JWH-122 N-(5-hydroxypentyl) metabolite is a metabolite of JWH 122 (a synthetic cannabinoid (CB) of the naphthoylindole class) that is characterized by monohydroxylation of the N-alkyl chain. Currently, there are no reports of its biological activity.

MAM-2201 has been recently detected in herbal products and has psychoactive and intoxicating effects in humans, suggesting that MAM-2201 alters brain function. MAM-2201 acts as an agonist of human cannabinoid receptor type 1 (CB1R) and thus to suppress neurotransmitter release. The reduction of neurotransmitter release from CB1R-containing synapses could contribute to some of the symptoms of synthetic cannabinoid intoxication including impairments in cerebellum-dependent motor coordination and motor learning.

QUCHIC or BB-22 (1-(cyclohexylmethyl)-8-quinolinyl ester-1H-indole-3-carboxylic acid), a quinoline derivative, is a synthetic cannabinoid. It is considered to be a constituent of illicit smoking mixtures "spice".

IPHOSPHORIC ACID, COMPD. WITH PIPERAZINE (1:1) is piperazine acidic salt, that used as Flame retardant agent.

Talo-Zanamivir is inactive enantiomer of Zanamivir, a medication used to treat and prevent influenza caused by influenza A and B viruses. Talo-Zanamivir is used as internal standard for Zanamivir analytical studies.

Arginine linoleate is more readily soluble in water, aqueous alcohol and other aqueous solutions than linoleic acid itself or the natural sources of the unsaturated acid. It is possess surface-active properties. When arginine linoleate was mixed with oxymyoglobin, the pigment was oxidized rapidly to metmyoglobin with some degradation of the heme moiety. Thus, the interaction of ferrous hemoproteins such as MbO2 with Arginine linoleate may participate to some extent in the color deterioration of meat during storage. Arginine linoleate is used as the component in the cosmetic materials.

2,5-Dimethoxy-4-chloroamphetamine (DOC) is a substituted alpha-methylated phenethylamine, a psychedelic drug. It was presumably first synthesized by Alexander Shulgin. DOC acts as a selective -hydroxytryptamine (5-HT2) receptor 5-HT2A and 5-HT2c agonist.

Ibotenic acid is an isoxazole originally isolated from Amanita mushrooms. The toxic fungi Amanita muscaria, commonly known as the fly agaric, was used to prepare the soma. The feelings of euphoria or invincibility experienced by those who drank it were eventually attributed to a group of isoxazoles centuries later. Two of these - ibotenic acid and muscimol - were first isolated from the Japanese mushroom Amanita ibotengutake in the 1960s, but found in abundance in all Amanita mushrooms. Ibotenic acid is a non-protein amino acid that is unstable and easily decarboxylated to muscimol. Ibotenic acid is a glutamate agonist, acting at glutamate receptors. Ibotenic acid is neurotoxic and used to induce cerebral lesioning in animal models.

ORM-15341 is an active main metabolite of ODM-201, which is structurally distinct from any known antiandrogens including the second-generation antiandrogens enzalutamide. ORM-15341 is a potent and full antagonist for human androgen receptor. It was shown, that in VCaP prostate cancer cells containing endogenous AR gene amplification and overexpressing AR, ORM-15341 inhibited cell proliferation more efficiently than enzalutamide or ARN-509.