NP-MRD: Showing NP-Card for (2s)-2-[(2-{[(2s)-2-amino-1-hydroxypropylidene]amino}-1-hydroxyethylidene)amino]-3-hydroxypropanoic acid (NP0205625)

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Record Information

Version

2.0

Created at

2022-09-05 01:34:46 UTC

Updated at

2022-09-05 01:34:46 UTC

NP-MRD ID

NP0205625

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s)-2-[(2-{[(2s)-2-amino-1-hydroxypropylidene]amino}-1-hydroxyethylidene)amino]-3-hydroxypropanoic acid

Description

Ala-Gly-Ser, also known as a-g-S or L-ala-gly-L-ser, belongs to the class of organic compounds known as peptides. Peptides are compounds containing an amide derived from two or more amino carboxylic acid molecules (the same or different) by formation of a covalent bond from the carbonyl carbon of one to the nitrogen atom of another. Ala-Gly-Ser is a secondary metabolite. Secondary metabolites are metabolically or physiologically non-essential metabolites that may serve a role as defense or signalling molecules. In some cases they are simply molecules that arise from the incomplete metabolism of other secondary metabolites. (2s)-2-[(2-{[(2s)-2-amino-1-hydroxypropylidene]amino}-1-hydroxyethylidene)amino]-3-hydroxypropanoic acid is found in Trypanosoma brucei. (2s)-2-[(2-{[(2s)-2-amino-1-hydroxypropylidene]amino}-1-hydroxyethylidene)amino]-3-hydroxypropanoic acid was first documented in 2017 (PMID: 27768593). Based on a literature review a small amount of articles have been published on Ala-Gly-Ser (PMID: 35788005) (PMID: 33750140) (PMID: 32882279) (PMID: 31226655).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 31 30  0  0  0  0  0  0  0  0999 V2000
   -4.4563   -0.5015    0.6826 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4402    0.3888   -0.0332 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.8009    0.4859   -1.4354 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1236   -0.2769    0.1048 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9837   -1.5517   -0.4222 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1556    0.3140    0.6922 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.1119   -0.3841    0.7993 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8372   -0.3919   -0.4721 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3147   -0.9651   -1.6350 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9895    0.1292   -0.5758 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.7663    0.7791    0.4266 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4826   -0.2893    1.2414 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2929   -0.9894    0.3206 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7736    1.6443   -0.2701 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5559    2.3019    0.4543 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8734    1.7447   -1.6371 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5177   -0.2580    1.7632 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4479   -0.4179    0.2204 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1365   -1.5715    0.5431 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4383    1.3913    0.4505 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9769    0.8899   -1.9402 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6695    1.0175   -1.5625 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4162   -1.8517   -1.2871 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6901    0.1122    1.5840 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1069   -1.4595    1.0617 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2354   -0.4083   -2.4718 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1551    1.3828    1.1226 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0928    0.1602    2.0517 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7918   -1.0016    1.7075 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0649   -1.4033    0.7815 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6422    0.9799   -2.2655 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  4  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 11 14  1  0
 14 16  1  0
 14 15  2  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  2 20  1  1
  3 21  1  0
  3 22  1  0
  5 23  1  0
  7 24  1  0
  7 25  1  0
  9 26  1  0
 11 27  1  1
 12 28  1  0
 12 29  1  0
 13 30  1  0
 16 31  1  0
M  END


  Mrv1652309052203342D          

 16 15  0  0  1  0            999 V2000
    3.7125   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000    0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7125    0.7145    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4750    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625   -0.7145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625    0.7145    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375   -0.7145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125   -0.7145    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2375   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6500   -1.4289    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125   -2.1434    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250   -1.4289    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  1  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  2  0  0  0  0
  6  7  1  4  0  0  0
  7  8  1  0  0  0  0
  8  9  1  4  0  0  0
  8 10  2  0  0  0  0
 11 10  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 11 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0205625

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H](N)C(O)=NCC(O)=N[C@@H](CO)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C8H15N3O5/c1-4(9)7(14)10-2-6(13)11-5(3-12)8(15)16/h4-5,12H,2-3,9H2,1H3,(H,10,14)(H,11,13)(H,15,16)/t4-,5-/m0/s1

> <INCHI_KEY>
NBTGEURICRTMGL-WHFBIAKZSA-N

> <FORMULA>
C8H15N3O5

> <MOLECULAR_WEIGHT>
233.224

> <EXACT_MASS>
233.101170595

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
31

> <JCHEM_AVERAGE_POLARIZABILITY>
22.46246546234342

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S)-2-[(2-{[(2S)-2-amino-1-hydroxypropylidene]amino}-1-hydroxyethylidene)amino]-3-hydroxypropanoic acid

> <JCHEM_LOGP>
-4.224192622880669

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
3.7727062629784633

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.1392954587646646

> <JCHEM_PKA_STRONGEST_BASIC>
9.570033397743224

> <JCHEM_POLAR_SURFACE_AREA>
148.73

> <JCHEM_REFRACTIVITY>
53.18530000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-2-[(2-{[(2S)-2-amino-1-hydroxypropylidene]amino}-1-hydroxyethylidene)amino]-3-hydroxypropanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0       6.930  -1.334   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.160   0.000   0.000  0.00  0.00           C+0
HETATM    3  N   UNK     0       6.930   1.334   0.000  0.00  0.00           N+0
HETATM    4  C   UNK     0       4.620   0.000   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       3.850  -1.334   0.000  0.00  0.00           O+0
HETATM    6  N   UNK     0       3.850   1.334   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0       2.310   1.334   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.540   0.000   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       2.310  -1.334   0.000  0.00  0.00           O+0
HETATM   10  N   UNK     0       0.000   0.000   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0      -0.770  -1.334   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.310  -1.334   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -3.080  -2.667   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       0.000  -2.667   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -0.770  -4.001   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0       1.540  -2.667   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   14                                                  
CONECT   12   11   13                                                       
CONECT   13   12                                                            
CONECT   14   11   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14                                                            
MASTER        0    0    0    0    0    0    0    0   16    0   30    0
END

View in JSmol

Synonyms

Value	Source
a-g-S	ChEBI
AGS	ChEBI
Alanyl-glycyl-serine	ChEBI
L-Ala-gly-L-ser	ChEBI

Chemical Formula

C₈H₁₅N₃O₅

Average Mass

233.2240 Da

Monoisotopic Mass

233.10117 Da

IUPAC Name

(2S)-2-[(2-{[(2S)-2-amino-1-hydroxypropylidene]amino}-1-hydroxyethylidene)amino]-3-hydroxypropanoic acid

Traditional Name

(2S)-2-[(2-{[(2S)-2-amino-1-hydroxypropylidene]amino}-1-hydroxyethylidene)amino]-3-hydroxypropanoic acid

CAS Registry Number

Not Available

SMILES

C[C@H](N)C(O)=NCC(O)=N[C@@H](CO)C(O)=O

InChI Identifier

InChI=1S/C8H15N3O5/c1-4(9)7(14)10-2-6(13)11-5(3-12)8(15)16/h4-5,12H,2-3,9H2,1H3,(H,10,14)(H,11,13)(H,15,16)/t4-,5-/m0/s1

InChI Key

NBTGEURICRTMGL-WHFBIAKZSA-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
Trypanosoma brucei	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as peptides. Peptides are compounds containing an amide derived from two or more amino carboxylic acid molecules (the same or different) by formation of a covalent bond from the carbonyl carbon of one to the nitrogen atom of another.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Peptides

Alternative Parents

Substituents

Alpha peptide
N-acyl-alpha-amino acid
N-acyl-alpha amino acid or derivatives
Serine or derivatives
Alpha-amino acid or derivatives
Beta-hydroxy acid
Hydroxy acid
Amino acid or derivatives
Amino acid
Carboximidic acid
Carboximidic acid derivative
Carboxylic acid
Monocarboxylic acid or derivatives
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Hydrocarbon derivative
Amine
Primary aliphatic amine
Organic oxide
Organic nitrogen compound
Alcohol
Carbonyl group
Organic oxygen compound
Organonitrogen compound
Organooxygen compound
Organopnictogen compound
Primary alcohol
Primary amine
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

tripeptide (CHEBI:73350 )

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	-4.2	ChemAxon
pKa (Strongest Acidic)	3.14	ChemAxon
pKa (Strongest Basic)	9.57	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	148.73 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	53.19 m³·mol⁻¹	ChemAxon
Polarizability	22.46 Å³	ChemAxon
Number of Rings	0	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

119047

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

135103

PDB ID

Not Available

ChEBI ID

73350

Good Scents ID

Not Available

References

General References

Asakura T, Naito A: Structure of silk I (Bombyx mori silk fibroin before spinning) in the dry and hydrated states studied using (13)C solid-state NMR spectroscopy. Int J Biol Macromol. 2022 Sep 1;216:282-290. doi: 10.1016/j.ijbiomac.2022.06.192. Epub 2022 Jul 2. [PubMed:35788005 ]
Donets S, Guskova O, Sommer JU: Searching for Aquamelt Behavior among Silklike Biomimetics during Fibrillation under Flow. J Phys Chem B. 2021 Apr 1;125(12):3238-3250. doi: 10.1021/acs.jpcb.1c00647. Epub 2021 Mar 22. [PubMed:33750140 ]
Asakura T, Ogawa T, Naito A, Williamson MP: Chain-folded lamellar structure and dynamics of the crystalline fraction of Bombyx mori silk fibroin and of (Ala-Gly-Ser-Gly-Ala-Gly)(n) model peptides. Int J Biol Macromol. 2020 Dec 1;164:3974-3983. doi: 10.1016/j.ijbiomac.2020.08.220. Epub 2020 Aug 31. [PubMed:32882279 ]
Watanabe M, Sugawara A, Noguchi Y, Hirose T, Omura S, Sunazuka T, Horie R: Jietacins, azoxy natural products, as novel NF-kappaB inhibitors: Discovery, synthesis, biological activity, and mode of action. Eur J Med Chem. 2019 Sep 15;178:636-647. doi: 10.1016/j.ejmech.2019.05.079. Epub 2019 May 29. [PubMed:31226655 ]
Redko B, Tuchinsky H, Segal T, Tobi D, Luboshits G, Ashur-Fabian O, Pinhasov A, Gerlitz G, Gellerman G: Toward the development of a novel non-RGD cyclic peptide drug conjugate for treatment of human metastatic melanoma. Oncotarget. 2017 Jan 3;8(1):757-768. doi: 10.18632/oncotarget.12748. [PubMed:27768593 ]
LOTUS database [Link]

Showing NP-Card for (2s)-2-[(2-{[(2s)-2-amino-1-hydroxypropylidene]amino}-1-hydroxyethylidene)amino]-3-hydroxypropanoic acid (NP0205625)

MOL for NP0205625 ((2s)-2-[(2-{[(2s)-2-amino-1-hydroxypropylidene]amino}-1-hydroxyethylidene)amino]-3-hydroxypropanoic acid)

3D MOL for NP0205625 ((2s)-2-[(2-{[(2s)-2-amino-1-hydroxypropylidene]amino}-1-hydroxyethylidene)amino]-3-hydroxypropanoic acid)

3D SDF for NP0205625 ((2s)-2-[(2-{[(2s)-2-amino-1-hydroxypropylidene]amino}-1-hydroxyethylidene)amino]-3-hydroxypropanoic acid)

3D-SDF for NP0205625 ((2s)-2-[(2-{[(2s)-2-amino-1-hydroxypropylidene]amino}-1-hydroxyethylidene)amino]-3-hydroxypropanoic acid)

PDB for NP0205625 ((2s)-2-[(2-{[(2s)-2-amino-1-hydroxypropylidene]amino}-1-hydroxyethylidene)amino]-3-hydroxypropanoic acid)

3D PDB for NP0205625 ((2s)-2-[(2-{[(2s)-2-amino-1-hydroxypropylidene]amino}-1-hydroxyethylidene)amino]-3-hydroxypropanoic acid)

SMILES for NP0205625 ((2s)-2-[(2-{[(2s)-2-amino-1-hydroxypropylidene]amino}-1-hydroxyethylidene)amino]-3-hydroxypropanoic acid)

INCHI for NP0205625 ((2s)-2-[(2-{[(2s)-2-amino-1-hydroxypropylidene]amino}-1-hydroxyethylidene)amino]-3-hydroxypropanoic acid)

Structure for NP0205625 ((2s)-2-[(2-{[(2s)-2-amino-1-hydroxypropylidene]amino}-1-hydroxyethylidene)amino]-3-hydroxypropanoic acid)

3D Structure for NP0205625 ((2s)-2-[(2-{[(2s)-2-amino-1-hydroxypropylidene]amino}-1-hydroxyethylidene)amino]-3-hydroxypropanoic acid)