NP-MRD: Showing NP-Card for (1s,2r,3s,5s,6s)-2-(hydroxymethyl)-3-[(2s)-2-hydroxypropyl]-8-azaspiro[bicyclo[3.2.1]octane-6,3'-indol]-2'-ol (NP0213484)

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Record Information

Version

2.0

Created at

2022-09-05 12:29:08 UTC

Updated at

2022-09-05 12:29:08 UTC

NP-MRD ID

NP0213484

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2r,3s,5s,6s)-2-(hydroxymethyl)-3-[(2s)-2-hydroxypropyl]-8-azaspiro[bicyclo[3.2.1]octane-6,3'-indol]-2'-ol

Description

CHEMBL3338226 belongs to the class of organic compounds known as beta amino acids and derivatives. These are amino acids having a (-NH2) group attached to the beta carbon atom. (1s,2r,3s,5s,6s)-2-(hydroxymethyl)-3-[(2s)-2-hydroxypropyl]-8-azaspiro[bicyclo[3.2.1]octane-6,3'-indol]-2'-ol is found in Alstonia angustifolia. Based on a literature review very few articles have been published on CHEMBL3338226.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 47 50  0  0  0  0  0  0  0  0999 V2000
   -4.2989    1.2516   -1.9666 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2488    1.2258   -0.8452 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6899    2.5250   -0.7585 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2214    0.2346   -1.2516 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0886    0.0354   -0.2992 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0957   -0.9710   -0.8443 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9122   -1.4348    0.1281 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3360   -1.8895    1.3919 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2522   -0.6887    1.8689 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8739    0.3344    1.6507 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8163   -0.3725    0.7180 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8203   -1.1405    1.5307 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4559   -2.0211    2.5313 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9702   -0.8111    1.1103 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9210    0.1368    0.0545 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9689    0.7027   -0.6223 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7378    1.6032   -1.6125 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4314    1.9213   -1.9062 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3687    1.3431   -1.2150 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5754    0.4242   -0.2035 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4908   -0.3323    1.1046 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5441   -1.3527    1.2425 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2822   -2.5954    0.6847 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1872    0.4060   -2.6525 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2620    2.1917   -2.5220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3317    1.1720   -1.5362 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7704    1.0779    0.0876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5418    2.7818    0.1945 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7573    0.6233   -2.2032 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7288   -0.7042   -1.5439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5700    1.0105   -0.2477 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4087   -0.5565   -1.7340 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6308   -1.8846   -1.2269 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5407   -2.1957   -0.3337 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1424   -2.7542    1.3996 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5223   -0.7484    2.9418 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5426    1.3163    1.3674 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3935    0.4312    2.6504 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3615   -1.7593    3.5073 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9994    0.4439   -0.3818 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5803    2.0432   -2.1402 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2202    2.6378   -2.6927 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3442    1.6070   -1.4572 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8836    0.6179    1.5674 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6871   -1.5104    2.3606 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5595   -1.0841    0.9007 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7920   -3.2914    1.2036 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  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 12  1  1
 12 13  1  0
 12 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
  9 21  1  0
 21 22  1  0
 22 23  1  0
 21  5  1  0
 11  7  1  0
 20 11  1  0
 20 15  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  2 27  1  1
  3 28  1  0
  4 29  1  0
  4 30  1  0
  5 31  1  1
  6 32  1  0
  6 33  1  0
  7 34  1  6
  8 35  1  0
  9 36  1  1
 10 37  1  0
 10 38  1  0
 13 39  1  0
 16 40  1  0
 17 41  1  0
 18 42  1  0
 19 43  1  0
 21 44  1  1
 22 45  1  0
 22 46  1  0
 23 47  1  0
M  END


  Mrv1652309052214292D          

 23 26  0  0  1  0            999 V2000
    6.5540    1.8494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0511    1.1954    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.2332    1.3040    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3660    0.4329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8631   -0.2211    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0557   -0.0518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4199   -0.5775    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0134   -1.3261    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.8894   -1.7075    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0885   -1.9052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4345   -1.4023    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3015   -2.2165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8821   -2.8027    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4861   -2.3417    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.1150   -1.6049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3192   -1.3876    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1094   -0.5897    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6956   -0.0091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4914   -0.2264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7012   -1.0243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2342   -0.9579    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.0590   -0.9434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4588   -0.2217    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  1  0  0  0
  2  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  9  8  1  1  0  0  0
  9 10  1  0  0  0  0
 11 10  1  6  0  0  0
  7 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 15 20  1  0  0  0  0
 11 20  1  0  0  0  0
  9 21  1  0  0  0  0
  5 21  1  0  0  0  0
 21 22  1  1  0  0  0
 22 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0213484

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H](O)C[C@@H]1C[C@@H]2N[C@@H](C[C@@]22C(O)=NC3=CC=CC=C23)[C@@H]1CO

> <INCHI_IDENTIFIER>
InChI=1S/C18H24N2O3/c1-10(22)6-11-7-16-18(8-15(19-16)12(11)9-21)13-4-2-3-5-14(13)20-17(18)23/h2-5,10-12,15-16,19,21-22H,6-9H2,1H3,(H,20,23)/t10-,11+,12+,15-,16-,18-/m0/s1

> <INCHI_KEY>
ZPMZMDMYYCLKMQ-NVMBSAOKSA-N

> <FORMULA>
C18H24N2O3

> <MOLECULAR_WEIGHT>
316.401

> <EXACT_MASS>
316.178692641

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
34.44882777505943

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2R,3S,5S,6S)-2-(hydroxymethyl)-3-[(2S)-2-hydroxypropyl]-8-azaspiro[bicyclo[3.2.1]octane-6,3'-indole]-2'-ol

> <JCHEM_LOGP>
-1.3506085588429266

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
15.413948744328323

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.84488352086466

> <JCHEM_PKA_STRONGEST_BASIC>
10.68727874591343

> <JCHEM_POLAR_SURFACE_AREA>
85.08

> <JCHEM_REFRACTIVITY>
89.17170000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,3S,5S,6S)-2-(hydroxymethyl)-3-[(2S)-2-hydroxypropyl]-8-azaspiro[bicyclo[3.2.1]octane-6,3'-indole]-2'-ol

> <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  C   UNK     0      12.234   3.452   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      11.295   2.231   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       9.769   2.434   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      11.883   0.808   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.944  -0.413   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.437  -0.097   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.250  -1.078   0.000  0.00  0.00           C+0
HETATM    8  N   UNK     0       9.358  -2.475   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0      10.994  -3.187   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.498  -3.556   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.278  -2.618   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.029  -4.138   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       9.113  -5.232   0.000  0.00  0.00           O+0
HETATM   14  N   UNK     0       6.507  -4.371   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0       5.815  -2.996   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.329  -2.590   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.938  -1.101   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.032  -0.017   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.517  -0.423   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.909  -1.912   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      11.637  -1.788   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      13.177  -1.761   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      13.923  -0.414   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   21                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   11                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   21                                                  
CONECT   10    9   11                                                       
CONECT   11   10    7   12   20                                             
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16   20                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   15   11                                                  
CONECT   21    9    5   22                                                  
CONECT   22   21   23                                                       
CONECT   23   22                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   52    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₂₄N₂O₃

Average Mass

316.4010 Da

Monoisotopic Mass

316.17869 Da

IUPAC Name

(1S,2R,3S,5S,6S)-2-(hydroxymethyl)-3-[(2S)-2-hydroxypropyl]-8-azaspiro[bicyclo[3.2.1]octane-6,3'-indole]-2'-ol

Traditional Name

(1S,2R,3S,5S,6S)-2-(hydroxymethyl)-3-[(2S)-2-hydroxypropyl]-8-azaspiro[bicyclo[3.2.1]octane-6,3'-indole]-2'-ol

CAS Registry Number

Not Available

SMILES

C[C@H](O)C[C@@H]1C[C@@H]2N[C@@H](C[C@@]22C(O)=NC3=CC=CC=C23)[C@@H]1CO

InChI Identifier

InChI=1S/C18H24N2O3/c1-10(22)6-11-7-16-18(8-15(19-16)12(11)9-21)13-4-2-3-5-14(13)20-17(18)23/h2-5,10-12,15-16,19,21-22H,6-9H2,1H3,(H,20,23)/t10-,11+,12+,15-,16-,18-/m0/s1

InChI Key

ZPMZMDMYYCLKMQ-NVMBSAOKSA-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
Alstonia angustifolia	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as beta amino acids and derivatives. These are amino acids having a (-NH2) group attached to the beta carbon atom.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Beta amino acids and derivatives

Alternative Parents

Substituents

Beta amino acid or derivatives
Indole or derivatives
Dihydroindole
Aralkylamine
Piperidine
Benzenoid
1,3-aminoalcohol
Pyrrolidine
Carboxamide group
Lactam
Secondary carboxylic acid amide
Secondary alcohol
Secondary aliphatic amine
Azacycle
Organoheterocyclic compound
Secondary amine
Organonitrogen compound
Alcohol
Hydrocarbon derivative
Organic oxide
Organic nitrogen compound
Organopnictogen compound
Carbonyl group
Organic oxygen compound
Organooxygen compound
Amine
Primary alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	-1.4	ChemAxon
pKa (Strongest Acidic)	3.84	ChemAxon
pKa (Strongest Basic)	10.69	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	85.08 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	89.17 m³·mol⁻¹	ChemAxon
Polarizability	34.45 Å³	ChemAxon
Number of Rings	4	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

58116506

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

118715148

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,2r,3s,5s,6s)-2-(hydroxymethyl)-3-[(2s)-2-hydroxypropyl]-8-azaspiro[bicyclo[3.2.1]octane-6,3'-indol]-2'-ol (NP0213484)

MOL for NP0213484 ((1s,2r,3s,5s,6s)-2-(hydroxymethyl)-3-[(2s)-2-hydroxypropyl]-8-azaspiro[bicyclo[3.2.1]octane-6,3'-indol]-2'-ol)

3D MOL for NP0213484 ((1s,2r,3s,5s,6s)-2-(hydroxymethyl)-3-[(2s)-2-hydroxypropyl]-8-azaspiro[bicyclo[3.2.1]octane-6,3'-indol]-2'-ol)

3D SDF for NP0213484 ((1s,2r,3s,5s,6s)-2-(hydroxymethyl)-3-[(2s)-2-hydroxypropyl]-8-azaspiro[bicyclo[3.2.1]octane-6,3'-indol]-2'-ol)

3D-SDF for NP0213484 ((1s,2r,3s,5s,6s)-2-(hydroxymethyl)-3-[(2s)-2-hydroxypropyl]-8-azaspiro[bicyclo[3.2.1]octane-6,3'-indol]-2'-ol)

PDB for NP0213484 ((1s,2r,3s,5s,6s)-2-(hydroxymethyl)-3-[(2s)-2-hydroxypropyl]-8-azaspiro[bicyclo[3.2.1]octane-6,3'-indol]-2'-ol)

3D PDB for NP0213484 ((1s,2r,3s,5s,6s)-2-(hydroxymethyl)-3-[(2s)-2-hydroxypropyl]-8-azaspiro[bicyclo[3.2.1]octane-6,3'-indol]-2'-ol)

SMILES for NP0213484 ((1s,2r,3s,5s,6s)-2-(hydroxymethyl)-3-[(2s)-2-hydroxypropyl]-8-azaspiro[bicyclo[3.2.1]octane-6,3'-indol]-2'-ol)

INCHI for NP0213484 ((1s,2r,3s,5s,6s)-2-(hydroxymethyl)-3-[(2s)-2-hydroxypropyl]-8-azaspiro[bicyclo[3.2.1]octane-6,3'-indol]-2'-ol)

Structure for NP0213484 ((1s,2r,3s,5s,6s)-2-(hydroxymethyl)-3-[(2s)-2-hydroxypropyl]-8-azaspiro[bicyclo[3.2.1]octane-6,3'-indol]-2'-ol)

3D Structure for NP0213484 ((1s,2r,3s,5s,6s)-2-(hydroxymethyl)-3-[(2s)-2-hydroxypropyl]-8-azaspiro[bicyclo[3.2.1]octane-6,3'-indol]-2'-ol)