CAS: 65-22-5; 3-Hydroxy-5-(Hydroxymethyl)-2-Methylisonicotinaldehyde Hydrochloride

相似化合物

66-72-8 58-56-0 65-23-6

上下游产品

Nα-(3-hydroxy-5-hydroxymethyl-2-methyl-pyridin-4-ylmethylene)-histidineNα-(3-hydroxy-5-hydroxymethyl-2-methyl-pyridin-4-ylmethylene)-histidine pyridoxal pyridoxal hydr°Chloridepyridine7-hydroxy-1-methoxy-6-methyl-1H,3H-furo3,4-cpyridine (E)-5-(hydroxymethyl)-2-methyl-4-((2-phenylhydra zono)methyl)pyridin-3-ol 4-deoxypyridoxine 4-pyridoxic acid

吡哆醛置于盐酸体系中,用 水 作为反应溶剂,化学反应 72.0H,反应生成 吡哆醛盐酸盐
参考文献:甲酰基吡啶和维生素b 6相关化合物中的宝石-二元醇和半缩醛形式:固态NMR和单晶x射线衍射研究
标题:甲酰基吡啶和维生素b 6相关化合物中的宝石-二元醇和半缩醛形式:固态NMR和单晶x射线衍射研究
摘要:很少分离或什至在固态下研究有机化合物的宝石二醇部分.在这里,液相和固态NMR以及单晶x射线衍射研究被用来显示不同的策略,有利于宝石-二醇或羰基部分以及分离与甲酰吡啶和维生素b 6相关的半缩醛结构.化合物.吡啶化合物中羰基的位置变化对水合具有明显和直接的影响,而三氟乙酸的加入则增强了水合作用.由于其生物化学重要性,因此研究了维生素b 6相关化合物,重点是阐明宝石.-二醇,环状半缩醛或羰基结构可以在不同的实验条件下获得.尤其是,据报道,吡fluoro醛具有环状半缩醛结构的新外消旋混合物,形式为三氟乙酸盐和盐酸盐衍生物.
DOI:10.1021/acs.Jpca.6B07898

专利信息

专利号:US-9382288-B2
优先权日:2010-10-06
标题 :Derivatives of steroid benzylamines, having an antiparasitic antibacterial, antimycotic and/or antiviral action
发明人：BECKER KATJA; KRIEG REIMAR; SCHÖNECKER BRUNO
权利人:BECKER KATJA; KRIEG REIMAR; SCHÖNECKER BRUNO; UNIV GIESSEN JUSTUS LIEBIG
摘要:The present invention relates to compounds derived from steroids of the general formula (I) n nwherein L represents a linker and R # represents a steroid residue, the use of compounds of the general formula (I) in medicine and for the prophylaxis and/or the treatment of infectious diseases. Furthermore described are pharmaceutical compositions containing at least one compound of the general formula (I). A further aspect of the invention relates to the synthesis of said compounds of the general formula (I).

专利号:WO-2007142222-A1
优先权日:2006-06-09
标 题 :Method for production of pyridoxamine
发明人：SAKAMOTO KEIJI; FUJIMOTO NOBORU; WADA KOUICHI; TSUZAKI KAZUYA
权利人:DAIICHI FINE CHEM CO LTD; SAKAMOTO KEIJI; FUJIMOTO NOBORU; WADA KOUICHI; TSUZAKI KAZUYA
摘要:Disclosed is an effective method for producing pyridoxamine by employing a fermentation technique. Pyridoxamine is one of the substances having a vitamin B6 activity and is useful as a pharmaceutical agent or an intermediate for the synthesis of the pharmaceutical agent. A microorganism strain capable of producing pyridoxamine is now found. Pyridoxamine and/or a salt thereof can be produced in a simple manner and with efficiency by using a cell, a culture, a cell treatment product or the like of the microorganism. The microorganism to be used for the production of pyridoxamine is selected from a bacterium, an yeast and a fungus.

专利号:US-5405772-A
优先权日:1993-06-18
标题 :Medium for long-term proliferation and development of cells
发明人：PONTING IAN L O
权利人:AMGEN INC
摘要:A serum-free or serum-depleted medium for the short- and long-term proliferation and development of cells, particularly hematopoietic cells and bone marrow stromal cells, the medium comprising cell proliferation and development effective amounts of: a standard culture medium such as Iscove's modified Dulbecco's medium; serum albumin; transferrin; a source of lipids and fatty acids; cholesterol; a reducing agent; pyruvate; a glucocorticoid (when the cells to be cultured are hematopoietic cells); nucleosides for synthesis of DNA and RNA; growth factors that stimulate the proliferation and development of stromal cells and cells from a variety of tissues or organs, such as epidermal growth factor, fibroblast growth factor, platelet derived growth factor, and insulin; and extracellular matrix materials, such as collagen, fibronectin, and laminin.

专利号:US-2023266302-A1
优先权日:2020-07-24
标 题:Synthesis and use of n-benzyl sulfonamides
发明人：LAMAR ANGUS A; SHEAFF ROBERT J
权利人:THE UNIV OF TULSA
摘要:Disclosed is a method for preparing N-benzyl sulfonamides. Also disclosed is a composition for treating cancer. The composition includes a N-benzyl sulfonamide and a metabolic inhibitor. Also disclosed is a method for determining the impact on cell ATP levels of a composition containing a N-benzyl sulfonamide with or without a metabolic inhibitor.

专利号:US-7628979-B1
优先权日:2005-04-20
标题 :Use of calco oil blue V in bait formulations for marking and controlling subterranean termites
发明人：MORALES-RAMOS JUAN A; ROJAS MARIA G
权利人:US AGRICULTURE
摘要:Termite bait matrix containing cellulose, calco oil blue V (solvent blue 58 or 9,10-anthracenedione, 1,4-bis[(2-ethylhexyl)amino]), and optionally a termite toxicant (e.g., chitin synthesis inhibitor). Methods of monitoring termite activity in a region involving placing a termite bait matrix in the region and assessing the presence of termites at the site of the termite matrix, the termite bait matrix contains cellulose and 9,10-anthracenedione, 1,4-bis[(2-ethylhexyl)amino]. Methods of killing termites, involving placing a termite bait matrix in a termite habitat and allowing termites to feed on the bait matrix, the termite bait matrix contains cellulose, 9,10-anthracenedione, 1,4-bis[(2-ethylhexyl)amino], and a termite toxicant (e.g., chitin synthesis inhibitor).

专利号:US-2006223147-A1
优先权日:2004-08-05
标题 :Process for producing glycoprotein composition
发明人：NISHIYA HARUE; SATOH MITSUO; MORI KATSUHIRO
权利人:KYOWA HAKKO KOGYO KK
摘要:The present invention relates to a cell into which an RNA capable of suppressing the function of an enzyme catalyzing a reaction which converts GDP-mannose into GDP-4-keto,6-deoxy-GDP-mannose is introduced; a process for producing a glycoprotein using the cell; a cell into which an RNA capable of suppressing the function of an enzyme relating to modification of a sugar chain in which 1-position of fucose is bound to 6-position of N-acetylglucosamine in the reducing end through α-bond in the complex type N-glycoside-linked sugar chain, and an RNA capable of suppressing the function of an enzyme relating to synthesis of an intracellular sugar nucleotide, GDP-fucose, or an RNA capable of suppressing the function of a protein relating to transport of an intracellular sugar nucleotide, GDP-fucose, to the Golgi body are introduced; a process for producing a glycoprotein composition using the cell; and the like.