
trans-4-Hydroxy-2-piperidinecarboxylic acid | CAS:1622-20-4
trans-4-Hydroxy-2-piperidinecarboxylic acid
- Name:trans-4-Hydroxy-2-piperidinecarboxylic acid
- CAS:1622-20-4
- Synonyms:rel-(2R,4R)-4-Hydroxy-2-piperidinecarboxylic acid; NSC 93088
- Molecular Formula:C6H11NO3
- Molecular Weight:145.16
- EINESC:
Description
Properties
Density | 1.299±0.06 g/cm3 (20 º |
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Safety
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SDS
Source | SDS/MSDS Samples |
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Synthetic Route
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More
Articles
Peer-Reviewed Papers
Probing the antimalarial mechanism of artemisinin and OZ277 (arterolane) with nonperoxidic isosteres and nitroxyl radicals.Matthias A Fügi et al.Antimicrobial agents and chemotherapy, 54(3), 1042-1046 (2009-12-24)
Molecular modeling studies of the artemisinin (qinghaosu)-hemin interaction: docking between the antimalarial agent and its putative receptor.K L Shukla et al.Journal of molecular graphics, 13(4), 215-222 (1995-08-01)
Bioconversion of artemisinin to its nonperoxidic derivative deoxyartemisinin through suspension cultures of Withania somnifera Dunal.Farzana Sabir et al.Zeitschrift fur Naturforschung. C, Journal of biosciences, 65(9-10), 607-612 (2010-12-09)
Microbial metabolism studies of the antimalarial sesquiterpene artemisinin.I S Lee et al.Journal of natural products, 52(2), 337-341 (1989-03-01)
[Thin layer chromatographic fluorometry of artemisinin and deoxyartemisinin].D R Wang et al.Zhongguo yao li xue bao = Acta pharmacologica Sinica, 8(4), 355-358 (1987-07-01)
Artemisinin directly targets malarial mitochondria through its specific mitochondrial activation.Juan Wang et al.PloS one, 5(3), e9582-e9582 (2010-03-12)
Biotransformation of artemisinin using cell suspension cultures of Catharanthus roseus (L.) G.Don and Lavandula officinalis L.Suman Patel et al.Biotechnology letters, 32(8), 1167-1171 (2010-04-07)
Antiulcerogenic activity of some sesquiterpene lactones isolated from Artemisia annua.Mary Ann Foglio et al.Planta medica, 68(6), 515-518 (2002-07-03)
Structure-activity relationships of the antimalarial agent artemisinin. 2. Effect of heteroatom substitution at O-11: synthesis and bioassay of N-alkyl-11-aza-9-desmethylartemisinins.M A Avery et al.Journal of medicinal chemistry, 38(26), 5038-5044 (1995-12-22)
Dihydroartemisinin inhibits the human erythroid cell differentiation by altering the cell cycle.Sara Finaurini et al.Toxicology, 300(1-2), 57-66 (2012-06-09)
Deoxyartemisinin derivatives from photooxygenation of anhydrodeoxydihydroartemisinin and their cytotoxic evaluation.Ahmed M Galal et al.Journal of natural products, 65(2), 184-188 (2002-02-23)
Peroxide bond-dependent antiplasmodial specificity of artemisinin and OZ277 (RBx11160).Marcel Kaiser et al.Antimicrobial agents and chemotherapy, 51(8), 2991-2993 (2007-06-15)
Topological study of the late steps of the artemisinin decomposition process: modeling the outcome of the experimentally obtained products.Pamela Moles et al.The journal of physical chemistry. B, 115(2), 333-346 (2010-12-24)
Remarks
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