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105467-77-4

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105467-77-4 Usage

Structure

Unique polycyclic structure

Applications

a. Medical and research applications
b. Potential anticancer properties
c. Anti-malarial agent

Mechanism of Action

Potent inhibitor of DNA topoisomerase II

DNA Interaction

Disrupts DNA structure and function

Tumor Cell Death

Induces tumor cell death by disrupting DNA

Plasmodium falciparum

Inhibits growth of the parasite

Toxicity

Known to be toxic and mutagenic

Laboratory Safety

Care must be taken when handling and using in laboratory settings

Check Digit Verification of cas no

The CAS Registry Mumber 105467-77-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,4,6 and 7 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 105467-77:
(8*1)+(7*0)+(6*5)+(5*4)+(4*6)+(3*7)+(2*7)+(1*7)=124
124 % 10 = 4
So 105467-77-4 is a valid CAS Registry Number.
InChI:InChI=1/C21H17N/c1-3-7-16-14(5-1)9-11-20-18(16)13-19-17-8-4-2-6-15(17)10-12-21(19)22-20/h1,3,5,7,9-13H,2,4,6,8H2

105467-77-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,3,4-tetrahydrodibenz<a,j>acridine

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:105467-77-4 SDS

105467-77-4Relevant articles and documents

Synthesis of Potential Metabolites of Dibenzacridine: Dihydro Diols and Phenols

Rosario, Christopher A.,Holder, Gerald M.,Duke, Colin C.

, p. 1064 - 1072 (2007/10/02)

The potential trans dihydro diol metabolites of the carcinogen dibenzacridine (1) were prepared.The dihydro diols trans-1,2-dihydroxydibenzacridine (12) and trans-3,4-dihydro-3,4-dihydroxydibenzacridine (13) were prepared by Prevost reactio

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