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2-[4-N,N-bis(2-chloroethyl)amino-phenyl]butanoic acid, also known as mechlorethamine, is an alkylating agent with the chemical formula C10H18Cl2N2O2. It is a nitrogen mustard derivative, which is a class of cytotoxic drugs used in cancer chemotherapy. Mechlorethamine works by cross-linking DNA strands, preventing cell division and ultimately leading to cell death. It is primarily used to treat Hodgkin's lymphoma and other lymphomas, as well as certain types of leukemia. Due to its highly reactive nature, it must be handled with extreme care to avoid exposure and potential health risks.

6555-38-0

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6555-38-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6555-38-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,5 and 5 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6555-38:
(6*6)+(5*5)+(4*5)+(3*5)+(2*3)+(1*8)=110
110 % 10 = 0
So 6555-38-0 is a valid CAS Registry Number.

6555-38-0Relevant academic research and scientific papers

Steroidal esters of the aromatic nitrogen mustard 2-[4-N,N-bis(2- chloroethyl)amino-phenyl]butanoic acid (2-PHE-BU): Synthesis and in-vivo biological evaluation

Papaconstantinou, Ioanna C.,Fousteris, Manolis A.,Koutsourea, Anna I.,Pairas, Georgios N.,Papageorgiou, Athanasios D.,Nikolaropoulos, Sotiris S.

, p. 52 - 65 (2013/02/25)

On the basis of the results of in-silico predictions and in an effort to extend our structure-activity relationship studies, the aromatic nitrogen mustard 2-[4-N,N-bis(2-chloroethyl) amino-phenyl]butanoic acid (2-PHE-BU) was synthesized and conjugated with various steroidal alcohols. The resulting steroidal esters were evaluated for their in-vivo toxicity and antileukemic activity in P388-leukemia-bearing mice. The new derivatives showed significantly reduced toxicity and marginally improved antileukemic activity compared with free 2-PHE-BU. Nevertheless, they did not prove to be superior either to the template steroidal ester used for in-silico predictions or to previously synthesized steroidal esters of aromatic nitrogen mustards. The results obtained indicate that in-silico design predictions may guide the design and synthesis of new bioactive steroidal esters, but further parameters should be considered aiming at the discovery of compounds with optimum activity.

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