56509-88-7|Viridinomycin|(4E,6E,8E,10Z,16Z,18Z,20E,22E,24R,25S,26R)-25,27-dihydroxy-26-methoxy-4,24-dimethyl-13-phenyl-3-oxa-14-azabicyclo[22.3.0]heptacosa-1(27),4,6,8,10,16,18,20,22-nonaene-2,15-dione|-范德生物科技公司

Viridinomycin

NMR下载 COA and HPLC MSDS下载
names：
(4E,6E,8E,10Z,16Z,18Z,20E,22E,24R,25S,26R)-25,27-dihydroxy-26-methoxy-4,24-dimethyl-13-phenyl-3-oxa-14-azabicyclo[22.3.0]heptacosa-1(27),4,6,8,10,16,18,20,22-nonaene-2,15-dione
CAS号：
56509-88-7
MDL Number：
MF(分子式)： C34H37NO6 MW(分子量)： 555.671
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	(4E,6E,8E,10Z,16Z,18Z,20E,22E,24R,25S,26R)-25,27-dihydroxy-26-methoxy-4,24-dimethyl-13-phenyl-3-oxa-14-azabicyclo[22.3.0]heptacosa-1(27),4,6,8,10,16,18,20,22-nonaene-2,15-dione
英文别名	Viridinomycin; Viridomycin; Antibiotic T-24146; Viridenomycin
CAS号	56509-88-7
SMILES	O=C(O/C(C)=C/C=C/C=C/C=C\CC(C1=CC=CC=C1)N2)C3=C(O)[C@H](OC)[C@@H](O)[C@]3(C)/C=C/C=C/C=C\C=C/C2=O
Inchi	InChI=1S/C34H37NO6/c1-25-19-13-8-4-5-9-16-22-27(26-20-14-12-15-21-26)35-28(36)23-17-10-6-7-11-18-24-34(2)29(33(39)41-25)30(37)31(40-3)32(34)38/h4-21,23-24,27,31-32,37-38H,22H2,1-3H3,(H,35,36)/b5-4+,10-6-,11-7+,13-8+,16-9-,23-17-,24-18+,25-19+/t27?,31-,32+,34+/m0/s1
InchiKey	GWYPHKYSRIAIBU-KGZNJIQESA-N
分子式 Formula	C34H37NO6
分子量 Molecular Weight	555.671
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	Viridinomycin(CAS:56509-88-7):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	Viridinomycin is a crystalline antibiotic that shows strong activity against Trichomonas vaginalis and gram-positive bacteria.
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]Batsanov AS, Knowles JP, Lightfoot AP, Maw G, Thirsk CE, Twiddle SJ, Whiting A. A novel, efficient, diastereo- and enantioselective Mukaiyama aldol-based synthesis of a vinyl cyclopentanone core derivative of viridenomycin. Org Lett. 2007 Dec 20;9(26):5565-8. Epub 2007 Nov 17. PubMed PMID: 18020354.

[2]Hasegawa T, Kamiya T, Henmi T, Iwasaki H, Yamatodani S. Viridenomycin, a new antibiotic. J Antibiot (Tokyo). 1975 Mar;28(3):167-75. PubMed PMID: 1079209.

[3] Knowles JP, O'Connor VE, Whiting A. Studies towards the synthesis of the northern polyene of viridenomycin and synthesis of Z-double bond analogues. Org Biomol Chem. 2011 Mar 21;9(6):1876-86. doi: 10.1039/c0ob00977f. Epub 2011 Jan 31. PubMed PMID: 21283899.

[4] Batsanov AS, Knowles JP, Whiting A. Mechanistic studies on the Heck-Mizoroki cross-coupling reaction of a hindered vinylboronate ester as a key approach to developing a highly stereoselective synthesis of a C1-C7 Z,Z,E-triene synthon for viridenomycin. J Org Chem. 2007 Mar 30;72(7):2525-32. Epub 2007 Mar 3. PubMed PMID: 17335239.

[5] Nakagawa M, Toda Y, Furihata K, Hayakawa Y, Seto H. Studies on viridenomycin, a novel 24-membered macrocyclic polyene lactam antibiotic. J Antibiot (Tokyo). 1992 Jul;45(7):1133-8. PubMed PMID: 1517159.

6: Trost BM, Jiang C. Pd-catalyzed asymmetric allylic alkylation. A short route to the cyclopentyl core of viridenomycin. Org Lett. 2003 May 1;5(9):1563-5. PubMed PMID: 12713324.

对不起，暂无产品评价！

MSDS

SDS 1.0 中文

展开

SDS 1.0 英文

展开