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Glp-Asn-Pro-d-Tyr-d-Trp-NH2_Molecular_structure_CAS_882400-49-9)
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Glp-Asn-Pro-d-Tyr-d-Trp-NH2

Catalog No. G5297 Name Sigma Aldrich
CAS Number 882400-49-9 Website http://www.sigmaaldrich.com
M. F. C34H40N8O8 Telephone 1-800-521-8956
M. W. 688.7302 Fax
Purity ≥98% (HPLC) Email
Storage Chembase ID: 154404

SYNONYMS

IUPAC name
(3S)-4-[(2S)-2-{[(1R)-1-{[(1R)-1-carbamoyl-2-(1H-indol-3-yl)ethyl]carbamoyl}-2-(4-hydroxyphenyl)ethyl]carbamoyl}pyrrolidin-1-yl]-4-oxo-3-{[(2S)-5-oxopyrrolidin-2-yl]formamido}butanamide
IUPAC Traditional name
(3S)-4-[(2S)-2-{[(1R)-1-{[(1R)-1-carbamoyl-2-(1H-indol-3-yl)ethyl]carbamoyl}-2-(4-hydroxyphenyl)ethyl]carbamoyl}pyrrolidin-1-yl]-4-oxo-3-{[(2S)-5-oxopyrrolidin-2-yl]formamido}butanamide
Synonyms
JAK4D

DATABASE IDS

MDL Number MFCD11114385
CAS Number 882400-49-9

PROPERTIES

Empirical Formula (Hill Notation) C34H40N8O8
Purity ≥98% (HPLC)
Gene Information rat ... TRH(7200), TRHDE(29953), TRHR(7201)
Apperance white solid
Solubility H2O: >2 mg/mL
MSDS Link Download
Personal Protective Equipment Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Storage Temperature -20°C
German water hazard class 2

DETAILS

Description (English)
Amino Acid Sequence
Glp-Asn-Pro-Tyr-Trp-NH2
Biochem/physiol Actions
The synthetic peptide Glp-Asn-Pro-d-Tyr-d-Trp-NH2 mimics and amplifies central actions of TRH in rat without releasing TSH. Glp-Asn-Pro-d-Tyr-d-Trp-NH2 has dual pharmacological activities: it inhibits TRH-DE and binds to central TRH receptors with nM affinity in rat hippocampus and cortex but not pituitary or heterologous cells expressing TRH receptor 1 (TRHR1) or TRH receptor 2 (TRHR2). The peptide can be a potent tool for probing the role of TRH actions in the CNS and a platform for development of novel TRH-based therapeutics for neuro diseases.
Description (简体中文)
Amino Acid Sequence
Glp-Asn-Pro-Tyr-Trp-NH2
Biochem/physiol Actions
The synthetic peptide Glp-Asn-Pro-d-Tyr-d-Trp-NH2 mimics and amplifies central actions of TRH in rat without releasing TSH. Glp-Asn-Pro-d-Tyr-d-Trp-NH2 has dual pharmacological activities: it inhibits TRH-DE and binds to central TRH receptors with nM affinity in rat hippocampus and cortex but not pituitary or heterologous cells expressing TRH receptor 1 (TRHR1) or TRH receptor 2 (TRHR2). The peptide can be a potent tool for probing the role of TRH actions in the CNS and a platform for development of novel TRH-based therapeutics for neuro diseases.

REFERENCES