Melanocyte-Stimulating Hormone R

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Melanocyte-Stimulating Hormone Release-Inhibiting Factor (trifluoroacetate salt)

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Cat No: 24476

Biochemicals - Peptides

Melanocyte-stimulating hormone release-inhibiting factor (MSH-R-IF) is a hypothalamic tripeptide that binds to rat striatum (Kd = 4.69 nM) and has diverse biological activities.{38774,38775,38776,38777} In vivo, MSH-R-IF (0.1 mg/kg) decreases immobili...

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Territorial Availability: Available through Bertin Technologies only in France

Synonyms:

L-prolyl-L-leucyl-glycinamide, trifluoroacetate salt

Correlated keywords:

15569-83-2 Melanostatin I Oxytocin C-terminal H-Pro-Leu-Gly-NH2 Prolyleucylglycinamide Prolyleucyl-glycinamide Prolylleucylglycine amide MIF1 MIF-I MIFI 3MT anti-depressant MSHRIF methoxytyramine antiopiate

Product Overview:
Melanocyte-stimulating hormone release-inhibiting factor (MSH-R-IF) is a hypothalamic tripeptide that binds to rat striatum (Kd = 4.69 nM) and has diverse biological activities.{38774,38775,38776,38777} In vivo, MSH-R-IF (0.1 mg/kg) decreases immobility of mice in the forced swim test, indicating antidepressant-like activity.{38775} MSH-R-IF (20 mg/kg) increases striatal concentration of dopamine (Item No. 21992) and the dopamine metabolites DOPAC, 3-methoxy tyramine (3-MT; Item No. 20511), and homovanillic acid (HVA) in a mouse model of Parkinson's disease induced by MPTP.{38776} It decreases vacuous chewing movements induced by haloperidol (Item No. 12014) in a rat model of tardive dyskinesia when administered at a dose of 2 mg/kg.{38777} MSH-R-IF also has anti-opiate effects, reversing analgesia induced by morphine (Item No. ISO60147) and an enkephalin in mice in a radiant heat tail-flick assay.{38774}

Size	10 mg
Shipping	dry ice
Molecular Formula	C₁₃H₂₄N₄O₃ • XCF₃COOH
SMILES	O=C([C@@H](NC([C@H]1NCCC1)=O)CC(C)C)NCC(N)=O.FC(F)(C(O)=O)F
Molecular Weight	284,4
Formulation	A lyophilized powder
Purity	≥95%
Custom Code	3504.00
UNSPSC code	12352100

Technical File

MSDS

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Cayman Chemical's mission is to help make research possible by supplying scientists worldwide with the basic research tools necessary for advancing human and animal health. Our utmost commitment to healthcare researchers is to offer the highest quality products with an affordable pricing policy.

Our scientists are experts in the synthesis, purification, and characterization of biochemicals ranging from small drug-like heterocycles to complex biolipids, fatty acids, and many others. We are also highly skilled in all aspects of assay and antibody development, protein expression, crystallization, and structure determination.

Over the past thirty years, Cayman developed a deep knowledge base in lipid biochemistry, including research involving the arachidonic acid cascade, inositol phosphates, and cannabinoids. This knowledge enabled the production of reagents of exceptional quality for cancer, oxidative injury, epigenetics, neuroscience, inflammation, metabolism, and many additional lines of research.

Our organic and analytical chemists specialize in the rapid development of manufacturing processes and analytical methods to carry out clinical and commercial GMP-API production. Pre-clinical drug discovery efforts are currently underway in the areas of bone restoration and repair, muscular dystrophy, oncology, and inflammation. A separate group of Ph.D.-level scientists are dedicated to offering Hit-to-Lead Discovery and Profiling Services for epigenetic targets. Our knowledgeable chemists can be contracted to perform complete sample analysis for analytes measured by the majority of our assays. We also offer a wide range of analytical services using LC-MS/MS, HPLC, GC, and many other techniques.

Accreditations
ISO/IEC 17025:2005
ISO Guide 34:2009

Cayman is a leader in the field of emerging drugs of abuse, providing high-purity Schedule I-V Controlled Substances to federally-licensed laboratories and qualified academic research institutions for forensic analyses. We are certified by ACLASS Accreditation Services with dual accreditation to ISO/IEC 17025:2005 and ISO Guide 34:2009.