Salicin

Template:Chembox new

WikiDoc Resources for Salicin

Articles

Most recent articles on Salicin

Most cited articles on Salicin

Review articles on Salicin

Articles on Salicin in N Eng J Med, Lancet, BMJ

Media

Powerpoint slides on Salicin

Images of Salicin

Photos of Salicin

Podcasts & MP3s on Salicin

Videos on Salicin

Evidence Based Medicine

Cochrane Collaboration on Salicin

Bandolier on Salicin

TRIP on Salicin

Clinical Trials

Ongoing Trials on Salicin at Clinical Trials.gov

Trial results on Salicin

Clinical Trials on Salicin at Google

Guidelines / Policies / Govt

US National Guidelines Clearinghouse on Salicin

NICE Guidance on Salicin

NHS PRODIGY Guidance

FDA on Salicin

CDC on Salicin

Books

Books on Salicin

News

Salicin in the news

Be alerted to news on Salicin

News trends on Salicin

Commentary

Blogs on Salicin

Definitions

Definitions of Salicin

Patient Resources / Community

Patient resources on Salicin

Discussion groups on Salicin

Patient Handouts on Salicin

Directions to Hospitals Treating Salicin

Risk calculators and risk factors for Salicin

Healthcare Provider Resources

Symptoms of Salicin

Causes & Risk Factors for Salicin

Diagnostic studies for Salicin

Treatment of Salicin

Continuing Medical Education (CME)

CME Programs on Salicin

International

Salicin en Espanol

Salicin en Francais

Business

Salicin in the Marketplace

Patents on Salicin

Experimental / Informatics

List of terms related to Salicin

## Overview

[edit | edit source]

Salicin (C13H18O7) is an alcoholic β-glycoside which contains D-glucose. Salicin is an anti-inflammatory which is produced from all willow barks. Salicin is closely related chemically to aspirin and has a very similar action in the human body. When consumed, it is metabolized to salicylic acid. The systematic (IUPAC) name of the molecule is 2-(Hydroxymethyl)phenyl β-D-glucopyranoside. It has the following classifications and chemical properties:

* CAS No. 138-52-3
* Merck index 11,8293
* Molecular weight 286.28 g/mol
* Melting point 197-200 °C

## References

[edit | edit source]

* www.emedicinal.com
* Aldrich: Catalog handbook of fine chemicals, Published by: Aldrich Chemical Company 1992
* Thomas Baker Chemicals
* [1] Uchytil, Ronald J. 1991. Salix drummondiana. In: Fire Effects Information System, Online. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/ 2006, July 19
* www.chemexper.com

* v
* t
* e

Analgesic products (N02A, N02B)

Opioids
See also: Opioids template|

Alphaprodine * Anileridine * Buprenorphine * Butorphanol * Codeine * Dextromoramide * Dextropropoxyphene * Dezocine * Desomorphine * Diamorphine * Dihydrocodeine * Dihydromorphine * Fentanyl * Hydrocodone * Hydromorphone * Ketobemidone * Levorphanol * Meptazinol * Methadone * Morphine * Nalbuphine * Nicomorphine * Opium * Oxycodone * Oxymorphone * Pethidine * Pentazocine * Pethidine * Piminodine * Piritramide * Tilidine * Tramadol * Tapentadol

Salicylic acid and derivatives|

Aspirin (Acetylsalicylic Acid) * Benorylate * Diflunisal * Ethenzamide * Magnesium Salicylate * Salicin * Salicylamide * Salsalate * See also: NSAIDs

Pyrazolones|

Ampyrone/Aminophenazone * Metamizole * Phenazone

Cannabinoids|

Cannabis * Tetrahydrocannabinol * AM404

Anilides|

Paracetamol (acetaminophen) * Phenacetin * Propacetamol

Non-Salicylate Non-Steroidal
Anti-Inflammatories
See also: NSAIDs template|

Template:Navbox subgroup

Atypical, Adjunct
& Miscellaneous|

Bicifadine * Clonidine * Cyclobenzaprine * Duloxetine * Flupirtine * Gabapentin * Nefopam * Orphenadrine * Trazadone * Ziconotide

* v
* t
* e

Non-steroidal anti-inflammatory drug (NSAID) products (primarily M01A and M02A, also N02BA)

Salicylates|

Aspirin (acetylsalicylic acid) * Aloxiprin * Benorylate * Diflunisal * Ethenzamide * Magnesium salicylate * Methyl salicylate * Salsalate * Salicin * Salicylamide * Sodium salicylate

Arylalkanoic acids|

Diclofenac * Aceclofenac * Acemetacin * Alclofenac * Bromfenac * Etodolac * Indometacin * Indomethacin farnesil * Nabumetone * Oxametacin * Proglumetacin * Sulindac * Tolmetin

2-Arylpropionic acids
(profens)|

Ibuprofen * Alminoprofen * Benoxaprofen * Carprofen * Dexibuprofen * Dexketoprofen * Fenbufen * Fenoprofen * Flunoxaprofen * Flurbiprofen * Ibuproxam * Indoprofen† * Ketoprofen * Ketorolac * Loxoprofen * Miroprofen * Naproxen * Oxaprozin * Pirprofen * Suprofen * Tarenflurbil * Tiaprofenic acid

N-Arylanthranilic acids
(fenamic acids)|

Mefenamic acid * Flufenamic acid * Meclofenamic acid * Tolfenamic acid

Pyrazolidine derivatives|

Phenylbutazone * Ampyrone * Azapropazone * Clofezone * Kebuzone * Metamizole† * Mofebutazone * Oxyphenbutazone * Phenazone * Sulfinpyrazone

Oxicams|

Piroxicam * Droxicam * Lornoxicam * Meloxicam * Tenoxicam

COX-2 inhibitors|

Celecoxib * Deracoxib‡ * Etoricoxib * Firocoxib‡ * Lumiracoxib† * Parecoxib * Rofecoxib† * Valdecoxib†

Sulphonanilides|

Nimesulide

Topically used products|

Bendazac * Diclofenac * Etofenamate * Felbinac * Flurbiprofen * Ibuprofen * Indometacin * Ketoprofen * Naproxen * Piroxicam * Suprofen

Others|

Fluproquazone * COX-inhibiting nitric oxide donator

Items listed in bold indicate initially developed compounds of specific groups. †Withdrawn drugs. ‡Veterinary use medications.

Template:Glycosides

de:Salicin

Template:WikiDoc Sources
*[v]: View this template
*[t]: Discuss this template
*[e]: Edit this template