
CAS 138-52-3: Salicin
Formula:C13H18O7
InChI:InChI=1S/C13H18O7/c14-5-7-3-1-2-4-8(7)19-13-12(18)11(17)10(16)9(6-15)20-13/h1-4,9-18H,5-6H2/t9-,10-,11+,12-,13-/m1/s1
InChI key:InChIKey=NGFMICBWJRZIBI-UJPOAAIJSA-N
SMILES:O([C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)C2=C(CO)C=CC=C2
Synonyms:- 1-β-<span class="text-smallcaps">D</span>-Glucosyloxy-2-hydroxymethylbenzene
- 1-β-D-Glucosyloxy-2-hydroxymethylbenzene
- 2-(Hydroxymethyl)Phenyl Hexopyranoside
- 2-(Hydroxymethyl)phenyl β-<span class="text-smallcaps">D</span>-glucopyranoside
- 2-(Hydroxymethyl)phenyl-β-D-glucopyranoside
- 2-(hydroxymethyl)phenyl beta-D-altropyranoside
- 2-(hydroxymethyl)phenyl beta-D-glucopyranoside
- 2-(hydroxymethyl)phenyl beta-L-glucopyranoside
- <span class="text-smallcaps">D</span>-Salicin
- D-Salicin (1.05055)
- Nsc 5751
- See more synonyms
Sort by
Salicin CRS
CAS:Salicin CRSFormula:C13H18O7Color and Shape:Crystalline Powder. White. Powder.Molecular weight:286.2778D-Salicin, natural
CAS:D-Salicin is a naturally occurring anti-inflammatory compound, which is derived from the bark of willow trees, primarily of the genus Salix. As a prodrug, D-Salicin is metabolized into salicylic acid in the body, where it acts by inhibiting the cyclooxygenase (COX) enzymes. This inhibition leads to a reduction in the synthesis of pro-inflammatory prostaglandins and thromboxanes, thereby exerting its anti-inflammatory and analgesic effects. Traditionally, extracts containing D-Salicin have been used for their pain-relieving and anti-inflammatory properties. In contemporary scientific contexts, it is utilized in research focusing on inflammation, pain management, and cardiovascular studies due to its effects on platelet aggregation. Furthermore, the presence of D-Salicin in natural supplements is of interest for the development of alternative therapeutics aimed at minimizing gastrointestinal side effects typically associated with synthetic non-steroidal anti-inflammatory drugs (NSAIDs). Its applications extend to pharmacological research, where it aids in the exploration of natural product-based drug discovery and development.Formula:C13H18O7Purity:Min. 90.0 Area-%Molecular weight:286.28 g/molRef: 3D-S-1498
1kgTo inquire5kgTo inquire250gTo inquire500gTo inquire2500gTo inquire-Unit-kgkgTo inquireSalicin
CAS:Salicin (Salicine), a phenol β-glycoside produced from willow bark, shows anti-inflammatory functions.Formula:C13H18O7Purity:98.2% - 99.86%Color and Shape:White Crystals Or PowderMolecular weight:286.28(2R,3S,4S,5R,6S)-2-(Hydroxymethyl)-6-(2-(hydroxymethyl)phenoxy)tetrahydro-2H-pyran-3,4,5-triol
CAS:Purity:95.0%Color and Shape:Solid, White to grey powderMolecular weight:286.2799987792969D-Salicin
CAS:Formula:C13H18O7Purity:≥ 98.0%Color and Shape:White to off-white powder or crystalsMolecular weight:286.28β-D-Glucopyranoside, 2-(hydroxymethyl)phenyl
CAS:Formula:C13H18O7Purity:98%Color and Shape:SolidMolecular weight:286.27781999999996D-Salicin
CAS:D-Salicin is a naturally occurring compound, classified as a biologically active glycoside. It is acquired from the bark of willow trees, primarily species within the genus Salix. The primary mode of action of D-Salicin involves its metabolic conversion into salicylic acid within the human body. This conversion occurs in the gastrointestinal tract and bloodstream, ultimately displaying effects similar to non-steroidal anti-inflammatory drugs (NSAIDs). The anti-inflammatory and analgesic properties of D-Salicin make it valuable for scientific research exploring natural alternatives to synthetic pain relievers. It is often studied for its capacity to inhibit cyclooxygenase enzymes, thereby reducing the biosynthesis of pro-inflammatory prostaglandins. Its applications extend into the fields of phytotherapy and pharmaceutical development, where it serves as a model compound for the study of natural anti-inflammatories. Furthermore, ongoing research investigates its potential antioxidant properties and effects on cardiovascular health, elucidating its multiple pharmacological benefits.Formula:C13H18O7Purity:Min. 98 Area-%Color and Shape:White Off-White PowderMolecular weight:286.28 g/molSalicin
CAS:Natural glycosideFormula:C13H18O7Purity:≥ 98.0 % (HPLC)Color and Shape:PowderMolecular weight:286.28D-(-)-Salicin
CAS:D-(-)-Salicin analytical standard provided with w/w absolute assay, to be used for quantitative titration.Formula:C13H18O7Purity:(HPLC) ≥99%Color and Shape:PowderMolecular weight:286.28D(-)-Salicin, 99+%
CAS:This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product portfolio. Some documentation and label information may refer to the legacy brand. The original Acros Organics product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.Formula:C13H18O7Purity:99+%Color and Shape:Crystalline powder, WhiteMolecular weight:286.28D-(-)-Salicin extrapure
CAS:Formula:C13H18O7Color and Shape:White, Crystalline powder, Clear, ColourlessMolecular weight:286.28D-(-)-Salicin, 99%
CAS:Salicin is used as an analgesic and antipyretic. It is also used as a substrate for beta-glucosidase and an inhibitor of Cox. It finds application as an anti-inflammatory agent. It is involved in antipyretic action without causing gastric injury. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.Formula:C13H18O7Purity:99%Color and Shape:Crystals or powder or crystalline powder, White to pale creamMolecular weight:286.28D-Salicin
CAS:Other glycosides, natural or reproduced by synthesis, and their salts, ethers, esters and other derivativesFormula:C13H18O7Color and Shape:White Off-White PowderMolecular weight:286.10525Salicin
CAS:Formula:C13H18O7Purity:>98.0%(HPLC)Color and Shape:White to Almost white powder to crystalMolecular weight:286.28D-Salicin
CAS:Applications Salicin is an anti-inflammatory agent produced by the bark of a willow tree. Analgesic. References Schmid, B. et al.: Eur J Pharmacol., 57, 387 (2001);Formula:C13H18O7Color and Shape:WhiteMolecular weight:286.28