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208255-51-0

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208255-51-0 Usage

Description

DAPM, or Diallyl Propyl Disulfide, is a naturally occurring organosulfur compound found in garlic and other Allium species. It is known for its potent bioactive properties and has been extensively studied for its potential health benefits and therapeutic applications.

Uses

Used in Pharmaceutical Industry:
DAPM is used as a bioactive compound for its potential therapeutic effects on various health conditions. Its properties include anti-inflammatory, antioxidant, and antimicrobial activities, making it a promising candidate for the development of new drugs and treatments.
Used in Cancer Research:
DAPM has shown potential as an anticancer agent, with studies suggesting that it may inhibit the growth and proliferation of cancer cells. It is currently being investigated for its possible use in the treatment of various types of cancer.
Used in Nutraceutical Industry:
Due to its antioxidant and anti-inflammatory properties, DAPM is also used in the development of nutraceutical products, such as dietary supplements and functional foods, aimed at promoting overall health and well-being.
Used in Cosmetic Industry:
The antimicrobial properties of DAPM make it a potential ingredient in the cosmetic industry for the development of products with antibacterial and antifungal properties, such as skincare and hair care products.
Used in Food Industry:
DAPM's natural origin and bioactive properties make it a valuable ingredient in the food industry, where it can be used to enhance the flavor, aroma, and shelf life of various food products, as well as provide potential health benefits.
Used in Gamma-Secretase Inhibitor XVI:
DAPM is used as a γ-secretase inhibitor for selectively blocking Aβ dimer and trimer formation. This application is particularly relevant in the context of Alzheimer's disease, where the inhibition of Aβ formation is a potential therapeutic strategy.

Check Digit Verification of cas no

The CAS Registry Mumber 208255-51-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,8,2,5 and 5 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 208255-51:
(8*2)+(7*0)+(6*8)+(5*2)+(4*5)+(3*5)+(2*5)+(1*1)=120
120 % 10 = 0
So 208255-51-0 is a valid CAS Registry Number.

208255-51-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl (2S)-2-[[(2S)-2-[[2-(3,5-difluorophenyl)acetyl]amino]propanoyl]amino]-2-phenylacetate

1.2 Other means of identification

Product number -
Other names N-(3,5-difluorophenylacetyl)-L-alanyl-(S)-phenylglycine-methylester

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:208255-51-0 SDS

208255-51-0Downstream Products

208255-51-0Relevant articles and documents

Parallel synthesis of DAPT derivatives and their γ-secretase- inhibitory activity

Kan, Toshiyuki,Tominari, Yusuke,Rikimaru, Kentaro,Morohashi, Yuichi,Natsugari, Hideaki,Tomita, Taisuke,Iwatsubo, Takeshi,Fukuyama, Tohru

, p. 1983 - 1985 (2007/10/03)

Parallel synthesis of the C-terminal-modified DAPT (1) derivatives was accomplished utilizing our novel resin 7. Condensation reaction of the N-acylamino acid 10 with the amines 11a-o proceeded smoothly to give the corresponding amides 6a-o without any epimerization. Among the analogues, the benzophenonemethyl amide derivative 6o showed 30 times more potent activity than the original DAPT (1).

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