NP-MRD: Showing NP-Card for 2,6-dimethyl-19-oxa-17-azapentacyclo[14.2.1.0²,¹⁴.0³,¹¹.0⁶,¹⁰]nonadecan-8-yl acetate (NP0247523)

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Record Information

Version

2.0

Created at

2022-09-07 09:24:26 UTC

Updated at

2022-09-07 09:24:27 UTC

NP-MRD ID

NP0247523

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2,6-dimethyl-19-oxa-17-azapentacyclo[14.2.1.0²,¹⁴.0³,¹¹.0⁶,¹⁰]nonadecan-8-yl acetate

Description

2,6-Dimethyl-19-oxa-17-azapentacyclo[14.2.1.0²,¹⁴.0³,¹¹.0⁶,¹⁰]Nonadecan-8-yl acetate belongs to the class of organic compounds known as samandarines. These are samamime-type alkaloids in which the A-ring of the steroidal backbone is an oxazolidine. 2,6-dimethyl-19-oxa-17-azapentacyclo[14.2.1.0²,¹⁴.0³,¹¹.0⁶,¹⁰]nonadecan-8-yl acetate is found in Salamandra salamandra. 2,6-Dimethyl-19-oxa-17-azapentacyclo[14.2.1.0²,¹⁴.0³,¹¹.0⁶,¹⁰]Nonadecan-8-yl acetate is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171514202D          

 25 29  0  0  0  0            999 V2000
   -5.5662    1.6690    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7661    1.8701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5402    2.6636    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1919    1.2778    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3918    1.4789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7588    0.9498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0600    1.3884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2665    1.1625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0654    0.3624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2719    0.1365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3204    0.7107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0714    0.3691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8067    0.7432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9726    1.5514    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4443    2.1850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6195    2.1669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3910    1.6035    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1193    1.5108    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1410    2.2937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6742    1.7367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8753    2.5368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6688    2.7627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2611    2.1885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5448    2.9632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0842    2.2444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  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
 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
 16 17  1  0  0  0  0
 13 17  1  0  0  0  0
 16 18  1  0  0  0  0
 11 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
  8 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
  7 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
  5 25  1  0  0  0  0
M  END

     RDKit          3D

 58 62  0  0  0  0  0  0  0  0999 V2000
    6.7664   -0.0022    2.1466 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8660   -0.0626    0.9693 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3424   -0.4524   -0.1281 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5400    0.2776    0.9856 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6658    0.2298   -0.1136 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5480   -0.7830    0.0915 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3189    0.0466    0.0478 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0890   -0.7154   -0.4707 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1442   -1.8547    0.4231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5421   -2.2149    0.7358 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5313   -1.5161   -0.1279 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.9476   -1.8985    0.1188 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8687   -0.8898   -0.5608 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.2955    0.0464    0.4383 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4767    1.2076    0.1890 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3970    0.6856   -0.6907 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.1330   -0.2097   -1.5052 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2863   -0.0205    0.0296 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2228    0.2997    1.4936 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9829    0.2767   -0.6575 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5784    1.6909   -0.2158 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6558    2.1639   -0.9412 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6863    1.0970   -1.0004 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8248    0.4739   -2.3541 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0457    1.5353   -0.4652 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1727   -0.2446    3.0769 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5867   -0.7193    2.1144 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1793    1.0074    2.3269 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2450   -0.1325   -0.9921 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7012   -1.2189    1.1032 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5729   -1.6052   -0.6231 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1480    0.5022    1.0186 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4216   -1.0828   -1.4883 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3483   -2.7766   -0.0136 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4023   -1.7308    1.4064 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7406   -3.3231    0.6333 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8212   -2.0018    1.8097 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3126   -1.7441   -1.2105 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2050   -1.9846    1.1994 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1636   -2.8749   -0.3739 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7744   -1.3698   -0.9792 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3133    0.2473    0.4171 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1671    1.7383    1.0780 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1019    1.9046   -0.4274 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0096    1.4534   -1.4157 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2393   -0.0483    1.8724 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2613    1.3859    1.7058 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0740   -0.1826    2.0343 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2415    0.4046   -1.7519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4413    1.7699    0.8601 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4238    2.3673   -0.4881 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3755    2.4952   -1.9398 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0698    3.0123   -0.3453 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6120    1.0714   -2.9013 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8598    0.5386   -2.9013 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2020   -0.5664   -2.3378 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5901    2.0816   -1.2713 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8604    2.2148    0.3660 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  1  1
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  6
 23 25  1  0
 25  5  1  0
 23  7  1  0
 20  8  1  0
 18 11  1  0
 17 13  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  5 29  1  6
  6 30  1  0
  6 31  1  0
  7 32  1  1
  8 33  1  6
  9 34  1  0
  9 35  1  0
 10 36  1  0
 10 37  1  0
 11 38  1  6
 12 39  1  0
 12 40  1  0
 13 41  1  6
 14 42  1  0
 15 43  1  0
 15 44  1  0
 16 45  1  6
 19 46  1  0
 19 47  1  0
 19 48  1  0
 20 49  1  6
 21 50  1  0
 21 51  1  0
 22 52  1  0
 22 53  1  0
 24 54  1  0
 24 55  1  0
 24 56  1  0
 25 57  1  0
 25 58  1  0
M  END


  Mrv1533004171514202D          

 25 29  0  0  0  0            999 V2000
   -5.5662    1.6690    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7661    1.8701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5402    2.6636    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1919    1.2778    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3918    1.4789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7588    0.9498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0600    1.3884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2665    1.1625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0654    0.3624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2719    0.1365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3204    0.7107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0714    0.3691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8067    0.7432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9726    1.5514    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4443    2.1850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6195    2.1669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3910    1.6035    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1193    1.5108    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1410    2.2937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6742    1.7367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8753    2.5368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6688    2.7627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2611    2.1885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5448    2.9632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0842    2.2444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  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
 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
 16 17  1  0  0  0  0
 13 17  1  0  0  0  0
 16 18  1  0  0  0  0
 11 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
  8 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
  7 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
  5 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0247523

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC1CC2C3CCC4CC5NCC(O5)C4(C)C3CCC2(C)C1

> <INCHI_IDENTIFIER>
InChI=1S/C21H33NO3/c1-12(23)24-14-9-17-15-5-4-13-8-19-22-11-18(25-19)21(13,3)16(15)6-7-20(17,2)10-14/h13-19,22H,4-11H2,1-3H3

> <INCHI_KEY>
LCDBBFJXTGHUHX-UHFFFAOYSA-N

> <FORMULA>
C21H33NO3

> <MOLECULAR_WEIGHT>
347.499

> <EXACT_MASS>
347.246043927

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
39.44287006477468

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2,6-dimethyl-19-oxa-17-azapentacyclo[14.2.1.0²,¹⁴.0³,¹¹.0⁶,¹⁰]nonadecan-8-yl acetate

> <ALOGPS_LOGP>
3.22

> <JCHEM_LOGP>
2.9601196609999993

> <ALOGPS_LOGS>
-4.95

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_BASIC>
9.020172077585848

> <JCHEM_POLAR_SURFACE_AREA>
47.56

> <JCHEM_REFRACTIVITY>
94.9353

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.90e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2,6-dimethyl-19-oxa-17-azapentacyclo[14.2.1.0²,¹⁴.0³,¹¹.0⁶,¹⁰]nonadecan-8-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0     -10.390   3.116   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -8.897   3.491   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -8.475   4.972   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      -7.825   2.385   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -6.331   2.761   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -5.150   1.773   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -3.845   2.592   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.364   2.170   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.989   0.676   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.508   0.255   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.598   1.327   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.000   0.689   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.372   1.387   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0       3.682   2.896   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0       2.696   4.079   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.156   4.045   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       2.597   2.993   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       0.223   2.820   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.263   4.282   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.258   3.242   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -1.634   4.735   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -3.115   5.157   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -4.221   4.085   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -4.750   5.531   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -5.757   4.190   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   25                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   23                                                  
CONECT    8    7    9   20                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   18                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   17                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16   13                                                       
CONECT   18   16   11   19   20                                             
CONECT   19   18                                                            
CONECT   20   18    8   21                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22    7   24   25                                             
CONECT   24   23                                                            
CONECT   25   23    5                                                       
MASTER        0    0    0    0    0    0    0    0   25    0   58    0
END

View in JSmol

Synonyms

Value	Source
2,6-Dimethyl-19-oxa-17-azapentacyclo[14.2.1.0,.0,.0,]nonadecan-8-yl acetic acid	Generator
2,6-Dimethyl-19-oxa-17-azapentacyclo[14.2.1.0²,¹⁴.0³,¹¹.0⁶,¹⁰]nonadecan-8-yl acetic acid	Generator

Chemical Formula

C₂₁H₃₃NO₃

Average Mass

347.4990 Da

Monoisotopic Mass

347.24604 Da

IUPAC Name

2,6-dimethyl-19-oxa-17-azapentacyclo[14.2.1.0²,¹⁴.0³,¹¹.0⁶,¹⁰]nonadecan-8-yl acetate

Traditional Name

2,6-dimethyl-19-oxa-17-azapentacyclo[14.2.1.0²,¹⁴.0³,¹¹.0⁶,¹⁰]nonadecan-8-yl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)OC1CC2C3CCC4CC5NCC(O5)C4(C)C3CCC2(C)C1

InChI Identifier

InChI=1S/C21H33NO3/c1-12(23)24-14-9-17-15-5-4-13-8-19-22-11-18(25-19)21(13,3)16(15)6-7-20(17,2)10-14/h13-19,22H,4-11H2,1-3H3

InChI Key

LCDBBFJXTGHUHX-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
Salamandra salamandra	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as samandarines. These are samamime-type alkaloids in which the A-ring of the steroidal backbone is an oxazolidine.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroidal alkaloids

Direct Parent

Samandarines

Alternative Parents

Substituents

Samandarin skeleton
Azasteroid
2-oxasteroid
Naphthopyran
Naphthalene
Alkaloid or derivatives
Azepane
Oxane
Pyran
Oxazolidine
Amino acid or derivatives
Carboxylic acid ester
Hemiaminal
Secondary amine
Oxacycle
Azacycle
Organoheterocyclic compound
Carboxylic acid derivative
Secondary aliphatic amine
Monocarboxylic acid or derivatives
Amine
Organopnictogen compound
Organic oxide
Organonitrogen compound
Organooxygen compound
Carbonyl group
Organic oxygen compound
Organic nitrogen compound
Hydrocarbon derivative
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	3.22	ALOGPS
logP	2.96	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Basic)	9.02	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	47.56 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	94.94 m³·mol⁻¹	ChemAxon
Polarizability	39.44 Å³	ChemAxon
Number of Rings	5	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

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 2,6-dimethyl-19-oxa-17-azapentacyclo[14.2.1.0²,¹⁴.0³,¹¹.0⁶,¹⁰]nonadecan-8-yl acetate (NP0247523)

MOL for NP0247523 (2,6-dimethyl-19-oxa-17-azapentacyclo[14.2.1.0²,¹⁴.0³,¹¹.0⁶,¹⁰]nonadecan-8-yl acetate)

3D MOL for NP0247523 (2,6-dimethyl-19-oxa-17-azapentacyclo[14.2.1.0²,¹⁴.0³,¹¹.0⁶,¹⁰]nonadecan-8-yl acetate)

3D SDF for NP0247523 (2,6-dimethyl-19-oxa-17-azapentacyclo[14.2.1.0²,¹⁴.0³,¹¹.0⁶,¹⁰]nonadecan-8-yl acetate)

3D-SDF for NP0247523 (2,6-dimethyl-19-oxa-17-azapentacyclo[14.2.1.0²,¹⁴.0³,¹¹.0⁶,¹⁰]nonadecan-8-yl acetate)

PDB for NP0247523 (2,6-dimethyl-19-oxa-17-azapentacyclo[14.2.1.0²,¹⁴.0³,¹¹.0⁶,¹⁰]nonadecan-8-yl acetate)

3D PDB for NP0247523 (2,6-dimethyl-19-oxa-17-azapentacyclo[14.2.1.0²,¹⁴.0³,¹¹.0⁶,¹⁰]nonadecan-8-yl acetate)

SMILES for NP0247523 (2,6-dimethyl-19-oxa-17-azapentacyclo[14.2.1.0²,¹⁴.0³,¹¹.0⁶,¹⁰]nonadecan-8-yl acetate)

INCHI for NP0247523 (2,6-dimethyl-19-oxa-17-azapentacyclo[14.2.1.0²,¹⁴.0³,¹¹.0⁶,¹⁰]nonadecan-8-yl acetate)

Structure for NP0247523 (2,6-dimethyl-19-oxa-17-azapentacyclo[14.2.1.0²,¹⁴.0³,¹¹.0⁶,¹⁰]nonadecan-8-yl acetate)

3D Structure for NP0247523 (2,6-dimethyl-19-oxa-17-azapentacyclo[14.2.1.0²,¹⁴.0³,¹¹.0⁶,¹⁰]nonadecan-8-yl acetate)