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Displaying drugs 501 - 525 of 874 in total
Arotinolol
Arotinolol is an alpha- and beta-receptor blocker developed in Japan. It is a thiopropanolamine with a tertiary butyl moiety. It has been studied for its potential to be an antihypertensive therapy. Artinolol is being developed by Sumitomo Pharmaceutical Co., Ltd. and it is currently under clinical trials.
Investigational
Matched Description: … Arotinolol is an alpha- and beta-receptor blocker developed in Japan. ... [T87] Artinolol is being developed by Sumitomo Pharmaceutical Co., Ltd. and it is currently under clinical …
Drostanolone
Drostanolone (also known as dromostanolone) is a potent synthetic androgenic anabolic steroid similar to testosterone. Drostanolone is indicated in postmenopausal women with recurrent breast cancer, in a combined hormone therapy.
Illicit
Lactaldehyde
Experimental
Andrographolide
Andrographolide (HMPL-004) is a botanical product extracted from a herb that occurs naturally in China. The herb has an extensive history of use in TCM for the treatment of upper respiratory tract infections and other inflammatory and infectious diseases.
Investigational
Matched Description: … other inflammatory and infectious diseases. ... herb has an extensive history of use in TCM for the treatment of upper respiratory tract infections and …
Hydroxyprogesterone
Experimental
Matched Categories: … Progesterone and Derivatives ... hydroxyprogesterone and estrogen ... Genito Urinary System and Sex Hormones ... Sex Hormones and Modulators of the Genital System ... Hormones, Hormone Substitutes, and Hormone Antagonists …
Lanatoside C
Experimental
Matched Iupac: … methyloxan-3-yl]oxy}-2-methyl-3-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-4-yl acetate …
1-Testosterone
1-Testosterone is an anabolic steroid that differs from testosterone by having a 1,2-double bond instead of 4,5-double bond in its A ring.
Experimental
Illicit
Investigational
Matched Categories: … Testosterone and derivatives ... Hormones, Hormone Substitutes, and Hormone Antagonists …
Ifenprodil
N-methyl-D-aspartate (NMDA) receptors (NMDARs) are members of the ionotropic glutamate receptor family, with key roles in brain development and neurological function.[A220118, A220128] NMDARs are heterotetramers that typically involve a dimer of dimers of both GluN1 and GluN2A-D subunits, with each subunit itself composed of an N-terminal domain (NTD), a ligand-binding...
Investigational
Withdrawn
Matched Description: … reduce pulmonary infiltration of neutrophils, natural killer cells, and T cells. ... NMDARs) are members of the ionotropic glutamate receptor family, with key roles in brain development and ... A220118, A220128] NMDARs are heterotetramers that typically involve a dimer of dimers of both GluN1 and …
Matched Categories: … Adrenergic alpha-Antagonists …
Matched Categories: … Adrenergic alpha-Antagonists …
Metribolone
A synthetic non-aromatizable androgen and anabolic steroid. It binds strongly to the androgen receptor and has therefore also been used as an affinity label for this receptor in the prostate and in prostatic tumors.
Experimental
Matched Description: … A synthetic non-aromatizable androgen and anabolic steroid. ... this receptor in the prostate and in prostatic tumors. ... It binds strongly to the androgen receptor and has therefore also been used as an affinity label for …
Adenosine-5'-Monophosphate Glucopyranosyl-Monophosphate Ester
Serves as the glycosyl donor for formation of bacterial glycogen, amylose in green algae, and amylopectin in higher plants. [PubChem]
Experimental
Matched Description: … Serves as the glycosyl donor for formation of bacterial glycogen, amylose in green algae, and amylopectin …
Neamine
Experimental
Synephrine
Synephrine, also referred to as, p-synephrine, is naturally occurring alkaloid. It is present in approved drug products as neo-synephrine, its m-substituted analog. p-synephrine and m-synephrine are known for their longer acting adrenergic effects compared to norepinephrine.
The similarity of naming between m-synephrine and the unsubstituted form, synephrine, is a source...
Experimental
Matched Description: … It is present in approved drug products as neo-synephrine, its m-substituted analog. p-synephrine and ... The similarity of naming between m-synephrine and the unsubstituted form, synephrine, is a source of ... While the compounds share some chemical and pharmacological similarities, they are in fact distinct chemical …
Matched Categories: … Adrenergic alpha-Agonists ... Adrenergic and Dopaminergic Agents ... Decongestants and Antiallergics …
Matched Categories: … Adrenergic alpha-Agonists ... Adrenergic and Dopaminergic Agents ... Decongestants and Antiallergics …
Implitapide
Implitapide is a microsomal triglyceride transfer protein (MTP)-inhibitor.
Investigational
17alpha-methyl-3beta,17beta-dihydroxyandrost-4-ene
Experimental
Illicit
Delorazepam
Delorazepam is a benzodiazepine which, like other drugs in its class, possesses anxiolytic, skeletal muscle relaxant, hypnotic and anticonvulsant properties. It may have adverse effects such as drowsiness, and cognitive impairments such as short term memory impairment.
Delorazepam is an active metabolite of the benzodiazepine known as cloxazolam. It is...
Experimental
Illicit
Matched Description: … benzodiazepine which, like other drugs in its class, possesses anxiolytic, skeletal muscle relaxant, hypnotic and ... It may have adverse effects such as drowsiness, and cognitive impairments such as short term memory impairment …
Matched Categories: … Benzodiazepines and benzodiazepine derivatives …
Matched Categories: … Benzodiazepines and benzodiazepine derivatives …
4,5-Dehydro-D-Glucuronic Acid
Experimental
(S)-acetoin
A product of fermentation. It is a component of the butanediol cycle in microorganisms. In mammals it is oxidized to carbon dioxide.
Experimental
(R)-acetoin
A product of fermentation. It is a component of the butanediol cycle in microorganisms. In mammals it is oxidized to carbon dioxide.
Experimental
Inosine
A purine nucleoside that has hypoxanthine linked by the N9 nitrogen to the C1 carbon of ribose. It is an intermediate in the degradation of purines and purine nucleosides to uric acid and in pathways of purine salvage. It also occurs in the anticodon of certain transfer RNA molecules. (Dorland,...
Experimental
Investigational
Matched Description: … It is an intermediate in the degradation of purines and purine nucleosides to uric acid and in pathways …
Matched Categories: … Genito Urinary System and Sex Hormones ... Gynecological Antiinfectives and Antiseptics ... Nucleic Acids, Nucleotides, and Nucleosides …
Matched Categories: … Genito Urinary System and Sex Hormones ... Gynecological Antiinfectives and Antiseptics ... Nucleic Acids, Nucleotides, and Nucleosides …
(S)-mandelonitrile
Experimental
3-Hydroxypyruvic Acid
Experimental
16,17-Androstene-3-Ol
Experimental
Lanosterol
Experimental
Displaying drugs 501 - 525 of 874 in total