NP-MRD: Showing NP-Card for (1r)-2-[(2s,6r)-6-[(2s)-2-hydroxy-2-phenylethyl]piperidin-2-yl]-1-phenylethanol (NP0153171)

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Record Information

Version

2.0

Created at

2022-09-02 09:46:31 UTC

Updated at

2022-09-02 09:46:31 UTC

NP-MRD ID

NP0153171

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r)-2-[(2s,6r)-6-[(2s)-2-hydroxy-2-phenylethyl]piperidin-2-yl]-1-phenylethanol

Description

ZINC4974918 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. (1r)-2-[(2s,6r)-6-[(2s)-2-hydroxy-2-phenylethyl]piperidin-2-yl]-1-phenylethanol is found in Lobelia inflata and Lobelia polyphylla. Based on a literature review very few articles have been published on ZINC4974918.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 51 53  0  0  0  0  0  0  0  0999 V2000
    4.0001    2.7648   -0.4433 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6657    1.6224    0.2678 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2386    1.4551    0.6202 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2160    1.4116   -0.4461 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3575    0.2974   -1.4366 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0092   -1.0395   -0.8068 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1865   -0.9001    0.1398 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355    0.3166   -0.2767 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3263    0.4731    0.2052 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2219   -0.6324   -0.2584 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9044   -1.8976    0.1358 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6423   -0.3960    0.1005 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4940    0.1808   -0.8029 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8272    0.3973   -0.4480 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2601    0.0314    0.7915 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4016   -0.5481    1.6972 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0880   -0.7579    1.3386 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1223    1.4825    0.0760 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.4396    0.4228   -0.0173 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6278   -0.4915    1.0308 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3686   -1.6447    0.8868 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9634   -1.9478   -0.3160 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7819   -1.0556   -1.3447 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0445    0.0887   -1.1954 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5720    2.8331   -1.3192 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1265    1.9389    1.3213 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8897    2.2678    1.3451 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1961    0.5178    1.2709 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3336    2.3693   -1.0508 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7218    0.4909   -2.3399 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3694    0.1988   -1.8396 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7480   -1.7743   -1.5679 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8539   -1.3637   -0.1740 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1651   -0.7205    1.1835 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7124   -1.8474    0.1460 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0196    0.2743   -1.4115 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7282    1.4102   -0.2892 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4032    0.6499    1.3039 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1191   -0.6341   -1.3936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8964   -2.0749    1.0937 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1563    0.4744   -1.7907 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4737    0.8520   -1.1771 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3038    0.1986    1.0752 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7809   -0.8246    2.6697 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4475   -1.2128    2.0749 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6290    2.3578   -0.1318 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1878   -0.3169    2.0074 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4870   -2.3257    1.7308 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5461   -2.8532   -0.4320 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2547   -1.2953   -2.3026 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9155    0.7762   -2.0197 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  1  0
 10 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
  8 18  1  0
  2 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  2  0
 18  4  1  0
 24 19  1  0
 17 12  1  0
  1 25  1  0
  2 26  1  1
  3 27  1  0
  3 28  1  0
  4 29  1  6
  5 30  1  0
  5 31  1  0
  6 32  1  0
  6 33  1  0
  7 34  1  0
  7 35  1  0
  8 36  1  6
  9 37  1  0
  9 38  1  0
 10 39  1  6
 11 40  1  0
 13 41  1  0
 14 42  1  0
 15 43  1  0
 16 44  1  0
 17 45  1  0
 18 46  1  0
 20 47  1  0
 21 48  1  0
 22 49  1  0
 23 50  1  0
 24 51  1  0
M  END


  Mrv1652309022211462D          

 24 26  0  0  1  0            999 V2000
    0.0000   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0000   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.9500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    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  0  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  1  1  6  0  0  0
  2  3  1  0  0  0  0
  4  3  1  1  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  1  0  0  0
  9 10  1  0  0  0  0
 10 11  1  1  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 12 17  1  0  0  0  0
  8 18  1  0  0  0  0
  4 18  1  0  0  0  0
  2 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>
NP0153171

> <DATABASE_NAME>
NP-MRD

> <SMILES>
O[C@@H](C[C@H]1CCC[C@@H](C[C@@H](O)C2=CC=CC=C2)N1)C1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C21H27NO2/c23-20(16-8-3-1-4-9-16)14-18-12-7-13-19(22-18)15-21(24)17-10-5-2-6-11-17/h1-6,8-11,18-24H,7,12-15H2/t18-,19+,20+,21-

> <INCHI_KEY>
UMXDEQATKLAHCQ-UJOPUZHASA-N

> <FORMULA>
C21H27NO2

> <MOLECULAR_WEIGHT>
325.452

> <EXACT_MASS>
325.204179113

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
51

> <JCHEM_AVERAGE_POLARIZABILITY>
38.09313758858018

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R)-2-[(2S,6R)-6-[(2S)-2-hydroxy-2-phenylethyl]piperidin-2-yl]-1-phenylethan-1-ol

> <ALOGPS_LOGP>
3.12

> <JCHEM_LOGP>
3.085217628666666

> <ALOGPS_LOGS>
-4.30

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
14.735666959958927

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.133611715683553

> <JCHEM_PKA_STRONGEST_BASIC>
9.559649157356585

> <JCHEM_POLAR_SURFACE_AREA>
52.49

> <JCHEM_REFRACTIVITY>
97.05680000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.64e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R)-2-[(2S,6R)-6-[(2S)-2-hydroxy-2-phenylethyl]piperidin-2-yl]-1-phenylethanol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  O   UNK     0       0.000  -3.080   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.667  -7.700   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.000  -7.700   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.000  -9.240   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       1.334 -10.010   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -1.334 -10.010   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.334 -11.550   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.667 -12.320   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -4.001 -11.550   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -4.001 -10.010   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -2.667  -9.240   0.000  0.00  0.00           C+0
HETATM   18  N   UNK     0       1.334  -5.390   0.000  0.00  0.00           N+0
HETATM   19  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   19                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   18                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   18                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   17                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   12                                                       
CONECT   18    8    4                                                       
CONECT   19    2   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   52    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₂₇NO₂

Average Mass

325.4520 Da

Monoisotopic Mass

325.20418 Da

IUPAC Name

(1R)-2-[(2S,6R)-6-[(2S)-2-hydroxy-2-phenylethyl]piperidin-2-yl]-1-phenylethan-1-ol

Traditional Name

(1R)-2-[(2S,6R)-6-[(2S)-2-hydroxy-2-phenylethyl]piperidin-2-yl]-1-phenylethanol

CAS Registry Number

Not Available

SMILES

O[C@@H](C[C@H]1CCC[C@@H](C[C@@H](O)C2=CC=CC=C2)N1)C1=CC=CC=C1

InChI Identifier

InChI=1S/C21H27NO2/c23-20(16-8-3-1-4-9-16)14-18-12-7-13-19(22-18)15-21(24)17-10-5-2-6-11-17/h1-6,8-11,18-24H,7,12-15H2/t18-,19+,20+,21-

InChI Key

UMXDEQATKLAHCQ-UJOPUZHASA-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
Lobelia inflata	LOTUS Database	35616633
Lobelia polyphylla	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
Piperidine
Benzenoid
1,3-aminoalcohol
Secondary alcohol
Secondary aliphatic amine
Azacycle
Organoheterocyclic compound
Secondary amine
Organooxygen compound
Organic oxygen compound
Alcohol
Hydrocarbon derivative
Aromatic alcohol
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	3.12	ALOGPS
logP	3.09	ChemAxon
logS	-4.3	ALOGPS
pKa (Strongest Acidic)	14.13	ChemAxon
pKa (Strongest Basic)	9.56	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	52.49 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	97.06 m³·mol⁻¹	ChemAxon
Polarizability	38.09 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

92245342

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r)-2-[(2s,6r)-6-[(2s)-2-hydroxy-2-phenylethyl]piperidin-2-yl]-1-phenylethanol (NP0153171)

MOL for NP0153171 ((1r)-2-[(2s,6r)-6-[(2s)-2-hydroxy-2-phenylethyl]piperidin-2-yl]-1-phenylethanol)

3D MOL for NP0153171 ((1r)-2-[(2s,6r)-6-[(2s)-2-hydroxy-2-phenylethyl]piperidin-2-yl]-1-phenylethanol)

3D SDF for NP0153171 ((1r)-2-[(2s,6r)-6-[(2s)-2-hydroxy-2-phenylethyl]piperidin-2-yl]-1-phenylethanol)

3D-SDF for NP0153171 ((1r)-2-[(2s,6r)-6-[(2s)-2-hydroxy-2-phenylethyl]piperidin-2-yl]-1-phenylethanol)

PDB for NP0153171 ((1r)-2-[(2s,6r)-6-[(2s)-2-hydroxy-2-phenylethyl]piperidin-2-yl]-1-phenylethanol)

3D PDB for NP0153171 ((1r)-2-[(2s,6r)-6-[(2s)-2-hydroxy-2-phenylethyl]piperidin-2-yl]-1-phenylethanol)

SMILES for NP0153171 ((1r)-2-[(2s,6r)-6-[(2s)-2-hydroxy-2-phenylethyl]piperidin-2-yl]-1-phenylethanol)

INCHI for NP0153171 ((1r)-2-[(2s,6r)-6-[(2s)-2-hydroxy-2-phenylethyl]piperidin-2-yl]-1-phenylethanol)

Structure for NP0153171 ((1r)-2-[(2s,6r)-6-[(2s)-2-hydroxy-2-phenylethyl]piperidin-2-yl]-1-phenylethanol)

3D Structure for NP0153171 ((1r)-2-[(2s,6r)-6-[(2s)-2-hydroxy-2-phenylethyl]piperidin-2-yl]-1-phenylethanol)