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1H-Pyrrole, 2-undecyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61930-40-3

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61930-40-3 Usage

Class

pyrrole derivatives

Structure

long chain alkyl derivative of pyrrole with an undecyl group attached to the second position of the pyrrole ring

Synthesis

used in the synthesis of various organic compounds

Applications

pharmaceutical and chemical industries, building block in the production of surfactants and polymers

Versatility

wide range of potential uses in different fields

Check Digit Verification of cas no

The CAS Registry Mumber 61930-40-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,9,3 and 0 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 61930-40:
(7*6)+(6*1)+(5*9)+(4*3)+(3*0)+(2*4)+(1*0)=113
113 % 10 = 3
So 61930-40-3 is a valid CAS Registry Number.

61930-40-3Downstream Products

61930-40-3Relevant academic research and scientific papers

Antimalarial activity of natural and synthetic prodiginines

Papireddy, Kancharla,Smilkstein, Martin,Kelly, Jane Xu,Shweta,Salem, Shaimaa M.,Alhamadsheh, Mamoun,Haynes, Stuart W.,Challis, Gregory L.,Reynolds, Kevin A.

, p. 5296 - 5306 (2011/10/02)

Prodiginines are a family of linear and cyclic oligopyrrole red-pigmented compounds. Herein we describe the in vitro antimalarial activity of four natural (IC50 = 1.7-8.0 nM) and three sets of synthetic prodiginines against Plasmodium falciparum. Set 1 compounds replaced the terminal nonalkylated pyrrole ring of natural prodiginines and had diminished activity (IC 50 > 2920 nM). Set 2 and set 3 prodiginines were monosubstituted or disubstituted at either the 3 or 5 position of the right-hand terminal pyrrole, respectively. Potent in vitro activity (IC50 = 0.9-16.0 nM) was observed using alkyl or aryl substituents. Metacycloprodiginine and more potent synthetic analogues were evaluated in a P. yoelii murine patent infection using oral administration. Each analogue reduced parasitemia by more than 90% after 25 (mg/kg)/day dosing and in some cases provided a cure. The most favorable profile was 92% parasite reduction at 5 (mg/kg)/day, and 100% reduction at 25 (mg/kg)/day without any evident weight loses or clinical overt toxicity.

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