ro 7

Ro 7-9767 is a biochemical.

RO-7 is a next-generation polymerase (PA) endonuclease inhibitor of influenza A and B viruses.

RO 7-0213 is a novel benzodiazepine (RO7-0213) containing a fully positive quaternary ammonium component.

Risdiplam (RG7916) is a centrally and peripherally distributed and orally administrable small molecule SMN2 pre-mRNA splicing modifier that increases survival motor neuron (SMN) protein levels.

HRO761 is a potent Werne r syndrome RecQ DNA deconjugase (WRN) inhibitor that can be used to study cancers such as colon and stomach cancer.

RO7185876 is a selective gamma secretase modulator, which can be used in the study of Alzheimer's disease.

Selnoflast (example 6) is a NLRP3 inhibitor[1].

2,4,5-Trichloro-7H-pyrrolo[2,3-d]pyrimid is a chemical agent.

Ornidazole (Tiberal) is a nitroimidazole antiprotozoal agent used in ameba and trichomonas infections. It is partially plasma-bound and also has radiation-sensitizing action.

6-Chloro-7-hydroxy-4-methylcoumarin ,with CAS No. 19492-02-5, is a fragment molecule that serves as an important scaffold for molecular linking, expansion, and modification. 6-Chloro-7-hydroxy-4-methylcoumarin 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.

3-Chloro-7-hydroxy-4-methylcoumarin ,with CAS No. 6174-86-3, is a fragment molecule that serves as an important scaffold for molecular linking, expansion, and modification. 3-Chloro-7-hydroxy-4-methylcoumarin 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.

7-Hydroxycarbostyril (3,4-Dihydro-7-hydroxycarbostyril) (3,4-Dihydro-7-hydroxycarbostyril) is a kind of pharmaceutical intermediate.

GDC-2992 is a selective and orally active androgen receptor (AR) degradator that degrades AR (DC50 = 2.7 nM) and inhibits proliferation (IC50 = 9.7 nM) in VCaP cells, making it suitable for studying castration-resistant prostate cancer (CRPC).

RO7567132 (FAP-LTBR) is a novel bispecific antibody that binds and agonizes LTBR bivalently while binds and antagonizes FAP monovalently, thereby limiting the activation of LTBR to the tumor microenvironment, inducing the formation of local tertiary lymphoid structures (TLS), and reducing systemic toxicity. Its mouse alternative can inhibit breast cancer growth, and the effect is better when combined with atezolizumab. In the mouse colorectal cancer model, it can also enhance immune cell infiltration and TLS-like structure formation.

1,8-Naphthyridine,1,2,3,4-tetrahydro-7-methyl- ,with CAS No. 274676-47-0, is a fragment molecule that serves as an important scaffold for molecular linking, expansion, and modification. 1,8-Naphthyridine,1,2,3,4-tetrahydro-7-methyl- 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-Chloro-7-deazapurine-β-D-riboside shows antifungal activity.

4-Chloro-7H-pyrrolo[2,3-d]pyrimidine ,with CAS No. 3680-69-1, is a fragment molecule that serves as an important scaffold for molecular linking, expansion, and modification. 4-Chloro-7H-pyrrolo[2,3-d]pyrimidine 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-Chloro-7H-pyrrolo[2,3-d]pyrimidine-5-carboxylic acid ,with CAS No. 186519-92-6, is a fragment molecule that serves as an important scaffold for molecular linking, expansion, and modification. 4-Chloro-7H-pyrrolo[2,3-d]pyrimidine-5-carboxylic acid 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.

1,4-Benzodioxin-6-amine, 2,3-dihydro-7-(phenylthio)- ,with CAS No. 1019584-14-5, is a fragment molecule that serves as an important scaffold for molecular linking, expansion, and modification. 1,4-Benzodioxin-6-amine, 2,3-dihydro-7-(phenylthio)- 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.

Misonidazole as a novel GPX inhibitors to cause oxidative stress in chemotherapy-resistant tumors.

Ruzotolimod (RO7020531) is an orally active Toll-like receptor 7 agonist that suppresses WHV replication and, in combination with RO-7049389, significantly reduces AAV-HBV viral load, while also serving as an experimental immunomodulatory agent for studying antiviral innate immune responses and therapeutic strategies relevant to SARS-CoV-2 and COVID-19 infection models.

Canrenone (SC14266) is an aldosterone antagonist with potassium-sparing diuretic activity.

RG7834 (RO 7020322) is a highly selective and orally bioavailable inhibitor of HBV, targeting HBsAg, HBeAg, and HBV DNA with IC50s of 2.8 nM, 2.6 nM, and 3.2 nM, respectively, in dHepaRG Cells.

4-{5-chloro-7-[(3,5-dihydroxyhexanoyl)oxy]-3-[(1E,3E,5E)-hepta-1,3,5-trien-1-yl]-7-methyl-6,8-dioxo-2,6,7,8-tetrahydroisoquinolin-2-yl}butanoic acid is a high-purity biochemical reagent suitable for biochemical experiments and drug synthesis research.