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Suriclone

Suriclone is a sedative and anxiolytic drug in the cyclopyrrolone family of drugs. It has a very similar pharmacological profile to the benzodiazepine family of drugs including sedative and anxiolytic properties but with less amnestic effects, and its chemical structure is quite different from that of the benzodiazepine drugs. The mechanism of action by which suriclone produces its sedative and anxiolytic effects is by modulating GABAA receptors, although suriclone is more subtype-selective than most benzodiazepines.

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Surinabant

Surinabant is a cannabinoid receptor type 1 antagonist. It is being investigated as a potential treatment for nicotine addiction, to assist smoking cessation. It may also be developed as an anorectic drug to assist with weight loss. It is at present mainly being developed as an anti-smoking drug, with possible application in the treatment of other addictive disorders such as alcoholism. Other potential applications such as treatment of ADHD have also been proposed.

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Suxibuzone

Suxibuzone is a drug used for joint and muscular pain. It is a prodrug of the non steroidal anti inflammatory drug phenylbutazone, and is commonly used in horses.

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Sweet Almond Oil

Sweet Almond oil is extracted from the seeds of Prunus amygdalus commonly known as Almond. Sweet almond oil is used as a carrier oil in Aromatherapy together with other essential oils. It is externally used in massage and skin care associated with eczema, dermatitis, psoriasis and sunburn.

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Synephrine

Synephrine is a drug commonly used for weight loss. While its effectiveness is widely debated, synephrine has gained significant popularity as an alternative to ephedrine, a related substance which has been made illegal or restricted in many countries due to health risks and its use as a precursor in the illicit manufacturing of methamphetamine. Products containing bitter orange or synephrine are suspected of causing adverse cardiovascular reactions. It is derived primarily from the immature fruit of Citrus aurantium.

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Synhexyl

Parahexyl is a synthetic homologue of THC, which was invented in 1949 during attempts to elucidate the structure of Δ9-THC, one of the active components of cannabis. It is similar in both structure and activity to THC, differing only in the position of one double bond, and the lengthening of the 3-pentyl chain by one CH2 group to n-hexyl. It produces classic cannabis agonist effects in animals. It has a somewhat higher oral bioavailability than THC itself but is otherwise very similar. Presumably it acts as a CB1 agonist in the same way as THC but as there has been no research published using parahexyl since the discovery of the CB1 receptor this has not been definitively confirmed.

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TAK-901

TAK-901 is a small-molecule inhibitor of the serine-threonine kinase Aurora B with potential antineoplastic activity.

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TAK875

TAK-875 is a potent, selective, and orally bioavailable GPR40 agonist, with a pharmacokinetic profile enabling long-acting drug efficacy. TAK-875 showed potent plasma glucose-lowering action and insulinotropic action during an oral glucose tolerance test in female Wistar fatty rats with impaired glucose tolerance. TAK-875 is currently in clinical trials for the treatment of type 2 diabetes mellitus.

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TGX-221

TGX-221 is a potent, selective, and cell membrane permeable inhibitor of the PI3K p110β catalytic subunit.

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TRIHEPTANOIN LAB GRADE 97%

Composed of three seven-carbon fatty acids,the triglyceride can produce ketone bodies with five carbon atoms, as opposed to even-carbon fatty acids which are metabolized to ketone bodies with four carbon atoms. http://www.bocsci.com/triheptanoin-cas-620-67-7-item-416071.html

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