NP-MRD: Showing NP-Card for [(1s,3r,17s,18r,19r,20r,21s,22s,23r,24r,25s)-19,21,24-tris(acetyloxy)-18,22,25-trihydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.0¹,²⁰.0³,²³.0⁷,¹²]pentacosa-7,9,11-trien-20-yl]methyl acetate (NP0243411)

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Record Information

Version

2.0

Created at

2022-09-07 03:57:11 UTC

Updated at

2022-09-07 03:57:11 UTC

NP-MRD ID

NP0243411

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[(1s,3r,17s,18r,19r,20r,21s,22s,23r,24r,25s)-19,21,24-tris(acetyloxy)-18,22,25-trihydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.0¹,²⁰.0³,²³.0⁷,¹²]pentacosa-7,9,11-trien-20-yl]methyl acetate

Description

Not Available

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072205572D          

 51 55  0  0  1  0            999 V2000
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M  END

     RDKit          3D

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 12 61  1  6
 13 62  1  0
 14 63  1  6
 15 64  1  6
 18 65  1  0
 18 66  1  0
 18 67  1  0
 23 68  1  0
 23 69  1  0
 23 70  1  0
 24 71  1  0
 24 72  1  0
 29 73  1  0
 30 74  1  0
 31 75  1  0
 50 91  1  0
 50 92  1  0
 50 93  1  0
 51 94  1  0
M  END


  Mrv1652309072205572D          

 51 55  0  0  1  0            999 V2000
   -1.9477   -4.0124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5551   -3.1293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3762   -2.6529    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8695   -2.5616    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9602   -1.6286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1794   -1.0608    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7677   -0.4185    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7007   -0.1338    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3435    0.5264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1999    0.3253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1720    1.4857    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4535    0.2631    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8295    1.1752    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3810    0.5204    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5106   -0.2187    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3007   -0.2173    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8789    0.5942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7140    0.9244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2394    1.3011    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6925   -0.8959    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4339   -0.3851    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2441    0.4782    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9315    1.3177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6789    1.2118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5203    1.2012    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1760    0.6723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5762    1.4551    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6385   -0.0292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2639    0.5089    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0425    0.2363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1958   -0.5743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5704   -1.1124    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.7917   -0.8398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6154   -1.6743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2674   -2.2559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1244   -2.3566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5288   -3.1278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4096   -2.7990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5158   -3.6675    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5719   -2.8816    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8978   -2.3664    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0679   -2.4828    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3913   -3.2965    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4621   -1.8455    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4415   -2.3312    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0323   -3.1813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3213   -3.8196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8774   -3.4801    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1775   -1.5800    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8311   -2.0423    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8887   -1.1282    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 14 15  1  6  0  0  0
 15 16  1  6  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
 15 20  1  0  0  0  0
  6 20  1  0  0  0  0
 20 21  1  1  0  0  0
 21 22  1  0  0  0  0
 14 22  1  0  0  0  0
 22 23  1  1  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  2  0  0  0  0
 26 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 28 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 38 39  2  0  0  0  0
 38 40  1  0  0  0  0
 41 40  1  1  0  0  0
 41 42  1  0  0  0  0
 42 43  1  6  0  0  0
 42 44  1  0  0  0  0
  6 44  1  0  0  0  0
 44 45  1  6  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 46 48  2  0  0  0  0
 41 49  1  0  0  0  0
 20 49  1  0  0  0  0
 49 50  1  0  0  0  0
 49 51  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0243411

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1C(C)C(=O)O[C@H]2[C@H](O)[C@H](OC(C)=O)[C@@]3(COC(C)=O)[C@H](OC(C)=O)[C@@H](O)[C@@H]4[C@@H](OC(C)=O)[C@]3(O[C@@]4(C)COC(=O)C3=CC=CN=C13)[C@@]2(C)O

> <INCHI_IDENTIFIER>
InChI=1S/C34H43NO16/c1-14-15(2)29(42)50-26-24(41)28(49-19(6)39)33(13-45-16(3)36)27(48-18(5)38)23(40)21-25(47-17(4)37)34(33,32(26,8)44)51-31(21,7)12-46-30(43)20-10-9-11-35-22(14)20/h9-11,14-15,21,23-28,40-41,44H,12-13H2,1-8H3/t14?,15?,21-,23+,24+,25?,26+,27-,28+,31+,32+,33-,34+/m1/s1

> <INCHI_KEY>
SHDBRMQJPSDFRT-SYNHGMGHSA-N

> <FORMULA>
C34H43NO16

> <MOLECULAR_WEIGHT>
721.709

> <EXACT_MASS>
721.258184309

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
94

> <JCHEM_AVERAGE_POLARIZABILITY>
70.63869027934885

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[(1S,3R,17S,18R,19R,20R,21S,22S,23R,24R,25S)-19,21,24-tris(acetyloxy)-18,22,25-trihydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.0^{1,20}.0^{3,23}.0^{7,12}]pentacosa-7,9,11-trien-20-yl]methyl acetate

> <JCHEM_LOGP>
-1.1252297256666686

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.200818581963176

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.532766364345154

> <JCHEM_PKA_STRONGEST_BASIC>
2.61183540810487

> <JCHEM_POLAR_SURFACE_AREA>
240.60999999999996

> <JCHEM_REFRACTIVITY>
164.4936

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
[(1S,3R,17S,18R,19R,20R,21S,22S,23R,24R,25S)-19,21,24-tris(acetyloxy)-18,22,25-trihydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.0^{1,20}.0^{3,23}.0^{7,12}]pentacosa-7,9,11-trien-20-yl]methyl acetate

> <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      -3.636  -7.490   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.903  -5.841   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -4.436  -4.952   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      -1.623  -4.782   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -1.792  -3.040   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.335  -1.980   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.433  -0.781   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -3.175  -0.250   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -4.375   0.983   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -5.973   0.607   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -4.054   2.773   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -0.846   0.491   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -1.548   2.194   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       0.711   0.971   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.953  -0.408   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -0.561  -0.406   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -1.641   1.109   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -3.199   1.726   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -0.447   2.429   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       1.293  -1.672   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       2.677  -0.719   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       2.322   0.893   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.739   2.460   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.134   2.262   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       4.705   2.242   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       5.928   1.255   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       6.676   2.716   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       6.792  -0.054   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       7.959   0.950   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       9.413   0.441   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       9.699  -1.072   0.000  0.00  0.00           C+0
HETATM   32  N   UNK     0       8.531  -2.076   0.000  0.00  0.00           N+0
HETATM   33  C   UNK     0       7.078  -1.568   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       6.749  -3.125   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       7.966  -4.211   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       5.832  -4.399   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       6.587  -5.838   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       4.498  -5.225   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       4.696  -6.846   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0       2.934  -5.379   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       1.676  -4.417   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       0.127  -4.635   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0       0.730  -6.153   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0      -0.863  -3.445   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0      -2.691  -4.352   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0      -3.794  -5.938   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      -2.466  -7.130   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0      -5.371  -6.496   0.000  0.00  0.00           O+0
HETATM   49  C   UNK     0       2.198  -2.949   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0       3.418  -3.812   0.000  0.00  0.00           C+0
HETATM   51  O   UNK     0       3.526  -2.106   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                                                       
CONECT    6    5    7   20   44                                             
CONECT    7    6    8   12                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    7   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   22                                                  
CONECT   15   14   16   20                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   15    6   21   49                                             
CONECT   21   20   22                                                       
CONECT   22   21   14   23   24                                             
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29   33                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   28   34                                                  
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38   41                                                       
CONECT   41   40   42   49                                                  
CONECT   42   41   43   44                                                  
CONECT   43   42                                                            
CONECT   44   42    6   45                                                  
CONECT   45   44   46                                                       
CONECT   46   45   47   48                                                  
CONECT   47   46                                                            
CONECT   48   46                                                            
CONECT   49   41   20   50   51                                             
CONECT   50   49                                                            
CONECT   51   49                                                            
MASTER        0    0    0    0    0    0    0    0   51    0  110    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₄H₄₃NO₁₆

Average Mass

721.7090 Da

Monoisotopic Mass

721.25818 Da

IUPAC Name

[(1S,3R,17S,18R,19R,20R,21S,22S,23R,24R,25S)-19,21,24-tris(acetyloxy)-18,22,25-trihydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.0^{1,20}.0^{3,23}.0^{7,12}]pentacosa-7,9,11-trien-20-yl]methyl acetate

Traditional Name

CAS Registry Number

Not Available

SMILES

CC1C(C)C(=O)O[C@H]2[C@H](O)[C@H](OC(C)=O)[C@@]3(COC(C)=O)[C@H](OC(C)=O)[C@@H](O)[C@@H]4[C@@H](OC(C)=O)[C@]3(O[C@@]4(C)COC(=O)C3=CC=CN=C13)[C@@]2(C)O

InChI Identifier

InChI=1S/C34H43NO16/c1-14-15(2)29(42)50-26-24(41)28(49-19(6)39)33(13-45-16(3)36)27(48-18(5)38)23(40)21-25(47-17(4)37)34(33,32(26,8)44)51-31(21,7)12-46-30(43)20-10-9-11-35-22(14)20/h9-11,14-15,21,23-28,40-41,44H,12-13H2,1-8H3/t14?,15?,21-,23+,24+,25?,26+,27-,28+,31+,32+,33-,34+/m1/s1

InChI Key

SHDBRMQJPSDFRT-SYNHGMGHSA-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

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	-1.1	ChemAxon
pKa (Strongest Acidic)	12.53	ChemAxon
pKa (Strongest Basic)	2.61	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	240.61 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	164.49 m³·mol⁻¹	ChemAxon
Polarizability	70.64 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for [(1s,3r,17s,18r,19r,20r,21s,22s,23r,24r,25s)-19,21,24-tris(acetyloxy)-18,22,25-trihydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.0¹,²⁰.0³,²³.0⁷,¹²]pentacosa-7,9,11-trien-20-yl]methyl acetate (NP0243411)

MOL for NP0243411 ([(1s,3r,17s,18r,19r,20r,21s,22s,23r,24r,25s)-19,21,24-tris(acetyloxy)-18,22,25-trihydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.0¹,²⁰.0³,²³.0⁷,¹²]pentacosa-7,9,11-trien-20-yl]methyl acetate)

3D MOL for NP0243411 ([(1s,3r,17s,18r,19r,20r,21s,22s,23r,24r,25s)-19,21,24-tris(acetyloxy)-18,22,25-trihydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.0¹,²⁰.0³,²³.0⁷,¹²]pentacosa-7,9,11-trien-20-yl]methyl acetate)

3D SDF for NP0243411 ([(1s,3r,17s,18r,19r,20r,21s,22s,23r,24r,25s)-19,21,24-tris(acetyloxy)-18,22,25-trihydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.0¹,²⁰.0³,²³.0⁷,¹²]pentacosa-7,9,11-trien-20-yl]methyl acetate)

3D-SDF for NP0243411 ([(1s,3r,17s,18r,19r,20r,21s,22s,23r,24r,25s)-19,21,24-tris(acetyloxy)-18,22,25-trihydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.0¹,²⁰.0³,²³.0⁷,¹²]pentacosa-7,9,11-trien-20-yl]methyl acetate)

PDB for NP0243411 ([(1s,3r,17s,18r,19r,20r,21s,22s,23r,24r,25s)-19,21,24-tris(acetyloxy)-18,22,25-trihydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.0¹,²⁰.0³,²³.0⁷,¹²]pentacosa-7,9,11-trien-20-yl]methyl acetate)

3D PDB for NP0243411 ([(1s,3r,17s,18r,19r,20r,21s,22s,23r,24r,25s)-19,21,24-tris(acetyloxy)-18,22,25-trihydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.0¹,²⁰.0³,²³.0⁷,¹²]pentacosa-7,9,11-trien-20-yl]methyl acetate)

SMILES for NP0243411 ([(1s,3r,17s,18r,19r,20r,21s,22s,23r,24r,25s)-19,21,24-tris(acetyloxy)-18,22,25-trihydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.0¹,²⁰.0³,²³.0⁷,¹²]pentacosa-7,9,11-trien-20-yl]methyl acetate)

INCHI for NP0243411 ([(1s,3r,17s,18r,19r,20r,21s,22s,23r,24r,25s)-19,21,24-tris(acetyloxy)-18,22,25-trihydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.0¹,²⁰.0³,²³.0⁷,¹²]pentacosa-7,9,11-trien-20-yl]methyl acetate)

Structure for NP0243411 ([(1s,3r,17s,18r,19r,20r,21s,22s,23r,24r,25s)-19,21,24-tris(acetyloxy)-18,22,25-trihydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.0¹,²⁰.0³,²³.0⁷,¹²]pentacosa-7,9,11-trien-20-yl]methyl acetate)

3D Structure for NP0243411 ([(1s,3r,17s,18r,19r,20r,21s,22s,23r,24r,25s)-19,21,24-tris(acetyloxy)-18,22,25-trihydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.0¹,²⁰.0³,²³.0⁷,¹²]pentacosa-7,9,11-trien-20-yl]methyl acetate)