NP-MRD: Showing NP-Card for 5-{[(1s,9as)-octahydro-1h-quinolizin-1-ylmethyl]-c-hydroxycarbonimidoyl}pentanoic acid (NP0202741)

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Record Information

Version

2.0

Created at

2022-09-04 22:01:11 UTC

Updated at

2022-09-04 22:01:11 UTC

NP-MRD ID

NP0202741

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-{[(1s,9as)-octahydro-1h-quinolizin-1-ylmethyl]-c-hydroxycarbonimidoyl}pentanoic acid

Description

5-({[(1S,9aS)-octahydro-1H-quinolizin-1-yl]methyl}-C-hydroxycarbonimidoyl)pentanoic acid belongs to the class of organic compounds known as quinolizines. Quinolizines are compounds containing a quinolizine moiety, which consists of two fused pyridine rings sharing a nitrogen atom. 5-{[(1s,9as)-octahydro-1h-quinolizin-1-ylmethyl]-c-hydroxycarbonimidoyl}pentanoic acid is found in Sophora alopecuroides. Based on a literature review very few articles have been published on 5-({[(1S,9aS)-octahydro-1H-quinolizin-1-yl]methyl}-C-hydroxycarbonimidoyl)pentanoic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 49 50  0  0  0  0  0  0  0  0999 V2000
    6.1591   -2.3031    0.1913 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8018   -1.1355   -0.1433 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0801   -0.7244   -1.4476 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1130   -0.2093    0.7699 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8568   -0.8265    1.3416 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8701   -1.1787    0.2460 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4637    0.0489   -0.5434 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4988   -0.3634   -1.5932 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8365   -1.3044   -2.5681 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3275    0.1526   -1.6110 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0975    1.1201   -0.6561 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5206    1.6026   -0.9282 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8522    2.6181    0.1452 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6973    2.0703    1.5105 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0362    0.6466    1.6987 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9313   -0.1917    0.5528 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5959   -1.4552    0.7769 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7295   -1.7155   -0.1712 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6245   -0.5367   -0.3722 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8551    0.7696   -0.4672 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4190    0.4124   -0.6715 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7771   -1.3637   -2.1818 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8031   -0.0659    1.6529 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9584    0.7598    0.2978 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3870   -0.1667    2.0922 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1413   -1.7718    1.8383 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2564   -1.9305   -0.4403 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9620   -1.5713    0.7420 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3299    0.4905   -1.0919 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9899    0.7411    0.1535 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9011   -2.2877   -2.3996 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0134    0.6914    0.3622 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6186    1.9846   -0.6861 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6257    2.0361   -1.9189 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8697    3.0638   -0.0365 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1471    3.4705   -0.0099 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6684    2.3010    1.8949 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3714    2.6715    2.1913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0507    0.5086    2.1461 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3259    0.2253    2.4712 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9087   -1.5763    1.8435 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8225   -2.2556    0.6057 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4199   -2.1127   -1.1475 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3728   -2.5259    0.2856 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1799   -0.6414   -1.3211 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3928   -0.5210    0.4447 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0200    1.2739    0.5298 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2435    1.4255   -1.2677 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3407   -0.3502   -1.4686 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
  8 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 12  1  0
 21 16  1  0
  3 22  1  0
  4 23  1  0
  4 24  1  0
  5 25  1  0
  5 26  1  0
  6 27  1  0
  6 28  1  0
  7 29  1  0
  7 30  1  0
  9 31  1  0
 11 32  1  0
 11 33  1  0
 12 34  1  6
 13 35  1  0
 13 36  1  0
 14 37  1  0
 14 38  1  0
 15 39  1  0
 15 40  1  0
 17 41  1  0
 17 42  1  0
 18 43  1  0
 18 44  1  0
 19 45  1  0
 19 46  1  0
 20 47  1  0
 20 48  1  0
 21 49  1  6
M  END


  Mrv1652309052200012D          

 21 22  0  0  1  0            999 V2000
    5.0013   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -4.1250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -2.8875    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.0026   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -1.6500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -2.4750    0.0000 C   0  0  1  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  0  0  0  0
  8  9  1  0  0  0  0
  8 10  2  0  0  0  0
 10 11  1  4  0  0  0
 12 11  1  6  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
 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  1  0  0  0  0
 12 21  1  0  0  0  0
 21 16  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0202741

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC(=O)CCCCC(O)=NC[C@@H]1CCCN2CCCC[C@@H]12

> <INCHI_IDENTIFIER>
InChI=1S/C16H28N2O3/c19-15(8-1-2-9-16(20)21)17-12-13-6-5-11-18-10-4-3-7-14(13)18/h13-14H,1-12H2,(H,17,19)(H,20,21)/t13-,14-/m0/s1

> <INCHI_KEY>
YCIRGKSLTJKAHS-KBPBESRZSA-N

> <FORMULA>
C16H28N2O3

> <MOLECULAR_WEIGHT>
296.411

> <EXACT_MASS>
296.20999277

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
49

> <JCHEM_AVERAGE_POLARIZABILITY>
34.67030349753318

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
5-({[(1S,9aS)-octahydro-1H-quinolizin-1-yl]methyl}-C-hydroxycarbonimidoyl)pentanoic acid

> <JCHEM_LOGP>
-1.1735550002947148

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
4.661416269695659

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.780117781987944

> <JCHEM_PKA_STRONGEST_BASIC>
9.368041061307988

> <JCHEM_POLAR_SURFACE_AREA>
73.13

> <JCHEM_REFRACTIVITY>
81.96209999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
5-{[(1S,9aS)-octahydro-1H-quinolizin-1-ylmethyl]-C-hydroxycarbonimidoyl}pentanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  O   UNK     0       9.336  -6.930   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      10.669  -7.700   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      10.669  -9.240   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      12.003  -6.930   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      13.337  -7.700   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      14.670  -6.930   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      16.004  -7.700   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      17.338  -6.930   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      17.338  -5.390   0.000  0.00  0.00           O+0
HETATM   10  N   UNK     0      18.672  -7.700   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0      20.005  -6.930   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      20.005  -5.390   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      18.672  -4.620   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      18.672  -3.080   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      20.005  -2.310   0.000  0.00  0.00           C+0
HETATM   16  N   UNK     0      21.339  -3.080   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0      22.673  -2.310   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      24.006  -3.080   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      24.006  -4.620   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      22.673  -5.390   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      21.339  -4.620   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                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   21                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   21                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   12   16                                                  
MASTER        0    0    0    0    0    0    0    0   21    0   44    0
END

View in JSmol

Synonyms

Value	Source
5-({[(1S,9as)-octahydro-1H-quinolizin-1-yl]methyl}-C-hydroxycarbonimidoyl)pentanoate	Generator

Chemical Formula

C₁₆H₂₈N₂O₃

Average Mass

296.4110 Da

Monoisotopic Mass

296.20999 Da

IUPAC Name

5-({[(1S,9aS)-octahydro-1H-quinolizin-1-yl]methyl}-C-hydroxycarbonimidoyl)pentanoic acid

Traditional Name

5-{[(1S,9aS)-octahydro-1H-quinolizin-1-ylmethyl]-C-hydroxycarbonimidoyl}pentanoic acid

CAS Registry Number

Not Available

SMILES

OC(=O)CCCCC(O)=NC[C@@H]1CCCN2CCCC[C@@H]12

InChI Identifier

InChI=1S/C16H28N2O3/c19-15(8-1-2-9-16(20)21)17-12-13-6-5-11-18-10-4-3-7-14(13)18/h13-14H,1-12H2,(H,17,19)(H,20,21)/t13-,14-/m0/s1

InChI Key

YCIRGKSLTJKAHS-KBPBESRZSA-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
Sophora alopecuroides	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as quinolizines. Quinolizines are compounds containing a quinolizine moiety, which consists of two fused pyridine rings sharing a nitrogen atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Quinolizines

Sub Class

Not Available

Direct Parent

Quinolizines

Alternative Parents

Substituents

Quinolizidine
Quinolizine
Medium-chain fatty acid
Amino fatty acid
Heterocyclic fatty acid
Piperidine
Fatty acid
Fatty acyl
Amino acid or derivatives
Tertiary amine
Tertiary aliphatic amine
Amino acid
Azacycle
Carboximidic acid
Carboximidic acid derivative
Carboxylic acid derivative
Carboxylic acid
Monocarboxylic acid or derivatives
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Organic oxygen compound
Carbonyl group
Hydrocarbon derivative
Organonitrogen compound
Organooxygen compound
Organopnictogen compound
Organic oxide
Amine
Organic nitrogen 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	-1.2	ChemAxon
pKa (Strongest Acidic)	3.78	ChemAxon
pKa (Strongest Basic)	9.37	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	73.13 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	81.96 m³·mol⁻¹	ChemAxon
Polarizability	34.67 Å³	ChemAxon
Number of Rings	2	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

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

162979704

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 5-{[(1s,9as)-octahydro-1h-quinolizin-1-ylmethyl]-c-hydroxycarbonimidoyl}pentanoic acid (NP0202741)

MOL for NP0202741 (5-{[(1s,9as)-octahydro-1h-quinolizin-1-ylmethyl]-c-hydroxycarbonimidoyl}pentanoic acid)

3D MOL for NP0202741 (5-{[(1s,9as)-octahydro-1h-quinolizin-1-ylmethyl]-c-hydroxycarbonimidoyl}pentanoic acid)

3D SDF for NP0202741 (5-{[(1s,9as)-octahydro-1h-quinolizin-1-ylmethyl]-c-hydroxycarbonimidoyl}pentanoic acid)

3D-SDF for NP0202741 (5-{[(1s,9as)-octahydro-1h-quinolizin-1-ylmethyl]-c-hydroxycarbonimidoyl}pentanoic acid)

PDB for NP0202741 (5-{[(1s,9as)-octahydro-1h-quinolizin-1-ylmethyl]-c-hydroxycarbonimidoyl}pentanoic acid)

3D PDB for NP0202741 (5-{[(1s,9as)-octahydro-1h-quinolizin-1-ylmethyl]-c-hydroxycarbonimidoyl}pentanoic acid)

SMILES for NP0202741 (5-{[(1s,9as)-octahydro-1h-quinolizin-1-ylmethyl]-c-hydroxycarbonimidoyl}pentanoic acid)

INCHI for NP0202741 (5-{[(1s,9as)-octahydro-1h-quinolizin-1-ylmethyl]-c-hydroxycarbonimidoyl}pentanoic acid)

Structure for NP0202741 (5-{[(1s,9as)-octahydro-1h-quinolizin-1-ylmethyl]-c-hydroxycarbonimidoyl}pentanoic acid)

3D Structure for NP0202741 (5-{[(1s,9as)-octahydro-1h-quinolizin-1-ylmethyl]-c-hydroxycarbonimidoyl}pentanoic acid)