9-Phenanthrol

9-Phenanthrol
Names
	IUPAC name 9-Phenanthrol
	Systematic IUPAC name 9-Hydroxyphenanthrene
	Other names 9-Phenanthrol; 9-Phenanthrenol; Phenanthren-9-ol; 9-Hydroxyphenanthrene;
Identifiers
CAS Number	484-17-3 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:28820;
ChEMBL	ChEMBL2407182;
ChemSpider	9812;
ECHA InfoCard	100.006.912
EC Number	207-602-4;
KEGG	C11430;
PubChem CID	10229;
UNII	9FYU45OV9H ;
CompTox Dashboard (EPA)	DTXSID9047592 ;
	InChI InChI=1S/C14H10O/c15-14-9-10-5-1-2-6-11(10)12-7-3-4-8-13(12)14/h1-9,15H Key: DZKIUEHLEXLYKM-UHFFFAOYSA-N;
	SMILES C1=CC=C2C(=C1)C=C(C3=CC=CC=C23)O;
Properties
Chemical formula	C14H10O
Molar mass	194.233 g·mol−1
Hazards
	GHS labelling:
Pictograms
Signal word	Warning
Hazard statements	H315, H319, H335
Precautionary statements	P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

9-Phenanthrol is an aromatic alcohol derived from phenanthrene, a tricyclic compound. It is a TRPM4 channel inhibitor.^[1] It can prevent the pancreas from secreting insulin when stimulated by glucose.^[2]

References

^ Guinamard, R; Hof, T; Del Negro, C A (2014). "The TRPM4 channel inhibitor 9-phenanthrol". British Journal of Pharmacology. 171 (7): 1600–1613. doi:10.1111/bph.12582. PMC 3966741. PMID 24433510.
^ Ma, Zuheng; Björklund, Anneli; Islam, Md. Shahidul (2017). "A TRPM4 Inhibitor 9-Phenanthrol Inhibits Glucose- and Glucagon-Like Peptide 1-Induced Insulin Secretion from Rat Islets of Langerhans". Journal of Diabetes Research. 2017: 1–5. doi:10.1155/2017/5131785. PMC 5643033. PMID 29098165.

[1] Guinamard, R; Hof, T; Del Negro, C A (2014). "The TRPM4 channel inhibitor 9-phenanthrol". British Journal of Pharmacology. 171 (7): 1600–1613. doi:10.1111/bph.12582. PMC 3966741. PMID 24433510.

[2] Ma, Zuheng; Björklund, Anneli; Islam, Md. Shahidul (2017). "A TRPM4 Inhibitor 9-Phenanthrol Inhibits Glucose- and Glucagon-Like Peptide 1-Induced Insulin Secretion from Rat Islets of Langerhans". Journal of Diabetes Research. 2017: 1–5. doi:10.1155/2017/5131785. PMC 5643033. PMID 29098165.

[1]

[2]