NP-MRD: Showing NP-Card for 21,22-dimethoxy-17-methyl-12,19-dioxa-5,16-diazaheptacyclo[14.7.1.1²,⁵.0²,¹⁵.0⁹,¹³.0²⁰,²⁴.0⁹,²⁵]pentacosa-1(24),7,20,22-tetraen-11-one (NP0310508)

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Record Information

Version

2.0

Created at

2022-09-11 05:52:13 UTC

Updated at

2022-09-11 05:52:14 UTC

NP-MRD ID

NP0310508

Secondary Accession Numbers

None

Natural Product Identification

Common Name

21,22-dimethoxy-17-methyl-12,19-dioxa-5,16-diazaheptacyclo[14.7.1.1²,⁵.0²,¹⁵.0⁹,¹³.0²⁰,²⁴.0⁹,²⁵]pentacosa-1(24),7,20,22-tetraen-11-one

Description

Obscurinervidine 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. Obscurinervidine is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004161506082D          

 31 37  0  0  0  0            999 V2000
    5.5200    2.7215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7004    2.8155    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2091    2.1527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3895    2.2468    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8982    1.5840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2266    0.8271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6083    0.2810    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.7722   -0.5276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1538   -1.0738    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5543   -0.7900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1726   -0.2438    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0463    0.7331    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375    1.3959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3571    1.3019    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8484    1.9647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8978    0.7002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1108    0.4528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5030    1.0106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3183    0.9322    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6467    1.6890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4520    1.8682    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0184    2.0020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6822    1.8159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0743    2.3737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2535    3.1790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0405    3.4265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6484    2.8687    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6315    2.7198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7953    1.9112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0770    1.5055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4692    2.0634    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
  4  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  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
  6 12  1  0  0  0  0
 12 13  2  0  0  0  0
  3 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
  7 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  2  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 18 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
  5 30  1  0  0  0  0
 16 30  1  0  0  0  0
 30 31  1  0  0  0  0
 23 31  1  0  0  0  0
 27 31  1  0  0  0  0
M  END

     RDKit          3D

 59 65  0  0  0  0  0  0  0  0999 V2000
    2.5098   -0.5253   -3.9065 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9593    0.1533   -2.7776 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3377    0.1904   -1.5603 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1317   -0.4888   -1.3351 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5275   -0.4368   -0.1081 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1402    0.2952    0.8729 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3251    0.9739    0.6900 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9282    0.9228   -0.5331 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1172    1.5898   -0.7599 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3510    0.8985   -0.5079 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8367    1.6825    1.8077 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5175    1.0207    3.0606 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0361    0.8659    3.2511 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4792    2.2591    3.4960 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4221    0.3146    2.0794 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8990   -0.2792    1.7888 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8479    0.8745    1.6880 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0486    0.6908    0.8394 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5246    1.9892    0.4628 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8141    2.4457   -0.6519 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9053    3.6015   -1.1169 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9606    1.3021   -1.1438 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6499    0.1493   -0.5373 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.8312   -0.2128   -1.3515 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7466   -1.3016   -2.1006 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5830   -2.1993   -2.2075 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4615   -1.8477   -1.4034 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8036   -2.9614   -0.7456 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4159   -2.4859    0.6644 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6698   -0.9962    0.5291 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8980   -1.0742   -0.2930 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8023    0.1351   -4.4629 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0481   -1.5153   -3.6719 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3522   -0.7546   -4.6077 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6622   -1.0625   -2.1239 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0747    1.0431   -1.3330 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7735    1.1740    0.4797 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1456   -0.1934   -0.4530 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9221    1.6982    3.8447 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0676    0.0624    3.1451 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8856    0.2208    4.1499 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2565    2.7804    4.1308 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4544    2.8292    2.5559 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5032    2.2713    3.9680 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2039   -0.9268    2.6385 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3355    1.8137    1.3424 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1829    1.0999    2.7430 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8523    0.0813    1.2929 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9467    1.5104   -0.8207 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0099    1.3442   -2.2504 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6995    0.3942   -1.3178 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6258   -1.5745   -2.7087 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9067   -3.2541   -2.0940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2405   -2.1284   -3.2836 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4980   -3.7994   -0.6512 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0979   -3.2947   -1.2991 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1234   -2.8823    1.4061 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6216   -2.7192    0.9065 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5960   -1.7638    0.2845 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 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
 22 23  1  0
 23 24  1  6
 24 25  2  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 30 29  1  1
 30 31  1  0
 15 13  1  0
 13 14  1  0
 13 12  1  0
 12 11  1  0
 11  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
  8  3  1  0
 30  5  1  0
  7  6  1  0
 30 16  1  0
 23 18  1  0
 31 23  1  0
 31 27  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  4 35  1  0
 16 45  1  1
 17 46  1  0
 17 47  1  0
 18 48  1  1
 22 49  1  0
 22 50  1  0
 24 51  1  0
 25 52  1  0
 26 53  1  0
 26 54  1  0
 28 55  1  0
 28 56  1  0
 29 57  1  0
 29 58  1  0
 31 59  1  1
 13 41  1  1
 14 42  1  0
 14 43  1  0
 14 44  1  0
 12 39  1  0
 12 40  1  0
 10 36  1  0
 10 37  1  0
 10 38  1  0
M  END


  Mrv1533004161506082D          

 31 37  0  0  0  0            999 V2000
    5.5200    2.7215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7004    2.8155    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2091    2.1527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3895    2.2468    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8982    1.5840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2266    0.8271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6083    0.2810    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.7722   -0.5276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1538   -1.0738    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5543   -0.7900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1726   -0.2438    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0463    0.7331    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375    1.3959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3571    1.3019    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8484    1.9647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8978    0.7002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1108    0.4528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5030    1.0106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3183    0.9322    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6467    1.6890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4520    1.8682    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0184    2.0020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6822    1.8159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0743    2.3737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2535    3.1790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0405    3.4265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6484    2.8687    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6315    2.7198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7953    1.9112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0770    1.5055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4692    2.0634    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
  4  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  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
  6 12  1  0  0  0  0
 12 13  2  0  0  0  0
  3 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
  7 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  2  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 18 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
  5 30  1  0  0  0  0
 16 30  1  0  0  0  0
 30 31  1  0  0  0  0
 23 31  1  0  0  0  0
 27 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0310508

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC2=C3N(C4CC5OC(=O)CC55C=CCN6CCC24C56)C(C)COC3=C1OC

> <INCHI_IDENTIFIER>
InChI=1S/C24H28N2O5/c1-13-12-30-21-19-14(9-15(28-2)20(21)29-3)24-6-8-25-7-4-5-23(22(24)25)11-18(27)31-17(23)10-16(24)26(13)19/h4-5,9,13,16-17,22H,6-8,10-12H2,1-3H3

> <INCHI_KEY>
DTJNFCUPFGKVAV-UHFFFAOYSA-N

> <FORMULA>
C24H28N2O5

> <MOLECULAR_WEIGHT>
424.497

> <EXACT_MASS>
424.19982201

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
45.21588782908456

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
21,22-dimethoxy-17-methyl-12,19-dioxa-5,16-diazaheptacyclo[14.7.1.1²,⁵.0²,¹⁵.0⁹,¹³.0²⁰,²⁴.0⁹,²⁵]pentacosa-1(24),7,20,22-tetraen-11-one

> <ALOGPS_LOGP>
2.84

> <JCHEM_LOGP>
1.5537191213333332

> <ALOGPS_LOGS>
-2.84

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_BASIC>
7.822473731164623

> <JCHEM_POLAR_SURFACE_AREA>
60.470000000000006

> <JCHEM_REFRACTIVITY>
114.70539999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.16e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
21,22-dimethoxy-17-methyl-12,19-dioxa-5,16-diazaheptacyclo[14.7.1.1²,⁵.0²,¹⁵.0⁹,¹³.0²⁰,²⁴.0⁹,²⁵]pentacosa-1(24),7,20,22-tetraen-11-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0      10.304   5.080   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       8.774   5.256   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       7.857   4.018   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.327   4.194   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.410   2.957   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.023   1.544   0.000  0.00  0.00           C+0
HETATM    7  N   UNK     0       4.869   0.524   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0       5.175  -0.985   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.021  -2.004   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.635  -1.475   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       7.789  -0.455   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       7.553   1.368   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.470   2.606   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      10.000   2.430   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      10.917   3.667   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.543   1.307   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.073   0.845   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.939   1.886   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -0.594   1.740   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -1.207   3.153   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -2.710   3.487   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -0.034   3.737   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.273   3.390   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.139   4.431   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.473   5.934   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.942   6.396   0.000  0.00  0.00           C+0
HETATM   27  N   UNK     0       3.077   5.355   0.000  0.00  0.00           N+0
HETATM   28  C   UNK     0       4.912   5.077   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       5.218   3.568   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       3.877   2.810   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       2.742   3.852   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   13                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   30                                                  
CONECT    6    5    7   12                                                  
CONECT    7    6    8   16                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11    6   13                                                  
CONECT   13   12    3   14                                                  
CONECT   14   13   15                                                       
CONECT   15   14                                                            
CONECT   16    7   17   30                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   23                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   18   24   31                                             
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   31                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29    5   16   31                                             
CONECT   31   30   23   27                                                  
MASTER        0    0    0    0    0    0    0    0   31    0   74    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₂₈N₂O₅

Average Mass

424.4970 Da

Monoisotopic Mass

424.19982 Da

IUPAC Name

21,22-dimethoxy-17-methyl-12,19-dioxa-5,16-diazaheptacyclo[14.7.1.1²,⁵.0²,¹⁵.0⁹,¹³.0²⁰,²⁴.0⁹,²⁵]pentacosa-1(24),7,20,22-tetraen-11-one

Traditional Name

21,22-dimethoxy-17-methyl-12,19-dioxa-5,16-diazaheptacyclo[14.7.1.1²,⁵.0²,¹⁵.0⁹,¹³.0²⁰,²⁴.0⁹,²⁵]pentacosa-1(24),7,20,22-tetraen-11-one

CAS Registry Number

Not Available

SMILES

COC1=CC2=C3N(C4CC5OC(=O)CC55C=CCN6CCC24C56)C(C)COC3=C1OC

InChI Identifier

InChI=1S/C24H28N2O5/c1-13-12-30-21-19-14(9-15(28-2)20(21)29-3)24-6-8-25-7-4-5-23(22(24)25)11-18(27)31-17(23)10-16(24)26(13)19/h4-5,9,13,16-17,22H,6-8,10-12H2,1-3H3

InChI Key

DTJNFCUPFGKVAV-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

Not Available

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
Benzomorpholine
Benzoxazine
Anisole
Tertiary aliphatic/aromatic amine
Dialkylarylamine
Alkyl aryl ether
Aralkylamine
Gamma butyrolactone
Oxazinane
N-alkylpyrrolidine
Benzenoid
Tetrahydrofuran
Pyrrolidine
Tertiary amine
Amino acid or derivatives
Tertiary aliphatic amine
Lactone
Carboxylic acid ester
Oxacycle
Azacycle
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Ether
Amine
Organic nitrogen compound
Carbonyl group
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Organonitrogen compound
Organooxygen compound
Organic oxygen 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	2.84	ALOGPS
logP	1.55	ChemAxon
logS	-2.8	ALOGPS
pKa (Strongest Basic)	7.82	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	60.47 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	114.71 m³·mol⁻¹	ChemAxon
Polarizability	45.22 Å³	ChemAxon
Number of Rings	7	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

550060

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 21,22-dimethoxy-17-methyl-12,19-dioxa-5,16-diazaheptacyclo[14.7.1.1²,⁵.0²,¹⁵.0⁹,¹³.0²⁰,²⁴.0⁹,²⁵]pentacosa-1(24),7,20,22-tetraen-11-one (NP0310508)

MOL for NP0310508 (21,22-dimethoxy-17-methyl-12,19-dioxa-5,16-diazaheptacyclo[14.7.1.1²,⁵.0²,¹⁵.0⁹,¹³.0²⁰,²⁴.0⁹,²⁵]pentacosa-1(24),7,20,22-tetraen-11-one)

3D MOL for NP0310508 (21,22-dimethoxy-17-methyl-12,19-dioxa-5,16-diazaheptacyclo[14.7.1.1²,⁵.0²,¹⁵.0⁹,¹³.0²⁰,²⁴.0⁹,²⁵]pentacosa-1(24),7,20,22-tetraen-11-one)

3D SDF for NP0310508 (21,22-dimethoxy-17-methyl-12,19-dioxa-5,16-diazaheptacyclo[14.7.1.1²,⁵.0²,¹⁵.0⁹,¹³.0²⁰,²⁴.0⁹,²⁵]pentacosa-1(24),7,20,22-tetraen-11-one)

3D-SDF for NP0310508 (21,22-dimethoxy-17-methyl-12,19-dioxa-5,16-diazaheptacyclo[14.7.1.1²,⁵.0²,¹⁵.0⁹,¹³.0²⁰,²⁴.0⁹,²⁵]pentacosa-1(24),7,20,22-tetraen-11-one)

PDB for NP0310508 (21,22-dimethoxy-17-methyl-12,19-dioxa-5,16-diazaheptacyclo[14.7.1.1²,⁵.0²,¹⁵.0⁹,¹³.0²⁰,²⁴.0⁹,²⁵]pentacosa-1(24),7,20,22-tetraen-11-one)

3D PDB for NP0310508 (21,22-dimethoxy-17-methyl-12,19-dioxa-5,16-diazaheptacyclo[14.7.1.1²,⁵.0²,¹⁵.0⁹,¹³.0²⁰,²⁴.0⁹,²⁵]pentacosa-1(24),7,20,22-tetraen-11-one)

SMILES for NP0310508 (21,22-dimethoxy-17-methyl-12,19-dioxa-5,16-diazaheptacyclo[14.7.1.1²,⁵.0²,¹⁵.0⁹,¹³.0²⁰,²⁴.0⁹,²⁵]pentacosa-1(24),7,20,22-tetraen-11-one)

INCHI for NP0310508 (21,22-dimethoxy-17-methyl-12,19-dioxa-5,16-diazaheptacyclo[14.7.1.1²,⁵.0²,¹⁵.0⁹,¹³.0²⁰,²⁴.0⁹,²⁵]pentacosa-1(24),7,20,22-tetraen-11-one)

Structure for NP0310508 (21,22-dimethoxy-17-methyl-12,19-dioxa-5,16-diazaheptacyclo[14.7.1.1²,⁵.0²,¹⁵.0⁹,¹³.0²⁰,²⁴.0⁹,²⁵]pentacosa-1(24),7,20,22-tetraen-11-one)

3D Structure for NP0310508 (21,22-dimethoxy-17-methyl-12,19-dioxa-5,16-diazaheptacyclo[14.7.1.1²,⁵.0²,¹⁵.0⁹,¹³.0²⁰,²⁴.0⁹,²⁵]pentacosa-1(24),7,20,22-tetraen-11-one)