NP-MRD: Showing NP-Card for (2z)-n-(4-amino-2,3-dihydroxybutyl)-3-(4-hydroxyphenyl)prop-2-enimidic acid (NP0326157)

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Record Information

Version

2.0

Created at

2022-09-12 07:28:17 UTC

Updated at

2022-09-12 07:28:17 UTC

NP-MRD ID

NP0326157

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2z)-n-(4-amino-2,3-dihydroxybutyl)-3-(4-hydroxyphenyl)prop-2-enimidic acid

Description

(2z)-n-(4-amino-2,3-dihydroxybutyl)-3-(4-hydroxyphenyl)prop-2-enimidic acid is found in Ipomoea nil.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 37 37  0  0  0  0  0  0  0  0999 V2000
    5.7380    1.6109   -0.3154 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.5151    1.0676    0.2732 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3196   -0.3302   -0.2973 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4582   -1.0579    0.0779 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1291   -1.0143    0.3123 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2727   -1.0240    1.6831 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8315   -0.2899   -0.0304 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7276   -0.9796    0.5758 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5347   -0.6564    0.3144 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4377   -1.4216    0.9823 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7083    0.4229   -0.5946 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8278    0.8733   -1.0465 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1413    0.4062   -0.7769 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6051   -0.8412   -0.5268 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9225   -1.1413   -0.1437 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8454   -0.1329   -0.0027 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1480   -0.4251    0.3758 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4093    1.1458   -0.2530 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1204    1.4285   -0.6248 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1540    0.9492   -1.0058 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5338    2.5288   -0.7909 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6621    0.9314    1.3668 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6796    1.7454    0.0263 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2383   -0.3146   -1.3937 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2834   -1.6737    0.8293 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0892   -2.0483   -0.0367 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5211   -1.5049    2.1132 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7241   -0.3956   -1.1497 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8925    0.7778    0.1844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7018   -1.2771    1.9361 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2453    0.9553   -0.9669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7457    1.7672   -1.7664 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9255   -1.6874   -0.7225 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1808   -2.1766    0.0335 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8329   -0.6180   -0.3706 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1336    1.9581   -0.1464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7945    2.4418   -0.8181 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  3  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
  9 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 16 18  1  0
 18 19  2  0
 19 13  1  0
  1 20  1  0
  1 21  1  0
  2 22  1  0
  2 23  1  0
  3 24  1  6
  4 25  1  0
  5 26  1  6
  6 27  1  0
  7 28  1  0
  7 29  1  0
 10 30  1  0
 11 31  1  0
 12 32  1  0
 14 33  1  0
 15 34  1  0
 17 35  1  0
 18 36  1  0
 19 37  1  0
M  END


  Mrv1652309122209282D          

 19 19  0  0  0  0            999 V2000
    3.5724   -1.2375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -0.8250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -2.4750    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
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  0  0  0  0
  8  7  1  4  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 13 19  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0326157

> <DATABASE_NAME>
NP-MRD

> <SMILES>
NCC(O)C(O)CN=C(O)\C=C/C1=CC=C(O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C13H18N2O4/c14-7-11(17)12(18)8-15-13(19)6-3-9-1-4-10(16)5-2-9/h1-6,11-12,16-18H,7-8,14H2,(H,15,19)/b6-3-

> <INCHI_KEY>
LXMCDWFRMKYSHE-UTCJRWHESA-N

> <FORMULA>
C13H18N2O4

> <MOLECULAR_WEIGHT>
266.297

> <EXACT_MASS>
266.126657068

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
37

> <JCHEM_AVERAGE_POLARIZABILITY>
27.775123680845702

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2Z)-N-(4-amino-2,3-dihydroxybutyl)-3-(4-hydroxyphenyl)prop-2-enimidic acid

> <JCHEM_LOGP>
-2.2351377191605954

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
9.691008521703775

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.196709320167011

> <JCHEM_PKA_STRONGEST_BASIC>
9.036865058089194

> <JCHEM_POLAR_SURFACE_AREA>
119.30000000000001

> <JCHEM_REFRACTIVITY>
72.1562

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2Z)-N-(4-amino-2,3-dihydroxybutyl)-3-(4-hydroxyphenyl)prop-2-enimidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  N   UNK     0       6.668  -2.310   0.000  0.00  0.00           N+0
HETATM    2  C   UNK     0       8.002  -1.540   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.336  -2.310   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       9.336  -3.850   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      10.669  -1.540   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      10.669   0.000   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      12.003  -2.310   0.000  0.00  0.00           C+0
HETATM    8  N   UNK     0      13.337  -1.540   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0      14.670  -2.310   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      14.670  -3.850   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      16.004  -1.540   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      17.338  -2.310   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      17.338  -3.850   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      18.672  -4.620   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      18.672  -6.160   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      17.338  -6.930   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      17.338  -8.470   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      16.004  -6.160   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      16.004  -4.620   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   19                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   13                                                       
MASTER        0    0    0    0    0    0    0    0   19    0   38    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₃H₁₈N₂O₄

Average Mass

266.2970 Da

Monoisotopic Mass

266.12666 Da

IUPAC Name

(2Z)-N-(4-amino-2,3-dihydroxybutyl)-3-(4-hydroxyphenyl)prop-2-enimidic acid

Traditional Name

(2Z)-N-(4-amino-2,3-dihydroxybutyl)-3-(4-hydroxyphenyl)prop-2-enimidic acid

CAS Registry Number

Not Available

SMILES

NCC(O)C(O)CN=C(O)\C=C/C1=CC=C(O)C=C1

InChI Identifier

InChI=1S/C13H18N2O4/c14-7-11(17)12(18)8-15-13(19)6-3-9-1-4-10(16)5-2-9/h1-6,11-12,16-18H,7-8,14H2,(H,15,19)/b6-3-

InChI Key

LXMCDWFRMKYSHE-UTCJRWHESA-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
Ipomoea nil	LOTUS Database	35616633

Chemical Taxonomy

Classification

Not classified

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	-2.2	ChemAxon
pKa (Strongest Acidic)	6.2	ChemAxon
pKa (Strongest Basic)	9.04	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	119.3 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	72.16 m³·mol⁻¹	ChemAxon
Polarizability	27.78 Å³	ChemAxon
Number of Rings	1	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

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2z)-n-(4-amino-2,3-dihydroxybutyl)-3-(4-hydroxyphenyl)prop-2-enimidic acid (NP0326157)

MOL for NP0326157 ((2z)-n-(4-amino-2,3-dihydroxybutyl)-3-(4-hydroxyphenyl)prop-2-enimidic acid)

3D MOL for NP0326157 ((2z)-n-(4-amino-2,3-dihydroxybutyl)-3-(4-hydroxyphenyl)prop-2-enimidic acid)

3D SDF for NP0326157 ((2z)-n-(4-amino-2,3-dihydroxybutyl)-3-(4-hydroxyphenyl)prop-2-enimidic acid)

3D-SDF for NP0326157 ((2z)-n-(4-amino-2,3-dihydroxybutyl)-3-(4-hydroxyphenyl)prop-2-enimidic acid)

PDB for NP0326157 ((2z)-n-(4-amino-2,3-dihydroxybutyl)-3-(4-hydroxyphenyl)prop-2-enimidic acid)

3D PDB for NP0326157 ((2z)-n-(4-amino-2,3-dihydroxybutyl)-3-(4-hydroxyphenyl)prop-2-enimidic acid)

SMILES for NP0326157 ((2z)-n-(4-amino-2,3-dihydroxybutyl)-3-(4-hydroxyphenyl)prop-2-enimidic acid)

INCHI for NP0326157 ((2z)-n-(4-amino-2,3-dihydroxybutyl)-3-(4-hydroxyphenyl)prop-2-enimidic acid)

Structure for NP0326157 ((2z)-n-(4-amino-2,3-dihydroxybutyl)-3-(4-hydroxyphenyl)prop-2-enimidic acid)

3D Structure for NP0326157 ((2z)-n-(4-amino-2,3-dihydroxybutyl)-3-(4-hydroxyphenyl)prop-2-enimidic acid)