NP-MRD: Showing NP-Card for (1s,6r,8r,12r,13s,23r)-16-methoxy-4-methyl-7,10-dioxa-4,14-diazaheptacyclo[10.8.3.2¹¹,¹⁴.0¹,¹³.0⁶,⁸.0⁶,²³.0¹⁵,²⁰]pentacosa-11(25),15(20),16,18-tetraene-21,24-dione (NP0247652)

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Record Information

Version

2.0

Created at

2022-09-07 09:34:43 UTC

Updated at

2022-09-07 09:34:43 UTC

NP-MRD ID

NP0247652

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,6r,8r,12r,13s,23r)-16-methoxy-4-methyl-7,10-dioxa-4,14-diazaheptacyclo[10.8.3.2¹¹,¹⁴.0¹,¹³.0⁶,⁸.0⁶,²³.0¹⁵,²⁰]pentacosa-11(25),15(20),16,18-tetraene-21,24-dione

Description

(1S,6R,8R,12R,13S,23R)-16-methoxy-4-methyl-7,10-dioxa-4,14-diazaheptacyclo[10.8.3.2¹¹,¹⁴.0¹,¹³.0⁶,⁸.0⁶,²³.0¹⁵,²⁰]Pentacosa-11(25),15(20),16,18-tetraene-21,24-dione 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. (1s,6r,8r,12r,13s,23r)-16-methoxy-4-methyl-7,10-dioxa-4,14-diazaheptacyclo[10.8.3.2¹¹,¹⁴.0¹,¹³.0⁶,⁸.0⁶,²³.0¹⁵,²⁰]pentacosa-11(25),15(20),16,18-tetraene-21,24-dione is found in Strychnos icaja. Based on a literature review very few articles have been published on (1S,6R,8R,12R,13S,23R)-16-methoxy-4-methyl-7,10-dioxa-4,14-diazaheptacyclo[10.8.3.2¹¹,¹⁴.0¹,¹³.0⁶,⁸.0⁶,²³.0¹⁵,²⁰]Pentacosa-11(25),15(20),16,18-tetraene-21,24-dione.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072211342D          

 30 36  0  0  1  0            999 V2000
   -1.8720    2.4330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1136    2.1081    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0157    1.2890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6762    0.7946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5784   -0.0245    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8200   -0.3494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1595    0.1450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2574    0.9641    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4484    1.4472    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6921    2.2740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0767    2.8234    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4664    2.6013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0316    1.9410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8408    2.2360    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5687    1.7923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4973    0.9583    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8114    0.1965    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9685    0.2546    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1283   -0.5746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7002   -1.3055    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.1777   -1.9783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8706   -1.4679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1645   -0.9828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6653   -0.1227    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5878   -0.8527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1564   -1.5559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3929   -0.3296    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0679    0.2970    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7235    1.1016    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9320    0.7282    0.0000 C   0  0  2  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
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  1  0  0  0
 18 17  1  1  0  0  0
 16 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
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24  7  1  6  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 28 27  1  6  0  0  0
 18 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 13  1  6  0  0  0
 29 30  1  0  0  0  0
 30  9  1  1  0  0  0
 24 30  1  0  0  0  0
M  END

     RDKit          3D

 54 60  0  0  0  0  0  0  0  0999 V2000
    5.5233   -1.2856   -1.9101 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1616   -1.0982   -1.6275 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7575   -0.1352   -0.7015 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6878    0.6360   -0.0599 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2522    1.5750    0.8464 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9158    1.7463    1.1118 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9759    0.9765    0.4719 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4016    0.0334   -0.4368 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2903   -0.6387   -0.9661 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.0719   -1.6627   -1.9259 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8502   -1.7635   -2.8862 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0964   -2.5415   -1.6793 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8561   -2.3557   -0.6051 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9137   -3.2778   -0.5701 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1053   -3.0882    0.1439 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6250   -1.6935    0.0774 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1271   -1.2754    1.3456 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9290   -0.6627    0.7073 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.2077    0.7801    0.5261 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3167    1.5146   -0.3008 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9932    2.2696   -1.3459 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4520    2.4420    0.4024 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0099    2.2741   -0.0262 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4945    0.9756    0.5714 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0257    0.8515    1.9280 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4788    1.5470    2.8058 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1259   -0.0456    2.3772 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6239   -0.9912    1.3393 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5350   -1.2944    0.3453 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0489   -0.1271   -0.3512 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.9080   -0.4706   -2.5647 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0761   -1.3521   -0.9518 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6599   -2.2876   -2.3979 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7559    0.5330   -0.2408 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9790    2.1892    1.3588 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6085    2.5049    1.8405 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2926   -3.3142   -2.3922 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9993   -3.4889    1.1949 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8631   -3.7913   -0.3137 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3707   -1.5062   -0.7185 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3257    1.3429    1.4782 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2280    0.8553    0.0416 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6422    3.0142   -0.7975 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6231    1.6526   -1.9874 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2499    2.8731   -1.8877 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7033    3.5020    0.1512 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5621    2.3756    1.4927 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0103    2.2265   -1.1316 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5830    3.1017    0.3877 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6518   -0.6216    3.2336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9484    0.5004    2.8801 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7895   -1.9799    1.8741 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2959   -1.7481    1.0032 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5944    0.2046   -1.1600 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
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 30  1  0
 30 29  1  0
 29 28  1  0
 28 27  1  0
 27 25  1  0
 25 26  2  0
 25 24  1  0
 24 23  1  6
 23 22  1  0
 22 20  1  0
 20 21  1  0
 20 19  1  0
 19 18  1  0
 18 17  1  1
 17 16  1  0
 16 15  1  0
 15 14  1  0
 14 13  1  0
 13 12  2  0
 12 10  1  0
 10 11  2  0
  8  3  1  0
 10  9  1  0
 24  7  1  0
 16 18  1  0
 24 30  1  0
 13 29  1  0
 18 28  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  4 34  1  0
  5 35  1  0
  6 36  1  0
 30 54  1  6
 29 53  1  1
 28 52  1  1
 27 50  1  0
 27 51  1  0
 23 48  1  0
 23 49  1  0
 22 46  1  0
 22 47  1  0
 21 43  1  0
 21 44  1  0
 21 45  1  0
 19 41  1  0
 19 42  1  0
 16 40  1  6
 15 38  1  0
 15 39  1  0
 12 37  1  0
M  END


  Mrv1652309072211342D          

 30 36  0  0  1  0            999 V2000
   -1.8720    2.4330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1136    2.1081    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0157    1.2890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6762    0.7946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5784   -0.0245    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8200   -0.3494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1595    0.1450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2574    0.9641    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4484    1.4472    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6921    2.2740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0767    2.8234    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4664    2.6013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0316    1.9410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8408    2.2360    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5687    1.7923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4973    0.9583    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8114    0.1965    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9685    0.2546    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1283   -0.5746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7002   -1.3055    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.1777   -1.9783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8706   -1.4679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1645   -0.9828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6653   -0.1227    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5878   -0.8527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1564   -1.5559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3929   -0.3296    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0679    0.2970    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7235    1.1016    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9320    0.7282    0.0000 C   0  0  2  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
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  1  0  0  0
 18 17  1  1  0  0  0
 16 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
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24  7  1  6  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 28 27  1  6  0  0  0
 18 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 13  1  6  0  0  0
 29 30  1  0  0  0  0
 30  9  1  1  0  0  0
 24 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0247652

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=CC2=C1N1[C@H]3[C@H]4[C@H]5CC(=O)[C@@]23CCN(C)C[C@]52O[C@@H]2COC4=CC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C23H24N2O5/c1-24-7-6-22-12-4-3-5-14(28-2)20(12)25-18(27)9-15-19(21(22)25)13(8-16(22)26)23(11-24)17(30-23)10-29-15/h3-5,9,13,17,19,21H,6-8,10-11H2,1-2H3/t13-,17-,19+,21+,22-,23+/m1/s1

> <INCHI_KEY>
CJXJFPZVDOJEAR-BQMRLHQHSA-N

> <FORMULA>
C23H24N2O5

> <MOLECULAR_WEIGHT>
408.454

> <EXACT_MASS>
408.168521881

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
41.8720693673294

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,6R,8R,12R,13S,23R)-16-methoxy-4-methyl-7,10-dioxa-4,14-diazaheptacyclo[10.8.3.2^{11,14}.0^{1,13}.0^{6,8}.0^{6,23}.0^{15,20}]pentacosa-11(25),15(20),16,18-tetraene-21,24-dione

> <JCHEM_LOGP>
0.2523226620000003

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
18.25404498513351

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.008241019175742

> <JCHEM_PKA_STRONGEST_BASIC>
8.304601944243297

> <JCHEM_POLAR_SURFACE_AREA>
71.61

> <JCHEM_REFRACTIVITY>
108.33250000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,6R,8R,12R,13S,23R)-16-methoxy-4-methyl-7,10-dioxa-4,14-diazaheptacyclo[10.8.3.2^{11,14}.0^{1,13}.0^{6,8}.0^{6,23}.0^{15,20}]pentacosa-11(25),15(20),16,18-tetraene-21,24-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0      -3.379   4.673   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -1.989   4.009   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -1.870   2.474   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -3.139   1.603   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -3.020   0.067   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.630  -0.597   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.361   0.274   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.480   1.810   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0       0.843   2.732   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0       1.264   4.277   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       0.114   5.302   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       2.722   4.860   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.772   3.645   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       5.270   4.204   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       6.625   3.404   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.466   1.839   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       7.058   0.437   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       5.483   0.539   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.837  -1.028   0.000  0.00  0.00           C+0
HETATM   20  N   UNK     0       5.002  -2.368   0.000  0.00  0.00           N+0
HETATM   21  C   UNK     0       5.860  -3.647   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.453  -2.629   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.087  -1.808   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.199  -0.163   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.001  -1.528   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       0.162  -2.820   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       2.520  -0.568   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.806   0.550   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.234   2.077   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       1.758   1.399   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   24                                                  
CONECT    8    7    3    9                                                  
CONECT    9    8   10   30                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   29                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16   18                                                       
CONECT   18   17   16   19   28                                             
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23    7   25   30                                             
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27   18   29                                                  
CONECT   29   28   13   30                                                  
CONECT   30   29    9   24                                                  
MASTER        0    0    0    0    0    0    0    0   30    0   72    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₂₄N₂O₅

Average Mass

408.4540 Da

Monoisotopic Mass

408.16852 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

COC1=CC=CC2=C1N1[C@H]3[C@H]4[C@H]5CC(=O)[C@@]23CCN(C)C[C@]52O[C@@H]2COC4=CC1=O

InChI Identifier

InChI=1S/C23H24N2O5/c1-24-7-6-22-12-4-3-5-14(28-2)20(12)25-18(27)9-15-19(21(22)25)13(8-16(22)26)23(11-24)17(30-23)10-29-15/h3-5,9,13,17,19,21H,6-8,10-11H2,1-2H3/t13-,17-,19+,21+,22-,23+/m1/s1

InChI Key

CJXJFPZVDOJEAR-BQMRLHQHSA-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 icaja	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
Anisole
Alkyl aryl ether
Oxepane
Aralkylamine
Benzenoid
Tertiary carboxylic acid amide
Vinylogous ester
Amino acid or derivatives
Carboxamide group
Ketone
Lactam
Tertiary amine
Tertiary aliphatic amine
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Oxacycle
Azacycle
Organooxygen compound
Organonitrogen compound
Organic oxygen compound
Organic nitrogen compound
Amine
Carbonyl group
Organic oxide
Hydrocarbon derivative
Organopnictogen compound
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	0.25	ChemAxon
pKa (Strongest Acidic)	14.01	ChemAxon
pKa (Strongest Basic)	8.3	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	71.61 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	108.33 m³·mol⁻¹	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

162866784

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,6r,8r,12r,13s,23r)-16-methoxy-4-methyl-7,10-dioxa-4,14-diazaheptacyclo[10.8.3.2¹¹,¹⁴.0¹,¹³.0⁶,⁸.0⁶,²³.0¹⁵,²⁰]pentacosa-11(25),15(20),16,18-tetraene-21,24-dione (NP0247652)

MOL for NP0247652 ((1s,6r,8r,12r,13s,23r)-16-methoxy-4-methyl-7,10-dioxa-4,14-diazaheptacyclo[10.8.3.2¹¹,¹⁴.0¹,¹³.0⁶,⁸.0⁶,²³.0¹⁵,²⁰]pentacosa-11(25),15(20),16,18-tetraene-21,24-dione)

3D MOL for NP0247652 ((1s,6r,8r,12r,13s,23r)-16-methoxy-4-methyl-7,10-dioxa-4,14-diazaheptacyclo[10.8.3.2¹¹,¹⁴.0¹,¹³.0⁶,⁸.0⁶,²³.0¹⁵,²⁰]pentacosa-11(25),15(20),16,18-tetraene-21,24-dione)

3D SDF for NP0247652 ((1s,6r,8r,12r,13s,23r)-16-methoxy-4-methyl-7,10-dioxa-4,14-diazaheptacyclo[10.8.3.2¹¹,¹⁴.0¹,¹³.0⁶,⁸.0⁶,²³.0¹⁵,²⁰]pentacosa-11(25),15(20),16,18-tetraene-21,24-dione)

3D-SDF for NP0247652 ((1s,6r,8r,12r,13s,23r)-16-methoxy-4-methyl-7,10-dioxa-4,14-diazaheptacyclo[10.8.3.2¹¹,¹⁴.0¹,¹³.0⁶,⁸.0⁶,²³.0¹⁵,²⁰]pentacosa-11(25),15(20),16,18-tetraene-21,24-dione)

PDB for NP0247652 ((1s,6r,8r,12r,13s,23r)-16-methoxy-4-methyl-7,10-dioxa-4,14-diazaheptacyclo[10.8.3.2¹¹,¹⁴.0¹,¹³.0⁶,⁸.0⁶,²³.0¹⁵,²⁰]pentacosa-11(25),15(20),16,18-tetraene-21,24-dione)

3D PDB for NP0247652 ((1s,6r,8r,12r,13s,23r)-16-methoxy-4-methyl-7,10-dioxa-4,14-diazaheptacyclo[10.8.3.2¹¹,¹⁴.0¹,¹³.0⁶,⁸.0⁶,²³.0¹⁵,²⁰]pentacosa-11(25),15(20),16,18-tetraene-21,24-dione)

SMILES for NP0247652 ((1s,6r,8r,12r,13s,23r)-16-methoxy-4-methyl-7,10-dioxa-4,14-diazaheptacyclo[10.8.3.2¹¹,¹⁴.0¹,¹³.0⁶,⁸.0⁶,²³.0¹⁵,²⁰]pentacosa-11(25),15(20),16,18-tetraene-21,24-dione)

INCHI for NP0247652 ((1s,6r,8r,12r,13s,23r)-16-methoxy-4-methyl-7,10-dioxa-4,14-diazaheptacyclo[10.8.3.2¹¹,¹⁴.0¹,¹³.0⁶,⁸.0⁶,²³.0¹⁵,²⁰]pentacosa-11(25),15(20),16,18-tetraene-21,24-dione)

Structure for NP0247652 ((1s,6r,8r,12r,13s,23r)-16-methoxy-4-methyl-7,10-dioxa-4,14-diazaheptacyclo[10.8.3.2¹¹,¹⁴.0¹,¹³.0⁶,⁸.0⁶,²³.0¹⁵,²⁰]pentacosa-11(25),15(20),16,18-tetraene-21,24-dione)

3D Structure for NP0247652 ((1s,6r,8r,12r,13s,23r)-16-methoxy-4-methyl-7,10-dioxa-4,14-diazaheptacyclo[10.8.3.2¹¹,¹⁴.0¹,¹³.0⁶,⁸.0⁶,²³.0¹⁵,²⁰]pentacosa-11(25),15(20),16,18-tetraene-21,24-dione)