NP-MRD: Showing NP-Card for Penazetidine A (NP0070294)

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Record Information

Version

2.0

Created at

2022-04-28 15:37:07 UTC

Updated at

2022-04-28 15:37:07 UTC

NP-MRD ID

NP0070294

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Penazetidine A

Description

(2S,3R,4R)-2-(hydroxymethyl)-4-[(12S)-12-methyloctadecyl]azetidin-3-ol belongs to the class of organic compounds known as azetidines. These are organic compounds containing a saturated four-member heterocycle where one nitrogen atom replaces a carbon atom. Penazetidine A is found in Panares sollasi and Penares sollasi. Based on a literature review very few articles have been published on (2S,3R,4R)-2-(hydroxymethyl)-4-[(12S)-12-methyloctadecyl]azetidin-3-ol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282217372D          

 26 26  0  0  1  0            999 V2000
   -2.3082    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0947    1.2094    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2978    0.9959    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5114    0.1990    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5834    1.4084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1311    0.9959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8456    1.4084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5600    0.9959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2745    1.4084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9890    0.9959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7035    1.4084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4179    0.9959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1324    1.4084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8469    0.9959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5613    1.4084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2758    0.9959    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.2758    0.1709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9903    1.4084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7048    0.9959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4192    1.4084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1337    0.9959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8482    1.4084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.5626    0.9959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5072    1.9239    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0227   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0227   -0.8250    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  0  0  0  0
  3  4  1  0  0  0  0
  1  4  1  0  0  0  0
  3  5  1  1  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  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  6  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
  2 24  1  6  0  0  0
  1 25  1  1  0  0  0
 25 26  1  0  0  0  0
M  END

     RDKit          3D

 73 73  0  0  0  0  0  0  0  0999 V2000
   -4.9020    2.9773   -0.1640 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2685    2.7720    0.3812 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1592    1.8059   -0.2908 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7724    0.3886   -0.3055 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4643    0.1010   -0.9840 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1923   -1.4031   -1.0005 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9094   -1.6980   -1.7048 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.6116   -3.1838   -1.7352 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7882   -0.8993   -1.1325 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4690   -1.2331   -1.8563 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3657   -0.4185   -1.2741 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1089   -0.6317    0.1851 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2540   -2.0622    0.4936 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5182   -2.2749    1.9451 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6570   -1.4995    2.5170 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9871   -1.8180    1.8939 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0715   -1.0167    2.5520 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8460    0.4593    2.3729 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8465    0.8102    0.9107 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1922    0.4515    0.3292 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2907    0.7673   -1.1122 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.7101    1.0402   -0.8408 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.2852    2.1331   -1.7075 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6234    3.3224   -1.5291 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2668    1.4970    0.5409 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.1639    1.2357    1.5492 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7843    2.6933   -1.2239 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7056    4.0999   -0.1193 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0900    2.5809    0.5010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1487    2.4604    1.4724 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8199    3.7689    0.3789 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2670    2.1386   -1.3798 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1988    1.8978    0.1449 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5447   -0.2652   -0.8275 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6554   -0.0401    0.7454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4639    0.5071   -1.9978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6135    0.5491   -0.4183 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0584   -1.9559   -1.4117 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0383   -1.6898    0.0812 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0531   -1.3705   -2.7698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1342   -3.5365   -0.8147 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0027   -3.4139   -2.6519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5698   -3.7200   -1.8847 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7003   -0.9546   -0.0467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9708    0.1885   -1.3903 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3449   -2.3096   -1.7555 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5770   -0.9599   -2.9254 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6014   -0.5583   -1.8105 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5802    0.6843   -1.3921 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9976   -0.3127    0.8024 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6874    0.0723    0.4885 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1895   -2.2768   -0.0874 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4983   -2.7731    0.1026 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6937   -3.3696    2.1091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3816   -2.0422    2.5622 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7187   -1.7295    3.5929 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4227   -0.4167    2.3990 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2088   -2.9052    2.0866 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0056   -1.7224    0.7976 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0664   -1.3613    2.2127 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0682   -1.2745    3.6555 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7639    0.9577    2.7947 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9403    0.7987    2.9117 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0234    0.2713    0.4176 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6539    1.9008    0.8499 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5359   -0.5722    0.4573 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8080    1.6971   -1.2519 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2878    0.1162   -0.8156 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2081    1.7593   -2.7695 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3711    2.1754   -1.4948 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1745    4.0348   -1.9524 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8358    2.5246    0.5264 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2332    2.0308    2.1276 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
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 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
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 22 25  1  0
 25 26  1  0
 25 20  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  2 30  1  0
  2 31  1  0
  3 32  1  0
  3 33  1  0
  4 34  1  0
  4 35  1  0
  5 36  1  0
  5 37  1  0
  6 38  1  0
  6 39  1  0
  7 40  1  6
  8 41  1  0
  8 42  1  0
  8 43  1  0
  9 44  1  0
  9 45  1  0
 10 46  1  0
 10 47  1  0
 11 48  1  0
 11 49  1  0
 12 50  1  0
 12 51  1  0
 13 52  1  0
 13 53  1  0
 14 54  1  0
 14 55  1  0
 15 56  1  0
 15 57  1  0
 16 58  1  0
 16 59  1  0
 17 60  1  0
 17 61  1  0
 18 62  1  0
 18 63  1  0
 19 64  1  0
 19 65  1  0
 20 66  1  6
 21 67  1  0
 22 68  1  1
 23 69  1  0
 23 70  1  0
 24 71  1  0
 25 72  1  6
 26 73  1  0
M  END


  Mrv1652304282217372D          

 26 26  0  0  1  0            999 V2000
   -2.3082    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0947    1.2094    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2978    0.9959    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5114    0.1990    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5834    1.4084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1311    0.9959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8456    1.4084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5600    0.9959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2745    1.4084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9890    0.9959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7035    1.4084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4179    0.9959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1324    1.4084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8469    0.9959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5613    1.4084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2758    0.9959    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.2758    0.1709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9903    1.4084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7048    0.9959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4192    1.4084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1337    0.9959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8482    1.4084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.5626    0.9959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5072    1.9239    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0227   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0227   -0.8250    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  0  0  0  0
  3  4  1  0  0  0  0
  1  4  1  0  0  0  0
  3  5  1  1  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  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  6  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
  2 24  1  6  0  0  0
  1 25  1  1  0  0  0
 25 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0070294

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCC[C@H](C)CCCCCCCCCCC[C@H]1N[C@@H](CO)[C@@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C23H47NO2/c1-3-4-5-13-16-20(2)17-14-11-9-7-6-8-10-12-15-18-21-23(26)22(19-25)24-21/h20-26H,3-19H2,1-2H3/t20-,21+,22-,23+/m0/s1

> <INCHI_KEY>
MXSVVKSZJQKNBC-GSPCLOLRSA-N

> <FORMULA>
C23H47NO2

> <MOLECULAR_WEIGHT>
369.634

> <EXACT_MASS>
369.360679757

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
73

> <JCHEM_AVERAGE_POLARIZABILITY>
49.82794041350795

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,3R,4R)-2-(hydroxymethyl)-4-[(12S)-12-methyloctadecyl]azetidin-3-ol

> <ALOGPS_LOGP>
6.83

> <JCHEM_LOGP>
6.714141857

> <ALOGPS_LOGS>
-5.88

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
15.179323217759446

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.02942150707771

> <JCHEM_PKA_STRONGEST_BASIC>
8.596024883621169

> <JCHEM_POLAR_SURFACE_AREA>
52.489999999999995

> <JCHEM_REFRACTIVITY>
111.75679999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
18

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.87e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3R,4R)-2-(hydroxymethyl)-4-[(12S)-12-methyloctadecyl]azetidin-3-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      -4.309   0.770   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -3.910   2.258   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.423   1.859   0.000  0.00  0.00           C+0
HETATM    4  N   UNK     0      -2.821   0.371   0.000  0.00  0.00           N+0
HETATM    5  C   UNK     0      -1.089   2.629   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.245   1.859   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.578   2.629   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.912   1.859   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.246   2.629   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.579   1.859   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.913   2.629   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.247   1.859   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.580   2.629   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.914   1.859   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      12.248   2.629   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      13.582   1.859   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      13.582   0.319   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      14.915   2.629   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      16.249   1.859   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      17.583   2.629   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      18.916   1.859   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      20.250   2.629   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      21.584   1.859   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -4.680   3.591   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -5.642  -0.000   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -5.642  -1.540   0.000  0.00  0.00           O+0
CONECT    1    2    4   25                                                  
CONECT    2    1    3   24                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3    1                                                       
CONECT    5    3    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                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22                                                            
CONECT   24    2                                                            
CONECT   25    1   26                                                       
CONECT   26   25                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   52    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₄₇NO₂

Average Mass

369.6340 Da

Monoisotopic Mass

369.36068 Da

IUPAC Name

(2S,3R,4R)-2-(hydroxymethyl)-4-[(12S)-12-methyloctadecyl]azetidin-3-ol

Traditional Name

(2S,3R,4R)-2-(hydroxymethyl)-4-[(12S)-12-methyloctadecyl]azetidin-3-ol

CAS Registry Number

Not Available

SMILES

CCCCCC[C@H](C)CCCCCCCCCCC[C@H]1N[C@@H](CO)[C@@H]1O

InChI Identifier

InChI=1S/C23H47NO2/c1-3-4-5-13-16-20(2)17-14-11-9-7-6-8-10-12-15-18-21-23(26)22(19-25)24-21/h20-26H,3-19H2,1-2H3/t20-,21+,22-,23+/m0/s1

InChI Key

MXSVVKSZJQKNBC-GSPCLOLRSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Panares sollasi	-	KNApSAcK
Penares sollasi	-	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as azetidines. These are organic compounds containing a saturated four-member heterocycle where one nitrogen atom replaces a carbon atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Azetidines

Sub Class

Not Available

Direct Parent

Azetidines

Alternative Parents

Substituents

Secondary alcohol
Azetidine
1,2-aminoalcohol
Azacycle
Secondary amine
Secondary aliphatic amine
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Organonitrogen compound
Amine
Alcohol
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic 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	6.83	ALOGPS
logP	6.71	ChemAxon
logS	-5.9	ALOGPS
pKa (Strongest Acidic)	14.03	ChemAxon
pKa (Strongest Basic)	8.6	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	18	ChemAxon
Refractivity	111.76 m³·mol⁻¹	ChemAxon
Polarizability	49.83 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	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

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

162822773

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Penazetidine A (NP0070294)

MOL for NP0070294 (Penazetidine A)

3D MOL for NP0070294 (Penazetidine A)

3D SDF for NP0070294 (Penazetidine A)

3D-SDF for NP0070294 (Penazetidine A)

PDB for NP0070294 (Penazetidine A)

3D PDB for NP0070294 (Penazetidine A)

SMILES for NP0070294 (Penazetidine A)

INCHI for NP0070294 (Penazetidine A)

Structure for NP0070294 (Penazetidine A)

3D Structure for NP0070294 (Penazetidine A)