NP-MRD: Showing NP-Card for (2e)-3-(2h-1,3-benzodioxol-5-yl)-n-cyclohexylprop-2-enimidic acid (NP0228060)

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Record Information

Version

2.0

Created at

2022-09-06 07:34:37 UTC

Updated at

2022-09-06 07:34:37 UTC

NP-MRD ID

NP0228060

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2e)-3-(2h-1,3-benzodioxol-5-yl)-n-cyclohexylprop-2-enimidic acid

Description

CHEMBL2203918 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. (2e)-3-(2h-1,3-benzodioxol-5-yl)-n-cyclohexylprop-2-enimidic acid is found in Piper nigrum. Based on a literature review very few articles have been published on CHEMBL2203918.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 39 41  0  0  0  0  0  0  0  0999 V2000
   -1.3037   -0.3402    0.7491 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8869    0.4403   -0.3171 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5333    0.5239   -0.6867 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4683   -0.1271   -0.0354 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8914   -0.0895   -0.3473 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4093    0.6547   -1.3864 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7833    0.6128   -1.5883 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6396   -0.1250   -0.8125 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1027   -0.8582    0.2161 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7502   -0.8329    0.4351 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1357   -1.5299    0.8754 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3394   -0.9014    0.4886 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0121   -0.3608   -0.7686 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7569    1.0906   -0.9794 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1766    1.0734   -0.6940 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6963   -0.3017   -0.8781 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8336   -0.7010   -0.0243 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8688   -0.1216    1.3399 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7633    1.4030    1.2296 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3977    1.6824    0.6458 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8506   -1.2411    0.9043 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8263    1.1397   -1.5212 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1239   -0.7335    0.7967 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7691    1.2407   -2.0099 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2094    1.1873   -2.3954 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3492   -1.4164    1.2488 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1195   -1.6802    0.4069 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6122   -0.0926    1.2044 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6389    1.7638   -1.4623 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0326   -0.3965   -1.9538 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8906   -1.0798   -0.7919 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8296   -0.4908   -0.5074 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8278   -1.8256    0.0871 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8724   -0.3156    1.7804 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1103   -0.4948    2.0365 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5528    1.7778    0.5560 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7901    1.8576    2.2371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6440    1.4510    1.4079 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3513    2.8040    0.5144 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
  6  7  1  0
  7  8  2  0
  8 13  1  0
 13 12  1  0
 12 11  1  0
 11  9  1  0
  9 10  2  0
  2 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 10  5  1  0
 20 15  1  0
  9  8  1  0
  1 21  1  0
  3 22  1  0
  4 23  1  0
  6 24  1  0
  7 25  1  0
 12 27  1  0
 12 28  1  0
 10 26  1  0
 15 29  1  0
 16 30  1  0
 16 31  1  0
 17 32  1  0
 17 33  1  0
 18 34  1  0
 18 35  1  0
 19 36  1  0
 19 37  1  0
 20 38  1  0
 20 39  1  0
M  END


  Mrv1652309062209342D          

 20 22  0  0  0  0            999 V2000
    6.2102    1.9354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    2.1904    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    0.8555    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957    3.1729    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.2102    3.5854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2102    4.4104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9246    4.8229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6391    4.4104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6391    3.5854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9246    3.1729    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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  5 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
  8 13  1  0  0  0  0
  2 14  2  0  0  0  0
 14 15  1  4  0  0  0
 15 16  1  0  0  0  0
 16 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
 15 20  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0228060

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC(\C=C\C1=CC=C2OCOC2=C1)=NC1CCCCC1

> <INCHI_IDENTIFIER>
InChI=1S/C16H19NO3/c18-16(17-13-4-2-1-3-5-13)9-7-12-6-8-14-15(10-12)20-11-19-14/h6-10,13H,1-5,11H2,(H,17,18)/b9-7+

> <INCHI_KEY>
HEVXIAMRBRLSEJ-VQHVLOKHSA-N

> <FORMULA>
C16H19NO3

> <MOLECULAR_WEIGHT>
273.332

> <EXACT_MASS>
273.136493476

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
30.70506743694495

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2E)-3-(2H-1,3-benzodioxol-5-yl)-N-cyclohexylprop-2-enimidic acid

> <JCHEM_LOGP>
3.3988998501003165

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.276282495198178

> <JCHEM_PKA_STRONGEST_BASIC>
4.363247360718351

> <JCHEM_POLAR_SURFACE_AREA>
51.05

> <JCHEM_REFRACTIVITY>
77.08160000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2E)-3-(2H-1,3-benzodioxol-5-yl)-N-cyclohexylprop-2-enimidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  O   UNK     0      11.592   3.613   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      10.259   4.383   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.925   3.613   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.591   4.383   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.258   3.613   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.258   2.073   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.924   1.303   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.590   2.073   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.590   3.613   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.924   4.383   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       2.126   4.089   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       1.220   2.843   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       2.126   1.597   0.000  0.00  0.00           O+0
HETATM   14  N   UNK     0      10.259   5.923   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0      11.592   6.693   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      11.592   8.233   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      12.926   9.003   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      14.260   8.233   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      14.260   6.693   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      12.926   5.923   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   14                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   10                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   13                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9    5                                                       
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12    8                                                       
CONECT   14    2   15                                                       
CONECT   15   14   16   20                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   15                                                       
MASTER        0    0    0    0    0    0    0    0   20    0   44    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₆H₁₉NO₃

Average Mass

273.3320 Da

Monoisotopic Mass

273.13649 Da

IUPAC Name

(2E)-3-(2H-1,3-benzodioxol-5-yl)-N-cyclohexylprop-2-enimidic acid

Traditional Name

(2E)-3-(2H-1,3-benzodioxol-5-yl)-N-cyclohexylprop-2-enimidic acid

CAS Registry Number

Not Available

SMILES

OC(\C=C\C1=CC=C2OCOC2=C1)=NC1CCCCC1

InChI Identifier

InChI=1S/C16H19NO3/c18-16(17-13-4-2-1-3-5-13)9-7-12-6-8-14-15(10-12)20-11-19-14/h6-10,13H,1-5,11H2,(H,17,18)/b9-7+

InChI Key

HEVXIAMRBRLSEJ-VQHVLOKHSA-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
Piper nigrum	LOTUS Database	35616633

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
Styrene
Benzenoid
Carboxamide group
Secondary carboxylic acid amide
Oxacycle
Carboxylic acid derivative
Acetal
Organopnictogen compound
Organic oxygen compound
Organooxygen compound
Organonitrogen compound
Carbonyl group
Organic nitrogen compound
Hydrocarbon derivative
Organic oxide
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	3.4	ChemAxon
pKa (Strongest Acidic)	6.28	ChemAxon
pKa (Strongest Basic)	4.36	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	51.05 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	77.08 m³·mol⁻¹	ChemAxon
Polarizability	30.71 Å³	ChemAxon
Number of Rings	3	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

603568

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

692702

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2e)-3-(2h-1,3-benzodioxol-5-yl)-n-cyclohexylprop-2-enimidic acid (NP0228060)

MOL for NP0228060 ((2e)-3-(2h-1,3-benzodioxol-5-yl)-n-cyclohexylprop-2-enimidic acid)

3D MOL for NP0228060 ((2e)-3-(2h-1,3-benzodioxol-5-yl)-n-cyclohexylprop-2-enimidic acid)

3D SDF for NP0228060 ((2e)-3-(2h-1,3-benzodioxol-5-yl)-n-cyclohexylprop-2-enimidic acid)

3D-SDF for NP0228060 ((2e)-3-(2h-1,3-benzodioxol-5-yl)-n-cyclohexylprop-2-enimidic acid)

PDB for NP0228060 ((2e)-3-(2h-1,3-benzodioxol-5-yl)-n-cyclohexylprop-2-enimidic acid)

3D PDB for NP0228060 ((2e)-3-(2h-1,3-benzodioxol-5-yl)-n-cyclohexylprop-2-enimidic acid)

SMILES for NP0228060 ((2e)-3-(2h-1,3-benzodioxol-5-yl)-n-cyclohexylprop-2-enimidic acid)

INCHI for NP0228060 ((2e)-3-(2h-1,3-benzodioxol-5-yl)-n-cyclohexylprop-2-enimidic acid)

Structure for NP0228060 ((2e)-3-(2h-1,3-benzodioxol-5-yl)-n-cyclohexylprop-2-enimidic acid)

3D Structure for NP0228060 ((2e)-3-(2h-1,3-benzodioxol-5-yl)-n-cyclohexylprop-2-enimidic acid)