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Thienamycin (>80%)

NMR下載 COA and HPLC MSDS下載
names：
Thienamycin (>80%)
CAS號：
59995-64-1
MDL Number：
MF(分子式)： C11H16N2O4S MW(分子量)： 272.321
EINECS: Reaxys Number:
Pubchem ID: Brand:BIOFOUNT

貨品編碼	規(guī)格	純度	價格 (￥)	現(xiàn)價(￥)	特價(￥)	庫存描述	數(shù)量	總計 (￥)
HCC348005-1mg	1mg	97%	￥ 2660.00	￥ 2660.00		4-7周	- +	￥ 0.00

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中文別名	Thienamycin (>80%);(59995-64-1)
英文別名	59995-64-1;Thienamycin (>80%)
CAS號	59995-64-1
Inchi	InChI=1S/C11H16N2O4S/c1-5(14)8-6-4-7(18-3-2-12)9(11(16)17)13(6)10(8)15/h5-6,8,14H,2-4,12H2,1H3,(H,16,17)/t5-,6-,8-/m1/s1
InchiKey	WKDDRNSBRWANNC-ATRFCDNQSA-N
分子式 Formula	C11H16N2O4S
分子量 Molecular Weight	272.321
溶解度Solubility	Chloroform (Slightly), Water (Sparingly)
性狀
儲藏條件 Storage conditions	Hygroscopic, -86°C Freezer, Under inert atmosphere

實驗注意事項：
1.實驗前需戴好防護眼鏡，穿戴防護服和口罩，佩戴手套，避免與皮膚接觸。
2.實驗過程中如遇到有毒或者刺激性物質及有害物質產(chǎn)生，必要時實驗操作需要手套箱內完成以免對實驗人員造成傷害
3.實驗后產(chǎn)生的廢棄物需分類存儲，并交于專業(yè)生物廢氣物處理公司處理，以免造成環(huán)境污染Experimental considerations:
1. Wear protective glasses, protective clothing and masks, gloves, and avoid contact with the skin during the experiment.
2. The waste generated after the experiment needs to be stored separately, and handed over to a professional biological waste gas treatment company to avoid environmental pollution.

產(chǎn)品說明	Thienamycin (>80%);(59995-64-1)可以作為藥物雜質對照品以及生物醫(yī)藥類試劑。
Introduction	59995-64-1;Thienamycin (>80%) can be used as a reference substance for drug impurities and reagents，only for research.
Application1
Application2
Application3

警示圖
危險性	warning
危險性警示	Not available
安全聲明	H303+H313+H333
安全防護	P264+P280+P305+P351+P338+P337+P313
備注	實驗過程中防止吸入、食入，做好安全防護

Hodgson S.Synthesis of the ?2-lactam antibiotic (+)- thienamycin via an intermediate ?€-allyltricarbonyliron lactone complex,Tetrahedron, 1985[DOI: 10.1016S0040-4020(01)91426-7]

Christian Ducho, Refaat B. Hamed, Edward T. Batchelar, John L. Sorensen, Barbara Odell and Christopher J. Schofield.Synthesis of regio- and stereoselectively deuterium-labelled derivatives of l-glutamate semialdehyde for studies on carbapenembiosynthesis,Org. Biomol. Chem., 2009, 7, 2770.[DOI: 10.1039b903312b]

Butler Mark S., Robertson Avril A. B., Cooper Matthew A..Natural product and natural product derived drugs in clinical trials,Nat. Prod. Rep., 2014[DOI: 10.1039C4NP00064A]

Activation and silencing of secondary metabolites in Streptomyces albus and Streptomyces lividans after transformation with cosmids containing the thienamycin gene cluster from Streptomyces cattleya,Archives of Microbiology[DOI: 10.1007s00203-014-0977-z]

The in vitro activity of N-formimidoyl thienamycin compared with other broad-spectrum cephalosporins and with clindamycin and metronidazole,Infection[DOI: 10.1007BF01641202]

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