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5-methoxy-2-(pyridin-3-ylmethoxy)benzaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

923255-75-8

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923255-75-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 923255-75-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,3,2,5 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 923255-75:
(8*9)+(7*2)+(6*3)+(5*2)+(4*5)+(3*5)+(2*7)+(1*5)=168
168 % 10 = 8
So 923255-75-8 is a valid CAS Registry Number.

923255-75-8Downstream Products

923255-75-8Relevant academic research and scientific papers

Rational design of pyridyl derivatives of vanillin for the treatment of sickle cell disease

Pagare, Piyusha P.,Ghatge, Mohini S.,Musayev, Faik N.,Deshpande, Tanvi M.,Chen, Qiukan,Braxton, Courtney,Kim, Solyi,Venitz, Jürgen,Zhang, Yan,Abdulmalik, Osheiza,Safo, Martin K.

, p. 2530 - 2538 (2018/04/16)

Hypoxia-induced polymerization of sickle hemoglobin (Hb S) is the principal phenomenon that underlays the pathophysiology and morbidity associated with sickle cell disease (SCD). Opportunely, as an allosteric protein, hemoglobin (Hb) serves as a convenient and potentially critical druggable target. Consequently, molecules that prevent Hb S polymerization (Hb modifiers), and the associated erythrocyte sickling have been investigated–and retain significant interest–as a viable therapeutic strategy for SCD. This group of molecules, including aromatic aldehydes, form high oxygen affinity Schiff-base adducts with Hb S, which are resistant to polymerization. Here, we report the design and synthesis of novel potent antisickling agents (SAJ-009, SAJ-310 and SAJ-270) based on the pharmacophore of vanillin and INN-312, a previously reported pyridyl derivative of vanillin. These novel derivatives exhibited superior in vitro binding and pharmacokinetic properties compared to vanillin, which translated into significantly enhanced allosteric and antisickling properties. Crystal structure studies of liganded Hb in the R2 quaternary state in complex with SAJ-310 provided important insights into the allosteric and antisickling properties of this group of compounds. While these derivatives generally show similar in vitro biological potency, significant structure-dependent differences in their biochemical profiles would help predict the most promising candidates for successful in vivo pre-clinical translational studies and inform further structural modifications to improve on their pharmacologic properties.

Compounds and uses thereof for the modulation of hemoglobin

-

, (2014/09/30)

Provide herein are compounds and pharmaceutical compositions suitable as modulators of hemoglobin, methods and intermediates for their preparation, and methods for their use in treating disorders mediated by hemoglobin and disorders that would benefit from tissue and/or cellular oxygenation.

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