7577-62-0|Fucosamine|(2S,3S,4R,5S)-2-amino-3,4,5-trihydroxyhexanal|-范德生物科技公司

Fucosamine

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names：
(2S,3S,4R,5S)-2-amino-3,4,5-trihydroxyhexanal
CAS号：
7577-62-0
MDL Number：
MF(分子式)： C6H13NO4 MW(分子量)： 163.17
EINECS: Reaxys Number:
Pubchem ID: Brand:BIOFOUNT

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询价

中文别名	Fucosamine
英文别名	Fucosamine;
CAS号	7577-62-0
Inchi	InChI=1S/C6H13NO4/c1-3(9)5(10)6(11)4(7)2-8/h2-6,9-11H,7H2,1H3/t3-,4+,5+,6-/m0/s1
InchiKey	NTBYIQWZAVDRHA-KCDKBNATSA-N
分子式 Formula	C6H13NO4
分子量 Molecular Weight	163.17
溶解度Solubility
性状	Solid powder
储藏条件 Storage conditions	Dry, dark and store at 0-4℃ for short term (days to weeks) or -20℃ for long term (Store correctly 2-3years).

产品说明	Fucosamine(CAS:7577-62-0):仅限应用于工业或者科学研究过程中非医疗目的，不应用于人类或动物的临床诊断以及治过程疗，该产品非药用，非食用。
Introduction	Fucosamine is an amino sugar derived from fucose.
Application1
Application2
Application3

警示图
危险性	Warning
危险性警示
安全声明
安全防护
备注

[1]Flamm D, Blaschek W. Exopolysaccharides of Synechocystis aquatilis are sulfated arabinofucans containing N-acetyl-fucosamine. Carbohydr Polym. 2014 Jan 30;101:301-6. doi: 10.1016/j.carbpol.2013.09.036. Epub 2013 Sep 2[1]PubMed PMID: 24299777.

[2]Leonori D, Seeberger PH. De novo synthesis of D- and L-fucosamine containing disaccharides. Beilstein J Org Chem. 2013;9:332-41. doi: 10.3762/bjoc.9.38. Epub 2013 Feb 14. PubMed PMID: 23503315; PubMed Central PMCID: PMC3596053.

[3] Leonori D, Seeberger PH. De novo synthesis of the bacterial 2-amino-2,6-dideoxy sugar building blocks D-fucosamine, D-bacillosamine, and D-xylo-6-deoxy-4-ketohexosamine. Org Lett. 2012 Sep 21;14(18):4954-7. Epub 2012 Sep 6. PubMed PMID: 22954071.

[4] Hung MN, Rangarajan E, Munger C, Nadeau G, Sulea T, Matte A. Crystal structure of TDP-fucosamine acetyltransferase (WecD) from Escherichia coli, an enzyme required for enterobacterial common antigen synthesis. J Bacteriol. 2006 Aug;188(15):5606-17. PubMed PMID: 16855251; PubMed Central PMCID: PMC1540030.

[5] Mulrooney EF, Poon KK, McNally DJ, Brisson JR, Lam JS. Biosynthesis of UDP-N-acetyl-L-fucosamine, a precursor to the biosynthesis of lipopolysaccharide in Pseudomonas aeruginosa serotype O11. J Biol Chem. 2005 May 20;280(20):19535-42. Epub 2005 Mar 18. PubMed PMID: 15778500.

6: Druzhinina TN, Kalinchuk NA, Shibaev VN. Biosynthesis of uridine diphosphate N-acetyl-L-fucosamine in a cell-free system from Salmonella arizonae O:59. Biochemistry (Mosc). 2005 Jan;70(1):85-91. PubMed PMID: 15701053.7: Kneidinger B, O'Riordan K, Li J, Brisson JR, Lee JC, Lam JS. Three highly conserved proteins catalyze the conversion of UDP-N-acetyl-D-glucosamine to precursors for the biosynthesis of O antigen in Pseudomonas aeruginosa O11 and capsule in Staphylococcus aureus type 5. Implications for the UDP-N-acetyl-L-fucosamine biosynthetic pathway. J Biol Chem. 2003 Feb 7;278(6):3615-27. Epub 2002 Dec 2. PubMed PMID: 12464616.8: Vinogradov EV, Kaca W, Knirel YA, Rózalski A, Kochetkov NK. Structural studies on the fucosamine-containing O-specific polysaccharide of Proteus vulgaris O19. Eur J Biochem. 1989 Mar 1;180(1):95-9. PubMed PMID: 2651127.9: Aono R, Uramoto M. Presence of fucosamine in teichuronic acid of the alkalophilic Bacillus strain C-125. Biochem J. 1986 Jan 1;233(1):291-4. PubMed PMID: 3006662; PubMed Central PMCID: PMC1153020.10: Yaguchi M, Daoust V, Perry MB. Ion-exchange chromatography of 2-amino-2,6-dideoxyhexoses and of the methyl ethers of 2-amino-2,6-dideoxy-D-glucopyranose (quinovosamine) and 2-amino-2,6-dideoxy-D-galactopyranose (fucosamine). Carbohydr Res. 1975 Jan;39(1):131-5. PubMed PMID: 1111960.1

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