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ChemicalBook--->CAS DataBase List--->412961-36-5

412961-36-5

412961-36-5 Structure

412961-36-5 Structure
IdentificationBack Directory
[Name]

BAM (8-22)
[CAS]

412961-36-5
[Synonyms]

BAM (8-22)
BAM-22P (8-22)
Bovine Adrenal Medulla 8-22
BAM8-22 trifluoroacetate salt
BAM (8-22) trifluoroacetate salt
VGRPEWWMDYQKRYG trifluoroacetate salt
Bovine Adrenal Medulla 8-22 trifluoroacetate salt
Bovine adrenal medulla peptide (8-22) trifluoroacetate salt
Val-Gly-Arg-Pro-Glu-Trp-Trp-Met-Asp-Tyr-Gln-Lys-Arg-Tyr-Gly
Val-Gly-Arg-Pro-Glu-Trp-Trp-Met-Asp-Tyr-Gln-Lys-Arg-Tyr-Gly trifluoroace
BAM-22P (8-22) trifluoroacetate salt H-Val-Gly-Arg-Pro-Glu-Trp-Trp-Met-Asp-Tyr-Gln-Lys-Arg-Tyr-Gly-OH trifluoroacetate salt
L-Valyl-glycyl-L-arginyl-L-prolyl-L-α-glutamyl-L-tryptophyl-L-tryptophyl-L-methionyl-L-α-aspartyl-L-tyrosyl-L-glutaminyl-L-lysyl-L-arginyl-L-tyrosyl-glycine trifluoroacetate salt
[Molecular Formula]

C91H127N25O23S
[MDL Number]

MFCD04974822
[MOL File]

412961-36-5.mol
[Molecular Weight]

1971.2
Chemical PropertiesBack Directory
[storage temp. ]

Desiccate at -20°C
[form ]

powder
[color ]

white to off-white
[Water Solubility ]

Soluble to 1 mg/ml in water
Safety DataBack Directory
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

BAM8-22 trifluoroacetate salt has been used in the study to identify the functions of Mas-related gene (Mrg) C in the pathogenesis and treatment of bone cancer pain (BCP).
[Biochem/physiol Actions]

BAM8-22 is a selective agonist for the sensory neuron specific G-protein coupled receptors (SNSRs). BAM8-22 inhibits development of morphine tolerance in rats. BAM8-22 is inactive at opioid receptors. Also, BAM8–22 is a potent activator of Mas-related G-protein-coupled receptors (Mrgprs), MrgprC11 and hMrgprX1. BAM8-22 produces itch and nociceptive sensations in humans in a histamine-independent manner.
[storage]

-20°C (desiccate)
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