DICL_CP_0307979 - DICL Database

Basic Molecular Information

Basic Information

DICL ID

DICL_CP_0307979

PubChem CID

876

Molecular Formula

C₅H₁₁NO₂S

Molecular Weight

149.215 g/mol

Synonyms/Alias

[DL-METHIONINE; 59-51-8; methionine; Racemethionine; Acimetion; Lobamine; Urimeth; Banthionine; Cynaron; Meonine; Mertionin; Metione; Pedameth; Dyprin; Neston; DL-Methioninum; (+-)-Methionine; 2-amino...[DL-METHIONINE; 59-51-8; methionine; Racemethionine; Acimetion; Lobamine; Urimeth; Banthionine; Cynaron; Meonine; Mertionin; Metione; Pedameth; Dyprin; Neston; DL-Methioninum; (+-)-Methionine; 2-amino-4-(methylthio)butanoic acid; D;L-methionine; H-DL-Met-OH; Methionine; DL-; DL-2-Amino-4-(methylthio)butanoic acid; FEMA No. 3301; (+/-)-Methionine; 2-amino-4-methylsulfanylbutanoic acid; Methionine dl-form; 2-amino-4-(methylsulfanyl)butanoic acid; NSC 9241; 2-Amino-4-(methylthio)butyric acid; Methilonin; Racemethionine [USAN]; CCRIS 3717; dl-methionin; DL-2-Amino-4-(methylthio)-butyric acid; alpha-Amino-gamma-methylmercaptobutyric acid; NSC-9241; EINECS 200-432-1; UNII-73JWT2K6T3; MFCD00063096; DL-2-Amino-4-(methylthio)butyric acid; 73JWT2K6T3; 26062-47-5; CHEBI:16811; alpha-Amino-gamma-(methylthio)butyric acid; AI3-18475; 2-amino-4-methylsulfanyl-butanoic acid; DL-Methionine (Racemethionine); 7005-18-7; Racemethionine [USAN:USP:NF]; DTXSID9020821; (+/-)-2-Amino-4-(methylmercapto)butyric acid; 2-Amino-4-methylthiobutanoic acid; NSC22946; 2-Amino-4-(methylmercapto)butyric acid; NCGC00159431-02; DL-Methionine (JAN); Racemethionine (USAN); .alpha.-Amino-.gamma.-methylmercaptobutyric acid; DL-METHIONINE [JAN]; Hmet; R-Methionine; Methionine; amorphous; Racemethionine (USAN:USP:NF); RACEMETHIONINE (USP-RS); RACEMETHIONINE [USP-RS]; Methionine DL-; Padameth; Petameth; Amurex; dl-Methionine; (2RS)-2-amino-4-(methylsulfanyl)butanoic acid; Metion; Methio-Form; NSC-45689; DL-Methionine;; Padameth (TN); alpha-Amino-gamma-methylmercaptobutyric acid (VAN); DL-Met; DL-2-Amino-4-methylthiobutanoic acid; Racemethionine; USAN; METHIONINE;L-; 2-amino-4-(methylthio)-butyric acid; (.+-.)-Methionine; (.+/-.)-Methionine; Met248; DL-Methionine; >=99%; SCHEMBL4225; DL-METHIONINE [FCC]; WLN: QVYZ2S1 -L; DTXCID50821; D;L-METHIONINE [FHFI]; DL-METHIONINE [MART.]; CHEMBL274119; DL-METHIONINE [WHO-DD]; DL-METHIONINE [WHO-IP]; H3CSCH2CH2CH(NH2)COOH; METHIONINE DL-FORM [MI]; BDBM86195; FEMA 3301; NSC9241; DL-CH3SCH2CH2CH(NH2)COOH; DL-Methionine; 99%; FCC; FG; CAS_6137; DL-METHIONINE [EP IMPURITY]; HY-N0325; NSC_6137; NSC45689; Tox21_111663; BBL009323; CAS_84815; DL-METHIONINE [EP MONOGRAPH]; DL-Methionine; >=99.0% (NT); NSC_84815; NSC118113; NSC522406; s9344; STK802463; 2-amino-4-(methylthio) butyric acid; AKOS000118924; AKOS016050523; DL-METHIONINUM [WHO-IP LATIN]; CCG-266195; DB13972; NSC-118113; NSC-522406; CAS-59-51-8; Butyric acid; 2-amino-4-(methylthio)-; NCGC00159431-03; NCGC00159431-04; DS-16180; SY004418; L(-)-Amino-.gamma.-methylthiobutyric acid; DB-029693; DB-227226; .gamma.-Methylthio-.alpha.-aminobutyric acid; AM20100433; CS-0008889; M0463; NS00006428; EN300-17984; C01733; D04983; D72471; DL-Methionine; SAJ special grade; >=99.0%; DL-Methionine; Vetec(TM) reagent grade; 98%; L-.gamma.-Methylthio-.alpha.-aminobutyric acid; Z00115; AB00373904-02; Q180341; SR-01000944495; J-300193; L-.alpha.-Amino-.gamma.-methylmercaptobutyric acid; Q-201029; SR-01000944495-1; Z57127440; F0001-1544; C6115881-E914-4EA8-A21A-DCBF67783824; DL-Methionine; European Pharmacopoeia (EP) Reference Standard; Racemethionine; United States Pharmacopeia (USP) Reference Standard; 33807-07-7; DL-Methionine; BioReagent; suitable for cell culture; suitable for insect cell culture; >=99%]

InChI Key

FFEARJCKVFRZRR-UHFFFAOYSA-N

InChI

InChI=1S/C5H11NO2S/c1-9-3-2-4(6)5(7)8/h4H,2-3,6H2,1H3,(H,7,8)

IUPAC Name

2-amino-4-methylsulfanylbutanoic acid

CAS Number

2922060-79-3

Structure Information

Chemical Structure Visualization

SMILES Notation

2D Molecular Drawing

Carbon (C)

Hydrogen (H)

Oxygen (O)

Nitrogen (N)

Sulfur (S)

SDF

20 19 0 0 0 0 0 0 0 0999 V2000
3.5167 0.8220 -0.5732 C 0 0 0 0 0 0 0 0 0 0 0 0
2.5066 -0.6246 -1.0223 S 0 0 0 0 0 0 0 0 0 0 0 0
1.0041 -0.024...

Download SDF File (1724 bytes)

Experimental Data

Activity Data

Target Ion Channel

5-hydroxytryptamine receptor 3A

Uniprot Accession Number

P35563

Function

Antagonist

Species

Rattus norvegicus (Rat)

IC₅₀

N/A (Not available)

EC₅₀

N/A (Not available)

K_i

K_i: >10000 nM

K_d

N/A (Not available)

Inhibition

N/A (Not available)

Experimental Conditions

Not mention

Holding Potential

Not specified

Temperature

Not mention

Test Method

Binding assay

Test Species

CHO cell (Chinese hamster ovary cell)

Binding Information

Binding Site

Not specified

Binding Site Residue

Not specified

Disease Information

Related Disease

Not specified

References

DOI

10.1124/jpet.102.047092

URL

N/A (Not available)

PMID

12649361

Patent

N/A (Not available)

Computed Properties

Heavy Atom Count

Rotatable Bonds

logP

0.1514

Complexity

38.6102

TPSA (Å²)

63.32

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