NP-MRD: Showing NP-Card for Songoramine (NP0067245)

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Record Information

Version

2.0

Created at

2022-04-28 11:44:20 UTC

Updated at

2022-04-28 11:44:20 UTC

NP-MRD ID

NP0067245

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Songoramine

Description

(1R,2S,4R,5S,8R,10S,12S,13R,14R,17R,19S)-11-ethyl-19-hydroxy-5-methyl-18-methylidene-9-oxa-11-azaheptacyclo[15.2.1.0¹,¹⁴.0²,¹².0⁴,¹³.0⁵,¹⁰.0⁸,¹³]Icosan-16-one belongs to the class of organic compounds known as kaurane diterpenoids. These are diterpene alkaloids with a structure that is based on the kaurane skeleton. Kaurane is a tetracyclic compound that arises by cyclisation of a pimarane precursor followed by rearrangement. It possesses a [3,2,1]-bicyclic ring system with C15-C16 bridge connected to C13, forming the five-membered ring D. Songoramine is found in Aconitum carmichaeli Debx , Aconitum karakolicum, Aconitum monticola, Aconitum napellus, Aconitum napellus L.ssp.vulgare , Aconitum soongaricum, Aconitum soongoricum, Acotinum carmichaeli and Acotinum nagarum var.lasiandrum. Based on a literature review very few articles have been published on (1R,2S,4R,5S,8R,10S,12S,13R,14R,17R,19S)-11-ethyl-19-hydroxy-5-methyl-18-methylidene-9-oxa-11-azaheptacyclo[15.2.1.0¹,¹⁴.0²,¹².0⁴,¹³.0⁵,¹⁰.0⁸,¹³]Icosan-16-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282213442D          

 26 32  0  0  1  0            999 V2000
    3.1341   -0.1369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0584    0.8333    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.7606    1.3102    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6412    1.9437    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5511    0.9539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2989    1.2528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4852    2.3704    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5171    2.4341    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2267    1.4068    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7017    1.4451    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5061    1.9730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1158    2.6686    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5756    1.6635    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8710    1.9914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1921    2.2012    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5012    3.0273    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1067    3.6361    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3317    3.2341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7760    2.5250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1657    1.3207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5810    0.9021    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9810    1.0129    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7682    0.1677    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1470    1.9967    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5321    1.6025    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7360   -0.7843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  6  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
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  9  2  1  6  0  0  0
  9 10  1  0  0  0  0
 10 11  1  6  0  0  0
 12 11  1  1  0  0  0
  4 12  1  0  0  0  0
  8 12  1  0  0  0  0
 10 13  1  0  0  0  0
 13 14  1  1  0  0  0
 15 14  1  1  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 19 18  1  1  0  0  0
  8 19  1  0  0  0  0
 13 19  1  0  0  0  0
 15 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 13 22  1  0  0  0  0
 22 23  1  1  0  0  0
  7 24  1  6  0  0  0
  3 24  1  0  0  0  0
  4 25  1  6  0  0  0
  1 26  1  0  0  0  0
M  END

     RDKit          3D

 55 61  0  0  0  0  0  0  0  0999 V2000
    5.0797    1.2583    0.5473 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8951    0.6634    0.4987 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6466    1.2518   -0.0666 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4772    2.5751    0.2885 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5331    0.3539    0.3936 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1399   -0.3991    1.5679 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5265   -0.6951    0.9742 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2744   -1.6352   -0.1421 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2066   -2.1625   -0.6881 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8712   -1.8952   -0.5519 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2025   -0.5762   -0.7655 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2643   -0.5557   -0.7597 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4878    0.9687   -0.5889 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2668    1.0463    0.7530 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5867    0.0908    1.5604 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8850   -1.0113    0.5584 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3785   -1.1135    0.2535 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.2295   -0.9750    1.4816 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5807   -2.4152   -0.4885 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4358   -2.5671   -1.4820 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0046   -1.1530   -1.8651 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2331   -0.4573   -1.9894 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6630    0.0160   -0.7461 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8592    1.1513   -0.4613 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4341    2.3022    0.0283 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2563    3.4502   -0.9410 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9380    0.7698    0.9667 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2054    2.2486    0.1655 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7692    1.2310   -1.1681 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6149    3.2062   -0.4815 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2025    0.2846    2.4107 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6067   -1.3201    1.8317 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2203   -1.0819    1.7377 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8798   -2.4286   -1.5287 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3424   -2.5498    0.1666 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5622   -0.1600   -1.7156 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0433    1.4588   -1.4021 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3450    2.0413    1.1383 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0496   -0.3039    2.4596 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5108    0.5467    1.9439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5147   -1.9906    0.8870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9849   -1.7925    1.4533 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6728   -1.0987    2.4340 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8038   -0.0254    1.4478 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6796   -3.2773    0.1833 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5267   -2.2774   -1.0838 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6622   -3.1430   -0.9875 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7920   -3.1308   -2.3872 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4678   -1.1435   -2.8384 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7336    0.2335   -0.7914 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5214    2.2038    0.2211 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9971    2.6926    1.0018 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4434    4.4064   -0.3742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9852    3.3994   -1.7780 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2054    3.4840   -1.2813 H   0  0  0  0  0  0  0  0  0  0  0  0
 26 25  1  0
 25 24  1  0
 24 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 12  1  0
 12 11  1  0
 11 10  1  0
 10  8  1  0
  8  9  2  0
  8  7  1  0
  7  6  1  0
  5  6  1  1
  5  3  1  0
  3  4  1  0
  3  2  1  0
  2  1  2  3
 12 21  1  6
 21 20  1  0
 20 19  1  0
 19 17  1  0
 17 18  1  1
 17 23  1  0
 23 22  1  0
 23 24  1  0
 12 13  1  0
  5 11  1  0
 22 21  1  0
  5 14  1  0
 17 16  1  0
  2  7  1  0
 26 53  1  0
 26 54  1  0
 26 55  1  0
 25 51  1  0
 25 52  1  0
 13 37  1  6
 14 38  1  1
 15 39  1  0
 15 40  1  0
 16 41  1  1
 11 36  1  6
 10 34  1  0
 10 35  1  0
  7 33  1  1
  6 31  1  0
  6 32  1  0
  3 29  1  6
  4 30  1  0
  1 27  1  0
  1 28  1  0
 21 49  1  6
 20 47  1  0
 20 48  1  0
 19 45  1  0
 19 46  1  0
 18 42  1  0
 18 43  1  0
 18 44  1  0
 23 50  1  6
M  END


  Mrv1652304282213442D          

 26 32  0  0  1  0            999 V2000
    3.1341   -0.1369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0584    0.8333    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.7606    1.3102    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6412    1.9437    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5511    0.9539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2989    1.2528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4852    2.3704    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5171    2.4341    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2267    1.4068    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7017    1.4451    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5061    1.9730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1158    2.6686    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5756    1.6635    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8710    1.9914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1921    2.2012    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5012    3.0273    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1067    3.6361    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3317    3.2341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7760    2.5250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1657    1.3207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5810    0.9021    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9810    1.0129    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7682    0.1677    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1470    1.9967    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5321    1.6025    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7360   -0.7843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  6  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
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  9  2  1  6  0  0  0
  9 10  1  0  0  0  0
 10 11  1  6  0  0  0
 12 11  1  1  0  0  0
  4 12  1  0  0  0  0
  8 12  1  0  0  0  0
 10 13  1  0  0  0  0
 13 14  1  1  0  0  0
 15 14  1  1  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 19 18  1  1  0  0  0
  8 19  1  0  0  0  0
 13 19  1  0  0  0  0
 15 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 13 22  1  0  0  0  0
 22 23  1  1  0  0  0
  7 24  1  6  0  0  0
  3 24  1  0  0  0  0
  4 25  1  6  0  0  0
  1 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0067245

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCN1[C@H]2[C@H]3C[C@@H]4[C@@]2([C@@H]2CC(=O)[C@@H]5C[C@]32[C@@H](O)C5=C)[C@H]2CC[C@]4(C)[C@@H]1O2

> <INCHI_IDENTIFIER>
InChI=1S/C22H29NO3/c1-4-23-17-12-7-14-20(3)6-5-16(26-19(20)23)22(14,17)15-8-13(24)11-9-21(12,15)18(25)10(11)2/h11-12,14-19,25H,2,4-9H2,1,3H3/t11-,12-,14+,15-,16-,17+,18+,19+,20+,21+,22-/m1/s1

> <INCHI_KEY>
YSSPOBAEOOLGAT-GHXMPSAKSA-N

> <FORMULA>
C22H29NO3

> <MOLECULAR_WEIGHT>
355.478

> <EXACT_MASS>
355.214743798

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
39.13518219080487

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,2S,4R,5S,8R,10S,12S,13R,14R,17R,19S)-11-ethyl-19-hydroxy-5-methyl-18-methylidene-9-oxa-11-azaheptacyclo[15.2.1.0^{1,14}.0^{2,12}.0^{4,13}.0^{5,10}.0^{8,13}]icosan-16-one

> <ALOGPS_LOGP>
1.63

> <JCHEM_LOGP>
1.7138801713333338

> <ALOGPS_LOGS>
-2.57

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.437509136898303

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.679533203362794

> <JCHEM_PKA_STRONGEST_BASIC>
5.663771287769157

> <JCHEM_POLAR_SURFACE_AREA>
49.77000000000001

> <JCHEM_REFRACTIVITY>
96.2832

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.64e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,4R,5S,8R,10S,12S,13R,14R,17R,19S)-11-ethyl-19-hydroxy-5-methyl-18-methylidene-9-oxa-11-azaheptacyclo[15.2.1.0^{1,14}.0^{2,12}.0^{4,13}.0^{5,10}.0^{8,13}]icosan-16-one

> <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       5.850  -0.255   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0       5.709   1.555   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0       7.020   2.446   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.930   3.628   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.762   1.781   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.158   2.339   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.506   4.425   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.699   4.544   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.157   2.626   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.043   2.698   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.545   3.683   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.816   4.981   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.941   3.105   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.626   3.717   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.359   4.109   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.936   5.651   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -0.199   6.787   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       2.486   6.037   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.315   4.713   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.309   2.465   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -1.085   1.684   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.831   1.891   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       1.434   0.313   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       7.741   3.727   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       6.593   2.991   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.974  -1.464   0.000  0.00  0.00           C+0
CONECT    1    2   26                                                       
CONECT    2    1    3    9                                                  
CONECT    3    2    4   24                                                  
CONECT    4    3    5   12   25                                             
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   24                                                  
CONECT    8    7    9   12   19                                             
CONECT    9    8    2   10                                                  
CONECT   10    9   11   13                                                  
CONECT   11   10   12                                                       
CONECT   12   11    4    8                                                  
CONECT   13   10   14   19   22                                             
CONECT   14   13   15                                                       
CONECT   15   14   16   20                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18    8   13                                                  
CONECT   20   15   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   13   23                                                  
CONECT   23   22                                                            
CONECT   24    7    3                                                       
CONECT   25    4                                                            
CONECT   26    1                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₂₉NO₃

Average Mass

355.4780 Da

Monoisotopic Mass

355.21474 Da

IUPAC Name

(1R,2S,4R,5S,8R,10S,12S,13R,14R,17R,19S)-11-ethyl-19-hydroxy-5-methyl-18-methylidene-9-oxa-11-azaheptacyclo[15.2.1.0^{1,14}.0^{2,12}.0^{4,13}.0^{5,10}.0^{8,13}]icosan-16-one

Traditional Name

(1R,2S,4R,5S,8R,10S,12S,13R,14R,17R,19S)-11-ethyl-19-hydroxy-5-methyl-18-methylidene-9-oxa-11-azaheptacyclo[15.2.1.0^{1,14}.0^{2,12}.0^{4,13}.0^{5,10}.0^{8,13}]icosan-16-one

CAS Registry Number

Not Available

SMILES

CCN1[C@H]2[C@H]3C[C@@H]4[C@@]2([C@@H]2CC(=O)[C@@H]5C[C@]32[C@@H](O)C5=C)[C@H]2CC[C@]4(C)[C@@H]1O2

InChI Identifier

InChI=1S/C22H29NO3/c1-4-23-17-12-7-14-20(3)6-5-16(26-19(20)23)22(14,17)15-8-13(24)11-9-21(12,15)18(25)10(11)2/h11-12,14-19,25H,2,4-9H2,1,3H3/t11-,12-,14+,15-,16-,17+,18+,19+,20+,21+,22-/m1/s1

InChI Key

YSSPOBAEOOLGAT-GHXMPSAKSA-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 carmichaeli Debx	Plant	KNApSAcK
Aconitum karakolicum	Plant	KNApSAcK
Aconitum monticola	Plant	KNApSAcK
Aconitum napellus	LOTUS Database	35616633
Aconitum napellus L.ssp.vulgare	Plant	KNApSAcK
Aconitum soongaricum	Plant	KNApSAcK
Aconitum soongoricum	Plant	KNApSAcK
Acotinum carmichaeli	-	KNApSAcK
Acotinum nagarum var.lasiandrum	-	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as kaurane diterpenoids. These are diterpene alkaloids with a structure that is based on the kaurane skeleton. Kaurane is a tetracyclic compound that arises by cyclisation of a pimarane precursor followed by rearrangement. It possesses a [3,2,1]-bicyclic ring system with C15-C16 bridge connected to C13, forming the five-membered ring D.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Kaurane diterpenoids

Alternative Parents

Substituents

Kaurane diterpenoid
Naphthopyran
Naphthalene
Azepane
Pyran
Piperidine
Oxazinane
Oxane
1,3-oxazinane
Cyclic alcohol
Secondary alcohol
Ketone
Hemiaminal
Oxacycle
Azacycle
Organoheterocyclic compound
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
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	1.63	ALOGPS
logP	1.71	ChemAxon
logS	-2.6	ALOGPS
pKa (Strongest Acidic)	13.68	ChemAxon
pKa (Strongest Basic)	5.66	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	49.77 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	96.28 m³·mol⁻¹	ChemAxon
Polarizability	39.14 Å³	ChemAxon
Number of Rings	7	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

162944214

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Songoramine (NP0067245)

MOL for NP0067245 (Songoramine)

3D MOL for NP0067245 (Songoramine)

3D SDF for NP0067245 (Songoramine)

3D-SDF for NP0067245 (Songoramine)

PDB for NP0067245 (Songoramine)

3D PDB for NP0067245 (Songoramine)

SMILES for NP0067245 (Songoramine)

INCHI for NP0067245 (Songoramine)

Structure for NP0067245 (Songoramine)

3D Structure for NP0067245 (Songoramine)