NP-MRD: Showing NP-Card for 6-trans-Piperamide-C-7-1 (NP0046941)

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Record Information

Version

2.0

Created at

2022-03-17 20:32:01 UTC

Updated at

2022-03-17 20:32:01 UTC

NP-MRD ID

NP0046941

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6-trans-Piperamide-C-7-1

Description

6-trans-Piperamide-C-7-1 is found in Piper nigrum.

Structure

MOL SDF PDB SMILES InChI


  Mrv0541 02241212572D          

 22 24  0  0  0  0            999 V2000
   -4.7437    0.3536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4582   -0.0589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4582   -0.8839    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7437   -1.2964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0293   -0.8839    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0293   -0.0589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2428    0.1960    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7277   -0.4715    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2428   -1.1389    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3148    0.3536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6003   -0.0589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8859    0.3536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1714   -0.0589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4569    0.3536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2575   -0.0589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9720    0.3536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6865   -0.0589    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3539    0.4260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9414   -0.8435    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7664   -0.8435    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0213   -0.0589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9720    1.1786    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  1  6  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  9  3  1  0  0  0  0
  2  3  1  0  0  0  0
  7  2  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  6 10  1  0  0  0  0
 10 11  2  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
 18 17  1  0  0  0  0
 17 19  1  0  0  0  0
 18 21  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 16 22  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0046941

> <DATABASE_NAME>
NP-MRD

> <SMILES>
O=C(CCCC\C=C\C1=CC=C2OCOC2=C1)N1CCCC1

> <INCHI_IDENTIFIER>
InChI=1S/C18H23NO3/c20-18(19-11-5-6-12-19)8-4-2-1-3-7-15-9-10-16-17(13-15)22-14-21-16/h3,7,9-10,13H,1-2,4-6,8,11-12,14H2/b7-3+

> <INCHI_KEY>
UUHCCOYKUNWUQJ-XVNBXDOJSA-N

> <FORMULA>
C18H23NO3

> <MOLECULAR_WEIGHT>
301.3801

> <EXACT_MASS>
301.167793607

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_AVERAGE_POLARIZABILITY>
34.89406853712768

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(6E)-7-(2H-1,3-benzodioxol-5-yl)-1-(pyrrolidin-1-yl)hept-6-en-1-one

> <ALOGPS_LOGP>
3.77

> <JCHEM_LOGP>
3.2240562256666676

> <ALOGPS_LOGS>
-3.60

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
0.12429010231280802

> <JCHEM_POLAR_SURFACE_AREA>
38.77

> <JCHEM_REFRACTIVITY>
86.41069999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.64e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(6E)-7-(2H-1,3-benzodioxol-5-yl)-1-(pyrrolidin-1-yl)hept-6-en-1-one

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0      -8.855   0.660   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -10.189  -0.110   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -10.189  -1.650   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -8.855  -2.420   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -7.521  -1.650   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -7.521  -0.110   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0     -11.653   0.366   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0     -12.558  -0.880   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0     -11.653  -2.126   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -6.188   0.660   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -4.854  -0.110   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -3.520   0.660   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.187  -0.110   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.853   0.660   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.481  -0.110   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.814   0.660   0.000  0.00  0.00           C+0
HETATM   17  N   UNK     0       3.148  -0.110   0.000  0.00  0.00           N+0
HETATM   18  C   UNK     0       4.394   0.795   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.624  -1.575   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.164  -1.575   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.640  -0.110   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       1.814   2.200   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3    7                                                  
CONECT    3    4    9    2                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    1    5   10                                                  
CONECT    7    2    8                                                       
CONECT    8    7    9                                                       
CONECT    9    3    8                                                       
CONECT   10    6   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   22                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17   21                                                       
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   18   20                                                       
CONECT   22   16                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   48    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₂₃NO₃

Average Mass

301.3801 Da

Monoisotopic Mass

301.16779 Da

IUPAC Name

(6E)-7-(2H-1,3-benzodioxol-5-yl)-1-(pyrrolidin-1-yl)hept-6-en-1-one

Traditional Name

(6E)-7-(2H-1,3-benzodioxol-5-yl)-1-(pyrrolidin-1-yl)hept-6-en-1-one

CAS Registry Number

Not Available

SMILES

O=C(CCCC\C=C\C1=CC=C2OCOC2=C1)N1CCCC1

InChI Identifier

InChI=1S/C18H23NO3/c20-18(19-11-5-6-12-19)8-4-2-1-3-7-15-9-10-16-17(13-15)22-14-21-16/h3,7,9-10,13H,1-2,4-6,8,11-12,14H2/b7-3+

InChI Key

UUHCCOYKUNWUQJ-XVNBXDOJSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Piper nigrum	LOTUS Database	35616633
Piper nigrum L.	FooDB	Dr. Duke's Phytochemical and Ethnobotanical Databases

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzodioxoles. These are organic compounds containing a benzene ring fused to either isomers of dioxole. Dioxole is a five-membered unsaturated ring of two oxygen atoms and three carbon atoms.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzodioxoles

Sub Class

Not Available

Direct Parent

Benzodioxoles

Alternative Parents

Substituents

Benzodioxole
N-acylpyrrolidine
Styrene
Benzenoid
Pyrrolidine
Tertiary carboxylic acid amide
Carboxamide group
Acetal
Carboxylic acid derivative
Oxacycle
Azacycle
Organooxygen compound
Organonitrogen compound
Organopnictogen compound
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organic nitrogen compound
Carbonyl group
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	3.77	ALOGPS
logP	3.22	ChemAxon
logS	-3.6	ALOGPS
pKa (Strongest Basic)	0.12	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	38.77 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	86.41 m³·mol⁻¹	ChemAxon
Polarizability	34.89 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB006610

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

10957591

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 6-trans-Piperamide-C-7-1 (NP0046941)

MOL for NP0046941 (6-trans-Piperamide-C-7-1)

3D MOL for NP0046941 (6-trans-Piperamide-C-7-1)

3D SDF for NP0046941 (6-trans-Piperamide-C-7-1)

3D-SDF for NP0046941 (6-trans-Piperamide-C-7-1)

PDB for NP0046941 (6-trans-Piperamide-C-7-1)

3D PDB for NP0046941 (6-trans-Piperamide-C-7-1)

SMILES for NP0046941 (6-trans-Piperamide-C-7-1)

INCHI for NP0046941 (6-trans-Piperamide-C-7-1)

Structure for NP0046941 (6-trans-Piperamide-C-7-1)

3D Structure for NP0046941 (6-trans-Piperamide-C-7-1)