NP-MRD: Showing NP-Card for 1-(6-hydroxy-8-phenyl-1,5,10-triazacyclotetradec-5-en-1-yl)ethanone (NP0246547)

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Record Information

Version

2.0

Created at

2022-09-07 08:03:46 UTC

Updated at

2022-09-07 08:03:46 UTC

NP-MRD ID

NP0246547

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-(6-hydroxy-8-phenyl-1,5,10-triazacyclotetradec-5-en-1-yl)ethanone

Description

1-(6-Hydroxy-8-phenyl-1,5,10-triazacyclotetradec-5-en-1-yl)ethan-1-one belongs to the class of organic compounds known as aralkylamines. These are alkylamines in which the alkyl group is substituted at one carbon atom by an aromatic hydrocarbyl group. 1-(6-hydroxy-8-phenyl-1,5,10-triazacyclotetradec-5-en-1-yl)ethanone is found in Maytenus buxifolia. 1-(6-Hydroxy-8-phenyl-1,5,10-triazacyclotetradec-5-en-1-yl)ethan-1-one is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 53 54  0  0  0  0  0  0  0  0999 V2000
   -5.8645   -1.0677    0.2616 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2804    0.2359   -0.1467 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9224    1.2976    0.0788 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0215    0.2294   -0.7746 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3282   -1.0033   -1.0104 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4974   -1.4503    0.1661 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1408   -1.8683   -0.3794 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0689   -1.8057    0.6580 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2170   -1.7470   -0.0268 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2542   -1.4088    0.9020 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6765    0.0341    0.7377 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0331    0.1435    0.1423 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0912    0.7040    0.8265 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3592    0.8191    0.3009 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5744    0.3482   -0.9735 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5330   -0.2142   -1.6728 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2599   -0.3310   -1.1482 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6540    0.8394   -0.0384 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0198    1.8782    0.8143 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7720    2.5352    1.5788 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3639    2.1699    0.8181 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1647    2.0749   -0.4068 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6324    2.1241   -0.0618 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4207    1.4714   -1.1857 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1552   -1.5608    0.9740 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9537   -1.7720   -0.6020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8684   -0.9392    0.7145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7049   -0.8898   -1.9453 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0200   -1.8503   -1.2469 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4096   -0.7085    0.9577 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9216   -2.3774    0.6520 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9245   -1.2435   -1.2678 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2293   -2.9128   -0.7566 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0766   -2.7672    1.2227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1649   -0.9716    1.3639 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3908   -2.6264   -0.5503 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1083   -2.1117    0.7407 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8763   -1.6222    1.9262 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7308    0.4699    1.7567 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9259    1.0802    1.8403 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1547    1.2700    0.8863 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5604    0.4255   -1.4116 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6965   -0.5885   -2.6810 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4269   -0.7594   -1.6556 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2071    1.3528   -0.8571 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8984    0.1988   -0.5232 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8333    2.4598    1.7082 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8890    1.1258   -0.8869 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8990    2.8865   -1.1179 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8905    3.2130    0.0409 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8610    1.6709    0.9145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7442    1.3207   -2.0778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1689    2.2191   -1.5278 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  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
 10 11  1  0
 11 18  1  0
 18 19  1  0
 19 20  2  0
 19 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 24  4  1  0
 17 12  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  5 28  1  0
  5 29  1  0
  6 30  1  0
  6 31  1  0
  7 32  1  0
  7 33  1  0
  8 34  1  0
  8 35  1  0
  9 36  1  0
 10 37  1  0
 10 38  1  0
 11 39  1  1
 18 45  1  0
 18 46  1  0
 21 47  1  0
 22 48  1  0
 22 49  1  0
 23 50  1  0
 23 51  1  0
 24 52  1  0
 24 53  1  0
 13 40  1  0
 14 41  1  0
 15 42  1  0
 16 43  1  0
 17 44  1  0
M  END


  Mrv1533004161523522D          

 24 25  0  0  0  0            999 V2000
    4.2868    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    5.7750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    4.5375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    4.5375    0.0000 C   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
    5.7158    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    2.4750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    3.3000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    1.6500    0.0000 C   0  0  0  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
    5.0013    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    0.4125    0.0000 C   0  0  0  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
  1  2  1  0  0  0  0
  2  3  2  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
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 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
  4 18  1  0  0  0  0
 11 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 19 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0246547

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)N1CCCCNCC(CC(=O)NCCC1)C1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C19H29N3O2/c1-16(23)22-12-6-5-10-20-15-18(17-8-3-2-4-9-17)14-19(24)21-11-7-13-22/h2-4,8-9,18,20H,5-7,10-15H2,1H3,(H,21,24)

> <INCHI_KEY>
OJHBIIMDJHZZCQ-UHFFFAOYSA-N

> <FORMULA>
C19H29N3O2

> <MOLECULAR_WEIGHT>
331.46

> <EXACT_MASS>
331.225977186

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
37.215175318051735

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1-acetyl-8-phenyl-1,5,10-triazacyclotetradecan-6-one

> <ALOGPS_LOGP>
1.34

> <JCHEM_LOGP>
0.43758509466666684

> <ALOGPS_LOGS>
-3.47

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.867532400762613

> <JCHEM_PKA_STRONGEST_BASIC>
8.009830980916394

> <JCHEM_POLAR_SURFACE_AREA>
61.440000000000005

> <JCHEM_REFRACTIVITY>
96.2146

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.12e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-acetyl-8-phenyl-1,5,10-triazacyclotetradecan-6-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0       8.002  10.780   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.336  10.010   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      10.669  10.780   0.000  0.00  0.00           O+0
HETATM    4  N   UNK     0       9.336   8.470   0.000  0.00  0.00           N+0
HETATM    5  C   UNK     0      10.669   9.240   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      12.003   8.470   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      12.003   6.930   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      10.669   6.160   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0      10.669   4.620   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0       9.336   3.850   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.002   4.620   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.668   3.850   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.335   4.620   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       4.001   3.850   0.000  0.00  0.00           O+0
HETATM   15  N   UNK     0       5.335   6.160   0.000  0.00  0.00           N+0
HETATM   16  C   UNK     0       6.668   6.930   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.668   8.470   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.002   9.240   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.002   3.080   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.336   2.310   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.336   0.770   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.002  -0.000   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.668   0.770   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   18                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   19                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17    4                                                       
CONECT   19   11   20   24                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   19                                                       
MASTER        0    0    0    0    0    0    0    0   24    0   50    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₂₉N₃O₂

Average Mass

331.4600 Da

Monoisotopic Mass

331.22598 Da

IUPAC Name

1-acetyl-8-phenyl-1,5,10-triazacyclotetradecan-6-one

Traditional Name

1-acetyl-8-phenyl-1,5,10-triazacyclotetradecan-6-one

CAS Registry Number

Not Available

SMILES

CC(=O)N1CCCCNCC(CC(=O)NCCC1)C1=CC=CC=C1

InChI Identifier

InChI=1S/C19H29N3O2/c1-16(23)22-12-6-5-10-20-15-18(17-8-3-2-4-9-17)14-19(24)21-11-7-13-22/h2-4,8-9,18,20H,5-7,10-15H2,1H3,(H,21,24)

InChI Key

OJHBIIMDJHZZCQ-UHFFFAOYSA-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
Maytenus buxifolia	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as aralkylamines. These are alkylamines in which the alkyl group is substituted at one carbon atom by an aromatic hydrocarbyl group.

Kingdom

Organic compounds

Super Class

Organic nitrogen compounds

Class

Organonitrogen compounds

Sub Class

Amines

Direct Parent

Aralkylamines

Alternative Parents

Substituents

Aralkylamine
Monocyclic benzene moiety
Benzenoid
Tertiary carboxylic acid amide
Acetamide
Cyclic carboximidic acid
Amino acid or derivatives
Carboxamide group
Carboxylic acid derivative
Secondary aliphatic amine
Secondary amine
Azacycle
Propargyl-type 1,3-dipolar organic compound
Organic 1,3-dipolar compound
Organoheterocyclic compound
Organooxygen compound
Organopnictogen compound
Hydrocarbon derivative
Carbonyl group
Organic oxide
Organic oxygen compound
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic 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	1.34	ALOGPS
logP	0.44	ChemAxon
logS	-3.5	ALOGPS
pKa (Strongest Acidic)	14.87	ChemAxon
pKa (Strongest Basic)	8.01	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	61.44 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	96.21 m³·mol⁻¹	ChemAxon
Polarizability	37.22 Å³	ChemAxon
Number of Rings	2	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

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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1-(6-hydroxy-8-phenyl-1,5,10-triazacyclotetradec-5-en-1-yl)ethanone (NP0246547)

MOL for NP0246547 (1-(6-hydroxy-8-phenyl-1,5,10-triazacyclotetradec-5-en-1-yl)ethanone)

3D MOL for NP0246547 (1-(6-hydroxy-8-phenyl-1,5,10-triazacyclotetradec-5-en-1-yl)ethanone)

3D SDF for NP0246547 (1-(6-hydroxy-8-phenyl-1,5,10-triazacyclotetradec-5-en-1-yl)ethanone)

3D-SDF for NP0246547 (1-(6-hydroxy-8-phenyl-1,5,10-triazacyclotetradec-5-en-1-yl)ethanone)

PDB for NP0246547 (1-(6-hydroxy-8-phenyl-1,5,10-triazacyclotetradec-5-en-1-yl)ethanone)

3D PDB for NP0246547 (1-(6-hydroxy-8-phenyl-1,5,10-triazacyclotetradec-5-en-1-yl)ethanone)

SMILES for NP0246547 (1-(6-hydroxy-8-phenyl-1,5,10-triazacyclotetradec-5-en-1-yl)ethanone)

INCHI for NP0246547 (1-(6-hydroxy-8-phenyl-1,5,10-triazacyclotetradec-5-en-1-yl)ethanone)

Structure for NP0246547 (1-(6-hydroxy-8-phenyl-1,5,10-triazacyclotetradec-5-en-1-yl)ethanone)

3D Structure for NP0246547 (1-(6-hydroxy-8-phenyl-1,5,10-triazacyclotetradec-5-en-1-yl)ethanone)