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Showing NP-Card for 2-Amino-5-chloro-5-hexenoic acid (NP0078192)

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Record Information
Version2.0
Created at2022-04-28 23:18:45 UTC
Updated at2022-04-28 23:18:45 UTC
NP-MRD IDNP0078192
Secondary Accession NumbersNone
Natural Product Identification
Common Name2-Amino-5-chloro-5-hexenoic acid
Description(2R)-2-amino-5-chlorohex-5-enoic acid belongs to the class of organic compounds known as d-alpha-amino acids. These are alpha amino acids which have the D-configuration of the alpha-carbon atom. 2-Amino-5-chloro-5-hexenoic acid is found in Amanita miculifera. Based on a literature review very few articles have been published on (2R)-2-amino-5-chlorohex-5-enoic acid.
Structure
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MOL3D MOLSDFPDBSMILESInChI

MOL for NP0078192 (2-Amino-5-chloro-5-hexenoic acid)


  Mrv1652304292201182D          

 10  9  0  0  1  0            999 V2000
    1.7605    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4750    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4750    0.6039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1895    1.8414    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9039    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6184    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3329    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0474    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3329    0.6039    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    3.1895    2.6664    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  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
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  4 10  1  6  0  0  0
M  END
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3D MOL for NP0078192 (2-Amino-5-chloro-5-hexenoic acid)

     RDKit          3D

 20 19  0  0  0  0  0  0  0  0999 V2000
    2.7817   -0.9563    0.7883 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4986   -0.4626   -0.3971 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7592   -0.2962   -1.6204 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    1.1302   -0.0170   -0.7906 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1676   -0.2125    0.3314 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2098    0.2410   -0.0784 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7350   -0.4616   -1.2002 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1023    0.0727    1.0866 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8460    0.6019    2.1927 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2508   -0.6835    0.9699 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9951   -1.0516    1.5284 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7796   -1.2598    1.0166 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1650    1.0459   -1.0793 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8455   -0.6313   -1.6696 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4738    0.4383    1.1866 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1345   -1.2654    0.6454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1266    1.3416   -0.2864 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1542   -0.4700   -2.0391 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2549   -1.3163   -0.9894 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0513   -0.4378    0.4046 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  2  1  0
  2  3  1  0
  2  1  2  3
  6  8  1  0
  8 10  1  0
  8  9  2  0
  7 18  1  0
  7 19  1  0
  6 17  1  6
  5 15  1  0
  5 16  1  0
  4 13  1  0
  4 14  1  0
  1 11  1  0
  1 12  1  0
 10 20  1  0
M  END
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3D SDF for NP0078192 (2-Amino-5-chloro-5-hexenoic acid)


  Mrv1652304292201182D          

 10  9  0  0  1  0            999 V2000
    1.7605    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4750    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4750    0.6039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1895    1.8414    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9039    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6184    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3329    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0474    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3329    0.6039    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    3.1895    2.6664    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  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
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  4 10  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0078192

> <DATABASE_NAME>
NP-MRD

> <SMILES>
N[C@H](CCC(Cl)=C)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C6H10ClNO2/c1-4(7)2-3-5(8)6(9)10/h5H,1-3,8H2,(H,9,10)/t5-/m1/s1

> <INCHI_KEY>
IFFHOISHOWGDDA-RXMQYKEDSA-N

> <FORMULA>
C6H10ClNO2

> <MOLECULAR_WEIGHT>
163.6

> <EXACT_MASS>
163.0400063

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
20

> <JCHEM_AVERAGE_POLARIZABILITY>
15.502588947802966

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R)-2-amino-5-chlorohex-5-enoic acid

> <ALOGPS_LOGP>
-1.89

> <JCHEM_LOGP>
-1.652648048912468

> <ALOGPS_LOGS>
-0.53

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.1122025349748887

> <JCHEM_PKA_STRONGEST_BASIC>
9.515887939737581

> <JCHEM_POLAR_SURFACE_AREA>
63.31999999999999

> <JCHEM_REFRACTIVITY>
39.13759999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.87e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R)-2-amino-5-chlorohex-5-enoic acid

> <JCHEM_VEBER_RULE>
0

$$$$
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3D-SDF for NP0078192 (2-Amino-5-chloro-5-hexenoic acid)

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PDB for NP0078192 (2-Amino-5-chloro-5-hexenoic acid)
HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  O   UNK     0       3.286   3.437   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       4.620   2.667   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       4.620   1.127   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       5.954   3.437   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.287   2.667   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.621   3.437   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.955   2.667   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      11.288   3.437   0.000  0.00  0.00           C+0
HETATM    9 Cl   UNK     0       9.955   1.127   0.000  0.00  0.00          Cl+0
HETATM   10  N   UNK     0       5.954   4.977   0.000  0.00  0.00           N+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   10                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    4                                                            
MASTER        0    0    0    0    0    0    0    0   10    0   18    0
END

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3D PDB for NP0078192 (2-Amino-5-chloro-5-hexenoic acid)
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SMILES for NP0078192 (2-Amino-5-chloro-5-hexenoic acid)
N[C@H](CCC(Cl)=C)C(O)=O
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INCHI for NP0078192 (2-Amino-5-chloro-5-hexenoic acid)
InChI=1S/C6H10ClNO2/c1-4(7)2-3-5(8)6(9)10/h5H,1-3,8H2,(H,9,10)/t5-/m1/s1
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View in JSmol
Synonyms
ValueSource
(2R)-2-Amino-5-chlorohex-5-enoateGenerator
Chemical FormulaC6H10ClNO2
Average Mass163.6000 Da
Monoisotopic Mass163.04001 Da
IUPAC Name(2R)-2-amino-5-chlorohex-5-enoic acid
Traditional Name(2R)-2-amino-5-chlorohex-5-enoic acid
CAS Registry NumberNot Available
SMILES
N[C@H](CCC(Cl)=C)C(O)=O
InChI Identifier
InChI=1S/C6H10ClNO2/c1-4(7)2-3-5(8)6(9)10/h5H,1-3,8H2,(H,9,10)/t5-/m1/s1
InChI KeyIFFHOISHOWGDDA-RXMQYKEDSA-N
Experimental Spectra
Not Available
Predicted Spectra
Spectrum TypeDescriptionDepositor IDDepositor OrganizationDepositorDeposition DateView
1D NMR13C NMR Spectrum (1D, 25 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 252 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 1000 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 50 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 200 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 75 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 300 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 101 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 400 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 126 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 500 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 151 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 600 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 176 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 700 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 201 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 800 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 226 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
Chemical Shift Submissions
Not Available
Species
Species of Origin
Species NameSourceReference
Amanita miculiferaFungi
Chemical Taxonomy
Description Belongs to the class of organic compounds known as d-alpha-amino acids. These are alpha amino acids which have the D-configuration of the alpha-carbon atom.
KingdomOrganic compounds  
Super ClassOrganic acids and derivatives  
ClassCarboxylic acids and derivatives  
Sub ClassAmino acids, peptides, and analogues  
Direct ParentD-alpha-amino acids  
Alternative Parents
Substituents
  • D-alpha-amino acid
    • 

  • Medium-chain fatty acid
    • 

  • Halogenated fatty acid
    • 

  • Fatty acyl
    • 

  • Fatty acid
    • 

  • Unsaturated fatty acid
    • 

  • Amino acid
    • 

  • Chloroalkene
    • 

  • Haloalkene
    • 

  • Vinyl halide
    • 

  • Vinyl chloride
    • 

  • Monocarboxylic acid or derivatives
    • 

  • Carboxylic acid
    • 

  • Organic nitrogen compound
    • 

  • Organic oxygen compound
    • 

  • Organopnictogen compound
    • 

  • Organic oxide
    • 

  • Hydrocarbon derivative
    • 

  • Primary amine
    • 

  • Organooxygen compound
    • 

  • Organonitrogen compound
    • 

  • Organochloride
    • 

  • Organohalogen compound
    • 

  • Primary aliphatic amine
    • 

  • Carbonyl group
    • 

  • Amine
    • 

  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic compounds
External DescriptorsNot Available
Physical Properties
StateNot Available
Experimental Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Predicted Properties
PropertyValueSource
logP-1.9ALOGPS
logP-1.7ChemAxon
logS-0.53ALOGPS
pKa (Strongest Acidic)2.11ChemAxon
pKa (Strongest Basic)9.52ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count3ChemAxon
Hydrogen Donor Count2ChemAxon
Polar Surface Area63.32 ŲChemAxon
Rotatable Bond Count4ChemAxon
Refractivity39.14 m³·mol⁻¹ChemAxon
Polarizability15.5 ųChemAxon
Number of Rings0ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
HMDB IDNot Available
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FoodDB IDNot Available
KNApSAcK IDNot Available
Chemspider IDNot Available
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound162980905  
PDB IDNot Available
ChEBI IDNot Available
Good Scents IDNot Available
References
General References