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4-(1-methylpiperidin-4-yl)-2-nitroaniline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

668423-23-2

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668423-23-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 668423-23-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,6,8,4,2 and 3 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 668423-23:
(8*6)+(7*6)+(6*8)+(5*4)+(4*2)+(3*3)+(2*2)+(1*3)=182
182 % 10 = 2
So 668423-23-2 is a valid CAS Registry Number.

668423-23-2Downstream Products

668423-23-2Relevant academic research and scientific papers

A class of fused ring triazole compounds, preparation method and applications thereof

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Paragraph 0279; 0280; 0283; 0284; 0287; 0288, (2020/03/12)

The invention discloses a class of fused ring triazole compounds, a preparation method and applications thereof, particularly a fused ring triazole compound represented by a formula (I), or a pharmaceutically acceptable salt thereof, or an enantiomer, a d

Nitrogen-containing fused ring compounds as well as preparation method and application thereof

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Paragraph 0189; 0190; 0193; 0197; 0198, (2019/05/16)

The invention discloses nitrogen-containing fused ring compounds as well as a preparation method and application thereof. The nitrogen-containing fused ring compounds have a structure represented by aformula (I) shown in the description, wherein each grou

A class of aniline imidazolylpyrimidine amine compounds having antitumor activity, preparation method and uses thereof

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Paragraph 0068; 007, (2019/05/16)

The invention relates to a class of aniline imidazolylpyrimidine amine compounds having antitumor activity, a preparation method and uses thereof, and discloses a compound represented by a general formula I, or a pharmaceutically acceptable salt, or an enantiomer, a diastereomer, a tautomer, a solvate, a polymorph or a prodrug thereof, a preparation method and pharmaceutical uses thereof, whereineach group is defined in the specification. The formula I is defined in the specification.

N-aryl-2-aminobenzimidazoles: Novel, efficacious, antimalarial lead compounds

Ramachandran, Sreekanth,Hameed P., Shahul,Srivastava, Abhishek,Shanbhag, Gajanan,Morayya, Sapna,Rautela, Nikhil,Awasthy, Disha,Kavanagh, Stefan,Bharath, Sowmya,Reddy, Jitendar,Panduga, Vijender,Prabhakar,Saralaya, Ramanatha,Nanduri, Robert,Raichurkar, Anandkumar,Menasinakai, Sreenivasaiah,Achar, Vijayashree,Jiménez-Díaz, María Belén,Martínez, María Santos,Angulo-Barturen, I?igo,Ferrer, Santiago,Sanz, Laura María,Gamo, Francisco Javier,Duffy, Sandra,Avery, Vicky M.,Waterson, David,Lee, Marcus C. S.,Coburn-Flynn, Olivia,Fidock, David A.,Iyer, Pravin S.,Narayanan, Shridhar,Hosagrahara, Vinayak,Sambandamurthy, Vasan K.

supporting information, p. 6642 - 6652 (2014/10/15)

From the phenotypic screening of the AstraZeneca corporate compound collection, N-aryl-2-aminobenzimidazoles have emerged as novel hits against the asexual blood stage of Plasmodium falciparum (Pf). Medicinal chemistry optimization of the potency against Pf and ADME properties resulted in the identification of 12 as a lead molecule. Compound 12 was efficacious in the P. berghei (Pb) model of malaria. This compound displayed an excellent pharmacokinetic profile with a long half-life (19 h) in rat blood. This profile led to an extended survival of animals for over 30 days following a dose of 50 mg/kg in the Pb malaria model. Compound 12 retains its potency against a panel of Pf isolates with known mechanisms of resistance. The fast killing observed in the in vitro parasite reduction ratio (PRR) assay coupled with the extended survival highlights the promise of this novel chemical class for the treatment of malaria.

Combination therapy with CHK1 inhibitors

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, (2008/06/13)

Compounds of Structure I, and salts, tautomers, stereoisomers, and mixtures thereof may be used in methods of inhibiting checkpoint kinase 1 in subjects, in methods for inducing cell cycle progression, and in methods for increasing apoptosis in cells. Such compounds may be used to prepare pharmaceutical compositions and may be used in conjunction with DNA damaging agents.

Inhibition of FGFR3 and treatment of multiple myeloma

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, (2008/06/13)

Methods of inhibiting fibroblast growth factor receptor 3 and treating various conditions mediated by fibroblast growth factor receptor 3 are provided that include administering to a subject a compound of Structure I, a pharmaceutically acceptable salt thereof, a tautomer thereof, or a pharmaceutically acceptable salt of the tautomer. Compounds having the Structure I have the following structure where and have the variables described herein. Such compounds may be used to prepare medicaments for use in inhibiting fibroblast growth factor receptor 3 and for use in treating conditions mediated by fibroblast growth factor receptor 3 such as multiple myeloma.

BENZIMIDAZOLE QUINOLINONES AND USES THEREOF

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Page 351-352, (2008/06/13)

Methods of inhibiting various enzymes and treating various conditions are provided that include administering to a subject a compound of Structure I or IB, a pharmaceutically acceptable salt thereof, a tautomer thereof, or a pharmaceutically acceptable salt of the tautomer. Compounds having the Structure I and IB have the following structures and have the variables described herein. Such compounds may be used to prepare medicaments for use in inhibiting various enzymes and for use in treating conditions mediated by such enzymes.

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