216167-92-9
Chemical Structure
Camobucol
Synonym(s): AGIX 4207
- CAS No.: 216167-92-9
- Formula:C33H50O4S2
- Molecular Weight:574.88
IUPAC Name: 2-(2,6-di-tert-butyl-4-((2-((3,5-di-tert-butyl-4-hydroxyphenyl)thio)propan-2-yl)thio)phenoxy)acetic acid
InChIKey: FGBGXESDYFKUFX-UHFFFAOYSA-N
SMILES: CC(C)(C)C1=CC(SC(C)(C)SC2=CC(C(C)(C)C)=C(OCC(O)=O)C(C(C)(C)C)=C2)=CC(C(C)(C)C)=C1O
Biological Activity: Camobucol (AGIX 4207) is an orally active, phenolic antioxidant and anti-inflammatory compound with antirheumatic properties.
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Camobucol | 99.50% | Camobucol (AGIX 4207) is an orally active, phenolic antioxidant and anti-inflammatory compound with antirheumatic properties. | ||||||||||||||||||||
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Probucol disuccinate | 99.14% | Probucol Disuccinate is a derivative of Probucol (HY-B0388), a lipid-regulating agent and can reduce LDL-cholesterol levels. | ||||||||||||||||||||
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Elsibucol | 99.35% | Elsibucol is a VCAM1 inhibitor for the study of organ transplant rejection. Elsibucol is a metabolically stable propanol derivative with antioxidant, anti-inflammatory and anti-proliferative properties. Elsibucol lowers blood cholesterol levels and reduces oxidative stress and inflammatory responses in injured arteries, thereby inhibiting atherosclerosis and protecting endothelial healing after arterial injury. | ||||||||||||||||||||
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Succinobucol (Standard) | ≥98% | Succinobucol (Standard) is the analytical standard of Succinobucol. This product is intended for research and analytical applications. Succinobucol is a phenolic antioxidant with anti-inflammatory and antiplatelet effects. | ||||||||||||||||||||
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FA-15 | FA-15 is an phenolic antioxidant. FA-15 has effect on stabilization of reactive fuels. | |||||||||||||||||||||
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S-15176 | S-15176 is an inhibitor of the mitochondrial permeability transition pore (PTP). S-15176 inhibits mitochondrial swelling induced by tert-butylhydroperoxide with an IC50 value of 45.7 μM. S-15176 inhibits PTP opening, prevents mitochondrial membrane potential dissipation and NAD(P)H oxidation, and increases mitochondrial calcium loading capacity. S-15176 is promising for research of ischemia-reperfusion injury. | |||||||||||||||||||||
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SC-45662 | SC-45662 is a 5-lipoxygenase inhibitor. SC-45662 inhibits the response of monocytes to phytohemagglutinin (PHA). SC-45662 inhibits superoxide production in neutrophils. SC-45662 slows early changes in lung mechanics and pulmonary hypertension in a sheep model of impaired lung function. SC-45662 can be used in research on diseases of the immune system, respiratory system, etc. | |||||||||||||||||||||
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Probucol | 99.85% | Probucol (DH-581) is an anti-hyperlipidemic agent. Probucol activates glutathione peroxidase. Probucol promotes low density lipoprotein (LDL) catabolism, inhibits ABCA1-dependent cholesterol efflux, and decreases HDL-C levels. Probucol also has anti-inflammatory, antioxidant and neuroprotective properties. Probucol can be used for researches on bone, cardiovascular, cancer, neurological, and metabolism-related diseases. | ||||||||||||||||||||
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Probucol-13C3 | Probucol-13C3 is the 13C-labeled Probucol. Probucol (DH-581) is an anti-hyperlipidemic agent by lowering the level of cholesterol in the bloodstream by increasing the rate of LDL catabolism. | |||||||||||||||||||||
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4,4'-Methylenebis(2,6-di-tert-butylphenol) | 99.83% | 4,4'-Methylenebis(2,6-di-tert-butylphenol) (4,4-MBP) is a bisphenol compound. 4,4'-Methylenebis(2,6-di-tert-butylphenol) acts as an inhibitor of sarco/endoplasmic reticulum calcium ATPase (SERCA) with an IC50 value of 17 μM. 4,4'-Methylenebis(2,6-di-tert-butylphenol) can be used in the research of diseases related to calcium homeostasis. | ||||||||||||||||||||
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Probucol dithiobisphenol | Probucol dithiobisphenol (DTBP) is the derivative of Probucol (HY-B0388). Probucol dithiobisphenol induces the production of heme oxygenase 1 (HO-1), and exhibits antioxidant activity. Probucol dithiobisphenol inhibits atherosclerotic lesions in Apoe−/− mice aorta, promotes re-endothelialization of aorta and inhibits restenosis in rabbit arterial injury models. Probucol dithiobisphenol is orally active. | |||||||||||||||||||||
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