Hypertensinogen

Base Information

• Chemical Name: Hypertensinogen
• CAS No.: 20845-02-7
• Molecular Formula: C₈₅H₁₂₃N₂₁O₂₀
• Molecular Weight: 1759.04
• European Community (EC) Number: 690-382-0
• DSSTox Substance ID: DTXSID701346983
• Mol file: 20845-02-7.mol

Synonyms:angiotensinogen (1-14);porcine renin substrate tetradecapeptide;renin substrate tetradecapeptide, porcine;Angiotensinogen;Hypertensinogen;Proangiotensin;Renin Substrate;Renin Substrate Tetradecapeptide;Renin-Substrate;Serpin A8;SERPINA8;Tetradecapeptide, Renin Substrate

Chemical Property of Hypertensinogen

Chemical Property:

• Appearance/Colour: White lyophilized powder
• PSA: 650.08000
• LogP: 4.97830
• Storage Temp.: −20°C
• Solubility.: H2O: 0.3 mg/mL, clear, colorless
• XLogP3: 0.8
• Hydrogen Bond Donor Count: 23
• Hydrogen Bond Acceptor Count: 24
• Rotatable Bond Count: 52
• Exact Mass: 1757.92532540
• Heavy Atom Count: 126
• Complexity: 3610

Purity/Quality:

99%, ^*data from raw suppliers

Renin Substrate Tetradecapeptide porcine ≥97%(HPLC) ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: CCC(C)C(C(=O)NC(CC1=CN=CN1)C(=O)N2CCCC2C(=O)NC(CC3=CC=CC=C3)C(=O)NC(CC4=CN=CN4)C(=O)NC(CC(C)C)C(=O)NC(CC(C)C)C(=O)NC(C(C)C)C(=O)NC(CC5=CC=C(C=C5)O)C(=O)NC(CO)C(=O)O)NC(=O)C(CC6=CC=C(C=C6)O)NC(=O)C(C(C)C)NC(=O)C(CCCNC(=N)N)NC(=O)C(CC(=O)O)N
• Isomeric SMILES: CC[C@H](C)[C@@H](C(=O)N[C@@H](CC1=CN=CN1)C(=O)N2CCC[C@H]2C(=O)N[C@@H](CC3=CC=CC=C3)C(=O)N[C@@H](CC4=CN=CN4)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC5=CC=C(C=C5)O)C(=O)N[C@@H](CO)C(=O)O)NC(=O)[C@H](CC6=CC=C(C=C6)O)NC(=O)[C@H](C(C)C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(=O)O)N

Technology Process of Hypertensinogen

There total 1 articles about Hypertensinogen which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

→ Asp-Arg-Val-Tyr-Ile-His-Pro-Phe-His-Leu-Leu-Val-Tyr-Ser (20845-02-7)

Guidance literature:

Boc-Asp(OCH2Ph)-Arg(NO2)-Val-Tyr(OCH2Ph)-Ile-His(CH2Ph)-Pro-Phe-His(CH2Ph)-Leu-Leu-Val-Tyr(OCH2Ph)-Ser(OCH2Ph) (Merrifield Festphasen-Synthese), 1) TFA/HBr(Gas); 2) H2/Pd (Me./Eg./W.);

DOI:10.1139/o74-018

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