NP-MRD: Showing NP-Card for Planchonelline (NP0067734)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-04-28 12:35:04 UTC

Updated at

2022-04-28 12:35:04 UTC

NP-MRD ID

NP0067734

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Planchonelline

Description

[(1S,7aS)-hexahydro-1H-pyrrolizin-1-yl]methyl (2E)-3-(methylsulfanyl)prop-2-enoate 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. Planchonelline is found in Planchonella anteridifera, Planchonella thyrsoidea, Planchonella thyrsoides and Planchonella thysoidea C.T.White. Based on a literature review very few articles have been published on [(1S,7aS)-hexahydro-1H-pyrrolizin-1-yl]methyl (2E)-3-(methylsulfanyl)prop-2-enoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 35 36  0  0  0  0  0  0  0  0999 V2000
    7.0336    0.2317    0.5458 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0651   -0.5241   -0.7937 S   0  0  0  0  0  0  0  0  0  0  0  0
    4.4455    0.2375   -0.9184 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4707   -0.1074   -0.0937 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1452    0.5042   -0.1826 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8793    1.3657   -1.0280 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1739    0.1056    0.7006 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1438    0.5983    0.7408 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8761    0.3452   -0.5631 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8964   -1.1708   -0.7729 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3331   -1.5720   -0.8487 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0539   -0.3645   -1.1903 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3741   -0.4241   -0.6380 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4059    0.4630    0.5829 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9097    0.5844    0.8937 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3275    0.6705   -0.4794 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.3992    0.4117    1.4539 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4948    1.1991    0.2211 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8289   -0.4666    0.8779 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2179    0.9934   -1.6627 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7043   -0.8609    0.6454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1600    1.6777    1.0121 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6575    0.0722    1.5720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3558    0.8123   -1.4018 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4069   -1.7083    0.0651 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3210   -1.4391   -1.6844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4465   -2.2965   -1.6818 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7336   -1.9789    0.0868 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1655   -0.1267   -1.3761 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6352   -1.4552   -0.3134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7351    1.4759    0.2939 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9390    0.0404    1.4317 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7384    1.4552    1.5236 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6362   -0.3797    1.3745 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6073    1.6308   -0.9353 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  5  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  9  1  0
 16 12  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  3 20  1  0
  4 21  1  0
  8 22  1  0
  8 23  1  0
  9 24  1  6
 10 25  1  0
 10 26  1  0
 11 27  1  0
 11 28  1  0
 13 29  1  0
 13 30  1  0
 14 31  1  0
 14 32  1  0
 15 33  1  0
 15 34  1  0
 16 35  1  6
M  END


  Mrv1652304282214352D          

 16 17  0  0  1  0            999 V2000
   -0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4849   -0.6674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -1.3349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7846   -1.0799    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7846   -0.2549    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5692    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0542   -0.6674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5692   -1.3349    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8242   -2.1195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6312   -2.2910    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8861   -3.0756    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3341   -3.6887    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6931   -3.2472    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9480   -4.0318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7550   -4.2033    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    5.3070   -3.5902    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  6  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  6  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0067734

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CS\C=C\C(=O)OC[C@H]1CCN2CCC[C@@H]12

> <INCHI_IDENTIFIER>
InChI=1S/C12H19NO2S/c1-16-8-5-12(14)15-9-10-4-7-13-6-2-3-11(10)13/h5,8,10-11H,2-4,6-7,9H2,1H3/b8-5+/t10-,11+/m1/s1

> <INCHI_KEY>
CSBNFFCXWVMDOG-GGMAAXRASA-N

> <FORMULA>
C12H19NO2S

> <MOLECULAR_WEIGHT>
241.35

> <EXACT_MASS>
241.11365003

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
35

> <JCHEM_AVERAGE_POLARIZABILITY>
27.00610716824598

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
[(1S,7aS)-hexahydro-1H-pyrrolizin-1-yl]methyl (2E)-3-(methylsulfanyl)prop-2-enoate

> <ALOGPS_LOGP>
1.80

> <JCHEM_LOGP>
1.6955402853333335

> <ALOGPS_LOGS>
-2.81

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_BASIC>
10.23354971825914

> <JCHEM_POLAR_SURFACE_AREA>
29.54

> <JCHEM_REFRACTIVITY>
67.69010000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.77e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,7aS)-hexahydro-1H-pyrrolizin-1-ylmethyl (2E)-3-(methylsulfanyl)prop-2-enoate

> <JCHEM_VEBER_RULE>
1

$$$$

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      -0.000  -0.000   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.905  -1.246   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.000  -2.492   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.465  -2.016   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0       1.465  -0.476   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0       2.929   0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.834  -1.246   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.929  -2.492   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.405  -3.956   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       4.911  -4.277   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       5.387  -5.741   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       4.357  -6.886   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       6.894  -6.061   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.370  -7.526   0.000  0.00  0.00           C+0
HETATM   15  S   UNK     0       8.876  -7.846   0.000  0.00  0.00           S+0
HETATM   16  C   UNK     0       9.906  -6.702   0.000  0.00  0.00           C+0
CONECT    1    2    5                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
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                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15                                                            
MASTER        0    0    0    0    0    0    0    0   16    0   34    0
END

View in JSmol

Synonyms

Value	Source
[(1S,7AS)-hexahydro-1H-pyrrolizin-1-yl]methyl (2E)-3-(methylsulfanyl)prop-2-enoic acid	Generator
[(1S,7AS)-hexahydro-1H-pyrrolizin-1-yl]methyl (2E)-3-(methylsulphanyl)prop-2-enoate	Generator
[(1S,7AS)-hexahydro-1H-pyrrolizin-1-yl]methyl (2E)-3-(methylsulphanyl)prop-2-enoic acid	Generator

Chemical Formula

C₁₂H₁₉NO₂S

Average Mass

241.3500 Da

Monoisotopic Mass

241.11365 Da

IUPAC Name

[(1S,7aS)-hexahydro-1H-pyrrolizin-1-yl]methyl (2E)-3-(methylsulfanyl)prop-2-enoate

Traditional Name

(1S,7aS)-hexahydro-1H-pyrrolizin-1-ylmethyl (2E)-3-(methylsulfanyl)prop-2-enoate

CAS Registry Number

Not Available

SMILES

CS\C=C\C(=O)OC[C@H]1CCN2CCC[C@@H]12

InChI Identifier

InChI=1S/C12H19NO2S/c1-16-8-5-12(14)15-9-10-4-7-13-6-2-3-11(10)13/h5,8,10-11H,2-4,6-7,9H2,1H3/b8-5+/t10-,11+/m1/s1

InChI Key

CSBNFFCXWVMDOG-GGMAAXRASA-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
Planchonella anteridifera	Plant	KNApSAcK
Planchonella thyrsoidea	LOTUS Database	35616633
Planchonella thyrsoides	Plant	KNApSAcK
Planchonella thysoidea C.T.White	Plant	KNApSAcK

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
Vinylogous thioester
N-alkylpyrrolidine
Acrylic acid or derivatives
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Pyrrolidine
Tertiary aliphatic amine
Thioenolether
Tertiary amine
Carboxylic acid ester
Amino acid or derivatives
Azacycle
Sulfenyl compound
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organosulfur compound
Organooxygen compound
Organonitrogen compound
Carbonyl group
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	1.8	ALOGPS
logP	1.7	ChemAxon
logS	-2.8	ALOGPS
pKa (Strongest Basic)	10.23	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	29.54 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	67.69 m³·mol⁻¹	ChemAxon
Polarizability	27.01 Å³	ChemAxon
Number of Rings	2	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

162930166

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Planchonelline (NP0067734)

MOL for NP0067734 (Planchonelline)

3D MOL for NP0067734 (Planchonelline)

3D SDF for NP0067734 (Planchonelline)

3D-SDF for NP0067734 (Planchonelline)

PDB for NP0067734 (Planchonelline)

3D PDB for NP0067734 (Planchonelline)

SMILES for NP0067734 (Planchonelline)

INCHI for NP0067734 (Planchonelline)

Structure for NP0067734 (Planchonelline)

3D Structure for NP0067734 (Planchonelline)