HTMT (maleate)

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HTMT (maleate)

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Cat No: 29018

Biochemicals - Receptor Pharmacology

HTMT is a histamine H1 receptor agonist.{47692} It also binds to the histamine H4 receptor (Ki = 1.2 µM) but does not increase calcium mobilization in HEK293 cells expressing the receptor at 10 µM.{47693} HTMT increases intracellular calcium and inosi...

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Territorial Availability: Available through Bertin Technologies only in France

Synonyms:

6-[[2-(1H-imidazol-5-yl)ethyl]amino]-N-[4-(trifluoromethyl)phenyl]-heptanamide, 2Z-butenedioate

Correlated keywords:

103827-16-3 tri-fluoro-methyl HT MT H 1 4 HEK 293 Ig G M

Product Overview:
HTMT is a histamine H1 receptor agonist.{47692} It also binds to the histamine H4 receptor (Ki = 1.2 µM) but does not increase calcium mobilization in HEK293 cells expressing the receptor at 10 µM.{47693} HTMT increases intracellular calcium and inositol phosphate levels (EC50s = 19 and 30 µM, respectively) in human peripheral blood lymphocytes.{47694} It increases proliferation of immortalized mouse small, but not large, cholangiocytes, when used at a concentration of 10 µM.{47696} HTMT (10 µg/kg twice per day) increases levels of sheep red blood cell-induced IgG and IgM antibodies in rabbit serum.{47697} It induces scratching in mice when administered at an intradermal dose of 0.2 µmol, an effect that is reduced by the H1 receptor antagonist terfenadine (Item No. 20305).{47695}

Size	1 mg
Shipping	dry ice
CAS Number	195867-54-0
Molecular Formula	C₁₉H₂₅F₃N₄O • 2C₄H₄O₄
SMILES	FC(F)(F)C1=CC=C(NC(CCCCC(C)NCCC2=CN=CN2)=O)C=C1.O=C(O)/C=C\C(O)=O.O=C(O)/C=C\C(O)=O
Molecular Weight	614,6
Formulation	A solid
Purity	≥98%
Custom Code	2933.29
UNSPSC code	12352100

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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.