16568-56-2Relevant articles and documents
Singlet oxygen reactivity of bilirubin and related tetrapyrroles
Lightner,Park
, p. 555 - 557 (1978)
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Version: 1.0
Creation Date: Aug 19, 2017
Revision Date: Aug 19, 2017
Product name | mesobilirubin |
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Product number | - |
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Other names | Mesobilirubin |
Identified uses | For industry use only. |
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Uses advised against | no data available |
Emergency phone number | - |
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Service hours | Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours). |
More Details:16568-56-2 SDS
Mesobilirubin or dihydromesobilirubin were converted by a pure strain of rat Clostridia to class II and III urobilinoid chromogens (l-half-stercobilinogen and l-stercobilinogen). This was also true in some experiments with various samples of human fecal flora; in others, only or mainly class I (...detailed
Mesobiliverdin IXα diesters of α,ω-dialkanols were obtained by reaction of mesobiliverdin IXα dicesium salt with diiodomethane, 1,3-dibromopropane and 1,4-dibromobutane. Mesobiliverdin IXα methylene diester was tested and compared to mesobiliverdin IXα dimethyl ester, for their photoisomer...detailed
Symmetric analogs of mesobilirubin-XIIIα, with propionic acid groups shortened and lengthened, exhibit induced circular dichroism (ICD) in CH2Cl2 solvent with excess S-(−)-methyl-p-tolylsulfoxide. The dimethyl esters of mesobilirubins with acetic, propionic, butyric, valeric and caproic acid ch...detailed
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