
2-Quinazolinamine | CAS:1687-51-0
2-Quinazolinamine
- Name:2-Quinazolinamine
- CAS:1687-51-0
- Synonyms:2-Aminoquinazoline; Quinazolin-2-ylamine
- Molecular Formula:C8H7N3
- Molecular Weight:145.16
- EINESC:
Description
Properties
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Safety
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SDS
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Synthetic Route
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More
Articles
Peer-Reviewed Papers
Comparing substrate specificity of two UDP-sugar pyrophosphorylases and efficient one-pot enzymatic synthesis of UDP-GlcA and UDP-GalAGuo Y, et al. Carbohydrate Research, 411, 1-5 (2015)
Simultaneous determination of intracellular UDP-sugars in hyaluronic acid-producing Streptococcus zooepidemicus.Lukáš Franke et al.Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 997, 194-199 (2015-06-27)
Biotransformation of glucoaurantio-obtusin towards aurantio-obtusin increases the toxicity of irinotecan through increased inhibition towards SN-38 glucuronidation.Jian Yu et al.Phytotherapy research : PTR, 28(10), 1577-1580 (2014-05-21)
In vitro and in vivo biotransformation of WMS-1410, a potent GluN2B selective NMDA receptor antagonist.Evamaria Falck et al.Journal of pharmaceutical and biomedical analysis, 94, 36-44 (2014-02-19)
In vitro inhibitory effects of Andrographis paniculata, Gynura procumbens, Ficus deltoidea, and Curcuma xanthorrhiza extracts and constituents on human liver glucuronidation activityHusni Z, et al. Pharmacognosy magazine, 13( 2), S236-S236 (2017)
Identification of UDP-glucuronosyltransferase isoforms responsible for leonurine glucuronidation in human liver and intestinal microsomes.Bo Tan et al.Xenobiotica; the fate of foreign compounds in biological systems, 44(9), 775-784 (2014-03-19)
Cytochrome P450 3A-mediated metabolism of the topoisomerase I inhibitor 9-aminocamptothecin: impact on cancer therapy.Alexandra Maier-Salamon et al.International journal of oncology, 45(2), 877-886 (2014-06-04)
Soy isoflavone metabolism in cats compared with other species: urinary metabolite concentrations and glucuronidation by liver microsomesRedmon J M, et al. Xenobiotica, 46(5), 406-415 (2016)
Metabolic drug-drug interaction potential of macrolactin A and 7-O-succinyl macrolactin A assessed by evaluating cytochrome P450 inhibition and induction and UDP-glucuronosyltransferase inhibition in vitro.Soo Hyeon Bae et al.Antimicrobial agents and chemotherapy, 58(9), 5036-5046 (2014-06-04)
Identifying drug targets in tissues and whole blood with thermal-shift profiling.Jessica Perrin et al.Nature biotechnology, 38(3), 303-308 (2020-01-22)
Glucuronidation of aurantio-obtusin: identification of human UDP-glucuronosyltransferases and species differences.Bao-Li Mi et al.Xenobiotica; the fate of foreign compounds in biological systems, 44(8), 716-721 (2014-03-13)
UDP-glucose 6-dehydrogenase regulates hyaluronic acid production and promotes breast cancer progression.James M Arnold et al.Oncogene, 39(15), 3089-3101 (2019-07-17)
Glutathione-dependent reduction of arsenate by glycogen phosphorylase responsiveness to endogenous and xenobiotic inhibitors.Zoltán Gregus et al.Toxicological sciences : an official journal of the Society of Toxicology, 100(1), 44-53 (2007-08-19)
Remarks
Products protected by valid patents are not offered for sale in countries where the sale of such products constitutes a patent infringement and its liability is at buyer's risk.
Products currently covered by valid US Patents are offered for R&D use in accordance with 35 USC 271 +A13(1).
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