Cayman Chemical

Cayman Chemical

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  • Linolein Hydroperoxides

    Linolein hydroperoxides are a mixture of 132 possible isomers of mono-, di-, and tri-hydroperoxides produced from the autoxidation of trilinolein. Autoxidation of linoleic acid containing triglycerides (for example, trilinolein) in vivo could result in the formation of these hydroperoxides. Unlike...

  • SGC0946

    Cayman Chemical

    A potent inhibitor of DOT1L (IC50 = 0.3 nM); over 100-fold selective over other PMTs; active in cells, reducing H3K79 dimethylation in A431 and MCF10A cells (IC50s = 2.6 and 8.8 nM, respectively).

  • DDA

    Cayman Chemical

    A prominent member of a class of reactive LO-catalyzed peroxidative decomposition products of unsaturated fatty acids that are formed when diatoms are crushed or eaten.

  • CUDC-101

    Cayman Chemical

    A multi-target inhibitor that potently blocks EGFR and HER2 (IC50s = 2.4 and 16.4 nM, respectively) and inhibits the activity of class I and class II HDACs at nanomolar concentrations (e.g., IC50s = 4.5, 12.6, 13.2, and 11.4 nM for HDAC1, 2, 4, and 5, respectively).

  • Kibdelone B

    Cayman Chemical

    A kibdelone whose mode of action and pharmacology have not been studied.

  • Colistin Methanesulfonate (sodium salt)

    A prodrug for colistin (also known as polymyxin E), an antibiotic that is effective against most Gram-negative bacteria but suffers from nephro- and neurotoxicity; used against infections caused by multidrug resistant Gram-negative bacteria.

  • PPARa (human) Reporter Assay Kit

    This nuclear receptor assay system utilizes proprietary non-human cells engineered to provide constitutive, high-level expression of the human peroxisome proliferator-activated receptor alpha (NR1C1), a ligand-dependent transcription factor commonly referred to as PPARA or PPARα....

  • A-922500

    Cayman Chemical

    A potent inhibitor of DGAT-1 (IC50s = 7 and 24 nM, for human and mouse, respectively); confers significant weight loss within seven days and significantly reduces plasma and liver triglycerides when administered at 3 mg/kg to DIO mice.

  • Lofexidine (hydrochloride)

    An α2-adrenergic receptor agonist (Kd = 7.6 nM for rat cerebral cortex membranes) that has transient antihypertensive effects; used in managing opioid withdrawal symptoms during detoxification from heroin and methadone.

  • Nitrate/Nitrite Colorimetric Assay Kit

    Cayman’s Nitrate/Nitrite Assay provides an accurate and convenient method for measurement of total nitrate/nitrite concentrations. This kit can be used to measure nitrate and nitrite in plasma/serum, urine, tissue culture media, and tissue homogenates. However, it cannot be used to analyze...

  • 1'-hydroxy Midazolam

    Cayman Chemical

    The major CYP3A metabolite of midazolam that has been shown to be equipotent to midazolam.

  • TBS Stock Solution (10X, pH 7.4) with Phenol Red

    TBS stock solution (10X, pH 7.4) contains filtered concentrated TBS. It is ready to use as supplied.

  • (1S,3R)-3-Hydroxycyclopentane carboxylic acid methyl ester

    A synthetic intermediate useful for pharmaceutical synthesis.

  • SMAD6 Polyclonal Antibody

    Antigen: synthetic peptides corresponding to amino acids 85-99 and amino acids 372-388 of human SMAD6 Cross Reactivity: (+) Human, new world monkey, mouse, rat, and ovine SMAD6; predicted to react with horse SMAD6 Application(s): IHC, WB SMAD6 is an inhibitory SMAD (I-SMAD) that is part of a family...

  • URMC-099

    Cayman Chemical

    An orally bioavailable, brain-penetrant inhibitor of MLKs (IC50s = 19, 42, 14, and 150 nM for MLK1, MLK2, MLK3, and the related MLK family member DLK, respectively); also inhibits LRRK2 activity (IC50 = 11 nM); demonstrates anti-inflammatory and neuroprotective effects both in...

  • IPA-3

    Cayman Chemical

    A cell-permeable allosteric inhibitor of PAK1 that is non-competitive with respect to ATP binding (IC50 = 2.5 µM); binds covalently to the PAK1 regulatory domain (apparent Kd = 1.9 uM) and prevents binding to the upstream activator Cdc42.

  • ?9-THC (CRM)

    Cayman Chemical
  • sPLA2 (Type III)

    Cayman Chemical

    EC 3.1.1.4 Active enzyme isolated from bee venom One unit of enzyme hydrolyzes one µmol of Diheptanoyl Thio-PC per minute at 25°C PLA2 catalyzes the hydrolysis of fatty acids at the sn-2 position of glycerophospholipids, yielding a free fatty acid and a lysophospholipid. PLA2 in bee venom...

  • Cannabigerol

    Cayman Chemical

    An analytical reference material categorized as a phytocannabinoid; intended for research and forensic applications

  • (±)11(12)-DiHET

    Cayman Chemical

    The diol resulting from the sEH opening of (±)11(12)-EET; contracts artery rings with approximately 70% of the magnitude of (±)11(12)-EET.

  • (±)-Felodipine

    Cayman Chemical

    An L-type calcium channel blocker that is selective over N-, R-, P/Q- and T-type calcium channels; displays antihypertensive activity, lowering arterial blood pressure without altering cardiac contractility.

  • Arachidonoyl Glycine-d8

    An internal standard for the quantification of NAGly by GC- or LC-MS.

  • Platycodin D

    Cayman Chemical

    A saponin isolated from the root of P. grandiflorum, which has been used extensively in Chinese herbal medicine for many applications.

  • PGDM-d4

    Cayman Chemical

    An internal standard for the quantification of PGDM by GC- or LC-MS.

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