NP-MRD: Showing NP-Card for [(1r,9s)-6-oxo-7,11-diazatricyclo[7.3.1.0²,⁷]trideca-2,4-dien-11-yl]acetic acid (NP0263336)

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Record Information

Version

2.0

Created at

2022-09-08 06:29:15 UTC

Updated at

2022-09-08 06:29:16 UTC

NP-MRD ID

NP0263336

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[(1r,9s)-6-oxo-7,11-diazatricyclo[7.3.1.0²,⁷]trideca-2,4-dien-11-yl]acetic acid

Description

(?)-12-Cytisineacetic acid belongs to the class of organic compounds known as cytisine and derivatives. These are lupin alkaloids with a structure based on the cytisine skeleton, which is a tetracyclic ketone containing fused pyridine and piperidine rings that form pyrido[1,2a][1,5]diazocin-8-one. [(1r,9s)-6-oxo-7,11-diazatricyclo[7.3.1.0²,⁷]trideca-2,4-dien-11-yl]acetic acid is found in Echinosophora koreensis. Based on a literature review very few articles have been published on (?)-12-Cytisineacetic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 34 36  0  0  0  0  0  0  0  0999 V2000
    4.1062   -0.5182    1.5332 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1395   -0.1300    0.3442 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3753    0.1250   -0.2899 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9528    0.1055   -0.5119 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7233    0.0102    0.1723 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2845   -1.2551    0.6257 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0507   -1.6708    0.0286 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1320   -1.0960   -1.3511 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2538    0.4070   -1.2280 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7266    0.9523   -0.2037 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6012    0.6526   -0.6498 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3393    1.7047   -1.1290 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5853    1.9524   -0.5853 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9978    1.1018    0.4196 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2148    0.0633    0.8588 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6704   -0.6634    1.7802 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9944   -0.1763    0.3235 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2341   -1.2781    0.8311 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4443    1.0752   -0.6701 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0545   -0.6083   -1.3674 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0239    1.1414   -0.9551 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0378   -2.0202    0.3623 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2278   -1.3073    1.7590 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0015   -2.7956   -0.0923 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0692   -1.4869   -1.8324 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6941   -1.4118   -2.0126 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1155    0.9293   -2.1933 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2305    1.2881    0.7411 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2447    1.8292   -0.6230 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9657    2.3379   -1.9169 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2144    2.7731   -0.9153 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9761    1.2862    0.8600 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9174   -1.1560    1.8813 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9351   -2.1610    0.8389 H   0  0  0  0  0  0  0  0  0  0  0  0
  3  2  1  0
  2  1  2  0
  2  4  1  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
  9 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 17 18  1  0
 10  5  1  0
 17 11  1  0
 18  7  1  0
  3 19  1  0
  4 20  1  0
  4 21  1  0
  6 22  1  0
  6 23  1  0
  7 24  1  6
  8 25  1  0
  8 26  1  0
  9 27  1  6
 10 28  1  0
 10 29  1  0
 12 30  1  0
 13 31  1  0
 14 32  1  0
 18 33  1  0
 18 34  1  0
M  END


  Mrv1652309082208292D          

 18 20  0  0  1  0            999 V2000
    7.1187    1.4963    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3325    1.7463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1558    2.5521    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7229    1.1904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9367    1.4403    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.8667    2.2624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2360    2.7942    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1662    1.6853    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5828    0.7397    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4049    0.8096    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9521    1.2715    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2752    0.7999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5283    1.1503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4584    1.9723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1353    2.4439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0654    3.2659    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8822    2.0935    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4140    2.7242    0.0000 C   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
  2  4  1  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  1  0  0  0
  9  8  1  1  0  0  0
  9 10  1  0  0  0  0
  5 10  1  0  0  0  0
  9 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
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 11 17  1  0  0  0  0
 17 18  1  0  0  0  0
  7 18  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0263336

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC(=O)CN1C[C@@H]2C[C@H](C1)C1=CC=CC(=O)N1C2

> <INCHI_IDENTIFIER>
InChI=1S/C13H16N2O3/c16-12-3-1-2-11-10-4-9(6-15(11)12)5-14(7-10)8-13(17)18/h1-3,9-10H,4-8H2,(H,17,18)/t9-,10+/m0/s1

> <INCHI_KEY>
UZCDOCUFLDOKIX-VHSXEESVSA-N

> <FORMULA>
C13H16N2O3

> <MOLECULAR_WEIGHT>
248.282

> <EXACT_MASS>
248.116092383

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
34

> <JCHEM_AVERAGE_POLARIZABILITY>
24.95988771390278

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-[(1R,9S)-6-oxo-7,11-diazatricyclo[7.3.1.0^{2,7}]trideca-2,4-dien-11-yl]acetic acid

> <JCHEM_LOGP>
-3.1490746326711645

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.5774969602803948

> <JCHEM_PKA_STRONGEST_BASIC>
9.7535313818095

> <JCHEM_POLAR_SURFACE_AREA>
60.85

> <JCHEM_REFRACTIVITY>
68.30760000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
[(1R,9S)-6-oxo-7,11-diazatricyclo[7.3.1.0^{2,7}]trideca-2,4-dien-11-yl]acetic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  O   UNK     0      13.288   2.793   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      11.821   3.260   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      11.491   4.764   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      10.683   2.222   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0       9.215   2.689   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0       9.085   4.223   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.907   5.216   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.777   3.146   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.688   1.381   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.222   1.511   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.511   2.373   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.247   1.493   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.853   2.147   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.722   3.682   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.986   4.562   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       3.855   6.096   0.000  0.00  0.00           O+0
HETATM   17  N   UNK     0       5.380   3.908   0.000  0.00  0.00           N+0
HETATM   18  C   UNK     0       6.373   5.085   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   10                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   18                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9    5                                                       
CONECT   11    9   12   17                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   11   18                                                  
CONECT   18   17    7                                                       
MASTER        0    0    0    0    0    0    0    0   18    0   40    0
END

View in JSmol

Synonyms

Value	Source
(?)-12-cytisineacetate	Generator

Chemical Formula

C₁₃H₁₆N₂O₃

Average Mass

248.2820 Da

Monoisotopic Mass

248.11609 Da

IUPAC Name

2-[(1R,9S)-6-oxo-7,11-diazatricyclo[7.3.1.0^{2,7}]trideca-2,4-dien-11-yl]acetic acid

Traditional Name

[(1R,9S)-6-oxo-7,11-diazatricyclo[7.3.1.0^{2,7}]trideca-2,4-dien-11-yl]acetic acid

CAS Registry Number

Not Available

SMILES

OC(=O)CN1C[C@@H]2C[C@H](C1)C1=CC=CC(=O)N1C2

InChI Identifier

InChI=1S/C13H16N2O3/c16-12-3-1-2-11-10-4-9(6-15(11)12)5-14(7-10)8-13(17)18/h1-3,9-10H,4-8H2,(H,17,18)/t9-,10+/m0/s1

InChI Key

UZCDOCUFLDOKIX-VHSXEESVSA-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
Echinosophora koreensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cytisine and derivatives. These are lupin alkaloids with a structure based on the cytisine skeleton, which is a tetracyclic ketone containing fused pyridine and piperidine rings that form pyrido[1,2a][1,5]diazocin-8-one.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Lupin alkaloids

Sub Class

Cytisine and derivatives

Direct Parent

Cytisine and derivatives

Alternative Parents

Substituents

Cytisine
Alpha-amino acid
Alpha-amino acid or derivatives
Pyridinone
Aralkylamine
Piperidine
Pyridine
Heteroaromatic compound
Amino acid or derivatives
Tertiary aliphatic amine
Tertiary amine
Amino acid
Lactam
Azacycle
Organoheterocyclic compound
Carboxylic acid derivative
Carboxylic acid
Monocarboxylic acid or derivatives
Organic oxide
Hydrocarbon derivative
Amine
Carbonyl group
Organic oxygen compound
Organonitrogen compound
Organooxygen compound
Organic nitrogen 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	-3.1	ChemAxon
pKa (Strongest Acidic)	1.58	ChemAxon
pKa (Strongest Basic)	9.75	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	60.85 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	68.31 m³·mol⁻¹	ChemAxon
Polarizability	24.96 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	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

103883536

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Bracket

METLIN ID

Not Available

PubChem Compound

92344070

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for [(1r,9s)-6-oxo-7,11-diazatricyclo[7.3.1.0²,⁷]trideca-2,4-dien-11-yl]acetic acid (NP0263336)

MOL for NP0263336 ([(1r,9s)-6-oxo-7,11-diazatricyclo[7.3.1.0²,⁷]trideca-2,4-dien-11-yl]acetic acid)

3D MOL for NP0263336 ([(1r,9s)-6-oxo-7,11-diazatricyclo[7.3.1.0²,⁷]trideca-2,4-dien-11-yl]acetic acid)

3D SDF for NP0263336 ([(1r,9s)-6-oxo-7,11-diazatricyclo[7.3.1.0²,⁷]trideca-2,4-dien-11-yl]acetic acid)

3D-SDF for NP0263336 ([(1r,9s)-6-oxo-7,11-diazatricyclo[7.3.1.0²,⁷]trideca-2,4-dien-11-yl]acetic acid)

PDB for NP0263336 ([(1r,9s)-6-oxo-7,11-diazatricyclo[7.3.1.0²,⁷]trideca-2,4-dien-11-yl]acetic acid)

3D PDB for NP0263336 ([(1r,9s)-6-oxo-7,11-diazatricyclo[7.3.1.0²,⁷]trideca-2,4-dien-11-yl]acetic acid)

SMILES for NP0263336 ([(1r,9s)-6-oxo-7,11-diazatricyclo[7.3.1.0²,⁷]trideca-2,4-dien-11-yl]acetic acid)

INCHI for NP0263336 ([(1r,9s)-6-oxo-7,11-diazatricyclo[7.3.1.0²,⁷]trideca-2,4-dien-11-yl]acetic acid)

Structure for NP0263336 ([(1r,9s)-6-oxo-7,11-diazatricyclo[7.3.1.0²,⁷]trideca-2,4-dien-11-yl]acetic acid)

3D Structure for NP0263336 ([(1r,9s)-6-oxo-7,11-diazatricyclo[7.3.1.0²,⁷]trideca-2,4-dien-11-yl]acetic acid)