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[5-[(9R,13R,14S,16R,17R)-2,16-dihydroxy-4,4,9,13,14-pentamethyl-3,11-dioxo-8,10,12,15,16,17-hexahydro-7H-cyclopenta[a]phenanthren-17-yl]-5-hydroxy-1,1-dimethyl-4-oxo-hexyl] acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

28973-67-3

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28973-67-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28973-67-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,9,7 and 3 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 28973-67:
(7*2)+(6*8)+(5*9)+(4*7)+(3*3)+(2*6)+(1*7)=163
163 % 10 = 3
So 28973-67-3 is a valid CAS Registry Number.

28973-67-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [6-[(9R,13R,14S,16R,17R)-2,16-dihydroxy-4,4,9,13,14-pentamethyl-3,11-dioxo-8,10,12,15,16,17-hexahydro-7H-cyclopenta[a]phenanthren-17-yl]-6-hydroxy-2-methyl-5-oxoheptan-2-yl] acetate

1.2 Other means of identification

Product number -
Other names 19-Norlanosta-1,5-diene-3,11,22-trione,25-(acetyloxy)-2,16,20-trihydroxy-9-methyl-,(9beta,10alpha,16alpha)

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:28973-67-3 SDS

28973-67-3Downstream Products

28973-67-3Relevant academic research and scientific papers

Synthesis and cytotoxic activity evaluation of dihydrocucurbitacin B and cucurbitacin B derivatives

Lang, Karen Luise,Silva, Izabella Thaís,Zimmermann, Lara Almida,MacHado, Vanessa Rocha,Teixeira, Marina Rodrigues,Lapuh, María Ivana,Galetti, Mariana Alejandra,Palermo, Jorge Alejandro,Cabrera, Gabriela Myriam,Bernardes, Lílian Sibelle Campos,Sim?es, Cláudia Maria Oliveira,Schenkel, Eloir Paulo,Caro, Miguel Soriano Balparda,Durán, Fernando Javier

experimental part, p. 3016 - 3030 (2012/06/18)

Two cucurbitacins, dihydrocucurbitacin B (1) and cucurbitacin B (2), which can be obtained in large amounts from the roots of Wilbrandia ebracteata and from the fruits of Luffa operculata, respectively, were used as starting materials for the preparation of a library of 29 semi-synthetic derivatives. The structural changes that were performed include the removal, modification or permutation of functional groups in rings A and B as well as in the side chain. All new semisynthetic compounds, as well as 1 and 2, were tested in vitro for their cytotoxic effects on non-small-cell lung cancer cells (A549 cells). Some of these compound displayed potent to moderate activity against A549 tumor cells, especially those cucurbitacin B derivatives which were modified at ring A.

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