H-Arg-Arg-Leu-Ile-Glu-Asp-Asn-Glu-Tyr-Thr-Ala-Arg-Gly-OH

Modify Date: 2025-09-06 18:45:56

H-Arg-Arg-Leu-Ile-Glu-Asp-Asn-Glu-Tyr-Thr-Ala-Arg-Gly-OH structure	Common Name	H-Arg-Arg-Leu-Ile-Glu-Asp-Asn-Glu-Tyr-Thr-Ala-Arg-Gly-OH
	CAS Number	81493-98-3	Molecular Weight	1592.71000
	Density	1.53g/cm3	Boiling Point	N/A
	Molecular Formula	C₆₆H₁₀₉N₂₃O₂₃	Melting Point	N/A
	MSDS	N/A	Flash Point	N/A

Use of H-Arg-Arg-Leu-Ile-Glu-Asp-Asn-Glu-Tyr-Thr-Ala-Arg-Gly-OH

pp60v-src Autophosphorylation site is a synthetic peptide. pp60v-src Autophosphorylation site can be used for various biochemical studies[1].

Name	pp60(v-SRC) Autophosphorylation Site,RRLIEDNEYTARG
Synonym	More Synonyms

Description	pp60v-src Autophosphorylation site is a synthetic peptide. pp60v-src Autophosphorylation site can be used for various biochemical studies[1].
Related Catalog	Research Areas >> Others Signaling Pathways >> Others >> Others
References	[1]. Ohguro H, et al. Separation of phospho- and non-phosphopeptides using reverse phase column chromatography. FEBS Lett. 1995 Jul 24;368(3):452-4. [2]. Ernould AP, et al. Purification and characterization of the major tyrosine protein kinase from the human promyelocytic cell line, HL60. Eur J Biochem. 1993 Jun 1;214(2):503-14. [3]. L J Pike, B Gallis, et al. Epidermal growth factor stimulates the phosphorylation of synthetic tyrosine-containing peptides by A431 cell membranes. Proc Natl Acad Sci U S A. 1982 Mar;79(5):1443-7.

Description

pp60v-src Autophosphorylation site is a synthetic peptide. pp60v-src Autophosphorylation site can be used for various biochemical studies[1].

Related Catalog

Research Areas >> Others

Signaling Pathways >> Others >> Others

References

Density	1.53g/cm3
Molecular Formula	C₆₆H₁₀₉N₂₃O₂₃
Molecular Weight	1592.71000
Exact Mass	1591.81000
PSA	793.67000
LogP	0.82220
Index of Refraction	1.663
InChIKey	FCOIFWGQVMAMSM-UHFFFAOYSA-N
SMILES	CCC(C)C(NC(=O)C(CC(C)C)NC(=O)C(CCCN=C(N)N)NC(=O)C(N)CCCN=C(N)N)C(=O)NC(CCC(=O)O)C(=O)NC(CC(=O)O)C(=O)NC(CC(N)=O)C(=O)NC(CCC(=O)O)C(=O)NC(Cc1ccc(O)cc1)C(=O)NC(C(=O)NC(C)C(=O)NC(CCCN=C(N)N)C(=O)NCC(=O)O)C(C)O
Storage condition	−20°C