NP-MRD: Showing NP-Card for 14-ethyl-9-methoxy-4,6,17-trioxa-14-azaoctacyclo[10.8.2.1²,⁸.0¹,¹³.0³,⁷.0³,¹¹.0¹⁶,¹⁸.0¹⁶,²¹]tricosane-11,20-diol (NP0215381)

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Record Information

Version

2.0

Created at

2022-09-05 14:59:05 UTC

Updated at

2022-09-05 14:59:05 UTC

NP-MRD ID

NP0215381

Secondary Accession Numbers

None

Natural Product Identification

Common Name

14-ethyl-9-methoxy-4,6,17-trioxa-14-azaoctacyclo[10.8.2.1²,⁸.0¹,¹³.0³,⁷.0³,¹¹.0¹⁶,¹⁸.0¹⁶,²¹]tricosane-11,20-diol

Description

14-Ethyl-9-methoxy-4,6,17-trioxa-14-azaoctacyclo[10.8.2.1²,⁸.0¹,¹³.0³,⁷.0³,¹¹.0¹⁶,¹⁸.0¹⁶,²¹]Tricosane-11,20-diol belongs to the class of organic compounds known as lappaconitine-type diterpenoid alkaloids. These are c18-bisnorditerpenoid alkaloids with a structure based on the heptacyclic lappaconitine skeleton. Lappaconitine similar to aconitane, with the difference that the former lacks a carbon atom at the 18-position. 14-ethyl-9-methoxy-4,6,17-trioxa-14-azaoctacyclo[10.8.2.1²,⁸.0¹,¹³.0³,⁷.0³,¹¹.0¹⁶,¹⁸.0¹⁶,²¹]tricosane-11,20-diol is found in Aconitum kirinense. 14-Ethyl-9-methoxy-4,6,17-trioxa-14-azaoctacyclo[10.8.2.1²,⁸.0¹,¹³.0³,⁷.0³,¹¹.0¹⁶,¹⁸.0¹⁶,²¹]Tricosane-11,20-diol is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004231514422D          

 29 36  0  0  0  0            999 V2000
    6.0276   -1.3799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2370   -1.1441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0459   -0.3415    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.6478    0.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4999    1.1503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1508    1.6892    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4057    2.0106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6683    2.4044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0365    1.8751    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2824    2.2096    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0705    0.9892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7437    0.9401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6210    0.0594    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5623   -0.0778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1614   -0.0293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7354    0.3416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6074   -0.4734    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9076    0.2097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3761    0.8753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5517    0.8419    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1684    0.1114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9265    1.6919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8561    2.2590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3989    1.5529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7458    1.2166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9703    0.9586    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2449    1.5077    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5203    2.2815    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3322    2.1192    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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
  5 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
  3 15  1  0  0  0  0
 11 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  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
 19 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 11 24  1  0  0  0  0
 24 25  1  0  0  0  0
 16 25  1  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
 22 29  1  0  0  0  0
 25 29  1  0  0  0  0
M  END

     RDKit          3D

 60 67  0  0  0  0  0  0  0  0999 V2000
   -3.4175   -3.2324    1.2511 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5902   -1.9751    1.4259 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1599   -1.4336    0.1739 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1413   -0.8919   -0.6594 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8770    0.3721   -1.3871 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.9246    1.0433   -1.8050 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3634    1.7279   -0.8333 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2126    1.5303    0.6107 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7817    1.2765    0.9358 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1645    2.4804    1.3633 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9199    0.5928   -0.0349 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8479   -0.9209    0.1468 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0634   -1.3081   -1.0788 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8279   -0.6003   -2.1659 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4203    0.6046   -1.4884 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3450   -0.7548   -1.1075 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8283   -1.1384   -2.3896 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2361   -1.4128   -0.1149 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1973   -0.5307    0.6192 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3987   -0.3579   -0.0977 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5027   -0.8001    0.5786 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6811    0.9000    0.7447 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2434    0.9545    1.2194 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4399    1.2128   -0.0053 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3170    0.7138   -1.1084 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1537    1.3673   -2.2976 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5676    2.6806   -2.0344 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3733    2.6588   -0.9008 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6590    1.3481   -0.6991 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.4883   -3.0251    1.0950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3242   -3.7879    2.2084 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9496   -3.8259    0.4424 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6835   -2.2141    2.0181 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2655   -1.2746    1.9970 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1286   -0.8150   -0.1133 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3814   -1.6689   -1.4518 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8302    2.6552   -1.1974 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4897    2.5138    1.1053 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9289    0.8202    1.0746 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7848    0.6500    1.8824 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5848    3.2229    0.8737 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3484   -1.2329    1.0687 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0938   -2.3950   -1.1661 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2188   -0.3542   -3.0486 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5954   -1.3206   -2.5273 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2124    1.5530   -1.9933 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4886   -0.4989   -2.7215 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6585   -1.9890    0.6601 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8804   -2.2173   -0.5864 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4561   -0.9868    1.5710 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3787   -0.5964   -0.1052 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4515   -1.9279    0.5866 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6946   -0.3614    1.5531 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3582    1.4889    1.3804 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1877    1.7974    1.9595 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0385    0.0489    1.7757 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2862    2.3238   -0.0599 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0957    3.1231   -2.9180 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6395    3.2641   -1.8498 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4631    0.9239   -1.2984 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  5  1  0
  5  6  1  6
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 11  9  1  1
 11 15  1  0
 15 14  1  0
 14 13  1  0
 13 12  1  0
 13 16  1  0
 16 17  1  6
 16 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 19 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  6
 26 27  1  0
 27 28  1  0
 28 29  1  0
 12  3  1  0
 25 16  1  0
 29 25  1  0
  7  5  1  0
 12 11  1  0
 29 22  1  0
 15  5  1  0
 24 11  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  2 33  1  0
  2 34  1  0
  4 35  1  0
  4 36  1  0
  7 37  1  6
  8 38  1  0
  8 39  1  0
  9 40  1  1
 10 41  1  0
 15 46  1  6
 14 44  1  0
 14 45  1  0
 13 43  1  6
 12 42  1  1
 17 47  1  0
 18 48  1  0
 18 49  1  0
 19 50  1  1
 21 51  1  0
 21 52  1  0
 21 53  1  0
 22 54  1  1
 23 55  1  0
 23 56  1  0
 24 57  1  6
 27 58  1  0
 27 59  1  0
 29 60  1  6
M  END


  Mrv1533004231514422D          

 29 36  0  0  0  0            999 V2000
    6.0276   -1.3799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2370   -1.1441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0459   -0.3415    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.6478    0.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4999    1.1503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1508    1.6892    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4057    2.0106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6683    2.4044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0365    1.8751    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2824    2.2096    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0705    0.9892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7437    0.9401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6210    0.0594    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5623   -0.0778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1614   -0.0293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7354    0.3416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6074   -0.4734    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9076    0.2097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3761    0.8753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5517    0.8419    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1684    0.1114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9265    1.6919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8561    2.2590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3989    1.5529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7458    1.2166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9703    0.9586    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2449    1.5077    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5203    2.2815    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3322    2.1192    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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
  5 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
  3 15  1  0  0  0  0
 11 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  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
 19 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 11 24  1  0  0  0  0
 24 25  1  0  0  0  0
 16 25  1  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
 22 29  1  0  0  0  0
 25 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0215381

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCN1CC23OC2CC(O)C24C3CC(C12)C1(O)CC(OC)C2CC4C11OCOC21

> <INCHI_IDENTIFIER>
InChI=1S/C22H31NO6/c1-3-23-8-19-13-5-11-17(23)21(13,15(24)6-16(19)29-19)14-4-10-12(26-2)7-20(11,25)22(14)18(10)27-9-28-22/h10-18,24-25H,3-9H2,1-2H3

> <INCHI_KEY>
AQELCJOMPNYNFK-UHFFFAOYSA-N

> <FORMULA>
C22H31NO6

> <MOLECULAR_WEIGHT>
405.491

> <EXACT_MASS>
405.215137722

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
42.24986988029612

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
14-ethyl-9-methoxy-4,6,17-trioxa-14-azaoctacyclo[10.8.2.1²,⁸.0¹,¹³.0³,⁷.0³,¹¹.0¹⁶,¹⁸.0¹⁶,²¹]tricosane-11,20-diol

> <ALOGPS_LOGP>
-0.18

> <JCHEM_LOGP>
-1.151273059666666

> <ALOGPS_LOGS>
-1.20

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
8

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
14.561292807669908

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.246800493415549

> <JCHEM_PKA_STRONGEST_BASIC>
8.814991211389172

> <JCHEM_POLAR_SURFACE_AREA>
83.92000000000002

> <JCHEM_REFRACTIVITY>
100.05190000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.58e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
14-ethyl-9-methoxy-4,6,17-trioxa-14-azaoctacyclo[10.8.2.1²,⁸.0¹,¹³.0³,⁷.0³,¹¹.0¹⁶,¹⁸.0¹⁶,²¹]tricosane-11,20-diol

> <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      11.252  -2.576   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.776  -2.136   0.000  0.00  0.00           C+0
HETATM    3  N   UNK     0       9.419  -0.638   0.000  0.00  0.00           N+0
HETATM    4  C   UNK     0      10.543   0.535   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.267   2.147   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      11.481   3.153   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      10.091   3.753   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.714   4.488   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.535   3.500   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       6.127   4.125   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       7.598   1.847   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.855   1.755   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.626   0.111   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.650  -0.145   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.768  -0.055   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.106   0.638   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       4.867  -0.884   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       3.561   0.392   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.569   1.634   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       1.030   1.572   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       0.314   0.208   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.596   3.158   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.331   4.217   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.345   2.899   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.125   2.271   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       3.678   1.789   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       2.324   2.814   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       2.838   4.259   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       4.353   3.956   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   15                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7   12                                             
CONECT    6    5    7                                                       
CONECT    7    6    5    8                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   15   24                                             
CONECT   12   11    5   13                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14    3   11                                                  
CONECT   16   14   17   18   25                                             
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20   22                                                  
CONECT   20   19   21                                                       
CONECT   21   20                                                            
CONECT   22   19   23   29                                                  
CONECT   23   22   24                                                       
CONECT   24   23   11   25                                                  
CONECT   25   24   16   26   29                                             
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   22   25                                                  
MASTER        0    0    0    0    0    0    0    0   29    0   72    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₃₁NO₆

Average Mass

405.4910 Da

Monoisotopic Mass

405.21514 Da

IUPAC Name

14-ethyl-9-methoxy-4,6,17-trioxa-14-azaoctacyclo[10.8.2.1²,⁸.0¹,¹³.0³,⁷.0³,¹¹.0¹⁶,¹⁸.0¹⁶,²¹]tricosane-11,20-diol

Traditional Name

14-ethyl-9-methoxy-4,6,17-trioxa-14-azaoctacyclo[10.8.2.1²,⁸.0¹,¹³.0³,⁷.0³,¹¹.0¹⁶,¹⁸.0¹⁶,²¹]tricosane-11,20-diol

CAS Registry Number

Not Available

SMILES

CCN1CC23OC2CC(O)C24C3CC(C12)C1(O)CC(OC)C2CC4C11OCOC21

InChI Identifier

InChI=1S/C22H31NO6/c1-3-23-8-19-13-5-11-17(23)21(13,15(24)6-16(19)29-19)14-4-10-12(26-2)7-20(11,25)22(14)18(10)27-9-28-22/h10-18,24-25H,3-9H2,1-2H3

InChI Key

AQELCJOMPNYNFK-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
Aconitum kirinense	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as lappaconitine-type diterpenoid alkaloids. These are c18-bisnorditerpenoid alkaloids with a structure based on the heptacyclic lappaconitine skeleton. Lappaconitine similar to aconitane, with the difference that the former lacks a carbon atom at the 18-position.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Lappaconitine-type diterpenoid alkaloids

Alternative Parents

Substituents

Lappaconitine-type diterpenoid alkaloid
Quinolidine
Alkaloid or derivatives
Azepane
Oxepane
Piperidine
Meta-dioxolane
Cyclic alcohol
Tertiary alcohol
Secondary alcohol
Tertiary amine
Tertiary aliphatic amine
Azacycle
Oxacycle
Ether
Oxirane
Dialkyl ether
Acetal
Organoheterocyclic compound
Organic nitrogen compound
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Organopnictogen compound
Organic oxygen compound
Amine
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	-0.18	ALOGPS
logP	-1.2	ChemAxon
logS	-1.2	ALOGPS
pKa (Strongest Acidic)	13.25	ChemAxon
pKa (Strongest Basic)	8.81	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	83.92 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	100.05 m³·mol⁻¹	ChemAxon
Polarizability	42.25 Å³	ChemAxon
Number of Rings	8	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	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

73834226

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 14-ethyl-9-methoxy-4,6,17-trioxa-14-azaoctacyclo[10.8.2.1²,⁸.0¹,¹³.0³,⁷.0³,¹¹.0¹⁶,¹⁸.0¹⁶,²¹]tricosane-11,20-diol (NP0215381)

MOL for NP0215381 (14-ethyl-9-methoxy-4,6,17-trioxa-14-azaoctacyclo[10.8.2.1²,⁸.0¹,¹³.0³,⁷.0³,¹¹.0¹⁶,¹⁸.0¹⁶,²¹]tricosane-11,20-diol)

3D MOL for NP0215381 (14-ethyl-9-methoxy-4,6,17-trioxa-14-azaoctacyclo[10.8.2.1²,⁸.0¹,¹³.0³,⁷.0³,¹¹.0¹⁶,¹⁸.0¹⁶,²¹]tricosane-11,20-diol)

3D SDF for NP0215381 (14-ethyl-9-methoxy-4,6,17-trioxa-14-azaoctacyclo[10.8.2.1²,⁸.0¹,¹³.0³,⁷.0³,¹¹.0¹⁶,¹⁸.0¹⁶,²¹]tricosane-11,20-diol)

3D-SDF for NP0215381 (14-ethyl-9-methoxy-4,6,17-trioxa-14-azaoctacyclo[10.8.2.1²,⁸.0¹,¹³.0³,⁷.0³,¹¹.0¹⁶,¹⁸.0¹⁶,²¹]tricosane-11,20-diol)

PDB for NP0215381 (14-ethyl-9-methoxy-4,6,17-trioxa-14-azaoctacyclo[10.8.2.1²,⁸.0¹,¹³.0³,⁷.0³,¹¹.0¹⁶,¹⁸.0¹⁶,²¹]tricosane-11,20-diol)

3D PDB for NP0215381 (14-ethyl-9-methoxy-4,6,17-trioxa-14-azaoctacyclo[10.8.2.1²,⁸.0¹,¹³.0³,⁷.0³,¹¹.0¹⁶,¹⁸.0¹⁶,²¹]tricosane-11,20-diol)

SMILES for NP0215381 (14-ethyl-9-methoxy-4,6,17-trioxa-14-azaoctacyclo[10.8.2.1²,⁸.0¹,¹³.0³,⁷.0³,¹¹.0¹⁶,¹⁸.0¹⁶,²¹]tricosane-11,20-diol)

INCHI for NP0215381 (14-ethyl-9-methoxy-4,6,17-trioxa-14-azaoctacyclo[10.8.2.1²,⁸.0¹,¹³.0³,⁷.0³,¹¹.0¹⁶,¹⁸.0¹⁶,²¹]tricosane-11,20-diol)

Structure for NP0215381 (14-ethyl-9-methoxy-4,6,17-trioxa-14-azaoctacyclo[10.8.2.1²,⁸.0¹,¹³.0³,⁷.0³,¹¹.0¹⁶,¹⁸.0¹⁶,²¹]tricosane-11,20-diol)

3D Structure for NP0215381 (14-ethyl-9-methoxy-4,6,17-trioxa-14-azaoctacyclo[10.8.2.1²,⁸.0¹,¹³.0³,⁷.0³,¹¹.0¹⁶,¹⁸.0¹⁶,²¹]tricosane-11,20-diol)