NP-MRD: Showing NP-Card for n,6,13-trimethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosa-5,18-dien-16-amine (NP0229333)

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Record Information

Version

2.0

Created at

2022-09-06 09:20:41 UTC

Updated at

2022-09-06 09:20:41 UTC

NP-MRD ID

NP0229333

Secondary Accession Numbers

None

Natural Product Identification

Common Name

n,6,13-trimethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosa-5,18-dien-16-amine

Description

N,6,13-trimethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]Icosa-5,18-dien-16-amine belongs to the class of organic compounds known as pyrrolines. Pyrrolines are compounds containing a pyrroline ring, which is a five-member unsaturated aliphatic ring with one nitrogen atom and four carbon atoms. n,6,13-trimethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosa-5,18-dien-16-amine is found in Holarrhena pubescens. N,6,13-trimethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]Icosa-5,18-dien-16-amine is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004161518422D          

 24 28  0  0  0  0            999 V2000
    6.2014   -0.2098    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7048   -0.8687    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.8860   -0.7681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3894   -1.4269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5706   -1.3263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2483   -0.5668    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7517   -1.2256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4295   -0.4662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9329   -1.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1141   -1.0244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7918   -0.2650    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7773   -1.0898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0117   -1.3310    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4848   -0.6551    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0117    0.0037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0262    0.8286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8152    1.0697    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2883    0.3939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1072    0.2932    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6037    0.9521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4226    0.8515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7449    0.0920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5637   -0.0086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3097   -0.6407    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
  6  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  2  0  0  0  0
 11 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 11 18  1  0  0  0  0
 18 19  1  0  0  0  0
  8 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
  6 22  1  0  0  0  0
 22 23  1  0  0  0  0
  3 23  1  0  0  0  0
 14 24  1  0  0  0  0
M  END

     RDKit          3D

 58 62  0  0  0  0  0  0  0  0999 V2000
    6.2905   -0.3723   -0.9223 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2552    0.0675   -1.7970 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9353    0.0777   -1.2743 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7579    1.0211   -0.0879 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2736    1.3054   -0.0057 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5127    0.0334    0.3784 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6326   -0.0991    1.8629 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0849   -1.1752   -0.2258 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3733   -2.2890   -0.2167 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0166   -2.2100    0.4237 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7430   -1.0294   -0.0768 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9115   -0.6394    0.7138 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9521   -1.5925    1.1238 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9852   -0.5193    1.6531 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0124    0.2832    0.3941 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7564    0.8440   -0.5260 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2332    0.9280   -0.5046 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8842    1.3733   -1.5616 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7457    0.3913   -1.4929 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6151    0.4400   -0.0044 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9165    1.7205    0.3455 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4731    1.4140    0.5660 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1128    0.2407   -0.1358 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4285   -1.2591   -0.8597 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8926    0.4908   -0.5074 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0457   -0.9217   -1.5599 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9602   -0.9740   -0.0765 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4988    1.0411   -2.1177 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2258    0.4646   -2.0508 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3414    1.9336   -0.1693 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0279    0.3990    0.8136 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9453    1.6868   -0.9910 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0788    2.0828    0.7834 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7080   -0.1805    2.4254 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1988    0.7574    2.3330 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2507   -0.9979    2.1637 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7387   -3.2059   -0.6430 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0652   -2.3021    1.5272 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5577   -3.1278    0.0931 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1038   -1.3034   -1.1137 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5631   -0.1534    1.7019 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6278   -2.2064    1.9770 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4412   -2.1638    0.3264 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4299    0.0546    2.3836 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9194   -0.9692    1.9178 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4893    1.9946   -0.2403 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7243    0.6084   -1.4226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6535    0.3168    0.3166 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0244    2.1768   -2.1511 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9520    0.8783   -2.0626 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0952   -0.5512   -1.9085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3225    2.2214    1.2431 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0245    2.4577   -0.4871 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2808    1.4237    1.6605 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1074    2.3120    0.1932 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2354    0.4988   -1.2136 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3168   -1.8905   -1.7786 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1262   -1.8064   -0.2045 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  1
  6 23  1  0
 23 22  1  0
 22 21  1  0
 20 21  1  6
 20 19  1  0
 19 18  1  0
 18 16  1  0
 16 17  1  0
 16 15  2  0
 15 14  1  0
 14 13  1  0
 13 12  1  0
 12 11  1  0
 11 10  1  0
 10  9  1  0
  9  8  2  0
  8 24  1  0
 24  3  1  0
  8  6  1  0
 11 23  1  0
 15 20  1  0
 12 20  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  2 28  1  0
  3 29  1  6
  4 30  1  0
  4 31  1  0
  5 32  1  0
  5 33  1  0
  7 34  1  0
  7 35  1  0
  7 36  1  0
 23 56  1  6
 22 54  1  0
 22 55  1  0
 21 52  1  0
 21 53  1  0
 19 50  1  0
 19 51  1  0
 18 49  1  0
 17 46  1  0
 17 47  1  0
 17 48  1  0
 14 44  1  0
 14 45  1  0
 13 42  1  0
 13 43  1  0
 12 41  1  1
 11 40  1  6
 10 38  1  0
 10 39  1  0
  9 37  1  0
 24 57  1  0
 24 58  1  0
M  END


  Mrv1533004161518422D          

 24 28  0  0  0  0            999 V2000
    6.2014   -0.2098    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7048   -0.8687    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.8860   -0.7681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3894   -1.4269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5706   -1.3263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2483   -0.5668    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7517   -1.2256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4295   -0.4662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9329   -1.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1141   -1.0244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7918   -0.2650    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7773   -1.0898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0117   -1.3310    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4848   -0.6551    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0117    0.0037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0262    0.8286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8152    1.0697    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2883    0.3939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1072    0.2932    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6037    0.9521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4226    0.8515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7449    0.0920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5637   -0.0086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3097   -0.6407    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
  6  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  2  0  0  0  0
 11 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 11 18  1  0  0  0  0
 18 19  1  0  0  0  0
  8 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
  6 22  1  0  0  0  0
 22 23  1  0  0  0  0
  3 23  1  0  0  0  0
 14 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0229333

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CNC1CCC2(C)C3CCC45CNC(C)=C4CCC5C3CC=C2C1

> <INCHI_IDENTIFIER>
InChI=1S/C22H34N2/c1-14-18-6-7-20-17-5-4-15-12-16(23-3)8-10-21(15,2)19(17)9-11-22(18,20)13-24-14/h4,16-17,19-20,23-24H,5-13H2,1-3H3

> <INCHI_KEY>
MWTHHJZKMUONAM-UHFFFAOYSA-N

> <FORMULA>
C22H34N2

> <MOLECULAR_WEIGHT>
326.528

> <EXACT_MASS>
326.272199103

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
41.037954366664195

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
N,6,13-trimethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosa-5,18-dien-16-amine

> <ALOGPS_LOGP>
3.97

> <JCHEM_LOGP>
2.8091925993333327

> <ALOGPS_LOGS>
-5.00

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
2

> <JCHEM_PKA_STRONGEST_BASIC>
10.782095054573517

> <JCHEM_POLAR_SURFACE_AREA>
24.06

> <JCHEM_REFRACTIVITY>
102.46619999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.27e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
N,6,13-trimethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosa-5,18-dien-16-amine

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0      11.576  -0.392   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0      10.649  -1.622   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0       9.120  -1.434   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.194  -2.664   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.665  -2.476   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.063  -1.058   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.137  -2.288   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.535  -0.870   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.608  -2.100   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.080  -1.912   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.478  -0.495   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.451  -2.034   0.000  0.00  0.00           C+0
HETATM   13  N   UNK     0      -0.022  -2.484   0.000  0.00  0.00           N+0
HETATM   14  C   UNK     0      -0.905  -1.223   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.022   0.007   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.049   1.547   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.522   1.997   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.405   0.735   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.933   0.547   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.860   1.777   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.389   1.589   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.990   0.172   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.519  -0.016   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -2.445  -1.196   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   23                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8   22                                             
CONECT    7    6                                                            
CONECT    8    6    9   19                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   15   18                                             
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   24                                                  
CONECT   15   14   11   16                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   11   19                                                  
CONECT   19   18    8   20                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21    6   23                                                  
CONECT   23   22    3                                                       
CONECT   24   14                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   56    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₃₄N₂

Average Mass

326.5280 Da

Monoisotopic Mass

326.27220 Da

IUPAC Name

N,6,13-trimethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosa-5,18-dien-16-amine

Traditional Name

N,6,13-trimethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosa-5,18-dien-16-amine

CAS Registry Number

Not Available

SMILES

CNC1CCC2(C)C3CCC45CNC(C)=C4CCC5C3CC=C2C1

InChI Identifier

InChI=1S/C22H34N2/c1-14-18-6-7-20-17-5-4-15-12-16(23-3)8-10-21(15,2)19(17)9-11-22(18,20)13-24-14/h4,16-17,19-20,23-24H,5-13H2,1-3H3

InChI Key

MWTHHJZKMUONAM-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
Holarrhena pubescens	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyrrolines. Pyrrolines are compounds containing a pyrroline ring, which is a five-member unsaturated aliphatic ring with one nitrogen atom and four carbon atoms.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Pyrrolines

Sub Class

Not Available

Direct Parent

Pyrrolines

Alternative Parents

Substituents

Pyrroline
Azacycle
Secondary amine
Enamine
Secondary aliphatic amine
Organic nitrogen compound
Organopnictogen compound
Hydrocarbon derivative
Organonitrogen compound
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	3.97	ALOGPS
logP	2.81	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Basic)	10.78	ChemAxon
Physiological Charge	2	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	24.06 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	102.47 m³·mol⁻¹	ChemAxon
Polarizability	41.04 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	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

12303828

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for n,6,13-trimethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosa-5,18-dien-16-amine (NP0229333)

MOL for NP0229333 (n,6,13-trimethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosa-5,18-dien-16-amine)

3D MOL for NP0229333 (n,6,13-trimethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosa-5,18-dien-16-amine)

3D SDF for NP0229333 (n,6,13-trimethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosa-5,18-dien-16-amine)

3D-SDF for NP0229333 (n,6,13-trimethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosa-5,18-dien-16-amine)

PDB for NP0229333 (n,6,13-trimethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosa-5,18-dien-16-amine)

3D PDB for NP0229333 (n,6,13-trimethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosa-5,18-dien-16-amine)

SMILES for NP0229333 (n,6,13-trimethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosa-5,18-dien-16-amine)

INCHI for NP0229333 (n,6,13-trimethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosa-5,18-dien-16-amine)

Structure for NP0229333 (n,6,13-trimethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosa-5,18-dien-16-amine)

3D Structure for NP0229333 (n,6,13-trimethyl-7-azapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icosa-5,18-dien-16-amine)