NP-MRD: Showing NP-Card for 24-(1,2-dihydroxy-3-methylpent-3-en-1-yl)-2,22,23-trihydroxy-5,7,14,21-tetramethyl-11,15,26-trioxa-25-azahexacyclo[23.2.2.0³,¹³.0⁴,⁹.0¹⁰,¹².0¹⁴,¹⁶]nonacos-1-ene-27,28-dione (NP0250333)

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Record Information

Version

2.0

Created at

2022-09-07 13:07:43 UTC

Updated at

2022-09-07 13:07:43 UTC

NP-MRD ID

NP0250333

Secondary Accession Numbers

None

Natural Product Identification

Common Name

24-(1,2-dihydroxy-3-methylpent-3-en-1-yl)-2,22,23-trihydroxy-5,7,14,21-tetramethyl-11,15,26-trioxa-25-azahexacyclo[23.2.2.0³,¹³.0⁴,⁹.0¹⁰,¹².0¹⁴,¹⁶]nonacos-1-ene-27,28-dione

Description

24-(1,2-Dihydroxy-3-methylpent-3-en-1-yl)-2,22,23-trihydroxy-5,7,14,21-tetramethyl-11,15,26-trioxa-25-azahexacyclo[23.2.2.0³,¹³.0⁴,⁹.0¹⁰,¹².0¹⁴,¹⁶]Nonacos-1-ene-27,28-dione belongs to the class of organic compounds known as oxepanes. Oxepanes are compounds containing an oxepane ring, which is a seven-member saturated aliphatic heterocycle with one oxygen and six carbon atoms. Based on a literature review very few articles have been published on 24-(1,2-dihydroxy-3-methylpent-3-en-1-yl)-2,22,23-trihydroxy-5,7,14,21-tetramethyl-11,15,26-trioxa-25-azahexacyclo[23.2.2.0³,¹³.0⁴,⁹.0¹⁰,¹².0¹⁴,¹⁶]Nonacos-1-ene-27,28-dione.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072215072D          

 46 51  0  0  0  0            999 V2000
   -0.1300   -2.7165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7225   -2.1424    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5215   -1.3422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1140   -0.7681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2719   -1.1162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8644   -1.6903    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4729   -0.3161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1195    0.2581    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2663   -0.0901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1442    0.7534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3247    0.8485    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4682    1.5766    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7894    2.0456    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1143    2.1624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7013    2.8766    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9599    2.4353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7852    2.3655    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5327    2.0020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  2  1  1  4  0  0  0
  2  3  2  0  0  0  0
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 45 46  2  0  0  0  0
M  END

     RDKit          3D

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  7 56  1  1
  8 57  1  0
  9 58  1  6
 10 59  1  1
 11 60  1  0
 12 61  1  6
 13 62  1  0
 14 63  1  1
 15 64  1  0
 15 65  1  0
 15 66  1  0
 16 67  1  0
 16 68  1  0
 17 69  1  0
 17 70  1  0
 18 71  1  0
 18 72  1  0
 19 73  1  0
 19 74  1  0
 20 75  1  1
 23 76  1  0
 23 77  1  0
 23 78  1  0
 24 79  1  6
 25 80  1  1
 27 81  1  1
 28 82  1  6
 29 83  1  0
 29 84  1  0
 30 85  1  6
 31 86  1  0
 31 87  1  0
 31 88  1  0
 32 89  1  0
 32 90  1  0
 33 91  1  6
 34 92  1  0
 34 93  1  0
 34 94  1  0
 35 95  1  1
 36 96  1  6
 38 97  1  0
 42 98  1  0
 42 99  1  0
M  END


  Mrv1652309072215072D          

 46 51  0  0  0  0            999 V2000
   -0.1300   -2.7165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7225   -2.1424    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5215   -1.3422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1140   -0.7681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2719   -1.1162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8644   -1.6903    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4729   -0.3161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1195    0.2581    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2663   -0.0901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1442    0.7534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3247    0.8485    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4682    1.5766    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7894    2.0456    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1143    2.1624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7013    2.8766    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9599    2.4353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7852    2.3655    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5327    2.0020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0980    1.3934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4054    0.6220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1243    0.2171    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4142   -0.2029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0494   -0.7294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1305   -0.9857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9405   -1.1426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7504   -1.2995    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2095   -1.9225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6686   -2.5455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9377   -3.3253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3968   -3.9483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6658   -4.7282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5869   -3.7914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3178   -3.0115    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5079   -2.8545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8587   -2.3885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5896   -1.6086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8431   -2.0254    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3120   -2.6568    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9625   -2.0053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1646   -2.2667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0041   -3.0759    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5434   -1.7346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6190   -0.8988    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4073   -0.6552    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0446   -1.1687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8053   -0.8494    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  4  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 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
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
 28 35  1  0  0  0  0
 35 36  1  0  0  0  0
 24 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  4  0  0  0
 37 39  2  0  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
 40 42  1  0  0  0  0
 42 43  1  0  0  0  0
  9 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 39 45  1  0  0  0  0
 45 46  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0250333

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC=C(C)C(O)C(O)C1C(O)C(O)C(C)CCCCC2OC2(C)C2C3OC3C3CC(C)CC(C)C3C2C(O)=C2C(=O)CN1OC2=O

> <INCHI_IDENTIFIER>
InChI=1S/C35H53NO10/c1-7-16(3)27(38)30(41)26-31(42)28(39)17(4)10-8-9-11-21-35(6,45-21)25-24(29(40)23-20(37)14-36(26)46-34(23)43)22-18(5)12-15(2)13-19(22)32-33(25)44-32/h7,15,17-19,21-22,24-28,30-33,38-42H,8-14H2,1-6H3

> <INCHI_KEY>
WRAVXSOFTDSTQL-UHFFFAOYSA-N

> <FORMULA>
C35H53NO10

> <MOLECULAR_WEIGHT>
647.806

> <EXACT_MASS>
647.366946911

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
99

> <JCHEM_AVERAGE_POLARIZABILITY>
70.08446904321852

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
24-(1,2-dihydroxy-3-methylpent-3-en-1-yl)-2,22,23-trihydroxy-5,7,14,21-tetramethyl-11,15,26-trioxa-25-azahexacyclo[23.2.2.0^{3,13}.0^{4,9}.0^{10,12}.0^{14,16}]nonacos-1-ene-27,28-dione

> <JCHEM_LOGP>
2.6126288923333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
11.758580273984862

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.6095511288909634

> <JCHEM_PKA_STRONGEST_BASIC>
-2.3542139661670616

> <JCHEM_POLAR_SURFACE_AREA>
172.82

> <JCHEM_REFRACTIVITY>
168.67110000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
24-(1,2-dihydroxy-3-methylpent-3-en-1-yl)-2,22,23-trihydroxy-5,7,14,21-tetramethyl-11,15,26-trioxa-25-azahexacyclo[23.2.2.0^{3,13}.0^{4,9}.0^{10,12}.0^{14,16}]nonacos-1-ene-27,28-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0      -0.243  -5.071   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.349  -3.999   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.973  -2.506   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.079  -1.434   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.508  -2.084   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       1.614  -3.155   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       0.883  -0.590   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -0.223   0.482   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       2.364  -0.168   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.136   1.406   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       0.606   1.584   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       2.741   2.943   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       1.474   3.818   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       3.947   4.037   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.176   5.370   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.525   4.546   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.066   4.416   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.461   3.737   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.516   2.601   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      10.090   1.161   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      11.432   0.405   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      10.107  -0.379   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      11.292  -1.362   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.577  -1.840   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      11.089  -2.133   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      12.601  -2.426   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      11.591  -3.589   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      10.581  -4.752   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      11.084  -6.207   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      10.074  -7.370   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      10.576  -8.826   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       8.562  -7.077   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       8.060  -5.621   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       6.548  -5.328   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       9.070  -4.459   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       8.567  -3.003   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       7.174  -3.781   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       6.182  -4.959   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       5.530  -3.743   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       4.041  -4.231   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       3.741  -5.742   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       2.881  -3.238   0.000  0.00  0.00           C+0
HETATM   43  N   UNK     0       3.022  -1.678   0.000  0.00  0.00           N+0
HETATM   44  O   UNK     0       4.494  -1.223   0.000  0.00  0.00           O+0
HETATM   45  C   UNK     0       5.683  -2.182   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0       7.103  -1.586   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   43                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20   22                                                       
CONECT   22   21   20   23   24                                             
CONECT   23   22                                                            
CONECT   24   22   25   36                                                  
CONECT   25   24   26   27                                                  
CONECT   26   25   27                                                       
CONECT   27   26   25   28                                                  
CONECT   28   27   29   35                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   28   36                                                  
CONECT   36   35   24   37                                                  
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40   45                                                  
CONECT   40   39   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40   43                                                       
CONECT   43   42    9   44                                                  
CONECT   44   43   45                                                       
CONECT   45   44   39   46                                                  
CONECT   46   45                                                            
MASTER        0    0    0    0    0    0    0    0   46    0  102    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₅H₅₃NO₁₀

Average Mass

647.8060 Da

Monoisotopic Mass

647.36695 Da

IUPAC Name

24-(1,2-dihydroxy-3-methylpent-3-en-1-yl)-2,22,23-trihydroxy-5,7,14,21-tetramethyl-11,15,26-trioxa-25-azahexacyclo[23.2.2.0^{3,13}.0^{4,9}.0^{10,12}.0^{14,16}]nonacos-1-ene-27,28-dione

Traditional Name

24-(1,2-dihydroxy-3-methylpent-3-en-1-yl)-2,22,23-trihydroxy-5,7,14,21-tetramethyl-11,15,26-trioxa-25-azahexacyclo[23.2.2.0^{3,13}.0^{4,9}.0^{10,12}.0^{14,16}]nonacos-1-ene-27,28-dione

CAS Registry Number

Not Available

SMILES

CC=C(C)C(O)C(O)C1C(O)C(O)C(C)CCCCC2OC2(C)C2C3OC3C3CC(C)CC(C)C3C2C(O)=C2C(=O)CN1OC2=O

InChI Identifier

InChI=1S/C35H53NO10/c1-7-16(3)27(38)30(41)26-31(42)28(39)17(4)10-8-9-11-21-35(6,45-21)25-24(29(40)23-20(37)14-36(26)46-34(23)43)22-18(5)12-15(2)13-19(22)32-33(25)44-32/h7,15,17-19,21-22,24-28,30-33,38-42H,8-14H2,1-6H3

InChI Key

WRAVXSOFTDSTQL-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oxepanes. Oxepanes are compounds containing an oxepane ring, which is a seven-member saturated aliphatic heterocycle with one oxygen and six carbon atoms.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Oxepanes

Sub Class

Not Available

Direct Parent

Oxepanes

Alternative Parents

Substituents

Oxepane
1,2-oxazinane
Oxazinane
Vinylogous acid
Ketone
Secondary alcohol
Carboxylic acid derivative
Dialkyl ether
Enol
Oxirane
Ether
Monocarboxylic acid or derivatives
Polyol
Oxacycle
Azacycle
Organic oxygen compound
Alcohol
Organonitrogen compound
Organooxygen compound
Organic oxide
Hydrocarbon derivative
Carbonyl group
Organic nitrogen compound
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	2.61	ChemAxon
pKa (Strongest Acidic)	3.61	ChemAxon
pKa (Strongest Basic)	-2.4	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	172.82 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	168.67 m³·mol⁻¹	ChemAxon
Polarizability	70.08 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	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

76215233

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 24-(1,2-dihydroxy-3-methylpent-3-en-1-yl)-2,22,23-trihydroxy-5,7,14,21-tetramethyl-11,15,26-trioxa-25-azahexacyclo[23.2.2.0³,¹³.0⁴,⁹.0¹⁰,¹².0¹⁴,¹⁶]nonacos-1-ene-27,28-dione (NP0250333)

MOL for NP0250333 (24-(1,2-dihydroxy-3-methylpent-3-en-1-yl)-2,22,23-trihydroxy-5,7,14,21-tetramethyl-11,15,26-trioxa-25-azahexacyclo[23.2.2.0³,¹³.0⁴,⁹.0¹⁰,¹².0¹⁴,¹⁶]nonacos-1-ene-27,28-dione)

3D MOL for NP0250333 (24-(1,2-dihydroxy-3-methylpent-3-en-1-yl)-2,22,23-trihydroxy-5,7,14,21-tetramethyl-11,15,26-trioxa-25-azahexacyclo[23.2.2.0³,¹³.0⁴,⁹.0¹⁰,¹².0¹⁴,¹⁶]nonacos-1-ene-27,28-dione)

3D SDF for NP0250333 (24-(1,2-dihydroxy-3-methylpent-3-en-1-yl)-2,22,23-trihydroxy-5,7,14,21-tetramethyl-11,15,26-trioxa-25-azahexacyclo[23.2.2.0³,¹³.0⁴,⁹.0¹⁰,¹².0¹⁴,¹⁶]nonacos-1-ene-27,28-dione)

3D-SDF for NP0250333 (24-(1,2-dihydroxy-3-methylpent-3-en-1-yl)-2,22,23-trihydroxy-5,7,14,21-tetramethyl-11,15,26-trioxa-25-azahexacyclo[23.2.2.0³,¹³.0⁴,⁹.0¹⁰,¹².0¹⁴,¹⁶]nonacos-1-ene-27,28-dione)

PDB for NP0250333 (24-(1,2-dihydroxy-3-methylpent-3-en-1-yl)-2,22,23-trihydroxy-5,7,14,21-tetramethyl-11,15,26-trioxa-25-azahexacyclo[23.2.2.0³,¹³.0⁴,⁹.0¹⁰,¹².0¹⁴,¹⁶]nonacos-1-ene-27,28-dione)

3D PDB for NP0250333 (24-(1,2-dihydroxy-3-methylpent-3-en-1-yl)-2,22,23-trihydroxy-5,7,14,21-tetramethyl-11,15,26-trioxa-25-azahexacyclo[23.2.2.0³,¹³.0⁴,⁹.0¹⁰,¹².0¹⁴,¹⁶]nonacos-1-ene-27,28-dione)

SMILES for NP0250333 (24-(1,2-dihydroxy-3-methylpent-3-en-1-yl)-2,22,23-trihydroxy-5,7,14,21-tetramethyl-11,15,26-trioxa-25-azahexacyclo[23.2.2.0³,¹³.0⁴,⁹.0¹⁰,¹².0¹⁴,¹⁶]nonacos-1-ene-27,28-dione)

INCHI for NP0250333 (24-(1,2-dihydroxy-3-methylpent-3-en-1-yl)-2,22,23-trihydroxy-5,7,14,21-tetramethyl-11,15,26-trioxa-25-azahexacyclo[23.2.2.0³,¹³.0⁴,⁹.0¹⁰,¹².0¹⁴,¹⁶]nonacos-1-ene-27,28-dione)

Structure for NP0250333 (24-(1,2-dihydroxy-3-methylpent-3-en-1-yl)-2,22,23-trihydroxy-5,7,14,21-tetramethyl-11,15,26-trioxa-25-azahexacyclo[23.2.2.0³,¹³.0⁴,⁹.0¹⁰,¹².0¹⁴,¹⁶]nonacos-1-ene-27,28-dione)

3D Structure for NP0250333 (24-(1,2-dihydroxy-3-methylpent-3-en-1-yl)-2,22,23-trihydroxy-5,7,14,21-tetramethyl-11,15,26-trioxa-25-azahexacyclo[23.2.2.0³,¹³.0⁴,⁹.0¹⁰,¹².0¹⁴,¹⁶]nonacos-1-ene-27,28-dione)