Synthesis and biological evaluation of 3-(4-aminophenyl)-coumarin derivatives as potential anti-Alzheimer's disease agents.
Hu YH, Yang J, Zhang Y, Liu KC, Liu T, Sun J, Wang XJ.
J Enzyme Inhib Med Chem. 2019 Dec;34(1):1083-1092. doi: 10.1080/14756366.2019.1615484.

Discovery of fluorescent coumarin-benzo[b]thiophene 1, 1-dioxide conjugates as mitochondria-targeting antitumor STAT3 inhibitors.
Cai G, Yu W, Song D, Zhang W, Guo J, Zhu J, Ren Y, Kong L.
Eur J Med Chem. 2019 Jul 15;174:236-251. doi: 10.1016/j.ejmech.2019.04.024. Epub 2019 Apr 16.

Design, Synthesis, and Mechanism of Dihydroartemisinin⁻Coumarin Hybrids as Potential Anti-Neuroinflammatory Agents.
Yu H, Hou Z, Yang X, Mou Y, Guo C.
Molecules. 2019 Apr 28;24(9). pii: E1672. doi: 10.3390/molecules24091672.

Discovery of coumarin Mannich base derivatives as multifunctional agents against monoamine oxidase B and neuroinflammation for the treatment of Parkinson's disease.
Tao D, Wang Y, Bao XQ, Yang BB, Gao F, Wang L, Zhang D, Li L.
Eur J Med Chem. 2019 Jul 1;173:203-212. doi: 10.1016/j.ejmech.2019.04.016. Epub 2019 Apr 12.

Triphenylethylene-Coumarin Hybrid TCH-5c Suppresses Tumorigenic Progression in Breast Cancer Mainly Through Its Inhibition of Angiogenesis.
Cui N, Lin DD, Shen Y, Shi JG, Wang B, Zhao MZ, Zheng L, Chen H, Shi JH.
Anticancer Agents Med Chem. 2019 Apr 4. doi: 10.2174/1871520619666190404155230

Anatolicin, a Highly Potent and Selective Cytotoxic Sesquiterpene Coumarin from the Root Extract of Heptaptera anatolica.
Tosun F, Beutler JA, Ransom TT, Miski M.
Molecules. 2019 Mar 23;24(6). pii: E1153. doi: 10.3390/molecules24061153.

Low-molecular-weight-heparin versus a coumarin for the prevention of recurrent venous thromboembolism in high- and low-risk patients with active cancer: a post hoc analysis of the CLOT Study.
Woodruff S, Lee AYY, Carrier M, Feugère G, Abreu P, Heissler J.
J Thromb Thrombolysis. 2019 May;47(4):495-504. doi: 10.1007/s11239-019-01833-w.

Coumarin Hybrids: Promising Scaffolds in the Treatment of Breast Cancer.
Bhatia R, Rawal RK.
Mini Rev Med Chem. 2019 Mar 8. doi: 10.2174/1389557519666190308122509.

Synthesis and Biological Evaluation of Novel Thiazolyl-Coumarin Derivatives as Potent Histone Deacetylase Inhibitors with Antifibrotic Activity.
Pardo-Jiménez V, Navarrete-Encina P, Díaz-Araya G.
Molecules. 2019 Feb 19;24(4). pii: E739. doi: 10.3390/molecules24040739.

Effectiveness and safety of a mixture of diosmin, coumarin and arbutin (Linfadren®) in addition to conventional treatment in the management of patients with post-trauma/surgery persistent hand edema: a randomized controlled trial.
Cacchio A, Di Carlo G, Vincenza C, Elisabetta B.
Clin Rehabil. 2019 May;33(5):904-912. doi: 10.1177/0269215519829797. Epub 2019 Feb 13.

Excellent antitumor and antimetastatic activities based on novel coumarin/pyrazole oxime hybrids.
Dai H, Huang M, Qian J, Liu J, Meng C, Li Y, Ming G, Zhang T, Wang S, Shi Y, Yao Y, Ge S, Zhang Y, Ling Y.
Eur J Med Chem. 2019 Mar 15;166:470-479. doi: 10.1016/j.ejmech.2019.01.070. Epub 2019 Jan 30

2H-chromen-2-one (Coumarin) is a chemical compound (benzopyran-2-one or chromen-2-one), an aromatic phenylpropanoid belonging to the chemical class of benzopyranes.

It occurs as a fine, white, odourless or crystalline powder.

Where is it ?

It was discovered in Odorata Dipteryx,  a tropical fruit-bearing tree, but is present in many plants, e.g. clover. Coumarins, organic heterocycles, are a large family of secondary metabolites found in the plant kingdom. They have a low molecular weight, good bioavailability, high solubility and a simple structure.

What is it for?

Coumarin displays diverse pharmacological properties. It has attracted the attention of chemists and medicinal chemists for decades. Many molecules based on the coumarin ring system have been described utilizing innovative synthetic methods. These synthetic routes have led to interesting analogues of coumarins which possess pharmacological activities like anti-HIV, antimicrobial, antiinflammatory, anticancer, anti-TB, anticonvulsant and inhibitory properties of monoamine oxidases. Details of these studies, correlating structure with biological activity are described in this review (1).

Litsea angulata is a plant species belonging to Lauraceae family that is distributed throughout Indonesia, Malaysia, and New Guinea. The seeds have been traditionally used by local people in Kalimantan, Indonesia for the treatment of boils; however, there is no information about the potency of its branch, bark and leaves yet. This study aimed to determine the antioxidant, antimicrobial activity as well as the phytochemical constituent of Litsea angulata branch, bark, and leaves. L. angulata contains secondary metabolites such as alkaloids, flavonoids, tannins, terpenoids, carotenoids, and coumarin. The antioxidant activity on different plant extracts was a range as very strong to weak capacity. All extracts in this study could inhibit the growth of S. aureus and S. mutans (2).

Used in the electroplating industry and in zinc, cadmium and nickel plating, it can reduce the porosity of the coating and increase the brightness of the coating.

Cosmetics

In the cosmetics and food industry is an antimicrobial flavouring and serves to impart taste or fragrance.

It can be chemically produced, but it can also be found in its natural state. No manufacturer specifies it on the label.

Safety in food and cosmetics

In 2004, the European Food Safety Authority ruled out the hypothesis that coumarin produces a genotoxic mechanism, but a tolerable daily intake (TDI) of 0.1 mg/kg body weight was established, however hepatotoxicity in humans cannot be completely excluded for sensitive individuals. Coumarin is known to penetrate easily through the skin and the European Cosmetics Regulation (EU) No 1223/2009 has not set a maximum limit in cosmetics for coumarin. This study considers that, considering an average daily consumption of several cosmetic products, the Tolerable Daily Intake (TDI) can easily be reached and exceeded (3).

It is a product that could give allergy and therefore must be indicated on the label.

The most relevant studies on the subject have been selected with a summary of their contents:

Coumarin studies

Optimal typical characteristics of the commercial product Coumarin

Appearance	Powder white crystalline
Melting point	69.0℃ ~ 71.0℃
Boiling Point	298.0±0.0 °C at 760 mmHg
Flash Point	118.3±16.1 °C
Density	1.2±0.1 g/cm3
Vapour Pressure	0.0±0.6 mmHg at 25°C
Index of Refraction	1.595
PSA	30.21000
LogP	1.39
Water Solubility	1.7 g/L (20 ºC)  1gram clearly dissolved in 8mlv 90% ethanol
Loss on drying	≤2.0%
Heavy metals	≤10 ppm
Water	≤1.0%
Sulphated ash	≤0.5% determined on 1.0 g.
Residue on ignition	≤0.1%
Safety

• Formula molecolare : C₉H₆O₂
• Peso molecolare : 146.145 g/mol
• CAS : 91-64-5
• UNII A4VZ22K1WT
• EC Number: 202-086-7
• DSSTox Substance ID: DTXSID7020348
• MDL number  
• PubChem Substance ID 
• InChI=1S/C9H6O2/c10-9-6-5-7-3-1-2-4-8(7)11-9/h1-6H
• InChl Key      ZYGHJZDHTFUPRJ-UHFFFAOYSA-N
• SMILES    C1=CC=C2C(=C1)C=CC(=O)O2
• IUPAC   chromen-2-one
• ChEBI   28794
• ICSC 1105
• NSC  755852    8774
• RTECS   GN4200000
• UN   2811
• NCI C397

• Coumarin
• 2H-Chromen-2-one
• 1-Benzopyran-2-one
• 1,2-Benzopyrone
• EINECS 202-086-7
• 2-Propenoic acid, 3-(2-hydroxyphenyl)-delta-lactone
• EC Number: 202-086-7
• MDL number: MFCD00006850
• PubChem Substance ID 329764209
• o-Coumaric acid lactone
• o-Hydroxyzimtsaure-lacton
• Coumarinic anhydride
• 2H-1-Benzopyran-2-one

References_____________________________________________________________________

(1) Srikrishna D, Godugu C, Dubey PK. A Review on Pharmacological Properties of Coumarins. Mini Rev Med Chem. 2018;18(2):113-141. doi: 10.2174/1389557516666160801094919. 

(2) Kuspradini H, Wulandari I, Putri AS, Tiya SY, Kusuma IW. Phytochemical, antioxidant and antimicrobial properties of Litsea angulata extracts. F1000Res. 2018 Nov 22;7:1839. doi: 10.12688/f1000research.16620.2.

(3) Stiefel C, Schubert T, Morlock GE. Bioprofiling of Cosmetics with Focus on Streamlined Coumarin Analysis. ACS Omega. 2017 Aug 31;2(8):5242-5250. doi: 10.1021/acsomega.7b00562.