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1426059-65-5

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1426059-65-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1426059-65-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,6,0,5 and 9 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1426059-65:
(9*1)+(8*4)+(7*2)+(6*6)+(5*0)+(4*5)+(3*9)+(2*6)+(1*5)=155
155 % 10 = 5
So 1426059-65-5 is a valid CAS Registry Number.

1426059-65-5Downstream Products

1426059-65-5Relevant articles and documents

Synthetic receptors induce anti angiogenic and stress signaling on human first trimester cytotrophoblast cells

Pantho, Ahmed F.,Price, Mason,Zuberi Ashraf,Wajid, Umaima,Khansari, Maryam Emami,Jahan, Afsana,Afroze, Syeda H.,Rhaman, Md Mhahabubur,Johnson, Corey R.,Kuehl, Thomas J.,Hossain, Md. Alamgir,Uddin, Mohammad Nasir

, (2017/05/18)

The cytotrophoblast (CTB) cells of the human placenta have membrane receptors that bind certain cardiotonic steroids (CTS) found in blood plasma. One of these, marinobufagenin, is a key factor in the etiology of preeclampsia. Herein, we used synthetic receptors (SR) to study their effectiveness on the angiogenic profile of human first trimester CTB cells. The humanextravillous CTB cells (Sw.71) use in this study were derived from first trimester chorionic villus tissue. Culture media of CTB cells treated with ≥1 nM SR level revealed sFlt-1 (Soluble fms-like tyrosine kinase-1) was significantly increased while VEGF (vascular endothelial growth factor) was significantly decreased in the culture media (*p 1 (Angiotensin II receptor, type 1) and VEGFR-1 (vascular endothelial growth factor receptor 1) receptor expression was significantly downregulated (* p 0.05 for each). Our results show that the anti-proliferative and anti-angiogenic effects of SR on CTB cells are similar to the effects of CTS. The observed anti angiogenic activity of SR on CTB cells demonstrates that the functionalized-urea/thiourea molecules may be useful as potent inhibitors to prevent CTS-induced impairment of CTB cells.

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