NP-MRD: Showing NP-Card for n-[(3s,7s,10e)-5,8-dihydroxy-7-(2-methylpropyl)-3-phenyl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),5,8,10,12,15-hexaen-4-yl]-1-[2-(dimethylamino)-3-(1h-indol-3-yl)propanoyl]pyrrolidine-2-carboximidic acid (NP0313430)

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Record Information

Version

2.0

Created at

2022-09-11 10:58:18 UTC

Updated at

2022-09-11 10:58:19 UTC

NP-MRD ID

NP0313430

Secondary Accession Numbers

None

Natural Product Identification

Common Name

n-[(3s,7s,10e)-5,8-dihydroxy-7-(2-methylpropyl)-3-phenyl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),5,8,10,12,15-hexaen-4-yl]-1-[2-(dimethylamino)-3-(1h-indol-3-yl)propanoyl]pyrrolidine-2-carboximidic acid

Description

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112212582D          

 52 57  0  0  1  0            999 V2000
    7.2308    0.2519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5536    1.0111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3726    1.1112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0575    1.6703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2386    1.5703    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.1493    0.7420    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.7139    0.0328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3047   -0.5431    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0149   -0.4213    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3006   -1.1953    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.1137   -1.3349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6411   -0.7005    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3993   -2.1089    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1934   -2.3327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2259   -3.1570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4519   -3.4427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9411   -2.7949    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.1167   -2.8274    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3171   -3.0306    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    3.9083   -3.5900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5243   -4.3202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8892   -5.0601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2984   -5.6358    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.5682   -5.2518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7942   -5.5374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1599   -5.0100    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2995   -4.1969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0735   -3.9112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7078   -4.4387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1730   -4.2552    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.7889   -4.9854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9973   -4.2227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1812   -0.5311    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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    2.3377    1.7540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.7094    1.5613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.2971    2.9523    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.9447    2.3741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6273    2.8374    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
  2  4  1  0  0  0  0
  5  4  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
 10  9  1  4  0  0  0
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 11 13  1  0  0  0  0
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 13 17  1  0  0  0  0
 17 18  1  0  0  0  0
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 20 21  1  0  0  0  0
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 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 22 30  1  0  0  0  0
 25 30  1  0  0  0  0
 20 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
  9 34  1  0  0  0  0
 34 35  1  6  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
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 41 42  1  0  0  0  0
 42 43  2  0  0  0  0
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 42 47  1  0  0  0  0
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 50 49  1  4  0  0  0
 50 51  2  0  0  0  0
  5 51  1  0  0  0  0
 51 52  1  0  0  0  0
M  END

     RDKit          3D

100105  0  0  0  0  0  0  0  0999 V2000
   -3.2581    2.8166   -0.6353 C   0  0  0  0  0  0  0  0  0  0  0  0
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 38 39  1  0
 39 40  2  0
 51  5  1  0
 40 35  1  0
 17 13  1  0
 30 22  1  0
 47 42  1  0
 30 25  1  0
  1 53  1  0
  1 54  1  0
  1 55  1  0
  2 56  1  0
  3 57  1  0
  3 58  1  0
  3 59  1  0
  4 60  1  0
  4 61  1  0
  5 62  1  1
  8 63  1  0
  9 64  1  6
 12 65  1  0
 13 66  1  1
 14 67  1  0
 14 68  1  0
 15 69  1  0
 15 70  1  0
 16 71  1  0
 16 72  1  0
 20 73  1  1
 21 74  1  0
 21 75  1  0
 23 76  1  0
 24 77  1  0
 26 78  1  0
 27 79  1  0
 28 80  1  0
 29 81  1  0
 32 82  1  0
 32 83  1  0
 32 84  1  0
 33 85  1  0
 33 86  1  0
 33 87  1  0
 34 88  1  1
 43 94  1  0
 44 95  1  0
 46 96  1  0
 47 97  1  0
 48 98  1  0
 49 99  1  0
 52100  1  0
 36 89  1  0
 37 90  1  0
 38 91  1  0
 39 92  1  0
 40 93  1  0
M  END


  Mrv1652309112212582D          

 52 57  0  0  1  0            999 V2000
    7.2308    0.2519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5536    1.0111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3726    1.1112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0575    1.6703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2386    1.5703    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.1493    0.7420    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.7139    0.0328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3047   -0.5431    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0149   -0.4213    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3006   -1.1953    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.1137   -1.3349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6411   -0.7005    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3993   -2.1089    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1934   -2.3327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2259   -3.1570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4519   -3.4427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9411   -2.7949    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.1167   -2.8274    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3171   -3.0306    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7327   -3.5575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9083   -3.5900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5243   -4.3202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8892   -5.0601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2984   -5.6358    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.5682   -5.2518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7942   -5.5374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1599   -5.0100    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2995   -4.1969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0735   -3.9112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7078   -4.4387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1730   -4.2552    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.7889   -4.9854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9973   -4.2227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1812   -0.5311    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1169   -1.3536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7971   -1.8206    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7328   -2.6431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9883   -2.9986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3082   -2.5317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3725   -1.7092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3688   -0.2913    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8347    0.3927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1897    0.9384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3377    1.7540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0976    2.1114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7094    1.5613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5900    0.7470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6657    2.7661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4479    3.1207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2971    2.9523    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.9447    2.3741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6273    2.8374    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
  2  4  1  0  0  0  0
  5  4  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
 10  9  1  4  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 13 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 22 30  1  0  0  0  0
 25 30  1  0  0  0  0
 20 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
  9 34  1  0  0  0  0
 34 35  1  6  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 38 39  1  0  0  0  0
 39 40  2  0  0  0  0
 35 40  1  0  0  0  0
 34 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  2  0  0  0  0
 43 44  1  0  0  0  0
 44 45  2  0  0  0  0
 45 46  1  0  0  0  0
 46 47  2  0  0  0  0
 42 47  1  0  0  0  0
 45 48  1  0  0  0  0
 48 49  2  0  0  0  0
 50 49  1  4  0  0  0
 50 51  2  0  0  0  0
  5 51  1  0  0  0  0
 51 52  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0313430

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C[C@@H]1N=C(O)C(N=C(O)C2CCCN2C(=O)C(CC2=CNC3=CC=CC=C23)N(C)C)[C@@H](OC2=CC=C(C=C2)\C=C/N=C1O)C1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C41H48N6O5/c1-26(2)23-33-38(48)42-21-20-27-16-18-30(19-17-27)52-37(28-11-6-5-7-12-28)36(40(50)44-33)45-39(49)34-15-10-22-47(34)41(51)35(46(3)4)24-29-25-43-32-14-9-8-13-31(29)32/h5-9,11-14,16-21,25-26,33-37,43H,10,15,22-24H2,1-4H3,(H,42,48)(H,44,50)(H,45,49)/b21-20-/t33-,34?,35?,36?,37-/m0/s1

> <INCHI_KEY>
SXBGDMUNBWTLBU-CSZGASKESA-N

> <FORMULA>
C41H48N6O5

> <MOLECULAR_WEIGHT>
704.872

> <EXACT_MASS>
704.36861867

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
100

> <JCHEM_AVERAGE_POLARIZABILITY>
74.84352547104143

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
N-[(3S,7S,10E)-5,8-dihydroxy-7-(2-methylpropyl)-3-phenyl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),5,8,10,12,15-hexaen-4-yl]-1-[2-(dimethylamino)-3-(1H-indol-3-yl)propanoyl]pyrrolidine-2-carboximidic acid

> <JCHEM_LOGP>
-0.8873493616932

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
-4.312271756278913

> <JCHEM_PKA_STRONGEST_ACIDIC>
-8.81374739069459

> <JCHEM_PKA_STRONGEST_BASIC>
14.954720989295607

> <JCHEM_POLAR_SURFACE_AREA>
146.34

> <JCHEM_REFRACTIVITY>
201.30009999999993

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
N-[(3S,7S,10E)-5,8-dihydroxy-7-(2-methylpropyl)-3-phenyl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),5,8,10,12,15-hexaen-4-yl]-1-[2-(dimethylamino)-3-(1H-indol-3-yl)propanoyl]pyrrolidine-2-carboximidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0      13.498   0.470   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      14.100   1.887   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      15.629   2.074   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      13.174   3.118   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      11.645   2.931   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0      11.479   1.385   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0      10.666   0.061   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      11.769  -1.014   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       9.361  -0.786   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0       9.894  -2.231   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0      11.412  -2.492   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      12.397  -1.308   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      11.945  -3.937   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      13.428  -4.354   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      13.488  -5.893   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      12.044  -6.426   0.000  0.00  0.00           C+0
HETATM   17  N   UNK     0      11.090  -5.217   0.000  0.00  0.00           N+0
HETATM   18  C   UNK     0       9.551  -5.278   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       8.059  -5.657   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       8.834  -6.641   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.295  -6.701   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.579  -8.064   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.260  -9.445   0.000  0.00  0.00           C+0
HETATM   24  N   UNK     0       6.157 -10.520   0.000  0.00  0.00           N+0
HETATM   25  C   UNK     0       4.794  -9.803   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.349 -10.337   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.165  -9.352   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.426  -7.834   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.870  -7.301   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.055  -8.286   0.000  0.00  0.00           C+0
HETATM   31  N   UNK     0       9.656  -7.943   0.000  0.00  0.00           N+0
HETATM   32  C   UNK     0       8.939  -9.306   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      11.195  -7.882   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       7.805  -0.991   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       7.685  -2.527   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       8.955  -3.398   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       8.835  -4.934   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       7.445  -5.597   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       6.175  -4.726   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       6.295  -3.191   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       6.288  -0.544   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       5.291   0.733   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       4.088   1.752   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       4.364   3.274   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       5.782   3.941   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       6.924   2.914   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       6.701   1.394   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       6.843   5.163   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0       8.303   5.825   0.000  0.00  0.00           C+0
HETATM   50  N   UNK     0       9.888   5.511   0.000  0.00  0.00           N+0
HETATM   51  C   UNK     0      11.097   4.432   0.000  0.00  0.00           C+0
HETATM   52  O   UNK     0      12.371   5.296   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   51                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   34                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   17                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   13   18                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   31                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   30                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   30                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   22   25                                                  
CONECT   31   20   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31                                                            
CONECT   34    9   35   41                                                  
CONECT   35   34   36   40                                                  
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   35                                                       
CONECT   41   34   42                                                       
CONECT   42   41   43   47                                                  
CONECT   43   42   44                                                       
CONECT   44   43   45                                                       
CONECT   45   44   46   48                                                  
CONECT   46   45   47                                                       
CONECT   47   46   42                                                       
CONECT   48   45   49                                                       
CONECT   49   48   50                                                       
CONECT   50   49   51                                                       
CONECT   51   50    5   52                                                  
CONECT   52   51                                                            
MASTER        0    0    0    0    0    0    0    0   52    0  114    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₁H₄₈N₆O₅

Average Mass

704.8720 Da

Monoisotopic Mass

704.36862 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(C)C[C@@H]1N=C(O)C(N=C(O)C2CCCN2C(=O)C(CC2=CNC3=CC=CC=C23)N(C)C)[C@@H](OC2=CC=C(C=C2)\C=C/N=C1O)C1=CC=CC=C1

InChI Identifier

InChI=1S/C41H48N6O5/c1-26(2)23-33-38(48)42-21-20-27-16-18-30(19-17-27)52-37(28-11-6-5-7-12-28)36(40(50)44-33)45-39(49)34-15-10-22-47(34)41(51)35(46(3)4)24-29-25-43-32-14-9-8-13-31(29)32/h5-9,11-14,16-21,25-26,33-37,43H,10,15,22-24H2,1-4H3,(H,42,48)(H,44,50)(H,45,49)/b21-20-/t33-,34?,35?,36?,37-/m0/s1

InChI Key

SXBGDMUNBWTLBU-CSZGASKESA-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
Paliurus hemsleyanus	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

External Links

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for n-[(3s,7s,10e)-5,8-dihydroxy-7-(2-methylpropyl)-3-phenyl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),5,8,10,12,15-hexaen-4-yl]-1-[2-(dimethylamino)-3-(1h-indol-3-yl)propanoyl]pyrrolidine-2-carboximidic acid (NP0313430)

MOL for NP0313430 (n-[(3s,7s,10e)-5,8-dihydroxy-7-(2-methylpropyl)-3-phenyl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),5,8,10,12,15-hexaen-4-yl]-1-[2-(dimethylamino)-3-(1h-indol-3-yl)propanoyl]pyrrolidine-2-carboximidic acid)

3D MOL for NP0313430 (n-[(3s,7s,10e)-5,8-dihydroxy-7-(2-methylpropyl)-3-phenyl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),5,8,10,12,15-hexaen-4-yl]-1-[2-(dimethylamino)-3-(1h-indol-3-yl)propanoyl]pyrrolidine-2-carboximidic acid)

3D SDF for NP0313430 (n-[(3s,7s,10e)-5,8-dihydroxy-7-(2-methylpropyl)-3-phenyl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),5,8,10,12,15-hexaen-4-yl]-1-[2-(dimethylamino)-3-(1h-indol-3-yl)propanoyl]pyrrolidine-2-carboximidic acid)

3D-SDF for NP0313430 (n-[(3s,7s,10e)-5,8-dihydroxy-7-(2-methylpropyl)-3-phenyl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),5,8,10,12,15-hexaen-4-yl]-1-[2-(dimethylamino)-3-(1h-indol-3-yl)propanoyl]pyrrolidine-2-carboximidic acid)

PDB for NP0313430 (n-[(3s,7s,10e)-5,8-dihydroxy-7-(2-methylpropyl)-3-phenyl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),5,8,10,12,15-hexaen-4-yl]-1-[2-(dimethylamino)-3-(1h-indol-3-yl)propanoyl]pyrrolidine-2-carboximidic acid)

3D PDB for NP0313430 (n-[(3s,7s,10e)-5,8-dihydroxy-7-(2-methylpropyl)-3-phenyl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),5,8,10,12,15-hexaen-4-yl]-1-[2-(dimethylamino)-3-(1h-indol-3-yl)propanoyl]pyrrolidine-2-carboximidic acid)

SMILES for NP0313430 (n-[(3s,7s,10e)-5,8-dihydroxy-7-(2-methylpropyl)-3-phenyl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),5,8,10,12,15-hexaen-4-yl]-1-[2-(dimethylamino)-3-(1h-indol-3-yl)propanoyl]pyrrolidine-2-carboximidic acid)

INCHI for NP0313430 (n-[(3s,7s,10e)-5,8-dihydroxy-7-(2-methylpropyl)-3-phenyl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),5,8,10,12,15-hexaen-4-yl]-1-[2-(dimethylamino)-3-(1h-indol-3-yl)propanoyl]pyrrolidine-2-carboximidic acid)

Structure for NP0313430 (n-[(3s,7s,10e)-5,8-dihydroxy-7-(2-methylpropyl)-3-phenyl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),5,8,10,12,15-hexaen-4-yl]-1-[2-(dimethylamino)-3-(1h-indol-3-yl)propanoyl]pyrrolidine-2-carboximidic acid)

3D Structure for NP0313430 (n-[(3s,7s,10e)-5,8-dihydroxy-7-(2-methylpropyl)-3-phenyl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),5,8,10,12,15-hexaen-4-yl]-1-[2-(dimethylamino)-3-(1h-indol-3-yl)propanoyl]pyrrolidine-2-carboximidic acid)