NP-MRD: Showing NP-Card for 7-(2-hydroxyethyl)-5-methyl-13-methylidene-9-oxa-7-azahexacyclo[8.6.2.2¹¹,¹⁴.0¹,⁸.0⁵,¹⁷.0¹¹,¹⁶]icosan-18-ol (NP0192350)

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Record Information

Version

2.0

Created at

2022-09-04 09:32:24 UTC

Updated at

2022-09-04 09:32:24 UTC

NP-MRD ID

NP0192350

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7-(2-hydroxyethyl)-5-methyl-13-methylidene-9-oxa-7-azahexacyclo[8.6.2.2¹¹,¹⁴.0¹,⁸.0⁵,¹⁷.0¹¹,¹⁶]icosan-18-ol

Description

7-(2-Hydroxyethyl)-5-methyl-13-methylidene-9-oxa-7-azahexacyclo[8.6.2.2¹¹,¹⁴.0¹,⁸.0⁵,¹⁷.0¹¹,¹⁶]Icosan-18-ol belongs to the class of organic compounds known as atisane diterpenoids. These are diterpenoids with a structure based on the atisane skeleton, which is a tetracyclic compound containing the [2,2,2]bicyc1ic ring system with the C15-C16 bridge attached at C12. 7-(2-hydroxyethyl)-5-methyl-13-methylidene-9-oxa-7-azahexacyclo[8.6.2.2¹¹,¹⁴.0¹,⁸.0⁵,¹⁷.0¹¹,¹⁶]icosan-18-ol is found in Spiraea formosana. 7-(2-Hydroxyethyl)-5-methyl-13-methylidene-9-oxa-7-azahexacyclo[8.6.2.2¹¹,¹⁴.0¹,⁸.0⁵,¹⁷.0¹¹,¹⁶]Icosan-18-ol is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004251513332D          

 26 31  0  0  0  0            999 V2000
    8.6667    1.5026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8508    1.3807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1430    0.5804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5904   -0.0586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7571    0.1152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2978    0.8692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4202    0.5830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9822   -0.1704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1328   -0.2001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2675    0.6332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0256    1.5303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7046    1.1361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7531    0.9198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3653    0.1501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5870   -0.1236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3026    1.7669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8258    2.4241    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4890    1.8597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0920    2.4850    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.8892    3.2846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4803    3.8602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2774    4.6598    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8963    2.2303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0811    1.4388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8492    0.6471    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9859    1.2824    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
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
  9 14  1  0  0  0  0
 14 15  2  0  0  0  0
 12 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
  6 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
 21 22  1  0  0  0  0
 19 23  1  0  0  0  0
  2 23  1  0  0  0  0
 16 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
  2 26  1  0  0  0  0
  6 26  1  0  0  0  0
M  END

     RDKit          3D

 59 64  0  0  0  0  0  0  0  0999 V2000
    5.1168   -0.2329    0.7948 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9033   -0.1286    0.3611 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6521   -0.3436    1.1523 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6671    0.6490    0.5704 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4449    1.9441    0.3430 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2567    1.7401   -0.9222 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6133    0.2473   -1.0546 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3415   -0.5642   -1.3957 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2294    0.2196   -0.8300 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1277   -0.3216   -0.7500 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5762   -0.9651   -2.0376 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1704   -2.3395   -1.8424 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3394   -2.2682   -0.8828 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9418   -1.5166    0.3954 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3396   -2.4340    1.5365 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7960   -0.2881    0.4480 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3577    0.6247   -0.5735 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1373    1.8214   -0.6741 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1955    2.6613    0.5602 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0037    3.7871    0.2832 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9891    0.9317   -0.4529 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5792    1.4723    0.7273 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4395    0.8145    1.3815 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1152   -0.5723    1.7089 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7133   -1.2918    2.5391 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4469   -1.2346    0.4119 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.0079   -0.0698    0.2122 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2871   -0.5096    1.8397 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3800   -1.4058    0.9353 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7925   -0.1406    2.2285 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6802    2.7174    0.1431 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0982    2.1844    1.2085 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2457    2.2405   -0.7533 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8466    2.1757   -1.8208 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4236    0.0689   -1.7455 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4345   -1.6038   -1.0863 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2989   -0.5155   -2.5240 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1526    1.1364   -1.4987 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2585   -1.0638   -2.7809 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3554   -0.3515   -2.5419 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4380   -3.0838   -1.4918 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6040   -2.6272   -2.8371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1594   -1.7588   -1.4255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6698   -3.2914   -0.6920 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0442   -3.4840    1.3399 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4698   -2.4097    1.5414 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0288   -2.0963    2.5210 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8348   -0.6022    0.1688 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8666    0.1797    1.4356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1494    1.6677   -1.0774 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6197    2.4508   -1.4543 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2506    3.0590    0.9212 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7261    2.1071    1.3684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3968    4.4984   -0.0827 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6926    1.6445   -1.2649 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6152    1.3087    2.3479 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0338   -0.3374    2.3272 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5255   -2.2596    2.4366 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0307   -2.2408    0.3039 H   0  0  0  0  0  0  0  0  0  0  0  0
 14 15  1  1
 14 13  1  0
 13 12  1  0
 12 11  1  0
 10 11  1  6
 10 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 24 26  1  0
 23  4  1  0
  4  5  1  6
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  7  2  1  0
  2  1  2  3
  2  3  1  0
 21 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 17 16  1  0
 26 14  1  0
  9  4  1  0
 16 14  1  0
 26 10  1  0
  3  4  1  0
  9 10  1  0
 15 45  1  0
 15 46  1  0
 15 47  1  0
 13 43  1  0
 13 44  1  0
 12 41  1  0
 12 42  1  0
 11 39  1  0
 11 40  1  0
 21 55  1  6
 23 56  1  1
 24 57  1  1
 25 58  1  0
 26 59  1  6
  5 31  1  0
  5 32  1  0
  6 33  1  0
  6 34  1  0
  7 35  1  6
  8 36  1  0
  8 37  1  0
  9 38  1  6
  1 27  1  0
  1 28  1  0
  3 29  1  0
  3 30  1  0
 18 50  1  0
 18 51  1  0
 19 52  1  0
 19 53  1  0
 20 54  1  0
 16 48  1  0
 16 49  1  0
M  END


  Mrv1533004251513332D          

 26 31  0  0  0  0            999 V2000
    8.6667    1.5026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8508    1.3807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1430    0.5804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5904   -0.0586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7571    0.1152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2978    0.8692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4202    0.5830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9822   -0.1704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1328   -0.2001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2675    0.6332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0256    1.5303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7046    1.1361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7531    0.9198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3653    0.1501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5870   -0.1236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3026    1.7669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8258    2.4241    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4890    1.8597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0920    2.4850    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.8892    3.2846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4803    3.8602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2774    4.6598    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8963    2.2303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0811    1.4388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8492    0.6471    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9859    1.2824    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
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
  9 14  1  0  0  0  0
 14 15  2  0  0  0  0
 12 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
  6 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
 21 22  1  0  0  0  0
 19 23  1  0  0  0  0
  2 23  1  0  0  0  0
 16 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
  2 26  1  0  0  0  0
  6 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0192350

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC12CCCC34C(OC(C(O)C13)C13CCC(CC41)C(=C)C3)N(CCO)C2

> <INCHI_IDENTIFIER>
InChI=1S/C22H33NO3/c1-13-11-21-7-4-14(13)10-15(21)22-6-3-5-20(2)12-23(8-9-24)19(22)26-18(21)16(25)17(20)22/h14-19,24-25H,1,3-12H2,2H3

> <INCHI_KEY>
OVBJGKKAXGRFJR-UHFFFAOYSA-N

> <FORMULA>
C22H33NO3

> <MOLECULAR_WEIGHT>
359.51

> <EXACT_MASS>
359.246043927

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
40.584891289260526

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
7-(2-hydroxyethyl)-5-methyl-13-methylidene-9-oxa-7-azahexacyclo[8.6.2.2¹¹,¹⁴.0¹,⁸.0⁵,¹⁷.0¹¹,¹⁶]icosan-18-ol

> <ALOGPS_LOGP>
1.71

> <JCHEM_LOGP>
2.161536129666666

> <ALOGPS_LOGS>
-2.85

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
15.59720530241998

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.880054760123702

> <JCHEM_PKA_STRONGEST_BASIC>
7.211354062146773

> <JCHEM_POLAR_SURFACE_AREA>
52.93000000000001

> <JCHEM_REFRACTIVITY>
99.27339999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.04e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
7-(2-hydroxyethyl)-5-methyl-13-methylidene-9-oxa-7-azahexacyclo[8.6.2.2¹¹,¹⁴.0¹,⁸.0⁵,¹⁷.0¹¹,¹⁶]icosan-18-ol

> <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      16.178   2.805   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      14.655   2.577   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      15.200   1.083   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      14.169  -0.109   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      12.613   0.215   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      11.756   1.622   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.118   1.088   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.300  -0.318   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.715  -0.373   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.966   1.182   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.514   2.857   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.782   2.121   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.006   1.717   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.282   0.280   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.829  -0.231   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.898   3.298   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      10.875   4.525   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      12.113   3.471   0.000  0.00  0.00           C+0
HETATM   19  N   UNK     0      13.238   4.639   0.000  0.00  0.00           N+0
HETATM   20  C   UNK     0      12.860   6.131   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      13.963   7.206   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      13.585   8.698   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      14.740   4.163   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      11.351   2.686   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      10.918   1.208   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      13.040   2.394   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   23   26                                             
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   18   26                                             
CONECT    7    6    8   12                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11    7   13   16                                             
CONECT   13   12   14                                                       
CONECT   14   13    9   15                                                  
CONECT   15   14                                                            
CONECT   16   12   17   24                                                  
CONECT   17   16   18                                                       
CONECT   18   17    6   19                                                  
CONECT   19   18   20   23                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21                                                            
CONECT   23   19    2                                                       
CONECT   24   16   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24    2    6                                                  
MASTER        0    0    0    0    0    0    0    0   26    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₃₃NO₃

Average Mass

359.5100 Da

Monoisotopic Mass

359.24604 Da

IUPAC Name

7-(2-hydroxyethyl)-5-methyl-13-methylidene-9-oxa-7-azahexacyclo[8.6.2.2¹¹,¹⁴.0¹,⁸.0⁵,¹⁷.0¹¹,¹⁶]icosan-18-ol

Traditional Name

7-(2-hydroxyethyl)-5-methyl-13-methylidene-9-oxa-7-azahexacyclo[8.6.2.2¹¹,¹⁴.0¹,⁸.0⁵,¹⁷.0¹¹,¹⁶]icosan-18-ol

CAS Registry Number

Not Available

SMILES

CC12CCCC34C(OC(C(O)C13)C13CCC(CC41)C(=C)C3)N(CCO)C2

InChI Identifier

InChI=1S/C22H33NO3/c1-13-11-21-7-4-14(13)10-15(21)22-6-3-5-20(2)12-23(8-9-24)19(22)26-18(21)16(25)17(20)22/h14-19,24-25H,1,3-12H2,2H3

InChI Key

OVBJGKKAXGRFJR-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
Spiraea formosana	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as atisane diterpenoids. These are diterpenoids with a structure based on the atisane skeleton, which is a tetracyclic compound containing the [2,2,2]bicyc1ic ring system with the C15-C16 bridge attached at C12.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Atisane diterpenoids

Alternative Parents

Substituents

Atisane diterpenoid
Alkaloid or derivatives
Oxane
Piperidine
Cyclic alcohol
Hemiaminal
Secondary alcohol
Alkanolamine
Oxacycle
Azacycle
Organoheterocyclic compound
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Organopnictogen compound
Organic oxygen compound
Primary alcohol
Alcohol
Organic nitrogen 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	1.71	ALOGPS
logP	2.16	ChemAxon
logS	-2.8	ALOGPS
pKa (Strongest Acidic)	13.88	ChemAxon
pKa (Strongest Basic)	7.21	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	52.93 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	99.27 m³·mol⁻¹	ChemAxon
Polarizability	40.58 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

73798917

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 7-(2-hydroxyethyl)-5-methyl-13-methylidene-9-oxa-7-azahexacyclo[8.6.2.2¹¹,¹⁴.0¹,⁸.0⁵,¹⁷.0¹¹,¹⁶]icosan-18-ol (NP0192350)

MOL for NP0192350 (7-(2-hydroxyethyl)-5-methyl-13-methylidene-9-oxa-7-azahexacyclo[8.6.2.2¹¹,¹⁴.0¹,⁸.0⁵,¹⁷.0¹¹,¹⁶]icosan-18-ol)

3D MOL for NP0192350 (7-(2-hydroxyethyl)-5-methyl-13-methylidene-9-oxa-7-azahexacyclo[8.6.2.2¹¹,¹⁴.0¹,⁸.0⁵,¹⁷.0¹¹,¹⁶]icosan-18-ol)

3D SDF for NP0192350 (7-(2-hydroxyethyl)-5-methyl-13-methylidene-9-oxa-7-azahexacyclo[8.6.2.2¹¹,¹⁴.0¹,⁸.0⁵,¹⁷.0¹¹,¹⁶]icosan-18-ol)

3D-SDF for NP0192350 (7-(2-hydroxyethyl)-5-methyl-13-methylidene-9-oxa-7-azahexacyclo[8.6.2.2¹¹,¹⁴.0¹,⁸.0⁵,¹⁷.0¹¹,¹⁶]icosan-18-ol)

PDB for NP0192350 (7-(2-hydroxyethyl)-5-methyl-13-methylidene-9-oxa-7-azahexacyclo[8.6.2.2¹¹,¹⁴.0¹,⁸.0⁵,¹⁷.0¹¹,¹⁶]icosan-18-ol)

3D PDB for NP0192350 (7-(2-hydroxyethyl)-5-methyl-13-methylidene-9-oxa-7-azahexacyclo[8.6.2.2¹¹,¹⁴.0¹,⁸.0⁵,¹⁷.0¹¹,¹⁶]icosan-18-ol)

SMILES for NP0192350 (7-(2-hydroxyethyl)-5-methyl-13-methylidene-9-oxa-7-azahexacyclo[8.6.2.2¹¹,¹⁴.0¹,⁸.0⁵,¹⁷.0¹¹,¹⁶]icosan-18-ol)

INCHI for NP0192350 (7-(2-hydroxyethyl)-5-methyl-13-methylidene-9-oxa-7-azahexacyclo[8.6.2.2¹¹,¹⁴.0¹,⁸.0⁵,¹⁷.0¹¹,¹⁶]icosan-18-ol)

Structure for NP0192350 (7-(2-hydroxyethyl)-5-methyl-13-methylidene-9-oxa-7-azahexacyclo[8.6.2.2¹¹,¹⁴.0¹,⁸.0⁵,¹⁷.0¹¹,¹⁶]icosan-18-ol)

3D Structure for NP0192350 (7-(2-hydroxyethyl)-5-methyl-13-methylidene-9-oxa-7-azahexacyclo[8.6.2.2¹¹,¹⁴.0¹,⁸.0⁵,¹⁷.0¹¹,¹⁶]icosan-18-ol)