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rdf:type
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http://linked.open...gbank/description
| - A drug used to lower LDL and HDL cholesterol yet has little effect on serum-triglyceride or VLDL cholesterol. (From Martindale, The Extra Pharmacopoeia, 30th ed, p993). (en)
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http://linked.open...gy/drugbank/group
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http://linked.open...drugbank/halfLife
| - Ranges from 12 hours to more than 500 hours, the longest half-life probably being in adipose tissue. (en)
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http://linked.open...ugbank/indication
| - Used to lower LDL and HDL cholesterol. (en)
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sameAs
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Title
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adms:identifier
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http://linked.open...mechanismOfAction
| - Probucol lowers serum cholesterol by increasing the fractional rate of low-density lipoprotein (LDL) catabolism in the final metabolic pathway for cholesterol elimination from the body. Additionally, probucol may inhibit early stages of cholesterol biosynthesis and slightly inhibit dietary cholesterol absorption. Recent information suggests that probucol may inhibit the oxidation and tissue deposition of LDL cholesterol, thereby inhibiting atherogenesis. It appears to inhibits ABCA1-mediated cellular lipid efflux. (en)
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http://linked.open...drugbank/packager
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http://linked.open.../drugbank/synonym
| - Biphenabid (en)
- Bisbid (en)
- Bisphenabid (en)
- Lesterol (en)
- Lorelco (en)
- Lurselle (en)
- Acetone bis(3,5-di-tert-butyl-4-hydroxyphenyl) mercaptole (en)
- DH-581 (en)
- Probucolum (en)
- Serterol (en)
- Superlipid (en)
- 4,4'- (Isopropylidenedithio)bis(2,6-di-tert-butylphenol) (en)
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http://linked.open.../drug/hasAHFSCode
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http://linked.open...k/foodInteraction
| - Take with food. Food increases availability. (en)
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http://linked.open...ynthesisReference
| - Claudio Giordano, Giuseppe Barreca, "Process for preparing an intermediate useful in the syntheis of probucol." U.S. Patent US5157156, issued July, 1988. (en)
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foaf:page
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http://linked.open...ugbank/IUPAC-Name
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http://linked.open...gy/drugbank/InChI
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http://linked.open...Molecular-Formula
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http://linked.open.../Molecular-Weight
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http://linked.open...noisotopic-Weight
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http://linked.open...y/drugbank/SMILES
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http://linked.open.../Water-Solubility
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http://linked.open...ogy/drugbank/logP
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http://linked.open...ogy/drugbank/logS
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http://linked.open...l/drug/hasATCCode
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http://linked.open...nd-Acceptor-Count
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http://linked.open...-Bond-Donor-Count
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http://linked.open...drugbank/InChIKey
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http://linked.open...urface-Area--PSA-
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http://linked.open...nk/Polarizability
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http://linked.open...bank/Refractivity
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http://linked.open...atable-Bond-Count
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http://linked.open...ugbank/absorption
| - Absorption from the gastrointestinal tract is limited and variable (about 7%). (en)
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http://linked.open.../affectedOrganism
| - Humans and other mammals (en)
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http://linked.open...casRegistryNumber
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http://linked.open...drugbank/category
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http://linked.open...gbank/containedIn
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http://linked.open...k/Bioavailability
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http://linked.open...bank/Ghose-Filter
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http://linked.open...nk/MDDR-Like-Rule
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http://linked.open...ank/Melting-Point
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http://linked.open...k/Number-of-Rings
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http://linked.open...siological-Charge
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http://linked.open...bank/Rule-of-Five
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http://linked.open...tional-IUPAC-Name
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http://linked.open...strongest-acidic-
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http://linked.open...-strongest-basic-
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