NP-MRD: Showing NP-Card for methyl (1r,11r,12r,17s)-12-acetyl-12-hydroxy-5-methoxy-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,9-tetraene-10-carboxylate (NP0270143)

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Record Information

Version

2.0

Created at

2022-09-08 15:52:39 UTC

Updated at

2022-09-08 15:52:39 UTC

NP-MRD ID

NP0270143

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (1r,11r,12r,17s)-12-acetyl-12-hydroxy-5-methoxy-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,9-tetraene-10-carboxylate

Description

Methyl (1R,11R,12R,17S)-12-acetyl-12-hydroxy-5-methoxy-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]Octadeca-2(7),3,5,9-tetraene-10-carboxylate belongs to the class of organic compounds known as strychnos alkaloids. These are alkaloids having a core structure based on the strychnan, stemmadenine (seco-curan), or the akuammicine (curan) skeleton. methyl (1r,11r,12r,17s)-12-acetyl-12-hydroxy-5-methoxy-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,9-tetraene-10-carboxylate is found in Alstonia angustifolia and Alstonia macrophylla. Based on a literature review very few articles have been published on methyl (1R,11R,12R,17S)-12-acetyl-12-hydroxy-5-methoxy-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]Octadeca-2(7),3,5,9-tetraene-10-carboxylate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082217522D          

 28 32  0  0  1  0            999 V2000
    1.4781    3.8783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4797    3.0533    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1949    2.6422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9086    3.0560    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1965    1.8172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0003    1.4016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7602    1.7571    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.3466    1.1735    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1713    1.1955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6027    0.4923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4274    0.5143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8588   -0.1889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2094   -0.2329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3847   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9533    0.4483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0766    0.5160    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2714   -0.3569    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5881   -0.8612    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8791   -0.3673    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.0348   -0.1521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8011    0.7067    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0636    0.3368    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2927    1.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5242    1.2409    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6011    2.1215    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3921    1.3975    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7871    0.9265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2946    0.3105    0.0000 C   0  0  1  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  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 10 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
  8 15  1  0  0  0  0
 16 15  1  6  0  0  0
  6 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  6  0  0  0
 21 23  1  1  0  0  0
 23 24  1  0  0  0  0
 23 25  2  0  0  0  0
 21 26  1  0  0  0  0
  5 26  1  0  0  0  0
 26 27  1  6  0  0  0
 28 27  1  1  0  0  0
 19 28  1  0  0  0  0
 16 28  1  0  0  0  0
M  END

     RDKit          3D

 52 56  0  0  0  0  0  0  0  0999 V2000
   -2.5352    4.1225    0.6417 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7219    3.0064    0.3294 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2279    1.9133   -0.3676 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4325    1.9929   -0.6897 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4664    0.7369   -0.7262 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1615    0.7578   -0.3459 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7968    1.8201   -0.3626 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1150    1.2510   -0.2021 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3786    1.8409   -0.2786 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5303    1.0924   -0.2312 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8006    1.6886   -0.3083 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9272    0.8535   -0.2527 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3824   -0.2684   -0.1049 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1557   -0.8849   -0.0242 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0083   -0.1079   -0.0715 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5627   -0.4314    0.1203 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3195   -0.7577    1.5898 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0222   -2.2054    1.5586 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7490   -2.3216    0.2766 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0282   -1.7364    0.5350 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6868   -1.4984   -0.7931 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3776   -2.6964   -1.5428 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1344   -1.4551   -0.7389 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0054   -0.5716    0.0750 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7665   -2.2540   -1.4545 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9483   -0.4283   -1.4901 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6136   -1.1298   -1.8986 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0856   -1.6077   -0.6500 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0478    5.0280    0.2497 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5789    4.2308    1.7532 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5612    3.9625    0.2194 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6170    2.8369   -0.4685 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4643    2.9126   -0.3776 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9177    0.1890    0.6483 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9376    0.1783   -1.1507 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8635    1.4096   -0.2554 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3139   -0.8515   -0.0708 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0579   -1.9589    0.0751 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4075   -0.0754    1.9983 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2694   -0.6087    2.1555 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7698   -2.4382    2.3612 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8304   -2.8799    1.6127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6465   -2.4810    1.0774 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9992   -0.7816    1.0653 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4198   -3.4747   -0.9231 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7867   -1.2100    0.5371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4200   -0.1398    0.9022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5313    0.1833   -0.5397 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4167   -0.1244   -2.4603 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0483   -0.3830   -2.3785 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8146   -1.9520   -2.5848 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8947   -2.2933   -0.9754 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 10 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  1
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  6
 21 26  1  0
 26 27  1  0
 27 28  1  0
 21 23  1  0
 23 24  1  0
 23 25  2  0
 26  5  1  0
 16  6  1  0
 28 16  1  0
 15  8  1  0
 28 19  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  7 32  1  0
  9 33  1  0
 12 34  1  0
 12 35  1  0
 12 36  1  0
 13 37  1  0
 14 38  1  0
 17 39  1  0
 17 40  1  0
 18 41  1  0
 18 42  1  0
 20 43  1  0
 20 44  1  0
 22 45  1  0
 26 49  1  6
 27 50  1  0
 27 51  1  0
 28 52  1  6
 24 46  1  0
 24 47  1  0
 24 48  1  0
M  END


  Mrv1652309082217522D          

 28 32  0  0  1  0            999 V2000
    1.4781    3.8783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4797    3.0533    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1949    2.6422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9086    3.0560    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1965    1.8172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0003    1.4016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7602    1.7571    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.3466    1.1735    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1713    1.1955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6027    0.4923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4274    0.5143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8588   -0.1889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2094   -0.2329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3847   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9533    0.4483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0766    0.5160    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2714   -0.3569    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5881   -0.8612    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8791   -0.3673    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.0348   -0.1521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8011    0.7067    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0636    0.3368    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2927    1.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5242    1.2409    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6011    2.1215    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3921    1.3975    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7871    0.9265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2946    0.3105    0.0000 C   0  0  1  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  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 10 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
  8 15  1  0  0  0  0
 16 15  1  6  0  0  0
  6 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  6  0  0  0
 21 23  1  1  0  0  0
 23 24  1  0  0  0  0
 23 25  2  0  0  0  0
 21 26  1  0  0  0  0
  5 26  1  0  0  0  0
 26 27  1  6  0  0  0
 28 27  1  1  0  0  0
 19 28  1  0  0  0  0
 16 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0270143

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C1=C2NC3=CC(OC)=CC=C3[C@@]22CCN3C[C@](O)([C@@H]1C[C@@H]23)C(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C21H24N2O5/c1-11(24)21(26)10-23-7-6-20-13-5-4-12(27-2)8-15(13)22-18(20)17(19(25)28-3)14(21)9-16(20)23/h4-5,8,14,16,22,26H,6-7,9-10H2,1-3H3/t14-,16+,20-,21-/m1/s1

> <INCHI_KEY>
HSSBHDYKSNNBQO-MGTBRSBRSA-N

> <FORMULA>
C21H24N2O5

> <MOLECULAR_WEIGHT>
384.432

> <EXACT_MASS>
384.168521881

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
40.31714899526394

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (1R,11R,12R,17S)-12-acetyl-12-hydroxy-5-methoxy-8,14-diazapentacyclo[9.5.2.0^{1,9}.0^{2,7}.0^{14,17}]octadeca-2,4,6,9-tetraene-10-carboxylate

> <JCHEM_LOGP>
0.3298746000000007

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
13.554112715183972

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.35583612150937

> <JCHEM_PKA_STRONGEST_BASIC>
8.694349646821848

> <JCHEM_POLAR_SURFACE_AREA>
88.1

> <JCHEM_REFRACTIVITY>
104.18529999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1R,11R,12R,17S)-12-acetyl-12-hydroxy-5-methoxy-8,14-diazapentacyclo[9.5.2.0^{1,9}.0^{2,7}.0^{14,17}]octadeca-2,4,6,9-tetraene-10-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0       2.759   7.240   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       2.762   5.700   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       4.097   4.932   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       5.429   5.705   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       4.100   3.392   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.601   2.616   0.000  0.00  0.00           C+0
HETATM    7  N   UNK     0       7.019   3.280   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0       8.114   2.191   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.653   2.232   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.458   0.919   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      11.998   0.960   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      12.803  -0.353   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.724  -0.435   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.185  -0.476   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.379   0.837   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.743   0.963   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.107  -0.666   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.831  -1.608   0.000  0.00  0.00           C+0
HETATM   19  N   UNK     0       3.508  -0.686   0.000  0.00  0.00           N+0
HETATM   20  C   UNK     0       1.932  -0.284   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.495   1.319   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       0.119   0.629   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       0.546   2.532   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -0.979   2.316   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       1.122   3.960   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       2.599   2.609   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       3.336   1.729   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.283   0.580   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   26                                                  
CONECT    6    5    7   16                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   15                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   13                                                  
CONECT   11   10   12                                                       
CONECT   12   11                                                            
CONECT   13   10   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14    8   16                                                  
CONECT   16   15    6   17   28                                             
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   28                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   23   26                                             
CONECT   22   21                                                            
CONECT   23   21   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23                                                            
CONECT   26   21    5   27                                                  
CONECT   27   26   28                                                       
CONECT   28   27   19   16                                                  
MASTER        0    0    0    0    0    0    0    0   28    0   64    0
END

View in JSmol

Synonyms

Value	Source
Methyl (1R,11R,12R,17S)-12-acetyl-12-hydroxy-5-methoxy-8,14-diazapentacyclo[9.5.2.0,.0,.0,]octadeca-2(7),3,5,9-tetraene-10-carboxylic acid	Generator

Chemical Formula

C₂₁H₂₄N₂O₅

Average Mass

384.4320 Da

Monoisotopic Mass

384.16852 Da

IUPAC Name

methyl (1R,11R,12R,17S)-12-acetyl-12-hydroxy-5-methoxy-8,14-diazapentacyclo[9.5.2.0^{1,9}.0^{2,7}.0^{14,17}]octadeca-2,4,6,9-tetraene-10-carboxylate

Traditional Name

methyl (1R,11R,12R,17S)-12-acetyl-12-hydroxy-5-methoxy-8,14-diazapentacyclo[9.5.2.0^{1,9}.0^{2,7}.0^{14,17}]octadeca-2,4,6,9-tetraene-10-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)C1=C2NC3=CC(OC)=CC=C3[C@@]22CCN3C[C@](O)([C@@H]1C[C@@H]23)C(C)=O

InChI Identifier

InChI=1S/C21H24N2O5/c1-11(24)21(26)10-23-7-6-20-13-5-4-12(27-2)8-15(13)22-18(20)17(19(25)28-3)14(21)9-16(20)23/h4-5,8,14,16,22,26H,6-7,9-10H2,1-3H3/t14-,16+,20-,21-/m1/s1

InChI Key

HSSBHDYKSNNBQO-MGTBRSBRSA-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
Alstonia angustifolia	LOTUS Database	35616633
Alstonia macrophylla	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as strychnos alkaloids. These are alkaloids having a core structure based on the strychnan, stemmadenine (seco-curan), or the akuammicine (curan) skeleton.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Strychnos alkaloids

Sub Class

Not Available

Direct Parent

Strychnos alkaloids

Alternative Parents

Substituents

Strychnan skeleton
Akuammicine-skeleton
Stemmadenine-skeleton
Carbazole
Indole or derivatives
Dihydroindole
Indolizidine
Anisole
Alkyl aryl ether
Aralkylamine
Secondary aliphatic/aromatic amine
Beta-aminoketone
Piperidine
Benzenoid
N-alkylpyrrolidine
Alpha-hydroxy ketone
Vinylogous amide
Pyrrolidine
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Methyl ester
Tertiary alcohol
Tertiary amine
Tertiary aliphatic amine
Amino acid or derivatives
Carboxylic acid ester
Ketone
Secondary amine
Carboxylic acid derivative
Enamine
Ether
Azacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Carbonyl group
Organic oxide
Organopnictogen compound
Organonitrogen compound
Organic nitrogen compound
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Alcohol
Amine
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	0.33	ChemAxon
pKa (Strongest Acidic)	12.36	ChemAxon
pKa (Strongest Basic)	8.69	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	88.1 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	104.19 m³·mol⁻¹	ChemAxon
Polarizability	40.32 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

163018354

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (1r,11r,12r,17s)-12-acetyl-12-hydroxy-5-methoxy-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,9-tetraene-10-carboxylate (NP0270143)

MOL for NP0270143 (methyl (1r,11r,12r,17s)-12-acetyl-12-hydroxy-5-methoxy-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,9-tetraene-10-carboxylate)

3D MOL for NP0270143 (methyl (1r,11r,12r,17s)-12-acetyl-12-hydroxy-5-methoxy-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,9-tetraene-10-carboxylate)

3D SDF for NP0270143 (methyl (1r,11r,12r,17s)-12-acetyl-12-hydroxy-5-methoxy-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,9-tetraene-10-carboxylate)

3D-SDF for NP0270143 (methyl (1r,11r,12r,17s)-12-acetyl-12-hydroxy-5-methoxy-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,9-tetraene-10-carboxylate)

PDB for NP0270143 (methyl (1r,11r,12r,17s)-12-acetyl-12-hydroxy-5-methoxy-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,9-tetraene-10-carboxylate)

3D PDB for NP0270143 (methyl (1r,11r,12r,17s)-12-acetyl-12-hydroxy-5-methoxy-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,9-tetraene-10-carboxylate)

SMILES for NP0270143 (methyl (1r,11r,12r,17s)-12-acetyl-12-hydroxy-5-methoxy-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,9-tetraene-10-carboxylate)

INCHI for NP0270143 (methyl (1r,11r,12r,17s)-12-acetyl-12-hydroxy-5-methoxy-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,9-tetraene-10-carboxylate)

Structure for NP0270143 (methyl (1r,11r,12r,17s)-12-acetyl-12-hydroxy-5-methoxy-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,9-tetraene-10-carboxylate)

3D Structure for NP0270143 (methyl (1r,11r,12r,17s)-12-acetyl-12-hydroxy-5-methoxy-8,14-diazapentacyclo[9.5.2.0¹,⁹.0²,⁷.0¹⁴,¹⁷]octadeca-2,4,6,9-tetraene-10-carboxylate)