Thiethylperazine Maleate is a dopamine antagonist which blocks postsynaptic dopamine 2 (D2) receptors.

Di-n-octyl phthalate is a plasticizer.

DEHP is an inducer of cell proliferation in lymphocytes.

Dexamethasone acetate is an anti-inflammatory glucocorticoid. Injectable and topical formulations containing dexamethasone acetate have been used to treat inflammation associated with carpal tunnel syndrome, ocular keratitis, asthma exacerbations, and infertility in men.

Hydroxy-PEG14-acid is a PEG derivative containing a hydroxyl group with a terminal carboxylic acid. The terminal carboxylic acid can be reacted with primary amine groups in the presence of activators (e.g. EDC, or DCC) to form a stable amide bond. The hydrophilic PEG spacer increases solubility in aqueous media. The hydroxyl group enables further derivatization or replacement with other reactive functional groups.

MMP9-IN-I is a cell-permeable, potent, and reversible MMP-9 inhibitor.

SKI-II HCl is a substrate competitive, reversible, and highly specific inhibitor of sphingosine kinase.

CKI-7 2HCl is a casein kinase 1 (CK1) inhibitor.

MM 47755 is a new benz[a]anthracene antibiotic from a streptomycete.

Paclitaxel-Succinic acid, also known as Paclitaxel Succinate or Paclitaxel-hemisuccinic acid, is a paclitaxel derivative with a succinic acid linker. The carboxy group of Paclitaxel-Succinic acid, after activiating, can be used to conjugate with other molecules such as peptides, proteins, antibodies or enzymes, or polymers. Paclitaxel-Succinic acid is a useful agent to make Paclitaxel-conjugate for drug delivery, nanodrug research.

1,7-Bis-Boc-1,4,7-Triazaheptane is a non-PEG crosslinker.

Aminolink phosphoramidite for oligonucleotide synthesis. DMS(O)MT is a special protective group similar to traditional MMT, but designed as an improved alternative to it. DMS(O)MT aminolink is fully compatible with standard coupling, deblock, and purification protocols. However, DMS(O)MT group is much better suited for DMT-on and cartridge purification of amino-oligonucleotides because of higher stability, and better oligonucleotide recovery. Oligonucleotides containing DMS(O)MT are more stable in solution than MMT analogs.

Aranorosin is an antibiotic which has been shown to circumvent arbekacin-resistance in MRSA by inhibiting the bifunctional enzyme AAC(6')/APH(2″).

Tecnazene is a giant myofibrillar protein; present in vertebrate & invertebrate striated muscle.

Saridegib HCl, also known as IPI-926 HCl, is a hedgehog pathway inhibitor which inhibits smoothened.

C.I. Disperse Red 15 is a Red dye used as a fluorescent indicator.

Avenanthramide C inhibits vascular smooth muscle cell proliferation and enhances nitric oxide production.

Azido-PEG12-acid is a PEG derivative containing an azide group with a terminal carboxylic acid. The hydrophilic PEG spacer increases solubility in aqueous media. The azide group can react with alkyne, BCN, DBCO via Click Chemistry to yield a stable triazole linkage. The terminal carboxylic acid can be reacted with primary amine groups in the presence of activators (e.g. EDC, or DCC) to form a stable amide bond.

Lauryl gallate is the ester of dodecanol and gallic acid. As a food additive it is used under the E number E312 as an antioxidant and preservative.

PEG2-bis(phosphonic acid) is a PEG Linker.

Dicloralurea is used in the preparation of monoaromatic derivatives of pulvinic acids which may display antioxidant activity. Component of early pesticides.

SR-3576 is a potent JNK3 inhibitor that is highly selective over p38.

Biotin-PEG5-azide is PEG derivative containing a biotin group and an azide group. The azide group can react to form a stable triazole linkage. The hydrophilic PEG spacer increases membrane impermeability of the molecules conjugated to the biotin compound and helps to minimize steric hindrance involved with the binding to avidin molecules. PEG Linkers may be useful in the development of antibody drug conjugates.

Decabromodiphenyl ether is a flame retardant.

Tetradifon is an acaride.

Propargyl-PEG5-CH2CO2-NHS is a PEG derivative containing a propargyl group and an NHS group. The hydrophilic PEG spacer increases solubility in aqueous media. This reagent has a terminal NHS ester and is an amine reactive reagent for derivatizing peptides, antibodies, amine coated surfaces etc. The propargyl group can be reacted with azide-bearing compounds or biomolecules via copper catalyzed azide-NHS ester Click Chemistry to yield a stable triazole linkage.

Carbobenzoxyphenylalanine is an inhibitor of thermolysin.

Pyr3 is a selective antagonist of the canonical transient receptor potential channel 3 (TRPC3).

Dolasetron mesylate is a selective 5-HT3 receptor antagonist.

Cythioate is a cholinesterase inhibitor used as an insecticide.