Salidroside - analytical standard, Moligand™, ≥98%(HPLC) , CAS No.10338-51-9

CAS: 10338-51-9 Cat. No.: S101157 Formula: C₁₄H₂₀O₇ Molecular Weight: 300.31 EC Number: 695-621-2 PubChem CID: 159278

GRADE & PURITY Analytical standard, Moligand™, ≥98%(HPLC)

Synonyms

2-(4-Hydroxyphenyl)ethyl beta-D-glucopyranoside | SALIDROSIDE (USP-RS) | NCGC00256072-01 | Tox21_113565 | NCGC00257931-01 | A800725 | NSC 741643 | s2396 | (2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[2-(4-hydroxyphenyl)ethoxy]tetrahydropyran-3,4,5-triol | AKOS00

Storage

Protected from light,Room temperature

Shipped In

Normal

Overview

Salidroside (Rhodioloside) is a prolyl endopeptidase inhibitor. Salidroside alleviates cachexia symptoms in mouse models of cancer cachexia via activating mTOR signalling. Salidroside protects dopaminergic neurons by enhancing PINK1/Parkin-mediated mitophagy.

Specifications

Synonyms

2-(4-Hydroxyphenyl)ethyl beta-D-glucopyranoside | SALIDROSIDE (USP-RS) | NCGC00256072-01 | Tox21_113565 | NCGC00257931-01 | A800725 | NSC 741643 | s2396 | (2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[2-(4-hydroxyphenyl)ethoxy]tetrahydropyran-3,4,5-triol | AKOS00

Specifications & Purity

analytical standard, Moligand™, ≥98%(HPLC)

Biochemical and Physiological Mechanisms

Salidroside, the 8-O-β-D-glucoside of tyrosol, is the main bioactive component of Rhodiola species and is found mainly in the plant roots. It is biosynthesised in the tyrosine metabolism, with glucosylation of tyrosol being the final step. It has been rep

Storage

Protected from light,Room temperature

Shipped In

Normal

Grade

Analytical standard, Moligand™

Purity

≥98%(HPLC)

Names and Identifiers

Pubchem Sid

504757437

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504757437

Canonical Smiles

C1=CC(=CC=C1CCOC2C(C(C(C(O2)CO)O)O)O)O

IUPAC Name

(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[2-(4-hydroxyphenyl)ethoxy]oxane-3,4,5-triol

InChIKey

ILRCGYURZSFMEG-RKQHYHRCSA-N

INCHI

1S/C14H20O7/c15-7-10-11(17)12(18)13(19)14(21-10)20-6-5-8-1-3-9(16)4-2-8/h1-4,10-19H,5-7H2/t10-,11-,12+,13-,14-/m1/s1

Isomeric SMILES

C1=CC(=CC=C1CCO[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O)O

PubChem CID

159278

Molecular Weight

300.31

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Class Organooxygen compounds
      • Subclass Carbohydrates and carbohydrate conjugates
        • Level5 Glycosyl compounds
          • Level6 O-glycosyl compounds

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Class: Organooxygen compounds
• Subclass: Carbohydrates and carbohydrate conjugates
• Intermediate Tree Nodes: Glycosyl compounds
• Direct Parent: O-glycosyl compounds
• Alternative Parents: Tyrosols and derivatives 1-hydroxy-2-unsubstituted benzenoids Oxanes Monosaccharides Benzene and substituted derivatives Secondary alcohols Polyols Oxacyclic compounds Acetals Primary alcohols Hydrocarbon derivatives
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: O-glycosyl compound - Tyrosol derivative - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Monocyclic benzene moiety - Monosaccharide - Oxane - Benzenoid - Secondary alcohol - Polyol - Oxacycle - Organoheterocyclic compound - Acetal - Hydrocarbon derivative - Alcohol - Primary alcohol - Aromatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond.
• External Descriptors: glycoside

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Associated Targets(Human)

MAOB Tclin Amine oxidase [flavin-containing] B (2 Activities)

Discover Target: MAOB

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

MAOA Tclin Monoamine oxidase A (11911 Activities)

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PTGS1 Tclin Cyclooxygenase-1 (9233 Activities)

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MAOB Tclin Monoamine oxidase B (8835 Activities)

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HUVEC (11049 Activities)

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HeLa (62764 Activities)

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MDA-MB-231 (73002 Activities)

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L02 (4864 Activities)

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Associated Targets(non-human)

Hdac6 Histone deacetylase 6 (222 Activities)

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Mus musculus (284745 Activities)

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Rattus norvegicus (775804 Activities)

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PC-12 (7051 Activities)

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L929 (3802 Activities)

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C2C12 (756 Activities)

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rep Replicase polyprotein 1ab (378 Activities)

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rnhA Ribonuclease HI (16 Activities)

Discover Target: rnhA

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SARS-CoV-2 (38078 Activities)

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Mechanisms of Action

Chemical and Physical Properties

• Sensitivity: Light sensitive
• Molecular Weight: 300.300 g/mol
• XLogP3: -0.600
• Hydrogen Bond Donor Count: 5
• Hydrogen Bond Acceptor Count: 7
• Rotatable Bond Count: 5
• Exact Mass: 300.121 Da
• Monoisotopic Mass: 300.121 Da
• Topological Polar Surface Area: 120.000 Ų
• Heavy Atom Count: 21
• Formal Charge: 0
• Complexity: 306.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 5
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1