[Glu3,4,7,10,14]-Conantokin G_Molecular_structure_CAS_)

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[Glu3,4,7,10,14]-Conantokin G
Catalog No.	C1733	Name	Sigma Aldrich
CAS Number		Website	http://www.sigmaaldrich.com
M. F.	C83H138N26O34	Telephone	1-800-521-8956
M. W.	2044.13762	Fax
Purity	>90% (HPLC)	Email
Storage		Chembase ID: 155607

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SYNONYMS

IUPAC name

(4S)-4-{[(1S)-1-{[(1S)-1-{[(1S)-1-{[(1S)-1-{[(1S)-1-{[(1S)-1-{[(1S)-1-{[(1S)-1-{[(1S)-1-{[(1S,2S)-1-{[(1S)-1-{[(1S)-1-{[(1S)-5-amino-1-{[(1S)-1-{[(1S)-1,2-dicarbamoylethyl]carbamoyl}-2-hydroxyethyl]carbamoyl}pentyl]carbamoyl}-3-carboxypropyl]carbamoyl}-4-carbamimidamidobutyl]carbamoyl}-2-methylbutyl]carbamoyl}-3-methylbutyl]carbamoyl}-3-carboxypropyl]carbamoyl}-3-carbamoylpropyl]carbamoyl}-2-carbamoylethyl]carbamoyl}-3-carboxypropyl]carbamoyl}-3-carbamoylpropyl]carbamoyl}-3-methylbutyl]carbamoyl}-3-carboxypropyl]carbamoyl}-3-carboxypropyl]carbamoyl}-4-(2-aminoacetamido)butanoic acid

IUPAC Traditional name

(4S)-4-{[(1S)-1-{[(1S)-1-{[(1S)-1-{[(1S)-1-{[(1S)-1-{[(1S)-1-{[(1S)-1-{[(1S)-1-{[(1S)-1-{[(1S,2S)-1-{[(1S)-1-{[(1S)-1-{[(1S)-5-amino-1-{[(1S)-1-{[(1S)-1,2-dicarbamoylethyl]carbamoyl}-2-hydroxyethyl]carbamoyl}pentyl]carbamoyl}-3-carboxypropyl]carbamoyl}-4-carbamimidamidobutyl]carbamoyl}-2-methylbutyl]carbamoyl}-3-methylbutyl]carbamoyl}-3-carboxypropyl]carbamoyl}-3-carbamoylpropyl]carbamoyl}-2-carbamoylethyl]carbamoyl}-3-carboxypropyl]carbamoyl}-3-carbamoylpropyl]carbamoyl}-3-methylbutyl]carbamoyl}-3-carboxypropyl]carbamoyl}-3-carboxypropyl]carbamoyl}-4-(2-aminoacetamido)butanoic acid

DATABASE IDS

MDL Number

MFCD00236929

PROPERTIES

Empirical Formula (Hill Notation)	C83H138N26O34
Purity	>90% (HPLC)
MSDS Link	Download
Personal Protective Equipment	Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Storage Temperature	-20°C
German water hazard class	3

DETAILS

Description (English)

Amino Acid Sequence
Gly-Glu-Glu-Glu-Leu-Gln-Glu-Asn-Gln-Glu-Leu-Ile-Arg-Glu-Lys-Ser-Asn
Biochem/physiol Actions
Highly conserved polypeptide NMDA glutamate receptor antagonist; acts through a potent noncompetitive inhibition of polyamine responses; approximately 7-fold more potent than spermine

Description (简体中文)