91-53-2
91-53-2
Chemical Structure
Ethoxyquin
- CAS. Nr.: 91-53-2
- Formula:C14H19NO
- Molecular Weight:217.31
IUPAC Name: 6-ethoxy-2,2,4-trimethyl-1,2-dihydroquinoline
InChIKey: DECIPOUIJURFOJ-UHFFFAOYSA-N
SMILES: CC1=CC(C)(C)NC2=C1C=C(OCC)C=C2
Biological Activity: Ethoxyquin is an antioxidant which has been used in animal feed for many years and also an inhibitor of heat shock protein 90 (Hsp90).
| Art. -Nr. | Produktname | Reinheit | Beschreibung | Pricing | |||||||||||||||||||
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Ethoxyquin | 98.76% | Ethoxyquin is an antioxidant which has been used in animal feed for many years and also an inhibitor of heat shock protein 90 (Hsp90). | ||||||||||||||||||||
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Ethoxyquin (Standard) | ≥98% | Ethoxyquin (Standard) is the analytical standard of Ethoxyquin. This product is intended for research and analytical applications. Ethoxyquin is an antioxidant which has been used in animal feed for many years and also an inhibitor of heat shock protein 90 (Hsp90). | ||||||||||||||||||||
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Oxeglitazar | Oxeglitazar is an orally active compound that can be used for the research of type II diabetes. | |||||||||||||||||||||
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Precocene II (Standard) | ≥98% | Precocene II (Standard) is the analytical standard of Precocene II (HY-122940). This product is intended for research and analytical applications. Precocene II (Ageratochromene) is a plant larva hormone antagonists that inhibits the biosynthesis of juvenile hormone. Precocene II inhibits corpora allata function and downregulates juvenile hormone levels, while exerting multiple effects including inducing precocious metamorphosis, forming macropterous morphs, inhibiting ovarian growth, producing cytotoxicity, disrupting insect development, and causing sterility and kidney damage. Precocene II blocks normal nymphal development, causes renal tubular damage and increases blood urea nitrogen levels, and also blocks juvenile hormone biosynthesis in vitro. Precocene II undergoes oxidative metabolism catalyzed by NADPH-dependent monooxygenase to generate a variety of metabolites. Precocene II can be applied in studies related to insect growth regulation and nephrotoxicity. | ||||||||||||||||||||
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LG-120753 | LG-120753 is an orally active nonsteroidal progesterone receptor (PR) antagonist, with an IC50 of 38 nM against hPR-B, a Ki of 19 nM against hPR-A, an IC50 of 227 nM against hAR, and IC50 values greater than 1000 nM against hGR, hER and hMR. LG-120753 blocks the action of progesterone, binds to and antagonizes hPR-A, and shows limited cross-reactivity with other steroid receptors. LG-120753 blocks blastocyst implantation, prevents the establishment of pregnancy, exhibits dose-dependent antiprogestogenic activity in vivo, and induces reversible antifertility effects. | |||||||||||||||||||||
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Bucetin | 98.47% | Bucetin (3-Hydroxy-p-butyrophenetidide) is an antipyretic compound and can also be used in pain relief studies. | ||||||||||||||||||||
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5,7-Dimethoxy-2,2-dimethylchromene | 5,7-Dimethoxy-2,2-dimethylchromene is a synthetic precocenoid, has potential insect control function. 5,7-Dimethoxy-2,2-dimethylchromene induces loss of pigmentation in hatching larvae of shield bug (Eurgaster integriceps). | |||||||||||||||||||||
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Aripiprazole impurity 35 | Aripiprazole impurity 35 is an impurity of Aripiprazole. | |||||||||||||||||||||
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Aripiprazole impurity 11 | Aripiprazole impurity 11 is an impurity of Aripiprazole. | |||||||||||||||||||||
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Aripiprazole impurity 2 | Aripiprazole impurity 2 is an impurity of Aripiprazole. | |||||||||||||||||||||
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Aripiprazole impurity 37 | Aripiprazole impurity 37 is an impurity of Aripiprazole. | |||||||||||||||||||||
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Tramadol impurity 1 | Tramadol impurity 1 is an impurity of Tramadol. | |||||||||||||||||||||
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