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98807-41-1

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98807-41-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98807-41-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,8,0 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 98807-41:
(7*9)+(6*8)+(5*8)+(4*0)+(3*7)+(2*4)+(1*1)=181
181 % 10 = 1
So 98807-41-1 is a valid CAS Registry Number.

98807-41-1Relevant academic research and scientific papers

Amino acids and peptides. XVIII. Synthetic peptides related to N-terminal portion of fibrin α-chain and their inhibitory effect on fibrinogen/thrombin cloning

Kawasaki,Miyano,Hirase,Iwamoto

, p. 975 - 977 (2007/10/02)

Peptide analogs of the N-terminal portion of fibrin α-chain were prepared and their inhibitory effects on fibrinogen/thrombin clotting were examined. Of the synthetic peptides, H-Gly-Pro-Arg-Pro-Pro-NH2 exhibited the most potent inhibitory effe

Amino acids and peptides. XVII. Synthesis of peptides related to N-terminal portion of fibrin alpha-chain and their inhibitory effect on fibrinogen/thrombin clotting.

Kawasaki,Tsuji,Hirase,Miyano,Inouye,Iwamoto

, p. 525 - 528 (2007/10/02)

Various peptides related to N-terminal portion of fibrin alpha-chain were synthesized by the solution method and the solid-phase method, and their inhibitory effect on fibrinogen/thrombin clotting was examined. Extension of peptide chain from N-terminal t

Amino acids and peptides. XVI. Synthesis of N-terminal tetrapeptide analogs of fibrin α-chain and their inhibitory effects on fibrinogen/thrombin clotting

Kawasaki,Hirase,Miyano,Tsuji,Iwamoto

, p. 3253 - 3260 (2007/10/02)

N-Terminal tetrapeptide analogs of fibrin α-chain were synthesized by the solution method using a new active ester, the ester of the oxime of p-nitroacetophenone, and by the solid-phase method. Their inhibitory effects on fibrinogen/thrombin clotting were examined. Of the synthetic peptides, amide analogs of Gly-Pro-Arg-Pro exhibited a more potent inhibitory effect.

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