DICL_CP_0307890 - DICL Database

Basic Molecular Information

Basic Information

DICL ID

DICL_CP_0307890

PubChem CID

33032

Molecular Formula

C₅H₉NO₄

Molecular Weight

147.13 g/mol

Synonyms/Alias

[L-glutamic acid; GLUTAMIC ACID; 56-86-0; (2S)-2-Aminopentanedioic acid; L-glutamate; (S)-2-Aminopentanedioic acid; Glutamidex; H-Glu-OH; Glutaminol; glutacid; Glutamicol; Glutaton; Aciglut; L-Glutami...[L-glutamic acid; GLUTAMIC ACID; 56-86-0; (2S)-2-Aminopentanedioic acid; L-glutamate; (S)-2-Aminopentanedioic acid; Glutamidex; H-Glu-OH; Glutaminol; glutacid; Glutamicol; Glutaton; Aciglut; L-Glutaminic acid; glutaminic acid; Glusate; (S)-Glutamic acid; L-glu; Acidum glutamicum; D-Glutamiensuur; L-(+)-glutamic acid; alpha-aminoglutaric acid; Glutamic acid; L-; (S)-(+)-Glutamic acid; Acido glutamico; Acide glutamique; Acidum glutaminicum; 1-Aminopropane-1;3-dicarboxylic acid; FEMA No. 3285; Glutamic acid (H-3); alpha-Glutamic acid; glut; glutamate; L-alpha-Aminoglutaric acid; L(+)-Glutamic acid; Glutamic acid; (S)-; 25513-46-6; CCRIS 7314; 2-Aminoglutaric acid; Pentanedioic acid; 2-amino-; (S)-; glu; AI3-18472; Acide glutamique [INN-French]; Acido glutamico [INN-Spanish]; Acidum glutamicum [INN-Latin]; EPA Pesticide Chemical Code 374350; NSC 143503; Glutamic Acid (L-glutamic acid); 2-Aminopentanedioic acid; (S)-; L-2-Aminoglutaric acid; aminoglutaric acid; EINECS 200-293-7; UNII-3KX376GY7L; Glutamic acid (VAN); 3KX376GY7L; INS NO.620; DTXSID5020659; Glutaminic acid (VAN); CHEBI:16015; Gamma-L-Glutamic Acid; INS-620; Glutamate; L-; MFCD00002634; Glutamic Acid [USAN:INN]; C5H9NO4; NSC-143503; L-2-amino-pentanedioic acid; E620; DTXCID30659; alpha-Aminoglutaric acid (VAN); HSDB 490; E 620; E-620; EC 200-293-7; NCGC00024502-03; a-Glutamic acid; (S)-2-AMINO-1;5-PENTANEDIOIC ACID; a-Aminoglutaric acid; Acide glutamique (INN-French); Acido glutamico (INN-Spanish); Acidum glutamicum (INN-Latin); GLUTAMIC ACID (USP-RS); GLUTAMIC ACID [USP-RS]; L-a-Aminoglutaric acid; GLUTAMIC ACID (EP MONOGRAPH); GLUTAMIC ACID [EP MONOGRAPH]; L-Glutaminsaeure; L-Acido glutamico; .alpha.-Glutamic acid; Polyglutamic acid(PGA); 6899-05-4; glt; 2-Amino-pentanedioic acid; 2-aminopentanedioate; 1-amino-propane-1;3-dicarboxylic acid; GLUTAMIC ACID [USAN]; L-Glutamic acid (9CI); L-Glutamic acid-13C5;15N; aminoglutarate; alpha-Glutamate; a-Glutamate; L-gluatmate; a-Aminoglutarate; L-glutamic-acid; NSC143503; L-Glutamic adid; 2-Aminoglutarate; 1ftj; 1xff; (S)-glutamate; L-a-Aminoglutarate; alpha-Aminoglutarate; GGL; (L)-glutamic acid; H-Glu; L-Glutamic;(S); L-(+)-Glutamate; L-alpha-Aminoglutarate; Glutamic acid (USP); Tocris-0218; [3h]-l-glutamic acid; 1ii5; (S)-(+)-Glutamate; (S)-Glu; L-[14C(U)]glutamate; (S)-2-Aminopentanedioate; Biomol-NT_000170; GLUTAMIC ACID [MI]; L-Glutamic acid (JP17); SCHEMBL2202; GLUTAMIC ACID [INN]; L-Glutamic acid; 98.5%; Lopac0_000529; S)-2-Aminopentanedioic acid; GLUTAMIC ACID [VANDF]; L-GLUTAMIC ACID [FCC]; L-GLUTAMIC ACID [JAN]; BPBio1_001132; CHEMBL575060; GTPL1369; GLUTAMIC ACID [WHO-DD]; L-GLUTAMIC ACID [FHFI]; L-Glutamic acid; 99%; FCC; BDBM17657; CHEBI:53374; 1-Aminopropane-1;3-dicarboxylate; Glutamic acid; L- (7CI;8CI); L (+)-glutamic acid; alpha-form; 1-amino-propane-1;3-dicarboxylate; 138-16-9; L-Glutamic acid; non-animal source; Pentanedioic acid; 2-amino-; (S); Tox21_113053; HB0383; HSCI1_000269; PDSP1_000128; PDSP1_001539; PDSP2_000127; PDSP2_001523; s6266; AKOS006238837; AKOS015854087; AM81690; CCG-204619; DB00142; SDCCGSBI-0050512.P002; CAS-56-86-0; ALANINE IMPURITY B [EP IMPURITY]; NCGC00024502-01; NCGC00024502-02; NCGC00024502-04; NCGC00024502-07; (2S)-2-aminopentanedioic acid;H-Glu-OH; AC-11294; DS-13284; HY-14608; (S)-1-Aminopropane-1;3-dicarboxylic acid; CS-0003473; G0059; NS00095129; EN300-52632; L-Glutamic acid; BioUltra; >=99.5% (NT); L-Glutamic acid; tested according to Ph.Eur.; C00025; D00007; L-Glutamic acid; NIST(R)RM 8573; USGS40; LYSINE ACETATE IMPURITY B [EP IMPURITY]; M02979; M03872; L-Glutamic acid; JIS special grade; >=99.0%; L-Glutamic acid; NIST(R) RM 8574; USGS41; A831210; SR-01000597730; J-502415; L-Glutamic acid; ReagentPlus(R); >=99% (HPLC); L-Glutamic acid; Vetec(TM) reagent grade; >=99%; SR-01000597730-1; L-Glutamic acid; >=99%; FCC; natural sourced; FG; Q26995161; F8889-8668; Z756440052; 27322E29-9696-49C1-B541-86BEF72DE2F3; Glutamic acid; European Pharmacopoeia (EP) Reference Standard; L-Glutamic acid; certified reference material; TraceCERT(R); Glutamic acid; United States Pharmacopeia (USP) Reference Standard; L-Glutamic acid; from non-animal source; meets EP testing specifications; suitable for cell culture; 98.5-100.5%]

InChI Key

WHUUTDBJXJRKMK-VKHMYHEASA-N

InChI

InChI=1S/C5H9NO4/c6-3(5(9)10)1-2-4(7)8/h3H,1-2,6H2,(H,7,8)(H,9,10)/t3-/m0/s1

IUPAC Name

(2S)-2-aminopentanedioic acid

CAS Number

59-30-3

Structure Information

Chemical Structure Visualization

SMILES Notation

2D Molecular Drawing

Carbon (C)

Hydrogen (H)

Oxygen (O)

Nitrogen (N)

Sulfur (S)

SDF

19 18 0 0 0 0 0 0 0 0999 V2000
0.1581 -0.3264 -0.5400 C 0 0 0 0 0 0 0 0 0 0 0 0
1.3399 0.0513 0.3637 C 0 0 0 0 0 0 0 0 0 0 0 0
2.5305 0.424...

Download SDF File (1641 bytes)

Experimental Data

Activity Data

Target Ion Channel

Glutamate receptor ionotropic subunit kainate 5

Uniprot Accession Number

Q16478

Function

Agonist

Species

Homo sapiens (Human)

IC₅₀

N/A (Not available)

EC₅₀

N/A (Not available)

K_i

K_i: 701 nM

K_d

N/A (Not available)

Inhibition

N/A (Not available)

Experimental Conditions

pH 7.5

Holding Potential

Not specified

Temperature

4 °C

Test Method

Binding assay

Test Species

HEK293 cell (Homo sapiens embryonic kidney 293 cell)

Binding Information

Binding Site

Not specified

Binding Site Residue

Not specified

Disease Information

Related Disease

Not specified

References

DOI

10.1021/jm9702387

URL

N/A (Not available)

PMID

9357531

Patent

N/A (Not available)

Computed Properties

Heavy Atom Count

Rotatable Bonds

logP

-0.7369

Complexity

32.481

TPSA (Å²)

100.62

H-Bond Donors

H-Bond Acceptors

Ring Count

New Search

Molecular Details

Basic Molecular Information

Basic Information

Structure Information

Chemical Structure Visualization

Experimental Data

Activity Data

Experimental Conditions

Binding Information

Disease Information

References

Computed Properties