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(S)-methyl-(5-guanidino-2-((3-(4-nitro-benzenesulfonylamino)thiophene-2-carbonyl)amino))pentanoate trifluoroacetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1207974-24-0

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1207974-24-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1207974-24-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,7,9,7 and 4 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1207974-24:
(9*1)+(8*2)+(7*0)+(6*7)+(5*9)+(4*7)+(3*4)+(2*2)+(1*4)=160
160 % 10 = 0
So 1207974-24-0 is a valid CAS Registry Number.

1207974-24-0Downstream Products

1207974-24-0Relevant articles and documents

Small molecule inhibitors of the neuropilin-1 vascular endothelial growth factor A (VEGF-A) interaction

Jarvis, Ashley,Allerston, Charles K.,Jia, Haiyan,Herzog, Birger,Garza-Garcia, Acely,Winfield, Natalie,Ellard, Katie,Aqil, Rehan,Lynch, Rosemary,Chapman, Chris,Hartzoulakis, Basil,Nally, James,Stewart, Mark,Cheng, Lili,Menon, Malini,Tickner, Michelle,Djordjevic, Snezana,Driscoll, Paul C.,Zachary, Ian,Selwood, David L.

, p. 2215 - 2226 (2010)

We report the molecular design and synthesis of EG00229,2, the first small molecule ligand for the VEGF-A receptor neuropilin 1 (NRPl) and the structural characterization of NRPl-ligand complexes by NMR spectroscopy and X-ray crystallography. Mutagenesis studies localized VEGF-A binding in the NRPl bl domain and a peptide fragment of VEGF-A was shown to bind at the same site by NMR, providing the basis for small molecule design. Compound 2 demonstrated inhibition of VEGF-A binding to NRPl and attenuated VEGFR2 phosphorylation in endothelial cells. Inhibition of migration of endothelial cells was also observed. The viability of A549 lung carcinoma cells was reduced by 2, and it increased the potency of the cytotoxic agents paclitaxel and 5-fluorouracil when given in combination. These studies provide the basis for design of specific small molecule inhibitors of ligand binding to NRP1.

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