Mechlorethamine (topical): Difference between revisions

Jump to navigation Jump to search
m (Protected "Mechlorethamine": Protecting pages from unwanted edits ([edit=sysop] (indefinite) [move=sysop] (indefinite)))
 
m (Robot: Automated text replacement (-{{SIB}} + & -{{EH}} + & -{{EJ}} + & -{{Editor Help}} + & -{{Editor Join}} +))
Line 18: Line 18:
}}
}}
{{SI}}
{{SI}}
{{EH}}
 


==Overview==
==Overview==
Line 31: Line 31:


{{Chemotherapeutic agents}}
{{Chemotherapeutic agents}}
{{SIB}}
 
[[Category:Chemotherapeutic agents]]
[[Category:Chemotherapeutic agents]]



Revision as of 17:14, 9 August 2012

Mechlorethamine (topical)
File:Mechlorethamine.png
Clinical data
Pregnancy
category
  • D (US)
Routes of
administration
IV, intracavitary, intrapericardially, topical
ATC code
Legal status
Legal status
  • In general: ℞ (Prescription only)
Pharmacokinetic data
Bioavailability?
MetabolismRapid hydrolysis and demethylation, possibly in plasma
Elimination half-life< 1 minute
ExcretionUrine (50% as metabolites, <0.01% as unchanged drug)
Identifiers
CAS Number
PubChem CID
DrugBank
E number{{#property:P628}}
ECHA InfoCard{{#property:P2566}}Lua error in Module:EditAtWikidata at line 36: attempt to index field 'wikibase' (a nil value).
Chemical and physical data
FormulaC5H11Cl2N
Molar mass156.055 g mol−1

WikiDoc Resources for Mechlorethamine (topical)

Articles

Most recent articles on Mechlorethamine (topical)

Most cited articles on Mechlorethamine (topical)

Review articles on Mechlorethamine (topical)

Articles on Mechlorethamine (topical) in N Eng J Med, Lancet, BMJ

Media

Powerpoint slides on Mechlorethamine (topical)

Images of Mechlorethamine (topical)

Photos of Mechlorethamine (topical)

Podcasts & MP3s on Mechlorethamine (topical)

Videos on Mechlorethamine (topical)

Evidence Based Medicine

Cochrane Collaboration on Mechlorethamine (topical)

Bandolier on Mechlorethamine (topical)

TRIP on Mechlorethamine (topical)

Clinical Trials

Ongoing Trials on Mechlorethamine (topical) at Clinical Trials.gov

Trial results on Mechlorethamine (topical)

Clinical Trials on Mechlorethamine (topical) at Google

Guidelines / Policies / Govt

US National Guidelines Clearinghouse on Mechlorethamine (topical)

NICE Guidance on Mechlorethamine (topical)

NHS PRODIGY Guidance

FDA on Mechlorethamine (topical)

CDC on Mechlorethamine (topical)

Books

Books on Mechlorethamine (topical)

News

Mechlorethamine (topical) in the news

Be alerted to news on Mechlorethamine (topical)

News trends on Mechlorethamine (topical)

Commentary

Blogs on Mechlorethamine (topical)

Definitions

Definitions of Mechlorethamine (topical)

Patient Resources / Community

Patient resources on Mechlorethamine (topical)

Discussion groups on Mechlorethamine (topical)

Patient Handouts on Mechlorethamine (topical)

Directions to Hospitals Treating Mechlorethamine (topical)

Risk calculators and risk factors for Mechlorethamine (topical)

Healthcare Provider Resources

Symptoms of Mechlorethamine (topical)

Causes & Risk Factors for Mechlorethamine (topical)

Diagnostic studies for Mechlorethamine (topical)

Treatment of Mechlorethamine (topical)

Continuing Medical Education (CME)

CME Programs on Mechlorethamine (topical)

International

Mechlorethamine (topical) en Espanol

Mechlorethamine (topical) en Francais

Business

Mechlorethamine (topical) in the Marketplace

Patents on Mechlorethamine (topical)

Experimental / Informatics

List of terms related to Mechlorethamine (topical)


Overview

Mechlorethamine also known as chlormethine, mustine, nitrogen mustard and HN2 and sold under the brand name Mustargen, is the prototype anticancer chemotherapeutic drug. Successful clinical use of mechlorethamine gave birth to the field of anticancer chemotherapy. The drug is an analogue of mustard gas and was derived from chemical warfare research, in particular a 1943 accident in Bari, Italy which exposed civilians and soldiers-- it was noted that white cell counts of exposed patients decreased, suggesting a possible therapy for the cancer Hodgkin's lymphoma. It belongs to the group of nitrogen mustard alkylating agents.

It has been derivatized into the estrogen analogue estramustine, used to treat prostate cancer.

It can also be used in chemical warfare where it has the code-name HN2. This chemical is a form of nitrogen mustard gas and therefore a powerful vesicant.

External links


de:Mechlorethamin it:Mecloretamina Template:WH Template:WS