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(R)-2,5,7,8-tetramethyl-2-((3'E,7'E)-4',8',12'-trimethyltrideca-3',7',11'-trienyl)chroman-6-yl phenylsulfonylcarbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1208120-80-2

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1208120-80-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1208120-80-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,8,1,2 and 0 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1208120-80:
(9*1)+(8*2)+(7*0)+(6*8)+(5*1)+(4*2)+(3*0)+(2*8)+(1*0)=102
102 % 10 = 2
So 1208120-80-2 is a valid CAS Registry Number.

1208120-80-2Downstream Products

1208120-80-2Relevant academic research and scientific papers

Design and preliminary structure-activity relationship of redox-silent semisynthetic tocotrienol analogues as inhibitors for breast cancer proliferation and invasion

Elnagar, Ahmed Y.,Wali, Vikram B.,Sylvester, Paul W.,El Sayed, Khalid A.

experimental part, p. 755 - 768 (2010/05/02)

Vitamin E (VE) is a generic term that represents a family of compounds composed of various tocopherol and tocotrienol isoforms. Tocotrienols display potent anti-angiogenic and antiproliferative activities. Redox-silent tocotrienol analogues also display potent anticancer activity. The ultimate objective of this study was to develop semisynthetically C-6-modified redox-silent tocotrienol analogues with enhanced antiproliferative and anti-invasive activities as compared to their parent compound. Examples of these are carbamate and ether analogues of α-, γ-, and δ-tocotrienols (1-3). Various aliphatic, olefinic, and aromatic substituents were used. Steric limitation, electrostatic, hydrogen bond donor (HBD) and hydrogen bond acceptor (HBA) properties were varied at this position and the biological activities of these derivatives were tested. Three-dimensional quantitative structure-activity relationship (3D QSAR) studies were performed using Comparative Molecular Field (CoMFA) and Comparative Molecular Similarity Indices Analyses (CoMSIA) to better understand the structural basis for biological activity and guide the future design of more potent VE analogues.

ANTI-CANCER TOCOTRIENOL ANALOGUES AND ASSOCIATED METHODS

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Page/Page column 19, (2010/11/05)

Compounds are disclosed relating to the treatment of cancer that include tocotrienols and derivatives of tocotrienols including 2,5,7,8-tetramethyl-2- ((3E,7E)-4,8,12-trimethyltrideca-3,7,l l-trienyl)chroman-6- ylphenylsulfonylcarbamate; (R)-2,8-dimethyl-2-((3E,7E)-4,8,12-trimethyltrideca- 3,7,1 l-trienyl)chroman-6-yl tosylcarbamate; and (R)-2,5,7,8-tetramethyl-2- ((3E,7E)-4,8, 12-trimethyltrideca-3,7, 1 l-trienyl)chroman-6-yl benzylcarbamate. Therapeutic uses of these types of compounds are also taught.

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