NP-MRD: Showing NP-Card for 11-acetyllepenine (NP0067216)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-04-28 11:37:22 UTC

Updated at

2022-04-28 11:37:22 UTC

NP-MRD ID

NP0067216

Secondary Accession Numbers

None

Natural Product Identification

Common Name

11-acetyllepenine

Description

(1R,2S,5R,8R,9R,10S,11R,13R,14S,15R,16R)-7-ethyl-2,11-dihydroxy-5-methyl-12-methylidene-7-azahexacyclo[7.6.2.2¹⁰,¹³.0¹,⁸.0⁵,¹⁶.0¹⁰,¹⁵]Nonadecan-14-yl acetate belongs to the class of organic compounds known as danudatine-type diterpenoid alkaloids. These are alkaloid diterpenoids with a structure based on the danudatine skeleton, which is a hexacyclic compound with an additional C-20-C7 bond in the atisine skeleton. 11-acetyllepenine is found in Aconitum barbatum, Aconitum kirinense, Aconitum leucostomum, Aconitum pseudohuilense and Aconitum pseudohuiliense. Based on a literature review very few articles have been published on (1R,2S,5R,8R,9R,10S,11R,13R,14S,15R,16R)-7-ethyl-2,11-dihydroxy-5-methyl-12-methylidene-7-azahexacyclo[7.6.2.2¹⁰,¹³.0¹,⁸.0⁵,¹⁶.0¹⁰,¹⁵]Nonadecan-14-yl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282213372D          

 29 34  0  0  1  0            999 V2000
    7.3921    1.1327    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.8095    0.3858    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4341   -0.3778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5888   -0.4301    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.0076    0.2243    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1411   -0.0518    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5274    0.6150    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1023    1.2561    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7266    0.7316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6233    0.7632    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.9612    1.2358    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.2934    2.0343    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.1301    1.9464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8722    2.7437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2759    3.4632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5550    0.5589    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1321   -0.1929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3367   -0.4118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8698   -0.6167    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7028   -0.7979    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0336   -1.5537    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5446   -2.2181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8754   -2.9738    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7246   -2.1268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0188    0.2084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9262    1.1253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1182    1.2588    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2742   -1.1927    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1485    1.4620    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  1  0  0  0
  6  7  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
 10  9  1  6  0  0  0
  1 10  1  0  0  0  0
  5 10  1  0  0  0  0
  8 11  1  0  0  0  0
  5 11  1  0  0  0  0
 11 12  1  1  0  0  0
 12 13  1  0  0  0  0
  1 13  1  0  0  0  0
 12 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  2  0  0  0  0
 19 17  1  1  0  0  0
 19 20  1  0  0  0  0
  6 20  1  0  0  0  0
 20 21  1  1  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 19 25  1  0  0  0  0
 25 26  1  0  0  0  0
  7 26  1  6  0  0  0
 16 27  1  1  0  0  0
  4 28  1  6  0  0  0
  1 29  1  1  0  0  0
M  END

     RDKit          3D

 64 69  0  0  0  0  0  0  0  0999 V2000
    3.9439   -1.1978    2.3182 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0741   -1.2947    1.3431 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3364   -0.6988    0.0044 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1111   -1.8257   -0.9871 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6555   -2.1849   -0.8444 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9821   -1.5539    0.3369 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7495   -2.0250    1.5262 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2881   -1.6056    2.7439 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4572   -1.7917    0.2639 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2545   -1.2825    1.4350 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1130    0.2265    1.3647 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4995    0.7550    1.1049 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.3713    0.4644    2.3198 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4302    2.2438    0.9548 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6884    2.5265   -0.3036 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4078    1.7887   -0.4876 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1979    1.7156   -1.8858 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2723    0.4672    0.0950 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8633   -0.6724   -0.7287 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2325   -0.5945   -0.9477 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7103   -1.7485   -1.6322 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7868   -1.4635   -2.6527 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0954    0.0534   -0.0730 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0804   -0.0344    0.3986 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2533    0.3542   -0.3789 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7855    1.6283   -0.1935 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0250    2.4422   -1.2855 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5852    3.8169   -1.1705 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7760    2.0591   -2.4708 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7941   -1.6155    3.3037 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8653   -0.6737    2.1377 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3307   -0.2632   -0.0552 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7966   -2.6552   -0.8272 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3144   -1.3867   -1.9963 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1775   -2.0826   -1.8024 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6436   -3.2937   -0.6131 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9230   -3.1124    1.5757 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8329   -0.9673    3.2303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7842   -2.7682   -0.1087 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0006   -1.7097    2.3943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3137   -1.6257    1.2365 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6372    0.6323    2.2559 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7970    0.3330    3.2399 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1149    1.2999    2.4472 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0085   -0.4431    2.1340 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0166    2.6771    1.8644 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4946    2.5866    0.8008 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4913    3.6195   -0.3544 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3841    2.3177   -1.1491 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4082    2.4491   -0.1011 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0989    2.6335   -2.1737 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3144   -0.7128   -1.6572 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8576   -2.2344   -2.1787 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1037   -2.5334   -0.9482 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6433   -2.0573   -3.5901 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7674   -0.3997   -2.9731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7858   -1.7322   -2.2668 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6852    0.8288   -0.6466 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8900   -0.6782    0.2594 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2897    0.3166    1.4623 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0421    0.2319   -1.4797 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6699    3.7607   -1.4727 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1119    4.4497   -1.9494 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5259    4.2409   -0.1657 H   0  0  0  0  0  0  0  0  0  0  0  0
 22 21  1  0
 21 20  1  0
 20 23  1  0
 23 12  1  0
 12 13  1  1
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 18 16  1  6
 18 11  1  0
 11 10  1  0
 10  9  1  0
  9 19  1  0
  9  6  1  0
  6  5  1  6
  5  4  1  0
  4  3  1  0
  3 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 27 29  2  0
 25 24  1  0
  3  2  1  0
  2  1  2  3
  2  7  1  0
  7  8  1  0
 19 20  1  0
 24  6  1  0
 11 12  1  0
  7  6  1  0
 19 18  1  0
 24 18  1  0
 22 55  1  0
 22 56  1  0
 22 57  1  0
 21 53  1  0
 21 54  1  0
 23 58  1  0
 23 59  1  0
 13 43  1  0
 13 44  1  0
 13 45  1  0
 14 46  1  0
 14 47  1  0
 15 48  1  0
 15 49  1  0
 16 50  1  1
 17 51  1  0
 11 42  1  1
 10 40  1  0
 10 41  1  0
  9 39  1  6
 19 52  1  6
  5 35  1  0
  5 36  1  0
  4 33  1  0
  4 34  1  0
  3 32  1  1
 25 61  1  6
 28 62  1  0
 28 63  1  0
 28 64  1  0
 24 60  1  1
  1 30  1  0
  1 31  1  0
  7 37  1  1
  8 38  1  0
M  END


  Mrv1652304282213372D          

 29 34  0  0  1  0            999 V2000
    7.3921    1.1327    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.8095    0.3858    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4341   -0.3778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5888   -0.4301    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.0076    0.2243    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1411   -0.0518    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5274    0.6150    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1023    1.2561    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7266    0.7316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6233    0.7632    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.9612    1.2358    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.2934    2.0343    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.1301    1.9464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8722    2.7437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2759    3.4632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5550    0.5589    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1321   -0.1929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3367   -0.4118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8698   -0.6167    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7028   -0.7979    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0336   -1.5537    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5446   -2.2181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8754   -2.9738    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7246   -2.1268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0188    0.2084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9262    1.1253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1182    1.2588    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2742   -1.1927    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1485    1.4620    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  1  0  0  0
  6  7  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
 10  9  1  6  0  0  0
  1 10  1  0  0  0  0
  5 10  1  0  0  0  0
  8 11  1  0  0  0  0
  5 11  1  0  0  0  0
 11 12  1  1  0  0  0
 12 13  1  0  0  0  0
  1 13  1  0  0  0  0
 12 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  2  0  0  0  0
 19 17  1  1  0  0  0
 19 20  1  0  0  0  0
  6 20  1  0  0  0  0
 20 21  1  1  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 19 25  1  0  0  0  0
 25 26  1  0  0  0  0
  7 26  1  6  0  0  0
 16 27  1  1  0  0  0
  4 28  1  6  0  0  0
  1 29  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0067216

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCN1C[C@]2(C)CC[C@H](O)[C@@]34[C@@H]2C[C@@H]([C@@H]13)[C@@]12CC[C@@H]([C@H](OC(C)=O)[C@@H]41)C(=C)[C@H]2O

> <INCHI_IDENTIFIER>
InChI=1S/C24H35NO4/c1-5-25-11-22(4)8-7-17(27)24-16(22)10-15(20(24)25)23-9-6-14(12(2)21(23)28)18(19(23)24)29-13(3)26/h14-21,27-28H,2,5-11H2,1,3-4H3/t14-,15+,16-,17+,18+,19-,20-,21-,22+,23+,24-/m1/s1

> <INCHI_KEY>
WYDGCJLTZZIEHA-RGBYBVADSA-N

> <FORMULA>
C24H35NO4

> <MOLECULAR_WEIGHT>
401.547

> <EXACT_MASS>
401.256608611

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
64

> <JCHEM_AVERAGE_POLARIZABILITY>
44.9452688363621

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,2S,5R,8R,9R,10S,11R,13R,14S,15R,16R)-7-ethyl-2,11-dihydroxy-5-methyl-12-methylidene-7-azahexacyclo[7.6.2.2^{10,13}.0^{1,8}.0^{5,16}.0^{10,15}]nonadecan-14-yl acetate

> <ALOGPS_LOGP>
1.75

> <JCHEM_LOGP>
1.0499654273333352

> <ALOGPS_LOGS>
-2.61

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
14.748971544222396

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.00675841166689

> <JCHEM_PKA_STRONGEST_BASIC>
9.997757217508797

> <JCHEM_POLAR_SURFACE_AREA>
70.0

> <JCHEM_REFRACTIVITY>
108.76310000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.75e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,5R,8R,9R,10S,11R,13R,14S,15R,16R)-7-ethyl-2,11-dihydroxy-5-methyl-12-methylidene-7-azahexacyclo[7.6.2.2^{10,13}.0^{1,8}.0^{5,16}.0^{10,15}]nonadecan-14-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      13.799   2.114   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      14.578   0.720   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      13.877  -0.705   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      12.299  -0.803   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      11.214   0.419   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.597  -0.097   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.451   1.148   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.524   2.345   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.690   1.366   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      12.363   1.425   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      11.128   2.307   0.000  0.00  0.00           C+0
HETATM   12  N   UNK     0      11.748   3.797   0.000  0.00  0.00           N+0
HETATM   13  C   UNK     0      13.309   3.633   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.961   5.122   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      11.715   6.465   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.636   1.043   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.847  -0.360   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.362  -0.769   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.224  -1.151   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.778  -1.489   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       9.396  -2.900   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       8.483  -4.140   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       9.101  -5.551   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       6.953  -3.970   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       7.502   0.389   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       7.329   2.101   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       5.821   2.350   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0      11.712  -2.226   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      15.211   2.729   0.000  0.00  0.00           C+0
CONECT    1    2   10   13   29                                             
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   28                                                  
CONECT    5    4    6   10   11                                             
CONECT    6    5    7   20                                                  
CONECT    7    6    8   16   26                                             
CONECT    8    7    9   11                                                  
CONECT    9    8   10                                                       
CONECT   10    9    1    5                                                  
CONECT   11    8    5   12                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12    1                                                       
CONECT   14   12   15                                                       
CONECT   15   14                                                            
CONECT   16    7   17   27                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   25                                                  
CONECT   20   19    6   21                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25   19   26                                                       
CONECT   26   25    7                                                       
CONECT   27   16                                                            
CONECT   28    4                                                            
CONECT   29    1                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   68    0
END

View in JSmol

Synonyms

Value	Source
(1R,2S,5R,8R,9R,10S,11R,13R,14S,15R,16R)-7-Ethyl-2,11-dihydroxy-5-methyl-12-methylidene-7-azahexacyclo[7.6.2.2,.0,.0,.0,]nonadecan-14-yl acetic acid	Generator

Chemical Formula

C₂₄H₃₅NO₄

Average Mass

401.5470 Da

Monoisotopic Mass

401.25661 Da

IUPAC Name

(1R,2S,5R,8R,9R,10S,11R,13R,14S,15R,16R)-7-ethyl-2,11-dihydroxy-5-methyl-12-methylidene-7-azahexacyclo[7.6.2.2^{10,13}.0^{1,8}.0^{5,16}.0^{10,15}]nonadecan-14-yl acetate

Traditional Name

(1R,2S,5R,8R,9R,10S,11R,13R,14S,15R,16R)-7-ethyl-2,11-dihydroxy-5-methyl-12-methylidene-7-azahexacyclo[7.6.2.2^{10,13}.0^{1,8}.0^{5,16}.0^{10,15}]nonadecan-14-yl acetate

CAS Registry Number

Not Available

SMILES

CCN1C[C@]2(C)CC[C@H](O)[C@@]34[C@@H]2C[C@@H]([C@@H]13)[C@@]12CC[C@@H]([C@H](OC(C)=O)[C@@H]41)C(=C)[C@H]2O

InChI Identifier

InChI=1S/C24H35NO4/c1-5-25-11-22(4)8-7-17(27)24-16(22)10-15(20(24)25)23-9-6-14(12(2)21(23)28)18(19(23)24)29-13(3)26/h14-21,27-28H,2,5-11H2,1,3-4H3/t14-,15+,16-,17+,18+,19-,20-,21-,22+,23+,24-/m1/s1

InChI Key

WYDGCJLTZZIEHA-RGBYBVADSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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 barbatum	LOTUS Database	35616633
Aconitum kirinense	Plant	KNApSAcK
Aconitum leucostomum	Plant	KNApSAcK
Aconitum pseudohuilense	Plant	KNApSAcK
Aconitum pseudohuiliense	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as danudatine-type diterpenoid alkaloids. These are alkaloid diterpenoids with a structure based on the danudatine skeleton, which is a hexacyclic compound with an additional C-20-C7 bond in the atisine skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Danudatine-type diterpenoid alkaloids

Alternative Parents

Substituents

Danudatine-type diterpenoid alkaloid
Alkaloid or derivatives
Azepane
Piperidine
Cyclic alcohol
Amino acid or derivatives
Carboxylic acid ester
Tertiary aliphatic amine
Tertiary amine
Secondary alcohol
Azacycle
Carboxylic acid derivative
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Organic oxide
Organonitrogen compound
Organooxygen compound
Alcohol
Organic oxygen compound
Organopnictogen compound
Carbonyl group
Organic nitrogen compound
Hydrocarbon derivative
Amine
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	1.75	ALOGPS
logP	1.05	ChemAxon
logS	-2.6	ALOGPS
pKa (Strongest Acidic)	14.01	ChemAxon
pKa (Strongest Basic)	10	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	70 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	108.76 m³·mol⁻¹	ChemAxon
Polarizability	44.95 Å³	ChemAxon
Number of Rings	6	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

163035351

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for 11-acetyllepenine (NP0067216)

MOL for NP0067216 (11-acetyllepenine)

3D MOL for NP0067216 (11-acetyllepenine)

3D SDF for NP0067216 (11-acetyllepenine)

3D-SDF for NP0067216 (11-acetyllepenine)

PDB for NP0067216 (11-acetyllepenine)

3D PDB for NP0067216 (11-acetyllepenine)

SMILES for NP0067216 (11-acetyllepenine)

INCHI for NP0067216 (11-acetyllepenine)

Structure for NP0067216 (11-acetyllepenine)

3D Structure for NP0067216 (11-acetyllepenine)