Chlorobutanol
Preservatives, Pharmaceutical
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Mutations in Drosophila heat shock cognate 4 are enhancers of Polycomb. (1/22)
The homeotic genes controlling segment identity in Drosophila are repressed by the Polycomb group of genes (PcG) and are activated by genes of the trithorax group (trxG). An F(1) screen for dominant enhancers of Polycomb yielded a point mutation in the heat shock cognate gene, hsc4, along with mutations corresponding to several known PcG loci. The new mutation is a more potent enhancer of Polycomb phenotypes than an apparent null allele of hsc4 is, although even the null allele occasionally displays homeotic phenotypes associated with the PcG. Previous biochemical results had suggested that HSC4 might interact with BRAHMA, a trxG member. Further analyses now show that there is no physical or genetic interaction between HSC4 and the Brahma complex. HSC4 might be needed for the proper folding of a component of the Polycomb repression complex, or it may be a functional member of that complex. (+info)Rapid stimulation of free glucuronate formation by non-glucuronidable xenobiotics in isolated rat hepatocytes. (2/22)
Vitamin C synthesis in rat liver is enhanced by several xenobiotics, including aminopyrine and chloretone. The effect of these agents has been linked to induction of enzymes potentially involved in the formation of glucuronate, a precursor of vitamin C. Using isolated rat hepatocytes as a model, we show that a series of agents (aminopyrine, antipyrine, chloretone, clotrimazole, metyrapone, proadifen, and barbital) induced in a few minutes an up to 15-fold increase in the formation of glucuronate, which was best observed in the presence of sorbinil, an inhibitor of glucuronate reductase. They also caused an approximately 2-fold decrease in the concentration of UDP-glucuronate but little if any change in the concentration of UDP-glucose. Depletion of UDP-glucuronate with resorcinol or d-galactosamine markedly decreased the formation of glucuronate both in the presence and in the absence of aminopyrine, confirming the precursor-product relationship between UDP-glucuronate and free glucuronate. Most of the agents did not induce the formation of detectable amounts of glucuronides, indicating that the formation of glucuronate is not due to a glucuronidation-deglucuronidation cycle. With the exception of barbital (which inhibits glucuronate reductase), all of the above mentioned agents also caused an increase in the concentration of ascorbic acid. They had little effect on glutathione concentration, and their effect on glucuronate and vitamin C formation was not mimicked by glutathione-depleting agents such as diamide and buthionine sulfoximine. It is concluded that the stimulation of vitamin C synthesis exerted by some xenobiotics is mediated through a rapid increase in the conversion of UDP-glucuronate to glucuronate, which does not apparently involve a glucuronidation-deglucuronidation cycle. (+info)Epithelial activity of hexokinase and glucose-6-phosphate dehydrogenase in cultured bovine lenses recovering from pharmaceutical-induced optical damage. (3/22)
PURPOSE: In a previous toxicological study, cultured bovine lenses exposed to three topical anesthetics displayed distinct patterns of optical damage and recovery. This work investigated the epithelial activity of the metabolic enzymes hexokinase (HK) and glucose-6-phosphate dehydrogenase (G6PD) in lenses recovering from anesthetic-induced damage. METHODS: Cultured bovine lenses were exposed to the anesthetics Alcaine, Fluress and Fluoracaine for 2 h. An automated laser scanner was used to determine the focal length variability (FLV) of the lenses at time-points up to 24 h following their return to fresh culture medium. The epithelial enzyme activities for HK and G6PD were then assayed at the 24 h time-point. RESULTS: Lenses exposed to Alcaine displayed an abrupt increase in FLV, while Fluoracaine treated lenses exhibited optical damage at a slower rate. The FLV in these two groups recovered to near-control levels after 24 h. Fluress treated lenses did not differ in FLV from controls at any time. The activities of both HK and G6PD were significantly reduced in epithelial samples from each of the three anesthetic treatment groups, relative to controls. CONCLUSIONS: These results show that lens optical quality can recover despite a severe reduction in epithelial HK and G6PD activity, indicating that the optical function of the lens may not be directly related to epithelial metabolic activity. The ScanTox In Vitro Assay System provides an objective measure of lens optical quality, enabling a direct comparison of optical damage and recovery to lens biochemical changes. (+info)Neurotoxicity of intra-arterial papaverine preserved with chlorobutanol used for the treatment of cerebral vasospasm after aneurysmal subarachnoid hemorrhage. (4/22)
BACKGROUND AND PURPOSE: Papaverine is used to vasodilate cerebral arteries undergoing vasospasm from subarachnoid hemorrhage. However, papaverine inhibits cellular respiration in vitro and could cause neurotoxicity in humans. METHODS: We studied 5 consecutive patients with cerebral vasospasm who were treated with intra-arterial papaverine preserved with chlorobutanol and imaged with MRI fluid-attenuated inversion recovery and diffusion-weighted imaging after treatment. One patient had histological analysis of the brain at autopsy. RESULTS: All 5 patients exhibited marked neurological decline immediately after treatment, and this was sustained through hospital discharge. In all cases, MRI images showed selective gray matter-only signal changes within the vascular territory treated with papaverine. Histological analysis of 1 case brought to autopsy showed selective injury to islands of neurons with relative sparing of white matter. CONCLUSIONS: Intra-arterial delivery of papaverine preserved with chlorobutanol into vasospastic anterior cerebral arteries may result in marked neurological deterioration with selective gray matter changes on MRI imaging. This effect is consistent with a permanent toxic effect to human brain. It is unclear whether this toxicity is caused by papaverine or chlorobutanol, and its use in the treatment of cerebral vasospasm should be reserved for cases without alternatives. (+info)Comparative toxicity of preservatives on immortalized corneal and conjunctival epithelial cells. (5/22)
(+info)GC determination of acetone, acetaldehyde, ethanol, and methanol in biological matrices and cell culture. (6/22)
A gas chromatography with flame ionization detection method (GC-FID) with direct injection, using a capillary column, was validated to determine ethanol, acetaldehyde, methanol, and acetone in different human matrices, such as whole blood, vitreous humour, and urine, with clinical and forensic interest. This method was also employed to quantify these compounds in cell culture medium, thus being useful in basic research. A good peak resolution was achieved, with linear correlation between concentration and peak areas for all the compounds in all the matrices. The inter- and intra-day precisions of the method were always under 15% and 10%, respectively. The accuracy of the method, calculated as the percentage of the target concentration, was within the acceptable limits. The obtained limits of detection were below 0.85 mg/L for acetaldehyde and below 0.75 mg/L for the other considered compounds. The small injection volume and the high split ratios applied, allied to the high performance of the GC column, resulted in very good peak resolution and high sensitivities. This method is easy to perform, making it suitable for the routine of clinical biochemistry and forensic laboratories. (+info)Interactions at human ether-a-go-go-related gene channels. (7/22)
(+info)A non-bronchoconstrictor, bacteriostatic preservative for nebuliser solutions. (8/22)
We have studied the bacteriostatic and airways effects of the preservatives chlorocresol and chlorbutol, to assess if they may be safely used in nebuliser solutions. The bacteriostatic study was carried out according to standard techniques, and the preservatives were able to inhibit the growth of a range of bacteria and yeasts for a period of 28 days. The airways effects were studied in eight asthmatic subjects, who were challenged with either the preservatives or saline (as placebo). Pulmonary function was followed as FEV1 for 60 min after inhalation, and there was no change in FEV1 following inhalation. We conclude that these preservatives may be used safely in nebuliser solutions. (+info)
Chlorobutanol - Wikipedia
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Chlorobutanol
... is highly toxic to the liver, is a skin irritant and a severe eye irritant. Chlorobutanol has proven effective at ... Chlorobutanol was first synthesized in 1881 by the German chemist Conrad Willgerodt (1841-1930). Chlorobutanol is formed by the ... Chlorobutanol has been used in anesthesia and euthanasia of invertebrates and fishes. It is a white, volatile solid with a ... Chlorobutanol is typically used at a concentration of 0.5% where it lends long term stability to multi-ingredient formulations ...
Chloral hydrate
Chlorobutanol Disulfiram-like drug Trichloroethanol Notes Vardanyan, R.S.; Hruby, V.J. (2006). "Soporific Agents (Hypnotics and ...
Conrad Willgerodt
Alongside the Willgerodt reaction, he had also discovered Iodosobenzene and chlorobutanol. As for his career, Conrad Willgerodt ...
Doxapram
Injectable products have a pH from 3.5-5. Benzyl alcohol or chlorobutanol is added as a preservative agent in the commercially ...
Caffeine
Brødbaek HB, Damkier P (May 2007). "[The treatment of hyperemesis gravidarum with chlorobutanol-caffeine rectal suppositories ... and of chlorobutanol and caffeine (for the treatment of hyperemesis). However, rectal absorption is less efficient than oral: ...
Artificial tears
Preservatives include benzalkonium chloride (BAK), ethylenediaminetetraacetic acid (EDTA), purite, chlorobutanol, sodium ...
2,2,2-Trichloroethanol
... and of chlorobutanol. Historically, it has been used as a sedative hypnotic. The hypnotic drug triclofos (2,2,2-trichloroethyl ...
Patulous Eustachian tube
Nasal medications containing diluted hydrochloric acid, chlorobutanol, and benzyl alcohol have been reported to be effective in ...
Menthol
Medicine portal Aroma compound Carvone Chlorobutanol Ethyl benzoate Ethyl salicylate Menthoxypropanediol Methyl salicylate ...
List of drugs: Cf-Ch
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Sedative
Dimenhydrinate Diphenhydramine Doxylamine Hydroxyzine Promethazine General anaesthetics Chloral hydrate Chlorobutanol ...
ATC code A04
... combinations A04AD54 Chlorobutanol, combinations QA04AD90 Maropitant "ATC (Anatomical Therapeutic Chemical Classification ... combinations A04AD01 Scopolamine A04AD02 Cerium oxalate A04AD04 Chlorobutanol A04AD05 Metopimazine A04AD10 Dronabinol A04AD11 ...
List of MeSH codes (D02)
... chlorobutanol MeSH D02.033.415.110.855 - tert-butyl alcohol MeSH D02.033.415.220 - dodecanol MeSH D02.033.415.220.720 - sodium ... chlorobutanol MeSH D02.033.260.335 - ethchlorvynol MeSH D02.033.260.350 - ethylene chlorohydrin MeSH D02.033.375.270 - ...
List of MeSH codes (D10)
... chlorobutanol MeSH D10.289.110.855 - tert-butyl alcohol MeSH D10.289.220.720 - sodium dodecyl sulfate MeSH D10.289.230.250 - ...
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Methaqualone - Wikipedia
Methaqualone became increasingly popular as a recreational drug in the late 1960s and 1970s, known variously as "ludes" or "sopers" (also "soaps") in the United States and "mandrakes" and "mandies" in the UK, Australia and New Zealand. Sopor is a Latin word for sleep. The drug was more tightly regulated in Britain under the Misuse of Drugs Act 1971 and in the U.S. from 1973. It was withdrawn from many developed markets in the early 1980s. In the United States it was withdrawn in 1983 and made a Schedule I drug in 1984. It has a DEA ACSCN of 2565 and in 2022 the aggregate annual manufacturing quota for the United States was 60[15] grams. Mention of its possible use in some types of cancer and AIDS treatments has periodically appeared in the literature since the late 1980s. Research does not appear to have reached an advanced stage. The DEA has also added the methaqualone analogue mecloqualone (also a result of some incomplete clandestine syntheses) to Schedule I as ACSCN 2572, with a ...
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Anhydrous2
- Chlorobutanol anhydrous (chloral derivative) added as a preservative may be habit forming. (pfizermedicalinformation.com)
- According to the Statement of Non-Compliance issued in EudraGMDP this statement is valid for all APIs: "The Plant I produced Metoprolol Tartrate, Metoprolol Succinate, Chlorobutanol Hemihydrate, Chlorobutanol Anhydrous and Fluconazole. (gmp-compliance.org)
Hemihydrate2
- Other ingredients include chlorobutanol hemihydrate, acetic acid glacial and water for injections. (who.int)
- All CEPs have been suspended: CEP 2009-112 (Chlorobutanol hemihydrate), CEP 2009-152 (Metoprolol tartarate), CEP 2009-170 (Metoprolol Succinate), CEP 2010-147 (Ferrous fumarate), CEP 2010-247 (Fluconazole), CEP 2011-304 (Metoprolol tartarate), CEP 2011-312 (Metoprolol Succinate). (gmp-compliance.org)
Preservative1
- Each gram of sterile ophthalmic ointment contains tobramycin 3 mg and dexamethasone 0.1% with chlorobutanol 0.5% as a preservative in a mineral oil and petrolatum base. (pharmachoice.com)
Chloral2
- 200 mg testosterone enanthate in sesame oil with 5 mg chlorobutanol (chloral. (enrique-calderon.com)
- Each ml of sterile, colorless to pale yellow solution provides 200 mg testosterone enanthate in sesame oil with 5 mg chlorobutanol (chloral derivative) as a. (blvcklxtus.com)
Chlorhexidine1
- antibacterial Chlorhexidine digluconate (0.1%) and Chlorobutanol (0.5%) helps maintain good oral hygiene. (pharmanatura.gr)
Derivative1
- Pitocin is composed of oxtocic acid/ml along with chlorobutanol , a chloroform derivative. (pharmawiki.in)
Exporter2
- Believe Chemical is a leading China Chlorobutanol CAS 57-15-8 manufacturer, supplier and exporter. (believechemical.com)
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Bacterial1
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Synthesis1
- A while ago i stumbled across a fairly easy looking synthesis for a chemical known as chlorobutanol. (sciencemadness.org)
Alcohol1
- Anyways after sorting out the fragmented directions at http://www.rhodium.ws/chemistry/chlorobutanol.txt i figured that all i needed was generic bleach, acetone, lye, denatured alcohol and a bit of equipment. (sciencemadness.org)
Quality1
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Benzalkonium1
- Benzalkonium chloride (BAK), chlorobutanol, chlorhexidine acetate (CHA), and phenylmercuric nitrate or acetate are some commonly used preservatives in eye preparations. (filonanotech.com)
Tobramycin 0.31
- Each gram of Tobrex ophthalmic ointment 0.3% contains tobramycin 0.3% (3 mg), chlorobutanol 0.5%, mineral oil, white petrolatum. (healthwiregeorgia.com)
Inactive Ingredients1
- Inactive Ingredients: Chlorobutanol (0.5%), Lanolin Alcohols. (universitypharmacy.ca)
Surfactants1
- Chlorobutanol [43] and 2-phenylethanol [37] are adversely affected by the presence of non-ionic surfactants, e.g. polysorbate 80. (chemistscorner.com)
Sesame Oil1
- chlorobutanol and sesame oil. (rxhealthmed.ca)
Drug1
- After the addition of chlorobutanol, the suicide effect of the drug preparation was significantly enhanced. (medical-steroids.com)
Found1
- 4-Chlorobutanol = 4 reactions were found. (tu-bs.de)
Activity1
- Although the antimicrobial activity of chlorobutanol is extensive, [ 18 ] its use has been limited due to the fact that it becomes unstable when stored at room temperature for extended periods of time. (medscape.com)
Human2
- [ 16 ] Human corneal epithelial cells exposed to chlorobutanol display a decreased amount of mitoses and deterioration of overall cell integrity. (medscape.com)
- The lethal human chlorobutanol dose is recovered in the past 1-6 weeks. (childbirthsolutions.com)
Skin1
- Chlorobutanol is highly toxic to the liver, is a skin irritant and a severe eye irritant. (psychonautwiki.org)
Method1
- [ 17 ] The method of action of chlorobutanol is cell lysis by way of disruption of microbial cell membrane lipid configuration. (medscape.com)