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1-(3,3-dimethyl-2-oxobutyl)-1H-indole-2,3-dione, also known as DIMBOA, is a chemical compound belonging to the class of indole alkaloids. It is predominantly found in maize and related plants, where it acts as a natural defense mechanism against herbivores and pathogens. DIMBOA is synthesized through the shikimate pathway and is recognized for its antipathogenic and allelopathic properties.

214417-82-0

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214417-82-0 Usage

Uses

Used in Agriculture:
1-(3,3-dimethyl-2-oxobutyl)-1H-indole-2,3-dione is used as a natural defense compound for protecting plants against herbivores and pathogens. Its application reason is due to its antipathogenic and allelopathic properties, which help inhibit the growth of certain insects, fungi, and bacteria.
Used in Pharmaceutical Applications:
1-(3,3-dimethyl-2-oxobutyl)-1H-indole-2,3-dione is used as a potential therapeutic agent for its anticancer and anti-inflammatory effects. The application reason is based on its pharmacological properties, which are currently under investigation for their potential to contribute to human health and well-being.

Check Digit Verification of cas no

The CAS Registry Mumber 214417-82-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,4,4,1 and 7 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 214417-82:
(8*2)+(7*1)+(6*4)+(5*4)+(4*1)+(3*7)+(2*8)+(1*2)=110
110 % 10 = 0
So 214417-82-0 is a valid CAS Registry Number.

214417-82-0Downstream Products

214417-82-0Relevant articles and documents

Parallel synthesis of isatin-based serine protease inhibitors

Shuttleworth, Stephen J.,Nasturica, Daniel,Gervais, Christian,Siddiqui, M. Arshad,Rando, Robert F.,Lee, Nola

, p. 2501 - 2504 (2007/10/03)

The synthesis of N-functionalised isatins using parallel, solution synthesis is described. Functionalised polymers were employed as stoichiometric and catalytic reagents as well as purification media in the exercise, and the derivatives were screened against a panel of serine proteases; high percentage inhibition was observed in several cases. (C) 2000 Elsevier Science Ltd.

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