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(3Z)-6-methoxy-3-[(4-methoxyphenyl)methylidene]-2,3-dihydro-4H-thiochromen-4-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

130689-04-2

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130689-04-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 130689-04-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,6,8 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 130689-04:
(8*1)+(7*3)+(6*0)+(5*6)+(4*8)+(3*9)+(2*0)+(1*4)=122
122 % 10 = 2
So 130689-04-2 is a valid CAS Registry Number.

130689-04-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (3Z)-6-methoxy-3-[(4-methoxyphenyl)methylidene]thiochromen-4-one

1.2 Other means of identification

Product number -
Other names -

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:130689-04-2 SDS

130689-04-2Relevant academic research and scientific papers

Structure-activity relationship study of tricyclic necroptosis inhibitors

Jagtap, Prakash G.,Degterev, Alexei,Choi, Sungwoon,Keys, Heather,Yuan, Junying,Cuny, Gregory D.

, p. 1886 - 1895 (2008/02/03)

Necroptosis is a regulated caspase-independent cell death mechanism that can be induced in multiple cell types and is characterized by morphological features resembling necrosis. Here we describe a series of tricyclic heterocycles (i.e., 3-phenyl-3,3a,4,5-tetrahydro-2H-benz[g]indazoles, 3-phenyl-2,3,3a,4-tetrahydro-[1]benzopyrano[4,3-c]pyrazoles, 3-phenyl-2,3,3a,4-tetrahydro[1]benzothiopyrano[4,3-c]pyrazoles, and 5,5-dioxo-3-phenyl-2,3,3a,4-tetrahydro[1]benzothiopyrano[4,3-c]pyrazoles], collectively termed Nec-3, that can potently inhibit necroptosis. For example, compounds 8, 22, 41, 53, and 55 inhibit necroptosis in an FADD-deficient variant of human Jurkat T cells treated for 24 h with TNF-α with EC50 values in the range 0.15-0.29 μM. Distinct from the previously described series of hydantoin-containing indole derivatives (Nec-1), the Nec-3 series exhibits specificity in inhibiting TNF-α-induced necroptosis. A structure-activity relationship (SAR) study revealed that the (3R,3aR)-rel-diastereomers were more active than the (3R,3aS)-rel-diastereomers for all four ring systems. Introduction of fluorine or methoxy to the 8-position of the tricyclic ring and a methoxy to the 4-position of the pendent phenyl ring increased activity. Amides at the 2-position of the tricyclic ring were best. The Nec-3 series provides new tools for elucidating caspase-independent cell death pathways and potentially lead compounds for therapeutic development.

COMPOUNDS, SCREENS, AND METHODS OF TREATMENT

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Page/Page column 210, (2008/06/13)

The present invention features compounds, pharmaceutical compositions, and methods for treating trauma, ischemia, stroke, degenerative diseases associated with cellular necrosis, and other conditions. Screening assays for identifying compounds useful for treating these conditions are also described.

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