NP-MRD: Showing NP-Card for (+)-Broussonetine N (NP0072756)

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Record Information

Version

2.0

Created at

2022-04-28 18:03:11 UTC

Updated at

2022-04-28 18:03:11 UTC

NP-MRD ID

NP0072756

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-Broussonetine N

Description

(10R)-1,10-Dihydroxy-10-[(3S,7aalpha)-5alpha-(hydroxymethyl)-6beta,7alpha-dihydroxyhexahydro-1H-pyrrolizine-3beta-yl]-5-decanone belongs to the class of organic compounds known as pyrrolizidines. Pyrrolizidines are compounds containing a pyrrolizidine, which is a bicyclic ring system made up of two fused pyrrolidine ring sharing a nitrogen atom. (+)-Broussonetine N is found in Broussonetia kazinoki, Broussonetia kazinoki SIEB. and Broussonetia papyrifera. Based on a literature review very few articles have been published on (10R)-1,10-Dihydroxy-10-[(3S,7aalpha)-5alpha-(hydroxymethyl)-6beta,7alpha-dihydroxyhexahydro-1H-pyrrolizine-3beta-yl]-5-decanone.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 58 59  0  0  0  0  0  0  0  0999 V2000
    2.8922   -3.0035   -0.4254 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3364   -1.8762   -0.3071 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8073   -1.7334   -0.1916 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2251   -0.2855   -0.0517 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7389   -0.2324    0.0606 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1632    1.2194    0.2024 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5451    1.2560    0.3053 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4139   -0.6984   -0.2814 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8050   -0.6306    1.0891 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8546    0.5153    1.2545 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3185    0.4781    0.3017 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0971   -0.7767    0.5204 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5486   -0.7852    1.8378 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3024   -0.8970   -0.3865 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9113   -0.7733   -1.8502 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6244    0.5043   -2.3340 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8372    0.4113   -1.4570 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.5074    1.6938   -1.1260 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.4954    2.0766   -2.0062 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0925    1.3108    0.2454 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.0015    2.3502    1.1420 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2525    0.1041    0.7046 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.0581   -1.1541    0.6784 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0969   -1.0376    1.6130 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1604    0.1814   -0.1652 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.2166   -2.2621    0.7151 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2945   -2.1536   -1.0962 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9141    0.3160   -0.9386 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8083    0.1590    0.8757 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0190   -0.7590    1.0063 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2151   -0.7083   -0.8198 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7092    1.6126    1.1401 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8269    1.7925   -0.6905 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8595    1.7353    1.1135 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6619   -0.8799   -1.0784 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9243    0.2365   -0.5154 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6521   -0.4339    1.8004 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3760   -1.5931    1.3993 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4213    1.4741    1.1725 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5038    0.4854    2.3262 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1301    0.4539   -0.7287 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8984    1.4030    0.4758 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4055   -1.6346    0.4114 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5650    0.1492    2.1592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7576   -1.8874   -0.1706 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8475   -0.7616   -2.0357 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4193   -1.6196   -2.3828 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0168    1.3653   -2.0357 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8386    0.4321   -3.4093 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5054   -0.3980   -1.7277 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7363    2.4667   -0.9434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1085    2.7456   -2.6188 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1041    0.9384    0.0530 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8718    2.4331    1.6050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9240    0.2640    1.7565 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5177   -1.4037   -0.2749 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4255   -1.9836    0.9941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0681   -0.2013    2.1179 H   0  0  0  0  0  0  0  0  0  0  0  0
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  2  0
  2  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 23 24  1  0
 22 25  1  0
 25 14  1  0
 25 17  1  0
  7 34  1  0
  6 32  1  0
  6 33  1  0
  5 30  1  0
  5 31  1  0
  4 28  1  0
  4 29  1  0
  3 26  1  0
  3 27  1  0
  8 35  1  0
  8 36  1  0
  9 37  1  0
  9 38  1  0
 10 39  1  0
 10 40  1  0
 11 41  1  0
 11 42  1  0
 12 43  1  1
 13 44  1  0
 14 45  1  6
 15 46  1  0
 15 47  1  0
 16 48  1  0
 16 49  1  0
 17 50  1  6
 18 51  1  1
 19 52  1  0
 20 53  1  6
 21 54  1  0
 22 55  1  1
 23 56  1  0
 23 57  1  0
 24 58  1  0
M  END


  Mrv1652304282220032D          

 25 26  0  0  1  0            999 V2000
   -0.9813    1.0689    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8950    0.2485    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0881    0.0769    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3244    0.7914    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2276    1.4045    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1849    2.1190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9919    1.9475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0781    1.1270    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7926    0.7145    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7926   -0.1105    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5070    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2215    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9360    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6505    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3649    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3649    1.9520    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0794    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7939    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5083    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2228    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9373    0.7145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2475   -0.6767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0680   -0.7630    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5081   -0.3036    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6958    1.4814    0.0000 O   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
  5  4  1  1  0  0  0
  1  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
  4  8  1  0  0  0  0
  8  9  1  1  0  0  0
  9 10  1  1  0  0  0
  9 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  2  0  0  0  0
 15 17  1  0  0  0  0
 17 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
  3 22  1  6  0  0  0
 22 23  1  0  0  0  0
  2 24  1  1  0  0  0
  1 25  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0072756

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OCCCCC(=O)CCCC[C@@H](O)[C@@H]1CC[C@@H]2[C@@H](O)[C@H](O)[C@@H](CO)N12

> <INCHI_IDENTIFIER>
InChI=1S/C18H33NO6/c20-10-4-3-6-12(22)5-1-2-7-16(23)13-8-9-14-17(24)18(25)15(11-21)19(13)14/h13-18,20-21,23-25H,1-11H2/t13-,14+,15+,16+,17+,18+/m0/s1

> <INCHI_KEY>
WGEIJHUJKRVXNI-IWGURSETSA-N

> <FORMULA>
C18H33NO6

> <MOLECULAR_WEIGHT>
359.463

> <EXACT_MASS>
359.230787787

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
40.21196454117981

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(10R)-10-[(3S,5R,6R,7R,7aR)-6,7-dihydroxy-5-(hydroxymethyl)-hexahydro-1H-pyrrolizin-3-yl]-1,10-dihydroxydecan-5-one

> <ALOGPS_LOGP>
-0.27

> <JCHEM_LOGP>
-0.6019489763333337

> <ALOGPS_LOGS>
-1.51

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
14.267244957589241

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.197296132418675

> <JCHEM_PKA_STRONGEST_BASIC>
8.665377589799897

> <JCHEM_POLAR_SURFACE_AREA>
121.46000000000001

> <JCHEM_REFRACTIVITY>
92.80019999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.12e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(10R)-10-[(3S,5R,6R,7R,7aR)-6,7-dihydroxy-5-(hydroxymethyl)-hexahydro-1H-pyrrolizin-3-yl]-1,10-dihydroxydecan-5-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      -1.832   1.995   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.671   0.464   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.164   0.144   0.000  0.00  0.00           C+0
HETATM    4  N   UNK     0       0.606   1.477   0.000  0.00  0.00           N+0
HETATM    5  C   UNK     0      -0.425   2.622   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.345   3.955   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.851   3.635   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.012   2.104   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.346   1.334   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       3.346  -0.206   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       4.680   2.104   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.013   1.334   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.347   2.104   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.681   1.334   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.015   2.104   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      10.015   3.644   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      11.348   1.334   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      12.682   2.104   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      14.016   1.334   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      15.349   2.104   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      16.683   1.334   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       0.462  -1.263   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       1.994  -1.424   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0      -2.815  -0.567   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0      -3.165   2.765   0.000  0.00  0.00           O+0
CONECT    1    2    5   25                                                  
CONECT    2    1    3   24                                                  
CONECT    3    2    4   22                                                  
CONECT    4    3    5    8                                                  
CONECT    5    4    1    6                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    4    9                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20                                                            
CONECT   22    3   23                                                       
CONECT   23   22                                                            
CONECT   24    2                                                            
CONECT   25    1                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   52    0
END

View in JSmol

Synonyms

Value	Source
(10R)-1,10-Dihydroxy-10-[(3S,7aalpha)-5a-(hydroxymethyl)-6b,7a-dihydroxyhexahydro-1H-pyrrolizine-3b-yl]-5-decanone	Generator
(10R)-1,10-Dihydroxy-10-[(3S,7aalpha)-5α-(hydroxymethyl)-6β,7α-dihydroxyhexahydro-1H-pyrrolizine-3β-yl]-5-decanone	Generator

Chemical Formula

C₁₈H₃₃NO₆

Average Mass

359.4630 Da

Monoisotopic Mass

359.23079 Da

IUPAC Name

(10R)-10-[(3S,5R,6R,7R,7aR)-6,7-dihydroxy-5-(hydroxymethyl)-hexahydro-1H-pyrrolizin-3-yl]-1,10-dihydroxydecan-5-one

Traditional Name

(10R)-10-[(3S,5R,6R,7R,7aR)-6,7-dihydroxy-5-(hydroxymethyl)-hexahydro-1H-pyrrolizin-3-yl]-1,10-dihydroxydecan-5-one

CAS Registry Number

Not Available

SMILES

OCCCCC(=O)CCCC[C@@H](O)[C@@H]1CC[C@@H]2[C@@H](O)[C@H](O)[C@@H](CO)N12

InChI Identifier

InChI=1S/C18H33NO6/c20-10-4-3-6-12(22)5-1-2-7-16(23)13-8-9-14-17(24)18(25)15(11-21)19(13)14/h13-18,20-21,23-25H,1-11H2/t13-,14+,15+,16+,17+,18+/m0/s1

InChI Key

WGEIJHUJKRVXNI-IWGURSETSA-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
Broussonetia kazinoki	LOTUS Database	35616633
Broussonetia kazinoki SIEB.	Plant	KNApSAcK
Broussonetia papyrifera	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyrrolizidines. Pyrrolizidines are compounds containing a pyrrolizidine, which is a bicyclic ring system made up of two fused pyrrolidine ring sharing a nitrogen atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Pyrrolizidines

Sub Class

Not Available

Direct Parent

Pyrrolizidines

Alternative Parents

Substituents

Pyrrolizidine
N-alkylpyrrolidine
Pyrrolidine
1,2-aminoalcohol
Ketone
Secondary alcohol
Tertiary amine
Tertiary aliphatic amine
Azacycle
Organic oxygen compound
Organic nitrogen compound
Primary alcohol
Organooxygen compound
Organonitrogen compound
Alcohol
Amine
Carbonyl group
Organic oxide
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	-0.27	ALOGPS
logP	-0.6	ChemAxon
logS	-1.5	ALOGPS
pKa (Strongest Acidic)	13.2	ChemAxon
pKa (Strongest Basic)	8.67	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	121.46 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	92.8 m³·mol⁻¹	ChemAxon
Polarizability	40.21 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	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

8174159

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

9998578

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (+)-Broussonetine N (NP0072756)

MOL for NP0072756 ((+)-Broussonetine N)

3D MOL for NP0072756 ((+)-Broussonetine N)

3D SDF for NP0072756 ((+)-Broussonetine N)

3D-SDF for NP0072756 ((+)-Broussonetine N)

PDB for NP0072756 ((+)-Broussonetine N)

3D PDB for NP0072756 ((+)-Broussonetine N)

SMILES for NP0072756 ((+)-Broussonetine N)

INCHI for NP0072756 ((+)-Broussonetine N)

Structure for NP0072756 ((+)-Broussonetine N)

3D Structure for NP0072756 ((+)-Broussonetine N)