Name | hemoglobin (protein family or complex) |
---|---|
Synonyms | Hemoglobin; Hemoglobins |
Name | methylene chloride |
---|---|
CAS | dichloromethane |
PubMed | Abstract | RScore(About this table) | |
---|---|---|---|
1900959 | Andersen ME, Clewell HJ 3rd, Gargas ML, MacNaughton MG, Reitz RH, Nolan RJ, McKenna MJ: Physiologically based pharmacokinetic modeling with dichloromethane, its metabolite, and blood carboxyhemoglobin in rats and humans. Toxicol Appl Pharmacol. 1991 Mar 15;108(1):14-27. Dichloromethane (methylene chloride, DCM) and other dihalomethanes are metabolized to (CO) which reversibly binds hemoglobin and is eliminated by exhalation. |
82(1,1,1,2) | Details |
9285047 | Cedrati N, Bonneaux F, Labrude P, Maincent P: Structure and stability of human hemoglobin microparticles prepared with a double emulsion technique. Artif Cells Blood Substit Immobil Biotechnol. 1997 Sep;25(5):457-62. Hemoglobin concentration, surfactant concentration i.e. poly (vinylic amounts of polymer and solvent (methylene chloride), duration and speed of stirring. |
14(0,0,1,9) | Details |
7994411 | Cedrati N, Maincent P, Thomas F, Labrude P, Vigneron C: Preparation and characterisation of poly (lactic acid) hemoglobin microspheres. Artif Cells Blood Substit Immobil Biotechnol. 1994;22(3):867-73. An aqueous solution of hemoglobin was emulsified into a solution of polymer in methylene chloride to form a W/O emulsion. |
12(0,0,1,7) | Details |
8286954 | Sakai H, Takeoka S, Yokohama H, Seino Y, Nishide H, Tsuchida E: Purification of concentrated hemoglobin using organic solvent and heat treatment. Protein Expr Purif. 1993 Dec;4(6):563-9. |
2(0,0,0,2) | Details |
2753027 | Manabe S, Kanai Y, Wada O: Exposure level monitor of 3-amino-1,4-dimethyl-5H-pyrido [4,3-b] The present investigation describes a method for the detection of minute amounts of 3-amino-1,4-dimethyl-5H-pyrido [4,3-b] (Trp-P-1), a carcinogenic pyrolysate, bound to the hemoglobin of erythrocytes and plasma from rabbits dosed orally with the dietary carcinogen. The method consists of the acid-induced release of the dietary carcinogen adducts as the free carcinogen and their extraction with methylene chloride and subsequent quantitation by high-performance liquid chromatography (HPLC). |
a dietary carcinogen, in rabbits. Environ Mol Mutagen. 1989;14(1):34-41.2(0,0,0,2) | Details |
8571372 | Krishnan K, Pelekis M: Hematotoxic interactions: occurrence, mechanisms and predictability. Toxicology. 1995 Dec 28;105(2-3):355-64. The available data on the binary chemical interactions involving hematotoxicants, particularly organic chemicals causing a reduction in either the number of white/red blood cells or the capacity of hemoglobin to transport are limited. |
1(0,0,0,1) | Details |