NP-MRD: Showing NP-Card for 11-ethyl-6-methoxy-13-methyl-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecane-4,8,9,16-tetrol (NP0200102)

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Record Information

Version

2.0

Created at

2022-09-04 18:52:27 UTC

Updated at

2022-09-04 18:52:27 UTC

NP-MRD ID

NP0200102

Secondary Accession Numbers

None

Natural Product Identification

Common Name

11-ethyl-6-methoxy-13-methyl-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecane-4,8,9,16-tetrol

Description

11-Ethyl-6-methoxy-13-methyl-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]Nonadecane-4,8,9,16-tetrol belongs to the class of organic compounds known as aconitane-type diterpenoid alkaloids. These are alkaloid diterpenoids with a structure based on the hexacyclic aconitane skeleton. These compounds have no oxygen functionality at the C7 atom. 11-ethyl-6-methoxy-13-methyl-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecane-4,8,9,16-tetrol is found in Aconitum napellus. 11-Ethyl-6-methoxy-13-methyl-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]Nonadecane-4,8,9,16-tetrol is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004251504392D          

 28 33  0  0  0  0            999 V2000
   -0.3274   -2.3893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4962   -2.3415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8666   -1.6043    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4197   -0.8647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7821   -0.0895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0090    0.1985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0155    0.7352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8202    0.9654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3453    0.3251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1498    0.5079    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1346   -0.5353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9178   -0.1091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6456    0.4548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4646   -0.2533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0354    0.0925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9630    0.9143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3899   -0.6478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3060   -1.4797    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3073   -2.3047    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1200   -1.6852    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7393   -1.0995    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5387   -1.3033    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7618   -2.0976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3984   -1.7119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3670   -2.5363    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3902   -1.3704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4816   -0.4669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8221   -1.5122    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
  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
 12 13  1  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
 15 17  1  0  0  0  0
 12 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 14 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 18 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
  5 27  1  0  0  0  0
 11 27  1  0  0  0  0
 24 28  1  0  0  0  0
  3 28  1  0  0  0  0
 11 28  1  0  0  0  0
M  END

     RDKit          3D

 63 68  0  0  0  0  0  0  0  0999 V2000
   -3.2757    2.3351   -2.7585 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9614    2.2191   -1.9749 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9985    0.9768   -1.2639 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9323    0.9242   -0.2389 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6707    0.0442    0.9254 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.1479    0.7494    2.1989 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3834   -1.2710    0.8805 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5945   -2.3954    0.3044 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7058   -1.8180   -0.7982 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4432   -1.3421   -1.8694 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7279   -0.8419   -0.2260 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1791   -0.1687    1.0442 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4312    1.1559    0.9906 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2546    1.2471   -0.3140 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2003    2.5822   -0.7796 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7231    0.3924   -1.1468 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6381    0.7073   -0.4714 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1460    1.4128   -1.6139 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5748    0.9938    0.6290 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4083   -0.1302    1.1519 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6855   -0.1700    0.6036 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7075   -0.2016    1.4998 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8011   -1.4923    0.8210 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3030   -1.5409    1.1403 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6010   -1.4635   -0.1564 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6220   -0.7029   -1.0020 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8433   -1.5185   -0.6946 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0066   -1.0831   -1.2454 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3528    3.3376   -3.2100 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1468    2.1499   -2.1044 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2488    1.6089   -3.5948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0349    3.0448   -1.2116 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1517    2.3328   -2.6897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1348    1.9810    0.1150 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9344    0.6170   -0.6649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1913   -0.0426    2.9752 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4197    1.4928    2.5557 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1462    1.2148    1.9977 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7496   -1.6002    1.8989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3173   -1.1471    0.2601 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2488   -3.1420   -0.1725 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8915   -2.8478    1.0468 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1653   -2.7280   -1.2015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6963   -2.0846   -2.4742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9969   -0.7388    1.9444 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1183    1.3734    1.8949 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2315    1.9641    0.9744 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8188    3.1296   -0.2590 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3386    0.1749   -2.1416 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0881    1.1376   -1.7236 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3255    1.8051    0.3623 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0976    1.4569    1.5459 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5382   -0.1301    2.2549 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6599   -0.2291    0.8919 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8242    0.7368    2.1127 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7439   -1.1136    2.1264 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3609   -2.2938    1.2839 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1401   -2.5656    1.5895 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0389   -0.8324    1.9116 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6049   -2.5036   -0.6008 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4416   -0.7943   -2.0751 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6155   -2.5605   -0.9929 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3632   -1.8038   -1.8556 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  1
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 11  9  1  6
 11 25  1  0
 25 24  1  0
 24 23  1  0
 23 27  1  0
 27 28  1  0
 27 26  1  0
 26 17  1  0
 17 18  1  6
 17 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 17 14  1  0
 14 15  1  6
 14 13  1  0
 13 12  1  0
 14 16  1  0
 16  3  1  0
 12  5  1  0
 12 11  1  0
 16 11  1  0
 26 25  1  0
 20 23  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  2 32  1  0
  2 33  1  0
  4 34  1  0
  4 35  1  0
  6 36  1  0
  6 37  1  0
  6 38  1  0
  7 39  1  0
  7 40  1  0
  8 41  1  0
  8 42  1  0
  9 43  1  6
 10 44  1  0
 25 60  1  6
 24 58  1  0
 24 59  1  0
 23 57  1  1
 27 62  1  6
 28 63  1  0
 26 61  1  6
 18 50  1  0
 19 51  1  0
 19 52  1  0
 20 53  1  1
 22 54  1  0
 22 55  1  0
 22 56  1  0
 15 48  1  0
 13 46  1  0
 13 47  1  0
 12 45  1  1
 16 49  1  6
M  END


  Mrv1533004251504392D          

 28 33  0  0  0  0            999 V2000
   -0.3274   -2.3893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4962   -2.3415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8666   -1.6043    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4197   -0.8647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7821   -0.0895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0090    0.1985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0155    0.7352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8202    0.9654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3453    0.3251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1498    0.5079    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1346   -0.5353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9178   -0.1091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6456    0.4548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4646   -0.2533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0354    0.0925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9630    0.9143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3899   -0.6478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3060   -1.4797    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3073   -2.3047    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1200   -1.6852    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7393   -1.0995    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5387   -1.3033    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7618   -2.0976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3984   -1.7119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3670   -2.5363    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3902   -1.3704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4816   -0.4669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8221   -1.5122    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
  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
 12 13  1  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
 15 17  1  0  0  0  0
 12 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 14 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 18 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
  5 27  1  0  0  0  0
 11 27  1  0  0  0  0
 24 28  1  0  0  0  0
  3 28  1  0  0  0  0
 11 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0200102

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCN1CC2(C)CCC(O)C34C5CC6C(O)C5C(O)(CC6OC)C(O)(CC23)C14

> <INCHI_IDENTIFIER>
InChI=1S/C22H35NO5/c1-4-23-10-19(2)6-5-15(24)22-12-7-11-13(28-3)8-20(26,16(12)17(11)25)21(27,18(22)23)9-14(19)22/h11-18,24-27H,4-10H2,1-3H3

> <INCHI_KEY>
XBAVRWWMTJPXJW-UHFFFAOYSA-N

> <FORMULA>
C22H35NO5

> <MOLECULAR_WEIGHT>
393.524

> <EXACT_MASS>
393.251523231

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
63

> <JCHEM_AVERAGE_POLARIZABILITY>
42.995431036749096

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
11-ethyl-6-methoxy-13-methyl-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecane-4,8,9,16-tetrol

> <ALOGPS_LOGP>
0.06

> <JCHEM_LOGP>
-1.0866686003333341

> <ALOGPS_LOGS>
-1.48

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
13.983770593964294

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.870122850148888

> <JCHEM_PKA_STRONGEST_BASIC>
9.45655145419349

> <JCHEM_POLAR_SURFACE_AREA>
93.39000000000001

> <JCHEM_REFRACTIVITY>
103.00219999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.29e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
11-ethyl-6-methoxy-13-methyl-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecane-4,8,9,16-tetrol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0      -0.611  -4.460   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.926  -4.371   0.000  0.00  0.00           C+0
HETATM    3  N   UNK     0       1.618  -2.995   0.000  0.00  0.00           N+0
HETATM    4  C   UNK     0       0.783  -1.614   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.460  -0.167   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.017   0.370   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.896   1.372   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.398   1.802   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.378   0.607   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       5.880   0.948   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       3.985  -0.999   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.447  -0.204   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.805   0.849   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.334  -0.473   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.533   0.173   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       7.398   1.707   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       6.328  -1.209   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.171  -2.762   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       6.174  -4.302   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       7.691  -3.146   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.847  -2.052   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      10.339  -2.433   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      10.755  -3.915   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.477  -3.195   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       4.418  -4.734   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       2.595  -2.558   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.766  -0.872   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.401  -2.823   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   28                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7   27                                             
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   27   28                                             
CONECT   12   11   13   17                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   21                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   12   18                                                  
CONECT   18   17   19   20   24                                             
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   14   22                                                  
CONECT   22   21   23                                                       
CONECT   23   22                                                            
CONECT   24   18   25   26   28                                             
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26    5   11                                                  
CONECT   28   24    3   11                                                  
MASTER        0    0    0    0    0    0    0    0   28    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₃₅NO₅

Average Mass

393.5240 Da

Monoisotopic Mass

393.25152 Da

IUPAC Name

11-ethyl-6-methoxy-13-methyl-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecane-4,8,9,16-tetrol

Traditional Name

11-ethyl-6-methoxy-13-methyl-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecane-4,8,9,16-tetrol

CAS Registry Number

Not Available

SMILES

CCN1CC2(C)CCC(O)C34C5CC6C(O)C5C(O)(CC6OC)C(O)(CC23)C14

InChI Identifier

InChI=1S/C22H35NO5/c1-4-23-10-19(2)6-5-15(24)22-12-7-11-13(28-3)8-20(26,16(12)17(11)25)21(27,18(22)23)9-14(19)22/h11-18,24-27H,4-10H2,1-3H3

InChI Key

XBAVRWWMTJPXJW-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 napellus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as aconitane-type diterpenoid alkaloids. These are alkaloid diterpenoids with a structure based on the hexacyclic aconitane skeleton. These compounds have no oxygen functionality at the C7 atom.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Aconitane-type diterpenoid alkaloids

Alternative Parents

Substituents

Aconitane-type diterpenoid alkaloid
Quinolidine
Alkaloid or derivatives
Azepane
Piperidine
Cyclic alcohol
Tertiary alcohol
1,2-aminoalcohol
Secondary alcohol
Tertiary aliphatic amine
Tertiary amine
Dialkyl ether
Ether
Polyol
Azacycle
Organoheterocyclic compound
Organonitrogen compound
Alcohol
Organic nitrogen compound
Organopnictogen compound
Organooxygen compound
Hydrocarbon derivative
Amine
Organic oxygen compound
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	0.06	ALOGPS
logP	-1.1	ChemAxon
logS	-1.5	ALOGPS
pKa (Strongest Acidic)	12.87	ChemAxon
pKa (Strongest Basic)	9.46	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	93.39 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	103 m³·mol⁻¹	ChemAxon
Polarizability	43 Å³	ChemAxon
Number of Rings	6	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 11-ethyl-6-methoxy-13-methyl-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecane-4,8,9,16-tetrol (NP0200102)

MOL for NP0200102 (11-ethyl-6-methoxy-13-methyl-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecane-4,8,9,16-tetrol)

3D MOL for NP0200102 (11-ethyl-6-methoxy-13-methyl-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecane-4,8,9,16-tetrol)

3D SDF for NP0200102 (11-ethyl-6-methoxy-13-methyl-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecane-4,8,9,16-tetrol)

3D-SDF for NP0200102 (11-ethyl-6-methoxy-13-methyl-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecane-4,8,9,16-tetrol)

PDB for NP0200102 (11-ethyl-6-methoxy-13-methyl-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecane-4,8,9,16-tetrol)

3D PDB for NP0200102 (11-ethyl-6-methoxy-13-methyl-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecane-4,8,9,16-tetrol)

SMILES for NP0200102 (11-ethyl-6-methoxy-13-methyl-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecane-4,8,9,16-tetrol)

INCHI for NP0200102 (11-ethyl-6-methoxy-13-methyl-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecane-4,8,9,16-tetrol)

Structure for NP0200102 (11-ethyl-6-methoxy-13-methyl-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecane-4,8,9,16-tetrol)

3D Structure for NP0200102 (11-ethyl-6-methoxy-13-methyl-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecane-4,8,9,16-tetrol)