1185117-79-6
1185117-79-6
Chemical Structure
Climbazole-d4
Synonym(s): BAY-e 6975-d4
- CAS No.: 1185117-79-6
- Formula:C15H13D4ClN2O2
- Molecular Weight:296.79
IUPAC Name: 1-(4-chlorophenoxy-2,3,5,6-d4)-1-(1H-imidazol-1-yl)-3,3-dimethylbutan-2-one
InChIKey: OWEGWHBOCFMBLP-UGWFXTGHSA-N
SMILES: ClC(C([2H])=C1[2H])=C([2H])C([2H])=C1OC(N2C=CN=C2)C(C(C)(C)C)=O
Biological Activity: Climbazole-d4 is the deuterium labeled Climbazole. Climbazole (BAY-e 6975) is a potent antifungal agent. Climbazole also is a potent inducer of rat hepatic cytochrome P450[2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
Climbazole-d4 | 99.91% | Climbazole-d4 is the deuterium labeled Climbazole. Climbazole (BAY-e 6975) is a potent antifungal agent. Climbazole also is a potent inducer of rat hepatic cytochrome P450. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Climbazole (Standard) | 97.78% | Climbazole (Standard) is the analytical standard of Climbazole. This product is intended for research and analytical applications. Climbazole (BAY-e 6975) is a potent antifungal agent. Climbazole also is a potent inducer of rat hepatic cytochrome P450. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Climbazole | 98.26% | Climbazole (BAY-e 6975) is a potent antifungal agent. Climbazole also is a potent inducer of rat hepatic cytochrome P450. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Vibunazole | 99.91% | Vibunazole (BAY-N-7133) is an antifungal azole agent. Vibunazole inhibits coccidioidostatic. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Dazoxiben | Dazoxiben is a potent and orally active thromboxane synthetase inhibitor. Dazoxiben has the potential for the research of Raynaud's syndrome. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Dazoxiben hydrochloride | 99.90% | Dazoxiben hydrochloride is a potent and orally active thromboxane (TX) synthase inhibitor. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Dulofibrate | Dulofibrate is a hypolipidaemic agent that induces microsomal drug-metabolizing enzymes. Dulofibrate is selective for a reduction in triglycerides. Dulofibrate decreases nopol conjugation. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Triadimefon | 98.12% | Triadimefon is an orally active fungicide. Triadimefon significantly reduces the phosphorylation of AKT1 and ERK1/2. Triadimefon significantly increases pAMPK levels, but does not affect total AMPK levels. Triadimefon inhibits the growth of Saccharomyces cerevisiae, disrupts hormone homeostasis (affecting the synthesis of testosterone, etc.), inhibits fetal adrenal development in rats, induces metabolic shifts in hepatocytes, and impairs spatial learning and memory. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Methyl clofenapate | 99.04% | Methyl clofenapate (Clofenapate methyl ester; MCP) is a peroxisome proliferator, which can induce hypolipidemia, peroxisome proliferation, and hepatocarcinogenesis. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Clofop | Clofop (HCG 004), a once-utilized post-emergence herbicide, was employed to manage annual grasses in various crop fields. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Triadimenol | 99.78% | Triadimenol is a triazole fungicide and has been widely used in agriculture. Triadimenol has certain toxicity to animals. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Fenirofibrate impurity 8 | Fenirofibrate impurity 8 (Fenirofibrate impurity F) is an impurity of Fenirofibrate. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
