Structure via PubChem · Public domain (PubChem)
orcinolo
Sign in to saveAlso known as 3-Hydroxy-5-methylphenol, Orcin, 5-Methyl-1,3-dihydroxybenzene, 1,3-Dihydroxy-5-methylbenzene
farmaco
Chemical data
- Formula
- C7H8O2
- Molecular weight
- 124.14 g/mol
- IUPAC name
- 5-methylbenzene-1,3-diol
- SMILES
- CC1=CC(=CC(=C1)O)O
- InChIKey
- OIPPWFOQEKKFEE-UHFFFAOYSA-N
- XLogP
- 1.6
- Polar surface area
- 40.5 Ų
- H-bond donors
- 2
- H-bond acceptors
- 2
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Molecule type
- Small molecule
via ChEMBL · EBI
Research
415 papers- Orcinol glucoside targeted p38 as an agonist to promote osteogenesis and protect glucocorticoid-induced osteoporosis.Phytomedicine : international journal of phytotherapy and phytopharmacology · 2023
- Production of the antidepressant orcinol glucoside in Yarrowia lipolytica with yields over 6,400-fold higher than plant extraction.PLoS biology · 2023
- Orcinol and resorcinol induce local ordering of water molecules near the liquid-vapor interface.Environmental science: atmospheres · 2022
- Orcinol gentiobioside inhibits RANKL-induced osteoclastogenesis by promoting apoptosis and suppressing autophagy via the JNK1 signaling.Journal of ethnopharmacology · 2024
- Orcinol Glucoside Facilitates the Shift of MSC Fate to Osteoblast and Prevents Adipogenesis via Wnt/β-Catenin Signaling Pathway [Retraction].Drug design, development and therapy · 2023
via PubMed
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 124.052429
Show 6 more facts
- described by source
- Brockhaus and Efron Encyclopedic Dictionary
- chemical formula
- C₇H₈O₂
- canonical SMILES
- CC1=CC(=CC(=C1)O)O
- melting point
- 107
- Commons category
- Orcinol
- boiling point
- 288.5
via Wikidata · CC0
Article · Italiano
L'orcinolo è un composto organico fenolico presente in molte specie di licheni, tra cui e . È stato ottenuto nel 1829 dal chimico francese Jean Pierre Robiquet, da un lichene del genere Roccella, trattando un estratto dello stesso con alcali.
Abstract from DBpedia / Wikipedia · CC BY-SA