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(5R,3aR,11bR)-4'α-Acetyloxy-3',3a,4',5',6',11b-hexahydro-3'α,7-dihydroxy-6'β-methylspiro[5H-furo[3,2-b]naphtho[2,3-d]pyran-5,2'-[2H]pyran]-2,6,11(3H)-trione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

59554-11-9

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59554-11-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59554-11-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,5,5 and 4 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 59554-11:
(7*5)+(6*9)+(5*5)+(4*5)+(3*4)+(2*1)+(1*1)=149
149 % 10 = 9
So 59554-11-9 is a valid CAS Registry Number.

59554-11-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name Griseucin A

1.2 Other means of identification

Product number -
Other names (-)-Griseusin A

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:59554-11-9 SDS

59554-11-9Downstream Products

59554-11-9Relevant academic research and scientific papers

A Divergent Enantioselective Strategy for the Synthesis of Griseusins

Zhang, Yinan,Ye, Qing,Wang, Xiachang,She, Qing-Bai,Thorson, Jon S.

, p. 11219 - 11222 (2015)

The first enantioselective total synthesis of griseusin A, griseusin C, 4′-deacetyl-griseusin A, and two non-native counterparts in 11–14 steps is reported. This strategy highlights a key hydroxy-directed C H olefination of 1-methylene isochroman with an

Total synthesis of griseusins and elucidation of the griseusin mechanism of action

Zhang, Yinan,Ye, Qing,Ponomareva, Larissa V.,Cao, Yanan,Liu, Yang,Cui, Zheng,Van Lanen, Steven G.,Voss, S. Randal,She, Qing-Bai,Thorson, Jon S.

, p. 7641 - 7648 (2019/08/21)

A divergent modular strategy for the enantioselective total synthesis of 12 naturally-occurring griseusin type pyranonaphthoquinones and 8 structurally-similar analogues is described. Key synthetic highlights include Cu-catalyzed enantioselective boration-hydroxylation and hydroxyl-directed C-H olefination to afford the central pharmacophore followed by epoxidation-cyclization and maturation via diastereoselective reduction and regioselective acetylation. Structural revision of griseusin D and absolute structural assignment of 2a,8a-epoxy-epi-4′-deacetyl griseusin B are also reported. Subsequent mechanistic studies establish, for the first time, griseusins as potent inhibitors of peroxiredoxin 1 (Prx1) and glutaredoxin 3 (Grx3). Biological evaluation, including comparative cancer cell line cytotoxicity and axolotl embryo tail inhibition studies, highlights the potential of griseusins as potent molecular probes and/or early stage leads in cancer and regenerative biology.

Griseusin derivatives and their use as antitumor agents

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Page/Page column 10, (2008/06/13)

The present invention relates to specific griseusin derivatives, pharmaceutical compositions comprising said griseusin derivatives and the use of these derivatives for the manufacture of a medicament for the treatment of cancers, particularly for the treatment of human solid cancers.

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