NP-MRD: Showing NP-Card for (2s)-n-[(2s)-1-[(3r,7r,10s,13z)-10-[(2s)-butan-2-yl]-8,11-dihydroxy-16-methoxy-2-oxa-6,9,12-triazatricyclo[13.3.1.0³,⁷]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-1-oxo-3-phenylpropan-2-yl]-2-(dimethylamino)-3-phenylpropanimidic acid (NP0236607)

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Record Information

Version

2.0

Created at

2022-09-06 19:32:53 UTC

Updated at

2022-09-06 19:32:53 UTC

NP-MRD ID

NP0236607

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s)-n-[(2s)-1-[(3r,7r,10s,13z)-10-[(2s)-butan-2-yl]-8,11-dihydroxy-16-methoxy-2-oxa-6,9,12-triazatricyclo[13.3.1.0³,⁷]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-1-oxo-3-phenylpropan-2-yl]-2-(dimethylamino)-3-phenylpropanimidic acid

Description

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062221322D          

 51 55  0  0  1  0            999 V2000
    4.9067    4.5442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7270    4.4563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0610    3.7020    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.8813    3.6141    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5748    3.0355    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.9582    2.2182    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.7037    1.8649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4277    2.2603    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5980    1.0467    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7872    0.8943    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.6815    0.0761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4271   -0.2772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9935    0.3226    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.8117    0.2169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3123    0.8727    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1293   -0.5445    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.6286   -1.2002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9462   -1.9617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7644   -2.0673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0820   -2.8288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5814   -3.4845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7632   -3.3788    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4456   -2.6174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9475   -0.6502    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.4481    0.0056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1305    0.7670    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.2663   -0.1001    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.7669    0.5557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4493    1.3171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6311    1.4228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3135    2.1842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8141    2.8399    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6323    2.7343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9499    1.9728    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5839   -0.8615    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   10.0833   -1.5173    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4021   -0.9672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2088    0.2012    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    3.2548    1.1739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0730    1.0683    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
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  5  3  1  6  0  0  0
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  6  7  2  0  0  0  0
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  9 10  1  0  0  0  0
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  9 13  1  6  0  0  0
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 22 23  2  0  0  0  0
 18 23  1  0  0  0  0
 16 24  1  1  0  0  0
 24 25  2  0  0  0  0
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 33 34  2  0  0  0  0
 29 34  1  0  0  0  0
 27 35  1  6  0  0  0
 35 36  1  0  0  0  0
 35 37  1  0  0  0  0
 10 38  1  0  0  0  0
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 41 42  2  0  0  0  0
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 49 48  1  4  0  0  0
 49 50  2  0  0  0  0
  5 50  1  0  0  0  0
 50 51  1  0  0  0  0
M  END

     RDKit          3D

100104  0  0  0  0  0  0  0  0999 V2000
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 34 29  1  0
 46 39  1  0
  1 52  1  0
  1 53  1  0
  1 54  1  0
  2 55  1  0
  2 56  1  0
  3 57  1  6
  4 58  1  0
  4 59  1  0
  4 60  1  0
  5 61  1  6
  8 62  1  0
  9 63  1  6
 10 64  1  1
 11 65  1  0
 11 66  1  0
 12 67  1  0
 12 68  1  0
 16 69  1  1
 17 70  1  0
 17 71  1  0
 19 72  1  0
 20 73  1  0
 21 74  1  0
 22 75  1  0
 23 76  1  0
 26 77  1  0
 27 78  1  6
 28 79  1  0
 28 80  1  0
 30 81  1  0
 31 82  1  0
 32 83  1  0
 33 84  1  0
 34 85  1  0
 36 86  1  0
 36 87  1  0
 36 88  1  0
 37 89  1  0
 37 90  1  0
 37 91  1  0
 40 92  1  0
 41 93  1  0
 44 94  1  0
 44 95  1  0
 44 96  1  0
 46 97  1  0
 47 98  1  0
 48 99  1  0
 51100  1  0
M  END


  Mrv1652309062221322D          

 51 55  0  0  1  0            999 V2000
    4.9067    4.5442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7270    4.4563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0610    3.7020    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.8813    3.6141    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5748    3.0355    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.9582    2.2182    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.7037    1.8649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4277    2.2603    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5980    1.0467    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7872    0.8943    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.6815    0.0761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4271   -0.2772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9935    0.3226    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.8117    0.2169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3123    0.8727    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1293   -0.5445    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.6286   -1.2002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9462   -1.9617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7644   -2.0673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0820   -2.8288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5814   -3.4845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7632   -3.3788    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4456   -2.6174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9475   -0.6502    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.4481    0.0056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1305    0.7670    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.2663   -0.1001    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.7669    0.5557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4493    1.3171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6311    1.4228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3135    2.1842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8141    2.8399    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6323    2.7343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9499    1.9728    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5839   -0.8615    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   10.0833   -1.5173    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4021   -0.9672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2088    0.2012    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3906    0.3068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8900   -0.3489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0717   -0.2433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7541    0.5182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9359    0.6238    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4353   -0.0319    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2548    1.1739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0730    1.0683    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9372    1.9353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4378    2.5911    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2560    2.4854    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.7566    3.1412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4390    3.9026    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  6  0  0  0
  5  3  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  4  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
  9 13  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  2  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  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 18 23  1  0  0  0  0
 16 24  1  1  0  0  0
 24 25  2  0  0  0  0
 25 26  1  4  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  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 29 34  1  0  0  0  0
 27 35  1  6  0  0  0
 35 36  1  0  0  0  0
 35 37  1  0  0  0  0
 10 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  2  0  0  0  0
 40 41  1  0  0  0  0
 41 42  2  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 42 45  1  0  0  0  0
 45 46  2  0  0  0  0
 39 46  1  0  0  0  0
 45 47  1  0  0  0  0
 47 48  2  0  0  0  0
 49 48  1  4  0  0  0
 49 50  2  0  0  0  0
  5 50  1  0  0  0  0
 50 51  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0236607

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@H](C)[C@@H]1N=C(O)[C@H]2[C@@H](CCN2C(=O)[C@H](CC2=CC=CC=C2)N=C(O)[C@H](CC2=CC=CC=C2)N(C)C)OC2=CC=C(OC)C(=C2)\C=C/N=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C40H49N5O6/c1-6-26(2)35-38(47)41-21-19-29-25-30(17-18-33(29)50-5)51-34-20-22-45(36(34)39(48)43-35)40(49)31(23-27-13-9-7-10-14-27)42-37(46)32(44(3)4)24-28-15-11-8-12-16-28/h7-19,21,25-26,31-32,34-36H,6,20,22-24H2,1-5H3,(H,41,47)(H,42,46)(H,43,48)/b21-19-/t26-,31-,32-,34+,35-,36+/m0/s1

> <INCHI_KEY>
YDFMRHVTUVJMHS-QYZWRBHNSA-N

> <FORMULA>
C40H49N5O6

> <MOLECULAR_WEIGHT>
695.861

> <EXACT_MASS>
695.368284318

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
100

> <JCHEM_AVERAGE_POLARIZABILITY>
75.55249404886163

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S)-N-[(2S)-1-[(3R,7R,10S,13Z)-10-[(2S)-butan-2-yl]-8,11-dihydroxy-16-methoxy-2-oxa-6,9,12-triazatricyclo[13.3.1.0^{3,7}]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-1-oxo-3-phenylpropan-2-yl]-2-(dimethylamino)-3-phenylpropanimidic acid

> <JCHEM_LOGP>
-1.384573488433087

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
-4.735937521780621

> <JCHEM_PKA_STRONGEST_ACIDIC>
-7.699488311699121

> <JCHEM_PKA_STRONGEST_BASIC>
14.955070223178945

> <JCHEM_POLAR_SURFACE_AREA>
139.78

> <JCHEM_REFRACTIVITY>
196.7102

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-N-[(2S)-1-[(3R,7R,10S,13Z)-10-[(2S)-butan-2-yl]-8,11-dihydroxy-16-methoxy-2-oxa-6,9,12-triazatricyclo[13.3.1.0^{3,7}]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-1-oxo-3-phenylpropan-2-yl]-2-(dimethylamino)-3-phenylpropanimidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0       9.159   8.483   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.690   8.319   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      11.314   6.910   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      12.845   6.746   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.406   5.666   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0      11.122   4.141   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0      12.514   3.481   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      13.865   4.219   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      12.316   1.954   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.803   1.669   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.606   0.142   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      11.997  -0.517   0.000  0.00  0.00           C+0
HETATM   13  N   UNK     0      13.054   0.602   0.000  0.00  0.00           N+0
HETATM   14  C   UNK     0      14.582   0.405   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      15.516   1.629   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      15.175  -1.016   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      14.240  -2.240   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      14.833  -3.662   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      16.360  -3.859   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      16.953  -5.280   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      16.019  -6.504   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      14.491  -6.307   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      13.898  -4.886   0.000  0.00  0.00           C+0
HETATM   24  N   UNK     0      16.702  -1.214   0.000  0.00  0.00           N+0
HETATM   25  C   UNK     0      17.636   0.010   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      17.044   1.432   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      19.164  -0.187   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      20.098   1.037   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      19.505   2.459   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      17.978   2.656   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      17.385   4.077   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      18.320   5.301   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      19.847   5.104   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      20.440   3.683   0.000  0.00  0.00           C+0
HETATM   35  N   UNK     0      19.757  -1.608   0.000  0.00  0.00           N+0
HETATM   36  C   UNK     0      18.822  -2.832   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      21.284  -1.805   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       9.723   0.376   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       8.196   0.573   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       7.261  -0.651   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       5.734  -0.454   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       5.141   0.967   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0       3.614   1.164   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0       2.679  -0.060   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       6.076   2.191   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       7.603   1.994   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       5.483   3.613   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       6.417   4.837   0.000  0.00  0.00           C+0
HETATM   49  N   UNK     0       7.944   4.639   0.000  0.00  0.00           N+0
HETATM   50  C   UNK     0       8.879   5.864   0.000  0.00  0.00           C+0
HETATM   51  O   UNK     0       8.286   7.285   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   50                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   13                                                  
CONECT   10    9   11   38                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12    9   14                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   24                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   23                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   18                                                       
CONECT   24   16   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   35                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30   34                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   29                                                       
CONECT   35   27   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35                                                            
CONECT   38   10   39                                                       
CONECT   39   38   40   46                                                  
CONECT   40   39   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   43   45                                                  
CONECT   43   42   44                                                       
CONECT   44   43                                                            
CONECT   45   42   46   47                                                  
CONECT   46   45   39                                                       
CONECT   47   45   48                                                       
CONECT   48   47   49                                                       
CONECT   49   48   50                                                       
CONECT   50   49    5   51                                                  
CONECT   51   50                                                            
MASTER        0    0    0    0    0    0    0    0   51    0  110    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₀H₄₉N₅O₆

Average Mass

695.8610 Da

Monoisotopic Mass

695.36828 Da

IUPAC Name

(2S)-N-[(2S)-1-[(3R,7R,10S,13Z)-10-[(2S)-butan-2-yl]-8,11-dihydroxy-16-methoxy-2-oxa-6,9,12-triazatricyclo[13.3.1.0^{3,7}]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-1-oxo-3-phenylpropan-2-yl]-2-(dimethylamino)-3-phenylpropanimidic acid

Traditional Name

CAS Registry Number

Not Available

SMILES

CC[C@H](C)[C@@H]1N=C(O)[C@H]2[C@@H](CCN2C(=O)[C@H](CC2=CC=CC=C2)N=C(O)[C@H](CC2=CC=CC=C2)N(C)C)OC2=CC=C(OC)C(=C2)\C=C/N=C1O

InChI Identifier

InChI=1S/C40H49N5O6/c1-6-26(2)35-38(47)41-21-19-29-25-30(17-18-33(29)50-5)51-34-20-22-45(36(34)39(48)43-35)40(49)31(23-27-13-9-7-10-14-27)42-37(46)32(44(3)4)24-28-15-11-8-12-16-28/h7-19,21,25-26,31-32,34-36H,6,20,22-24H2,1-5H3,(H,41,47)(H,42,46)(H,43,48)/b21-19-/t26-,31-,32-,34+,35-,36+/m0/s1

InChI Key

YDFMRHVTUVJMHS-QYZWRBHNSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Ziziphus jujuba	LOTUS Database	35616633

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	-1.4	ChemAxon
pKa (Strongest Acidic)	-7.7	ChemAxon
pKa (Strongest Basic)	14.96	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	139.78 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	196.71 m³·mol⁻¹	ChemAxon
Polarizability	75.55 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 (2s)-n-[(2s)-1-[(3r,7r,10s,13z)-10-[(2s)-butan-2-yl]-8,11-dihydroxy-16-methoxy-2-oxa-6,9,12-triazatricyclo[13.3.1.0³,⁷]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-1-oxo-3-phenylpropan-2-yl]-2-(dimethylamino)-3-phenylpropanimidic acid (NP0236607)

MOL for NP0236607 ((2s)-n-[(2s)-1-[(3r,7r,10s,13z)-10-[(2s)-butan-2-yl]-8,11-dihydroxy-16-methoxy-2-oxa-6,9,12-triazatricyclo[13.3.1.0³,⁷]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-1-oxo-3-phenylpropan-2-yl]-2-(dimethylamino)-3-phenylpropanimidic acid)

3D MOL for NP0236607 ((2s)-n-[(2s)-1-[(3r,7r,10s,13z)-10-[(2s)-butan-2-yl]-8,11-dihydroxy-16-methoxy-2-oxa-6,9,12-triazatricyclo[13.3.1.0³,⁷]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-1-oxo-3-phenylpropan-2-yl]-2-(dimethylamino)-3-phenylpropanimidic acid)

3D SDF for NP0236607 ((2s)-n-[(2s)-1-[(3r,7r,10s,13z)-10-[(2s)-butan-2-yl]-8,11-dihydroxy-16-methoxy-2-oxa-6,9,12-triazatricyclo[13.3.1.0³,⁷]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-1-oxo-3-phenylpropan-2-yl]-2-(dimethylamino)-3-phenylpropanimidic acid)

3D-SDF for NP0236607 ((2s)-n-[(2s)-1-[(3r,7r,10s,13z)-10-[(2s)-butan-2-yl]-8,11-dihydroxy-16-methoxy-2-oxa-6,9,12-triazatricyclo[13.3.1.0³,⁷]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-1-oxo-3-phenylpropan-2-yl]-2-(dimethylamino)-3-phenylpropanimidic acid)

PDB for NP0236607 ((2s)-n-[(2s)-1-[(3r,7r,10s,13z)-10-[(2s)-butan-2-yl]-8,11-dihydroxy-16-methoxy-2-oxa-6,9,12-triazatricyclo[13.3.1.0³,⁷]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-1-oxo-3-phenylpropan-2-yl]-2-(dimethylamino)-3-phenylpropanimidic acid)

3D PDB for NP0236607 ((2s)-n-[(2s)-1-[(3r,7r,10s,13z)-10-[(2s)-butan-2-yl]-8,11-dihydroxy-16-methoxy-2-oxa-6,9,12-triazatricyclo[13.3.1.0³,⁷]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-1-oxo-3-phenylpropan-2-yl]-2-(dimethylamino)-3-phenylpropanimidic acid)

SMILES for NP0236607 ((2s)-n-[(2s)-1-[(3r,7r,10s,13z)-10-[(2s)-butan-2-yl]-8,11-dihydroxy-16-methoxy-2-oxa-6,9,12-triazatricyclo[13.3.1.0³,⁷]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-1-oxo-3-phenylpropan-2-yl]-2-(dimethylamino)-3-phenylpropanimidic acid)

INCHI for NP0236607 ((2s)-n-[(2s)-1-[(3r,7r,10s,13z)-10-[(2s)-butan-2-yl]-8,11-dihydroxy-16-methoxy-2-oxa-6,9,12-triazatricyclo[13.3.1.0³,⁷]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-1-oxo-3-phenylpropan-2-yl]-2-(dimethylamino)-3-phenylpropanimidic acid)

Structure for NP0236607 ((2s)-n-[(2s)-1-[(3r,7r,10s,13z)-10-[(2s)-butan-2-yl]-8,11-dihydroxy-16-methoxy-2-oxa-6,9,12-triazatricyclo[13.3.1.0³,⁷]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-1-oxo-3-phenylpropan-2-yl]-2-(dimethylamino)-3-phenylpropanimidic acid)

3D Structure for NP0236607 ((2s)-n-[(2s)-1-[(3r,7r,10s,13z)-10-[(2s)-butan-2-yl]-8,11-dihydroxy-16-methoxy-2-oxa-6,9,12-triazatricyclo[13.3.1.0³,⁷]nonadeca-1(18),8,11,13,15(19),16-hexaen-6-yl]-1-oxo-3-phenylpropan-2-yl]-2-(dimethylamino)-3-phenylpropanimidic acid)