NP-MRD: Showing NP-Card for (20r)-20-ethoxy-15,17,18-trimethoxy-21-methyl-5,7-dioxa-21-azapentacyclo[11.8.0.0²,¹⁰.0⁴,⁸.0¹⁴,¹⁹]henicosa-1(13),2,4(8),9,11,14,16,18-octaene (NP0152779)

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Record Information

Version

2.0

Created at

2022-09-02 09:19:41 UTC

Updated at

2022-09-02 09:19:41 UTC

NP-MRD ID

NP0152779

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(20r)-20-ethoxy-15,17,18-trimethoxy-21-methyl-5,7-dioxa-21-azapentacyclo[11.8.0.0²,¹⁰.0⁴,⁸.0¹⁴,¹⁹]henicosa-1(13),2,4(8),9,11,14,16,18-octaene

Description

(20R)-20-ethoxy-15,17,18-trimethoxy-21-methyl-5,7-dioxa-21-azapentacyclo[11.8.0.0²,¹⁰.0⁴,⁸.0¹⁴,¹⁹]Henicosa-1(13),2,4(8),9,11,14(19),15,17-octaene belongs to the class of organic compounds known as dihydrobenzophenanthridine alkaloids. These are alkaloids containing a dihydrobenzophenanthridine skeleton, which is a tetracyclic compound containing a benzene fused to a dihydrophenanthridine moiety. (20r)-20-ethoxy-15,17,18-trimethoxy-21-methyl-5,7-dioxa-21-azapentacyclo[11.8.0.0²,¹⁰.0⁴,⁸.0¹⁴,¹⁹]henicosa-1(13),2,4(8),9,11,14,16,18-octaene is found in Chelidonium majus. Based on a literature review very few articles have been published on (20R)-20-ethoxy-15,17,18-trimethoxy-21-methyl-5,7-dioxa-21-azapentacyclo[11.8.0.0²,¹⁰.0⁴,⁸.0¹⁴,¹⁹]Henicosa-1(13),2,4(8),9,11,14(19),15,17-octaene.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022211192D          

 31 35  0  0  1  0            999 V2000
    4.9361   -5.3900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1399   -4.5905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5494   -4.0143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7532   -3.2149    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1628   -2.6387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3686   -2.8619    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1648   -3.6614    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3706   -3.8846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7781   -2.2857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9839   -2.5090    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3935   -1.9328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9819   -1.4863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7761   -1.2631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9799   -0.4636    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7742   -0.2404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3666   -1.8393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1608   -1.6160    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3646   -0.8166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1588   -0.5934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7493   -1.1696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5435   -0.9463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1339   -1.5225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9301   -2.3220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1359   -2.5452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5455   -1.9690    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7512   -2.1922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5475   -2.9917    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.1379   -3.5679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6275   -2.7628    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2622   -2.2359    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9572   -1.4693    0.0000 O   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
  4  3  1  6  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
  6  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  9 12  2  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
 13 16  2  0  0  0  0
  5 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 20 25  1  0  0  0  0
 25 26  2  0  0  0  0
 17 26  1  0  0  0  0
 26 27  1  0  0  0  0
  4 27  1  0  0  0  0
 27 28  1  0  0  0  0
 23 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 22 31  1  0  0  0  0
M  END

     RDKit          3D

 56 60  0  0  0  0  0  0  0  0999 V2000
   -1.7293    3.6977   -1.2423 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7852    3.7211   -0.0806 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7034    2.5516    0.6498 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3281    1.4619   -0.0772 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3129    0.3343    0.1155 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5486    0.6180    0.5586 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9057    1.8706    1.0442 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7766    2.2089    2.4320 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5192   -0.3708    0.5395 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7821   -0.0561    0.9987 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7674   -1.0723    0.9756 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1927   -1.6229    0.0670 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9284   -1.9293   -0.3858 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7010   -3.1916   -0.8311 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6839   -4.2065   -0.8580 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9700   -0.9389   -0.3592 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4306   -1.2661   -0.5904 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8127   -2.4813   -1.0716 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1808   -2.7326   -1.2470 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1328   -1.7939   -0.9541 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4718   -2.0445   -1.1624 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4096   -1.0788   -0.8972 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0078    0.1381   -0.4263 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6552    0.4349   -0.2020 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7301   -0.5303   -0.4615 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3925   -0.2773   -0.2748 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9820    0.9561    0.2805 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.7807    1.6319    1.3078 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1175    0.9101   -0.2466 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3056    0.1205   -0.3554 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8148   -1.0370   -1.0032 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6888    4.2400   -1.0340 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3014    4.1866   -2.1438 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0199    2.6473   -1.4435 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2195    4.1227   -0.3527 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1951    4.4947    0.6355 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2347    1.6969   -1.1793 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7139    1.9675    2.9718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5871    3.2814    2.5184 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9708    1.6390    2.9170 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7327   -0.6666    1.3498 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4004   -1.8728    1.6781 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8315   -1.4385   -0.0554 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9920   -2.3788    0.0655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3811   -5.0816   -1.4316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0353   -4.4718    0.1779 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6029   -3.7841   -1.3608 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1087   -3.2309   -1.3298 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4623   -3.7124   -1.6291 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7542   -3.0197   -1.5388 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4303    1.4136    0.0695 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9467    1.7455    2.1220 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0012    2.6709    1.1385 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4503    0.9976    1.8870 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0829    0.6367   -0.9517 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6418   -0.1086    0.6768 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4 27  1  0
 27 28  1  0
 27 26  1  0
 26 25  2  0
 25 24  1  0
 24 23  2  0
 23 29  1  0
 29 30  1  0
 30 31  1  0
 31 22  1  0
 22 21  2  0
 21 20  1  0
 20 19  2  0
 19 18  1  0
 18 17  2  0
 17 16  1  0
 16 13  2  0
 13 14  1  0
 14 15  1  0
 13 12  1  0
 12  9  2  0
  9 10  1  0
 10 11  1  0
  9  6  1  0
  6  7  1  0
  7  8  1  0
  6  5  2  0
  5  4  1  0
 17 26  1  0
  5 16  1  0
 20 25  1  0
 22 23  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  2 35  1  0
  2 36  1  0
  4 37  1  6
 28 52  1  0
 28 53  1  0
 28 54  1  0
 24 51  1  0
 30 55  1  0
 30 56  1  0
 21 50  1  0
 19 49  1  0
 18 48  1  0
 15 45  1  0
 15 46  1  0
 15 47  1  0
 12 44  1  0
 11 41  1  0
 11 42  1  0
 11 43  1  0
  8 38  1  0
  8 39  1  0
  8 40  1  0
M  END


  Mrv1652309022211192D          

 31 35  0  0  1  0            999 V2000
    4.9361   -5.3900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1399   -4.5905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5494   -4.0143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7532   -3.2149    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1628   -2.6387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3686   -2.8619    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1648   -3.6614    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3706   -3.8846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7781   -2.2857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9839   -2.5090    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3935   -1.9328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9819   -1.4863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7761   -1.2631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9799   -0.4636    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7742   -0.2404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3666   -1.8393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1608   -1.6160    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3646   -0.8166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1588   -0.5934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7493   -1.1696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5435   -0.9463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1339   -1.5225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9301   -2.3220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1359   -2.5452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5455   -1.9690    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7512   -2.1922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5475   -2.9917    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.1379   -3.5679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6275   -2.7628    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2622   -2.2359    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9572   -1.4693    0.0000 O   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
  4  3  1  6  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
  6  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  9 12  2  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
 13 16  2  0  0  0  0
  5 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 20 25  1  0  0  0  0
 25 26  2  0  0  0  0
 17 26  1  0  0  0  0
 26 27  1  0  0  0  0
  4 27  1  0  0  0  0
 27 28  1  0  0  0  0
 23 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 22 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0152779

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCO[C@H]1N(C)C2=C3C=C4OCOC4=CC3=CC=C2C2=C(OC)C=C(OC)C(OC)=C12

> <INCHI_IDENTIFIER>
InChI=1S/C24H25NO6/c1-6-29-24-21-20(18(26-3)11-19(27-4)23(21)28-5)14-8-7-13-9-16-17(31-12-30-16)10-15(13)22(14)25(24)2/h7-11,24H,6,12H2,1-5H3/t24-/m1/s1

> <INCHI_KEY>
LAOZQGDLCLVXDY-XMMPIXPASA-N

> <FORMULA>
C24H25NO6

> <MOLECULAR_WEIGHT>
423.465

> <EXACT_MASS>
423.168187529

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
45.72871028431811

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(20R)-20-ethoxy-15,17,18-trimethoxy-21-methyl-5,7-dioxa-21-azapentacyclo[11.8.0.0^{2,10}.0^{4,8}.0^{14,19}]henicosa-1,3,8,10,12,14,16,18-octaene

> <ALOGPS_LOGP>
4.10

> <JCHEM_LOGP>
4.255149282

> <ALOGPS_LOGS>
-4.09

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-3.958816067606872

> <JCHEM_POLAR_SURFACE_AREA>
58.620000000000005

> <JCHEM_REFRACTIVITY>
116.31380000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.43e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(20R)-20-ethoxy-15,17,18-trimethoxy-21-methyl-5,7-dioxa-21-azapentacyclo[11.8.0.0^{2,10}.0^{4,8}.0^{14,19}]henicosa-1,3,8,10,12,14,16,18-octaene

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0       9.214 -10.061   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.594  -8.569   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       8.492  -7.493   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       8.873  -6.001   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.771  -4.926   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.288  -5.342   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       5.908  -6.835   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       4.425  -7.251   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.186  -4.267   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       3.703  -4.683   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       2.601  -3.608   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.566  -2.774   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.049  -2.358   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       7.429  -0.865   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       8.912  -0.449   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.151  -3.433   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.633  -3.017   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      10.014  -1.524   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      11.496  -1.108   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      12.599  -2.183   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      14.081  -1.766   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      15.183  -2.842   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      14.803  -4.334   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      13.320  -4.751   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      12.218  -3.675   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      10.736  -4.092   0.000  0.00  0.00           C+0
HETATM   27  N   UNK     0      10.355  -5.584   0.000  0.00  0.00           N+0
HETATM   28  C   UNK     0      11.457  -6.660   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      16.105  -5.157   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      17.289  -4.174   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      16.720  -2.743   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   27                                                  
CONECT    5    4    6   16                                                  
CONECT    6    5    7    9                                                  
CONECT    7    6    8                                                       
CONECT    8    7                                                            
CONECT    9    6   10   12                                                  
CONECT   10    9   11                                                       
CONECT   11   10                                                            
CONECT   12    9   13                                                       
CONECT   13   12   14   16                                                  
CONECT   14   13   15                                                       
CONECT   15   14                                                            
CONECT   16   13    5   17                                                  
CONECT   17   16   18   26                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   25                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   31                                                  
CONECT   23   22   24   29                                                  
CONECT   24   23   25                                                       
CONECT   25   24   20   26                                                  
CONECT   26   25   17   27                                                  
CONECT   27   26    4   28                                                  
CONECT   28   27                                                            
CONECT   29   23   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   22                                                       
MASTER        0    0    0    0    0    0    0    0   31    0   70    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₂₅NO₆

Average Mass

423.4650 Da

Monoisotopic Mass

423.16819 Da

IUPAC Name

(20R)-20-ethoxy-15,17,18-trimethoxy-21-methyl-5,7-dioxa-21-azapentacyclo[11.8.0.0^{2,10}.0^{4,8}.0^{14,19}]henicosa-1,3,8,10,12,14,16,18-octaene

Traditional Name

(20R)-20-ethoxy-15,17,18-trimethoxy-21-methyl-5,7-dioxa-21-azapentacyclo[11.8.0.0^{2,10}.0^{4,8}.0^{14,19}]henicosa-1,3,8,10,12,14,16,18-octaene

CAS Registry Number

Not Available

SMILES

CCO[C@H]1N(C)C2=C3C=C4OCOC4=CC3=CC=C2C2=C(OC)C=C(OC)C(OC)=C12

InChI Identifier

InChI=1S/C24H25NO6/c1-6-29-24-21-20(18(26-3)11-19(27-4)23(21)28-5)14-8-7-13-9-16-17(31-12-30-16)10-15(13)22(14)25(24)2/h7-11,24H,6,12H2,1-5H3/t24-/m1/s1

InChI Key

LAOZQGDLCLVXDY-XMMPIXPASA-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
Chelidonium majus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as dihydrobenzophenanthridine alkaloids. These are alkaloids containing a dihydrobenzophenanthridine skeleton, which is a tetracyclic compound containing a benzene fused to a dihydrophenanthridine moiety.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Benzophenanthridine alkaloids

Sub Class

Dihydrobenzophenanthridine alkaloids

Direct Parent

Dihydrobenzophenanthridine alkaloids

Alternative Parents

Substituents

Dihydrobenzophenanthridine alkaloid skeleton
Benzoquinoline
Phenanthridine
Naphthalene
Quinoline
Benzodioxole
Anisole
Dialkylarylamine
Alkyl aryl ether
Benzenoid
Organoheterocyclic compound
Azacycle
Ether
Acetal
Oxacycle
Organooxygen compound
Organonitrogen compound
Organic nitrogen compound
Hydrocarbon derivative
Organopnictogen 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	4.1	ALOGPS
logP	4.26	ChemAxon
logS	-4.1	ALOGPS
pKa (Strongest Basic)	-4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	58.62 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	116.31 m³·mol⁻¹	ChemAxon
Polarizability	45.73 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

162950324

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (20r)-20-ethoxy-15,17,18-trimethoxy-21-methyl-5,7-dioxa-21-azapentacyclo[11.8.0.0²,¹⁰.0⁴,⁸.0¹⁴,¹⁹]henicosa-1(13),2,4(8),9,11,14,16,18-octaene (NP0152779)

MOL for NP0152779 ((20r)-20-ethoxy-15,17,18-trimethoxy-21-methyl-5,7-dioxa-21-azapentacyclo[11.8.0.0²,¹⁰.0⁴,⁸.0¹⁴,¹⁹]henicosa-1(13),2,4(8),9,11,14,16,18-octaene)

3D MOL for NP0152779 ((20r)-20-ethoxy-15,17,18-trimethoxy-21-methyl-5,7-dioxa-21-azapentacyclo[11.8.0.0²,¹⁰.0⁴,⁸.0¹⁴,¹⁹]henicosa-1(13),2,4(8),9,11,14,16,18-octaene)

3D SDF for NP0152779 ((20r)-20-ethoxy-15,17,18-trimethoxy-21-methyl-5,7-dioxa-21-azapentacyclo[11.8.0.0²,¹⁰.0⁴,⁸.0¹⁴,¹⁹]henicosa-1(13),2,4(8),9,11,14,16,18-octaene)

3D-SDF for NP0152779 ((20r)-20-ethoxy-15,17,18-trimethoxy-21-methyl-5,7-dioxa-21-azapentacyclo[11.8.0.0²,¹⁰.0⁴,⁸.0¹⁴,¹⁹]henicosa-1(13),2,4(8),9,11,14,16,18-octaene)

PDB for NP0152779 ((20r)-20-ethoxy-15,17,18-trimethoxy-21-methyl-5,7-dioxa-21-azapentacyclo[11.8.0.0²,¹⁰.0⁴,⁸.0¹⁴,¹⁹]henicosa-1(13),2,4(8),9,11,14,16,18-octaene)

3D PDB for NP0152779 ((20r)-20-ethoxy-15,17,18-trimethoxy-21-methyl-5,7-dioxa-21-azapentacyclo[11.8.0.0²,¹⁰.0⁴,⁸.0¹⁴,¹⁹]henicosa-1(13),2,4(8),9,11,14,16,18-octaene)

SMILES for NP0152779 ((20r)-20-ethoxy-15,17,18-trimethoxy-21-methyl-5,7-dioxa-21-azapentacyclo[11.8.0.0²,¹⁰.0⁴,⁸.0¹⁴,¹⁹]henicosa-1(13),2,4(8),9,11,14,16,18-octaene)

INCHI for NP0152779 ((20r)-20-ethoxy-15,17,18-trimethoxy-21-methyl-5,7-dioxa-21-azapentacyclo[11.8.0.0²,¹⁰.0⁴,⁸.0¹⁴,¹⁹]henicosa-1(13),2,4(8),9,11,14,16,18-octaene)

Structure for NP0152779 ((20r)-20-ethoxy-15,17,18-trimethoxy-21-methyl-5,7-dioxa-21-azapentacyclo[11.8.0.0²,¹⁰.0⁴,⁸.0¹⁴,¹⁹]henicosa-1(13),2,4(8),9,11,14,16,18-octaene)

3D Structure for NP0152779 ((20r)-20-ethoxy-15,17,18-trimethoxy-21-methyl-5,7-dioxa-21-azapentacyclo[11.8.0.0²,¹⁰.0⁴,⁸.0¹⁴,¹⁹]henicosa-1(13),2,4(8),9,11,14,16,18-octaene)