NP-MRD: Showing NP-Card for (1r,7s,9r,11r,13r,14r)-14-hydroxy-11-methyl-3-oxo-2,17-diazatetracyclo[7.7.1.0²,⁷.0¹³,¹⁷]heptadecan-17-ium-17-olate (NP0176148)

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Record Information

Version

2.0

Created at

2022-09-03 13:45:54 UTC

Updated at

2022-09-03 13:45:54 UTC

NP-MRD ID

NP0176148

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,7s,9r,11r,13r,14r)-14-hydroxy-11-methyl-3-oxo-2,17-diazatetracyclo[7.7.1.0²,⁷.0¹³,¹⁷]heptadecan-17-ium-17-olate

Description

(1R,7S,9R,11R,13R,14R)-14-hydroxy-11-methyl-2,17λ⁵-diazatetracyclo[7.7.1.0²,⁷.0¹³,¹⁷]Heptadecane-3,17-dione belongs to the class of organic compounds known as quinolizidines. Quinolizidines are compounds containing a quinolizidine moiety, which is a octahydro-2H-quinolizine derivative. (1r,7s,9r,11r,13r,14r)-14-hydroxy-11-methyl-3-oxo-2,17-diazatetracyclo[7.7.1.0²,⁷.0¹³,¹⁷]heptadecan-17-ium-17-olate is found in Palhinhaea cernua. Based on a literature review very few articles have been published on (1R,7S,9R,11R,13R,14R)-14-hydroxy-11-methyl-2,17λ⁵-diazatetracyclo[7.7.1.0²,⁷.0¹³,¹⁷]Heptadecane-3,17-dione.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 47 50  0  0  0  0  0  0  0  0999 V2000
   -3.9094    2.3686   -0.0331 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8428    1.4722    0.5509 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5122    1.9649    0.0275 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4553    1.0510    0.6088 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8715    1.7133    0.3528 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9377    0.6620    0.6938 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2693    1.3678    0.5691 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4003    0.3887    0.4931 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2704   -0.4311   -0.7432 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8737   -0.9190   -0.9793 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7849   -1.8699   -1.8159 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7642   -0.3526   -0.3148 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4489   -0.7800   -0.6444 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4103   -2.2822   -0.7869 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8040   -2.9311   -0.2299 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0484   -2.1235   -0.2452 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6803   -2.2852    1.0095 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8374   -0.6331   -0.4079 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0223    0.0634    0.1255 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5806   -0.2995    0.2280 N   0  0  2  0  0  4  0  0  0  0  0  0
   -0.5234   -1.1027    1.3450 O   0  0  0  0  0  1  0  0  0  0  0  0
   -4.9140    2.1337    0.3737 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9464    2.1876   -1.1248 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6199    3.4273    0.1154 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8847    1.5634    1.6583 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5317    1.9749   -1.0610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3443    2.9677    0.4798 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6070    1.1347    1.7282 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9928    2.0426   -0.7002 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9669    2.6040    0.9981 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7510    0.3209    1.7146 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2275    1.9762   -0.3573 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3442    2.0731    1.4144 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4665   -0.1981    1.4216 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3445    0.9995    0.3853 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4967    0.2417   -1.6167 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9948   -1.2671   -0.8112 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2148   -0.3709   -1.6710 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5646   -2.5935   -1.8454 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2978   -2.6985   -0.2249 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0077   -3.8550   -0.8502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5906   -3.3685    0.7908 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8033   -2.5006   -0.9844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2027   -2.9389    1.5754 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7012   -0.4499   -1.5111 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5066   -0.4907    0.9776 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8173    0.0427   -0.6786 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  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
 10 11  2  0
 10 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  1
 19  2  1  0
 20  4  1  0
 12  6  1  0
 20 13  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  2 25  1  1
  3 26  1  0
  3 27  1  0
  4 28  1  1
  5 29  1  0
  5 30  1  0
  6 31  1  1
  7 32  1  0
  7 33  1  0
  8 34  1  0
  8 35  1  0
  9 36  1  0
  9 37  1  0
 13 38  1  6
 14 39  1  0
 14 40  1  0
 15 41  1  0
 15 42  1  0
 16 43  1  6
 17 44  1  0
 18 45  1  6
 19 46  1  0
 19 47  1  0
M  CHG  2  20   1  21  -1
M  END


  Mrv1652309032215452D          

 21 24  0  0  1  0            999 V2000
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
    2.1434    0.4125    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  4  3  1  6  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  2  0  0  0  0
 10 12  1  0  0  0  0
  6 12  1  6  0  0  0
 13 12  1  1  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  1  0  0  0
 16 18  1  0  0  0  0
 18 19  1  1  0  0  0
  2 19  1  0  0  0  0
 18 20  1  0  0  0  0
  4 20  1  0  0  0  0
 13 20  1  0  0  0  0
 20 21  1  0  0  0  0
M  CHG  2  20   1  21  -1
M  END
> <DATABASE_ID>
NP0176148

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1C[C@@H]2C[C@@H]3CCCC(=O)N3[C@H]3CC[C@@H](O)[C@@H](C1)[N+]23[O-]

> <INCHI_IDENTIFIER>
InChI=1S/C16H26N2O3/c1-10-7-12-9-11-3-2-4-16(20)17(11)15-6-5-14(19)13(8-10)18(12,15)21/h10-15,19H,2-9H2,1H3/t10-,11+,12-,13-,14-,15-,18?/m1/s1

> <INCHI_KEY>
BIDUKOSIGHDYCM-NSKVRHJXSA-N

> <FORMULA>
C16H26N2O3

> <MOLECULAR_WEIGHT>
294.395

> <EXACT_MASS>
294.194342705

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
32.36804160570134

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,7S,9R,11R,13R,14R)-14-hydroxy-11-methyl-3-oxo-2,17-diazatetracyclo[7.7.1.0^{2,7}.0^{13,17}]heptadecan-17-ium-17-olate

> <ALOGPS_LOGP>
0.28

> <JCHEM_LOGP>
0.060665133999999454

> <ALOGPS_LOGS>
-1.72

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.255606968392932

> <JCHEM_PKA_STRONGEST_BASIC>
2.1239676912579473

> <JCHEM_POLAR_SURFACE_AREA>
63.60000000000001

> <JCHEM_REFRACTIVITY>
78.76870000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.59e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,7S,9R,11R,13R,14R)-14-hydroxy-11-methyl-3-oxo-2,17-diazatetracyclo[7.7.1.0^{2,7}.0^{13,17}]heptadecan-17-ium-17-olate

> <JCHEM_VEBER_RULE>
0

$$$$

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  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.336   2.310   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      10.669   1.540   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.669   0.000   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.336  -0.770   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       9.336  -2.310   0.000  0.00  0.00           O+0
HETATM   12  N   UNK     0       8.002   0.000   0.000  0.00  0.00           N+0
HETATM   13  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       2.667  -3.080   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   20  N   UNK     0       5.335   0.000   0.000  0.00  0.00           N+1
HETATM   21  O   UNK     0       4.001   0.770   0.000  0.00  0.00           O-1
CONECT    1    2                                                            
CONECT    2    1    3   19                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   20                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   12                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10    6   13                                                  
CONECT   13   12   14   20                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20                                                  
CONECT   19   18    2                                                       
CONECT   20   18    4   13   21                                             
CONECT   21   20                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   48    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₆H₂₆N₂O₃

Average Mass

294.3950 Da

Monoisotopic Mass

294.19434 Da

IUPAC Name

(1R,7S,9R,11R,13R,14R)-14-hydroxy-11-methyl-3-oxo-2,17-diazatetracyclo[7.7.1.0^{2,7}.0^{13,17}]heptadecan-17-ium-17-olate

Traditional Name

(1R,7S,9R,11R,13R,14R)-14-hydroxy-11-methyl-3-oxo-2,17-diazatetracyclo[7.7.1.0^{2,7}.0^{13,17}]heptadecan-17-ium-17-olate

CAS Registry Number

Not Available

SMILES

C[C@@H]1C[C@@H]2C[C@@H]3CCCC(=O)N3[C@H]3CC[C@@H](O)[C@@H](C1)[N+]23[O-]

InChI Identifier

InChI=1S/C16H26N2O3/c1-10-7-12-9-11-3-2-4-16(20)17(11)15-6-5-14(19)13(8-10)18(12,15)21/h10-15,19H,2-9H2,1H3/t10-,11+,12-,13-,14-,15-,18?/m1/s1

InChI Key

BIDUKOSIGHDYCM-NSKVRHJXSA-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
Palhinhaea cernua	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as quinolizidines. Quinolizidines are compounds containing a quinolizidine moiety, which is a octahydro-2H-quinolizine derivative.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Quinolizidines

Sub Class

Not Available

Direct Parent

Quinolizidines

Alternative Parents

Substituents

Pyridopyrimidine
Quinolizidine
Delta-lactam
Piperidinone
1,3-diazinane
Piperidine
Pyridine
Pyrimidine
Tertiary carboxylic acid amide
Trialkyl amine oxide
Secondary alcohol
Carboxamide group
Lactam
Trisubstituted n-oxide
Azacycle
N-oxide
Carboxylic acid derivative
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Alcohol
Organic nitrogen compound
Organic oxygen compound
Organic oxide
Organic zwitterion
Organic salt
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	0.28	ALOGPS
logP	0.061	ChemAxon
logS	-1.7	ALOGPS
pKa (Strongest Acidic)	13.26	ChemAxon
pKa (Strongest Basic)	2.12	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	63.6 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	78.77 m³·mol⁻¹	ChemAxon
Polarizability	32.37 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

8645130

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10469719

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,7s,9r,11r,13r,14r)-14-hydroxy-11-methyl-3-oxo-2,17-diazatetracyclo[7.7.1.0²,⁷.0¹³,¹⁷]heptadecan-17-ium-17-olate (NP0176148)

MOL for NP0176148 ((1r,7s,9r,11r,13r,14r)-14-hydroxy-11-methyl-3-oxo-2,17-diazatetracyclo[7.7.1.0²,⁷.0¹³,¹⁷]heptadecan-17-ium-17-olate)

3D MOL for NP0176148 ((1r,7s,9r,11r,13r,14r)-14-hydroxy-11-methyl-3-oxo-2,17-diazatetracyclo[7.7.1.0²,⁷.0¹³,¹⁷]heptadecan-17-ium-17-olate)

3D SDF for NP0176148 ((1r,7s,9r,11r,13r,14r)-14-hydroxy-11-methyl-3-oxo-2,17-diazatetracyclo[7.7.1.0²,⁷.0¹³,¹⁷]heptadecan-17-ium-17-olate)

3D-SDF for NP0176148 ((1r,7s,9r,11r,13r,14r)-14-hydroxy-11-methyl-3-oxo-2,17-diazatetracyclo[7.7.1.0²,⁷.0¹³,¹⁷]heptadecan-17-ium-17-olate)

PDB for NP0176148 ((1r,7s,9r,11r,13r,14r)-14-hydroxy-11-methyl-3-oxo-2,17-diazatetracyclo[7.7.1.0²,⁷.0¹³,¹⁷]heptadecan-17-ium-17-olate)

3D PDB for NP0176148 ((1r,7s,9r,11r,13r,14r)-14-hydroxy-11-methyl-3-oxo-2,17-diazatetracyclo[7.7.1.0²,⁷.0¹³,¹⁷]heptadecan-17-ium-17-olate)

SMILES for NP0176148 ((1r,7s,9r,11r,13r,14r)-14-hydroxy-11-methyl-3-oxo-2,17-diazatetracyclo[7.7.1.0²,⁷.0¹³,¹⁷]heptadecan-17-ium-17-olate)

INCHI for NP0176148 ((1r,7s,9r,11r,13r,14r)-14-hydroxy-11-methyl-3-oxo-2,17-diazatetracyclo[7.7.1.0²,⁷.0¹³,¹⁷]heptadecan-17-ium-17-olate)

Structure for NP0176148 ((1r,7s,9r,11r,13r,14r)-14-hydroxy-11-methyl-3-oxo-2,17-diazatetracyclo[7.7.1.0²,⁷.0¹³,¹⁷]heptadecan-17-ium-17-olate)

3D Structure for NP0176148 ((1r,7s,9r,11r,13r,14r)-14-hydroxy-11-methyl-3-oxo-2,17-diazatetracyclo[7.7.1.0²,⁷.0¹³,¹⁷]heptadecan-17-ium-17-olate)