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4-METHYLUMBELLIFERYL PROPIONATE is a fluorescent chemical compound that serves as a substrate for evaluating esterase or lipase activity. It is characterized by its ability to release a fluorescent moiety, 4-methylumbelliferone, upon enzymatic hydrolysis, which can be measured using fluorescence detection methods. This property makes it a valuable tool in various research and diagnostic applications.

3361-13-5

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3361-13-5 Usage

Uses

Used in Enzymatic Assays:
4-METHYLUMBELLIFERYL PROPIONATE is used as a substrate in enzymatic assays for assessing the activity and specificity of esterases and lipases. Its fluorescence upon hydrolysis allows for the quantification of enzyme activity in biological and environmental samples.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 4-METHYLUMBELLIFERYL PROPIONATE is used as a tool for evaluating the effects of compounds on enzyme activity. It aids in the identification of potential inhibitors or activators of esterases and lipases, contributing to drug discovery and development.
Used in Clinical Research:
4-METHYLUMBELLIFERYL PROPIONATE is employed in clinical research for drug screening purposes. Its ability to detect enzyme activity can help in the identification of potential therapeutic agents and the assessment of their efficacy in modulating esterase or lipase activity.
Used in Diagnostic Applications:
4-METHYLUMBELLIFERYL PROPIONATE can be utilized in diagnostic assays to detect and quantify esterase or lipase activity in clinical samples. This can be useful in the diagnosis and monitoring of various diseases and conditions associated with altered enzyme activity.

Check Digit Verification of cas no

The CAS Registry Mumber 3361-13-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,6 and 1 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3361-13:
(6*3)+(5*3)+(4*6)+(3*1)+(2*1)+(1*3)=65
65 % 10 = 5
So 3361-13-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H12O4/c1-3-12(14)16-9-4-5-10-8(2)6-13(15)17-11(10)7-9/h4-7H,3H2,1-2H3

3361-13-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-methyl-2-oxochromen-7-yl) propanoate

1.2 Other means of identification

Product number -
Other names 4-methyl-2-oxo-2H-chromen-7-yl propionate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3361-13-5 SDS

3361-13-5Relevant academic research and scientific papers

Highly Selective Hydrogenation of C═C Bonds Catalyzed by a Rhodium Hydride

Gu, Yiting,Lisnyak, Vladislav G.,Norton, Jack R.,Salahi, Farbod,Snyder, Scott A.,Zhou, Zhiyao

supporting information, p. 9657 - 9663 (2021/07/19)

Under mild conditions (room temperature, 80 psi of H2) Cp*Rh(2-(2-pyridyl)phenyl)H catalyzes the selective hydrogenation of the C═C bond in α,β-unsaturated carbonyl compounds, including natural product precursors with bulky substituents in the β position and substrates possessing an array of additional functional groups. It also catalyzes the hydrogenation of many isolated double bonds. Mechanistic studies reveal that no radical intermediates are involved, and the catalyst appears to be homogeneous, thereby affording important complementarity to existing protocols for similar hydrogenation processes.

Salivary hydrogen sulfide measured with a new highly sensitive self-immolative coumarin-based fluorescent probe

Zaorska, Ewelina,Konop, Marek,Ostaszewski, Ryszard,Koszelewski, Dominik,Ufnal, Marcin

, (2018/09/12)

Ample evidence suggests that H2S is an important biological mediator, produced by endogenous enzymes and microbiota. So far, several techniques including colorimetric methods, electrochemical analysis and sulfide precipitation have been developed for H2S detection. These methods provide sensitive detection, however, they are destructive for tissues and require tedious sequences of preparation steps for the analyzed samples. Here, we report synthesis of a new fluorescent probe for H2S detection, 4-methyl-2-oxo-2H-chromen-7-yl 5-azidopentanoate (1). The design of 1 is based on combination of two strategies for H2S detection, i.e., reduction of an azido group to an amine in the presence of H2S and intramolecular lactamization. Finally, we measured salivary H2S concentration in healthy, 18–40-year-old volunteers immediately after obtaining specimens. The newly developed self-immolative coumarin-based fluorescence probe (C15H15N3O4) showed high sensitivity to H2S detection in both sodium phosphate buffer at physiological pH and in saliva. Salivary H2S concentration in healthy volunteers was within a range of 1.641–7.124 μM.

Tris(pentafluorophenyl)borane catalyzed acylation of alcohols, phenols, amines, and thiophenols under solvent-free condition

Prajapti, Santosh Kumar,Nagarsenkar, Atulya,Babu, Bathini Nagendra

, p. 1784 - 1787 (2014/03/21)

The acylation of alcohols, phenols, amines, and thiophenols was accomplished with 0.5 mol % of tris(pentafluorophenyl)borane [B(C 6F5)3] at ambient temperature under solvent-free condition. Major advantages of this method include high yield, short reaction time, simple procedure, compatibility with sensitive protecting groups as well as other functional groups, absence of racemization of optical active compounds, and epimerization of sugars.

Synthesis of propiophenone derivatives as new class of antidiabetic agents reducing body weight in db/db mice

Kumar, Atul,Sharma, Siddharth,Gupta, Lalit Prakash,Ahmad, Pervez,Srivastava, Swayam Prakash,Rahuja, Neha,Tamrakar,Srivastava, Arvind K.

scheme or table, p. 2172 - 2179 (2012/04/23)

A series of propiophenone derivatives (6-23) have been synthesized and evaluated for their in vivo antihyperglycemic activities in sucrose loaded model (SLM), sucrose challenged streptozotocin (STZ-S) induced diabetic rat model and C57BL/KsJ db/db diabetic mice model. Compound 15 and 16 were emerged as potent antihyperglycemics and lipid lowering agents. These compounds (15, 16) further validate the potency by reducing body weight and food intake in db/db mice model. Possible mechanism of action for the propiophenone derivatives was established by the evaluation in various in vitro models. Interestingly some of the compounds were efficiently inhibiting PTP-1B.

Structure activity studies with xenobiotic substrates using carboxylesterases isolated from Arabidopsis thaliana

Cummins, Ian,Landrum, Marie,Steel, Patrick G.,Edwards, Robert

, p. 811 - 818 (2008/03/13)

Carboxylesterases (CXEs) catalyse the hydrolysis of xenobiotics and natural products radically altering their biological activities. Whereas the substrate selectivity of animal CXEs, such as porcine liver esterase (PLE) have been well studied, the respective enzymes in plants have yet to be defined and their activities determined. Using Arabidopsis thaliana (At) as a source, five representative members of the α/β hydrolase AtCXE family of proteins have been cloned, expressed and the purified recombinant proteins assayed for esterase activity with xenobiotic substrates. Two members, AtCXE5 and AtCXE18 were found to be active carboxylesterases, though AtCXE5 proved to be highly unstable as a soluble protein. AtCXE18 and the previously characterised S-formylglutathione hydrolase from Arabidopsis (AtSFGH) were assayed against a series of esters based on methylumbelliferone in which the acyl moiety was varied with respect to size and conformation. The same series was used to assay crude esterase preparation from Arabidopsis plants and the results compared with those obtained with the commonly used PLE. With straight chain esters, AtCXE18 behaved like PLE, but the Arabidopsis hydrolases proved less tolerant of branched chain acyl components than the mammalian enzyme. While none of the enzyme preparations accurately reflected all the activities determined with crude Arabidopsis protein extracts, the plant enzymes proved more useful than PLE in predicting the hydrolysis of the more sterically constrained esters.

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