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Cucumechinoside C

NMR下載 COA and HPLC MSDS下載
names：
Cucumechinoside C
CAS號(hào)：
125640-32-6
MDL Number：
MF(分子式)： C54H86O28S2 MW(分子量)： 1247.37
EINECS: Reaxys Number:
Pubchem ID: Brand:BIOFOUNT

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中文別名	((2R,3S,4S,5S,6S)-6-(((2R,3R,4R,5S,6R)-4,5-dihydroxy-6-(((2R,3R,4S,5R)-4-hydroxy-2-(((3R,3aS,5aS,7aS,9R,11aR,11bS,13aS)-3,5a,8,8,11a-pentamethyl-3-(4-methyl-2-oxopentyl)-1-oxo-3a,4,5,5a,7,7a,8,9,10,11,11a,11b,12,13-tetradecahydro-1H,3H-naphtho[2',1'4,5]indeno[1,7a-c]furan-9-yl)oxy)-5-(sulfooxy)tetrahydro-2H-pyran-3-yl)oxy)-2-methyltetrahydro-2H-pyran-3-yl)oxy)-4-(((2S,3R,4R,5R,6S)-3,5-dihydroxy-6-(hydroxymethyl)-4-methoxytetrahydro-2H-pyran-2-yl)oxy)-3,5-dihydroxytetrahydro-2H-pyran-2-yl)methyl hydrogen sulfate
英文別名	Cucumechinoside C;
CAS號(hào)	125640-32-6
Inchi	InChI=1S/C54H86O28S2/c1-23(2)18-25(56)19-53(8)32-13-16-52(7)27-10-11-31-50(4,5)33(14-15-51(31,6)26(27)12-17-54(32,52)49(64)81-53)77-48-44(36(59)30(21-72-48)82-84(68,69)70)80-45-38(61)37(60)41(24(3)74-45)78-47-40(63)43(35(58)29(76-47)22-73-83(65,66)67)79-46-39(62)42(71-9)34(57)28(20-55)75-46/h10,23-24,26,28-48,55,57-63H,11-22H2,1-9H3,(H,65,66,67)(H,68,69,70)/t24-,26-,28+,29-,30-,31-,32-,33-,34-,35+,36-,37-,38+,39-,40+,41+,42-,43+,44-,45-,46+,47+,48-,51-,52+,53-,54-/m1/s1
InchiKey	SUKVYAYIZXRRBY-SOACPDBGSA-N
分子式 Formula	C54H86O28S2
分子量 Molecular Weight	1247.37
溶解度Solubility
性狀	Solid powder
儲(chǔ)藏條件 Storage conditions	Dry, dark and store at 0-4℃ for short term (days to weeks) or -20℃ for long term (Store correctly 2-3years).

產(chǎn)品說(shuō)明	Cucumechinoside C(CAS:125640-32-6):僅限應(yīng)用于工業(yè)或者科學(xué)研究過(guò)程中非醫(yī)療目的，不應(yīng)用于人類或動(dòng)物的臨床診斷以及治過(guò)程療，該產(chǎn)品非藥用，非食用。
Introduction	Cucumechinoside C is a bioactive natural chemical.
Application1
Application2
Application3

警示圖
危險(xiǎn)性	Warning
危險(xiǎn)性警示
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[2]Basso AV, Nicotra VE, Parra A, Martínez A, Fernández-Vivas A. Biotransformation of Salpichrolides A, C, and G by Three Filamentous Fungi. J Nat Prod. 2016 Jun 24;79(6):1658-67. doi: 10.1021/acs.jnatprod.6b00310. Epub 2016 Jun 10. PubMed PMID: 27285201.

[3] Yamada M, Tanabe Y, Dang JS, Sato S, Mizorogi N, Hachiya M, Suzuki M, Abe T, Kurihara H, Maeda Y, Zhao X, Lian Y, Nagase S, Akasaka T. D(2d)(23)-C(84) versus Sc(2)C(2)@D(2d)(23)-C(84): Impact of Endohedral Sc(2)C(2) Doping on Chemical Reactivity in the Photolysis of Diazirine. J Am Chem Soc. 2016 Dec 21;138(50):16523-16532. doi: 10.1021/jacs.6b10751. Epub 2016 Dec 7. PubMed PMID: 27998084.

[4] Filho LC, Packer L. Revision of the Neotropical subgenera Coelioxys (Platycoelioxys) Mitchell and C. (Rhinocoelioxys) Mitchell (Hymenoptera; Megachilidae) with the description of one new species. Zootaxa. 2015 Mar 31;3941(2):151-203. doi: 10.11646/zootaxa.3941.2.1. PubMed PMID: 25947503.

[5] Bai Y, Li S, Zong YN, Li XL, Zhao ZH, Kong XD. [Mutation screening of 433 families with Duchenne/Becker muscular dystrophy]. Zhonghua Yi Xue Za Zhi. 2016 Apr 26;96(16):1261-9. doi: 10.3760/cma.j.issn.0376-2491.2016.16.008. Chinese. PubMed PMID: 27122458.

6: Zhang H, Timmermann BN. Withanolide Structural Revisions by (13)C NMR Spectroscopic Analysis Inclusive of the γ-Gauche Effect. J Nat Prod. 2016 Apr 22;79(4):732-42. doi: 10.1021/acs.jnatprod.5b00648. Epub 2016 Feb 19. PubMed PMID: 26894655.7: Henderson SJ, Timbs AT, McCarthy J, Gallienne AE, Proven M, Rugless MJ, Lopez H, Eglinton J, Dziedzic D, Beardsall M, Khalil MS, Old JM. Ten Years of Routine α- and β-Globin Gene Sequencing in UK Hemoglobinopathy Referrals Reveals 60 Novel Mutations. Hemoglobin. 2016;40(2):75-84. doi: 10.3109/03630269.2015.1113990. Epub 2015 Dec 4. Review. PubMed PMID: 26635043.8: Ding L, Ishida N, Murakami M, Morokuma K. sp3-sp2 vs sp3-sp3 C-C site selectivity in Rh-catalyzed ring opening of benzocyclobutenol: a DFT study. J Am Chem Soc. 2014 Jan 8;136(1):169-78. doi: 10.1021/ja407422q. Epub 2013 Dec 16. PubMed PMID: 24341735.9: Pavuluri CM, Kawamura K. Enrichment of (13)C in diacids and related compounds during photochemical processing of aqueous aerosols: New proxy for organic aerosols aging. Sci Rep. 2016 Nov 4;

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