NP-MRD: Showing NP-Card for methyl 14-acetyl-4,9-dimethyl-10-oxa-4,14-diazapentacyclo[11.7.0.0¹,⁵.0⁷,¹².0¹⁵,²⁰]icosa-15,17,19-triene-8-carboxylate (NP0160306)

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Record Information

Version

2.0

Created at

2022-09-02 18:13:42 UTC

Updated at

2022-09-02 18:13:42 UTC

NP-MRD ID

NP0160306

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 14-acetyl-4,9-dimethyl-10-oxa-4,14-diazapentacyclo[11.7.0.0¹,⁵.0⁷,¹².0¹⁵,²⁰]icosa-15,17,19-triene-8-carboxylate

Description

139682-33-0 Belongs to the class of organic compounds known as carbazoles. Carbazoles are compounds containing a three ring system containing a pyrrole ring fused on either side to a benzene ring. methyl 14-acetyl-4,9-dimethyl-10-oxa-4,14-diazapentacyclo[11.7.0.0¹,⁵.0⁷,¹².0¹⁵,²⁰]icosa-15,17,19-triene-8-carboxylate is found in Strychnos myrtoides. 139682-33-0 Is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004231520262D          

 29 33  0  0  0  0            999 V2000
    8.5998   -1.0916    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2288   -0.3547    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4051   -0.3076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9525   -0.9973    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0341    0.4293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4868    1.1190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3104    1.0719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1158    1.8559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2921    1.9031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8395    1.2133    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2105    0.4764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7578   -0.2133    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9342   -0.1661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3480   -0.7467    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.4731   -1.5621    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6147   -0.3686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7477    0.4456    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5632    0.5707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0158    1.2605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4997    1.9041    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.7171    2.7000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1365    3.2861    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5150    2.9096    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7281    1.6122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9948    1.9902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3008    1.5443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3400    0.7202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0733    0.3421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7673    0.7881    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
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  5 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  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 13 18  1  0  0  0  0
 18 19  1  0  0  0  0
 10 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 20 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 18 29  1  0  0  0  0
 24 29  1  0  0  0  0
M  END

     RDKit          3D

 59 63  0  0  0  0  0  0  0  0999 V2000
    5.3581    0.3569    1.9822 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6600    0.7676    0.8466 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2768    0.5058    0.7085 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7764   -0.1081    1.6780 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5641    0.9443   -0.4895 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1150    0.3007   -1.7560 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5897    1.3421   -2.7440 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1182   -0.4432   -2.4003 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5845   -1.4105   -1.5365 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7889   -0.7458   -0.4210 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0894    0.7417   -0.4212 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4011    1.3848    0.7204 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0986    1.1847    0.6650 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7744    2.4069    0.3082 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2367    3.5882    0.9014 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7528    2.4285   -1.1538 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8869    1.0086   -1.5817 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5555    0.2104   -0.3490 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8359   -0.4183    0.1319 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1123    0.0743    0.2866 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1547   -0.7238    0.7257 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9480   -2.0479    1.0245 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6657   -2.5358    0.8677 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5982   -1.7370    0.4241 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2139   -2.0523    0.2148 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5558   -3.1769    0.7405 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0985   -4.1710    1.6750 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6576   -3.3758    0.3785 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6707   -0.9597   -0.6151 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7811   -0.4651    2.4837 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3221   -0.1265    1.6675 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5402    1.1463    2.7232 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7301    2.0578   -0.6090 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9874   -0.3258   -1.4920 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1752    0.8321   -3.5239 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1332    2.1651   -2.2555 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6609    1.7199   -3.2625 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4044   -2.0184   -1.0901 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9602   -2.0790   -2.1456 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0813   -1.1551    0.5532 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7063    1.1235   -1.4174 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7750    0.9869    1.6796 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5928    2.4832    0.7567 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4623    0.9011    1.6917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7945    3.4317    1.8993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0735    4.3286    1.0736 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5107    4.1059    0.2163 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8366    2.9445   -1.4953 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6598    2.9933   -1.5170 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9652    0.7842   -1.9012 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3027    0.7938   -2.4674 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2708    1.1293    0.0469 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1540   -0.3333    0.8457 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7468   -2.7027    1.3717 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5285   -3.5909    1.0984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6595   -3.6165    2.4828 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2252   -4.6269    2.2527 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6636   -4.9886    1.2226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8178   -1.2380   -1.7000 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  1  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 29  1  0
 29 25  1  0
 25 26  1  0
 26 27  1  0
 26 28  2  0
 25 24  1  0
 24 23  2  0
 23 22  1  0
 22 21  2  0
 21 20  1  0
 20 19  2  0
 19 18  1  0
 18 17  1  6
 17 16  1  0
 16 14  1  0
 14 15  1  0
 14 13  1  0
 13 12  1  0
 12 11  1  0
 11  5  1  0
 11 10  1  0
 18 29  1  0
 13 18  1  0
 19 24  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  5 33  1  6
  6 34  1  1
  7 35  1  0
  7 36  1  0
  7 37  1  0
  9 38  1  0
  9 39  1  0
 10 40  1  1
 29 59  1  6
 27 56  1  0
 27 57  1  0
 27 58  1  0
 23 55  1  0
 22 54  1  0
 21 53  1  0
 20 52  1  0
 17 50  1  0
 17 51  1  0
 16 48  1  0
 16 49  1  0
 15 45  1  0
 15 46  1  0
 15 47  1  0
 13 44  1  1
 12 42  1  0
 12 43  1  0
 11 41  1  6
M  END


  Mrv1533004231520262D          

 29 33  0  0  0  0            999 V2000
    8.5998   -1.0916    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2288   -0.3547    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4051   -0.3076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9525   -0.9973    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0341    0.4293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4868    1.1190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3104    1.0719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1158    1.8559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2921    1.9031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8395    1.2133    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2105    0.4764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7578   -0.2133    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9342   -0.1661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3480   -0.7467    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.4731   -1.5621    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6147   -0.3686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7477    0.4456    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5632    0.5707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0158    1.2605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4997    1.9041    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.7171    2.7000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1365    3.2861    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5150    2.9096    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7281    1.6122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9948    1.9902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3008    1.5443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3400    0.7202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0733    0.3421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7673    0.7881    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
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  5 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  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 13 18  1  0  0  0  0
 18 19  1  0  0  0  0
 10 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 20 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 18 29  1  0  0  0  0
 24 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0160306

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C1C(C)OCC2C3N(C(C)=O)C4=CC=CC=C4C33CCN(C)C3CC12

> <INCHI_IDENTIFIER>
InChI=1S/C23H30N2O4/c1-13-20(22(27)28-4)15-11-19-23(9-10-24(19)3)17-7-5-6-8-18(17)25(14(2)26)21(23)16(15)12-29-13/h5-8,13,15-16,19-21H,9-12H2,1-4H3

> <INCHI_KEY>
MUNURTJJRWIXFH-UHFFFAOYSA-N

> <FORMULA>
C23H30N2O4

> <MOLECULAR_WEIGHT>
398.503

> <EXACT_MASS>
398.220557454

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
44.27231539882223

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl 14-acetyl-4,9-dimethyl-10-oxa-4,14-diazapentacyclo[11.7.0.0¹,⁵.0⁷,¹².0¹⁵,²⁰]icosa-15,17,19-triene-8-carboxylate

> <ALOGPS_LOGP>
1.93

> <JCHEM_LOGP>
1.1498119086666663

> <ALOGPS_LOGS>
-2.69

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_BASIC>
8.96134164233681

> <JCHEM_POLAR_SURFACE_AREA>
59.080000000000005

> <JCHEM_REFRACTIVITY>
108.612

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.07e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl 14-acetyl-4,9-dimethyl-10-oxa-4,14-diazapentacyclo[11.7.0.0¹,⁵.0⁷,¹².0¹⁵,²⁰]icosa-15,17,19-triene-8-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 23-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-APR-15         0                                  
HETATM    1  C   UNK     0      16.053  -2.038   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      15.360  -0.662   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      13.823  -0.574   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      12.978  -1.862   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      13.130   0.801   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      13.975   2.089   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      15.513   2.001   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      13.283   3.464   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      11.745   3.552   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.900   2.265   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      11.593   0.889   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.748  -0.398   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.210  -0.310   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0       8.116  -1.394   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0       8.350  -2.916   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.747  -0.688   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.996   0.832   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.518   1.065   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.363   2.353   0.000  0.00  0.00           C+0
HETATM   20  N   UNK     0       8.399   3.554   0.000  0.00  0.00           N+0
HETATM   21  C   UNK     0       8.805   5.040   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       7.722   6.134   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      10.295   5.431   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.959   3.009   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.590   3.715   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.295   2.883   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.368   1.344   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       5.737   0.639   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       7.032   1.471   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   11                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   19                                                  
CONECT   11   10    5   12                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   18                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   13   19   29                                             
CONECT   19   18   10   20                                                  
CONECT   20   19   21   24                                                  
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   20   25   29                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   18   24                                                  
MASTER        0    0    0    0    0    0    0    0   29    0   66    0
END

View in JSmol

Synonyms

Value	Source
Methyl 14-acetyl-4,9-dimethyl-10-oxa-4,14-diazapentacyclo[11.7.0.0¹,⁵.0⁷,¹².0¹⁵,²⁰]icosa-15,17,19-triene-8-carboxylic acid	Generator

Chemical Formula

C₂₃H₃₀N₂O₄

Average Mass

398.5030 Da

Monoisotopic Mass

398.22056 Da

IUPAC Name

methyl 14-acetyl-4,9-dimethyl-10-oxa-4,14-diazapentacyclo[11.7.0.0¹,⁵.0⁷,¹².0¹⁵,²⁰]icosa-15,17,19-triene-8-carboxylate

Traditional Name

methyl 14-acetyl-4,9-dimethyl-10-oxa-4,14-diazapentacyclo[11.7.0.0¹,⁵.0⁷,¹².0¹⁵,²⁰]icosa-15,17,19-triene-8-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)C1C(C)OCC2C3N(C(C)=O)C4=CC=CC=C4C33CCN(C)C3CC12

InChI Identifier

InChI=1S/C23H30N2O4/c1-13-20(22(27)28-4)15-11-19-23(9-10-24(19)3)17-7-5-6-8-18(17)25(14(2)26)21(23)16(15)12-29-13/h5-8,13,15-16,19-21H,9-12H2,1-4H3

InChI Key

MUNURTJJRWIXFH-UHFFFAOYSA-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
Strychnos myrtoides	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as carbazoles. Carbazoles are compounds containing a three ring system containing a pyrrole ring fused on either side to a benzene ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Carbazoles

Direct Parent

Carbazoles

Alternative Parents

Substituents

Carbazole
Aralkylamine
Oxane
N-alkylpyrrolidine
Benzenoid
Pyrrolidine
Tertiary carboxylic acid amide
Methyl ester
Acetamide
Carboxamide group
Carboxylic acid ester
Tertiary amine
Amino acid or derivatives
Tertiary aliphatic amine
Monocarboxylic acid or derivatives
Ether
Dialkyl ether
Carboxylic acid derivative
Azacycle
Oxacycle
Amine
Organic oxygen compound
Organooxygen compound
Organonitrogen compound
Organic nitrogen compound
Hydrocarbon derivative
Carbonyl group
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	1.93	ALOGPS
logP	1.15	ChemAxon
logS	-2.7	ALOGPS
pKa (Strongest Basic)	8.96	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	59.08 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	108.61 m³·mol⁻¹	ChemAxon
Polarizability	44.27 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

71343012

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 14-acetyl-4,9-dimethyl-10-oxa-4,14-diazapentacyclo[11.7.0.0¹,⁵.0⁷,¹².0¹⁵,²⁰]icosa-15,17,19-triene-8-carboxylate (NP0160306)

MOL for NP0160306 (methyl 14-acetyl-4,9-dimethyl-10-oxa-4,14-diazapentacyclo[11.7.0.0¹,⁵.0⁷,¹².0¹⁵,²⁰]icosa-15,17,19-triene-8-carboxylate)

3D MOL for NP0160306 (methyl 14-acetyl-4,9-dimethyl-10-oxa-4,14-diazapentacyclo[11.7.0.0¹,⁵.0⁷,¹².0¹⁵,²⁰]icosa-15,17,19-triene-8-carboxylate)

3D SDF for NP0160306 (methyl 14-acetyl-4,9-dimethyl-10-oxa-4,14-diazapentacyclo[11.7.0.0¹,⁵.0⁷,¹².0¹⁵,²⁰]icosa-15,17,19-triene-8-carboxylate)

3D-SDF for NP0160306 (methyl 14-acetyl-4,9-dimethyl-10-oxa-4,14-diazapentacyclo[11.7.0.0¹,⁵.0⁷,¹².0¹⁵,²⁰]icosa-15,17,19-triene-8-carboxylate)

PDB for NP0160306 (methyl 14-acetyl-4,9-dimethyl-10-oxa-4,14-diazapentacyclo[11.7.0.0¹,⁵.0⁷,¹².0¹⁵,²⁰]icosa-15,17,19-triene-8-carboxylate)

3D PDB for NP0160306 (methyl 14-acetyl-4,9-dimethyl-10-oxa-4,14-diazapentacyclo[11.7.0.0¹,⁵.0⁷,¹².0¹⁵,²⁰]icosa-15,17,19-triene-8-carboxylate)

SMILES for NP0160306 (methyl 14-acetyl-4,9-dimethyl-10-oxa-4,14-diazapentacyclo[11.7.0.0¹,⁵.0⁷,¹².0¹⁵,²⁰]icosa-15,17,19-triene-8-carboxylate)

INCHI for NP0160306 (methyl 14-acetyl-4,9-dimethyl-10-oxa-4,14-diazapentacyclo[11.7.0.0¹,⁵.0⁷,¹².0¹⁵,²⁰]icosa-15,17,19-triene-8-carboxylate)

Structure for NP0160306 (methyl 14-acetyl-4,9-dimethyl-10-oxa-4,14-diazapentacyclo[11.7.0.0¹,⁵.0⁷,¹².0¹⁵,²⁰]icosa-15,17,19-triene-8-carboxylate)

3D Structure for NP0160306 (methyl 14-acetyl-4,9-dimethyl-10-oxa-4,14-diazapentacyclo[11.7.0.0¹,⁵.0⁷,¹².0¹⁵,²⁰]icosa-15,17,19-triene-8-carboxylate)