UCSF

ZINC01532526

Draw Identity 99% 90% 80% 70%

Substance Information

In ZINC since Heavy atoms Benign functionality
October 6th, 2004 10 Yes

Popular Name: L-Glutamine L-Glutamine

Find On: PubMed — Wikipedia — Google

CAS Numbers: 39537-23-0 , 56-85-9 , 585-21-7 , 5959-95-5 , 6899-04-3 , [39537-23-0] , [585-21-7]

Other Names:

"L-Glutamine, 99%"

(2S)-2,5-diamino-5-oxopentanoate; (2S)-2,5-diamino-5-oxopentanoic acid; (2S)-2-amino-4-carbamoylbutanoate; (2S)-2-amino-4-carbamoylbutanoic acid; (S)-2,5-Diamino-5-oxopentanoate; (S)-2,5-Diamino-5-oxopentanoic acid; 2-Aminoglutaramic acid; Cebrogen; Glava

(2S)-2,5-diamino-5-oxopentanoate; L-glutamine anion

(2S)-2,5-diamino-5-oxopentanoate;(2S)-2,5-diamino-5-oxopentanoic acid;(2S)-2-amino-4-carbamoylbutanoate;(2S)-2-amino-4-carbamoylbutanoic acid;(S)-2,5-Diamino-5-oxopentanoate;(S)-2,5-Diamino-5-oxopentanoic acid;2-Aminoglutaramic acid;Cebrogen;gamma-Glutami

(2S)-2,5-diamino-5-oxopentanoate;(2S)-2,5-diamino-5-oxopentanoic acid;(2S)-2-amino-4-carbamoylbutanoate;(2S)-2-amino-4-carbamoylbutanoic acid;(S)-2,5-Diamino-5-oxopentanoate;(S)-2,5-Diamino-5-oxopentanoic acid;2-Aminoglutaramic acid;Cebrogen;Glavamin;Glum

(2S)-2,5-diamino-5-oxopentanoic acid; (2S)-2-amino-4-carbamoylbutanoic acid; (S)-2,5-diamino-5-oxopentanoic acid; Glutamic acid 5-amide; Glutamic acid amide; L-(+)-glutamine; L-2-aminoglutaramic acid; L-Glutamin; L-Glutaminsaeure-5-amid; L-glutamic acid g

(2S)-2-((2S)-2-Aminopropanoylamino)-4-carbamoylbutanoic acid

(2S)-2-amino-4-carbamoylbutanoate; (2S)-2-amino-4-carbamoylbutanoic acid; (2S)-2,5-diamino-5-oxopentanoate; (2S)-2,5-diamino-5-oxopentanoic acid; (S)-2,5-Diamino-5-oxopentanoate; (S)-2,5-Diamino-5-oxopentanoic acid; 2-Aminoglutaramic acid; gamma-glutamine

(2S)-2-amino-4-carbamoylbutanoic acid

(2S)-5-amino-2-ammonio-5-oxopentanoate; L-glutamine

(S)-2,5-diamino-5-oxopentanoic acid

(S)-2,5-Diamino-5-oxopentanoic acid; 2,5-Diamino-5-oxopentanoic acid, (S)-; 2-Aminoglutaramic acid; 2-Aminoglutaramic acid, L-; AI3-24392; BRN 1723797; Cebrogen; EINECS 200-292-1; FEMA No. 3684; Glavamin; Glumin; Glumin (amino acid); Glutamic acid 5-amide

(S)-2,5-Diamino-5-oxopentanoic acid; 2,5-Diamino-5-oxopentanoic acid, (S)-; 2-Aminoglutaramic acid; 2-Aminoglutaramic acid, L-; Cebrogen; GLUTAMINE, L-; Glavamin; Glumin; Glumin (amino acid); Glutamic acid 5-amide; Glutamic acid amide; Glutamine; L-(+)-Gl

2,5-Diamino-5-oxopentanoic acid

2-amino-4-carbamoylbutanoic acid

2-Amino-4-carbamoylbutyric acid

2-Aminoglutaramic acid

2-aminoglutaramic acid; 56-85-9; L-glutamine; gln; glum; glumin; glutamic acid 5-amide; glutamine; proglumide

2-Aminoglutaramic acid; 6899-04-3; C00303; Glutamine

56-85-9; D00015; Glutamine (USP); L-Glutamine (JP16); Levoglutamide; Nutrestore (TN)

AES-14

Ala-Gln

Cebrogen

CHEBI:21308; CHEBI:42899; CHEBI:42812; CHEBI:42814; CHEBI:42943; CHEBI:13110; CHEBI:6227

D-2-Aminoglutaramic acid

D-Glutamine

DIPEPTIVEN

DL-Glutamine

DL-Glutamine, 98%

Earthlink Science Glutamine Chews Chocolate

Earthlink Science Glutamine Chews Chocolate (Amerifit)

FDA

Glavamin

Glutamine

GLUTAMINE (D)

Glutamine (FDA

Glutamine (INN

GLUTAMINE (L)

GLUTAMINE DL-

Glutamine Express

Glutamine Express (Genetic Evolutionary Nutrition)

Glutamine Fuel Mega

Glutamine Fuel Mega (Twinlab)

Glutamine Fuel Powder

Glutamine Fuel Powder (Twinlab)

H-Gln-OH

INN

L(+)-Glutamine

L(+)-Glutamine, 99%

L(+)-Glutamine, specified according to the requirements of USP

L-(+)-glutamine

L-2-aminoglutaramic acid

L-Alanyl-L-glutamide

L-Glutamic acid 5-amide

L-glutamic acid γ-amide

L-glutaminate

L-Glutamine Power

L-Glutamine Power (Champion Nutrition)

L-glutamine zwitterion

L-Glutamine [56-85-9]; (H-Gln-OH)

L-Glutamine, 99%

L-GLUTAMINE; [56-85-9]

MFCD00008044

MFCD00065103

N/A

NA

NUTRESTORE

OR-3012

Saforis

Stimulina

USAN

USP); L-Glutamine (JAN); Levoglutamide (DCF)

Download: MOL2 SDF SMILES Flexibase

Annotations

Vendors

Physical Representations

Type pH range xlogP Des A‑Pol Apolar desolvation (kcal/mol) Des Pol Polar desolvation (kcal/mol) H Don H-bond donors H Acc H-bond acceptors Chg Net charge tPSA (Ų) MWT Molecular weight (g/mol) RB Rotatable bonds DL
Ref Reference (pH 7) -3.76 -2.13 -50.63 5 5 0 111 146.146 4 ↓
Hi High (pH 8-9.5) -3.76 -2.45 -53.15 4 5 -1 109 145.138 4 ↓

Vendor Notes

Note Type Comments Provided By
UniProt Database Links 050L_FRG3G; 073R_IIV3; 089R_FRG3G; 11S3_HELAN; 1433_NEOCA; 1A110_ARATH; 3CP1_STRS9; 3CP2_STRSQ; 3HAPM_CUPPJ; 4F2_HUMAN; 5HT2A_DROME; 5HT2B_HUMAN; 5NT1B_HUMAN; 7LESS_DROVI; 7TMK2_DICDI; A1AG1_HUMAN; A1CF_HUMAN; A1CF_MOUSE; A1CF_PONAB; A1CF_RAT; A4_HUMAN; A ChEBI
Melting_Point 177? Alfa-Aesar
MP 183 - 185 Enamine Building Blocks
MP 184 - 186 Enamine Building Blocks
MP 184...186 Enamine Building Blocks
Mp [°C] 185 Acros Organics
MP 185 °C (dec.)(lit.) Indofine
Melting_Point 185? dec. Alfa-Aesar
Melting_Point 185° dec. Alfa-Aesar
MP 186° Matrix Scientific
purity 9.500000000000000e+001 Enamine Building Blocks
ALOGPS_SOLUBILITY 9.78e+01 g/l DrugBank-experimental
purity 95 Enamine Building Blocks
Purity 95% Fluorochem
Purity 95+% Matrix Scientific
Purity 98% Fluorochem
UniProt Database Links AGLUS_ARCFU; AGLUS_DEHE1; AGLUS_METJA; AGLUS_THEMA; AGLUS_THENN; AGLUS_THESQ; ARCS_METJA; ARGA_MYCTU; CARB_STAAR; CARB_STAAS; CARB_STAAT; CARB_STAAW; CARB_STACT; CARB_STAEQ; CARB_STAES; CARB_STAHJ; CARB_STAS1; CARB_STRA1; CARB_STRA3; CARB_STRA5; CARB_STRA ChEBI
therap dietary suppliment MicroSource Spectrum
Patent Database Links EP0962459; EP1125925; EP1127869; EP1222920; EP1568283; EP1582208; EP1609462; EP1616963; EP1627884; EP1640381; EP1762232; EP1815856; EP1854486; EP1869977; EP1938798; GB1585736; US2002010195; US2002065299; US2003176448; US2004034080; US2004133013; US2004176 ChEBI
Therapy Excitatory amino acid SMDC Pharmakon
SOLUBILITY H2O: 25 mg/mL Indofine
Warnings IRRITANT Matrix Scientific
Target Others Selleck Chemicals
Notes Pyrogen free Apollo Scientific Bioactives
Reactome Database Links REACT_111140; REACT_111222; REACT_11135; REACT_1171; REACT_13419; REACT_13449; REACT_13482; REACT_13564; REACT_13590; REACT_13593; REACT_13611; REACT_13659; REACT_13763; REACT_13773; REACT_1427; REACT_14843; REACT_15361; REACT_15363; REACT_1700; REACT_193 ChEBI
Patent Database Links US2005171117 ChEBI

Activity (Go SEA)

Direct Reactome Annotations (via ChEBI)

Description Species
Amino acid synthesis and interconversion (transamination)
Amino acid transport across the plasma membrane
Antigen Presentation: Folding, assembly and peptide loading of class I MHC
Antigen processing: Ubiquitination & Proteasome degradation
Astrocytic Glutamate-Glutamine Uptake And Metabolism
Conjugation of phenylacetate with glutamine
Cross-presentation of soluble exogenous antigens (endosomes)
Cytosolic tRNA aminoacylation
De novo synthesis of GMP
De novo synthesis of IMP
De novo synthesis of UMP
Endosomal/Vacuolar pathway
ER-Phagosome pathway
Glutamate Neurotransmitter Release Cycle
Glutathione synthesis and recycling
Mitochondrial tRNA aminoacylation
Na+/Cl- dependent neurotransmitter transporters
Nicotinate metabolism
Proton/oligonucleotide cotransporters
Purine ribonucleoside monophosphate biosynthesis
Pyrimidine biosynthesis
Synthesis and interconversion of nucleotide di- and triphosphates
Synthesis of UDP-N-acetyl-glucosamine

Analogs ( Draw Identity 99% 90% 80% 70% )