NP-MRD: Showing NP-Card for (2s,3s)-n-[(2s)-1-(3-chloro-4-hydroxyphenyl)-3-oxopentan-2-yl]-2-hydroxy-3-methylpentanimidic acid (NP0297941)

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Record Information

Version

1.0

Created at

2022-09-10 08:44:51 UTC

Updated at

2022-09-10 08:44:51 UTC

NP-MRD ID

NP0297941

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s,3s)-n-[(2s)-1-(3-chloro-4-hydroxyphenyl)-3-oxopentan-2-yl]-2-hydroxy-3-methylpentanimidic acid

Description

Auriculamide belongs to the class of organic compounds known as amphetamines and derivatives. These are organic compounds containing or derived from 1-phenylpropan-2-amine. (2s,3s)-n-[(2s)-1-(3-chloro-4-hydroxyphenyl)-3-oxopentan-2-yl]-2-hydroxy-3-methylpentanimidic acid is found in Herpetosiphon aurantiacus. It was first documented in 2016 (PMID: 28144348). Based on a literature review very few articles have been published on Auriculamide.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 47 47  0  0  0  0  0  0  0  0999 V2000
    0.8156   -5.1142   -1.0750 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5398   -3.7906   -1.0269 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6035   -2.7683   -0.4755 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5287   -3.0834   -0.1570 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0163   -1.3497   -0.2990 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2579   -1.3462    0.5521 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7961    0.0168    0.7815 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3758    0.7540    1.8680 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8601    2.0348    2.1126 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7830    2.6139    1.2709 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2674    3.9055    1.5229 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2085    1.8836    0.1822 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3824    2.6264   -0.8841 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    3.7194    0.6109   -0.0502 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0671   -0.6167    0.2379 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5650    0.4687   -0.1455 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0486    1.1196   -1.2436 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7076    1.0690    0.5662 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4244    2.3270    1.0933 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9153    1.2271   -0.3418 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.3052   -0.0690   -1.0055 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1111    1.7418    0.4192 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2629    1.9746   -0.5320 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4927   -5.8727   -1.5107 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0863   -4.9828   -1.6819 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5231   -5.3595   -0.0277 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4295   -3.8105   -0.3645 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8091   -3.4434   -2.0505 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2606   -0.9318   -1.3040 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1503   -1.9038    1.4803 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0481   -1.8863   -0.0477 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6466    0.3355    2.5604 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5230    2.6156    2.9767 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9341    4.3589    0.9396 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0662    0.0397   -0.9207 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6504    1.5159   -1.9648 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0528    0.4409    1.4214 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9739    2.2059    1.9571 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6468    1.9571   -1.1259 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7199    0.0865   -2.0230 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4105   -0.7519   -1.0455 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0779   -0.6169   -0.4209 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4619    1.0186    1.1785 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8730    2.6783    0.9808 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1783    1.4070   -0.2312 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9994    1.6148   -1.5514 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4422    3.0493   -0.5950 H   0  0  0  0  0  0  0  0  0  0  0  0
 23 22  1  0
 22 20  1  0
 20 21  1  0
 20 18  1  0
 18 19  1  0
 18 16  1  0
 16 17  1  0
 16 15  2  0
 15  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 12 14  2  0
  5  3  1  0
  3  4  2  0
  3  2  1  0
  2  1  1  0
 14  7  1  0
 23 45  1  0
 23 46  1  0
 23 47  1  0
 22 43  1  0
 22 44  1  0
 20 39  1  6
 21 40  1  0
 21 41  1  0
 21 42  1  0
 18 37  1  1
 19 38  1  0
 17 36  1  0
  5 29  1  6
  6 30  1  0
  6 31  1  0
  8 32  1  0
  9 33  1  0
 11 34  1  0
 14 35  1  0
  2 27  1  0
  2 28  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
M  END


  Mrv1652309102210442D          

 23 23  0  0  1  0            999 V2000
   -2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4289   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.1250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -5.3625    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
  3  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
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  2  0  0  0  0
  7 14  1  0  0  0  0
  5 15  1  6  0  0  0
 15 16  2  0  0  0  0
 16 17  1  4  0  0  0
 16 18  1  0  0  0  0
 18 19  1  6  0  0  0
 18 20  1  0  0  0  0
 20 21  1  1  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0297941

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@H](C)[C@H](O)C(O)=N[C@@H](CC1=CC=C(O)C(Cl)=C1)C(=O)CC

> <INCHI_IDENTIFIER>
InChI=1S/C17H24ClNO4/c1-4-10(3)16(22)17(23)19-13(14(20)5-2)9-11-6-7-15(21)12(18)8-11/h6-8,10,13,16,21-22H,4-5,9H2,1-3H3,(H,19,23)/t10-,13-,16-/m0/s1

> <INCHI_KEY>
GQUNWFSEBZMTLB-NKFCBESUSA-N

> <FORMULA>
C17H24ClNO4

> <MOLECULAR_WEIGHT>
341.83

> <EXACT_MASS>
341.139386

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
35.92147106247883

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S,3S)-N-[(2S)-1-(3-chloro-4-hydroxyphenyl)-3-oxopentan-2-yl]-2-hydroxy-3-methylpentanimidic acid

> <JCHEM_LOGP>
4.13028659

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
7.939737709672209

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.5483399381621137

> <JCHEM_PKA_STRONGEST_BASIC>
0.9284857062842042

> <JCHEM_POLAR_SURFACE_AREA>
90.12

> <JCHEM_REFRACTIVITY>
89.8382

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3S)-N-[(2S)-1-(3-chloro-4-hydroxyphenyl)-3-oxopentan-2-yl]-2-hydroxy-3-methylpentanimidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0      -4.001  -2.310   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -1.334  -0.770   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       1.334   3.850   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   13 Cl   UNK     0       4.001   2.310   0.000  0.00  0.00          Cl+0
HETATM   14  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   15  N   UNK     0       0.000  -4.620   0.000  0.00  0.00           N+0
HETATM   16  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -2.667  -4.620   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -2.667  -7.700   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       0.000  -7.700   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.000  -9.240   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.334 -10.010   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   15                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   14                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12    7                                                       
CONECT   15    5   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   46    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₇H₂₄ClNO₄

Average Mass

341.8300 Da

Monoisotopic Mass

341.13939 Da

IUPAC Name

(2S,3S)-N-[(2S)-1-(3-chloro-4-hydroxyphenyl)-3-oxopentan-2-yl]-2-hydroxy-3-methylpentanimidic acid

Traditional Name

(2S,3S)-N-[(2S)-1-(3-chloro-4-hydroxyphenyl)-3-oxopentan-2-yl]-2-hydroxy-3-methylpentanimidic acid

CAS Registry Number

Not Available

SMILES

CC[C@H](C)[C@H](O)C(O)=N[C@@H](CC1=CC=C(O)C(Cl)=C1)C(=O)CC

InChI Identifier

InChI=1S/C17H24ClNO4/c1-4-10(3)16(22)17(23)19-13(14(20)5-2)9-11-6-7-15(21)12(18)8-11/h6-8,10,13,16,21-22H,4-5,9H2,1-3H3,(H,19,23)/t10-,13-,16-/m0/s1

InChI Key

GQUNWFSEBZMTLB-NKFCBESUSA-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
Herpetosiphon aurantiacus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as amphetamines and derivatives. These are organic compounds containing or derived from 1-phenylpropan-2-amine.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Phenethylamines

Direct Parent

Amphetamines and derivatives

Alternative Parents

Substituents

Amphetamine or derivatives
2-chlorophenol
2-halophenol
1-hydroxy-2-unsubstituted benzenoid
Phenol
Halobenzene
Chlorobenzene
Aryl halide
Aryl chloride
Secondary alcohol
Ketone
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Carboximidic acid derivative
Carboximidic acid
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Organochloride
Organohalogen compound
Carbonyl group
Alcohol
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic 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	4.13	ChemAxon
pKa (Strongest Acidic)	3.55	ChemAxon
pKa (Strongest Basic)	0.93	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	90.12 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	89.84 m³·mol⁻¹	ChemAxon
Polarizability	35.92 Å³	ChemAxon
Number of Rings	1	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

35000209

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

132933464

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Braga D, Hoffmeister D, Nett M: A non-canonical peptide synthetase adenylates 3-methyl-2-oxovaleric acid for auriculamide biosynthesis. Beilstein J Org Chem. 2016 Dec 16;12:2766-2770. doi: 10.3762/bjoc.12.274. eCollection 2016. [PubMed:28144348 ]
LOTUS database [Link]

Showing NP-Card for (2s,3s)-n-[(2s)-1-(3-chloro-4-hydroxyphenyl)-3-oxopentan-2-yl]-2-hydroxy-3-methylpentanimidic acid (NP0297941)

MOL for NP0297941 ((2s,3s)-n-[(2s)-1-(3-chloro-4-hydroxyphenyl)-3-oxopentan-2-yl]-2-hydroxy-3-methylpentanimidic acid)

3D MOL for NP0297941 ((2s,3s)-n-[(2s)-1-(3-chloro-4-hydroxyphenyl)-3-oxopentan-2-yl]-2-hydroxy-3-methylpentanimidic acid)

3D SDF for NP0297941 ((2s,3s)-n-[(2s)-1-(3-chloro-4-hydroxyphenyl)-3-oxopentan-2-yl]-2-hydroxy-3-methylpentanimidic acid)

3D-SDF for NP0297941 ((2s,3s)-n-[(2s)-1-(3-chloro-4-hydroxyphenyl)-3-oxopentan-2-yl]-2-hydroxy-3-methylpentanimidic acid)

PDB for NP0297941 ((2s,3s)-n-[(2s)-1-(3-chloro-4-hydroxyphenyl)-3-oxopentan-2-yl]-2-hydroxy-3-methylpentanimidic acid)

3D PDB for NP0297941 ((2s,3s)-n-[(2s)-1-(3-chloro-4-hydroxyphenyl)-3-oxopentan-2-yl]-2-hydroxy-3-methylpentanimidic acid)

SMILES for NP0297941 ((2s,3s)-n-[(2s)-1-(3-chloro-4-hydroxyphenyl)-3-oxopentan-2-yl]-2-hydroxy-3-methylpentanimidic acid)

INCHI for NP0297941 ((2s,3s)-n-[(2s)-1-(3-chloro-4-hydroxyphenyl)-3-oxopentan-2-yl]-2-hydroxy-3-methylpentanimidic acid)

Structure for NP0297941 ((2s,3s)-n-[(2s)-1-(3-chloro-4-hydroxyphenyl)-3-oxopentan-2-yl]-2-hydroxy-3-methylpentanimidic acid)

3D Structure for NP0297941 ((2s,3s)-n-[(2s)-1-(3-chloro-4-hydroxyphenyl)-3-oxopentan-2-yl]-2-hydroxy-3-methylpentanimidic acid)