NP-MRD: Showing NP-Card for 10,11-Dimethoxynareline (NP0068976)

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Record Information

Version

2.0

Created at

2022-04-28 14:15:12 UTC

Updated at

2022-04-28 14:15:12 UTC

NP-MRD ID

NP0068976

Secondary Accession Numbers

None

Natural Product Identification

Common Name

10,11-Dimethoxynareline

Description

Methyl (1R,10S,12R,13E,14S,17S,18S,19R)-13-ethylidene-17-hydroxy-4,6-dimethoxy-16-oxa-8,15-diazahexacyclo[10.6.1.0¹,⁹.0²,⁷.0¹⁰,¹⁵.0¹⁴,¹⁸]Nonadeca-2(7),3,5,8-tetraene-19-carboxylate belongs to the class of organic compounds known as 3-alkylindoles. 3-Alkylindoles are compounds containing an indole moiety that carries an alkyl chain at the 3-position. 10,11-Dimethoxynareline is found in Alstonia macrophylla . Based on a literature review very few articles have been published on methyl (1R,10S,12R,13E,14S,17S,18S,19R)-13-ethylidene-17-hydroxy-4,6-dimethoxy-16-oxa-8,15-diazahexacyclo[10.6.1.0¹,⁹.0²,⁷.0¹⁰,¹⁵.0¹⁴,¹⁸]Nonadeca-2(7),3,5,8-tetraene-19-carboxylate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282216152D          

 30 35  0  0  1  0            999 V2000
    2.3162    2.4351    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7700    2.3746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8078    1.4345    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4372    0.6998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8884    0.0091    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.6847    0.2247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7257    1.0487    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4598    1.4252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1529    0.9776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1119    0.1537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3778   -0.2228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3368   -1.0468    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0298   -1.4943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8870    1.3541    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5801    0.9066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9547    1.3423    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0752    1.9859    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8266    2.3266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4973    1.8463    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9072    3.1477    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6585    3.4884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9351    0.5027    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2959    1.3435    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2517    2.3635    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6371    2.9138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8063    3.7212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8867    1.0729    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6657    0.2224    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4127   -0.1357    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5919   -0.9410    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  6  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  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  2  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
  9 14  1  0  0  0  0
 14 15  1  0  0  0  0
  7 16  1  0  0  0  0
 16  4  1  6  0  0  0
 16 17  1  0  0  0  0
  1 17  1  0  0  0  0
 17 18  1  1  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 22 16  1  6  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
  1 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 23 27  1  6  0  0  0
  3 27  1  1  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 22 29  1  0  0  0  0
 29 30  1  1  0  0  0
M  END

     RDKit          3D

 54 59  0  0  0  0  0  0  0  0999 V2000
   -4.6957    1.6581    1.1647 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9436    0.4862    1.6673 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0766   -0.1079    0.8941 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3133   -1.2663    1.3490 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8206   -0.9126    1.2406 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3208   -2.3629    1.3653 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3127   -2.6367    2.7454 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2676   -3.1576    0.7871 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3652   -2.3996    0.4783 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1977   -2.0598   -0.9377 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0469   -0.9120   -1.3562 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7792    0.3320   -0.5215 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3275    0.6511   -0.6908 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9423    1.9691   -0.1599 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4438    2.8140   -0.9453 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0938    2.3442    1.1597 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6841    3.6406    1.5442 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4781   -0.4675   -0.1323 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7682   -1.6532   -1.0276 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2957   -1.9744   -1.6316 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.3889   -1.1646   -1.2632 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7128   -1.1807   -1.6635 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2084   -2.0736   -2.5914 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5759   -2.0106   -2.9350 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5693   -0.2470   -1.0944 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1432    0.6752   -0.1611 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9776    1.6094    0.4153 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3378    1.7601    0.1512 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8120    0.6748    0.2263 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9476   -0.2476   -0.3310 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9647    2.4952    1.0657 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4063    1.9759    1.9565 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2192    1.4516    0.2077 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0883    0.0933    2.6759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5220   -1.5979    2.3627 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4804   -0.2843    2.0569 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6939   -2.4807    0.9952 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3668   -3.3171    2.9719 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4372   -2.9347   -1.5390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1378   -1.1600   -1.3352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7801   -0.6492   -2.3936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4523    1.1234   -0.8429 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1349    0.6521   -1.7836 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5750    4.2936    1.7175 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1094    4.1494    0.7296 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0276    3.6419    2.4280 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8619   -0.9712   -3.2673 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8559   -2.7531   -3.6987 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1926   -2.2052   -2.0152 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6141   -0.2286   -1.3831 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8515    0.8328   -0.1399 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4994    2.5924   -0.5731 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8295    2.1036    1.1016 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4782    1.3963    0.9567 H   0  0  0  0  0  0  0  0  0  0  0  0
 17 16  1  0
 16 14  1  0
 14 15  2  0
 14 13  1  0
 13 12  1  0
 12 11  1  0
 11 10  1  0
 10  9  1  0
  9  8  1  0
  8  6  1  0
  6  7  1  0
  6  5  1  0
  5  4  1  0
  4  3  1  0
  3  2  2  0
  2  1  1  0
  5 18  1  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 30  2  0
 30 29  1  0
 29 26  2  0
 26 27  1  0
 27 28  1  0
 26 25  1  0
 25 22  2  0
 22 23  1  0
 23 24  1  0
 18 13  1  0
 18 30  1  1
  3 12  1  0
 22 21  1  0
 19 10  1  0
  4  9  1  0
 17 44  1  0
 17 45  1  0
 17 46  1  0
 13 43  1  6
 12 42  1  6
 11 40  1  0
 11 41  1  0
 10 39  1  6
  6 37  1  6
  7 38  1  0
  5 36  1  1
  4 35  1  1
  2 34  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
 29 54  1  0
 28 51  1  0
 28 52  1  0
 28 53  1  0
 25 50  1  0
 24 47  1  0
 24 48  1  0
 24 49  1  0
M  END


  Mrv1652304282216152D          

 30 35  0  0  1  0            999 V2000
    2.3162    2.4351    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7700    2.3746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8078    1.4345    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4372    0.6998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8884    0.0091    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.6847    0.2247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7257    1.0487    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4598    1.4252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1529    0.9776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1119    0.1537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3778   -0.2228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3368   -1.0468    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0298   -1.4943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8870    1.3541    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5801    0.9066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9547    1.3423    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0752    1.9859    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8266    2.3266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4973    1.8463    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9072    3.1477    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6585    3.4884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9351    0.5027    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2959    1.3435    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2517    2.3635    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6371    2.9138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8063    3.7212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8867    1.0729    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6657    0.2224    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4127   -0.1357    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5919   -0.9410    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  6  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  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  2  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
  9 14  1  0  0  0  0
 14 15  1  0  0  0  0
  7 16  1  0  0  0  0
 16  4  1  6  0  0  0
 16 17  1  0  0  0  0
  1 17  1  0  0  0  0
 17 18  1  1  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 22 16  1  6  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
  1 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 23 27  1  6  0  0  0
  3 27  1  1  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 22 29  1  0  0  0  0
 29 30  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0068976

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)[C@@H]1[C@H]2C[C@@H]3N4O[C@H](O)[C@H]([C@H]4\C2=C\C)[C@@]11C3=NC2=C1C=C(OC)C=C2OC

> <INCHI_IDENTIFIER>
InChI=1S/C22H24N2O6/c1-5-10-11-8-13-19-22(15(11)20(25)29-4,16-18(10)24(13)30-21(16)26)12-6-9(27-2)7-14(28-3)17(12)23-19/h5-7,11,13,15-16,18,21,26H,8H2,1-4H3/b10-5+/t11-,13-,15-,16-,18+,21-,22-/m0/s1

> <INCHI_KEY>
IZJXWXGTDBFHQB-KBAKQQQHSA-N

> <FORMULA>
C22H24N2O6

> <MOLECULAR_WEIGHT>
412.442

> <EXACT_MASS>
412.163436501

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
42.18196751866444

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (1R,10S,12R,13E,14S,17S,18S,19R)-13-ethylidene-17-hydroxy-4,6-dimethoxy-16-oxa-8,15-diazahexacyclo[10.6.1.0^{1,9}.0^{2,7}.0^{10,15}.0^{14,18}]nonadeca-2(7),3,5,8-tetraene-19-carboxylate

> <ALOGPS_LOGP>
1.79

> <JCHEM_LOGP>
1.5245651436666656

> <ALOGPS_LOGS>
-3.24

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.641431835231376

> <JCHEM_PKA_STRONGEST_BASIC>
4.039879648978776

> <JCHEM_POLAR_SURFACE_AREA>
89.82000000000001

> <JCHEM_REFRACTIVITY>
107.6766

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.39e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1R,10S,12R,13E,14S,17S,18S,19R)-13-ethylidene-17-hydroxy-4,6-dimethoxy-16-oxa-8,15-diazahexacyclo[10.6.1.0^{1,9}.0^{2,7}.0^{10,15}.0^{14,18}]nonadeca-2(7),3,5,8-tetraene-19-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       4.324   4.545   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.304   4.433   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.375   2.678   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.550   1.306   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0       5.392   0.017   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0       6.878   0.419   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.955   1.958   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.325   2.660   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.619   1.825   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.542   0.287   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.172  -0.416   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       8.095  -1.954   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       9.389  -2.789   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      10.989   2.528   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      12.283   1.692   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.516   2.506   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.740   3.707   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.143   4.343   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       8.395   3.446   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       7.293   5.876   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       8.696   6.512   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.612   0.938   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.419   2.508   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.337   4.412   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.189   5.439   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.505   6.946   0.000  0.00  0.00           C+0
HETATM   27  N   UNK     0       1.655   2.003   0.000  0.00  0.00           N+0
HETATM   28  O   UNK     0       1.243   0.415   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       2.637  -0.253   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       2.972  -1.756   0.000  0.00  0.00           O+0
CONECT    1    2   17   24                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4   27                                                  
CONECT    4    3    5   16                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   11                                                  
CONECT    7    6    8   16                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10    6   12                                                  
CONECT   12   11   13                                                       
CONECT   13   12                                                            
CONECT   14    9   15                                                       
CONECT   15   14                                                            
CONECT   16    7    4   17   22                                             
CONECT   17   16    1   18                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20                                                            
CONECT   22   16   23   29                                                  
CONECT   23   22   24   27                                                  
CONECT   24   23    1   25                                                  
CONECT   25   24   26                                                       
CONECT   26   25                                                            
CONECT   27   23    3   28                                                  
CONECT   28   27   29                                                       
CONECT   29   28   22   30                                                  
CONECT   30   29                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   70    0
END

View in JSmol

Synonyms

Value	Source
Methyl (1R,10S,12R,13E,14S,17S,18S,19R)-13-ethylidene-17-hydroxy-4,6-dimethoxy-16-oxa-8,15-diazahexacyclo[10.6.1.0,.0,.0,.0,]nonadeca-2(7),3,5,8-tetraene-19-carboxylic acid	Generator

Chemical Formula

C₂₂H₂₄N₂O₆

Average Mass

412.4420 Da

Monoisotopic Mass

412.16344 Da

IUPAC Name

methyl (1R,10S,12R,13E,14S,17S,18S,19R)-13-ethylidene-17-hydroxy-4,6-dimethoxy-16-oxa-8,15-diazahexacyclo[10.6.1.0^{1,9}.0^{2,7}.0^{10,15}.0^{14,18}]nonadeca-2(7),3,5,8-tetraene-19-carboxylate

Traditional Name

methyl (1R,10S,12R,13E,14S,17S,18S,19R)-13-ethylidene-17-hydroxy-4,6-dimethoxy-16-oxa-8,15-diazahexacyclo[10.6.1.0^{1,9}.0^{2,7}.0^{10,15}.0^{14,18}]nonadeca-2(7),3,5,8-tetraene-19-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)[C@@H]1[C@H]2C[C@@H]3N4O[C@H](O)[C@H]([C@H]4\C2=C\C)[C@@]11C3=NC2=C1C=C(OC)C=C2OC

InChI Identifier

InChI=1S/C22H24N2O6/c1-5-10-11-8-13-19-22(15(11)20(25)29-4,16-18(10)24(13)30-21(16)26)12-6-9(27-2)7-14(28-3)17(12)23-19/h5-7,11,13,15-16,18,21,26H,8H2,1-4H3/b10-5+/t11-,13-,15-,16-,18+,21-,22-/m0/s1

InChI Key

IZJXWXGTDBFHQB-KBAKQQQHSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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 macrophylla	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 3-alkylindoles. 3-Alkylindoles are compounds containing an indole moiety that carries an alkyl chain at the 3-position.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Indoles

Direct Parent

3-alkylindoles

Alternative Parents

Substituents

3-alkylindole
Anisole
Alkyl aryl ether
Ortho-oxazepine
Benzenoid
Piperidine
Methyl ester
Isoxazolidine
Ketimine
Carboxylic acid ester
Oxacycle
Azacycle
N-organohydroxylamine
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Monocarboxylic acid or derivatives
Ether
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Imine
Carbonyl group
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	1.79	ALOGPS
logP	1.52	ChemAxon
logS	-3.2	ALOGPS
pKa (Strongest Acidic)	11.64	ChemAxon
pKa (Strongest Basic)	4.04	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	89.82 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	107.68 m³·mol⁻¹	ChemAxon
Polarizability	42.18 Å³	ChemAxon
Number of Rings	6	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

163192964

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 10,11-Dimethoxynareline (NP0068976)

MOL for NP0068976 (10,11-Dimethoxynareline)

3D MOL for NP0068976 (10,11-Dimethoxynareline)

3D SDF for NP0068976 (10,11-Dimethoxynareline)

3D-SDF for NP0068976 (10,11-Dimethoxynareline)

PDB for NP0068976 (10,11-Dimethoxynareline)

3D PDB for NP0068976 (10,11-Dimethoxynareline)

SMILES for NP0068976 (10,11-Dimethoxynareline)

INCHI for NP0068976 (10,11-Dimethoxynareline)

Structure for NP0068976 (10,11-Dimethoxynareline)

3D Structure for NP0068976 (10,11-Dimethoxynareline)