Methoxybenzenes

Organic compounds that consist of a phenyl group with a methoxy functional group substitution; a methoxy group has an oxygen atom bonded to a methyl group.

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1,666 – 1,680 of 2,440 results

1,666

Aobchem AOBCHEM

5000931348 2 6-DIFLUORO-4-METHOXYPHENYL

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1,667

Aobchem AOBCHEM

5000930784 - 2-BROMO-4-METHOXYPHENYL -3-

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1,668

Aobchem AOBCHEM

5000930973 3-ETHOXY-5-METHOXYPHENYL PHE

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1,669

Medchemexpress LLC Gol-ntr | 2968461-58-5 | 99.4% | 467.40 | C24H16F3N3O4 | 10 MG

Gol-NTR is a Golgi-targetable fluorescent probe activated by nitroreductase (NTR), designed for selective and sensitive imaging of NTR activity in cells and in vivo. The probe is intended for fluorescent labeling and monitoring of disease models where NTR activity is relevant, including acute lung injury research.

Golgi-targetable probe for subcellular imaging
NTR-activated fluorescence for selective detection
Low detection limit of 54.8 ng/mL for high sensitivity
Suitable for fluorescent labeling in A549 cells and in vivo imaging
High reported purity (99.4%) for research applications
Solid, white to off-white form with recommended sealed storage

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1,670

Medchemexpress LLC 1-(3-Methoxyphenyl)piperazine | 16015-71-7 | 99.26% | 192.26 | 10 G

1-(3-Methoxyphenyl)piperazine is an analytical reference standard categorized as a piperazine. It is intended for research use only.

Categorized as a piperazine
Suitable for research use
Available in various pack sizes

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1,671

Accela Chembio Inc 3-methoxyphenylacetic Acid | 100g | 1798-09-0 | MFCD00004334 | 97+% | Shelf Life: 1260 Days | Regular

3-methoxyphenylacetic Acid | 100g | 1798-09-0 | MFCD00004334 | 97+% | Shelf Life: 1260 Days | Regular

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1,672

Medchemexpress LLC 7-Methylguanine | 578-76-7 | 99.9% | 165.15 | 100 MG

7-Methylguanine is an orally active and competitive PARP-1 inhibitor with a Ki value of 61 μM. As a metabolite of nucleic acids, it shows anticancer properties against uterine sarcoma and colon adenocarcinoma. It also acts as a valuable probe for investigating protein-DNA interactions and does not induce DNA damage in NKE-hTERT cells at tested concentrations.

Orally active and competitive PARP-1 inhibitor (Ki 61 μM)
Metabolite of nucleic acids
Anticancer activity against uterine sarcoma and colon adenocarcinoma
Probe for studying protein-DNA interactions
No DNA damage in NKE-hTERT cells at tested concentrations
Low in vivo toxicity at 50 mg/kg orally
Inhibits tumor growth in uterine sarcoma and colon adenocarcinoma models
Solid, white to light yellow form
Store at 4°C protected from light; in solvent, -80°C for 6 months or -20°C for 1 month