1689-99-2
1689-99-2
Chemical Structure
Bromoxynil octanoate
- CAS. Nr.: 1689-99-2
- Formula:C15H17Br2NO2
- Molecular Weight:403.11
IUPAC Name: 2,6-dibromo-4-cyanophenyl octanoate
InChIKey: DQKWXTIYGWPGOO-UHFFFAOYSA-N
SMILES: CCCCCCCC(OC1=C(Br)C=C(C#N)C=C1Br)=O
Biological Activity: Bromoxynil octanoate is an orally active Herbicide and Cx43 gap junction channel inhibitor. Bromoxynil octanoate activates ERK1/2 and NF-κB-P65. Bromoxynil octanoate induces Apoptosis. Bromoxynil octanoate induces oxidative stress and inflammation. Bromoxynil octanoate causes reproductive toxicity by reducing epididymal sperm count and motility as well as serum testosterone levels[1][2][3].
| Art. -Nr. | Produktname | Reinheit | Beschreibung | Pricing | |||||||||||||||||||
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Bromoxynil octanoate | 99.28% | Bromoxynil octanoate is an orally active Herbicide and Cx43 gap junction channel inhibitor. Bromoxynil octanoate activates ERK1/2 and NF-κB-P65. Bromoxynil octanoate induces Apoptosis. Bromoxynil octanoate induces oxidative stress and inflammation. Bromoxynil octanoate causes reproductive toxicity by reducing epididymal sperm count and motility as well as serum testosterone levels. | ||||||||||||||||||||
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Bromoxynil octanoate (Standard) | ≥98% | Bromoxynil octanoate (Standard) is the analytical standard of Bromoxynil octanoate (HY-136370). This product is intended for research and analytical applications. Bromoxynil octanoate is an orally active Herbicide and Cx43 gap junction channel inhibitor. Bromoxynil octanoate activates ERK1/2 and NF-κB-P65. Bromoxynil octanoate induces Apoptosis. Bromoxynil octanoate induces oxidative stress and inflammation. Bromoxynil octanoate causes reproductive toxicity by reducing epididymal sperm count and motility as well as serum testosterone levels. | ||||||||||||||||||||
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Bromoxynil octanoate-d15 | Bromoxynil octanoate-d15 is the d15-labeled Bromoxynil octanoate (HY-136370). Bromoxynil octanoate is an orally active Herbicide and Cx43 gap junction channel inhibitor. Bromoxynil octanoate activates ERK1/2 and NF-κB-P65. Bromoxynil octanoate induces Apoptosis. Bromoxynil octanoate induces oxidative stress and inflammation. Bromoxynil octanoate causes reproductive toxicity by reducing epididymal sperm count and motility as well as serum testosterone levels. | |||||||||||||||||||||
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Remetinostat | 98.0% | Remetinostat (SHP-141) is a hydroxamic acid-based histone deacetylase (HDAC) inhibitor. Remetinostat alleviates Imiquimod (HY-B0180)-induced psoriatic dermatitis. Remetinostat can be used for study of cutaneous T-cell lymphoma. | ||||||||||||||||||||
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2,4,6-Tribromophenyl caproate (Standard) | ≥98% | 2,4,6-Tribromophenyl caproate (Standard) is the analytical standard of 2,4,6-Tribromophenyl caproate (HY-101506). This product is intended for research and analytical applications. 2,4,6-Tribromophenyl caproate (2,4,6-tribromophenyl caproic acid ester) is an anti-fungal agent. | ||||||||||||||||||||
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Aplysamine-1 | Aplysamine-1 acts as an antagonist for the histamine H3 receptor. | |||||||||||||||||||||
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4-Nitrophenyl Laurate | 98.96% | 4-Nitrophenyl Laurate is a class of 4-nitrophenyl ester, which can be used as enzyme substrate. | ||||||||||||||||||||
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4-Nitrophenyl octanoate | 99.57% | 4-Nitrophenyl octanoate (p-Nitrophenyl caprylate) is an aromatic ester compound which can be used as a substrate for pancreatic lipase. 4-Nitrophenyl octanoate contains an ester bond that can be hydrolyzed under the action of lipase, releasing p-nitrophenol as a yellow product. 4-Nitrophenyl octanoate can be used to assay the activities of lipases and esterases. | ||||||||||||||||||||
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Paradol | 98.66% | Paradol is a pungent phenolic substance found in ginger and other Zingiberaceae plants. Paradol is an effective inhibitor of tumor promotion in mouse skin carcinogenesis, binds to cyclooxygenase (COX)-2 active site. | ||||||||||||||||||||
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4-Nitrophenyl decanoate | 98.04% | 4-Nitrophenyl decanoate is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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p-Tolyl octanoate | p-Tolyl n-Octanoate is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | |||||||||||||||||||||
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5-Bromo-1H-indol-3-yl octanoate | 5-Bromo-1H-indol-3-yl octanoate is a chromogenic substrate for esterase with C8 activity. 5-Bromo-1H-indol-3-yl octanoate yields a blue precipitate when cleaved. | |||||||||||||||||||||
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2-Naphthalenyl octanoate | 2-Naphthalenyl octanoate is a biochemical assay reagent. | |||||||||||||||||||||
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References
- [1]. Leithe E, et al. Inhibition of connexin 43 gap junction channels by the endocrine disruptor ioxynil. Toxicology and applied pharmacology. 2010 Aug 15;247(1):10-7.
- [2]. El-Nagar MMF, et al. Exposure to bromoxynil octanoate herbicide induces oxidative stress, inflammation, and apoptosis in testicular tissue via modulating NF-кB pathway. Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association. 2023 Oct;180:114008.
- [3]. El-Nagar MMF, et al. Protective effect of Spirulina platensis against testicular toxicity induced by bromoxynil octanoate herbicide through reducing oxidative stress, and inflammation and regulating PPAR-γ/FOXO1/NF-κB and Nrf-2/HO-1 signaling pathways. Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association. 2025 Oct;204:115616.
