hioc

Selective TrkB receptor agonist. Protects neurons from excitotoxicity. Protects retinas from light-induced retinal degeneration (LIRD) in vivo. Blood brain barrier and blood-retinal barrier penetrant.

Thioctamide (Thioctic acid amide) is a trivial name for 6, 8-dithiooctanoic amide. It is 6, 8-dithiooctanoic acid's functional form where the carboxyl group is attached to protein (or any other amine) by an amide linkage (containing -NH2).

Benzyl isothiocyanate (Benzoylthiocarbimide) (BITC) is an isothiocyanate originally found in cruciferous vegetables. It shows immunomodulatory, anti-parasitic, antibiotic, antioxidative, anti-atherosclerotic, anti-angiogenic, anti-metastatic, anticancer chemotherapeutic, and chemopreventive activities.

Phenylethyl isothiocyanate (JC5411) is an HDAC inhibitor. It potentially for the treatment of benign prostatic hypertrophy.

Pyrrolidinedithiocarbamate ammonium (1-Pyrrolidinedithiocarboxylic acid ammonium salt), a selective NF-κB inhibitor, inhibits translation of nitric oxide synthase mRNA to prevent induction.

Sodium Thiocyanate, one of the main sources of the thiocyanate anion, is used as a precursor for the synthesis of pharmaceuticals and other specialty chemicals.

DIETHYLDITHIOCARBAMIC ACID COPPER SALT is a widely used industrial compound. It has been used as a chelating agent in various biochemical and physiological experiments, including experiments involving metals, proteins, and enzymes.

Butyl isothiocyanate is an isothiocyanate having a butyl group attached to the nitrogen. It has a role as a hapten.

Ammonium thiocyanate is an inorganic salt commonly used to determine iron content, capable of binding with various metal ions (including copper, silver, zinc, lead, and mercury).

Naphthalene-1-thiocarboxamide, 97% ,with CAS No. 20300-10-1, is a fragment molecule that serves as an important scaffold for molecular linking, expansion, and modification. Naphthalene-1-thiocarboxamide, 97% provides a structural basis and research tool for the design and screening of novel drug candidates, and is commonly used in drug discovery, drug synthesis, and related research.

1,1-Dioxo-2,3-dihydrothiochromen-4-one ,with CAS No. 19446-96-9, is a fragment molecule that serves as an important scaffold for molecular linking, expansion, and modification. 1,1-Dioxo-2,3-dihydrothiochromen-4-one provides a structural basis and research tool for the design and screening of novel drug candidates, and is commonly used in drug discovery, drug synthesis, and related research.

(Nz)-n-(6-fluoro-2,3-dihydrothiochromen-4-ylidene)hydroxylamine ,with CAS No. 50596-11-7, is a fragment molecule that serves as an important scaffold for molecular linking, expansion, and modification. (Nz)-n-(6-fluoro-2,3-dihydrothiochromen-4-ylidene)hydroxylamine provides a structural basis and research tool for the design and screening of novel drug candidates, and is commonly used in drug discovery, drug synthesis, and related research.

6-Chlorothiochroman-4-one ,with CAS No. 13735-12-1, is a fragment molecule that serves as an important scaffold for molecular linking, expansion, and modification. 6-Chlorothiochroman-4-one provides a structural basis and research tool for the design and screening of novel drug candidates, and is commonly used in drug discovery, drug synthesis, and related research.

4-(Trifluoromethyl)pyridine-3-thiocarboxamide ,with CAS No. 158063-54-8, is a fragment molecule that serves as an important scaffold for molecular linking, expansion, and modification. 4-(Trifluoromethyl)pyridine-3-thiocarboxamide provides a structural basis and research tool for the design and screening of novel drug candidates, and is commonly used in drug discovery, drug synthesis, and related research.

6-Fluoro-2,3-dihydro-4H-thiochromen-4-one 1,1-dioxide ,with CAS No. 21243-22-1, is a fragment molecule that serves as an important scaffold for molecular linking, expansion, and modification. 6-Fluoro-2,3-dihydro-4H-thiochromen-4-one 1,1-dioxide provides a structural basis and research tool for the design and screening of novel drug candidates, and is commonly used in drug discovery, drug synthesis, and related research.

6-(2,2,2-Trifluoroethoxy)pyridine-3-thiocarboxamide ,with CAS No. 175277-59-5, is a fragment molecule that serves as an important scaffold for molecular linking, expansion, and modification. 6-(2,2,2-Trifluoroethoxy)pyridine-3-thiocarboxamide provides a structural basis and research tool for the design and screening of novel drug candidates, and is commonly used in drug discovery, drug synthesis, and related research.

Thiophene-2-thiocarboxamide ,with CAS No. 20300-02-1, is a fragment molecule that serves as an important scaffold for molecular linking, expansion, and modification. Thiophene-2-thiocarboxamide provides a structural basis and research tool for the design and screening of novel drug candidates, and is commonly used in drug discovery, drug synthesis, and related research.

D-alpha-Methylbenzyl isothiocyanate is an antioxidant. It induces phase II enzyme activity and is also used as a chiral agent.

3-Phenylpropyl isothiocyanate exhibits a potent inhibitory effect on N-nitrosomethyl-benzylamine (NMBA) tumorigenesis, thereby displaying strong chemopreventive properties [1] [2].

3-Isothiocyanato-tetrahydro-thiophene 1,1-dioxide ,with CAS No. 85109-44-0, is a fragment molecule that serves as an important scaffold for molecular linking, expansion, and modification. 3-Isothiocyanato-tetrahydro-thiophene 1,1-dioxide provides a structural basis and research tool for the design and screening of novel drug candidates, and is commonly used in drug discovery, drug synthesis, and related research.

Erythromycin thiocyanate acts by binding to bacterial 50S ribosomal subunits and inhibits RNA-dependent protein synthesis by blockage of transpeptidation and/or translocation reactions, without affecting synthesis of nucleic acid .Erythromycin thiocyanate

Sinapinethiocyanate is a useful organic compound for research related to life sciences and the catalog number is T130131.

Thiocillin I, a thiopeptide antibiotic, demonstrates potent in vitro antibacterial effects against Gram-positive bacteria. This compound exhibits minimum inhibitory concentrations (MICs) of 2 μg/mL, 0.5 μg/mL, 4 μg/mL, and 0.5 μg/mL against S. aureus 1974149, E. faecalis 1674621, B. subtilis ATCC 6633, and S. pyogenes 1744264, respectively.

Thiochrome is a selective enhancer of M4 muscarinic receptor of acetylcholine (ACh) affinity.