Salicin - Moligand™, 10mM in DMSO , Agonist of TAS2R16, CAS No.138-52-3, Agonist of TAS2R16

CAS: 138-52-3 Cat. No.: S408989 Formula: C13H18O7 Peso molecolare: 286.28 Beilstein Registry Number: 89593 Numero EC: 205-331-6 PubChem CID: 439503
Disponibile su ordine
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. 10mM in DMSO
Synonyms
Salicoside,Salicine | β-D-Glucopyranoside, 2-(hydroxymethyl)phenyl
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
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Size
Germania (EU)
USA*
Price
Qty
1ml
S408989-1ml
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1 Disponibile
25,08€
Enter a quantity for the sizes you want to add.
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Why this grade

Moligand™, 10mM in DMSO Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 5 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Panoramica

Information

Salicin (Salicoside, Salicine) is a phenol β-glycosid produced from willow bark that shows anti-inflammatory effects. It is a natural, non-selectiveCOX-1andCOX-2inhibitor.
In vitro

Salicin (Salicoside, Salicine) is a phenol β-glycosid produced from willow bark that shows anti-inflammatory effects. Salicin is a prodrug which is gradually transported to the lower part of the intestine, hydrolyzed to saligenin by intestinal bacteria, and converted to salicylic acid after absorption. It thus produces an antipyretic action without causing gastric injury.

In vivo


Cell Data

cell lines:

Concentrations:

Incubation Time:

Powder Purity:≥98%

Specifications

Sinonimi
Salicoside,Salicine | β-D-Glucopyranoside, 2-(hydroxymethyl)phenyl
Specifiche e purezza
Moligand™, 10mM in DMSO
Meccanismi biochimici e fisiologici
Salicin (Salicoside, Salicine) is a phenol β-glycosid produced from willow bark that shows anti-inflammatory effects. It is a natural, non-selective COX-1 and COX-2 inhibitor.
Condizioni di conservazione di stoccaggio
Store at -80°C
Spedito in
Dry ice packs + Cold packs
Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.
Grado
Moligand™
Tipo di azione
AGONIST
Meccanismo d'azione
Agonist of TAS2R16
Nomi e identificatori
Isomeri SMILES C1=CC=C(C(=C1)CO)O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O
WGK Germania 3
RTECS LZ5901700
CAS alternativo 138-52-3
PubChem CID 439503
Numero NSC 758201
Termini MeSH salicin;salicyl alcohol glucoside
Peso molecolare 286.28
Beilstein 89593
Reaxy-Rn 89593

Documentazione

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Obiettivi associati (umani)
TAS2R16 Tchem Taste receptor type 2 member 16 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
Certificati (CoA, COO, BSE/TSE e tabella di analisi)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Proprietà chimiche e fisiche
SolubilitàSolubility (25°C) In vitro DMSO: 41 mg/mL (197.79 mM); Ethanol: 41 mg/mL (197.79 mM); Water: Insoluble;
Rotazione specifica [α]-62 ° (C=3, H2O)
Punto di fusione (°C)199-202°C
Citations of This Product
Riferimenti
1. Lei Chen, Ning Li, Min-Hua Zong.  (2011)  A glucose-tolerant β-glucosidase from Prunus domestica seeds: Purification and characterization.  PROCESS BIOCHEMISTRY,      [PMID:] [10.1016/j.procbio.2011.10.023]
2. Zhenyue Wang, Faidah Arina Nur, Jingyi Ma, Jianguo Wang, Chuanwang Cao.  (2019)  Effects of poplar secondary metabolites on performance and detoxification enzyme activity of Lymantria dispar.  COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY C-TOXICOLOGY & PHARMACOLOGY,      [PMID:31401083] [10.1016/j.cbpc.2019.108587]
3. Xinqi Gao, Yafang Lei, Teng Sun, Yuanze Ma, Hao Guan, Li Yan.  (2025)  Evaluation of Anti-Fungal Activities of Environmentally Friendly Wood Preservative from Thermal-Induced Lignified Twigs.  Forests,  16  (1): (119).  [PMID:] [10.3390/f16010119]
4. Shangguang Du, Hao Wan, Jun Luo, Xiaohua Duan, Zhengrong Zou.  (2024)  Metabolic profiling of Citrus maxima L. seedlings in response to cadmium stress using UPLC-QTOF-MS.  PLANT PHYSIOLOGY AND BIOCHEMISTRY,      [PMID:38996714] [10.1016/j.plaphy.2024.108920]
5. Mingzhen Zhang, Cong Liu, Yan Zhang, Zhangyaoyu Yuan, Shi Chen, Huihui Zhang, Xianju Huang, Lvyi Chen, Zhinan Mei, Yuebin Ge.  (2025)  Bioactive Components, Untargeted Metabolomics and Bioinformatics of Chaenomeles speciosa Fruit on Uric Acid-Lowering Activity Assessment.  Foods,  15  (1): (20).  [PMID:41517086] [10.3390/foods15010020]
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