridec-4-en-6-one)

PDB for NP0224301 ((1s,9s)-7,11-diazatricyclo[7.3.1.0²,⁷]tridec-4-en-6-one)

3D PDB for NP0224301 ((1s,9s)-7,11-diazatricyclo[7.3.1.0²,⁷]tridec-4-en-6-one)

SMILES for NP0224301 ((1s,9s)-7,11-diazatricyclo[7.3.1.0²,⁷]tridec-4-en-6-one)

INCHI for NP0224301 ((1s,9s)-7,11-diazatricyclo[7.3.1.0²,⁷]tridec-4-en-6-one)

Structure for NP0224301 ((1s,9s)-7,11-diazatricyclo[7.3.1.0²,⁷]tridec-4-en-6-one)

3D Structure for NP0224301 ((1s,9s)-7,11-diazatricyclo[7.3.1.0²,⁷]tridec-4-en-6-one)