21884-44-6|Luteoskyrin|(5aS,6S,13aR,14S,17R,18S,19R,20R)-1,4,7,9,12,15,17,20-octahydroxy-3,11-dimethyl-14-hydro-5H,6H-6,13a,5a,14-(epibutane[1,2,3,4]tetrayl)cycloocta[1,2-b5,6-b']dinaphthalene-5,8,13,16-tetraone|-范德生物科技公司

Luteoskyrin

NMR下载 COA and HPLC MSDS下载
names：
(5aS,6S,13aR,14S,17R,18S,19R,20R)-1,4,7,9,12,15,17,20-octahydroxy-3,11-dimethyl-14-hydro-5H,6H-6,13a,5a,14-(epibutane[1,2,3,4]tetrayl)cycloocta[1,2-b5,6-b']dinaphthalene-5,8,13,16-tetraone
CAS号：
21884-44-6
MDL Number：
MF(分子式)： C30H22O12 MW(分子量)： 574.49
EINECS: Reaxys Number:
Pubchem ID: Brand:BIOFOUNT

货品编码	规格	纯度	价格 (¥)	现价(¥)	特价(¥)	库存描述	数量	总计 (¥)

大包装询价提供各种包装，敬请垂询
收藏商品商品点评加入购物车立即购买

快速询价

收起

你想询价的产品

*产品名称：

CAS号：

产品编号：

需求描述：

请准确填写您的联系方式，以便为您提供最好的服务。

*公司名称：

*电子邮箱：

联系人：

*电话：

*验证码：

询价

中文别名	Luteoskyrin
英文别名	Luteoskyrin; Flavomycelin;
CAS号	21884-44-6
SMILES	Cc1cc(O)c(C(C2=C(O)[C@@H]3[C@@H]4O)=O)c(C([C@]52[C@H]4[C@H]6[C@@]3(C(c7c(C8=O)c(O)cc(C)c7O)=O)C8=C(O)[C@@H]5[C@@H]6O)=O)c1O
Inchi	InChI=1S/C30H22O12/c1-5-3-7(31)9-11(19(5)33)27(41)29-13-14-24(38)17(29)26(40)16-22(36)10-8(32)4-6(2)20(34)12(10)28(42)30(14,16)18(23(13)37)25(39)15(29)21(9)35/h3-4,13-14,17-18,23-24,31-34,37-40H,1-2H3/t13-,14+,17-,18-,23+,24+,29-,30+/m0/s1
InchiKey	KXNUPFFSGSRABD-KCIWCSDFSA-N
分子式 Formula	C30H22O12
分子量 Molecular Weight	574.49
闪点 FP
熔点 Melting point
沸点 Boiling point
Polarizability极化度
密度 Density
蒸汽压 Vapor Pressure
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	Luteoskyrin(CAS:21884-44-6):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	Luteoskyrin is a hepatotoxic and hepatocarcinogenic bisdihydroanthraquinone produced by Penicillium islandicum Sopp.
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]Masuda T, Ito J, Akuzawa S, Ishii K, Takagi H, Ueno Y. Hepatic accumulation and hepatotoxicity of luteoskyrin in mice. Toxicol Lett. 1992 Jun;61(1):9-20. PubMed PMID: 1609444.

[2]Tseng HH, Tseng TC. Effects of naled and dichlorvos on growth and production of Luteoskyrin byPenicillium islandicum. Mycotoxin Res. 1993 Mar;9(1):35-40. doi: 10.1007/BF03192230. PubMed PMID: 23606065.

[3] Ueno Y, Ishikawa I. Production of luteoskyrin, a hepatotoxic pigment, by Penicillium islandicum Sopp. Appl Microbiol. 1969 Sep;18(3):406-9. PubMed PMID: 5373676; PubMed Central PMCID: PMC377994.

[4] Ueno I, Sekijima M, Hoshino M, Ohya-Nishiguchi H, Ueno Y. Spin-trapping and direct EPR investigations on the hepatotoxic and hepatocarcinogenic actions of luteoskyrin, an anthraquinoid mycotoxin produced by Penicillium islandicum Sopp. Generations of superoxide anion and luteoskyrin semiquinone radical in the redox systems consisted of luteoskyrin and liver NADPH- or NADH-dependent reductases. Free Radic Res. 1995 Jul;23(1):41-50. PubMed PMID: 7647918.

[5] Ueno I. Sex and age differences in luteoskyrin hepatotoxicity. Ann Nutr Aliment. 1977;31(4-6):789-802. PubMed PMID: 566069.

6: Ueno I, Hoshino M, Maitani T, Kanegasaki S, Ueno Y. Luteoskyrin, an anthraquinoid hepatotoxin, and ascorbic acid generate hydroxyl radical in vitro in the presence of a trace amount of ferrous iron. Free Radic Res Commun. 1993;19 Suppl 1:S95-100. PubMed PMID: 8282236.7: Ghosh AC, Manmade A, Kobbe B, Townsend JM, Demain AL. Production of luteoskyrin and isolation of a new metabolite, pibasterol, from Penicillium islandicum Sopp. Appl Environ Microbiol. 1978 Mar;35(3):563-6. PubMed PMID: 565188; PubMed Central PMCID: PMC242880.8: Mizutani K, Kumagai S, Mochizuki N, Kitagawa Y, Sugita-Konishi Y. Determination of a yellow rice toxin, luteoskyrin, in rice by using liquid chromatography-tandem mass spectrometry with electrospray ionization. J Food Prot. 2009 Jun;72(6):1321-6. PubMed PMID: 19610349.9: Tseng HH, Tseng TC. Effects of butylated hydroxyanisole, butylated hydroxytoluene and tertiary butylhydroquinone on growth and luteoskyrin production byPenicillium islandicum. Mycopathologia. 1995;129(2):73-8. doi: 10.1007/BF01103463. PubMed PMID: 20878563.10: KITAGAWA I, SHIBATA S. Metabolic products of fungi. X. The structure of rubroskyrin and its relation to the structure of luteoskyrin. Pharm Bull. 1956 Aug;4(4):309-13. PubMed PMID: 13378957.1

对不起，暂无产品评价！

MSDS

SDS 1.0 中文

展开

SDS 1.0 英文

展开