NP-MRD: Showing NP-Card for (1r,2r,10s)-7,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadecan-6-one (NP0185281)

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Record Information

Version

2.0

Created at

2022-09-04 00:38:22 UTC

Updated at

2022-09-04 00:38:22 UTC

NP-MRD ID

NP0185281

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2r,10s)-7,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadecan-6-one

Description

(1R,2R,10S)-7,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]Heptadecan-6-one belongs to the class of organic compounds known as sparteine, lupanine, and related alkaloids. These are alkaloids with a structure based on either sparteine, lupanine, or derivatives thereof. These are tetracyclic compounds made of two fused quinolizidine ring systems. (1r,2r,10s)-7,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadecan-6-one is found in Argyrolobium lunare, Aspalathus perfoliata, Baptisia simplicifolia, Clathrotropis brachypetala, Cytisophyllum sessilifolium, Cytisus hirsutus, Dichilus strictus, Euphorbia larica, Genista albida, Haplormosia monophylla, Laburnum alpinum, Laburnum watereri, Lebeckia plukenetiana, Calobota pungens, Liparia splendens, Lotononis listii, Lupinus argenteus, Lupinus latifolius, Lupinus mutabilis, Lupinus sericeus, Lupinus texensis, Melolobium wilmsii, Pearsonia sessilifolia, Petteria ramentacea, Polhillia brevicalyx, Rothia hirsuta, Sophora davidii, Sophora flavescens, Sophora secundiflora, Spartium junceum, Thermopsis chinensis and Ulex minor. Based on a literature review very few articles have been published on (1R,2R,10S)-7,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]Heptadecan-6-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 42 45  0  0  0  0  0  0  0  0999 V2000
   -2.6614   -2.8944    0.8660 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7439   -1.7169    0.4298 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0747   -1.2413   -0.0914 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2219    0.1836    0.3312 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1141    1.0758   -0.1492 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7482    0.6088    0.2006 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7145    0.9616   -0.8695 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3605   -0.2708   -1.6714 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4208   -1.1658   -0.7153 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3222   -1.3562    0.5951 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6501   -0.8167    0.4040 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.7031   -0.4251   -0.4809 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6965   -1.2309    0.3311 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0381   -0.5521    0.1525 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9981    0.9172    0.3852 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7789    1.6064   -0.0926 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5505    0.8488    0.1146 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4668    1.6450   -0.3178 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0841   -1.2891   -1.2050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8638   -1.8373    0.3721 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1678    0.5700   -0.1481 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3854    0.2430    1.4178 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3009    2.0867    0.3048 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1938    1.1980   -1.2516 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4283    1.1070    1.1476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2474    1.6470   -1.5787 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2401   -0.7468   -2.0881 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3280    0.0395   -2.4800 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6373   -2.1438   -1.1414 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3598   -2.3937    0.9189 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1879   -0.7244    1.3807 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1847   -0.2830   -1.4917 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7538   -2.2561   -0.0696 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4487   -1.2110    1.4114 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7939   -1.0029    0.8283 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3827   -0.8088   -0.8883 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8804    1.3647   -0.1613 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1956    1.1286    1.4566 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6860    2.5821    0.4439 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8054    1.8654   -1.1781 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1320    2.2789    0.5558 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8138    2.4090   -1.0746 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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  1  0
  9 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
 11  2  1  0
 17 12  1  0
 11  6  1  0
 18  7  1  0
  3 19  1  0
  3 20  1  0
  4 21  1  0
  4 22  1  0
  5 23  1  0
  5 24  1  0
  6 25  1  1
  7 26  1  6
  8 27  1  0
  8 28  1  0
  9 29  1  6
 10 30  1  0
 10 31  1  0
 12 32  1  6
 13 33  1  0
 13 34  1  0
 14 35  1  0
 14 36  1  0
 15 37  1  0
 15 38  1  0
 16 39  1  0
 16 40  1  0
 18 41  1  0
 18 42  1  0
M  END


  Mrv1652309042202382D          

 18 21  0  0  1  0            999 V2000
    6.1269   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1269   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8413    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8413    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1269    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4124    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8290    1.4084    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6655    0.3094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0040   -0.5834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8290   -0.5834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4124   -0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4207   -0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7062   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9917    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9917    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7062    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4207    0.8250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.0040    1.4084    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
  3  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
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  2 11  1  0  0  0  0
  6 11  1  1  0  0  0
  9 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
 16 17  1  0  0  0  0
 12 17  1  6  0  0  0
 17 18  1  0  0  0  0
  7 18  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0185281

> <DATABASE_NAME>
NP-MRD

> <SMILES>
O=C1CCC[C@@H]2[C@@H]3CC(CN12)[C@@H]1CCCCN1C3

> <INCHI_IDENTIFIER>
InChI=1S/C15H24N2O/c18-15-6-3-5-14-11-8-12(10-17(14)15)13-4-1-2-7-16(13)9-11/h11-14H,1-10H2/t11-,12?,13+,14-/m1/s1

> <INCHI_KEY>
JYIJIIVLEOETIQ-NIWMIYJQSA-N

> <FORMULA>
C15H24N2O

> <MOLECULAR_WEIGHT>
248.37

> <EXACT_MASS>
248.188863401

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
28.34013297518259

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,2R,10S)-7,15-diazatetracyclo[7.7.1.0^{2,7}.0^{10,15}]heptadecan-6-one

> <JCHEM_LOGP>
1.0759273119999997

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_BASIC>
9.75154362875031

> <JCHEM_POLAR_SURFACE_AREA>
23.550000000000004

> <JCHEM_REFRACTIVITY>
71.4485

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,10S)-7,15-diazatetracyclo[7.7.1.0^{2,7}.0^{10,15}]heptadecan-6-one

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  O   UNK     0      11.437  -2.310   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      11.437  -0.770   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      12.770   0.000   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      12.770   1.540   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      11.437   2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.103   1.540   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.014   2.629   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.709   0.577   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.474  -1.089   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.014  -1.089   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0      10.103  -0.000   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0       6.385  -0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.052  -0.770   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.718   0.000   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.718   1.540   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.052   2.310   0.000  0.00  0.00           C+0
HETATM   17  N   UNK     0       6.385   1.540   0.000  0.00  0.00           N+0
HETATM   18  C   UNK     0       7.474   2.629   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   11                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   11                                                  
CONECT    7    6    8   18                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   12                                                  
CONECT   10    9   11                                                       
CONECT   11   10    2    6                                                  
CONECT   12    9   13   17                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   12   18                                                  
CONECT   18   17    7                                                       
MASTER        0    0    0    0    0    0    0    0   18    0   42    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₂₄N₂O

Average Mass

248.3700 Da

Monoisotopic Mass

248.18886 Da

IUPAC Name

(1R,2R,10S)-7,15-diazatetracyclo[7.7.1.0^{2,7}.0^{10,15}]heptadecan-6-one

Traditional Name

(1R,2R,10S)-7,15-diazatetracyclo[7.7.1.0^{2,7}.0^{10,15}]heptadecan-6-one

CAS Registry Number

Not Available

SMILES

O=C1CCC[C@@H]2[C@@H]3CC(CN12)[C@@H]1CCCCN1C3

InChI Identifier

InChI=1S/C15H24N2O/c18-15-6-3-5-14-11-8-12(10-17(14)15)13-4-1-2-7-16(13)9-11/h11-14H,1-10H2/t11-,12?,13+,14-/m1/s1

InChI Key

JYIJIIVLEOETIQ-NIWMIYJQSA-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
Argyrolobium lunare	LOTUS Database	35616633
Aspalathus perfoliata	LOTUS Database	35616633
Baptisia simplicifolia	LOTUS Database	35616633
Clathrotropis brachypetala	LOTUS Database	35616633
Cytisophyllum sessilifolium	LOTUS Database	35616633
Cytisus hirsutus	LOTUS Database	35616633
Dichilus strictus	LOTUS Database	35616633
Euphorbia larica	LOTUS Database	35616633
Genista albida	LOTUS Database	35616633
Haplormosia monophylla	LOTUS Database	35616633
Laburnum alpinum	LOTUS Database	35616633
Laburnum watereri	LOTUS Database	35616633
Lebeckia plukenetiana	LOTUS Database	35616633
Lebeckia pungens	LOTUS Database	35616633
Liparia splendens	LOTUS Database	35616633
Lotononis listii	LOTUS Database	35616633
Lupinus argenteus	LOTUS Database	35616633
Lupinus latifolius	LOTUS Database	35616633
Lupinus mutabilis	LOTUS Database	35616633
Lupinus sericeus	LOTUS Database	35616633
Lupinus texensis	LOTUS Database	35616633
Melolobium wilmsii	LOTUS Database	35616633
Pearsonia sessilifolia	LOTUS Database	35616633
Petteria ramentacea	LOTUS Database	35616633
Polhillia brevicalyx	LOTUS Database	35616633
Rothia hirsuta	LOTUS Database	35616633
Sophora davidii	LOTUS Database	35616633
Sophora flavescens	LOTUS Database	35616633
Sophora secundiflora	LOTUS Database	35616633
Spartium junceum	LOTUS Database	35616633
Thermopsis chinensis	LOTUS Database	35616633
Ulex minor	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sparteine, lupanine, and related alkaloids. These are alkaloids with a structure based on either sparteine, lupanine, or derivatives thereof. These are tetracyclic compounds made of two fused quinolizidine ring systems.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Lupin alkaloids

Sub Class

Sparteine, lupanine, and related alkaloids

Direct Parent

Sparteine, lupanine, and related alkaloids

Alternative Parents

Substituents

Sparteine-lupanine skeleton
Quinolizidinone
Quinolizidine
Piperidinone
Delta-lactam
Piperidine
Tertiary carboxylic acid amide
Tertiary aliphatic amine
Tertiary amine
Lactam
Carboxamide group
Amino acid or derivatives
Azacycle
Organoheterocyclic compound
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Amine
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	1.08	ChemAxon
pKa (Strongest Basic)	9.75	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	23.55 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	71.45 m³·mol⁻¹	ChemAxon
Polarizability	28.34 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	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

64860009

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

163184988

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,2r,10s)-7,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadecan-6-one (NP0185281)

MOL for NP0185281 ((1r,2r,10s)-7,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadecan-6-one)

3D MOL for NP0185281 ((1r,2r,10s)-7,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadecan-6-one)

3D SDF for NP0185281 ((1r,2r,10s)-7,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadecan-6-one)

3D-SDF for NP0185281 ((1r,2r,10s)-7,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadecan-6-one)

PDB for NP0185281 ((1r,2r,10s)-7,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadecan-6-one)

3D PDB for NP0185281 ((1r,2r,10s)-7,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadecan-6-one)

SMILES for NP0185281 ((1r,2r,10s)-7,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadecan-6-one)

INCHI for NP0185281 ((1r,2r,10s)-7,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadecan-6-one)

Structure for NP0185281 ((1r,2r,10s)-7,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadecan-6-one)

3D Structure for NP0185281 ((1r,2r,10s)-7,15-diazatetracyclo[7.7.1.0²,⁷.0¹⁰,¹⁵]heptadecan-6-one)