NP-MRD: Showing NP-Card for (1s,2r,3s,5s,16z,18z,20r,21s)-11-chloro-21,23-dihydroxy-12,20-dimethoxy-2,5,9,16-tetramethyl-8-oxo-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1¹⁰,¹⁴.0³,⁵]hexacosa-10(26),11,13,16,18,22-hexaen-6-yl (2s)-2-(n-methylpropanamido)propanoate (NP0217093)

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Record Information

Version

2.0

Created at

2022-09-05 17:19:12 UTC

Updated at

2022-09-05 17:19:12 UTC

NP-MRD ID

NP0217093

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2r,3s,5s,16z,18z,20r,21s)-11-chloro-21,23-dihydroxy-12,20-dimethoxy-2,5,9,16-tetramethyl-8-oxo-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1¹⁰,¹⁴.0³,⁵]hexacosa-10(26),11,13,16,18,22-hexaen-6-yl (2s)-2-(n-methylpropanamido)propanoate

Description

Maytanprine belongs to the class of organic compounds known as macrolactams. These are cyclic amides of amino carboxylic acids, having a 1-azacycloalkan-2-one structure, or analogues having unsaturation or heteroatoms replacing one or more carbon atoms of the ring. They are nitrogen analogues (the a nitrogen atom replacing the o atom of the cyclic carboxylic acid group ) of the naturally occurring macrolides. (1s,2r,3s,5s,16z,18z,20r,21s)-11-chloro-21,23-dihydroxy-12,20-dimethoxy-2,5,9,16-tetramethyl-8-oxo-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1¹⁰,¹⁴.0³,⁵]hexacosa-10(26),11,13,16,18,22-hexaen-6-yl (2s)-2-(n-methylpropanamido)propanoate was first documented in 2004 (PMID: 15305028). Based on a literature review very few articles have been published on Maytanprine (PMID: 27521896).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052219192D          

 49 52  0  0  1  0            999 V2000
   -3.3832   -3.6076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6688   -4.0201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.9543   -2.7826    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2398   -4.0201    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2398   -4.8451    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5253   -3.6076    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5253   -2.7826    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1891   -4.0201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1891   -4.8451    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.1425   -3.3833    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
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
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  5  7  1  0  0  0  0
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 39 38  1  6  0  0  0
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 47 48  1  0  0  0  0
 12 48  1  0  0  0  0
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 48 49  1  6  0  0  0
M  END

     RDKit          3D

 97100  0  0  0  0  0  0  0  0999 V2000
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 25 26  1  0
 48 12  1  0
 25 18  1  0
 43 36  1  0
 48 46  1  0
  1 50  1  0
  1 51  1  0
  1 52  1  0
  2 53  1  0
  2 54  1  0
  6 55  1  0
  6 56  1  0
  6 57  1  0
  7 58  1  1
  8 59  1  0
  8 60  1  0
  8 61  1  0
 12 62  1  1
 13 63  1  0
 13 64  1  0
 17 65  1  0
 17 66  1  0
 17 67  1  0
 19 68  1  0
 27 73  1  0
 27 74  1  0
 29 75  1  0
 29 76  1  0
 29 77  1  0
 30 78  1  0
 31 79  1  0
 32 80  1  0
 33 81  1  1
 35 82  1  0
 35 83  1  0
 35 84  1  0
 37 85  1  0
 38 86  1  0
 38 87  1  0
 39 88  1  6
 42 89  1  0
 44 90  1  1
 45 91  1  0
 45 92  1  0
 45 93  1  0
 46 94  1  6
 49 95  1  0
 49 96  1  0
 49 97  1  0
 21 69  1  0
 24 70  1  0
 24 71  1  0
 24 72  1  0
M  END


  Mrv1652309052219192D          

 49 52  0  0  1  0            999 V2000
   -3.3832   -3.6076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6688   -4.0201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9543   -3.6076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9543   -2.7826    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2398   -4.0201    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2398   -4.8451    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5253   -3.6076    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5253   -2.7826    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1891   -4.0201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1891   -4.8451    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9036   -3.6076    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6181   -4.0201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1425   -3.3833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8454   -2.9513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5349   -2.1869    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6504   -2.7709    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.6050   -1.9471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4704   -2.8616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2926   -2.9298    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6447   -3.6758    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1746   -4.3538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3524   -4.2857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8823   -4.9637    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0601   -4.8955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0003   -3.5396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1781   -3.4715    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    6.1804   -4.5251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2937   -5.3423    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1184   -5.3650    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1355   -6.1520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7230   -6.8664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1009   -7.4083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3365   -7.7187    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5169   -8.5238    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3043   -8.7700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5128   -7.7642    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9735   -8.4485    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0427   -7.0862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2205   -7.1543    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8684   -7.9004    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3385   -8.5784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9864   -9.3245    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1607   -8.5103    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5523   -6.4048    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8346   -6.8116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3061   -5.6175    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6032   -5.1854    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3288   -4.7928    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7067   -4.2509    0.0000 C   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  2  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  1  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  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
 16 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  1  0  0  0  0
 23 24  1  0  0  0  0
 22 25  2  0  0  0  0
 18 25  1  0  0  0  0
 25 26  1  0  0  0  0
 20 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 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  1  1  0  0  0
 34 35  1  0  0  0  0
 33 36  1  0  0  0  0
 36 37  1  1  0  0  0
 36 38  1  0  0  0  0
 39 38  1  6  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 41 43  2  0  0  0  0
 36 43  1  0  0  0  0
 39 44  1  0  0  0  0
 44 45  1  1  0  0  0
 44 46  1  0  0  0  0
 46 47  1  6  0  0  0
 47 48  1  0  0  0  0
 12 48  1  0  0  0  0
 46 48  1  0  0  0  0
 48 49  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0217093

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC(=O)N(C)[C@@H](C)C(=O)OC1CC(=O)N(C)C2=CC(C\C(C)=C/C=C\[C@@H](OC)[C@@]3(O)C[C@H](OC(O)=N3)[C@@H](C)[C@@H]3O[C@@]13C)=CC(OC)=C2Cl

> <INCHI_IDENTIFIER>
InChI=1S/C35H48ClN3O10/c1-10-28(40)38(6)21(4)32(42)48-27-17-29(41)39(7)23-15-22(16-24(45-8)30(23)36)14-19(2)12-11-13-26(46-9)35(44)18-25(47-33(43)37-35)20(3)31-34(27,5)49-31/h11-13,15-16,20-21,25-27,31,44H,10,14,17-18H2,1-9H3,(H,37,43)/b13-11-,19-12-/t20-,21+,25+,26-,27?,31+,34+,35+/m1/s1

> <INCHI_KEY>
BVXGVRDMHBYRCQ-HTRYSSCQSA-N

> <FORMULA>
C35H48ClN3O10

> <MOLECULAR_WEIGHT>
706.23

> <EXACT_MASS>
705.3028225

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
97

> <JCHEM_AVERAGE_POLARIZABILITY>
72.65152382020435

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2R,3S,5S,16Z,18Z,20R,21S)-11-chloro-21,23-dihydroxy-12,20-dimethoxy-2,5,9,16-tetramethyl-8-oxo-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1^{10,14}.0^{3,5}]hexacosa-10(26),11,13,16,18,22-hexaen-6-yl (2S)-2-(N-methylpropanamido)propanoate

> <JCHEM_LOGP>
4.5133392166666635

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.643378803868941

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.7488678380102245

> <JCHEM_PKA_STRONGEST_BASIC>
-1.651315885764177

> <JCHEM_POLAR_SURFACE_AREA>
159.96

> <JCHEM_REFRACTIVITY>
181.5709

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,3S,5S,16Z,18Z,20R,21S)-11-chloro-21,23-dihydroxy-12,20-dimethoxy-2,5,9,16-tetramethyl-8-oxo-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1^{10,14}.0^{3,5}]hexacosa-10(26),11,13,16,18,22-hexaen-6-yl (2S)-2-(N-methylpropanamido)propanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0      -6.315  -6.734   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.982  -7.504   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.648  -6.734   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -3.648  -5.194   0.000  0.00  0.00           O+0
HETATM    5  N   UNK     0      -2.314  -7.504   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0      -2.314  -9.044   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.981  -6.734   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.981  -5.194   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.353  -7.504   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       0.353  -9.044   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0       1.687  -6.734   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       3.020  -7.504   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.999  -6.316   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.311  -5.509   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       4.732  -4.082   0.000  0.00  0.00           O+0
HETATM   16  N   UNK     0       6.814  -5.172   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0       6.729  -3.635   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.345  -5.342   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.879  -5.469   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      10.537  -6.862   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.659  -8.127   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.124  -8.000   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       7.247  -9.265   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       5.712  -9.138   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       7.467  -6.607   0.000  0.00  0.00           C+0
HETATM   26 Cl   UNK     0       5.933  -6.480   0.000  0.00  0.00          Cl+0
HETATM   27  C   UNK     0      11.537  -8.447   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      11.748  -9.972   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      13.288 -10.015   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      11.453 -11.484   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      10.683 -12.817   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       9.522 -13.829   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       8.095 -14.408   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       8.432 -15.911   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       9.901 -16.371   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       6.557 -14.493   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       7.417 -15.771   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       5.680 -13.228   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       4.145 -13.355   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       3.488 -14.747   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       4.365 -16.013   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       3.708 -17.406   0.000  0.00  0.00           O+0
HETATM   43  N   UNK     0       5.900 -15.886   0.000  0.00  0.00           N+0
HETATM   44  C   UNK     0       2.898 -11.956   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       1.558 -12.715   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       2.438 -10.486   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0       1.126  -9.679   0.000  0.00  0.00           O+0
HETATM   48  C   UNK     0       2.480  -8.946   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0       1.319  -7.935   0.000  0.00  0.00           C+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   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   48                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   25                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   27                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   25                                                  
CONECT   23   22   24                                                       
CONECT   24   23                                                            
CONECT   25   22   18   26                                                  
CONECT   26   25                                                            
CONECT   27   20   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34   36                                                  
CONECT   34   33   35                                                       
CONECT   35   34                                                            
CONECT   36   33   37   38   43                                             
CONECT   37   36                                                            
CONECT   38   36   39                                                       
CONECT   39   38   40   44                                                  
CONECT   40   39   41                                                       
CONECT   41   40   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41   36                                                       
CONECT   44   39   45   46                                                  
CONECT   45   44                                                            
CONECT   46   44   47   48                                                  
CONECT   47   46   48                                                       
CONECT   48   47   12   46   49                                             
CONECT   49   48                                                            
MASTER        0    0    0    0    0    0    0    0   49    0  104    0
END

View in JSmol

Synonyms

Value	Source
N(2')-Deacetyl-N(2')-(1-oxopropyl)maytansine	MeSH

Chemical Formula

C₃₅H₄₈ClN₃O₁₀

Average Mass

706.2300 Da

Monoisotopic Mass

705.30282 Da

IUPAC Name

(1S,2R,3S,5S,16Z,18Z,20R,21S)-11-chloro-21,23-dihydroxy-12,20-dimethoxy-2,5,9,16-tetramethyl-8-oxo-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1^{10,14}.0^{3,5}]hexacosa-10(26),11,13,16,18,22-hexaen-6-yl (2S)-2-(N-methylpropanamido)propanoate

Traditional Name

CAS Registry Number

Not Available

SMILES

CCC(=O)N(C)[C@@H](C)C(=O)OC1CC(=O)N(C)C2=CC(C\C(C)=C/C=C\[C@@H](OC)[C@@]3(O)C[C@H](OC(O)=N3)[C@@H](C)[C@@H]3O[C@@]13C)=CC(OC)=C2Cl

InChI Identifier

InChI=1S/C35H48ClN3O10/c1-10-28(40)38(6)21(4)32(42)48-27-17-29(41)39(7)23-15-22(16-24(45-8)30(23)36)14-19(2)12-11-13-26(46-9)35(44)18-25(47-33(43)37-35)20(3)31-34(27,5)49-31/h11-13,15-16,20-21,25-27,31,44H,10,14,17-18H2,1-9H3,(H,37,43)/b13-11-,19-12-/t20-,21+,25+,26-,27?,31+,34+,35+/m1/s1

InChI Key

BVXGVRDMHBYRCQ-HTRYSSCQSA-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 macrolactams. These are cyclic amides of amino carboxylic acids, having a 1-azacycloalkan-2-one structure, or analogues having unsaturation or heteroatoms replacing one or more carbon atoms of the ring. They are nitrogen analogues (the a nitrogen atom replacing the o atom of the cyclic carboxylic acid group ) of the naturally occurring macrolides.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Macrolactams

Sub Class

Not Available

Direct Parent

Macrolactams

Alternative Parents

Substituents

Macrolactam
Alpha-amino acid ester
Alanine or derivatives
Alpha-amino acid or derivatives
Anisole
Phenol ether
Alkyl aryl ether
1,3-oxazinane
Oxazinane
Aryl chloride
Benzenoid
Aryl halide
Tertiary carboxylic acid amide
Carbamic acid ester
Carboxylic acid ester
Carboxamide group
Lactam
Alkanolamine
Oxacycle
Azacycle
Organoheterocyclic compound
Carboxylic acid derivative
Dialkyl ether
Oxirane
Ether
Monocarboxylic acid or derivatives
Carbonyl group
Organooxygen compound
Hydrocarbon derivative
Organonitrogen compound
Organic nitrogen compound
Organic oxygen compound
Organochloride
Organohalogen compound
Organic oxide
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	4.51	ChemAxon
pKa (Strongest Acidic)	1.75	ChemAxon
pKa (Strongest Basic)	-1.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	159.96 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	181.57 m³·mol⁻¹	ChemAxon
Polarizability	72.65 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00051515

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

101306858

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Eckelmann D, Kusari S, Spiteller M: Occurrence and spatial distribution of maytansinoids in Putterlickia pyracantha, an unexplored resource of anticancer compounds. Fitoterapia. 2016 Sep;113:175-81. doi: 10.1016/j.fitote.2016.08.006. Epub 2016 Aug 10. [PubMed:27521896 ]
Nakao H, Senokuchi K, Umebayashi C, Kanemaru K, Masuda T, Oyama Y, Yonemori S: Cytotoxic activity of maytanprine isolated from Maytenus diversifolia in human leukemia K562 cells. Biol Pharm Bull. 2004 Aug;27(8):1236-40. doi: 10.1248/bpb.27.1236. [PubMed:15305028 ]
LOTUS database [Link]

Showing NP-Card for (1s,2r,3s,5s,16z,18z,20r,21s)-11-chloro-21,23-dihydroxy-12,20-dimethoxy-2,5,9,16-tetramethyl-8-oxo-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1¹⁰,¹⁴.0³,⁵]hexacosa-10(26),11,13,16,18,22-hexaen-6-yl (2s)-2-(n-methylpropanamido)propanoate (NP0217093)

MOL for NP0217093 ((1s,2r,3s,5s,16z,18z,20r,21s)-11-chloro-21,23-dihydroxy-12,20-dimethoxy-2,5,9,16-tetramethyl-8-oxo-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1¹⁰,¹⁴.0³,⁵]hexacosa-10(26),11,13,16,18,22-hexaen-6-yl (2s)-2-(n-methylpropanamido)propanoate)

3D MOL for NP0217093 ((1s,2r,3s,5s,16z,18z,20r,21s)-11-chloro-21,23-dihydroxy-12,20-dimethoxy-2,5,9,16-tetramethyl-8-oxo-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1¹⁰,¹⁴.0³,⁵]hexacosa-10(26),11,13,16,18,22-hexaen-6-yl (2s)-2-(n-methylpropanamido)propanoate)

3D SDF for NP0217093 ((1s,2r,3s,5s,16z,18z,20r,21s)-11-chloro-21,23-dihydroxy-12,20-dimethoxy-2,5,9,16-tetramethyl-8-oxo-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1¹⁰,¹⁴.0³,⁵]hexacosa-10(26),11,13,16,18,22-hexaen-6-yl (2s)-2-(n-methylpropanamido)propanoate)

3D-SDF for NP0217093 ((1s,2r,3s,5s,16z,18z,20r,21s)-11-chloro-21,23-dihydroxy-12,20-dimethoxy-2,5,9,16-tetramethyl-8-oxo-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1¹⁰,¹⁴.0³,⁵]hexacosa-10(26),11,13,16,18,22-hexaen-6-yl (2s)-2-(n-methylpropanamido)propanoate)

PDB for NP0217093 ((1s,2r,3s,5s,16z,18z,20r,21s)-11-chloro-21,23-dihydroxy-12,20-dimethoxy-2,5,9,16-tetramethyl-8-oxo-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1¹⁰,¹⁴.0³,⁵]hexacosa-10(26),11,13,16,18,22-hexaen-6-yl (2s)-2-(n-methylpropanamido)propanoate)

3D PDB for NP0217093 ((1s,2r,3s,5s,16z,18z,20r,21s)-11-chloro-21,23-dihydroxy-12,20-dimethoxy-2,5,9,16-tetramethyl-8-oxo-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1¹⁰,¹⁴.0³,⁵]hexacosa-10(26),11,13,16,18,22-hexaen-6-yl (2s)-2-(n-methylpropanamido)propanoate)

SMILES for NP0217093 ((1s,2r,3s,5s,16z,18z,20r,21s)-11-chloro-21,23-dihydroxy-12,20-dimethoxy-2,5,9,16-tetramethyl-8-oxo-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1¹⁰,¹⁴.0³,⁵]hexacosa-10(26),11,13,16,18,22-hexaen-6-yl (2s)-2-(n-methylpropanamido)propanoate)

INCHI for NP0217093 ((1s,2r,3s,5s,16z,18z,20r,21s)-11-chloro-21,23-dihydroxy-12,20-dimethoxy-2,5,9,16-tetramethyl-8-oxo-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1¹⁰,¹⁴.0³,⁵]hexacosa-10(26),11,13,16,18,22-hexaen-6-yl (2s)-2-(n-methylpropanamido)propanoate)

Structure for NP0217093 ((1s,2r,3s,5s,16z,18z,20r,21s)-11-chloro-21,23-dihydroxy-12,20-dimethoxy-2,5,9,16-tetramethyl-8-oxo-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1¹⁰,¹⁴.0³,⁵]hexacosa-10(26),11,13,16,18,22-hexaen-6-yl (2s)-2-(n-methylpropanamido)propanoate)

3D Structure for NP0217093 ((1s,2r,3s,5s,16z,18z,20r,21s)-11-chloro-21,23-dihydroxy-12,20-dimethoxy-2,5,9,16-tetramethyl-8-oxo-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1¹⁰,¹⁴.0³,⁵]hexacosa-10(26),11,13,16,18,22-hexaen-6-yl (2s)-2-(n-methylpropanamido)propanoate)