NP-MRD: Showing NP-Card for 2-hydroxy-3-{[3-methoxy-2-(3-methyl-2,5-dioxopyrrolidin-1-yl)-3-oxopropyl]sulfanyl}propanoic acid (NP0258015)

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Record Information

Version

2.0

Created at

2022-09-07 23:18:19 UTC

Updated at

2022-09-07 23:18:19 UTC

NP-MRD ID

NP0258015

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-hydroxy-3-{[3-methoxy-2-(3-methyl-2,5-dioxopyrrolidin-1-yl)-3-oxopropyl]sulfanyl}propanoic acid

Description

2-Hydroxy-3-{[3-methoxy-2-(3-methyl-2,5-dioxopyrrolidin-1-yl)-3-oxopropyl]sulfanyl}propanoic acid belongs to the class of organic compounds known as alpha amino acid esters. These are ester derivatives of alpha amino acids. 2-hydroxy-3-{[3-methoxy-2-(3-methyl-2,5-dioxopyrrolidin-1-yl)-3-oxopropyl]sulfanyl}propanoic acid is found in Aspergillus violaceus. Based on a literature review very few articles have been published on 2-hydroxy-3-{[3-methoxy-2-(3-methyl-2,5-dioxopyrrolidin-1-yl)-3-oxopropyl]sulfanyl}propanoic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 38 38  0  0  0  0  0  0  0  0999 V2000
   -0.4030    4.2129    0.5354 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0599    2.9030    0.3346 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8144    1.8483    0.3086 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0436    2.0521    0.4656 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3765    0.4354    0.0989 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4687    0.2979   -1.1467 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9445    1.3118   -1.0421 S   0  0  0  0  0  0  0  0  0  0  0  0
    3.0783    0.7665    0.2403 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6654   -0.5987   -0.0627 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3743   -0.5929   -1.2612 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6118   -0.9892    1.0137 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2001   -1.0667    2.2024 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9538   -1.2772    0.7603 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4919   -0.4739    0.1091 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6904   -1.4958    1.0808 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8347   -1.9174    1.8955 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1069   -1.9317    0.9068 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1997   -1.8498   -0.6249 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.6053   -1.9499   -1.1115 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5845   -0.5194   -0.8359 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8716    0.4093   -1.6201 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2934    4.9265    0.0489 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3872    4.4755    1.6320 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4449    4.3738    0.1905 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2761    0.1974    0.9597 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1023    0.6162   -2.0434 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7108   -0.7737   -1.2875 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9469    1.4842    0.2308 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6621    0.8111    1.2591 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8508   -1.3467   -0.0966 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1186    0.0476   -1.2007 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2415   -1.7553   -0.0859 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8129   -1.1390    1.2682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3199   -2.9252    1.2914 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5662   -2.6785   -1.0133 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1968   -2.4955   -0.3659 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5806   -2.4701   -2.1051 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0236   -0.9231   -1.1956 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
  3  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
  9 11  1  0
 11 13  1  0
 11 12  2  0
  5 14  1  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  2  0
 20 14  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  5 25  1  1
  6 26  1  0
  6 27  1  0
  8 28  1  0
  8 29  1  0
  9 30  1  6
 10 31  1  0
 13 32  1  0
 17 33  1  0
 17 34  1  0
 18 35  1  6
 19 36  1  0
 19 37  1  0
 19 38  1  0
M  END


  Mrv1652309082201182D          

 21 21  0  0  0  0            999 V2000
    0.7664   -0.2756    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0364   -1.0552    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8465   -1.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3866   -0.5874    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1166   -1.9906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9267   -2.1465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4668   -1.5229    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    4.2769   -1.6788    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8170   -1.0552    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5470   -0.2756    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6272   -1.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1672   -0.5874    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8972   -1.9906    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5765   -2.6143    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.7636   -3.4178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5236   -3.7387    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0572   -3.8440    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4336   -3.3039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3700   -3.4910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7545   -2.5439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3283   -1.8375    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
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  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
 11 13  1  0  0  0  0
  5 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 14 20  1  0  0  0  0
 20 21  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0258015

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C(CSCC(O)C(O)=O)N1C(=O)CC(C)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C12H17NO7S/c1-6-3-9(15)13(10(6)16)7(12(19)20-2)4-21-5-8(14)11(17)18/h6-8,14H,3-5H2,1-2H3,(H,17,18)

> <INCHI_KEY>
KMOGJXSUBZHITP-UHFFFAOYSA-N

> <FORMULA>
C12H17NO7S

> <MOLECULAR_WEIGHT>
319.33

> <EXACT_MASS>
319.072573065

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
38

> <JCHEM_AVERAGE_POLARIZABILITY>
30.21576572817083

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-hydroxy-3-{[3-methoxy-2-(3-methyl-2,5-dioxopyrrolidin-1-yl)-3-oxopropyl]sulfanyl}propanoic acid

> <JCHEM_LOGP>
-0.8584542713333335

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
13.961407727452116

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.3700919857327105

> <JCHEM_PKA_STRONGEST_BASIC>
-3.932276510741528

> <JCHEM_POLAR_SURFACE_AREA>
121.20999999999998

> <JCHEM_REFRACTIVITY>
71.80290000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
2-hydroxy-3-{[3-methoxy-2-(3-methyl-2,5-dioxopyrrolidin-1-yl)-3-oxopropyl]sulfanyl}propanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0       1.431  -0.515   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       1.935  -1.970   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       3.447  -2.261   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       4.455  -1.097   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       3.951  -3.716   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.463  -4.007   0.000  0.00  0.00           C+0
HETATM    7  S   UNK     0       6.471  -2.843   0.000  0.00  0.00           S+0
HETATM    8  C   UNK     0       7.984  -3.134   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.992  -1.970   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       8.488  -0.515   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      10.504  -2.261   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      11.512  -1.097   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0      11.008  -3.716   0.000  0.00  0.00           O+0
HETATM   14  N   UNK     0       2.943  -4.880   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0       3.292  -6.380   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       4.711  -6.979   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       1.973  -7.175   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.809  -6.167   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.691  -6.517   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.408  -4.749   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       0.613  -3.430   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   14                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14    5   15   20                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   14   21                                                  
CONECT   21   20                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   42    0
END

View in JSmol

Synonyms

Value	Source
2-Hydroxy-3-{[3-methoxy-2-(3-methyl-2,5-dioxopyrrolidin-1-yl)-3-oxopropyl]sulfanyl}propanoate	Generator
2-Hydroxy-3-{[3-methoxy-2-(3-methyl-2,5-dioxopyrrolidin-1-yl)-3-oxopropyl]sulphanyl}propanoate	Generator
2-Hydroxy-3-{[3-methoxy-2-(3-methyl-2,5-dioxopyrrolidin-1-yl)-3-oxopropyl]sulphanyl}propanoic acid	Generator

Chemical Formula

C₁₂H₁₇NO₇S

Average Mass

319.3300 Da

Monoisotopic Mass

319.07257 Da

IUPAC Name

2-hydroxy-3-{[3-methoxy-2-(3-methyl-2,5-dioxopyrrolidin-1-yl)-3-oxopropyl]sulfanyl}propanoic acid

Traditional Name

2-hydroxy-3-{[3-methoxy-2-(3-methyl-2,5-dioxopyrrolidin-1-yl)-3-oxopropyl]sulfanyl}propanoic acid

CAS Registry Number

Not Available

SMILES

COC(=O)C(CSCC(O)C(O)=O)N1C(=O)CC(C)C1=O

InChI Identifier

InChI=1S/C12H17NO7S/c1-6-3-9(15)13(10(6)16)7(12(19)20-2)4-21-5-8(14)11(17)18/h6-8,14H,3-5H2,1-2H3,(H,17,18)

InChI Key

KMOGJXSUBZHITP-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
Aspergillus violaceus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as alpha amino acid esters. These are ester derivatives of alpha amino acids.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Alpha amino acid esters

Alternative Parents

Substituents

Alpha-amino acid ester
Cysteine or derivatives
Hydroxy fatty acid
Heterocyclic fatty acid
Fatty acyl
Fatty acid
N-alkylpyrrolidine
2-pyrrolidone
Pyrrolidone
Carboxylic acid imide, n-substituted
Monosaccharide
Hydroxy acid
Dicarboxylic acid or derivatives
Alpha-hydroxy acid
Methyl ester
Pyrrolidine
Dicarboximide
Carboxylic acid imide
Secondary alcohol
Lactam
Carboxylic acid ester
Azacycle
Organoheterocyclic compound
Dialkylthioether
Sulfenyl compound
Thioether
Carboxylic acid
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organosulfur compound
Organooxygen compound
Organonitrogen compound
Carbonyl group
Alcohol
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic 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	-0.86	ChemAxon
pKa (Strongest Acidic)	3.37	ChemAxon
pKa (Strongest Basic)	-3.9	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	121.21 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	71.8 m³·mol⁻¹	ChemAxon
Polarizability	30.22 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

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

162814817

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-hydroxy-3-{[3-methoxy-2-(3-methyl-2,5-dioxopyrrolidin-1-yl)-3-oxopropyl]sulfanyl}propanoic acid (NP0258015)

MOL for NP0258015 (2-hydroxy-3-{[3-methoxy-2-(3-methyl-2,5-dioxopyrrolidin-1-yl)-3-oxopropyl]sulfanyl}propanoic acid)

3D MOL for NP0258015 (2-hydroxy-3-{[3-methoxy-2-(3-methyl-2,5-dioxopyrrolidin-1-yl)-3-oxopropyl]sulfanyl}propanoic acid)

3D SDF for NP0258015 (2-hydroxy-3-{[3-methoxy-2-(3-methyl-2,5-dioxopyrrolidin-1-yl)-3-oxopropyl]sulfanyl}propanoic acid)

3D-SDF for NP0258015 (2-hydroxy-3-{[3-methoxy-2-(3-methyl-2,5-dioxopyrrolidin-1-yl)-3-oxopropyl]sulfanyl}propanoic acid)

PDB for NP0258015 (2-hydroxy-3-{[3-methoxy-2-(3-methyl-2,5-dioxopyrrolidin-1-yl)-3-oxopropyl]sulfanyl}propanoic acid)

3D PDB for NP0258015 (2-hydroxy-3-{[3-methoxy-2-(3-methyl-2,5-dioxopyrrolidin-1-yl)-3-oxopropyl]sulfanyl}propanoic acid)

SMILES for NP0258015 (2-hydroxy-3-{[3-methoxy-2-(3-methyl-2,5-dioxopyrrolidin-1-yl)-3-oxopropyl]sulfanyl}propanoic acid)

INCHI for NP0258015 (2-hydroxy-3-{[3-methoxy-2-(3-methyl-2,5-dioxopyrrolidin-1-yl)-3-oxopropyl]sulfanyl}propanoic acid)

Structure for NP0258015 (2-hydroxy-3-{[3-methoxy-2-(3-methyl-2,5-dioxopyrrolidin-1-yl)-3-oxopropyl]sulfanyl}propanoic acid)

3D Structure for NP0258015 (2-hydroxy-3-{[3-methoxy-2-(3-methyl-2,5-dioxopyrrolidin-1-yl)-3-oxopropyl]sulfanyl}propanoic acid)