NP-MRD: Showing NP-Card for 2-{[5-hydroxy-5-(hydroxymethyl)-2-methoxy-3-oxocyclohex-1-en-1-yl]amino}pentanedioic acid (NP0251084)

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Record Information

Version

2.0

Created at

2022-09-07 14:09:20 UTC

Updated at

2022-09-07 14:09:20 UTC

NP-MRD ID

NP0251084

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-{[5-hydroxy-5-(hydroxymethyl)-2-methoxy-3-oxocyclohex-1-en-1-yl]amino}pentanedioic acid

Description

2-{[5-Hydroxy-5-(hydroxymethyl)-2-methoxy-3-oxocyclohex-1-en-1-yl]amino}pentanedioic acid belongs to the class of organic compounds known as glutamic acid and derivatives. Glutamic acid and derivatives are compounds containing glutamic acid or a derivative thereof resulting from reaction of glutamic acid at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom. 2-{[5-hydroxy-5-(hydroxymethyl)-2-methoxy-3-oxocyclohex-1-en-1-yl]amino}pentanedioic acid is found in Colletotrichum gloeosporioides. 2-{[5-Hydroxy-5-(hydroxymethyl)-2-methoxy-3-oxocyclohex-1-en-1-yl]amino}pentanedioic acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 41 41  0  0  0  0  0  0  0  0999 V2000
    0.7800   -0.2228   -3.2408 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5051    0.7081   -2.2204 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5810    0.4900   -1.3894 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5157    0.7108   -0.0637 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7266    1.1861    0.4549 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5851    0.5431    1.3732 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2485   -0.7239    0.9927 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1616   -0.6540   -0.1737 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3097    0.2358   -0.0692 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5950    0.8734    0.9562 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1399    0.3840   -1.1754 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0708    0.4560    2.7810 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2211    1.2865    3.1450 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5156   -0.5192    3.6655 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6541    0.4904    0.8501 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9390    0.4564    0.0447 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0165    1.7023   -0.5841 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1591    0.1446    0.8438 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9807   -1.1070    1.4265 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8014   -0.5926   -1.0412 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8083    0.0098   -1.9992 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0954    0.0552   -3.1953 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9398   -1.2076   -2.7241 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0178   -0.2699   -3.9719 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7713    0.0369   -3.7011 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9683    2.1580    0.0497 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4628    1.2828    1.5168 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5345   -1.5682    0.8726 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8877   -1.0178    1.8840 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6188   -1.7032   -0.2589 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6408   -0.5461   -1.1425 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9934    0.9421   -1.1326 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4584   -0.7097    3.9142 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5889   -0.4717    1.3960 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8172    1.3448    1.5621 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7726    1.7172   -1.2258 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0017    0.0430    0.1147 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4140    0.9199    1.5991 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7487   -1.3314    2.0250 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4313   -1.5462   -0.6494 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7915   -0.7440   -1.5088 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 15  1  0
 15 16  1  0
 16 17  1  6
 16 18  1  0
 18 19  1  0
 16 20  1  0
 20 21  1  0
 21 22  2  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 11  1  0
  9 10  2  0
  6 12  1  0
 12 14  1  0
 12 13  2  0
 21  3  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
 15 34  1  0
 15 35  1  0
 17 36  1  0
 18 37  1  0
 18 38  1  0
 19 39  1  0
 20 40  1  0
 20 41  1  0
  5 26  1  0
  6 27  1  1
  7 28  1  0
  7 29  1  0
  8 30  1  0
  8 31  1  0
 11 32  1  0
 14 33  1  0
M  END


  Mrv1533004251515432D          

 22 22  0  0  0  0            999 V2000
    1.5691    4.2059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1566    4.9204    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3316    4.9204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0809    4.2059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9059    4.2059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3184    4.9204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9504    4.3901    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9504    5.4507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7256    5.1685    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9059    5.6349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0809    5.6349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3316    6.3493    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3316    3.4914    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0809    2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9059    2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3184    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5559    1.3480    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5559    2.7770    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3316    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0809    1.3480    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1566    2.0625    0.0000 O   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  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  6 10  1  0  0  0  0
 10 11  1  0  0  0  0
  3 11  1  0  0  0  0
 11 12  2  0  0  0  0
  4 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
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 14 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0251084

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(CC(O)(CO)CC1=O)NC(CCC(O)=O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C13H19NO8/c1-22-11-8(4-13(21,6-15)5-9(11)16)14-7(12(19)20)2-3-10(17)18/h7,14-15,21H,2-6H2,1H3,(H,17,18)(H,19,20)

> <INCHI_KEY>
DYTYGLGPPCXREZ-UHFFFAOYSA-N

> <FORMULA>
C13H19NO8

> <MOLECULAR_WEIGHT>
317.294

> <EXACT_MASS>
317.111066576

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
41

> <JCHEM_AVERAGE_POLARIZABILITY>
30.022048641318158

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-{[5-hydroxy-5-(hydroxymethyl)-2-methoxy-3-oxocyclohex-1-en-1-yl]amino}pentanedioic acid

> <ALOGPS_LOGP>
-1.22

> <JCHEM_LOGP>
-2.327508939666667

> <ALOGPS_LOGS>
-1.44

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
4.27271089017744

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.5679263391066938

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0845878442649246

> <JCHEM_POLAR_SURFACE_AREA>
153.39

> <JCHEM_REFRACTIVITY>
73.56039999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.15e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-{[5-hydroxy-5-(hydroxymethyl)-2-methoxy-3-oxocyclohex-1-en-1-yl]amino}pentanedioic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0       2.929   7.851   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       2.159   9.185   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       0.619   9.185   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.151   7.851   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.691   7.851   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.461   9.185   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -3.641   8.195   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -3.641  10.175   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -5.088   9.648   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -1.691  10.518   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.151  10.518   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       0.619  11.852   0.000  0.00  0.00           O+0
HETATM   13  N   UNK     0       0.619   6.517   0.000  0.00  0.00           N+0
HETATM   14  C   UNK     0      -0.151   5.184   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.691   5.184   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.461   3.850   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -4.001   3.850   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -4.771   2.516   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0      -4.771   5.184   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       0.619   3.850   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -0.151   2.516   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       2.159   3.850   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   11                                                  
CONECT    4    3    5   13                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8   10                                             
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8                                                            
CONECT   10    6   11                                                       
CONECT   11   10    3   12                                                  
CONECT   12   11                                                            
CONECT   13    4   14                                                       
CONECT   14   13   15   20                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   14   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   44    0
END

View in JSmol

Synonyms

Value	Source
2-{[5-hydroxy-5-(hydroxymethyl)-2-methoxy-3-oxocyclohex-1-en-1-yl]amino}pentanedioate	Generator

Chemical Formula

C₁₃H₁₉NO₈

Average Mass

317.2940 Da

Monoisotopic Mass

317.11107 Da

IUPAC Name

2-{[5-hydroxy-5-(hydroxymethyl)-2-methoxy-3-oxocyclohex-1-en-1-yl]amino}pentanedioic acid

Traditional Name

2-{[5-hydroxy-5-(hydroxymethyl)-2-methoxy-3-oxocyclohex-1-en-1-yl]amino}pentanedioic acid

CAS Registry Number

Not Available

SMILES

COC1=C(CC(O)(CO)CC1=O)NC(CCC(O)=O)C(O)=O

InChI Identifier

InChI=1S/C13H19NO8/c1-22-11-8(4-13(21,6-15)5-9(11)16)14-7(12(19)20)2-3-10(17)18/h7,14-15,21H,2-6H2,1H3,(H,17,18)(H,19,20)

InChI Key

DYTYGLGPPCXREZ-UHFFFAOYSA-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
Colletotrichum gloeosporioides	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as glutamic acid and derivatives. Glutamic acid and derivatives are compounds containing glutamic acid or a derivative thereof resulting from reaction of glutamic acid at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Glutamic acid and derivatives

Alternative Parents

Substituents

Glutamic acid or derivatives
Alpha-amino acid
Hydroxy fatty acid
Amino fatty acid
Cyclohexenone
Dicarboxylic acid or derivatives
Fatty acyl
Vinylogous amide
Tertiary alcohol
1,2-diol
Cyclic ketone
Ketone
Amino acid
Secondary aliphatic amine
Secondary amine
Enamine
Carboxylic acid
Organic nitrogen compound
Organonitrogen compound
Organooxygen compound
Primary alcohol
Hydrocarbon derivative
Organic oxide
Carbonyl group
Organopnictogen compound
Amine
Organic oxygen compound
Alcohol
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic 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	-1.2	ALOGPS
logP	-2.3	ChemAxon
logS	-1.4	ALOGPS
pKa (Strongest Acidic)	3.57	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	153.39 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	73.56 m³·mol⁻¹	ChemAxon
Polarizability	30.02 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

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

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BiGG ID

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Wikipedia Link

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METLIN ID

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PubChem Compound

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PDB ID

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ChEBI ID

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Good Scents ID

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References

General References

LOTUS database [Link]

Showing NP-Card for 2-{[5-hydroxy-5-(hydroxymethyl)-2-methoxy-3-oxocyclohex-1-en-1-yl]amino}pentanedioic acid (NP0251084)

MOL for NP0251084 (2-{[5-hydroxy-5-(hydroxymethyl)-2-methoxy-3-oxocyclohex-1-en-1-yl]amino}pentanedioic acid)

3D MOL for NP0251084 (2-{[5-hydroxy-5-(hydroxymethyl)-2-methoxy-3-oxocyclohex-1-en-1-yl]amino}pentanedioic acid)

3D SDF for NP0251084 (2-{[5-hydroxy-5-(hydroxymethyl)-2-methoxy-3-oxocyclohex-1-en-1-yl]amino}pentanedioic acid)

3D-SDF for NP0251084 (2-{[5-hydroxy-5-(hydroxymethyl)-2-methoxy-3-oxocyclohex-1-en-1-yl]amino}pentanedioic acid)

PDB for NP0251084 (2-{[5-hydroxy-5-(hydroxymethyl)-2-methoxy-3-oxocyclohex-1-en-1-yl]amino}pentanedioic acid)

3D PDB for NP0251084 (2-{[5-hydroxy-5-(hydroxymethyl)-2-methoxy-3-oxocyclohex-1-en-1-yl]amino}pentanedioic acid)

SMILES for NP0251084 (2-{[5-hydroxy-5-(hydroxymethyl)-2-methoxy-3-oxocyclohex-1-en-1-yl]amino}pentanedioic acid)

INCHI for NP0251084 (2-{[5-hydroxy-5-(hydroxymethyl)-2-methoxy-3-oxocyclohex-1-en-1-yl]amino}pentanedioic acid)

Structure for NP0251084 (2-{[5-hydroxy-5-(hydroxymethyl)-2-methoxy-3-oxocyclohex-1-en-1-yl]amino}pentanedioic acid)

3D Structure for NP0251084 (2-{[5-hydroxy-5-(hydroxymethyl)-2-methoxy-3-oxocyclohex-1-en-1-yl]amino}pentanedioic acid)