Ononetin Knowpia

Ononetin
Identifiers
	IUPAC name 1-(2,4-dihydroxyphenyl)-2-(4-methoxyphenyl)ethanone;
CAS Number	487-49-0;
PubChem CID	259632;
ChemSpider	227880;
UNII	4S084Z7YS4;
ChEMBL	ChEMBL241858;
CompTox Dashboard (EPA)	DTXSID50197590 ;
Chemical and physical data
Formula	C15H14O4
Molar mass	258.273 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES COC1=CC=C(C=C1)CC(=O)C2=C(C=C(C=C2)O)O;
	InChI InChI=1S/C15H14O4/c1-19-12-5-2-10(3-6-12)8-14(17)13-7-4-11(16)9-15(13)18/h2-7,9,16,18H,8H2,1H3; Key:XHBZOAYMBBUURD-UHFFFAOYSA-N;

Ononetin is a natural product from the deoxybenzoin group, which is found in the Russian traditional medicine plant Ononis spinosa. It acts as an inhibitor of the transient receptor potential ion channel TRPM3 and has analgesic effects in animal studies,^[1]^[2] as well as being used for research into the role of TRPM3 in the immune system dysfunction associated with chronic fatigue syndrome.^[3]^[4]

References edit

^ Straub I, Mohr F, Stab J, Konrad M, Philipp SE, Oberwinkler J, Schaefer M (April 2013). "Citrus fruit and fabacea secondary metabolites potently and selectively block TRPM3". British Journal of Pharmacology. 168 (8): 1835–50. doi:10.1111/bph.12076. PMC 3623054. PMID 23190005.
^ Straub I, Krügel U, Mohr F, Teichert J, Rizun O, Konrad M, et al. (November 2013). "Flavanones that selectively inhibit TRPM3 attenuate thermal nociception in vivo". Molecular Pharmacology. 84 (5): 736–50. doi:10.1124/mol.113.086843. PMID 24006495. S2CID 20522738.
^ Cabanas H, Muraki K, Balinas C, Eaton-Fitch N, Staines D, Marshall-Gradisnik S (April 2019). "Validation of impaired Transient Receptor Potential Melastatin 3 ion channel activity in natural killer cells from Chronic Fatigue Syndrome/ Myalgic Encephalomyelitis patients". Molecular Medicine. 25 (1): 14. doi:10.1186/s10020-019-0083-4. PMC 6480905. PMID 31014226.
^ Cabanas H, Muraki K, Staines D, Marshall-Gradisnik S (2019). "Naltrexone Restores Impaired Transient Receptor Potential Melastatin 3 Ion Channel Function in Natural Killer Cells From Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Patients". Frontiers in Immunology. 10: 2545. doi:10.3389/fimmu.2019.02545. PMC 6834647. PMID 31736966.

[1] Straub I, Mohr F, Stab J, Konrad M, Philipp SE, Oberwinkler J, Schaefer M (April 2013). "Citrus fruit and fabacea secondary metabolites potently and selectively block TRPM3". British Journal of Pharmacology. 168 (8): 1835–50. doi:10.1111/bph.12076. PMC 3623054. PMID 23190005.

[2] Straub I, Krügel U, Mohr F, Teichert J, Rizun O, Konrad M, et al. (November 2013). "Flavanones that selectively inhibit TRPM3 attenuate thermal nociception in vivo". Molecular Pharmacology. 84 (5): 736–50. doi:10.1124/mol.113.086843. PMID 24006495. S2CID 20522738.

[3] Cabanas H, Muraki K, Balinas C, Eaton-Fitch N, Staines D, Marshall-Gradisnik S (April 2019). "Validation of impaired Transient Receptor Potential Melastatin 3 ion channel activity in natural killer cells from Chronic Fatigue Syndrome/ Myalgic Encephalomyelitis patients". Molecular Medicine. 25 (1): 14. doi:10.1186/s10020-019-0083-4. PMC 6480905. PMID 31014226.

[4] Cabanas H, Muraki K, Staines D, Marshall-Gradisnik S (2019). "Naltrexone Restores Impaired Transient Receptor Potential Melastatin 3 Ion Channel Function in Natural Killer Cells From Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Patients". Frontiers in Immunology. 10: 2545. doi:10.3389/fimmu.2019.02545. PMC 6834647. PMID 31736966.

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Identifiers

IUPAC name 1-(2,4-dihydroxyphenyl)-2-(4-methoxyphenyl)ethanone
CAS Number	487-49-0
PubChem CID	259632
ChemSpider	227880
UNII	4S084Z7YS4
ChEMBL	ChEMBL241858
CompTox Dashboard (EPA)	DTXSID50197590
Chemical and physical data
Formula	C₁₅H₁₄O₄
Molar mass	258.273 g·mol⁻¹
3D model (JSmol)	Interactive image
SMILES COC1=CC=C(C=C1)CC(=O)C2=C(C=C(C=C2)O)O
InChI InChI=1S/C15H14O4/c1-19-12-5-2-10(3-6-12)8-14(17)13-7-4-11(16)9-15(13)18/h2-7,9,16,18H,8H2,1H3 Key:XHBZOAYMBBUURD-UHFFFAOYSA-N

Summary

References edit