Tin Mesoporphyrin IX (chloride)

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Cat No: 19071

Biochemicals - Small Molecule Inhibitors

Heme oxygenases (HOs) convert protoheme to biliverdin, which in turn is enzymatically metabolized to bilirubin (Item No. 17161). Tin mesoporphyrin IX is a potent, competitive inhibitor of HO activity in vitro (Ki = 14 nM).{30698} It inhibits hepatic, r...

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Territorial Availability: Available through Bertin Technologies only in France

Synonyms:

(OC-6-13)-dichloro[7,12-diethyl-3,8,13,17-tetramethyl-21H,23H-porphine-2,18-dipropanoato(4-)-?N21,?N22,?N23,?N24]-stannate(2-), dihydrogen

Correlated keywords:

749168-44-3 110946-74-2 B 992 B992 Stanate Stannsoporfin NSC267099 heme oxygenase HO Sn(IV) SINIV SIN IV

Product Overview:
Heme oxygenases (HOs) convert protoheme to biliverdin, which in turn is enzymatically metabolized to bilirubin (Item No. 17161). Tin mesoporphyrin IX is a potent, competitive inhibitor of HO activity in vitro (Ki = 14 nM).{30698} It inhibits hepatic, renal, and splenic HO activity in vivo for extended periods of time.{30698} Tin mesoporphyrin IX blocks bilirubin production in vivo, decreasing HO activity in animal models of hyperbilirubinemia.{30698,26672,30699} Tin mesoporphyrin IX can be used to study the physiological roles of induced HO-1 expression in animal models.{30697,30700,30701}

Size	1 mg
Shipping	dry ice
CAS Number	106344-20-1
Molecular Formula	C₃₄H₃₄Cl₂N₄O₄Sn • 2H
SMILES	[Cl-][Sn+4]1([N-]2C3=CC(C(C)=C4CCC([O-])=O)=[N]1C4=CC5=C6CCC([O-])=O)([N](C7=C8)=C(C(C)=C7CC)C=C2C(CC)=C3C)([N-]5C8=C6C)[Cl-].[H+].[H+]
Molecular Weight	754,3
Formulation	A crystalline solid
Purity	≥95%
Custom Code	2933.49
UNSPSC code	12352100

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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.