NP-MRD: Showing NP-Card for [(1s,5r,10z,12e,16r,17s)-3,17-dihydroxy-5,17-dimethyl-14-methylidene-11-propyl-7,20-dithia-4,21-diazatricyclo[14.3.1.1⁶,⁹]henicosa-3,6(21),8,10,12-pentaen-1-yl]acetic acid (NP0268147)

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Record Information

Version

2.0

Created at

2022-09-08 13:10:32 UTC

Updated at

2022-09-08 13:10:33 UTC

NP-MRD ID

NP0268147

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[(1s,5r,10z,12e,16r,17s)-3,17-dihydroxy-5,17-dimethyl-14-methylidene-11-propyl-7,20-dithia-4,21-diazatricyclo[14.3.1.1⁶,⁹]henicosa-3,6(21),8,10,12-pentaen-1-yl]acetic acid

Description

Based on a literature review very few articles have been published on 2-[(1S,5R,10Z,12Z,16R,17S)-3,17-dihydroxy-5,17-dimethyl-14-methylidene-11-propyl-7,20-dithia-4,21-diazatricyclo[14.3.1.1⁶,⁹]Henicosa-3,6(21),8,10,12-pentaen-1-yl]acetic acid.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242104233D          

 67 69  0  0  0  0            999 V2000
    1.0474   -3.4014   -1.3843 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7972   -2.1242   -1.0084 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3812   -1.0375   -1.7623 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3380   -0.2013   -1.4051 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.4787   -0.5212   -0.0297 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0576   -0.2334    1.3144 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.5200   -0.6768    1.3606 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4703    0.4252    0.9320 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5976    1.6476    0.9740 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6836    2.5379    2.0477 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4995    3.7051    1.6099 S   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.1328   -2.0486    0.1709 C   0  0  2  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

 67 69  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1652306242104233D          

 67 69  0  0  0  0            999 V2000
    1.0474   -3.4014   -1.3843 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7972   -2.1242   -1.0084 C   0  0  0  0  0  0  0  0  0  0  0  0
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  5  6  1  0  0  0  0
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 32  2  1  0  0  0  0
 14 10  1  0  0  0  0
 33 21  1  0  0  0  0
  1 34  1  0  0  0  0
  1 35  1  0  0  0  0
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  4 37  1  0  0  0  0
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 32 66  1  0  0  0  0
 32 67  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0268147

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC(=O)C([H])([H])[C@@]12S[C@]([H])(C([H])([H])C(=C([H])[H])\C([H])=C(\[H])/C(=C([H])\C3=C([H])SC(=N3)[C@]([H])(N([H])C(=O)C1([H])[H])C([H])([H])[H])/C([H])([H])C([H])([H])C([H])([H])[H])[C@](O[H])(C([H])([H])[H])C([H])([H])C2([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C25H34N2O4S2/c1-5-6-18-8-7-16(2)11-20-24(4,31)9-10-25(33-20,14-22(29)30)13-21(28)26-17(3)23-27-19(12-18)15-32-23/h7-8,12,15,17,20,31H,2,5-6,9-11,13-14H2,1,3-4H3,(H,26,28)(H,29,30)/b8-7-,18-12-/t17-,20-,24+,25+/m1/s1

> <INCHI_KEY>
AJDKITCLGCYCKZ-LECOWXBGSA-N

> <FORMULA>
C25H34N2O4S2

> <MOLECULAR_WEIGHT>
490.68

> <EXACT_MASS>
490.195999931

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
67

> <JCHEM_AVERAGE_POLARIZABILITY>
52.635219479943295

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-[(1S,5R,10Z,12Z,16R,17S)-17-hydroxy-5,17-dimethyl-14-methylidene-3-oxo-11-propyl-7,20-dithia-4,21-diazatricyclo[14.3.1.1^{6,9}]henicosa-6(21),8,10,12-tetraen-1-yl]acetic acid

> <ALOGPS_LOGP>
3.58

> <JCHEM_LOGP>
3.5251216430000007

> <ALOGPS_LOGS>
-5.16

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
11.868221859579203

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.602948953353368

> <JCHEM_PKA_STRONGEST_BASIC>
1.2514217251914563

> <JCHEM_POLAR_SURFACE_AREA>
99.52000000000001

> <JCHEM_REFRACTIVITY>
134.42599999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.36e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[(1S,5R,10Z,12Z,16R,17S)-17-hydroxy-5,17-dimethyl-14-methylidene-3-oxo-11-propyl-7,20-dithia-4,21-diazatricyclo[14.3.1.1^{6,9}]henicosa-6(21),8,10,12-tetraen-1-yl]acetic acid

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 67 69  0  0  0  0  0  0  0  0999 V2000
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    1.6836    2.5379    2.0477 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.3560   -2.7760    0.9143 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
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  5  6  1  0
  6  7  1  0
  7  8  1  0
  5  9  2  0
  9 10  1  0
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 28 31  1  0
 31 32  1  0
 31 33  1  0
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 33 21  1  0
  1 34  1  0
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  9 45  1  0
 11 46  1  0
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 29 61  1  0
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 31 65  1  1
 32 66  1  0
 32 67  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0       1.047  -3.401  -1.384  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.797  -2.124  -1.008  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.381  -1.038  -1.762  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.338  -0.201  -1.405  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.011  -0.088  -0.156  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.479  -0.521  -0.030  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.058  -0.233   1.314  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.520  -0.677   1.361  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.470   0.425   0.932  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.598   1.648   0.974  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.684   2.538   2.048  0.00  0.00           C+0
HETATM   12  S   UNK     0       0.500   3.705   1.610  0.00  0.00           S+0
HETATM   13  C   UNK     0      -0.019   3.012   0.136  0.00  0.00           C+0
HETATM   14  N   UNK     0       0.734   1.947   0.065  0.00  0.00           N+0
HETATM   15  C   UNK     0      -1.056   3.506  -0.763  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.569   3.145  -2.183  0.00  0.00           C+0
HETATM   17  N   UNK     0      -2.425   3.194  -0.527  0.00  0.00           N+0
HETATM   18  C   UNK     0      -3.263   2.540   0.347  0.00  0.00           C+0
HETATM   19  O   UNK     0      -3.917   3.346   1.154  0.00  0.00           O+0
HETATM   20  C   UNK     0      -3.647   1.129   0.636  0.00  0.00           C+0
HETATM   21  C   UNK     0      -2.407   0.238   0.673  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.704   0.666   1.858  0.00  0.00           C+0
HETATM   23  C   UNK     0      -2.505   0.393   3.137  0.00  0.00           C+0
HETATM   24  O   UNK     0      -3.577  -0.237   3.146  0.00  0.00           O+0
HETATM   25  O   UNK     0      -2.030   0.862   4.350  0.00  0.00           O+0
HETATM   26  C   UNK     0      -1.978   0.167  -0.705  0.00  0.00           C+0
HETATM   27  C   UNK     0      -2.655  -0.925  -1.550  0.00  0.00           C+0
HETATM   28  C   UNK     0      -2.278  -2.326  -1.240  0.00  0.00           C+0
HETATM   29  C   UNK     0      -1.859  -3.148  -2.411  0.00  0.00           C+0
HETATM   30  O   UNK     0      -3.536  -2.956  -0.920  0.00  0.00           O+0
HETATM   31  C   UNK     0      -1.505  -2.429   0.012  0.00  0.00           C+0
HETATM   32  C   UNK     0      -0.133  -2.049   0.171  0.00  0.00           C+0
HETATM   33  S   UNK     0      -2.734  -1.511   1.080  0.00  0.00           S+0
HETATM   34  H   UNK     0       1.652  -3.697  -2.209  0.00  0.00           H+0
HETATM   35  H   UNK     0       0.599  -4.201  -0.805  0.00  0.00           H+0
HETATM   36  H   UNK     0       0.943  -0.938  -2.810  0.00  0.00           H+0
HETATM   37  H   UNK     0       2.684   0.464  -2.241  0.00  0.00           H+0
HETATM   38  H   UNK     0       5.046   0.075  -0.782  0.00  0.00           H+0
HETATM   39  H   UNK     0       4.643  -1.578  -0.207  0.00  0.00           H+0
HETATM   40  H   UNK     0       5.040   0.815   1.632  0.00  0.00           H+0
HETATM   41  H   UNK     0       4.556  -0.856   2.107  0.00  0.00           H+0
HETATM   42  H   UNK     0       6.928  -0.238   2.300  0.00  0.00           H+0
HETATM   43  H   UNK     0       6.998  -0.208   0.464  0.00  0.00           H+0
HETATM   44  H   UNK     0       6.580  -1.772   1.357  0.00  0.00           H+0
HETATM   45  H   UNK     0       2.699  -0.114   1.857  0.00  0.00           H+0
HETATM   46  H   UNK     0       2.333   2.506   2.941  0.00  0.00           H+0
HETATM   47  H   UNK     0      -0.954   4.668  -0.876  0.00  0.00           H+0
HETATM   48  H   UNK     0       0.398   3.673  -2.323  0.00  0.00           H+0
HETATM   49  H   UNK     0      -1.315   3.609  -2.888  0.00  0.00           H+0
HETATM   50  H   UNK     0      -0.524   2.082  -2.370  0.00  0.00           H+0
HETATM   51  H   UNK     0      -3.001   3.674  -1.344  0.00  0.00           H+0
HETATM   52  H   UNK     0      -4.260   1.103   1.529  0.00  0.00           H+0
HETATM   53  H   UNK     0      -4.273   0.665  -0.166  0.00  0.00           H+0
HETATM   54  H   UNK     0      -0.726   0.298   2.160  0.00  0.00           H+0
HETATM   55  H   UNK     0      -1.721   1.817   1.865  0.00  0.00           H+0
HETATM   56  H   UNK     0      -2.691   1.140   5.063  0.00  0.00           H+0
HETATM   57  H   UNK     0      -0.917   0.237  -0.958  0.00  0.00           H+0
HETATM   58  H   UNK     0      -2.381   1.041  -1.329  0.00  0.00           H+0
HETATM   59  H   UNK     0      -3.742  -0.719  -1.579  0.00  0.00           H+0
HETATM   60  H   UNK     0      -2.292  -0.744  -2.589  0.00  0.00           H+0
HETATM   61  H   UNK     0      -1.141  -2.701  -3.086  0.00  0.00           H+0
HETATM   62  H   UNK     0      -1.626  -4.174  -2.043  0.00  0.00           H+0
HETATM   63  H   UNK     0      -2.742  -3.358  -3.104  0.00  0.00           H+0
HETATM   64  H   UNK     0      -3.397  -3.785  -0.446  0.00  0.00           H+0
HETATM   65  H   UNK     0      -1.662  -3.496   0.377  0.00  0.00           H+0
HETATM   66  H   UNK     0       0.090  -1.110   0.629  0.00  0.00           H+0
HETATM   67  H   UNK     0       0.356  -2.776   0.914  0.00  0.00           H+0
CONECT    1    2   34   35                                                  
CONECT    2    1    3   32                                                  
CONECT    3    2    4   36                                                  
CONECT    4    3    5   37                                                  
CONECT    5    4    6    9                                                  
CONECT    6    5    7   38   39                                             
CONECT    7    6    8   40   41                                             
CONECT    8    7   42   43   44                                             
CONECT    9    5   10   45                                                  
CONECT   10    9   11   14                                                  
CONECT   11   10   12   46                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13   10                                                       
CONECT   15   13   16   17   47                                             
CONECT   16   15   48   49   50                                             
CONECT   17   15   18   51                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   52   53                                             
CONECT   21   20   22   26   33                                             
CONECT   22   21   23   54   55                                             
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   56                                                       
CONECT   26   21   27   57   58                                             
CONECT   27   26   28   59   60                                             
CONECT   28   27   29   30   31                                             
CONECT   29   28   61   62   63                                             
CONECT   30   28   64                                                       
CONECT   31   28   32   33   65                                             
CONECT   32   31    2   66   67                                             
CONECT   33   31   21                                                       
CONECT   34    1                                                            
CONECT   35    1                                                            
CONECT   36    3                                                            
CONECT   37    4                                                            
CONECT   38    6                                                            
CONECT   39    6                                                            
CONECT   40    7                                                            
CONECT   41    7                                                            
CONECT   42    8                                                            
CONECT   43    8                                                            
CONECT   44    8                                                            
CONECT   45    9                                                            
CONECT   46   11                                                            
CONECT   47   15                                                            
CONECT   48   16                                                            
CONECT   49   16                                                            
CONECT   50   16                                                            
CONECT   51   17                                                            
CONECT   52   20                                                            
CONECT   53   20                                                            
CONECT   54   22                                                            
CONECT   55   22                                                            
CONECT   56   25                                                            
CONECT   57   26                                                            
CONECT   58   26                                                            
CONECT   59   27                                                            
CONECT   60   27                                                            
CONECT   61   29                                                            
CONECT   62   29                                                            
CONECT   63   29                                                            
CONECT   64   30                                                            
CONECT   65   31                                                            
CONECT   66   32                                                            
CONECT   67   32                                                            
MASTER        0    0    0    0    0    0    0    0   67    0  138    0
END

RDKit          3D

67 69  0  0  0  0  0  0  0  0999 V2000
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  1  2  2  0
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  6  7  1  0
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  5  9  2  0
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 31 33  1  0
 32  2  1  0
 14 10  1  0
 33 21  1  0
  1 34  1  0
  1 35  1  0
  3 36  1  0
  4 37  1  0
  6 38  1  0
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  7 40  1  0
  7 41  1  0
  8 42  1  0
  8 43  1  0
  8 44  1  0
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 11 46  1  0
 15 47  1  6
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 29 61  1  0
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 30 64  1  0
 31 65  1  1
 32 66  1  0
 32 67  1  0
M  END

View in JSmol

Synonyms

Value	Source
2-[(1S,5R,10Z,12Z,16R,17S)-3,17-Dihydroxy-5,17-dimethyl-14-methylidene-11-propyl-7,20-dithia-4,21-diazatricyclo[14.3.1.1,]henicosa-3,6(21),8,10,12-pentaen-1-yl]acetate	Generator

Chemical Formula

C₂₅H₃₄N₂O₄S₂

Average Mass

490.6800 Da

Monoisotopic Mass

490.19600 Da

IUPAC Name

2-[(1S,5R,10Z,12Z,16R,17S)-17-hydroxy-5,17-dimethyl-14-methylidene-3-oxo-11-propyl-7,20-dithia-4,21-diazatricyclo[14.3.1.1^{6,9}]henicosa-6(21),8,10,12-tetraen-1-yl]acetic acid

Traditional Name

[(1S,5R,10Z,12Z,16R,17S)-17-hydroxy-5,17-dimethyl-14-methylidene-3-oxo-11-propyl-7,20-dithia-4,21-diazatricyclo[14.3.1.1^{6,9}]henicosa-6(21),8,10,12-tetraen-1-yl]acetic acid

CAS Registry Number

Not Available

SMILES

[H]OC(=O)C([H])([H])[C@@]12S[C@]([H])(C([H])([H])C(=C([H])[H])\C([H])=C(\[H])/C(=C([H])\C3=C([H])SC(=N3)[C@]([H])(N([H])C(=O)C1([H])[H])C([H])([H])[H])/C([H])([H])C([H])([H])C([H])([H])[H])[C@](O[H])(C([H])([H])[H])C([H])([H])C2([H])[H]

InChI Identifier

InChI=1S/C25H34N2O4S2/c1-5-6-18-8-7-16(2)11-20-24(4,31)9-10-25(33-20,14-22(29)30)13-21(28)26-17(3)23-27-19(12-18)15-32-23/h7-8,12,15,17,20,31H,2,5-6,9-11,13-14H2,1,3-4H3,(H,26,28)(H,29,30)/b8-7-,18-12-/t17-,20-,24+,25+/m1/s1

InChI Key

AJDKITCLGCYCKZ-LECOWXBGSA-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
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

Not Available

Chemical Taxonomy

Classification

Not classified

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	3.58	ALOGPS
logP	3.53	ChemAxon
logS	-5.2	ALOGPS
pKa (Strongest Acidic)	4.6	ChemAxon
pKa (Strongest Basic)	1.25	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	99.52 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	134.43 m³·mol⁻¹	ChemAxon
Polarizability	52.64 Å³	ChemAxon
Number of Rings	3	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

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 [(1s,5r,10z,12e,16r,17s)-3,17-dihydroxy-5,17-dimethyl-14-methylidene-11-propyl-7,20-dithia-4,21-diazatricyclo[14.3.1.1⁶,⁹]henicosa-3,6(21),8,10,12-pentaen-1-yl]acetic acid (NP0268147)

MOL for NP0268147 ([(1s,5r,10z,12e,16r,17s)-3,17-dihydroxy-5,17-dimethyl-14-methylidene-11-propyl-7,20-dithia-4,21-diazatricyclo[14.3.1.1⁶,⁹]henicosa-3,6(21),8,10,12-pentaen-1-yl]acetic acid)

3D MOL for NP0268147 ([(1s,5r,10z,12e,16r,17s)-3,17-dihydroxy-5,17-dimethyl-14-methylidene-11-propyl-7,20-dithia-4,21-diazatricyclo[14.3.1.1⁶,⁹]henicosa-3,6(21),8,10,12-pentaen-1-yl]acetic acid)

3D SDF for NP0268147 ([(1s,5r,10z,12e,16r,17s)-3,17-dihydroxy-5,17-dimethyl-14-methylidene-11-propyl-7,20-dithia-4,21-diazatricyclo[14.3.1.1⁶,⁹]henicosa-3,6(21),8,10,12-pentaen-1-yl]acetic acid)

3D-SDF for NP0268147 ([(1s,5r,10z,12e,16r,17s)-3,17-dihydroxy-5,17-dimethyl-14-methylidene-11-propyl-7,20-dithia-4,21-diazatricyclo[14.3.1.1⁶,⁹]henicosa-3,6(21),8,10,12-pentaen-1-yl]acetic acid)

PDB for NP0268147 ([(1s,5r,10z,12e,16r,17s)-3,17-dihydroxy-5,17-dimethyl-14-methylidene-11-propyl-7,20-dithia-4,21-diazatricyclo[14.3.1.1⁶,⁹]henicosa-3,6(21),8,10,12-pentaen-1-yl]acetic acid)

3D PDB for NP0268147 ([(1s,5r,10z,12e,16r,17s)-3,17-dihydroxy-5,17-dimethyl-14-methylidene-11-propyl-7,20-dithia-4,21-diazatricyclo[14.3.1.1⁶,⁹]henicosa-3,6(21),8,10,12-pentaen-1-yl]acetic acid)

SMILES for NP0268147 ([(1s,5r,10z,12e,16r,17s)-3,17-dihydroxy-5,17-dimethyl-14-methylidene-11-propyl-7,20-dithia-4,21-diazatricyclo[14.3.1.1⁶,⁹]henicosa-3,6(21),8,10,12-pentaen-1-yl]acetic acid)

INCHI for NP0268147 ([(1s,5r,10z,12e,16r,17s)-3,17-dihydroxy-5,17-dimethyl-14-methylidene-11-propyl-7,20-dithia-4,21-diazatricyclo[14.3.1.1⁶,⁹]henicosa-3,6(21),8,10,12-pentaen-1-yl]acetic acid)

Structure for NP0268147 ([(1s,5r,10z,12e,16r,17s)-3,17-dihydroxy-5,17-dimethyl-14-methylidene-11-propyl-7,20-dithia-4,21-diazatricyclo[14.3.1.1⁶,⁹]henicosa-3,6(21),8,10,12-pentaen-1-yl]acetic acid)

3D Structure for NP0268147 ([(1s,5r,10z,12e,16r,17s)-3,17-dihydroxy-5,17-dimethyl-14-methylidene-11-propyl-7,20-dithia-4,21-diazatricyclo[14.3.1.1⁶,⁹]henicosa-3,6(21),8,10,12-pentaen-1-yl]acetic acid)