UCSF

ZINC01532529

Substance Information

In ZINC since Heavy atoms Benign functionality
October 6th, 2004 9 No

Other Names:

"L-Methionine, 99%"

(+-)-Methionine; AI3-18475; Acimetion; Banthionine; C5H11NO2S; CCRIS 3717; Cynaron; D,L-methionine; DL-2-Amino-4-(methylthio)-butyric acid; DL-2-Amino-4-(methylthio)butanoic acid; DL-Methioninum; Dyprin; EINECS 200-432-1; FEMA No. 3301; LS-7491; Lobamine

(+-)-Methionine;(+/-)-2-Amino-4-(methylmercapto)butyric acid;2-Amino-4-(methylmercapto)butyric acid;2-Amino-4-(methylsulfanyl)butanoic acid;2-Amino-4-(methylthio)-Butyric acid;2-Amino-4-(methylthio)butanoic acid;2-Amino-4-(methylthio)butyric acid;2-Amino-

(+/-)-2-Amino-4-(methylthio)butyric acid

(2S)-2-amino-4-(methylsulfanyl)butanoate; (2S)-2-amino-4-(methylsulfanyl)butanoic acid; (l)-methionine; (s)-(+)-methionine; (S)-2-amino-4-(methylthio)-Butanoate; (S)-2-amino-4-(methylthio)-Butanoic acid; (S)-2-Amino-4-(methylthio)butanoate; (S)-2-Amino-4-

(2S)-2-amino-4-(methylsulfanyl)butanoate; (2S)-2-amino-4-(methylsulfanyl)butanoic acid; (L)-methionine; (S)-(+)-methionine; (S)-2-Amino-4-(methylthio)butanoate; (S)-2-Amino-4-(methylthio)butanoic acid; (S)-2-amino-4-(methylthio)-Butanoate; (S)-2-amino-4-(

(2S)-2-amino-4-(methylsulfanyl)butanoate; L-methionine anion

(2S)-2-amino-4-(methylsulfanyl)butanoate;(2S)-2-amino-4-(methylsulfanyl)butanoic acid;(L)-methionine;(S)-(+)-methionine;(S)-2-amino-4-(methylthio)-Butanoate;(S)-2-amino-4-(methylthio)-Butanoic acid;(S)-2-Amino-4-(methylthio)butanoate;(S)-2-Amino-4-(methyl

(2S)-2-amino-4-(methylsulfanyl)butanoate;(2S)-2-amino-4-(methylsulfanyl)butanoic acid;(L)-methionine;(S)-(+)-methionine;(S)-2-Amino-4-(methylthio)butanoate;(S)-2-Amino-4-(methylthio)butanoic acid;(S)-2-amino-4-(methylthio)-Butanoate;(S)-2-amino-4-(methylt

(2S)-2-amino-4-(methylsulfanyl)butanoic acid

(2S)-2-amino-4-(methylsulfanyl)butanoic acid; (S)-2-amino-4-(methylthio)butanoic acid; (S)-2-amino-4-(methylthio)butyric acid; (S)-methionine; L-(-)-methionine; L-Methionin; L-alpha-amino-gamma-methylmercaptobutyric acid; Methionine

(2S)-2-amino-4-methylsulfanyl-butanoic acid

(2S)-2-ammonio-4-(methylsulfanyl)butanoate; L-methionine

(L)-Methionine; (S)-2-Amino-4-(methylthio)butanoic acid; 2-Amino-4-(methylthio)butyric acid, (S)-; 2-Amino-4-methylthiobutanoic acid (S)-; Butanoic acid, 2-amino-4-(methylthio)-, (S)-; C5H11NO2S; CCRIS 5528; CCRIS 5536; Cymethion; EINECS 200-562-9; HSDB 4

(L)-Methionine; (S)-2-Amino-4-(methylthio)butanoic acid; 2-Amino-4-(methylthio)butyric acid, (S)-; 2-Amino-4-methylthiobutanoic acid (S)-; Butanoic acid, 2-amino-4-(methylthio)-, (S)-; Cymethion; L(-)-Amino-gamma-methylthiobutyric acid; L-(-)-Methionine

(R)-Methionine; C5H11NO2S; D-Methionine; D-Metionien [Australian]; EINECS 206-483-6; LS-91364; Methionine D-; Methionine, D-; NSC 45689

(S)-((2-Amino-4-(methylthio)butanoyl)oxy)zinc(II) hydrogensulfate

(S)-2-Amino-4-(methylmercapto)butyric acid, L-2-Amino-4-(methilthio)butanoic acid

(S)-2-Amino-4-(methylthio)butanoic acid

(S)-2-Amino-4-(methylthio)butyric acid

(S)-2-Amino-4-methylmercaptobutyric acid

(S)-methionine

2-amino-4-(methylsulfanyl)butanoic acid

2-Amino-4-(methylthio)butyric acid

2-Amino-4-(methylthio)butyric acid; 59-51-8; C01733; Methionine

2-ammonio-4-(methylsulfanyl)butanoate; methionine

58576-49-1; Carbon-11 methionine; D04984; Methionine C 11 (USAN)

63-68-3; D00019; L-Methionine (JP16); L-Methionine Z (TN); Methionine (USP)

63-68-3; L-methionine; met; methionine

a-Amino-g-methylmercaptobutyric acid

Acimethin

AMINOMETHYLTHIOBUTANOICACI

CHEBI:43990; CHEBI:21360; CHEBI:13141; CHEBI:6271

Cymethion

Dichloro(L-methioninato-N,S)platinate(1-) hydrogen (SP-4-3)-; Dichloro-L-methionineplatinum(II); LS-117469; Methionine platinum dichloride; Platinate(1-), dichloro(L-methioninato-N,S)-, hydrogen, (SP-4-3)-; Platinum, dichloro(L-methionine)-; Platinum, dic

DL-Methionine

Dl-Methionine (JAN); Methionine (INN

DL-Methionine methylsulfonium chloride

DL-Methionine [59-51-8]

DL-Methionine, 99%

DL-Methionine, 99+%

DL-METHIONINE-D3

DL-METHIONINE; [59-51-8]

DL-MethionineMethylsulfoniuMChloride

g-Methylthio-a-aminobutyric acid

H-D-Met-OH

H-DL-Met-OH

H-Met-OH

INN); Methionine (11C) (USP)

L-(-)-Methionine

L-a-Amino-g-methylthiobutyric acid

L-methioninate

L-Methionine (JAN); Methionine (INN

L-Methionine (JAN); Methionine (USAN

L-Methionine methylsulfonium iodide

L-Methionine methylsulfonium iodide, 99%

L-methionine zwitterion

L-Methionine [63-68-3]

L-Methionine, 98+%

L-METHIONINE, [METHYL-14C]

L-METHIONINE,[METHYL-14C]

L-methionine-methyl-13c,d3

L-methionine-methyl-d3

L-METHIONINE; [63-68-3]

methionine

methionine zwitterion

MFCD00002622

MFCD00002624

MFCD00002625

MFCD00031700

MFCD00050272

MFCD00063096

MFCD00063097

MFCD04118310

NF); Racemethionine (USAN

Racemethionine

USAN

USP

USP)

USP); Methionine (11C) (USP)

USP); Methionine C 11 (USP)

Zinc Monomethionine

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) -2.24 2.24 -40.54 3 3 0 68 149.215 4
Hi High (pH 8-9.5) -2.24 1.91 -44.84 2 3 -1 66 148.207 4

Vendor Notes

Note Type Comments Provided By
SOLUBILITY 1 M HCl: 0.5 M at 20 C, clear, colorless Indofine
UniProt Database Links 13SB_FAGES; 1A111_ARATH; 1A11_CUCMA; 1A11_CUCPE; 1A11_ORYSI; 1A11_ORYSJ; 1A11_PRUMU; 1A12_ARATH; 1A12_CUCMA; 1A12_CUCPE; 1A12_SOLLC; 1A13_SOLLC; 1A14_ARATH; 1A14_SOLLC; 1A15_ARATH; 1A16_ARATH; 1A17_ARATH; 1A18_ARATH; 1A19_ARATH; 1A1C_DIACA; 1A1C_MALDO; 1A ChEBI
Melting_Point 156-157? Alfa-Aesar
Melting_Point 156-157° Alfa-Aesar
UniProt Database Links 1A111_ARATH; 1A11_CUCMA; 1A11_CUCPE; 1A11_ORYSI; 1A11_ORYSJ; 1A11_PRUMU; 1A12_ARATH; 1A12_CUCMA; 1A12_CUCPE; 1A12_SOLLC; 1A13_SOLLC; 1A14_ARATH; 1A14_SOLLC; 1A15_ARATH; 1A16_ARATH; 1A17_ARATH; 1A18_ARATH; 1A19_ARATH; 1A1C_DIACA; 1A1C_MALDO; 1A1C_SOYBN; 1A ChEBI
ALOGPS_SOLUBILITY 2.39e+01 g/l DrugBank-nutriceuticals
Mp [°C] 270 - 273 Acros Organics
MP 273 - 275 Enamine Building Blocks
MP 273...275 Enamine Building Blocks
MP 280° Oakwood Chemical
MP 284 °C (dec.)(lit.) Indofine
purity 9.500000000000000e+001 Enamine Building Blocks Enamine Building Blocks
Purity 95% Fluorochem
Purity 95+% Matrix Scientific
Purity 98% Fluorochem
UniProt Database Links AATR1_DICDI; AATR1_SCHPO; AATR2_DICDI; AATR2_SCHPO; AATR3_SCHPO; AK1H_ECOLI; AK1H_SERMA; AK1_ARATH; AK1_BACSU; AK2H_ECOLI; AK2_ARATH; AK2_BACSU; AK3_ARATH; AK3_BACSU; AKH1_ARATH; AKH1_MAIZE; AKH2_ARATH; AKH2_MAIZE; AKH_BUCAI; AKH_BUCAP; AKH_BUCBP; AKH_DAU ChEBI
Melting_Point ca 272? dec. Alfa-Aesar
Melting_Point ca 272° dec. Alfa-Aesar
Melting_Point ca 280? dec. Alfa-Aesar
Melting_Point ca 280° dec. Alfa-Aesar
Patent Database Links EP1552838; EP1568283; EP1609462; EP1616963; EP1627884; EP1632233; EP1656931; EP1762232; EP1774858; EP1808184; EP1849466; EP1869977; EP1875921; EP1983044; GB1212533; US2004034080; US2004248776; US2005101540; US2005130274; US2005256031; US2006178430; US2006 ChEBI
Warnings IRRITANT Matrix Scientific
Notes Ph.Eur, Pyrogen free Apollo Scientific Bioactives
Reactome Database Links REACT_111140; REACT_111222; REACT_115861; REACT_13449; REACT_13479; REACT_13482; REACT_13590; REACT_13593; REACT_13642; REACT_13741; REACT_14802; REACT_14843; REACT_15420; REACT_15446; REACT_163720; REACT_19313; REACT_19377; REACT_25068; REACT_6739; REACT ChEBI
S phrase S24/25: Avoid contact with skin and eyes. Acros Organics

Activity (Go SEA)

Direct Reactome Annotations (via ChEBI)

Description Species
Amino acid transport across the plasma membrane
Antigen Presentation: Folding, assembly and peptide loading of class I MHC
Antigen processing: Ubiquitination & Proteasome degradation
Cobalamin (Cbl, vitamin B12) transport and metabolism
Cross-presentation of soluble exogenous antigens (endosomes)
Cytosolic tRNA aminoacylation
Endosomal/Vacuolar pathway
ER-Phagosome pathway
Glutathione synthesis and recycling
Inactivation, recovery and regulation of the phototransduction cascade
Methionine salvage pathway
Methylation
Mitochondrial tRNA aminoacylation
Molybdenum cofactor biosynthesis
Na+/Cl- dependent neurotransmitter transporters
Proton/oligonucleotide cotransporters
Sulfur amino acid metabolism

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